JP3192631B2 - Pharmaceuticals consisting of saturated heterocyclic compounds - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION

[0001]

The present invention relates to a novel saturated heterocyclic compound having an excellent antagonistic action on substance P and neurokinin A.

[0002]

2. Description of the Related Art A compound relatively similar to the structure of the compound of the present invention is disclosed in FR 2729952 (published on Aug. 2, 1996).
Sun), FR2729953 (release date August 2, 1996
Sun), FR2729954 (release date August 2, 1996
Day). However, they are those having a selective antagonism against receptor of substance P (hereinafter referred to as "NK ₁ receptor.").

[0003] In addition, NK ₁ receptor and neurokinin A
There are few reported examples of low-molecular-weight, non-peptidic compounds that antagonize both of these receptors (hereinafter referred to as “NK ₂ receptors”), and the following compounds are known. However, these compounds have problems such as poor oral absorbability.

[0004]

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Further, spiro [benzo [c] thiophene-
Synthesis of 1 (3H), 4'-piperidine] -2-oxide has been described in J. Org. Chem. 41, 2628 (1976) and W.
Although it is known in O95 / 28389 and the like, there is no report on the synthesis of an optically active substance based on the asymmetry of the sulfoxide portion, the optically active resolution, and the like.

[0006]

SUMMARY OF THE INVENTION The inventors of the present invention have been dedicated to the synthesis of derivatives having tachykinin antagonism (particularly, substance P antagonism, and antagonism to neurokinin A and B) and their pharmacological activities for many years. As a result of research, a novel saturated heterocyclic compound having a structure different from that of a known compound, in particular, S of spiro [benzo [c] thiophen-1 (3H), 4′-piperidine] -2-oxide
The optically active substance having an absolute configuration of has an outstanding antagonism to the tachykinin receptor, and further, the compound of the present invention has a better oral absorbability as compared with the above-mentioned known compounds. , found that antagonism to both NK ₁ receptors and NK ₂ receptors is better, and completed the present invention.

Further, another object of the present invention is to provide a preventive or therapeutic agent for tachykinin-mediated diseases, comprising the above compound as an active ingredient, and to manufacture a preventive or therapeutic agent for tachykinin-mediated diseases. lies in the use of the compounds for, as such prophylactic or therapeutic agents, e.g., a NK ₁ receptor and / or NK ₂ receptor inhibitors, such diseases, such as anxiety Diseases of the central nervous system, including depression, depression, psychiatric disorders and schizophrenia; dementia in AIDS, senile dementia of the Alzheimer type, Alzheimer's disease, Down's syndrome, demyelinating disease, amyotrophic lateral sclerosis, neuropathy, peripheral Neurodegenerative diseases including neuropathy and neuralgia; chronic obstructive pulmonary disease, bronchitis, pneumonia, bronchoconstriction, respiratory diseases including asthma, cough; inflammatory bowel disease (I
BD), psoriasis, fibrotitis, osteoarthritis, degenerative arthritis,
And inflammatory diseases including rheumatoid arthritis; eczema; and allergic diseases including rhinitis; hypersensitivity diseases including hypersensitivity diseases to vine plants; conjunctivitis, spring conjunctivitis, spring catarrh, blood-eye chamber with various inflammatory eye diseases. Ophthalmic diseases including disruption of the water barrier, increased intraocular pressure, miosis; skin diseases including contact dermatitis, atopic dermatitis, hives and other eczema-like dermatitis; addiction including alcoholism; Somatic disorders due to stress; Reflex sympathetic dystrophy including shoulder-hand syndrome; Mood swings; Unwanted immune response including graft rejection and immune enhancement including systemic lupus erythematosus or diseases associated with immunosuppression Diseases caused by abnormalities of nerves regulating internal organs, gastrointestinal diseases including colitis, ulcerative colitis, Crohn's disease; X-ray irradiation and chemotherapeutic agents, poisons, toxins, pregnancy, vestibular disorders, postoperative diseases, Intestinal obstruction, gastrointestinal hypokinesia, visceral pain, migraine, intracranial pressure increase, vomiting include vomiting induced by intracranial pressure reduction or side effects associated with various drug administration; cystitis,
Bladder dysfunction, including urinary incontinence; Eosinophilia due to collagen disease, scleroderma, fluke infection; Vasodilation, including angina, migraine, and Raynaud's disease, due to abnormal blood flow due to contraction Diseases: Pain nociceptive pain including migraine, headache, toothache.

[0008]

Means for Solving the Problems The novel medicine of the present invention comprises:
(1) The following general formula (I):

[0009]

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Wherein R ¹ and R ² are the same or different and are an aryl group, a heteroaryl group, an aryl group substituted by 1 to 3 groups selected from a substituent group A, or
Represents a heteroaryl group substituted by 1 to 3 groups selected from a substituent group A, A represents a methylene group, a carbonyl group or a sulfonyl group, and B represents a single bond, 1 to 4 carbon atoms. An alkylene group or an alkenylene group having 2 to 4 carbon atoms, D represents an oxygen atom or a sulfur atom,
Represents an alkylene group having 1 to 6 carbon atoms which may be substituted with a halogen atom, or an alkylene group having 3 to 8 carbon atoms including a cycloalkane ring having 3 to 6 carbon atoms; L represents an alkylene group having 1 to 4 alkylene groups or an alkenylene group having 2 to 4 carbon atoms;
A group having (R ³ ) —, wherein R ³ is an aryl group, a heteroaryl group, an aryl group substituted by 1 to 3 groups selected from a substituent group A, or a substituent group A A heteroaryl group substituted with 1 to 3 selected groups is shown. Or a group having the general formula —C (R ⁴ ) (R ⁵ ) —, wherein R ⁴ is a group selected from a hydrogen atom, an aryl group, a heteroaryl group, and a substituent group A. to 3 substituted aryl groups, or represents a 1 to 3 substituted heteroaryl group by a group selected from substituent group a, R ⁵
It is a group (wherein having the general formula -CO-R ^6, R ⁶ is a lower alkyl group, a lower alkoxy group, an amine residue, 1 to 3 substituted aryl groups selected from Substituent group A Group or a group selected from substituent group A, from 1 to 3
It represents a monosubstituted heteroaryl group. ), A lower alkyl group, an amino group, an acylamino group, an acylamino lower alkyl group, an acylamino group in which a nitrogen atom is substituted with a lower alkyl group, a hydroxyl group, a hydroxy lower alkyl group in which an oxygen atom may be substituted with an aralkyl group, or Or a lower alkoxy group, or R ⁴ and R ⁵ together
A 5- to 8-membered saturated heterocyclic ring including the carbon atom to which they are bonded (the heterocyclic ring may be substituted with one or two groups selected from a substituent group B, an aryl ring, a heterocyclic ring, An aryl ring, an aryl ring substituted by 1 to 3 groups with a group selected from substituent group A, or a heterocyclic ring substituted with 1 to 3 groups with a group selected from substituent group A good.) R ⁴ group is an aryl group, a heteroaryl group, substituent group A
An aryl group substituted by 1 to 3 groups selected from
Alternatively, when a heteroaryl group substituted by 1 to 3 groups selected from the substituent group A is shown, both of one hydrogen atom of the R ⁴ group and one hydrogen atom of the R ⁶ group are replaced with each other. Shows a group connected by a single bond. R ⁷ represents a lower alkyl group. And a pharmacologically acceptable salt thereof, an ester thereof and other derivatives.

[Substituent group A] A halogen atom, a lower alkyl group, a halogeno lower alkyl group, a lower alkoxy group, a lower alkoxycarbonyl group, a carboxy group, a hydroxyl group, a lower aliphatic acyl group, a lower aliphatic acylamino group, an amino group, And a cyano group [Substituent group B] an oxo group; and a lower alkyl, aryl and aralkyl group, a lower aliphatic acyl group, a lower alkyl group which may be substituted with a substituent group A as a substituent on a nitrogen atom. Alkanesulfonyl group Among these, preferred drugs include (2) R ¹ is an aryl group, a heteroaryl group or a group selected from the following Substituent Group A, from 1 to 3
A compound which is an individually substituted aryl group, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, (3) wherein R ¹ is an aryl group or the following substituent group A
^A compound which is an aryl group substituted by 1 to 3 groups selected from 1; a pharmacologically acceptable salt thereof; a medicament comprising an ester or other derivative thereof; (4) R ² is an aryl group or a substituent A compound comprising an aryl group substituted by 1 to 3 groups selected from group A, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, (5) R ² is an aryl group, or A compound which is an aryl group substituted by 1 to 3 halogen atoms, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, (6) a compound wherein A is a carbonyl group, (7) a compound comprising B as a single bond, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, ) D is a compound which is an oxygen atom, a pharmacologically acceptable salt, pharmaceutical consisting of esters or other derivatives, is (9) E, 1 carbon atoms
Which is a compound having 1 to 4 alkylene groups or an alkylene group having 3 to 8 carbon atoms containing a cycloalkane ring having 3 to 6 carbon atoms, a pharmacologically acceptable salt thereof, an ester thereof or another derivative thereof (10) E is a methylene group, an ethylene group, a dimethylmethylene group, a 1,1-dimethylethylene group, a 2,2-dimethylethylene group, a cyclopropane-1,1-diyl group, a cyclobutane-1,1
-Diyl group, cyclopentane-1,1-diyl group, cyclohexane-1,1-diyl group, cyclopropane-1,
A compound which is a 1-diylmethyl group, a cyclobutane-1,1-diylmethyl group, a cyclopentane-1,1-diylmethyl group or a cyclohexane-1,1-diylmethyl group, a pharmaceutically acceptable salt thereof, an ester thereof, or another derivative thereof A pharmaceutical comprising (11) a compound, wherein G is an alkylene group having 1 to 4 carbon atoms, a pharmacologically acceptable salt thereof, an ester thereof or another derivative thereof;
(12) a compound wherein G is an alkylene group having 2 or 3 carbon atoms, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, (13) a compound wherein R ³ is a heteroaryl group or a substituent A compound which is an aryl group substituted by 1 to 3 groups selected from group A, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, (14) L is a compound represented by the general formula -C ( R ⁴ ) (R ⁵ )-
(15) a pharmaceutical comprising a compound which is a group having the formula, a pharmacologically acceptable salt thereof, an ester thereof, or another derivative thereof;
R ⁴ is an aryl group or compound is a heteroaryl group, a pharmacologically acceptable salt, pharmaceutical consisting of esters or other derivatives, is (16) R ^5, formula -C
A compound comprising a group having OR ⁶ (wherein R ⁶ represents a lower alkyl group or an amine residue), a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, (17) A compound wherein R ⁵ is an amino group, an acylamino group or a hydroxyl group, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof;
^{When 4} groups represent an aryl group, a compound in which both one hydrogen atom of the R ⁴ group and one hydrogen atom of the R ⁶ group are connected to each other by a single bond, A pharmaceutical comprising a salt, an ester or other derivative thereof,
(19) L is the following formula (I _L ):

[0012]

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(Wherein J represents an alkylene group having 1 to 6 carbon atoms, and ring Ar is substituted with 1 to 4 rings selected from an aryl ring, a heteroaryl ring and a substituent group A) An aryl ring or a heteroaryl ring substituted with 1 to 3 substituent (s) selected from substituent group A)), a pharmacologically acceptable salt thereof, an ester thereof, or another derivative thereof. A medicine, (20) a medicine comprising a compound wherein J is an alkylene group having 1 to 4 carbon atoms, a pharmacologically acceptable salt thereof, an ester thereof, or another derivative; (21) a medicament comprising a methylene group or an ethylene group (22) a compound consisting of a compound represented by the formula:
Wherein the compound is an aryl ring, a heteroaryl ring or an aryl ring substituted by 1 to 3 groups selected from a substituent group A, a pharmacologically acceptable salt thereof, a medicament comprising an ester or other derivative thereof, (23) a compound wherein ring Ar is an aryl ring or an aryl ring substituted by 1 to 3 groups selected from substituent group A, a pharmacologically acceptable salt thereof, an ester thereof or another derivative thereof (24) A drug comprising a compound in which the oxygen atom of the sulfoxide group of the group having the formula (I _L ) is bonded to a sulfur atom in the S configuration, a pharmaceutically acceptable salt thereof, an ester thereof, or another derivative thereof. It is.

[Substituent group A] A halogen atom, a lower alkyl group, a halogeno lower alkyl group, a lower alkoxy group, a lower alkoxycarbonyl group, a carboxy group, a hydroxyl group, a lower aliphatic acyl group, a lower aliphatic acylamino group, an amino group, And a cyano group [Substituent group B] an oxo group; and a lower alkyl, aryl and aralkyl group, a lower aliphatic acyl group, a lower alkyl group which may be substituted with a substituent group A as a substituent on a nitrogen atom. Alkanesulfonyl group [Substituent group A ¹ ] Lower alkyl group, halogeno lower alkyl group, lower alkoxy group.

Further preferred medicaments are medicaments consisting of the following compounds: 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-
4-carboxylic acid amide, 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-
4-carboxylic acid dimethylamide, 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (2-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (3,4- Dichlorophenyl) -3
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (3-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (3,4- Dichlorophenyl) -3
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (4-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (4-chlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxamide, 1- {2- [5- (4-chlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxylic acid dimethylamide;-1- {2- [5- (4-chlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (2-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (4-chlorophenyl)- 3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (3-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (4-chlorophenyl)- 3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (4-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (4-fluorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxylic acid amide, 1- {2- [5- (4-fluorophenyl) -3-]
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxylic acid dimethylamide, 1- {2- [5- (4-fluorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (2-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (4-fluorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (3-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (4-fluorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (4-pyridyl) piperidine-4-carboxylic acid amide; 1- {2- [5- (3,4-dichlorophenyl) ) -3
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] -2-oxide; 1- {2- [ 2- (3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxamide, 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxylic acid dimethylamide, 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxylic acid pyrrolidineamide, 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxylic acid morpholinamide, 1- {2- [2- (4-chlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid amide; 1- {2- [2- (4-chlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid dimethylamide; 1- {2- [2- (4-fluorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid amide; 1- {2- [2- (4-fluorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid dimethylamide; 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl} -4-phenylpiperidine-4-carboxylic acid amide; 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl｝ -4-phenylpiperidine-4-carboxylic acid
Dimethylamide, 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [isobenzofuran-1
(3H), 4'-piperidine], 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine], 1- {2- [2- (3 , 4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] -2-oxide; 1- {2- [ 2- (3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [isoquinoline-1 (2
H), 4'-Piperidin] -3 (4H) -one; 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl @ spiro [isobenzofuran-1 (3H), 4 '
-Piperidine], 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-piperidine], 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] -2-oxide, 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl @ spiro [isoquinolin-1 (2H), 4'-piperidin] -3 (4H) -one.

The most preferred medicaments are those consisting of the following compounds: 1- {2-[(5R)-(3,4-dichlorophenyl) -3- (3,4,5-trimethoxybenzoyl) Oxazolidin-5-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-
(2S) -oxide, 1- {2-[(5R)-(4-chlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide; -[(5R)-(4-fluorophenyl)-
3- (3,4,5-trimethoxybenzoyl) oxazolidine-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide, 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [benzo [c] thiophene- 1 (3H), 4'-piperidine]-(2S)
-Oxide, 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide; -[(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) morpholin-5-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide; 2-[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophene- 1 (3H),
4'-piperidine]-(2S) -oxide, 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S) -oxide · 1- {2-[(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)- Oxide, 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl} spiro [benzo [c] thiophen-1 ( 3H), 4'-piperidine]-
(2S) -oxide, 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide, 1- {2-[(2R)-(4-fluorophenyl)-
4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)
-Oxide, 1- {2-[(2R)-(3,4-dichlorophenyl) -5,5-dimethyl-4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [Benzo [c] thiophene-1 (3H), 4′-piperidine]-(2S) -oxide.

The novel agent for preventing or treating tachykinin-mediated diseases of the present invention is a medicament selected from the above, and the novel inhibitor of the NK ₁ receptor and / or NK ₂ receptor of the present invention comprises The medicament selected from the above, the novel prophylactic or therapeutic agent for asthma and / or bronchitis of the present invention is the medicament selected from the above, and the novel prophylactic or therapeutic agent for rhinitis of the present invention is The therapeutic agent is a medicament selected from the above, and the novel preventive or therapeutic agent for allergy of the present invention is a therapeutic agent is a medicament selected from the above, and further, the novel preventive agent for urinary incontinence of the present invention. The therapeutic agent is a medicament selected from the above.

Further, the novel use of the present invention is as follows: (1) The following general formula (I) for producing a medicament:

[0019]

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In the formula, R ¹ and R ² are the same or different and are an aryl group, a heteroaryl group, an aryl group substituted with 1 to 3 groups selected from a substituent group A, or
Represents a heteroaryl group substituted by 1 to 3 groups selected from a substituent group A, A represents a methylene group, a carbonyl group or a sulfonyl group, and B represents a single bond, 1 to 4 carbon atoms. An alkylene group or an alkenylene group having 2 to 4 carbon atoms, D represents an oxygen atom or a sulfur atom,
Represents an alkylene group having 1 to 6 carbon atoms which may be substituted with a halogen atom, or an alkylene group having 3 to 8 carbon atoms including a cycloalkane ring having 3 to 6 carbon atoms; L represents an alkylene group having 1 to 4 alkylene groups or an alkenylene group having 2 to 4 carbon atoms;
A group having (R ³ ) —, wherein R ³ is an aryl group, a heteroaryl group, an aryl group substituted by 1 to 3 groups selected from a substituent group A, or a substituent group A A heteroaryl group substituted with 1 to 3 selected groups is shown. Or a group having the general formula —C (R ⁴ ) (R ⁵ ) —, wherein R ⁴ is a group selected from a hydrogen atom, an aryl group, a heteroaryl group, and a substituent group A. to 3 substituted aryl groups, or represents a 1 to 3 substituted heteroaryl group by a group selected from substituent group a, R ⁵
It is a group (wherein having the general formula -CO-R ^6, R ⁶ is a lower alkyl group, a lower alkoxy group, an amine residue, 1 to 3 substituted aryl groups selected from Substituent group A Group or a group selected from substituent group A, from 1 to 3
It represents a monosubstituted heteroaryl group. ), A lower alkyl group, an amino group, an acylamino group, an acylamino lower alkyl group, an acylamino group in which a nitrogen atom is substituted with a lower alkyl group, a hydroxyl group, a hydroxy lower alkyl group in which an oxygen atom may be substituted with an aralkyl group, or Or a lower alkoxy group, or R ⁴ and R ⁵ together
A 5- to 8-membered saturated heterocyclic ring including the carbon atom to which they are bonded (the heterocyclic ring may be substituted with one or two groups selected from a substituent group B, an aryl ring, a heterocyclic ring, An aryl ring, an aryl ring substituted by 1 to 3 groups with a group selected from substituent group A, or a heterocyclic ring substituted with 1 to 3 groups with a group selected from substituent group A good.) R ⁴ group is an aryl group, a heteroaryl group, substituent group A
An aryl group substituted by 1 to 3 groups selected from
Alternatively, when a heteroaryl group substituted by 1 to 3 groups selected from the substituent group A is shown, both of one hydrogen atom of the R ⁴ group and one hydrogen atom of the R ⁶ group are replaced with each other. Shows a group connected by a single bond. R ⁷ represents a lower alkyl group.化合物, pharmacologically acceptable salts thereof, esters and other derivatives thereof.

[Substituent group A] A halogen atom, a lower alkyl group, a halogeno lower alkyl group, a lower alkoxy group, a lower alkoxycarbonyl group, a carboxy group, a hydroxyl group, a lower aliphatic acyl group, a lower aliphatic acylamino group, an amino group, And a cyano group [Substituent group B] an oxo group; and a lower alkyl, aryl and aralkyl group, a lower aliphatic acyl group, a lower alkyl group which may be substituted with a substituent group A as a substituent on a nitrogen atom. Alkanesulfonyl group Among these, preferably, (2) a compound wherein R ¹ is an aryl group, a heteroaryl group, or an aryl group substituted by 1 to 3 groups selected from the following Substituent Group A, Use of pharmacologically acceptable salts, esters or other derivatives thereof, (3)
A compound wherein R ¹ is an aryl group or an aryl group substituted by 1 to 3 groups selected from the following substituent group A ¹ , a pharmacologically acceptable salt thereof, use of an ester or other derivative thereof, (4) Use of a compound in which R ² is an aryl group or an aryl group substituted by 1 to 3 groups selected from a substituent group A, a pharmacologically acceptable salt thereof, an ester or other derivative thereof, (5) Use of a compound in which R ² is an aryl group or an aryl group substituted with 1 to 3 halogen atoms, a pharmacologically acceptable salt thereof, an ester or other derivative thereof, and (6) A is Use of a compound that is a carbonyl group, a pharmacologically acceptable salt thereof, an ester or other derivative thereof, (7) B is
(8) Use of a compound having a single bond, a pharmaceutically acceptable salt thereof, an ester thereof or another derivative thereof; (8) a compound wherein D is an oxygen atom, a pharmaceutically acceptable salt thereof, an ester thereof or another derivative thereof; Use, (9) a compound wherein E is an alkylene group having 1 to 4 carbon atoms or an alkylene group having 3 to 8 carbon atoms containing a cycloalkane ring having 3 to 6 carbon atoms, a pharmacologically acceptable compound thereof; (10) E is a methylene group, an ethylene group, a dimethylmethylene group, a 1,1-dimethylethylene group, a 2,2-dimethylethylene group, a cyclopropane-1,1- Diyl group, cyclobutane-1,1-diyl group, cyclopentane-1,1-diyl group, cyclohexane-1,1-diyl group, cyclopropane-1,1-
Use of a compound which is a diylmethyl group, a cyclobutane-1,1-diylmethyl group, a cyclopentane-1,1-diylmethyl group or a cyclohexane-1,1-diylmethyl group, a pharmacologically acceptable salt thereof, an ester thereof, or another derivative thereof (11) Use of a compound in which G is an alkylene group having 1 to 4 carbon atoms, a pharmaceutically acceptable salt thereof, an ester or other derivative thereof, (12) G is a compound having 2 or 3 carbon atoms. Use of a compound which is an alkylene group, a pharmaceutically acceptable salt thereof, an ester or other derivative thereof, (13) R ³ is substituted with 1 to 3 heteroaryl groups or a group selected from substituent group A. (14) use of a compound which is an aryl group, a pharmacologically acceptable salt thereof, an ester or other derivative thereof,
Use of a compound which is a group having C (R ⁴ ) (R ⁵ )-, a pharmacologically acceptable salt thereof, use of an ester or other derivative thereof, (15) a compound wherein R ⁴ is an aryl group or a heteroaryl group Use of a pharmacologically acceptable salt thereof, an ester or other derivative thereof, (16) a group in which R ⁵ has a general formula —CO—R ⁶ (wherein R ⁶ is a lower alkyl group or an amine residue Or a pharmacologically acceptable salt thereof, use of an ester or other derivative thereof, (17) a compound wherein R ⁵ is an amino group, an acylamino group or a hydroxyl group, or a pharmacologically acceptable salt thereof. Use of an ester or other derivative thereof. (18) When the R ⁴ group represents an aryl group, instead of one hydrogen atom of the R ⁴ group and one hydrogen atom of the R ⁶ group, both are a single bond Compound that is a group Pharmacologically acceptable salts, the use of esters or other derivatives, (19) L
Is the following formula (I _L ):

[0022]

Embedded image

(Wherein J represents an alkylene group having 1 to 6 carbon atoms, and ring Ar is substituted by 1 to 4 rings selected from an aryl ring, a heteroaryl ring, and a substituent group A. Which is a group having an aryl ring or a heteroaryl ring substituted by 1 to 3 groups selected from a substituent group A), a pharmacologically acceptable salt thereof, an ester thereof, or another derivative thereof. , (20) J is 1 carbon atom
Use of a compound having from 4 to 4 alkylene groups, a pharmaceutically acceptable salt thereof, an ester or other derivative thereof,
(21) Use of a compound in which J is a methylene group or an ethylene group, a pharmacologically acceptable salt thereof, an ester or other derivative thereof, and (22) a ring Ar is an aryl ring, a heteroaryl ring or a substituent group A Use of a compound which is an aryl ring substituted by 1 to 3 groups selected from a group selected therefrom, a pharmacologically acceptable salt thereof, use of an ester or other derivative thereof, (23) ring Ar is an aryl ring or a group of substituents A
Use of a compound which is an aryl ring substituted by 1 to 3 groups with a group selected from the group consisting of: a pharmacologically acceptable salt thereof, use of an ester or other derivative thereof, (24) a sulfoxide group of a group having the formula ( _IL ) Or a pharmacologically acceptable salt thereof, an ester or other derivative thereof, wherein the oxygen atom is bonded to a sulfur atom in the S configuration. [Substituent group A] halogen atom, lower alkyl group, halogeno lower alkyl group, lower alkoxy group, lower alkoxycarbonyl group, carboxy group, hydroxyl group, lower aliphatic acyl group, lower aliphatic acylamino group, amino group, and cyano Group [Substituent group B] oxo group; and a lower alkyl, aryl and aralkyl group, lower aliphatic acyl group, lower alkane sulfonyl group which may be substituted with substituent group A as a substituent on the nitrogen atom. [Substituent group A ¹ ] a lower alkyl group, a halogeno lower alkyl group, a lower alkoxy group.

Further preferred is the use of the following compounds, their pharmaceutically acceptable salts, their esters or other derivatives: 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-
4-carboxylic acid amide 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-
4-carboxylic acid dimethylamide 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (2-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (3,4-dichlorophenyl) ) -3
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (3-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (3,4-dichlorophenyl) ) -3
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (4-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (4-chlorophenyl)- 3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxamide-1- {2- [5- (4-chlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxylic acid dimethylamide 1- {2- [5- (4-chlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (2-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (4-chlorophenyl) -3] −
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (3-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (4-chlorophenyl) -3] −
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (4-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (4-fluorophenyl)- 3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxamide-1- {2- [5- (4-fluorophenyl) -3-]
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4-phenylpiperidine-4
-Carboxylic acid dimethylamide 1- {2- [5- (4-fluorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (2-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (4-fluorophenyl)- 3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (3-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (4-fluorophenyl)- 3-
(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} -4- (4-pyridyl) piperidine-4-carboxylic acid amide 1- {2- [5- (3,4-dichlorophenyl) -3
-(3,4,5-trimethoxybenzoyl) oxazolidine-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] -2-oxide 1- {2- [2 -(3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxamide-1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxylic acid dimethylamide 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxylic acid pyrrolidineamide 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} -4-phenylpiperidine-4-
Carboxylic acid morpholinamide 1- {2- [2- (4-chlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid amide 1- {2- [2- (4-chlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid dimethylamide 1- {2- [2- (4-fluorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid amide 1- {2- [2- (4-fluorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl} -4-phenylpiperidine-4-carboxylic acid dimethylamide 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl} -4-phenylpiperidine-4-carboxylic acid amide ・ 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl｝ -4-phenylpiperidine-4-carboxylic acid
Dimethylamide 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [isobenzofuran-1
(3H), 4'-piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] 1- {2- [2- (3 4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine] -2-oxide 1- {2- [2 -(3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [isoquinoline-1 (2
H), 4'-Piperidine] -3 (4H) -one 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl @ spiro [isobenzofuran-1 (3H), 4 '
-Piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] -2-oxide 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl @ spiro [isoquinolin-1 (2H), 4'-piperidin] -3 (4H) -one.

Most preferred is the use of the following compounds, their pharmaceutically acceptable salts, their esters or other derivatives: 1- {2-[(5R)-(3,4-dichlorophenyl)- 3- (3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-
(2S) -oxide, 1- {2-[(5R)-(4-chlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide; -[(5R)-(4-fluorophenyl)-
3- (3,4,5-trimethoxybenzoyl) oxazolidine-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide, 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [benzo [c] thiophene- 1 (3H), 4'-piperidine]-(2S)
-Oxide, 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide; -[(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) morpholin-5-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide; 2-[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophene- 1 (3H),
4'-piperidine]-(2S) -oxide, 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S) -oxide · 1- {2-[(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)- Oxide, 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl} spiro [benzo [c] thiophen-1 ( 3H), 4'-piperidine]-
(2S) -oxide, 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide, 1- {2-[(2R)-(4-fluorophenyl)-
4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)
-Oxide, 1- {2-[(2R)-(3,4-dichlorophenyl) -5,5-dimethyl-4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [Benzo [c] thiophene-1 (3H), 4′-piperidine]-(2S) -oxide.

On the other hand, the use of the present invention for producing a prophylactic or therapeutic agent for a tachykinin-mediated disease is a use wherein the medicament is a prophylactic or therapeutic agent for a tachykinin-mediated disease in the use selected from the above. NK _{1 of the} present invention
For the manufacture of a receptor and / or NK ₂ receptor inhibitors, as used to be selected from the above, the medicament is NK
₁ use and / or an NK ₂ receptor inhibitor. The use of the present invention for producing a prophylactic or therapeutic agent for asthma and / or bronchitis is the use selected from the above, The use wherein the medicament is a prophylactic or therapeutic agent for asthma and / or bronchitis. The use of the present invention for producing a prophylactic or therapeutic agent for rhinitis is the use selected from the above, wherein The use of the present invention for producing a prophylactic or therapeutic agent for allergy is a use in which the medicament is a prophylactic or therapeutic agent for allergy. Use of the present invention for producing a prophylactic or therapeutic agent for urinary incontinence according to the present invention is a use wherein the medicament is a prophylactic or therapeutic agent for urinary incontinence in the use selected from the above.

In the above general formula (I), R ¹ , R ² ,
“Aryl group” in the definition of R ³ and R ⁴ , R ¹ , R
“Aryl group” of “aryl group substituted by 1 to 3 groups selected from substituent group A” in the definition of ² , R ³ , R ⁴ and R ⁶ , and definition of [substituent group B] The "aryl group" of the "aryl group optionally substituted by substituent group A as a substituent on a nitrogen atom" in the above is, for example, a group having 5 to 5 carbon atoms such as phenyl, indenyl, naphthyl, phenanthrenyl and anthracenyl There may be mentioned 14 aromatic hydrocarbon groups, preferably a phenyl group.

The "aryl group" may be condensed with a cycloalkyl group having 3 to 10 carbon atoms, and examples thereof include a group such as 2-indanyl.

[0029] R ^1, R ^2, "heteroaryl group" in the definition of R ³ and R ⁴ and R ^1, R ^2, R ^3, groups selected from "Substituent group A in the definition of R ⁴ and R ⁶ The “heteroaryl group” of the “heteroaryl group substituted by 1 to 3” represents a 5- to 7-membered aromatic heterocyclic group containing 1 to 3 sulfur atoms, oxygen atoms and / or nitrogen atoms,
For example, a group such as furyl, thienyl, pyrrolyl, azepinyl, pyrazolyl, imidazolyl, oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl, triazolyl, tetrazolyl, thiadiazolyl, pyranyl, pyridyl, pyridazinyl, pyrimidinyl, pyrimidinyl, pyrazinyl. And preferably a 5- to 7-membered aromatic heterocyclic group containing at least one nitrogen atom and optionally containing an oxygen atom or a sulfur atom, for example, pyrrolyl, azepinyl, pyrazolyl, imidazolyl, Oxazolyl, isoxazolyl, thiazolyl, isothiazolyl, 1,2,3-oxadiazolyl,
Examples include groups such as triazolyl, tetrazolyl, thiadiazolyl, pyridyl, pyridazinyl, pyrimidinyl, pyrazinyl, and more preferably pyridyl, imidazolyl, oxazolyl, pyrazinyl and thiazolyl. The above “heteroaryl group” may be condensed with another cyclic group, and examples thereof include groups such as indolyl, benzofuryl, benzothienyl, benzoxazolyl, benzimidazolyl, isoquinolyl, quinolyl, and quinoxalyl. Can be mentioned.

In the definition of B and G, “C 1 to C 4
"Alkylene groups" means, for example, 1 to 4 carbon atoms such as methylene, methylmethylene, ethylene, propylene, trimethylene, tetramethylene, 1-methyltrimethylene, 2-methyltrimethylene, and 3-methyltrimethylene. Or a straight-chain or branched-chain alkylene group. B is preferably a linear or branched alkylene group having 1 to 3 carbon atoms. For G, preferably
It is a linear or branched alkylene group having 1 to 3 carbon atoms, more preferably ethylene and trimethylene, and most preferably ethylene.

In the definition of B and G, “C 2 to C 4
"Alkenylene groups" means ethenylene, 2-propenylene, 1-methyl-2-propenylene, 2-methyl-2
-Propenylene, 2-ethyl-2-propenylene, 2-
Examples thereof include linear or branched alkenylene groups having 2 to 4 carbon atoms such as butenylene, preferably ethenylene, 2-propenylene or 3-butenylene, more preferably ethenylene or 2-butenylene. It is propenylene.

The "alkylene group having 1 to 6 carbon atoms" in the definition of J and the "alkylene group having 1 to 6 carbon atoms which may be substituted by halogen" in the definition of E, "1 to 6 carbon atoms""Alkylenegroup" is a linear or branched alkylene group having 1 to 6 carbon atoms, for example,
The “alkylene group having 1 to 4 carbon atoms”, pentamethylene, hexamethylene, 1,1-dimethyltetramethylene, 2,2-dimethyltrimethylene, 1,1-dimethyltetramethylene, and 2,2-dimethyltetramethylene; Groups such as methylene can be mentioned. Preferably, it is an alkylene group having 1 to 4 carbon atoms. More preferably, E is methylene, ethylene, trimethylene, dimethylmethylene or 1,1-dimethylethylene, most preferably methylene, ethylene.

For J, more preferably, methylene, ethylene, dimethylmethylene or 1,1-dimethylethylene, more preferably methylene or ethylene,
Most preferably, it is methylene.

In the definition of E, "an alkylene group having 3 to 8 carbon atoms containing a cycloalkane ring having 3 to 6 carbon atoms" means a cycloalkane-1,1-diyl group having 3 to 6 carbon atoms, or C3-C6 cycloalkane-1,
A group in which methylene is bonded to one or both bonds of a 1-diyl group, that is, a group having the following formula.

[0035]

Embedded image

(In the formula, m represents an integer of 2 to 5.) Examples of such a group include cyclopropane-1,1
-Diyl, cyclobutane-1,1-diyl, cyclopentane-1,1-diyl, cyclohexane-1,1-diyl, cyclopropane-1,1-diylmethyl, cyclobutane-1,1-diylmethyl, cyclopentane-1, 1
-Diylmethyl, cyclohexane-1,1-diylmethyl, cyclopropane-1,1-di (ylmethyl), cyclobutane-1,1-di (ylmethyl), cyclopentane-1,1-di (ylmethyl), cyclohexane-1, 1
Groups such as -di (ylmethyl).
Preferably, it is cyclopropane-1,1-diyl, cyclobutane-1,1-diyl, cyclopropane-1,1-diylmethyl or cyclobutane-1,1-diylmethyl.

R ⁵ , R ⁶ , R ⁷ , “lower alkyl group” in the definition of [Substituent group A] and [Substituent group A ¹ ];
In the definition of R ⁵ in the "nitrogen atom acylamino group substituted with a lower alkyl group", "lower alkyl group"; in the definition of R ⁵ of the "aralkyl optionally hydroxy-lower alkyl group oxygen atom optionally substituted by a group""Lower alkyl group";"lower alkyl group" of "acylamino lower alkyl group" in the definition of R ⁵ and "substituent group A as a substituent on a nitrogen atom in the definition of [substituent group B]. The "lower alkyl group" of the "lower alkyl group" which may be, for example, methyl, ethyl, n-propyl,
Isopropyl, n-butyl, isobutyl, s-butyl,
tert-butyl, n-pentyl, isopentyl, 2-methylbutyl, neopentyl, 1-ethylpropyl, n-hexyl, isohexyl, 4-methylpentyl, 3-methylpentyl, 2-methylpentyl, 1-methylpentyl, 3,3 1 to 6 carbon atoms such as dimethylbutyl, 2,2-dimethylbutyl, 1,1-dimethylbutyl, 1,2-dimethylbutyl, 1,3-dimethylbutyl, 2,3-dimethylbutyl and 2-ethylbutyl And represents a straight-chain or branched-chain alkyl group, preferably a straight-chain or branched-chain alkyl group having 1 to 4 carbon atoms.

An “acylamino group” in the definition of R ⁵ ,
The `` acyl group '' of the `` acylamino lower alkyl group '' and the `` acyl group '' of the `` acylamino group having a nitrogen atom substituted by a lower alkyl group '' include, for example, formyl, acetyl, propionyl, butyryl, isobutyryl, pentanoyl, pivaloyl, Valeryl, isovaleryl, octanoyl, nonylcarbonyl, decylcarbonyl, 3-methylnonylcarbonyl, 8-methylnonylcarbonyl, 3
-Ethyloctylcarbonyl, 3,7-dimethyloctylcarbonyl, undecylcarbonyl, dodecylcarbonyl, tridecylcarbonyl, tetradecylcarbonyl, pentadecylcarbonyl, hexadecylcarbonyl, 1-methylpentadecylcarbonyl, 14-methylpentadecylcarbonyl, Alkylcarbonyl groups such as 13,13-dimethyltetradecylcarbonyl, heptadecylcarbonyl, 15-methylhexadecylcarbonyl, octadecylcarbonyl, 1-methylheptadecylcarbonyl, nonadecylcarbonyl, eicosylcarbonyl, henicosylcarbonyl, chloro Acetyl,
Halogenated alkylcarbonyl groups such as dichloroacetyl, trichloroacetyl and trifluoroacetyl, lower alkoxyalkylcarbonyl groups such as methoxyacetyl, acrylcarbonyl, propionylcarbonyl, methacrylcarbonyl, crotonylcarbonyl, isocrotonylcarbonyl, (E) “Aliphatic acyl group” such as unsaturated alkylcarbonyl group such as -2-methyl-2-butenoyl; arylcarbonyl group such as benzoyl, α-naphthoyl and β-naphthoyl, 2-bromobenzoyl, 4-chlorobenzoyl A lower alkylated arylcarbonyl group such as 2,4,6-trimethylbenzoyl, 4-toluoyl, and a lower alkoxylated arylcarbonyl group such as 4-anisoyl , 4-nitrobenzoyl, a nitrated arylcarbonyl group such as 2-nitrobenzoyl, a lower alkoxycarbonylated arylcarbonyl group such as 2- (methoxycarbonyl) benzoyl,
An “aromatic acyl group” such as an arylated arylcarbonyl group such as phenylbenzoyl; methoxycarbonyl,
Ethoxycarbonyl, propoxycarbonyl, butoxycarbonyl, s-butoxycarbonyl, tert-butoxycarbonyl, lower alkoxycarbonyl groups such as isobutoxycarbonyl, 2,2,2-trichloroethoxycarbonyl, halogen such as 2-trimethylsilylethoxycarbonyl, or An "alkoxycarbonyl group" such as a lower alkoxycarbonyl group substituted with a tri-lower alkylsilyl group; an "alkenylcarbonyl group" such as vinylcarbonyl and allylcarbonyl; benzylcarbonyl, phenacyl, 4-methoxybenzylcarbonyl,
An “aralkylcarbonyl group” in which the aryl ring may be substituted with one or two lower alkoxy or nitro groups such as 3,4-dimethoxybenzylcarbonyl, 2-nitrobenzylcarbonyl, 4-nitrobenzylcarbonyl; methane "Lower alkanesulfonyl" such as sulfonyl, ethanesulfonyl, 1-propanesulfonyl; fluorinated "lower alkanesulfonyl" such as trifluoromethanesulfonyl, pentafluoroethanesulfonyl and benzenesulfonyl, p-toluenesulfonyl Preferred examples include an "aliphatic acyl group", an "aromatic acyl group" and a "lower alkanesulfonyl group".

R ⁵ , [Substituent group A] and [Substituent group A]
¹ ] The term "lower alkoxy group" of the "lower alkoxy group" in the definition of [ ¹ ] and the "lower alkoxycarbonyl group" in the definition of [Substituent group A] refers to a group in which the above "lower alkyl group" is bonded to an oxygen atom. For example, methoxy, ethoxy, n-propoxy, isopropoxy, n-
Butoxy, isobutoxy, s-butoxy, tert-butoxy, n-pentoxy, isopentoxy, 2-methylbutoxy, neopentoxy, n-hexyloxy, 4-methylpentoxy, 3-methylpentoxy, 2-methylpentoxy, 3, A straight chain having 1 to 6 carbon atoms such as 3-dimethylbutoxy, 2,2-dimethylbutoxy, 1,1-dimethylbutoxy, 1,2-dimethylbutoxy, 1,3-dimethylbutoxy, 2,3-dimethylbutoxy. It represents a chain or branched alkoxy group, preferably a straight or branched alkoxy group having 1 to 4 carbon atoms.

R ⁴ and R ⁵ together form a “5- to 8-membered saturated heterocyclic ring (including a carbon atom to which they are bonded) (the heterocyclic ring is a group selected from Substituent Group B) At 1
An aryl ring, a heteroaryl ring, an aryl ring substituted with 1 to 3 groups selected from the substituent group A or 1 to 3 groups optionally substituted with the group selected from the substituent group A It may be condensed with an individually substituted heteroaryl ring. )) "Is a 5- to 8-membered saturated heterocyclic ring containing 1 to 3 sulfur atoms, oxygen atoms and / or nitrogen atoms, preferably a sulfur atom, an oxygen atom And / or a 5- or 6-membered saturated heterocyclic ring containing 1 to 3 nitrogen atoms, most preferably a 5-membered saturated heterocyclic ring containing 1 or 2 sulfur atoms, oxygen atoms and / or nitrogen atoms. Examples of such a ring include rings such as an imidazolidine ring, an oxazolidine ring and a thiolane ring. One or two of these rings may be substituted with a group selected from the substituent group B, and further, an “aryl ring”, a “heteroaryl ring”, a “substituent group” in the definition of the ring Ar described below. 1 to 3 with a group selected from A
It may be condensed with the same ring as the “substituted aryl ring” or the “heteroaryl ring substituted by 1 to 3 groups selected from the substituent group A”.

The “amine residue” in the definition of R ⁶ is:
Amino group; amino group substituted by one or two “lower alkyl groups” such as methylamino, ethylamino, isopropylamino, butylamino, dimethylamino, diethylamino, diisopropylamino, and dibutylamino; cyclopentylamino, cyclohexylamino, An amino group substituted by one or two “cycloalkyl groups having 5 to 7 carbon atoms” such as cyclopentylamino and dicyclohexylamino; pyrrolidino, piperidino, piperazino,
A saturated cyclic amine residue having a nitrogen atom in the ring such as N-methylpiperazino, morpholino, and thiomorpholino; a nitrogen atom having a "lower alkyl group" such as anilino, benzylamino, N-methylanilino and N-methylbenzylamino; An aryl or aralkylamino group which may be substituted with; a nitrogen atom such as a heteroarylamino group in which a nitrogen atom such as pyridylamino, N-methylpyridylamino or N-ethylpyridylamino may be substituted with a “lower alkyl group”; And an amino group substituted with one or two "lower alkyl groups"; pyrrolidino, piperidino, piperazino, N-methylpiperazino, morpholino, thiomorpholino, and the like. A saturated cyclic amine residue having a nitrogen atom in the ring; and Nirino, benzylamino, N-
Such as methylanilino, N-methylbenzylamino,
An aryl or aralkylamino group in which a nitrogen atom may be substituted by a “lower alkyl group”.

The “halogen atom” in the definition of the “substituent group A” and the “halogen atom” in the “alkylene group having 1 to 6 carbon atoms which may be substituted by a halogen atom” in the definition of E include fluorine. It is an atom, a chlorine atom, a bromine atom or an iodine atom, preferably a fluorine atom or a chlorine atom.

The “halogeno lower alkyl group” in the definition of [Substituent group A] and [Substituent group A ¹ ] refers to a group in which the above “halogen atom” is bonded to “lower alkyl group”. Fluoromethyl, trichloromethyl,
Difluoromethyl, dichloromethyl, dibromomethyl,
Fluoromethyl, 2,2,2-trichloroethyl, 2,
2,2-trifluoroethyl, 2-bromoethyl, 2-
Examples include groups such as chloroethyl, 2-fluoroethyl, and 2,2-dibromoethyl, and preferred are trifluoromethyl, 2-bromoethyl, 2-chloroethyl and 2-fluoroethyl.

"Lower aliphatic acyl group" in the definition of [Substituent group A]; "Lower aliphatic acyl group" in "lower aliphatic acylamino group"; and "nitrogen atom" in the definition of [Substituent group B] As the above substituent, the “lower aliphatic acyl group” of the “lower aliphatic acyl group” means an aliphatic acyl group having 1 to 6 carbon atoms, for example, formyl, acetyl, propionyl, butyryl, isobutyryl, pentanoyl , Pivaloyl, valeryl and isovaleryl, preferably acetyl and propionyl.

As the "aralkyl group" of the "hydroxy lower alkyl group optionally substituted with an aralkyl group for an oxygen atom" in the definition of R ⁵ and the "substituent on the nitrogen atom" in the definition of the "substituent group B", The “aralkyl group” of the “aralkyl group which may be substituted with the substituent group A” refers to a group in which the “aryl group” is bonded to the “lower alkyl group”, for example, benzyl, α-naphthylmethyl , Β-naphthylmethyl, indenylmethyl, phenanthrenylmethyl, anthracenylmethyl, diphenylmethyl, triphenylmethyl, 1-phenethyl, 2-phenethyl, 1-naphthylethyl, 2-naphthylethyl, 1
-Phenylpropyl, 2-phenylpropyl, 3-phenylpropyl, 1-naphthylpropyl, 2-naphthylpropyl, 3-naphthylpropyl, 1-phenylbutyl,
2-phenylbutyl, 3-phenylbutyl, 4-phenylbutyl, 1-naphthylbutyl, 2-naphthylbutyl,
3-naphthylbutyl, 4-naphthylbutyl, 1-phenylpentyl, 2-phenylpentyl, 3-phenylpentyl, 4-phenylpentyl, 5-phenylpentyl,
1-naphthylpentyl, 2-naphthylpentyl, 3-naphthylpentyl, 4-naphthylpentyl, 5-naphthylpentyl, 1-phenylhexyl, 2-phenylhexyl, 3-phenylhexyl, 4-phenylhexyl, 5
-Phenylhexyl, 6-phenylhexyl, 1-naphthylhexyl, 2-naphthylhexyl, 3-naphthylhexyl, 4-naphthylhexyl, 5-naphthylhexyl, and 6-naphthylhexyl. The "group" portion is benzene, and the "lower alkyl group" is an "aralkyl group" having 1 to 4 carbon atoms, more preferably a benzyl group and a phenethyl group.

The “lower alkanesulfonyl group” of the “lower alkanesulfonyl group as a substituent on a nitrogen atom” in the definition of [Substituent group B] is the same group as the above “lower alkanesulfonyl group”.

The “aryl ring” in the definition of the ring Ar and the “aryl ring” of the “aryl ring substituted by 1 to 4 groups selected from the substituent group A” include, for example, a benzene ring, an indene ring, Naphthalene ring, phenanthrene ring,
An aromatic hydrocarbon group having 6 to 14 carbon atoms such as an anthracenyl ring can be mentioned, and a benzene ring is preferable.

The “heteroaryl ring” in the definition of the ring Ar and the “heteroaryl ring” of the “heteroaryl ring substituted with one to three groups selected from the substituent group A”
Is, for example, a 5- to 7-membered aromatic heterocycle containing 1 to 3 sulfur atoms, oxygen atoms and / or nitrogen atoms, for example, a furan ring, a thiophene ring, a pyrrole ring, an azepine ring, a pyrazole ring, an imidazole Ring, oxazole ring,
Isoxazole ring, thiazole ring, isothiazole ring,
Rings such as a 1,2,3-oxadiazole ring, a triazole ring, a tetrazole ring, a thiadiazole ring, a pyran ring, a pyridine ring, a pyridazine ring, a pyrimidine ring and a pyrazine ring can be mentioned, and preferably a nitrogen atom And a 5- to 7-membered aromatic heterocyclic group optionally containing an oxygen atom or a sulfur atom, such as a pyrrole ring, an azepine ring, a pyrazole ring, an imidazole ring, an oxazole ring, an isoxazole ring, and a thiazole. Ring, isothiazole ring, 1,2,3-oxadiazole ring, triazole ring, tetrazole ring, thiadiazole ring, pyridine ring, pyridazine ring, pyrimidine ring and pyrazine ring, and more preferably. Is a pyridine ring,
An imidazole ring, an oxazole ring, a pyrazine ring and a thiazole ring.

Regarding the "aryl group substituted by 1 to 3 groups selected from the substituent group A" in the definition of R ¹ , preferably 1 to 3 groups by the group selected from the substituent group A ¹ A substituted phenyl group, more preferably a phenyl group substituted by 1 to 3 groups with a group selected from the substituent group A ¹ , most preferably a “lower alkoxy”
A phenyl group substituted with 1 to 3 phenyl groups.

The “aryl group substituted by 1 to 3 groups selected from the substituent group A” in the definition of R ² is preferably an aryl group substituted by 1 to 3 “halogen atoms”. Yes, more preferably "halogen atom"
Is a phenyl group substituted by 1 to 3 groups.

R ⁴ and R ⁵ together form a “5- to 8-membered saturated heterocyclic ring (including a carbon atom to which they are bonded) (the heterocyclic ring is a group selected from Substituent Group B) At 1
An aryl ring, a heteroaryl ring, an aryl ring substituted with 1 to 3 groups selected from the substituent group A or 1 to 3 groups optionally substituted with the group selected from the substituent group A It may be condensed with an individually substituted heteroaryl ring. )) Is preferably a compound of the formula (I _L ):

[0052]

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(Wherein J represents an alkylene group having 1 to 6 carbon atoms, and ring Ar is substituted with 1 to 4 rings selected from an aryl ring, a heteroaryl ring, and a substituent group A) An aryl ring or a heteroaryl ring substituted with 1 to 3 substituent (s) selected from a substituent group A). More preferably, the sulfoxide group of the above formula (I _L ) is S A ring that is a sulfoxide in a configuration.

"Pharmacologically acceptable salt" means a salt of compound (I) of the present invention when it has an amino group and / or a carboxy group, which can be converted into a salt.
As the salt based on an amino group, preferably, hydrofluoride, hydrochloride, hydrobromide, hydrohalide such as hydroiodide, nitrate, perchlorate, sulfate And inorganic salts such as phosphates; arylsulfones such as lower alkanesulfonates such as methanesulfonate, trifluoromethanesulfonate and ethanesulfonate, benzenesulfonate and p-toluenesulfonate. Acid salts, acetic acid,
Organic acid salts such as malic acid, fumarate, succinate, citrate, tartrate, oxalate, and maleate; and glycine, lysine, arginine, ornithine, glutamate, and asparagine Amino acid salts such as acid salts can be mentioned. On the other hand, as a salt based on a carboxy group, preferably, an alkali metal salt such as a sodium salt, a potassium salt, a lithium salt, an alkaline earth metal salt such as a calcium salt and a magnesium salt, an aluminum salt,
Metal salts such as iron salts; inorganic salts such as ammonium salts; t-
Octylamine salt, dibenzylamine salt, morpholine salt, glucosamine salt, phenylglycine alkyl ester salt, ethylenediamine salt, N-methylglucamine salt,
Guanidine salt, diethylamine salt, triethylamine salt, dicyclohexylamine salt, N, N′-dibenzylethylenediamine salt, chloroprocaine salt, procaine salt, diethanolamine salt, N-benzylphenethylamine salt, piperazine salt, tetramethylammonium salt,
Amine salts such as organic salts such as tris (hydroxymethyl) aminomethane salt; and amino acid salts such as glycine salt, lysine salt, arginine salt, ornithine salt, glutamate and aspartate.

The compound (I) of the present invention can be obtained by modifying the nitrogen atom of the piperidino group in the molecule with an R ³ group.
Since it can be a quaternary amine, a compound having such a cation and an anion (there is no particular limitation as long as it becomes an anion. it can.)
Are included in the present invention.

Further, when the compound (I) of the present invention is left in the air, it may absorb water and may absorb adsorbed water or form hydrates. Included in the invention.

The “ester” means the ester of the compound (I) of the present invention, since it can be converted into an ester. Such esters include “esters of hydroxyl group” and “esters of carboxy group”. And an ester residue in which each ester residue is a “general protecting group” or a “protecting group that can be cleaved in vivo by a biological method such as hydrolysis”.

"General protecting group" means a protecting group that can be cleaved by a chemical method such as hydrogenolysis, hydrolysis, electrolysis, or photolysis.

The “general protecting group” for the “ester of a hydroxyl group” is preferably the above “lower aliphatic acyl group”; the above “aromatic acyl group”;
2-yl, 3-bromotetrahydropyran-2-yl,
"Tetrahydropyranyl or tetrahydrothiopyranyl group" such as 4-methoxytetrahydropyran-4-yl, tetrahydrothiopyran-2-yl, 4-methoxytetrahydrothiopyran-4-yl; tetrahydrofuran-2-yl, tetrahydro "Tetrahydrofuranyl or tetrahydrothiofuranyl group" such as thiofuran-2-yl; such as trimethylsilyl, triethylsilyl, isopropyldimethylsilyl, t-butyldimethylsilyl, methyldiisopropylsilyl, methyldi-t-butylsilyl, triisopropylsilyl Tri-lower alkyl substituted with one or two aryl groups such as tri-lower alkylsilyl, diphenylmethylsilyl, diphenylbutylsilyl, diphenylisopropylsilyl and phenyldiisopropylsilyl A "silyl group" such as a killsilyl group;
Lower alkoxymethyl groups such as methoxymethyl, 1,1-dimethyl-1-methoxymethyl, ethoxymethyl, propoxymethyl, isopropoxymethyl, butoxymethyl, tert-butoxymethyl, lower alkoxylation such as 2-methoxyethoxymethyl Lower alkoxymethyl group, 2,2,2-trichloroethoxymethyl, bis (2
"Alkoxymethyl group" such as halogeno lower alkoxymethyl such as -chloroethoxy) methyl; lower alkoxylated ethyl group such as 1-ethoxyethyl and 1- (isopropoxy) ethyl; and 2,2,2-trichloroethyl. "Substituted ethyl group" such as an ethyl halide group; 1 to 3 such as benzyl, α-naphthylmethyl, β-naphthylmethyl, diphenylmethyl, triphenylmethyl, α-naphthyldiphenylmethyl, 9-anthrylmethyl;
Lower alkyl groups substituted with two aryl groups, 4-methylbenzyl, 2,4,6-trimethylbenzyl, 3,
4,5-trimethylbenzyl, 4-methoxybenzyl,
4-methoxyphenyldiphenylmethyl, 2-nitrobenzyl, 4-nitrobenzyl, 4-chlorobenzyl,
Lower alkyl such as -bromobenzyl, 4-cyanobenzyl, lower alkoxy, nitro, halogen, lower alkyl having 1 to 3 aryl groups substituted with an aryl ring having a cyano group, etc. "Aralkyl group";"alkoxycarbonylgroup";"alkenyloxycarbonylgroup" such as vinyloxycarbonyl and allyloxycarbonyl; benzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 3,4-dimethoxybenzyloxycarbonyl, And an "aralkyloxycarbonyl group" in which the aryl ring may be substituted with one or two lower alkoxy or nitro groups such as -nitrobenzyloxycarbonyl and 4-nitrobenzyloxycarbonyl.

As the “general protecting group” for the “ester of a carboxy group”, preferably the above “lower alkyl group”; ethenyl, 1-propenyl, 2-propenyl,
-Methyl-2-propenyl, 1-methyl-1-propenyl, 2-methyl-1-propenyl, 2-methyl-2-propenyl, 2-ethyl-2-propenyl, 1-butenyl, 2-butenyl, 1-methyl -2-butenyl, 1-methyl-1-butenyl, 3-methyl-2-butenyl, 1-
Ethyl-2-butenyl, 3-butenyl, 1-methyl-3
-Butenyl, 2-methyl-3-butenyl, 1-ethyl-
3-butenyl, 1-pentenyl, 2-pentenyl, 1-
Methyl-2-pentenyl, 2-methyl-2-pentenyl, 3-pentenyl, 1-methyl-3-pentenyl, 2
-Methyl-3-pentenyl, 4-pentenyl, 1-methyl-4-pentenyl, 2-methyl-4-pentenyl 1-
Lower alkenyl groups such as hexenyl, 2-hexenyl, 3-hexenyl, 4-hexenyl, 5-hexenyl;
Ethynyl, 2-propynyl, 1-methyl-2-propynyl, 2-methyl-2-propenyl, 2-ethyl-2-propenyl, 2-butynyl, 1-methyl-2-butynyl,
2-methyl-2-butynyl, 1-ethyl-2-butynyl, 3-butynyl, 1-methyl-3-butynyl, 2-methyl-3-butynyl 1-ethyl-3-butynyl, 2-pentynyl, 1-methyl -2-pentynyl, 2-methyl-
2-pentynyl, 3-pentynyl, 1-methyl-3-pentynyl, 2-methyl-3-pentynyl, 4-pentynyl, 1-methyl-4-pentynyl, 2-methyl-4-pentynyl, 2-hexynyl, 3- Lower alkynyl groups such as hexynyl, 4-hexynyl and 5-hexynyl; the above-mentioned "halogeno lower alkyl";2-hydroxyethyl;
Hydroxy "lower alkyl group" such as 2,3-dihydroxypropyl, 3-hydroxypropyl, 3,4-dihydroxybutyl and 4-hydroxybutyl; "lower aliphatic acyl" such as acetylmethyl- "lower alkyl group" The “aralkyl group”; the “silyl group”.

The term "protecting group that can be cleaved in vivo by a biological method such as hydrolysis" means that it is cleaved in a human body by a biological method such as hydrolysis to produce a free acid or a salt thereof. Refers to a protecting group, whether such a derivative is administered by intravenous injection to experimental animals such as rats and mice,
Subsequent examination of the body fluids of the animals allows the determination of the ability to detect the original compound or a pharmacologically acceptable salt thereof, which can be determined by the "esters of hydroxyl groups" and such "biological methods such as hydrolysis in vivo." As the protecting group which can be cleaved by, preferably, formyloxymethyl, acetoxymethyl, dimethylaminoacetoxymethyl, propionyloxymethyl, butyryloxymethyl, pivaloyloxymethyl, valeryloxymethyl, isovaleryloxy Methyl, hexanoyloxymethyl, 1-formyloxyethyl, 1-acetoxyethyl, 1-propionyloxyethyl, 1-butyryloxyethyl, 1-pivaloyloxyethyl, 1-valeryloxyethyl, 1-isovale Ryloxyethyl, 1-hexanoyloxyethyl,
1-formyloxypropyl, 1-acetoxypropyl, 1-propionyloxypropyl, 1-butyryloxypropyl, 1-pivaloyloxypropyl, 1-valeryloxypropyl, 1-isovaleryloxypropyl, 1-hexa Noyloxypropyl, 1-acetoxybutyl, 1-propionyloxybutyl, 1-butyryloxybutyl, 1-pivaloyloxybutyl, 1-acetoxypentyl, 1-propionyloxypentyl, 1
1- such as butyryloxypentyl, 1-pivaloyloxypentyl, 1-pivaloyloxyhexyl
("Lower aliphatic acyl" oxy) "lower alkyl",
Cyclopentylcarbonyloxymethyl, cyclohexylcarbonyloxymethyl, 1-cyclopentylcarbonyloxyethyl, 1-cyclohexylcarbonyloxyethyl, 1-cyclopentylcarbonyloxypropyl, 1-cyclohexylcarbonyloxypropyl, 1
1-("cycloalkyl" carbonyloxy) "lower alkyl" such as -cyclopentylcarbonyloxybutyl, 1-cyclohexylcarbonyloxybutyl,
1- (acyloxy) "lower alkyl group" such as 1-("aromatic acyl" oxy) "lower alkyl group" such as benzoyloxymethyl; methoxycarbonyloxymethyl, ethoxycarbonyloxymethyl, propoxycarbonyloxymethyl, Propoxycarbonyloxymethyl, butoxycarbonyloxymethyl, isobutoxycarbonyloxymethyl, pentyloxycarbonyloxymethyl, hexyloxycarbonyloxymethyl, cyclohexyloxycarbonyloxymethyl, cyclohexyloxycarbonyloxy (cyclohexyl) methyl, 1- (methoxycarbonyloxy) Ethyl, 1- (ethoxycarbonyloxy) ethyl, 1-
(Propoxycarbonyloxy) ethyl, 1- (isopropoxycarbonyloxy) ethyl, 1- (butoxycarbonyloxy) ethyl, 1- (isobutoxycarbonyloxy) ethyl, 1- (tert-butoxycarbonyloxy) ethyl, 1- ( Pentyloxycarbonyloxy) ethyl, 1- (hexyloxycarbonyloxy)
Ethyl, 1- (cyclopentyloxycarbonyloxy) ethyl, 1- (cyclopentyloxycarbonyloxy) propyl, 1- (cyclohexyloxycarbonyloxy) propyl, 1- (cyclopentyloxycarbonyloxy) butyl, 1- (cyclohexyloxycarbonyloxy) Butyl, 1- (cyclohexyloxycarbonyloxy) ethyl, 1- (ethoxycarbonyloxy) propyl, 2- (methoxycarbonyloxy)
Ethyl, 2- (ethoxycarbonyloxy) ethyl, 2
-(Propoxycarbonyloxy) ethyl, 2- (isopropoxycarbonyloxy) ethyl, 2- (butoxycarbonyloxy) ethyl, 2- (isobutoxycarbonyloxy) ethyl, 2- (pentyloxycarbonyloxy) ethyl, 2- ( Hexyloxycarbonyloxy) ethyl, 1- (methoxycarbonyloxy) propyl, 1- (ethoxycarbonyloxy) propyl, 1-
(Propoxycarbonyloxy) propyl, 1- (isopropoxycarbonyloxy) propyl, 1- (butoxycarbonyloxy) propyl, 1- (isobutoxycarbonyloxy) propyl, 1- (pentyloxycarbonyloxy) propyl, 1- (hexyl Oxycarbonyloxy) propyl, 1- (methoxycarbonyloxy) butyl, 1- (ethoxycarbonyloxy) butyl, 1- (propoxycarbonyloxy) butyl,
(Isopropoxycarbonyloxy) butyl, 1- (butoxycarbonyloxy) butyl, 1- (isobutoxycarbonyloxy) butyl, 1- (methoxycarbonyloxy) pentyl, 1- (ethoxycarbonyloxy)
(Lower alkoxycarbonyloxy) alkyl groups such as pentyl, 1- (methoxycarbonyloxy) hexyl, 1- (ethoxycarbonyloxy) hexyl;
(5-phenyl-2-oxo-1,3-dioxolene-
4-yl) methyl, [5- (4-methylphenyl) -2
-Oxo-1,3-dioxolen-4-yl] methyl,
[5- (4-methoxyphenyl) -2-oxo-1,3
-Dioxolen-4-yl] methyl, [5- (4-fluorophenyl) -2-oxo-1,3-dioxolene-
4-yl] methyl, [5- (4-chlorophenyl) -2
-Oxo-1,3-dioxolen-4-yl] methyl,
(2-oxo-1,3-dioxolen-4-yl) methyl, (5-methyl-2-oxo-1,3-dioxolen-4-yl) methyl, (5-ethyl-2-oxo-1,
3-dioxolen-4-yl) methyl, (5-propyl-2-oxo-1,3-dioxolen-4-yl) methyl, (5-isopropyl-2-oxo-1,3-dioxolen-4-yl) "Carbonyloxyalkyl groups" such as methyl, oxodioxorenylmethyl groups such as (5-butyl-2-oxo-1,3-dioxolen-4-yl) methyl; phthalidyl, dimethylphthalidyl, dimethoxyphthalic; “Phthalidyl group” such as jill: the above “lower aliphatic acyl group”: the above “aromatic acyl group”: “half ester salt residue of succinic acid”: “phosphate ester residue”: “ester of amino acid or the like” "Forming residue": carbamoyl group: carbamoyl group substituted with 1 to 2 lower alkyl groups: and 1-carboxy group such as pivaloyloxymethyloxycarbonyl It can be exemplified acyloxy) alkyloxycarbonyl group ", preferably a" carbonyloxy alkyl group ".

On the other hand, the “protecting group that can be cleaved in vivo by a biological method such as hydrolysis” as the “ester of a carboxy group” is preferably methoxyethyl,
1-ethoxyethyl, 1-methyl-1-methoxyethyl, 1- (isopropoxy) ethyl, 2-methoxyethyl, 2-ethoxyethyl, 1,1-dimethyl-1-methoxyethyl, ethoxymethyl, n-propoxymethyl ,
Lower alkoxy lower alkyl groups such as isopropoxymethyl, n-butoxymethyl, tert-butoxymethyl,
Lower alkoxylated lower alkoxy lower alkyl groups such as 2-methoxyethoxymethyl, “aryl” oxy “lower alkyl groups” such as phenoxymethyl,
“Alkoxy lower alkyl groups” such as halogenated lower alkoxy lower alkyl groups such as 2-trichloroethoxymethyl and bis (2-chloroethoxy) methyl; “lower alkoxy” carbonyl “lower alkyl groups” such as methoxycarbonylmethyl "Cyano" lower alkyl "such as cyanomethyl and 2-cyanoethyl;""loweralkyl" thiomethyl "such as methylthiomethyl and ethylthiomethyl;" aryl "such as phenylthiomethyl and naphthylthiomethyl Thiomethyl group "; 2-
"" Lower alkyl optionally substituted with halogen "sulfonyl" lower alkyl group "such as methanesulfonylethyl and 2-trifluoromethanesulfonylethyl;
“Aryl” sulfonyl “lower alkyl group” such as 2-benzenesulfonylethyl and 2-toluenesulfonylethyl; the “1- (acyloxy)“ lower alkyl group ””; the “phthalidyl group”; "The lower alkyl group";"carboxyalkylgroup" such as carboxymethyl; and "amino acid amide-forming residue" such as phenylalanine.

The “other derivative” is a derivative other than the above “pharmacologically acceptable salts” and the above “esters thereof” when the compound (I) of the present invention has an amino group and / or a carboxy group. Derivatives are shown because Such derivatives include, for example, amide derivatives.

The compound (I) of the present invention has an asymmetric carbon in the molecule, and there are stereoisomers each of which is R-coordinate or S-coordinate. Are included in the present invention.

[0065]

BEST MODE FOR CARRYING OUT THE INVENTION The saturated heterocyclic compound of the present invention can be produced by the method described below.

[Method A]

[0067]

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In the above formula, R ¹ , R ² , A, B, D, E,
G and L are as defined above.

Y and Y ′ are not particularly limited as long as they are groups which can be eliminated as nucleophilic residues.
Halogen atoms such as bromine and iodine; trihalogenomethyloxy groups such as trichloromethyloxy; lower alkanesulfonyloxy groups such as methanesulfonyloxy and ethanesulfonyloxy; such as trifluoromethanesulfonyloxy and pentafluoroethanesulfonyloxy Halogeno lower alkanesulfonyloxy group; arylsulfonyloxy group such as benzenesulfonyloxy, p-toluenesulfonyloxy and p-nitrobenzenesulfonyloxy; more preferably, halogen atom and lower alkanesulfonyloxy group; It is.

R ⁸ represents a hydrogen atom or a protecting group for a hydroxyl group. The hydroxyl-protecting group refers to a “protecting group in a reaction” that can be cleaved by a chemical method such as hydrogenolysis, hydrolysis, electrolysis, or photolysis. And the same groups as described above.

Step A1 is a reaction of the compound (II) with the compound (III) in a solvent in the presence of a base, and the imino group of the compound (II) is converted to a compound represented by the formula -ABR ¹ . This is a step of producing a compound (IV) modified with a group (wherein, A, B and R ¹ have the same meanings as described above).

The solvent used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent, but is preferably an aliphatic hydrocarbon such as hexane, heptane, ligroin or petroleum ether. Hydrogens; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethyl formate, ethyl acetate, propyl acetate; Esters such as butyl acetate and diethyl carbonate; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; acetone, methyl ethyl ketone, methyl isobutyl ketone, isophorone, cyclohexane Ketones such as xanone; nitro compounds such as nitroethane and nitrobenzene; nitriles such as acetonitrile and isobutyronitrile; and more preferably halogenated hydrocarbons and ethers. And most preferably,
Methylene chloride and tetrahydrofuran. The base to be used is not particularly limited as long as it is used as a base in a normal reaction.
N-methylmorpholine, triethylamine, tripropylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline,
-(N, N-dimethylamino) pyridine, 2,6-di (t-butyl) -4-methylpyridine, quinoline, N,
N-dimethylaniline, N, N-diethylaniline,
1,5-diazabicyclo [4.3.0] non-5-ene (DBN), 1,4-diazabicyclo [2.2.2] octane (DABCO), 1,8-diazabicyclo [5.
4.0] Undec-7-ene (DBU), and more preferably, triethylamine and diisopropylethylamine. The reaction is carried out at a temperature of -20 ° C to 100 ° C, preferably,
0 ° C. to 20 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually 5 minutes to 24 hours, preferably 10 minutes to 12 hours.

The compound (II) wherein A represents a carbonyl group
When reacting with I), the compound represented by the general formula R ¹ -B-A-OH
(Wherein A, B and R ¹ have the same meanings as described above), and the reaction is carried out with a "condensing agent" in a solvent in the presence or absence of a base. Is done. Examples of the "condensing agent" used include: (1) a combination of a phosphoric ester such as diethylphosphoryl cyanide or diphenylphosphoryl azide and the following base; (2) 1,3-dicyclohexylcarbodiimide,
3-diisopropylcarbodiimide, 1-ethyl-3-
Carbodiimides such as (3-dimethylaminopropyl) carbodiimide; combinations of the carbodiimides with the following bases; the carbodiimides and N-hydroxysuccinimide, 1-hydroxybenzotriazole, N-hydroxy-5-norbornene-2,3-di Combinations of N-hydroxys such as carboximides; (3) 2,2′-dipyridyl disulfide, 2,
Combination of disulfides such as 2'-dibenzothiazolyl disulfide and phosphines such as triphenylphosphine and tributylphosphine; (4) N, N'-disuccinimidyl carbonate, di-2-pyridyl carbonate , S, S'-bis (1-
Carbonates such as phenyl-1H-tetrazol-5-yl) dithiocarbonate; (5) phosphinic chlorides such as N, N′-bis (2-oxo-3-oxazolidinyl) phosphinic chloride; 6) N, N'-disuccinimidyl oxalate,
N, N'-diphthalimide oxalate, N, N'-bis (5-norbornene-2,3-dicarboximidyl) oxalate, 1,1'-bis (benzotriazolyl) oxalate, 1,1 Oxalates such as' -bis (6-chlorobenzotriazolyl) oxalate and 1,1'-bis (6-trifluoromethylbenzotriazolyl) oxalate; (7) the phosphines and diethyl azodicarboxylate;
Combinations of azodicarboxylic acid esters such as 1,1 '-(azodicarbonyl) dipiperidine or azodicarboxamides; combinations of the above phosphines and the following bases; (8) N-ethyl-5-phenylisoxazolium −
N-lower alkyl-5-arylisoxazolium-3'-sulfonates such as 3'-sulfonate; (9) diheteroaryldiselenides such as di-2-pyridyldiselenide; (10 ) Arylsulfonyltriazolides such as p-nitrobenzenesulfonyltriazolide; (11) 2-halo-1-lower alkylpyridinium halides such as 2-chloro-1-methylpyridinium iodide; 1'-oxalyldiimidazole, N,
Imidazoles such as N'-carbonyldiimidazole; (13) 3-lower alkyl-2-halogen-benzothiazolium fluoroborates such as 3-ethyl-2-chloro-benzothiazolium fluoroborate (14) 3-lower alkyl-benzothiazole-2-cellones such as 3-methyl-benzothiazole-2-cellone; (15) phosphates such as phenyldichlorophosphate and polyphosphate ester; (16) chloro; (17) halogenosilanes such as trimethylsilyl chloride and triethylsilyl chloride; (18) combinations of lower alkanesulfonyl halides such as methanesulfonyl chloride and the following bases; (19) N, N, N, N, N ', N'-tetra-lower alkylhalogenoformamidium chlorides, such as N', N'-tetramethylchloroformamidium chloride; ).

The solvent to be used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent, but is preferably an aliphatic hydrocarbon such as hexane or heptane; Aromatic hydrocarbons such as toluene and xylene; methylene chloride, chloroform,
Halogenated hydrocarbons such as carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; esters such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate and diethyl carbonate; diethyl ether, diisopropyl ether, tetrahydrofuran; Ethers such as dioxane, dimethoxyethane and diethylene glycol dimethyl ether; nitriles such as acetonitrile and isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide;
Examples include amides such as N-methyl-2-pyrrolidone, N-methylpyrrolidinone, and hexamethylphosphorotriamide. The base to be used is not particularly limited as long as it is used as a base in a usual reaction. Preferably, N-methylmorpholine, triethylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methyl Piperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4- (N, N-dimethylamino) pyridine, 2,6
Organic bases such as -di (tert-butyl) -4-methylpyridine, quinoline, N, N-dimethylaniline and N, N-diethylaniline can be mentioned. Incidentally, 4
-(N, N-dimethylamino) pyridine and 4-pyrrolidinopyridine can be used in combination with other bases in a catalytic amount, and in order to carry out the reaction effectively, a molecular sieve such as molecular sieve is used. Dehydrating agents, quaternary ammonium salts such as benzyltriethylammonium chloride and tetrabutylammonium chloride, dibenzo-1
Crown ethers such as 8-crown-6, 3,4
-Dihydro-2H-pyrido [1,2-a] pyrimidine-
An acid scavenger such as 2-one can also be added.
The reaction is carried out at a temperature of -20 ° C to 80 ° C, preferably 0 ° C to room temperature. The reaction time depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 10 minutes to 3 days, preferably from 30 minutes to 1 day.

Step A2 is a compound represented by the formula ( ⁸ )
After removing the group, the produced hydroxyl group is converted to a leaving group Y ′ in the presence of a base, in the presence or absence of a solvent, to produce a compound (V).

The removal of the R ⁸ group depends on its type, but is generally carried out as follows by methods well known in the art.

When a silyl group is used as the R ⁸ group, a compound which generates a fluorine anion such as tetrabutylammonium fluoride, hydrofluoric acid, hydrofluoric acid-pyridine and potassium fluoride is usually used. Treated or acetic acid,
It can be removed by treatment with an organic acid such as methanesulfonic acid, paratoluenesulfonic acid, trifluoroacetic acid, trifluoromethanesulfonic acid, B-bromocatecholborane or an inorganic acid such as hydrochloric acid. In addition, when removing with a fluorine anion, the reaction may be accelerated by adding an organic acid such as formic acid, acetic acid, or propionic acid. The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Preferably, the solvent is diethyl ether, diisopropyl ether.
Ethers such as ter, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; nitriles such as acetonitrile and isobutyronitrile; water; organic acids such as acetic acid; and mixed solvents thereof. Although the reaction temperature and the reaction time are not particularly limited, the reaction is usually carried out at 0 ° C. to 150 ° C. (preferably 10 ° C. to 100 ° C.) for 1 hour to 48 hours (preferably 2 hours to 12 hours). Is done.

When the R ⁸ group is an aralkyl group or an aralkyloxycarbonyl group, it is usually removed by contacting with a reducing agent in a solvent (preferably catalytic reduction at room temperature under a catalyst). Alternatively, a method of removing using an oxidizing agent is preferable. The solvent used in the removal by catalytic reduction is not particularly limited as long as it does not participate in the present reaction, but alcohols such as methanol, ethanol and isopropanol, diethyl ether, Ethers such as tetrahydrofuran and dioxane, aromatic hydrocarbons such as toluene, benzene and xylene;
Hexane, aliphatic hydrocarbons such as cyclohexane,
Ethyl acetate, esters such as propyl acetate, formamide, dimethylformamide, dimethylacetamide, N-methyl-2-pyrrolidone, amides such as hexamethylphosphorotriamide, formic acid, fatty acids such as acetic acid, water, or These mixed solvents are preferred, more preferably alcohols, fatty acids, a mixed solvent of alcohols and ethers, a mixed solvent of alcohols and water, or a mixed solvent of fatty acids and fatty acids. It is a mixed solvent with water. The catalyst to be used is not particularly limited as long as it is usually used for a catalytic reduction reaction, but is preferably palladium carbon, palladium black, Raney nickel, platinum oxide, platinum black, rhodium oxide. Aluminum, triphenylphosphine-rhodium chloride, palladium-barium sulfate are used. The pressure is not particularly limited, but it is usually 1 to 10 atm. The reaction temperature and reaction time depend on the starting materials,
Although it depends on the type of the solvent and the catalyst, it is usually 0 ° C to 100 ° C (preferably 20 ° C to 70 ° C), and 5 minutes to 4 minutes.
8 hours (preferably 1 hour to 24 hours).

The solvent used in the removal by oxidation is not particularly limited as long as it does not participate in the present reaction, but is preferably a water-containing organic solvent. Suitable examples of such organic solvents include ketones such as acetone, methylene chloride, chloroform, halogenated hydrocarbons such as carbon tetrachloride, nitriles such as acetonitrile, diethyl ether, tetrahydrofuran, and dioxane. And ethers, amides such as dimethylformamide, dimethylacetamide and hexamethylphosphorotriamide, and sulfoxides such as dimethylsulfoxide. The oxidizing agent to be used is not particularly limited as long as it is a compound used for oxidation, but is preferably potassium persulfate, sodium persulfate, ammonium cerium nitrate (CAN), 2,3-
Dichloro-5,6-dicyano-p-benzoquinone (DD
Q) is used. The reaction temperature and reaction time vary depending on the starting material, solvent, type of catalyst and the like, but are usually carried out at 0 to 150 ° C. for 10 minutes to 24 hours.

Further, in liquid ammonia or methanol
In alcohols such as ethanol and ethanol, -78
It can also be removed by applying alkali metals such as metallic lithium and metallic sodium at a temperature of from -20 ° C to -20 ° C.

Further, it can also be removed by using an alkylsilyl halide such as aluminum chloride-sodium iodide or trimethylsilyl iodide in a solvent. The solvent used is not particularly limited as long as it does not participate in the reaction, but is preferably a nitrile such as acetonitrile, a methylene chloride, a halogenated hydrocarbon such as chloroform, or a mixed solvent thereof. Is used. The reaction temperature and reaction time vary depending on the starting material, solvent, etc., but are usually 0 to 50 ° C. and 5 minutes to 3 minutes.
Implemented for days.

When the reaction substrate has a sulfur atom,
Preferably, aluminum chloride-sodium iodide is used.

When R ⁸ is an aliphatic acyl group, an aromatic acyl group or a lower alkoxycarbonyl group, it is removed by treating with a base in a solvent.

The base to be used is not particularly limited as long as it does not affect the other parts of the compound. Preferably, metal alkoxides such as sodium methoxide; sodium carbonate, potassium carbonate, carbonate Alkali metal carbonates such as lithium; alkali metal hydroxides such as sodium hydroxide, potassium hydroxide, lithium hydroxide, barium hydroxide or ammonia such as ammonia water and concentrated ammonia-methanol are used. . The solvent to be used is not particularly limited as long as it is used in a usual hydrolysis reaction. Water; methanol, ethanol
Preferred are organic solvents such as alcohols such as toluene and n-propanol, ethers such as tetrahydrofuran and dioxane, or mixed solvents of water and the above organic solvents. The reaction temperature and reaction time vary depending on the starting material, solvent and base used, and are not particularly limited. However, in order to suppress a side reaction, the reaction is usually carried out at 0 to 150 ° C. for 1 to 10 hours.

When R ⁸ is a lower alkoxymethyl group, a tetrahydropyranyl group, a tetrahydrothiopyranyl group, a tetrahydrofuranyl group, a tetrahydrothiofuranyl group or a substituted ethyl group, it is usually added in a solvent.
Removed by treatment with acid. The acid used is not particularly limited as long as it is usually used as a Bronsted acid or Lewis acid, and is preferably hydrogen chloride; an inorganic acid such as hydrochloric acid, sulfuric acid, or nitric acid; Bronsted acids such as organic acids such as fluoroacetic acid, methanesulfonic acid and p-toluenesulfonic acid: Lewis acids such as boron trifluoride, but strongly acidic cation exchange resins such as Dowex 50W Can be used. The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent.
Preferably, aliphatic hydrocarbons such as hexane, heptane, ligroin, petroleum ether; benzene, toluene,
Aromatic hydrocarbons such as xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate, and diethyl carbonate Esters such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; methano-
, Ethanol, n-propanol, isopropanol
, N-butanol, isobutanol, tert-butanol
Alcohols such as alcohol, isoamyl alcohol, diethylene glycol, glycerin, octanol, cyclohexanol, methyl cellosolve; acetone, methyl ethyl ketone, methyl isobutyl ketone, isophorone,
Ketones such as cyclohexanone; water or a mixed solvent thereof are preferred, and halogenated hydrocarbons, esters or ethers are more preferred. The reaction temperature and reaction time vary depending on the starting material, the solvent, the type and concentration of the acid used, and the like.
(Preferably −5 to 50 ° C.) for 5 minutes to 48 hours (preferably 30 minutes to 10 hours).

When the R ⁸ group is an alkenyloxycarbonyl group, the same conditions as those for the removal reaction when the R ⁸ group is an aliphatic acyl group, an aromatic acyl group or a lower alkoxycarbonyl group are usually used. And by treating with a base.

In the case of allyloxycarbonyl, palladium and triphenylphosphine or bis (methyldiphenylphosphine) (1,5-cyclooctadiene) iridium (I) hexafluorophosphate are particularly used. And the method can be carried out with few side reactions.

The solvent used in the subsequent reaction is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent, but is preferably an aromatic solvent such as benzene, toluene or xylene. Hydrocarbons; halogenated hydrocarbons such as methylene chloride and chloroform;
Diethyl ether, tetrahydrofuran, dioxane,
Ethers such as dimethoxyethane or nitriles such as acetonitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-
Amides such as methyl-2-pyrrolidone, N-methylpyrrolidinone, and hexamethylphosphorotriamide; and pyridine. As the base used,
There is no particular limitation as long as it is used as a base in a usual reaction. , 4-pyrrolidinopyridine, picoline, 4- (N, N-dimethylamino) pyridine, 2,6-di (t-butyl) -4-methylpyridine, quinoline, N, N-dimethylaniline,
N, N-diethylaniline, 1,5-diazabicyclo [4.3.0] non-5-ene (DBN), 1,4-diazabicyclo [2.2.2] octane (DABCO),
1,8-diazabicyclo [5.4.0] undec-7-
Organic bases such as ene (DBU); more preferably, triethylamine, pyridine and 4
-(N, N-dimethylamino) pyridine.

Most preferably, it is achieved by using pyridine as a solvent and adding a catalytic amount of 4- (N, N-dimethylamino) pyridine. The reaction temperature is from -20 ° C to 50 ° C, preferably from -10 ° C to 20 ° C.
The reaction time varies depending mainly on the reaction temperature, the starting compound, the reagent or the type of the solvent used, but is usually from 15 minutes to 24 hours, preferably from 30 minutes to 6 hours.

As the reagent for forming the leaving group Y ', a corresponding halide is used. Examples of such a reagent include sulfonyl halides such as methanesulfonyl chloride and P-toluenesulfonyl chloride.

Step A3 is a step of reacting compound (V) with compound (VI) in a solvent in the presence of a base to produce saturated heterocyclic compound (I) of the present invention.

The solvent used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent. Preferably, the solvent is an aliphatic hydrocarbon such as hexane, heptane, ligroin or petroleum ether. Hydrogens; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethyl formate, ethyl acetate, propyl acetate; Esters such as butyl acetate and diethyl carbonate; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; acetone, methyl ethyl ketone, methyl isobutyl ketone, isophorone, cyclohexane Ketones such as xanone; nitro compounds such as nitroethane and nitrobenzene; nitriles such as acetonitrile and isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2 −
Examples include amides such as pyrrolidone, N-methylpyrrolidinone, and hexamethyl phosphorotriamide; and sulfoxides such as dimethyl sulfoxide and sulfolane. More preferred are amides, ethers and nitriles. , Most preferably amides. The base to be used is not particularly limited as long as it is used as a base in a usual reaction, but preferably, a metal iodide such as potassium iodide, sodium carbonate, potassium carbonate, lithium carbonate Alkali metal carbonates such as sodium hydrogen carbonate, potassium hydrogen carbonate and lithium hydrogen carbonate; alkali metal hydrides such as lithium hydride, sodium hydride and potassium hydride; Combinations with inorganic bases such as alkali metal hydroxides such as sodium, potassium hydroxide, barium hydroxide, lithium hydroxide or alkali metal fluorides such as sodium fluoride and potassium fluoride, or , N-methylmorpholine, triethylamine,
Tripropylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4- (N, N-dimethylamino) pyridine, 2,
6-di (t-butyl) -4-methylpyridine, quinoline, N, N-dimethylaniline, N, N-diethylaniline, 1,5-diazabicyclo [4.3.0] nona-5
-Ene (DBN), 1,4-diazabicyclo [2.2.
2] Organic bases such as octane (DABCO) and 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU), and more preferably, metal iodide and inorganic base And most preferably,
A combination of metal iodides and alkali metal bicarbonates. The reaction temperature is from 0 ° C. to 150 ° C.,
Preferably, it is between 20 ° C and 120 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually 30 minutes to 48 hours, preferably 1 hour to 12 hours.

[Method B]

[0094]

Embedded image

In the above formula, R ¹ , R ² , A, B, D, E,
G and L are as defined above. G ′ represents a corresponding group having one less carbon atom than “an alkylene group having 1 to 4 carbon atoms or an alkenylene group having 2 to 4 carbon atoms” in the definition of G.

[Method B] is a separate method for synthesizing the saturated heterocyclic compound (I) from the compound (VII).

Step B1 is an alcohol derivative (VI
By oxidizing I), the aldehyde derivative (VII)
This is a step of producing I), which is usually performed in a solvent in the presence of an oxidizing agent.

The oxidation reaction in this step is not particularly limited as long as it is an oxidation reaction for producing an aldehyde from a primary alcohol. For example, Collins oxidation carried out using pyridine and chromic acid in methylene chloride; ,
Pyridinium chlorochromat
e, PCC); PCC oxidation; pyridinium dichromate (methylene chloride)
PDC oxidation using PDC) in methylene chloride
Electrophiles (eg acetic anhydride, trifluoroacetic anhydride, thionyl chloride, sulfuryl chloride, oxalyl chloride, dicyclohexylcarbodiimide, diphenylketene-p-tolylimine, N, N-diethylaminoacetylene, N,
N-dimethylaminophenylacetylene, sulfur trioxide
Pyridine complex) and dimethyl sulfoxide (DMS
O), such as Swern oxidation, DMSO
Oxidation; and manganese dioxide oxidation using manganese dioxide in methylene chloride or benzene. Suitably Swern oxidation with oxalyl chloride and DMSO in methylene chloride. The reaction temperature is usually from -100 ° C to room temperature, preferably from -78 ° C to -20 ° C. The reaction time is usually 1
It is carried out for 0 minutes to 2 days, preferably for 10 minutes to 6 days.
Time.

Step B2 is a step of reacting the compound (VIII) with the compound (VI) by reductive amination to produce a saturated heterocyclic compound (I).

The solvent to be used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent. Preferably, alcohols such as methanol, ethanol and propanol, diethyl ether, Ethers such as tetrahydrofuran and dioxane can be mentioned. More preferably, it is an alcohol,
Most preferably, it is methanol or ethanol. The reducing agent to be used is not particularly limited as long as it is generally used as a reducing agent, but preferably, hydrogenating agents such as sodium cyanoborohydride, sodium borohydride, and lithium borohydride Boron alkali metal; lithium aluminum hydride, lithium hydride tri-tert-
Aluminum hydride compounds such as aluminum butoxide; sodium telluride hydride; hydride reagents such as di (isobutyl) aluminum hydride and organoaluminum hydride reducing agents such as bis (methoxyethoxy) aluminum sodium hydride; More preferably, it is an alkali metal borohydride, most preferably sodium cyanoborohydride.

The reaction is carried out at a temperature from -10 ° C to 100 ° C, preferably from room temperature to 80 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 10 minutes to 2 minutes.
Days, preferably 1 hour to 6 hours.

[Method C]

[0103]

Embedded image

In the above formula, R ² , D and G are as defined above.

R ⁹ represents a hydroxyl-protecting group, and is the same as the “hydroxyl-protecting group” in the definition of R ⁸ . [C
Method] is the same as in the above compound (II),

[0106]

Embedded image

Is a method for producing a compound having a 5-membered ring.

Step C1 is a step of oxidizing the exo-methylene group of the compound (IX) to a diol form with an oxidizing agent in a solvent to produce the compound (X).

The oxidizing agent to be used is not particularly limited as long as it is usually used in an oxidation reaction. Preferably, manganese oxides such as potassium permanganate and manganese dioxide; ruthenium oxide ( Ruthenium oxides such as IV); selenium compounds such as selenium dioxide; osmium tetroxide, potassium osmate dihydrate (K ₂ OsO _4.
Osmium compounds such as (2H ₂ O).
More preferably, it is a catalytic amount of osmium tetroxide and an oxidizing agent for reoxidizing osmium, such oxidizing agents include metal ferricyanides such as potassium ferricyanide; 4-methylmorpholine N-oxide N-oxides of amines such as; inorganic oxidizing agents such as persulfate compounds such as potassium persulfate and sodium persulfate; peroxides such as t-butyl hydroperoxide; t-butyl hypochlorite Examples of suitable hypochlorous acid compounds include nitrites such as methyl nitrite, and more preferred are metal ferricyanides and N-oxides of amines.

The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting materials to some extent. Preferably, aromatic solvents such as benzene, toluene and xylene; Halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as ether, tetrahydrofuran, dioxane and dimethoxyethane; amides such as dimethylformamide, dimethylacetamide and hexamethylphosphorotriamide; dimethyl sulfoxide Sulfoxides such as methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutanol, and t-butanol.
And alcohols such as isoamyl alcohol; esters such as ethyl acetate, propyl acetate, butyl acetate and diethyl carbonate; diluent acids such as sulfuric acid; diluent bases such as sodium hydroxide; water. Ketones such as acetone and methyl ethyl ketone; organic bases such as pyridine or nitriles such as acetonitrile, and the above-mentioned mixed solvents, and more preferably acetone or a mixed solvent of acetone-water.

The reaction is carried out at a temperature from -20 ° C to 80 ° C, preferably from -5 ° C to 50 ° C. The reaction time is
Although it depends mainly on the reaction temperature, the starting compound, the type of the reagent or the solvent used, it is usually 1 hour to 24 hours, preferably 2 hours to 12 hours. If desired, an optically active diol derivative having a specific absolute configuration can be produced by carrying out an asymmetric dihydroxylation reaction using an asymmetric ligand. Such an asymmetric dihydroxylation reaction is known, for example, from the method of Sharpless et al. (Chemical Review, Vol. 94, p. 2483 (1994)), and can be achieved by carrying out the reaction according to the method. .

For example, the oxidizing agent used in such a reaction is, for example, 0.0001 equivalent to 0.1 equivalent.
1 equivalent (preferably 0.001 equivalent to 0.005 equivalent) of osmium tetroxide and, as asymmetric ligands, hydroquinidine 1,4-phthalazinediyl diether ((DHQD) ₂ -PHAL), hydroquinidine
To reoxidize hydroquinidines such as 2,5-diphenyl-4,6-pyrimidinediyl diether ((DHQD) ₂ -PYR) (preferably (DHQD) ₂ -PHAL), and osmium Examples of the oxidizing agent include potassium ferricyanide and potassium carbonate.

The solvent used includes water and halogenated hydrocarbons such as methylene chloride and chloroform;
Ethers such as ether, tetrahydrofuran, dioxane, dimethoxyethane; dimethylformamide;
Amides such as dimethylacetamide and hexamethylphosphorotriamide; sulfoxides such as dimethylsulfoxide; methanol, ethanol, n-propanol, isopropanol, n-butanol and t-butanol. Alcohols such as toluene, isobutanol and isoamyl alcohol; ketones such as acetone and methyl ethyl ketone; esters such as ethyl acetate, propyl acetate, butyl acetate and diethyl carbonate or nitriles such as acetonitrile. A mixed solvent of water and an alcohol is preferable, and a mixed solvent of water and t-butanol is more preferable.

Further, the exo-methylene group of the compound (IX) is converted into thiirane according to a conventional method, followed by ring opening with a hydroxy ion to produce a compound (X) wherein D is a sulfur atom. Can be.

Step C2 converts a primary hydroxyl group of compound (X) into a leaving group in the presence of a base in the presence or absence of a solvent, and then converts the primary hydroxyl group in a solvent in the presence or absence of a catalyst. In this step, the compound is reacted with an azide reagent and converted into an azide group to produce a compound (XI).

The solvent to be used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent. Preferably, aromatic solvents such as benzene, toluene and xylene; Halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as ether, tetrahydrofuran, dioxane and dimethoxyethane or nitriles such as acetonitrile; formamide, N, N-dimethylformamide, N, N −
Dimethylacetamide, N-methyl-2-pyrrolidone,
Amides such as N-methylpyrrolidinone and hexamethylphosphorotriamide can be mentioned. More preferably, in the first-stage reaction, halogenated hydrocarbons and ethers are used, and in the second-stage reaction, And amides.

The first-stage reaction is carried out according to the second-stage process of Step A2 .

The reagent used in the subsequent reaction is not particularly limited as long as it is usually used for azidation, but is preferably a diarylphosphoric acid azide derivative such as diphenylphosphoric acid azide; trimethylsilyl azide; Examples thereof include trialkylsilyl azides such as triethylsilyl azide and alkali metal azides such as sodium azide, potassium azide and lithium azide, and more preferably alkali metal azide.

Examples of the catalyst used include trialkylsilyl triflates such as trimethylsilyl triflate and triethylsilyl triflate, and trifluoroborane etherates, Lewis such as aluminum chloride and zinc chloride. Acids can be mentioned.

The reaction temperature is between 20 ° C. and 180 ° C.
Preferably, it is 50 ° C to 150 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the reagent or the type of the solvent used, but is usually from 10 minutes to 24 hours, preferably from 30 minutes to 8 hours.

Step C3 is a step of reducing the azide group of compound (XI) in a solvent to produce an amino compound (XII).

The reduction method is not particularly limited as long as it is a reagent capable of reducing an azide group to an amino group. Preferably, the reduction method is carried out in an aqueous solvent (preferably, ethers such as tetrahydrofuran). Phosphine is used as a reducing agent at 20 ° C. to 150 ° C. (preferably 50 ° C. to 100 ° C.), usually for 15 minutes to 1 day (preferably 1 hour to 12 hours). Reaction, or using a catalyst such as palladium carbon, platinum, and Raney nickel, and using an alcohol such as methanol or ethanol.
Esters such as ethyl acetate, propyl acetate, butyl acetate and diethyl carbonate; ethers such as tetrahydrofuran and dioxane; fatty acids such as acetic acid; or a mixed solvent of these organic solvents with water (preferably Is an alcohol
It is a class. ), -10 ° C to 100 ° C (preferably,
0 ° C to 50 ° C. ) Is usually carried out for 1 hour to 4 days (preferably 2 hours to 2 days) by carrying out catalytic reduction.

Step C4 reacts the amino group and the DH group of compound (XII) with an aldehyde, ketone or acetal in the presence or absence of a solvent, in the presence or absence of an acid catalyst, In this step, an oxazolidine ring or a thiazolidine ring is formed to produce the compound (II).

Examples of the aldehyde used include formaldehyde, paraformaldehyde, and acetaldehyde. Examples of the ketones include acetone and cyclopropanone. Examples of the acetal include acetone. Dimethyl acetal and the like can be mentioned.

The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Preferably, the solvent is an aliphatic hydrocarbon such as hexane, heptane, ligroin or petroleum ether. Hydrogens; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethyl formate, ethyl acetate, propyl acetate; Esters such as butyl acetate and diethyl carbonate; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; acetone, methyl ethyl ketone, methyl isobutyl ketone, isophorone, cyclohexane Ketones such as xanone; nitro compounds such as nitroethane and nitrobenzene; nitriles such as acetonitrile and isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2 −
Amides such as pyrrolidone, N-methylpyrrolidinone, and hexamethyl phosphorotriamide; dimethyl sulfoxides and sulfoxides such as sulfolane; and more preferably, aromatic hydrocarbons, and most preferably, aromatic hydrocarbons. , Benzene and toluene.

The acid catalyst to be used is not particularly limited as long as it is used as an acid catalyst in a usual reaction, but is preferably hydrochloric acid, hydrobromic acid, sulfuric acid, perchloric acid,
Examples include inorganic acids such as phosphoric acid or Bronsted acids such as acetic acid, formic acid, oxalic acid, methanesulfonic acid, p-toluenesulfonic acid, camphorsulfonic acid, trifluoroacetic acid, and organic acids such as trifluoromethanesulfonic acid. , More preferably an organic acid, most preferably p-
It is toluenesulfonic acid.

The reaction is carried out at a temperature of from 50 ° C. to 200 ° C., preferably from 80 ° C. to 150 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 30 minutes to 4 minutes.
8 hours, preferably 1 hour to 12 hours.

[Method D]

[0129]

Embedded image

In the above formula, R ² , R ⁹ , D, E and G are
The meaning is as defined above.

R ¹⁰ represents a protecting group for a hydroxyl group, and is the same as the “protecting group in the reaction” in the definition of R ⁸ .

R ¹¹ represents a protecting group for an imino group, for example, the above “lower aliphatic acyl group”; the above “aromatic acyl group”; the above “lower alkoxycarbonyl group”; the above “alkenyloxycarbonyl group”; The "aralkyloxycarbonyl group"; or the "silyl group" can be mentioned, preferably a lower alkoxycarbonyl group, and more preferably tert-butoxycarbonyl.

[Method D] is based on the compound (II).
ring

[0134]

Embedded image

Is a method for producing a compound having a 6- to 8-membered ring.

Step D1 is a diol compound (X)
Is converted to a leaving group, and then substituted with an amino group of the amino alcohol compound (XIII). The resulting secondary amino group is protected with an R ¹¹ group to give the compound (XI
V).

The reaction for converting the primary hydroxyl group of the diol compound (X) into a leaving group is carried out in accordance with the subsequent reaction of Step A2 .

The compound obtained by converting the primary hydroxyl group of the diol compound (X) into a leaving group is converted to an amino alcohol compound (XII
The reaction of substituting with the amino group of I) is usually performed using a metal salt in a solvent. The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Examples thereof include aromatic hydrocarbons such as benzene, toluene and xylene; methylene chloride, chloroform, Halogenated hydrocarbons such as carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; acetone, methyl ethyl ketone, methyl Ketones such as isobutyl ketone, isophorone and cyclohexanone: nitriles such as acetonitrile, propionitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetate Bromide,
Examples include amides such as N-methyl-2-pyrrolidone, N-methylpyrrolidinone, and hexamethylphosphorotriamide. Preferably, it is a nitrile,
More preferably, it is acetonitrile. Examples of the metal salt used include metal perchlorates such as lithium perchlorate, magnesium perchlorate and sodium perchlorate; metal chlorides such as calcium chloride, zinc chloride and cobalt chloride; lithium tetrafluoroborate Metal tetrafluoroborate such as potassium tetrafluoroborate; zinc trifluoromethanesulfonate; Preferably it is a metal perchlorate, more preferably lithium perchlorate.

The reaction is carried out at a temperature of -20 ° C to 150 ° C, preferably room temperature to 100 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually 30 minutes to 2 days, preferably 2 hours to 1 day.

The secondary amino group at the subsequent stage is represented by R¹¹To protect the base
The process is performed as follows. <Method 1> General formula R¹¹A compound having -X or
General formula R¹¹-OR¹¹(R)¹¹Is an acyl group
In the above formula, R¹¹Is as defined above, and X is
Represents a group, and such a leaving group is usually a nucleophilic residue.
There is no particular limitation as long as it is a leaving group.
Halogen atoms such as iodine, bromine and iodine; methoxycarbo
Lower alcohols such as niloxy and ethoxycarbonyloxy
Alkoxycarbonyloxy group; chloroacetyloxy,
Dichloroacetyloxy, trichloroacetyloxy,
Halogenated alkyls such as trifluoroacetyloxy
Carbonyloxy group; methanesulfonyloxy, eta
Lower alkanesulfonyloxy such as sulfonyloxy
Xy group; trifluoromethanesulfonyloxy, penta
Halogeno lower such as fluoroethanesulfonyloxy
Alkanesulfonyloxy group; benzenesulfonyloxy
Si, p-toluenesulfonyloxy, p-nitrobenze
Arylsulfonyloxy such as sulfonyloxy
And more preferably a halogen atom,
Halogeno lower alkane sulfonyloxy group and ant
-Sulfonyloxy group. 1 to 4 equivalents (good
Suitably 2 to 3 equivalents) and the resulting compound in a solvent
In, in the presence or absence of a base, a method of reacting,<Method 2> General formula R¹¹-OH-containing compound (R¹¹
Is an acyl group) [In the above formula, R¹¹Has the same significance as described above. ] And generate
In a solvent in the presence of the above-mentioned "condensing agent"
A method of reacting in the presence or absence of a group.

<Method 3> In particular, when R ¹¹ is a tert-butoxycarbonyl group or a benzyloxycarbonyl group, the tert-butoxycarbonyl agent or the benzyloxycarbonylating agent and the resulting compound are dissolved in a solvent,
By reacting in the presence of a base, a secondary amino group can be protected with an R ¹¹ group.

The solvent used in <Method 1> is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, but is preferably an aliphatic carbon such as hexane or heptane. Hydrogens: benzene, toluene,
Aromatic hydrocarbons such as xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate, and diethyl carbonate Esters: ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; nitriles such as acetonitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N- Dimethylacetamide, N-methyl-2-pyrrolidone, N-
Amides such as methylpyrrolidinone and hexamethylphosphorotriamide can be mentioned. The base used in <Method 1> is not particularly limited as long as it is used as a base in a normal reaction.
Preferably, N-methylmorpholine, triethylamine,
Tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4- (N, N
Organic bases such as -dimethylamino) pyridine, 2,6-di (tert-butyl) -4-methylpyridine, quinoline, N, N-dimethylaniline and N, N-diethylaniline. In addition, 4- (N, N-dimethylamino) pyridine and 4-pyrrolidinopyridine can be used in combination with other bases in a catalytic amount.
In order to carry out the reaction effectively, quaternary ammonium salts such as benzyltriethylammonium chloride and tetrabutylammonium chloride, dibenzo-18-
Crown ethers such as crown-6 can also be added. The reaction is usually carried out at a temperature from -20 ° C to the reflux temperature of the solvent used, preferably from 0 ° C to room temperature. The reaction time mainly depends on the reaction temperature, the starting compound,
Although it depends on the type of the base or the solvent used, it is usually from 10 minutes to 3 days,
Hours to one day.

Specific examples of the compound having the general formula R ¹¹ -X include, for example, aliphatic acyl halides such as acetyl chloride, propionyl chloride, butyryl bromide, valeryl chloride, and hexanoyl chloride; methoxycarbonyl chloride, methoxycarbonyl bromide Ethoxycarbonyl chloride, propoxycarbonyl chloride, butoxycarbonyl chloride, lower alkoxycarbonyl halide such as hexyloxycarbonyl chloride or benzoyl chloride, benzoyl bromide, acyl halides such as arylcarbonyl halide such as naphthoyl chloride, tert-butyl Dimethylsilyl chloride, trimethylsilyl chloride, triethylsilyl chloride, triethylsilyl bromide, triisopropylsilyl chloride Chloride, dimethylisopropylsilyl chloride, diethylisopropylsilyl chloride,
Silyl halides such as tert-butyldiphenylsilyl chloride, diphenylmethylsilyl chloride, triphenylsilyl chloride or corresponding silyltrifluoromethanesulfonates, aralkyl halides such as benzyl chloride, benzyl bromide or pivaloyloxy Examples thereof include carbonyloxy lower alkyl halides such as methyl chloride and ethoxycarbonyloxymethyl chloride.

Specific examples of the compound having the general formula R ¹¹ —O—R ¹¹ include, for example, aliphatic carboxylic anhydrides such as acetic anhydride, propionic anhydride, valeric anhydride and hexanoic anhydride. In addition, mixed anhydrides such as formic acid and acetic acid can be used.

The solvent used in <Method 2> is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Hydrogens: benzene, toluene,
Aromatic hydrocarbons such as xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate, and diethyl carbonate Esters: ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; nitriles such as acetonitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N- Dimethylacetamide, N-methyl-2-pyrrolidone, N-
Amides such as methylpyrrolidinone and hexamethylphosphorotriamide can be mentioned. As the base used in <Method 2> , the same base as described in <Method 1> can be used. The reaction is carried out at a temperature of -20 ° C to 80 ° C, preferably 0 ° C to room temperature. The reaction time mainly depends on the reaction temperature,
Although it depends on the type of the starting compound, the reaction reagent or the solvent used, it is usually 10 minutes to 3 days, preferably
30 minutes to 1 day.

The solvent used in <Method 3> is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Hydrogens, benzene, toluene,
Aromatic hydrocarbons such as xylene, methylene chloride, chloroform, carbon tetrachloride, halogenated hydrocarbons such as dichloroethane, chlorobenzene, dichlorobenzene, ethyl formate, ethyl acetate, propyl acetate, butyl acetate, and diethyl carbonate Esters, diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, ethers such as diethylene glycol dimethyl ether, nitriles such as acetonitrile, isobutyronitrile, formamide, N, N-dimethylformamide, N, N- Dimethylacetamide, N-methyl-2-pyrrolidone, N-
Organic solvents such as amides such as methylpyrrolidinone and hexamethylphosphorotriamide; water; and mixed solvents of water and the above organic solvents. As the base used in <Method 3> , the same base as described in <Method 1> can be used. <Person
The tert-butoxycarbonylating agent used in the method 3> is preferably di-tert-butyl dicarbonate, 2- (tert-butoxycarbonyloxyimino)-
2-phenylacetonitrile, S- (4,6-dimethylpyrimidin-2-yl) thiolcarboxylic acid tert-butyl ester, 1,2,2,2-tetrachloroethyl
Tert-butyl carbonate and the like can be mentioned, and more preferably di-tert-butyl dicarbonate. <
Preferred examples of the benzyloxycarbonylating agent used in the method 3> include benzyloxycarbonyl chloride, benzyloxycarbonyl cyanide, dibenzyl dicarbonate and the like. The reaction temperature is from -20 ° C to 80 ° C, preferably,
0 ° C to room temperature. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually 10 minutes to 3 days, preferably 30 minutes.
Minutes to one day.

Step D2 performs a dehydration reaction from compound (XIV) by a Mitsunobu reaction, closes the ring, and forms compound (X
V).

The reagent used for the Mitsunobu reaction is not particularly limited as long as it can be used for the Mitsunobu reaction. Preferably, however, a reagent such as diethyl azodicarboxylate or diisopropyl azodicarboxylate is preferably used. Azo compounds such as lower alkyl azodicarboxylates or azodicarbonyls such as 1,1 '-(azodicarbonyl) dipiperidine and triarylphosphines such as triphenylphosphine or tri-n-butylphosphine. It is a combination of phosphines such as tri-lower alkyl phosphines, more preferably a combination of di-lower alkyl azodicarboxylates and triaryl phosphines, most preferably diethyl azodicarboxylate and triphenyl. It is a combination of phosphines. The solvent used is not particularly limited as long as it does not hinder the reaction and dissolves the starting material to some extent. Preferably, aromatic hydrocarbons such as benzene, toluene and xylene; methylene chloride, Halogenated hydrocarbons such as chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; esters such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate and diethyl carbonate; diethyl ether, diisopropyl ether
Ethers such as ter, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; nitriles such as acetonitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl Amides such as -2-pyrrolidone, N-methylpyrrolidinone, and hexamethyl phosphorotriamide; sulfoxides such as dimethyl sulfoxide and sulfolane; and aromatic hydrocarbons and ethers are preferable. It is. The reaction temperature is from -20 ° C to 100 ° C, preferably from 0 ° C to 50 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 10 minutes to 3 days, preferably from 30 minutes to 12 hours.

In the course of carrying out this step, R ⁹
Group and R ¹¹ group may be removed, in which case,
If desired, the imino group can be protected again with the R ¹¹ group according to the subsequent step of Step D1 , and the hydroxyl group can be protected again with the R ⁹ group according to any of the following methods. .

<Method 1> A compound having the general formula R ⁹ —X or a compound having the general formula R ⁹ —O—R ⁹ (R
^In the case where ⁹ is an acyl group, wherein R ⁹ has the same meaning as described above,
"Silyl group", most preferably a tert-butyldimethylsilyl group. X represents a leaving group, and such a leaving group is not particularly limited as long as it is a group capable of leaving as a nucleophilic residue, and preferably, such as chlorine, bromine, and iodine. Halogen atoms; lower alkoxycarbonyloxy groups such as methoxycarbonyloxy and ethoxycarbonyloxy; halogenated alkylcarbonyloxy groups such as chloroacetyloxy, dichloroacetyloxy, trichloroacetyloxy and trifluoroacetyloxy; methanesulfonyloxy, ethane Lower alkane sulfonyloxy groups such as sulfonyloxy; halogeno lower alkane sulfonyloxy groups such as trifluoromethanesulfonyloxy and pentafluoroethanesulfonyloxy; benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfo Ants, such as aryloxy - can be exemplified Le sulfonyloxy group, more preferably a halogen atom, a lower alkanesulfonyloxy group, and, ants - a le sulfonyloxy group. 1 to 4 equivalents (preferably 2 to 3 equivalents)
A method of reacting in a solvent in the presence or absence of a base.

<Method 2> Compound having the general formula R ⁹ —OH (when R ⁹ is an acyl group) [In the above formula, R ⁹ has the same meaning as described above. And a solvent in the presence of the above-mentioned “condensing agent”, in the presence or absence of a base.

<Method 3> Compound having the general formula R ⁹ —OH (when R ⁹ is an acyl group) [In the above formula, R ⁹ has the same meaning as described above. And a base in the presence of a dialkyl halide, such as diethyl chloride phosphate, and a base in a solvent.

The method is performed according to any one of the above methods.

The solvent used in <Method 1> is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent, but is preferably an aliphatic carbon such as hexane or heptane. Hydrogens: benzene, toluene,
Aromatic hydrocarbons such as xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate, and diethyl carbonate Esters: ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; nitriles such as acetonitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N- Dimethylacetamide, N-methyl-2-pyrrolidone, N-
Methyl pyrrolidinone, amides such as hexamethyl phosphorotriamide can be mentioned, more preferably,
Amides. The base used in <Method 1> is not particularly limited as long as it is used as a base in a usual reaction, but is preferably N-methylmorpholine, triethylamine, tributylamine, diisopropylethylamine, dicyclohexyl. Amine, N
-Methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4- (N, N-dimethylamino) pyridine, 2,6-di (tert-butyl) -4-methylpyridine, imidazole, quinoline, N, N- Organic bases such as dimethylaniline and N, N-diethylaniline can be mentioned, and more preferably, triethylamine and 4- (N, N-dimethylamino) pyridine. still,
4- (N, N-dimethylamino) pyridine and 4-pyrrolidinopyridine can be used in combination with other bases in a catalytic amount, and in order to make the reaction run effectively,
Quaternary ammonium salts such as benzyltriethylammonium chloride and tetrabutylammonium chloride, and crown ethers such as dibenzo-18-crown-6 can also be added. The reaction temperature is usually from -20 ° C to 100 ° C.
-10 ° C to 50 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound, the base used or the type of the solvent used, but is usually from 10 minutes to 1 day, preferably from 30 minutes to 10 hours.

Specific examples of the compound having the general formula R ⁹ -X include, for example, aliphatic acyl halides such as acetyl chloride, propionyl chloride, butyryl bromide, valeryl chloride, and hexanoyl chloride; methoxycarbonyl chloride, methoxycarbonyl bromide ,
Acyl halides such as ethoxycarbonyl chloride, propoxycarbonyl chloride, butoxycarbonyl chloride, lower alkoxycarbonyl halides such as hexyloxycarbonyl chloride or arylcarbonyl halides such as benzoyl chloride, benzoyl bromide and naphthoyl chloride, t-butyldimethyl Silyl chloride, trimethylsilyl chloride, triethylsilyl chloride, triethylsilyl bromide, triisopropylsilyl chloride, dimethylisopropylsilyl chloride, diethylisopropylsilyl chloride,
Silyl halides such as t-butyldiphenylsilyl chloride, diphenylmethylsilyl chloride, triphenylsilyl chloride or corresponding silyltrifluoromethanesulfonates, aralkyl halides such as benzyl chloride, benzyl bromide or pivaloyloxy Examples thereof include carbonyloxy lower alkyl halides such as methyl chloride and ethoxycarbonyloxymethyl chloride.

Specific examples of the compound having the general formula R ⁹ —O—R ⁹ include, for example, aliphatic carboxylic anhydrides such as acetic anhydride, propionic anhydride, valeric anhydride and hexanoic anhydride. Alternatively, mixed acid anhydrides such as formic acid and acetic acid can be used.

The solvent used in <Method 2> is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Hydrogens: benzene, toluene,
Aromatic hydrocarbons such as xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate, and diethyl carbonate Esters: ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; nitriles such as acetonitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N- Dimethylacetamide, N-methyl-2-pyrrolidone, N-
Amides such as methylpyrrolidinone and hexamethylphosphorotriamide can be mentioned. As the base used in <Method 2> , the same base as described in <Method 1> can be used. The reaction is carried out at a temperature of -20 ° C to 80 ° C, preferably 0 ° C to room temperature. The reaction time mainly depends on the reaction temperature,
Although it depends on the type of the starting compound, the reaction reagent or the solvent used, it is usually 10 minutes to 3 days, preferably
30 minutes to 1 day.

The solvent used in <Method 3> is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Preferably, the solvent is an aliphatic carbon such as hexane or heptane. Hydrogens: benzene, toluene,
Aromatic hydrocarbons such as xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate, and diethyl carbonate Esters: ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; nitriles such as acetonitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N- Dimethylacetamide, N-methyl-2-pyrrolidone, N-
Amides such as methylpyrrolidinone and hexamethylphosphorotriamide can be mentioned. As the base used in <Method 3> , the same base as described in <Method 1> can be used. The reaction is carried out at a temperature from 0 ° C. to the reflux temperature of the solvent used, preferably from room temperature to 50 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 10 minutes to 3 minutes.
Days, preferably 30 minutes to 1 day.

Step D3 is a compound represented by the formula ( ¹¹ )
This is a step of producing a compound (II) by removing a group.

The removal of the R ¹¹ group depends on its type, but is generally carried out by a method well known in the art as follows. When R ¹¹ is a silyl group, it is usually removed by treating with a compound generating a fluorine anion such as tetrabutylammonium fluoride. The reaction solvent is not particularly limited as long as it does not inhibit the reaction, but ethers such as tetrahydrofuran and dioxane are preferable. The reaction temperature and reaction time are
Although not particularly limited, the reaction is usually performed at room temperature for 10 minutes to 18 hours.

When R ¹¹ is an aliphatic acyl group, an aromatic acyl group, an alkoxycarbonyl group or a substituted methylene group forming a Schiff base, treatment with an acid or a base in the presence of a solvent. Can be removed. The acid to be used is not particularly limited as long as it does not inhibit the reaction, and is not particularly limited as long as it does not inhibit the reaction. Preferably, an inorganic acid such as hydrochloric acid, sulfuric acid, phosphoric acid, or hydrobromic acid is used. Alternatively, a Lewis acid such as B-bromocatecholborane is used, and more preferably, hydrochloric acid or B-bromocatecholborane. The solvent used in the reaction with the acid is not particularly limited as long as it is used in a usual hydrolysis reaction, and examples thereof include aromatic hydrocarbons such as benzene, toluene and xylene; methylene chloride, Chloroform, carbon tetrachloride, dichloroethane,
Halogenated hydrocarbons such as chlorobenzene and dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; nitrated hydrocarbons such as nitroethane and nitrobenzene Can be mentioned. Preferred are aromatic hydrocarbons and halogenated hydrocarbons.

The base to be used is not particularly limited as long as it does not affect the other parts of the compound, but is preferably a metal alkoxide such as sodium methoxide, sodium carbonate, potassium carbonate, or the like. Alkali metal carbonates such as lithium carbonate, alkali metal hydroxides such as sodium hydroxide, potassium hydroxide and lithium hydroxide or ammonia such as aqueous ammonia and concentrated ammonia-methanol are used. It should be noted that isomerization may occur in hydrolysis with a base. The solvent used in the reaction with the base is not particularly limited as long as it is used in a usual hydrolysis reaction. Water; alcohols such as methanol, ethanol and n-propanol -Such as alcohols, tetrahydrofuran and dioxane
An organic solvent such as ters or a mixed solvent of water and the above organic solvent is preferable. The reaction temperature and reaction time vary depending on the starting material, the solvent and the acid or base used, and are not particularly limited. However, in order to suppress a side reaction, the reaction is usually performed at 0 to 150 ° C. for 1 to 10 hours. You.

When R ¹¹ is an aralkyl group or an aralkyloxycarbonyl group, it is usually removed by contacting with a reducing agent in a solvent (preferably catalytic reduction at room temperature under a catalyst). Alternatively, a method of removing using an oxidizing agent is preferable. The solvent used in the removal by catalytic reduction is not particularly limited as long as it does not participate in the present reaction, but alcohols such as methanol, ethanol and isopropanol, diethyl ether, Ethers such as tetrahydrofuran and dioxane, aromatic hydrocarbons such as toluene, benzene and xylene;
Hexane, aliphatic hydrocarbons such as cyclohexane,
Esters such as ethyl acetate and propyl acetate, fatty acids such as acetic acid, and mixed solvents of these organic solvents and water are preferred. The catalyst to be used is not particularly limited as long as it is usually used for a catalytic reduction reaction.
Preferably, palladium carbon, Raney nickel, platinum oxide, platinum black, rhodium-aluminum oxide, triphenylphosphine-rhodium chloride, and palladium-barium sulfate are used. The pressure is not particularly limited, but it is usually 1 to 10 atm. The reaction temperature and reaction time vary depending on the starting material, the type of the solvent and the catalyst, and the like.
Performed at 0 to 100 ° C. for 5 minutes to 24 hours.

The solvent used in the removal by oxidation is not particularly limited as long as it does not participate in the present reaction, but is preferably a water-containing organic solvent. Suitable examples of such organic solvents include ketones such as acetone, methylene chloride, chloroform, halogenated hydrocarbons such as carbon tetrachloride, nitriles such as acetonitrile, diethyl ether, tetrahydrofuran, and dioxane. And ethers, amides such as dimethylformamide, dimethylacetamide and hexamethylphosphorotriamide, and sulfoxides such as dimethylsulfoxide. The oxidizing agent to be used is not particularly limited as long as it is a compound used for oxidation, but is preferably potassium persulfate, sodium persulfate, ammonium cerium nitrate (CAN), 2,3-
Dichloro-5,6-dicyano-p-benzoquinone (DD
Q) is used. The reaction temperature and reaction time vary depending on the starting material, solvent, type of catalyst and the like, but are usually carried out at 0 to 150 ° C. for 10 minutes to 24 hours.

When R ¹¹ is an alkenyloxycarbonyl group, the protecting group for the amino group is usually the above-mentioned aliphatic acyl group, aromatic acyl group, alkoxycarbonyl group or a substituted methylene group forming a Schiff base. It is achieved by treating with a base in the same manner as in the removal reaction in some cases.

In the case of allyloxycarbonyl, the removal method using palladium and triphenylphosphine or nickel tetracarbonyl is particularly simple and can be carried out with few side reactions.

[Method E]

[0168]

Embedded image

In the above formula, R ² , R ⁹ , D and G are as defined above.

X ′ and X ″ represent the same groups as in the definition of Y.

E ′ is an “alkylene group having 1 to 4 carbon atoms which may be substituted by a halogen atom” in the definition of E, or “3 to 8 carbon atoms containing a cycloalkane ring having 3 to 6 carbon atoms”. And a corresponding group having one less carbon atom than "alkylene groups".

[Method E] is the same as Compound [I], as in Method D.
In I), the ring

[0173]

Embedded image

Is a method for producing a compound having a 6- to 8-membered ring.

Step E1 is to react an amino group of compound (XII) with compound (XVI) in a solvent in the presence of a base, perform acylation, and then carry out alkylation to DH group. To form a cyclic amide, and the compound (X
VII).

In the acylation in the first step, the solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Preferably, it is an aliphatic solvent such as hexane or heptane. Hydrocarbons; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethyl formate, ethyl acetate and propyl acetate Esters such as acetic acid, butyl acetate and diethyl carbonate; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; nitriles such as acetonitrile and isobutyronitrile;
Formamide, N, N-dimethylformamide, N, N
Amides such as -dimethylacetamide, N-methyl-2-pyrrolidone, N-methylpyrrolidinone, and hexamethylphosphorotriamide. The base to be used is not particularly limited as long as it is used as a base in a normal reaction.
N-methylmorpholine, triethylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine, pyridine, 4-pyrrolidinopyridine, picoline, 4- (N, N-dimethylamino) pyridine, 2,6-di (tert -Butyl) -4-methylpyridine, quinoline, N, N-dimethylaniline,
Organic bases such as N, N-diethylaniline can be mentioned. In addition, 4- (N, N-dimethylamino) pyridine and 4-pyrrolidinopyridine can be used in combination with other bases in a catalytic amount. Dehydrating agents such as sieves, quaternary ammonium salts such as benzyltriethylammonium chloride, tetrabutylammonium chloride, crown ethers such as dibenzo-18-crown-6, 3,4-dihydro-2H-pyrido [1 ,
2-a] An acid scavenger such as pyrimidin-2-one can also be added. Reaction temperature is -20 ° C to 80 ° C
The temperature is preferably 0 ° C. to room temperature. The reaction time depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 10 minutes to 3 days, preferably from 30 minutes to 1 day.

In the case of the carboxylic acid derivative in which the X ″ group of the compound (XVI) represents a hydroxyl group, the compound is reacted with the above-mentioned “condensing agent” in the above-mentioned solvent in the presence or absence of the above-mentioned base. Can also be achieved.

The solvent used in the subsequent alkylation reaction is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent, but is preferably a solvent such as benzene, toluene and xylene. Aromatic hydrocarbons; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, and dichlorobenzene; diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane,
Ethers such as dimethoxyethane and diethylene glycol dimethyl ether; nitriles such as acetonitrile, propionitrile and isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2 -Pyrrolidone, N
-Amides such as methylpyrrolidinone and hexamethylphosphorotriamide; sulphoxides such as dimethylsulfoxide and sulfolane; more preferably, ethers and amides; most preferably, Tetrahydrofuran and N, N-dimethylformamide. The base used is not particularly limited as long as it is used as a base in a usual reaction, but preferably, alkali metal carbonates such as sodium carbonate, potassium carbonate and lithium carbonate; sodium hydrogen carbonate Alkali metal hydrogencarbonates such as potassium, hydrogencarbonate and lithium hydrogencarbonate; alkali metal hydrides such as lithium hydride, sodium hydride and potassium hydride; sodium hydroxide, potassium hydroxide, barium hydroxide, water Alkali metal hydroxides such as lithium oxide; inorganic bases such as alkali metal fluorides such as sodium fluoride and potassium fluoride; sodium methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, potassium Alkali metal alkoxy such as t-butoxide and lithium methoxide There may be mentioned earth, more preferably, an alkali metal hydrides and alkali metal alkoxides. The reaction temperature is from -20 ° C to 100 ° C, preferably from 0 ° C to 50 ° C.
It is. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 10 minutes to 24 hours, preferably from 30 minutes to 12 hours.

Step E2 is a step in which the amide group of compound (XVII) is reduced to an imino group using a reducing agent in a solvent to produce compound (II).

The solvent to be used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent. Preferably, aromatic solvents such as benzene, toluene and xylene; Methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene,
Halogenated hydrocarbons such as dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, and diethylene glycol dimethyl ether; and more preferably, ether And most preferably, diethyl ether and tetrahydrofuran. The reducing agent to be used is not particularly limited as long as it is usually used as a reducing agent, but is preferably an alkali metal borohydride such as sodium borohydride or lithium borohydride; Aluminum hydride compounds such as lithium aluminum and lithium tri-tert-butoxide aluminum; sodium tellurium hydride; organoaluminum hydride reducing agents such as di (isobutyl) aluminum hydride and bis (methoxyethoxy) aluminum sodium hydride And hydride reagents such as borane-dimethylsulfide complex and borane-tetrahydrofuran complex. More preferably, they are aluminum hydride compounds and boron-based reducing agents. , A boron-based reducing agent, most suitable Is a borane-dimethyl sulfide complex. The reaction is carried out at a temperature of -78 ° C to 150 ° C, preferably -20 ° C to 100 ° C.
The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 5 minutes to 24 hours, preferably from 10 minutes to 2 hours.

[0181] In the present process, may R ⁹ groups are removed, in which case, optionally, the Step
The hydroxyl group can be protected again with the R ⁹ group in the same manner as in <Method 1> to <Method 3> of D2 .

[Method F]

[0183]

Embedded image

In the above formula, R ² , R ⁹ and G are as defined above.

[Method F] is a method for producing compound (IX) which is a raw material compound in the above [Method C].

Step F1 is a reaction between compound (XVIII) and metallic magnesium according to a conventional method to produce a Grignard reagent, and then cross-coupling of the Grignard reagent and compound (XIX) using a palladium catalyst or a nickel catalyst. In this step, the reaction is carried out to produce compound (IX).

The palladium catalyst to be used is not particularly limited as long as it is a catalyst containing palladium, but is preferably tetrakis (triphenylphosphine) palladium (0), bis (triphenylphosphene) palladium (II) chloride. ), Bis (acetonitrile) palladium (I
I) chloride, [1,1′-bis (diphenylphosphino) ferrocene] palladium (II) chloride, tris (dibenzylideneacetone) dipalladium (0),
[1,2-bis (diphenylphosphino) ethane] dichloropalladium (II) and palladium acetate can be mentioned. The nickel catalyst to be used is not particularly limited as long as it is a catalyst containing nickel, but is preferably bis (triphenylphosphine) nickel (II) chloride,
[1,3-bis (diphenylphosphino) propanedichloronickel (II) and nickel (II) acetylacetonate.

The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. And ethers such as dimethyl ether, and more preferably diethyl ether or tetrahydrofuran.

The reaction is carried out at a temperature of 0 ° C. to 120 ° C., preferably room temperature to 80 ° C.

The reaction time depends mainly on the reaction temperature, the starting materials, the reaction reagents and the type of the solvent used, but is usually from 10 minutes to 24 hours, preferably from 30 minutes to 5 hours. [Method G]

[0191]

Embedded image

In the above formula, R ² and G ′ have the same meaning as described above.

W represents the same group as the group in the definition of Y.

W may form a single bond together with R ¹² , in which case the compound (XXI) is an acid anhydride.

R ¹² represents a carboxy-protecting group, and represents a “protecting group in the reaction” which can be cleaved by a chemical method such as hydrogenolysis, hydrolysis, electrolysis, or photolysis.
As the “protecting group in the reaction”, preferably, the “lower alkyl group”; the “lower alkenyl group”; the “lower alkynyl group”; the “halogeno lower alkyl group”; and the hydroxy “lower alkyl group” "Aliphatic acyl" such as acetylmethyl- "lower alkyl";
The “aralkyl group” in the definition of the “ester” thereof; the “silyl group” can be mentioned. [G
Method] is a method for producing a compound in which the G group has 3 or 4 carbon atoms in the compound (IX).

Step G1 is a reaction between the compound (XX) and the acid derivative (XXI) by a Friedel-Crafts reaction in the presence or absence of a solvent in the presence of a Lewis acid. When XXI) is an acid anhydride,
If desired, the resulting free carboxylic acid is esterified with an R ¹² group, and then the carbonyl group is converted to an exomethylene group by a Wittig reaction in a solvent in the presence of a base to produce compound (XXII). It is a process.

The Lewis acid used in the former Friedel-Crafts reaction is not particularly limited as long as it is generally used as a Lewis acid.
Tri-lower alkylsilyl trifluoromethanesulfonates such as trimethylsilyltrifluoromethanesulfonate, aluminums such as aluminum chloride and aluminum bromide, tins such as tin tetrachloride, zincs such as zinc bromide, titanium tetrachloride Titanium or a perchloric acid such as trimethylsilyl perchlorate and triphenylmethyl perchlorate, more preferably aluminum and titanium, and particularly preferably aluminum chloride and bromide. Aluminum.

The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting materials to some extent. Preferably, aromatic solvents such as benzene, toluene and xylene; Methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene,
Halogenated hydrocarbons such as dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; and nitro compounds such as nitroethane and nitrobenzene. And more preferably halogenated hydrocarbons.

The reaction is carried out at a temperature of from -10 ° C to 150 ° C, preferably from 0 ° C to 100 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually 30 minutes to 24 hours, preferably 1 hour to 12 hours.

In the middle stage of esterification, when such a reaction belongs to alkylation, the carboxylic acid can be esterified by treating with any of the following methods.

<Method 1> Compound having the general formula R ¹² —W ′ (wherein R ¹² has the same meaning as described above, and W ′
Is a halogen atom such as, for example, chlorine, bromine, iodine;
Lower alkanesulfonyloxy groups such as methanesulfonyloxy and ethanesulfonyloxy; halogeno lower alkanesulfonyloxy groups such as trifluoromethanesulfonyloxy and pentafluoroethanesulfonyloxy; benzenesulfonyloxy, p-toluenesulfonyloxy, p-nitrobenzenesulfonyl It represents a group leaving as a nucleophilic residue, such as an arylsulfonyloxy group such as oxy. ) And a solvent (the solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Preferably, aliphatic hydrocarbons such as hexane and heptane are used. Aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; diethyl ether, diisopropyl ether, tetrahydrofuran; Ethers such as dioxane, dimethoxyethane and diethylene glycol dimethyl ether; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone, isophorone and cyclohexanone; nitriles such as acetonitrile and isobutyronitrile; formamide, N, N- The Chill formamide, N, N- dimethylacetamide, N- methyl -
Examples include amides such as 2-pyrrolidone, N-methylpyrrolidinone, and hexamethylphosphorotriamide. ), In the presence of a base (as the base used,
There is no particular limitation as long as it is used as a base in a normal reaction, but preferably, alkali metal carbonates such as sodium carbonate, potassium carbonate, and lithium carbonate; sodium hydrogen carbonate, potassium hydrogen carbonate, and hydrogen carbonate Alkali metal bicarbonates such as lithium; alkali metal hydrides such as lithium hydride, sodium hydride, potassium hydride; alkali metals such as sodium hydroxide, potassium hydroxide, barium hydroxide, lithium hydroxide Hydroxides; inorganic bases such as alkali metal fluorides such as sodium fluoride and potassium fluoride; sodium methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, potassium tert-butoxide, lithium methoxide Metal alkoxides such as methyl mercap Mercaptans alkali metals such as emissions sodium, ethyl mercaptan sodium; N- methylmorpholine, triethylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N- methylpiperidine, pyridine, 4-
Pyrrolidinopyridine, picoline, 4- (N, N-dimethylamino) pyridine, 2,6-di (tert-butyl) -4
-Methylpyridine, quinoline, N, N-dimethylaniline, N, N-diethylaniline, 1,5-diazabicyclo [4.3.0] non-5-ene (DBN), 1,4-
Diazabicyclo [2.2.2] octane (DABC
O), organic bases such as 1,8-diazabicyclo [5.4.0] undec-7-ene (DBU) or organic metal bases such as butyllithium, lithium diisopropylamide, lithium bis (trimethylsilyl) amide Can be mentioned. ), Usually from -20 ° C to 12
A method of reacting at 0 ° C. (preferably 0 to 80 ° C.) for 0.5 to 10 hours.

<Method 2> Compound having the general formula R ¹² —OH [wherein R ¹² has the same meaning as described above. ]When,
A method of reacting with the above-mentioned "condensing agent" in a solvent in the presence or absence of a base.

The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Preferably, the solvent is an aliphatic hydrocarbon such as hexane or heptane; Aromatic hydrocarbons such as toluene and xylene; methylene chloride, chloroform,
Halogenated hydrocarbons such as carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; esters such as ethyl formate, ethyl acetate, propyl acetate, butyl acetate and diethyl carbonate; diethyl ether, diisopropyl ether, tetrahydrofuran; Ethers such as dioxane, dimethoxyethane and diethylene glycol dimethyl ether; nitriles such as acetonitrile and isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide;
Examples include amides such as N-methyl-2-pyrrolidone, N-methylpyrrolidinone, and hexamethylphosphorotriamide.

The base to be used is not particularly limited as long as it is used as a base in a usual reaction, but is preferably N-methylmorpholine, triethylamine, tributylamine, diisopropylethylamine, dicyclohexylamine, N-methylpiperidine,
Pyridine, 4-pyrrolidinopyridine, picoline, 4-
(N, N-dimethylamino) pyridine, 2,6-di (te
rt-butyl) -4-methylpyridine, quinoline, N, N
Organic bases such as -dimethylaniline and N, N-diethylaniline.

It is to be noted that 4- (N, N-dimethylamino) pyridine and 4-pyrrolidinopyridine may be used in combination with other bases in a catalytic amount. , Dehydrating agents such as molecular sieves, quaternary ammonium salts such as benzyltriethylammonium chloride, tetrabutylammonium chloride, crown ethers such as dibenzo-18-crown-6, 3,4-dihydro-2H- Pyrido [1,
2-a] An acid scavenger such as pyrimidin-2-one can also be added.

The reaction is carried out at a temperature from -20 ° C to 80 ° C, preferably from 0 ° C to room temperature. The reaction time is
Although it depends mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, it is usually from 10 minutes to 3 days, preferably from 30 minutes to 1 day.

<Method 3> When the protecting group is a lower alkyl group, it is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent in a solvent. Alcohols such as hexane and heptane; aromatic hydrocarbons such as benzene, toluene and xylene; methylene chloride, chloroform,
Halogenated hydrocarbons such as carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; acetone;
Ketones such as methyl ethyl ketone, methyl isobutyl ketone, isophorone and cyclohexanone; nitriles such as acetonitrile and isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone , N-
Amides such as methylpyrrolidinone and hexamethylphosphorotriamide can be mentioned, and are preferably the same alcohol as the reagent. ), In the presence of an acid catalyst (there is no particular limitation as long as it is used as an acid catalyst in a normal reaction, but preferably, such as hydrogen chloride, hydrobromic acid, sulfuric acid, perchloric acid, and phosphoric acid). Inorganic acid or Brönsted acid such as acetic acid, formic acid, oxalic acid, methanesulfonic acid, organic acid such as paratoluenesulfonic acid, trifluoroacetic acid, trifluoromethanesulfonic acid or boron trichloride, boron trifluoride, boron tribromide And a corresponding alcohol such as methanol, ethanol, propanol and butanol, and 0 ° C to 15 ° C.
The reaction is carried out at 0 ° C. (preferably 50 ° C. to 100 ° C.) for 10 minutes to 24 hours (preferably 30 minutes to 5 hours).

The reagents used in the latter Wittig reaction are not particularly limited as long as they are usually used in the Wittig reaction. Preferably, methyltriphenylphosphonium bromide, methyltriphenyl iodide are used. Methyltriphenylphosphonium halides such as phosphonium. The solvent used is not particularly limited as long as it does not hinder the reaction and dissolves the starting material to some extent, but is preferably aromatic hydrocarbons such as benzene, toluene and xylene; methylene chloride, Chloroform, carbon tetrachloride, dichloroethane, chlorobenzene,
Halogenated hydrocarbons such as dichlorobenzene; ethers such as diethyl ether, diisopropyl ether and tetrahydrofuran; nitriles such as acetonitrile and isobutyronitrile; formamide, dimethylformamide, dimethylacetamide, hexa Examples include amides such as methyl phosphorotriamide; sulfoxides such as dimethyl sulfoxide and sulfolane, more preferably aromatic hydrocarbons, and most preferably benzene. The base used is not particularly limited as long as it is used as a base in a usual reaction, but preferably, sodium carbonate,
Alkali metal carbonates such as potassium carbonate and lithium carbonate; alkali metal hydrogen carbonates such as sodium hydrogen carbonate, potassium hydrogen carbonate and lithium hydrogen carbonate; alkali metal hydrogen such as lithium hydride, sodium hydride and potassium hydride Alkali metal hydroxides such as sodium hydroxide, potassium hydroxide, barium hydroxide and lithium hydroxide; inorganic bases such as alkali metal fluorides such as sodium fluoride and potassium fluoride; sodium Methoxide, sodium ethoxide, potassium methoxide, potassium ethoxide, potassium t-butoxide,
Examples thereof include alkali metal alkoxides such as lithium methoxide, more preferably alkali metal hydrides and alkali metal alkoxides, and most preferably alkali metal alkoxides. The reaction is carried out at a temperature of -20 ° C to 100 ° C, preferably 0 ° C.
C. to 50.degree. The reaction time depends mainly on the reaction temperature, the starting compound, the solvent used or the type of the base used, but is usually from 10 minutes to 24 hours, preferably from 30 minutes to 12 hours.

Step G2 is an ester compound (XX
The carboxyl group of II) is subjected to a reduction reaction using a reducing agent in a solvent to convert it into a primary hydroxyl group, and then, this hydroxyl group is protected with an R ⁹ group to produce a compound (IX). is there.

The reducing agent used in the first-stage reduction reaction is not particularly limited as long as it is generally used as a reducing agent. Preferably, such reducing agents as sodium borohydride and lithium borohydride are used. Alkali metal borohydride; aluminum hydride compounds such as lithium aluminum hydride and lithium tri-tert-butoxide aluminum; sodium tellurium hydride; di (isobutyl) aluminum hydride, bis (methoxyethoxy) aluminum sodium hydride Hydride reagents such as organoaluminum hydride-based reducing agents can be used. More preferred are aluminum hydride compounds and organoaluminum hydride-based reducing agents, and most preferred are aluminum hydride compounds.

The solvent used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent, but is preferably an aromatic hydrocarbon such as benzene, toluene or xylene; Methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene,
Halogenated hydrocarbons such as dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, and diethylene glycol dimethyl ether; and more preferably, ether And most preferably, diethyl ether and tetrahydrofuran. The reaction is carried out at a temperature of -78 ° C to 50 ° C, preferably -20 ° C to 20 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 5 minutes to 24 hours, preferably from 10 minutes to 2 hours.

The protection reaction at the subsequent R ⁹ group is carried out according to the above-mentioned Ste.
or <Method 1> of p D2 are carried out according to <Method 3>.

[Method H]

[0214]

Embedded image

In the above formula, R ² has the same meaning as described above.

R ¹³ represents a protecting group for a carboxy group;
The same groups as the groups in the definition of ¹² are shown. R ¹⁴ is
The term "lower alkyl group" refers to such a group, preferably, methyl, ethyl, propyl, isopropyl and the like. The two R ¹⁴ groups may together represent a lower alkylene group, and such groups preferably include methylene, ethylene, trimethylene and the like. R ¹⁵ represents a hydroxyl-protecting group, and is the same as the group in the definition of R ⁹ . W '' is
It represents a halogen atom, and is preferably a chlorine atom.

[Method H] is a method for producing a compound (XXVII) in which the G group has 2 carbon atoms in the above compound (IX).

Step H1 is a step of producing a β-ketoester derivative (XXIV) from the compound (XXIII). For example, the method of J. Wemple et al. (Synthesis, 290)
(1993)).

Step H2 is an alcohol having the β-ketoester derivative (XXIV) and the formula R ¹⁴ —OH (where R ¹⁴ has the same meaning as described above), the formula HO—R ¹⁴ ′ —O
An alkanediol having H (wherein R ¹⁴ ′ represents a lower alkylene group formed by two R ¹⁴ groups together), or a compound of the formula (R ¹⁴ —O) ₃ CH, wherein R ¹⁴ is A ketal (XXV) by reacting with an orthoformate having the same meaning as described above). The reaction is performed, for example, in an alcohol or alkanediol.
It is carried out by heating in the presence or absence of an acid catalyst.

Examples of the alcohol having the formula R ¹⁴ -OH include methanol, ethanol, propanol and isopropanol. Preferably it is ethanol. The alkanediol having the formula HO-R ¹⁴ '-OH, such as ethylene glycol and propylene glycol. Formula (R ¹⁴ -O) (wherein, R ¹⁴ is. Showing the same meaning as defined above) ₃ CH The orthoformate ester with, can be, for example, trimethoxy methane, and triethoxymethane.

A preferred method is heating in ethanol in the presence of ethyl orthoformate using p-toluenesulfonic acid as a catalyst.

The reaction temperature is usually from 40 ° C. to 150 ° C., preferably from 50 ° C. to 100 ° C.

The reaction time varies depending mainly on the reaction temperature, the starting materials and the solvent used, but is usually from 30 minutes to 2 days, preferably from 2 hours to 12 hours.

Step H3 is a step of reducing the ester of the compound (XXV), deprotecting the ketal group, and then protecting the primary hydroxyl group with the R ¹⁵ group to produce the compound (XXVI).

[0225] The reaction of reducing the ester, Step G
The process is performed according to the previous step of No. 2 .

The deprotection of the ketal group is usually carried out in a solvent in the presence of an acid, preferably using trifluoroacetic acid in chloroform.

The reaction temperature is usually from -20 ° C to 100 ° C.
The temperature is preferably −10 ° C. to room temperature. The reaction time varies depending mainly on the reaction temperature, the starting materials and the solvent used, but is usually from 10 minutes to 1 day, preferably from 30 minutes to 2 hours.

[0228] to protect the primary hydroxyl group reaction, Step
This is performed according to <Method 1> to <Method 3> of D2 . Preferably, it is performed according to <Method 1>.

Step H4 converts the carbonyl group of compound (XXVI) into an exo-methylene group by a Wittig reaction in a solvent in the presence of a base to give compound (XXVI).
This is the step of manufacturing I). The reaction of this step is performed by the above St.
The reaction is performed according to the reaction in the latter stage of ep G1 .

[Method I]

[0231]

Embedded image

In the above formula, R ² and R ¹⁵ are as defined above.

[Method I] is a separate method for producing compound (XXVII).

Step I1 is described in Ito et al. (Bull. Chem.
Soc. Jpn., 64, 3746 (1991))
Compound (XVIII) is reacted with magnesium metal to produce a Grignard reagent according to a conventional method, and then in the presence or absence of a Lewis acid, in a catalytic amount (preferably 0.1 to 0). .5 equivalents) under palladium catalyst
In a solvent, the resulting carboxylic acid is coupled with diketene, and then the resulting carboxylic acid is subjected to a reaction according to a desired step of Step G1 , esterified, and the ester is reduced to protect a generated primary hydroxyl group. This is a method for producing compound (XXVII).

The Lewis acid used in the main step is not particularly limited as long as it is usually used as a Lewis acid, and the reaction is carried out in the presence of the Lewis acid, since the amount of by-products is small, and the yield is low. Although achieved at a high rate, preferably as a Lewis acid, tri-lower alkylsilyltrifluoromethanesulfonates such as trimethylsilyltrifluoromethanesulfonate, aluminums such as aluminum chloride, tins such as tin tetrachloride, zinc chloride, Zincs such as zinc bromide, titaniums such as titanium tetrachloride or perchloric acids such as trimethylsilyl perchlorate and triphenylmethyl perchlorate, more preferably zincs And most preferably zinc chloride. The palladium catalyst used is
There is no particular limitation as long as the catalyst contains palladium,
Preferably, organophosphorus palladium such as bis (triphenylphosphine) palladium chloride can be mentioned. The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent.
Preferred are ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether, and more preferred is diethyl ether. The reaction is carried out at a temperature of -20 ° C to 50 ° C, preferably 0 ° C to 20 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reaction reagent or the type of the solvent used, but is usually from 15 minutes to 8 minutes.
Time, preferably 30 minutes to 2 hours.

The reduction of the ester in the latter step is carried out in accordance with the desired step of Step G1 , and the protection of the primary hydroxyl group is carried out according to the <Method 1> to <Method 3> of Step D2. It will be implemented in accordance with it.

[Method J]

[0238]

Embedded image

In the above formula, R ¹⁶ , J and ring Ar are as defined above. Q represents a hydroxyl group or the aforementioned halogen atom.

Q 'represents a halogen atom, preferably a bromine atom.

[Method J] In compound (VI), L is the following formula (I _L ):

[0242]

Embedded image

(Wherein J and ring Ar have the same meanings as described above).

Step J1 is a process for producing a compound (XXX) from the compound (XXIX).

(1) When Q is a hydroxyl group, this step comprises the steps of:
This is achieved by converting the hydroxyl group of compound (XXIX) to an acetylthio group, and then hydrolyzing with a base to remove the acetyl group.

In the first reaction, the compound (XXIX)
Is converted to a leaving group, followed by reaction with a salt of thioacetic acid, or (b) Mitsunobu reaction using thioacetic acid. The reaction for converting a hydroxyl group to a leaving group in the above (a) is performed according to the latter step of Step A2 , and the reaction for substituting with a thioacetyl group is usually performed by reacting with a salt of thioacetic acid in a solvent. Achieved by The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Examples thereof include aromatic hydrocarbons such as benzene, toluene and xylene; methylene chloride, chloroform, Halogenated hydrocarbons such as carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; acetone, methyl ethyl ketone, methyl Ketones such as isobutyl ketone, isophorone and cyclohexanone: nitriles such as acetonitrile, propionitrile, isobutyronitrile; formamide, N, N-dimethylformamide, N, N-dimethylacetate Bromide,
Examples include amides such as N-methyl-2-pyrrolidone, N-methylpyrrolidinone, and hexamethylphosphorotriamide. Preferably, they are amides, and more preferably, N, N-dimethylformamide. The thioacetic acid salt to be used preferably includes metal salts of thioacetic acid such as lithium thioacetate, sodium thioacetate and potassium thioacetate. The reaction temperature is-
The reaction is carried out at a temperature of from 20 ° C. to 150 ° C., preferably from room temperature to 100 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound and the type of the solvent used, but is usually 30 minutes to 2 days, preferably 2 hours to 1 day.

The Mitsunobu reaction using thioacetic acid in the above (b) is carried out in the same manner as in Step D2 , except that the compound (XXIX) and thioacetic acid are used. The reaction for removing the acetyl group of the acetylthio group is achieved by treating with a base in a solvent.

The base used is not particularly limited as long as it does not affect the other parts of the compound, but is preferably an alkali metal alkoxide such as sodium methoxide; sodium carbonate, potassium carbonate, or the like. Alkali metal carbonates such as lithium carbonate; sodium hydroxide,
Alkali metal hydroxides such as potassium hydroxide, lithium hydroxide and barium hydroxide or ammonia water, and ammonias such as concentrated ammonia-methanol are used.
The solvent to be used is not particularly limited as long as it is one used in a usual hydrolysis reaction. Water; alcohols such as methanol, ethanol, and n-propanol, tetrahydrofuran, An organic solvent such as ethers such as dioxane or a mixed solvent of water and the above organic solvent is preferable. The reaction temperature and the reaction time vary depending on the starting material, the solvent, the base used, and the like, and are not particularly limited.
Implemented for hours.

(2) When Q is a halogen atom, this step is achieved by reacting compound (XXIX) with thiourea by heating in a solvent, followed by hydrolysis. As the solvent used in the first reaction, alcohols such as methanol, ethanol, isopropanol and the like can be preferably mentioned.

The reaction temperature is usually from room temperature to 150 ° C.
And preferably 50 to 100 ° C. The reaction time varies mainly depending on the type of the solvent and the starting material, but is usually 30 minutes to 4 days, preferably 12 hours to 24 hours.

The latter hydrolysis is usually carried out in a mixed solvent of water and the above alcohols. The reaction temperature is usually from room temperature to 150 ° C, preferably from 50 ° C to 100 ° C. The reaction time varies depending mainly on the type of the solvent and the starting material, but is usually 30 minutes to 6 hours, preferably 30 minutes to 2 hours.

Step J2 is a step of producing compound (XXXII) by reacting compound (XXX) with compound (XXXI) in a solvent in the presence of a base.

The solvent to be used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Preferably, the solvent is an aliphatic hydrocarbon such as hexane or heptane; Aromatic hydrocarbons such as toluene and xylene; methylene chloride, chloroform,
Halogenated hydrocarbons such as carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; acetonitrile, isobutyro Nitriles such as nitriles; formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone, N-
Amides such as methylpyrrolidinone and hexamethylphosphorotriamide can be mentioned. More preferred are ethers, most preferably tetrahydrofuran. The base used is not particularly limited as long as it is used as a base in a normal reaction.
Preferably, alkali metal hydrides such as lithium hydride, sodium hydride, potassium hydride, and n-butyllithium, sec-butyllithium, tert-butyllithium, lithium diisopropylamide, lithium bis (trimethylsilyl) amide And organic metal bases such as More preferred are organometallic bases, most preferably butyllithium. The reaction temperature is usually from -100 ° C to 100 ° C, preferably from -78 ° C to 0 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the reagent, or the type of the solvent used, but is usually 0.5 to 10 hours.
Preferably, it is 1 hour to 6 hours.

Step J3 is a step of producing a compound (XXIII) by performing a dehydration reaction from the compound (XXXII) in the presence or absence of a solvent in the presence of an acid, followed by ring closure.

The solvent to be used is not particularly limited as long as it does not hinder the reaction and dissolves the starting materials to some extent, but is preferably alcohols such as methanol and ethanol; and alcohols such as hexane and heptane. Aliphatic hydrocarbons; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene and dichlorobenzene; diethyl ether, diisopropyl Ethers such as ether, tetrahydrofuran, dioxane, dimethoxyethane, diethylene glycol dimethyl ether; acetone, methyl ethyl ketone, methyl isobutyl ketone, isophorone,
Ketones such as cyclohexanone; acetonitrile,
Nitriles such as isobutyronitrile; amides such as formamide, N, N-dimethylformamide, N, N-dimethylacetamide, N-methyl-2-pyrrolidone, N-methylpyrrolidinone, hexamethylphosphorotriamide; And more preferably methanol or ethanol. As the acid used,
There is no particular limitation as long as it is used as an acid in a usual reaction, but preferably, hydrogen chloride, hydrobromic acid, sulfuric acid, perchloric acid, an inorganic acid such as phosphoric acid or acetic acid, formic acid, oxalic acid, Bronsted acids such as organic acids such as methanesulfonic acid, paratoluenesulfonic acid, trifluoroacetic acid and trifluoromethanesulfonic acid, or Lewis acids such as boron trichloride, boron trifluoride and boron tribromide, or acidic ion exchange resins Can be mentioned. More preferably, it is an inorganic acid, most preferably sulfuric acid. The reaction temperature is usually from 0 ° C to 150 ° C, preferably from 50 ° C to 120 ° C. The reaction time varies depending mainly on the reaction temperature, the starting compound, the reagent, or the type of the solvent used, but is usually from 10 minutes to 24 hours, preferably from 5 hours to 24 hours.

Step J4 is a compound (XXXIII)
Is oxidized to give a sulfoxide derivative (XXX
IV), which is usually performed using an oxidizing agent in the presence or absence of a solvent. The oxidizing agent to be used is not particularly limited as long as it is usually used in a reaction for oxidizing a sulfide to form a sulfoxide, and preferably, m-chloroperbenzoic acid, 3,5-dinitro Peracids such as perbenzoic acid, o-carboxyperbenzoic acid, peracetic acid, pertrifluoroacetic acid, perphthalic acid; and N
Combinations of succinimides such as -bromosuccinimide and alkali can be mentioned, more preferably peracids, and most preferably m-chloroperbenzoic acid. The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent.
Preferably, aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as diethyl ether, tetrahydrofuran, dioxane and dimethoxyethane; dimethyl Amides such as formamide, dimethylacetamide, hexamethyl phosphorotriamide; sulfoxides such as dimethyl sulfoxide; methanol, ethanol, n-propanol, isopropanol, n-butanol and isobutanol. Alcohols such as isoamyl alcohol; dilute acids such as sulfuric acid; dilute bases such as sodium hydroxide; water; ketones such as acetone and methyl ethyl ketone; organic bases such as pyridine; Nitriles such as acetonitrile or the above mixed solvent It can be a gel, more preferably,
Halogenated hydrocarbons, most preferably methylene chloride. The reaction temperature is from -20 ° C to 80 ° C, preferably from -5 ° C to 50 ° C. The reaction time depends mainly on the reaction temperature, the starting compound, the oxidizing agent or the type of the solvent used, but is usually from 1 hour to 24 hours.
Hours, preferably 2 hours to 12 hours.

In the above compound (XXXIV), an optically active sulfoxide derivative (XXXIVa) in which the oxygen atom of the sulfoxide group is bonded to the sulfur atom in the S configuration,
(A) direct asymmetric oxidation of compound (XXXIII),
Alternatively, the compound (XXXIII) can be produced by oxidizing the compound (XXXIII) to give the compound (XXXIV) and then performing optical resolution by a diastereomer method.

(A) The asymmetric oxidation of directly obtaining the optically active sulfoxide (XXXIVa) from the compound (XXXIII) includes the optically active oxidizing agent and a chemical method using a combination of an optically active ligand and an oxidizing agent. Biological techniques using baker's yeast and microorganisms are known.
Such asymmetric oxidation is described, for example, in the following literature. 1) G. Solladie, Synthesis 185 (1981): 2) KK Andersen, The Chemistry of Sulfones and Su
lfoxides: S. Patai, Z. Rappoport, CJMStirling., E
ds. Wiley & Sons, Ltd .; Chichester, England, 1988,
Chapter 3, pp55-94: GHPosner., Ibid. Chapter 1
6, pp823-849: 3) HBKagan et al., Synlett 643 (1990): 4) HBKagan, "Asymmetric Oxidation of Sulfides"
in "Catalytic Asymmetric Synthesis" 1, Ojima Ed. V
CH, pp203-226 (1993): 5) FADavis et al., J. Am. Chem. Soc., 114 , 1428 (1
992)).

Of these, F.I. A. Davis
(3'S, 2R)-(-)-
Asymmetric oxidation using N- (phenylsulfonyl) (3,3-dichlorocampholyl) oxaziridine or (+)-[(8,8-dimethoxycamphoryl) sulfonyl] oxaziridine is preferred.

F. A. When asymmetric oxidation is carried out according to the method of Davis et al., The solvent used is not particularly limited as long as it does not inhibit the reaction and dissolves the starting material to some extent. Aliphatic hydrocarbons such as benzene; toluene and xylene; aromatic hydrocarbons such as methylene chloride, chloroform, carbon tetrachloride, halogenated hydrocarbons such as cycloethane, chlorobenzene and dichlorobenzene; ethyl formate Esters such as acetic acid, propyl acetate, butyl acetate and diethyl carbonate; ethers such as diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, dimethoxyethane and diethylene glycol dimethyl ether; nitriles such as acetonitrile and isobutyronitrile; pyridine and the like To mention Can.
The reaction temperature is from -50 ° C to 50 ° C, preferably from -20 ° C to room temperature. The reaction time mainly depends on the reaction temperature,
Although it depends on the type of the starting compound, the reaction reagent and the solvent used, it is usually 10 minutes to 3 days, preferably 2 minutes.
Hours to one day.

[0261] In the method of performing optical resolution by (b) Diastereomer method, first, the Step J
The compound (XXXIII) is oxidized according to 4 to synthesize a racemic sulfoxide derivative (XXXIV). Next, after removing the protecting group, an appropriate optically active carboxylic acid is used as an optical resolving agent to form a salt, and fractional crystallization is performed to obtain an optically active sulfoxide derivative (XXXIVa).

The optical resolving agent used for performing the optical resolution is not particularly limited, but preferably includes tartaric acid, camphor-10-sulfonic acid, and mandelic acid, and particularly preferably, mandelic acid. Is an acid. The solvent used is not particularly limited, but is particularly preferably acetonitrile.

The salt obtained by the division is converted into a free form by using an aqueous alkali solution such as an aqueous sodium hydroxide solution as a free solvent (eg, aromatic hydrocarbons such as benzene, toluene and xylene; Halogenated hydrocarbons such as methylene chloride and chloroform; ethers such as ether, tetrahydrofuran, dioxane and dimethoxyethane; amides such as dimethylformamide, dimethylacetamide and hexamethylphosphorotriamide; dimethyl sulfoxide , Etc.), the optically active sulfoxide derivative (XXIXa) can be isolated.

Step J5 is a process for producing a compound (VI) by removing the protecting group when the R ¹⁶ group of the compound (XXXIV) is a protecting group for an amino group. The reaction is carried out according to the step at the preceding stage of Step D3 .

After completion of each of the above reactions, the target compound is collected from the reaction mixture according to a conventional method. For example, the reaction mixture is appropriately neutralized, and if insolubles are present, they are removed by filtration, and then an immiscible organic solvent such as water and ethyl acetate is added. The organic layer is separated, dried over anhydrous magnesium sulfate or the like, and then obtained by distilling off the solvent. The obtained target compound may be used in a conventional manner, for example, recrystallization, reprecipitation, or a method usually used for separation and purification of organic compounds, if necessary, such as silica gel, alumina, magnesium-silica gel florisil. Column chromatography using a suitable carrier; Sephadex LH-20 (manufactured by Pharmacia), Amberlite XAD-11 (Rohm and
A method using a synthetic adsorbent such as distribution column chromatography using a carrier such as Haas Co., Ltd., Diaion HP-20 (manufactured by Mitsubishi Kasei), a method using ion exchange chromatography, or silica gel or alkylation. Separation and purification can be achieved by appropriately combining a normal phase / reverse phase column chromatography method with silica gel (preferably high performance liquid chromatography) and eluting with a suitable eluent.

The starting compounds (for example, compound (XXI)
X)) can be purchased commercially or easily synthesized according to known production methods.

The novel saturated heterocyclic compounds of the present invention have excellent antagonistic activity against substance P and neurokinin A and have low toxicity, and therefore, they are useful for preventing or treating tachykinin-mediated diseases, for example, anxiety. Diseases of the central nervous system, including depression, psychiatric disorders and schizophrenia; dementia in AIDS, senile dementia of the Alzheimer type, Alzheimer's disease, Down's syndrome, demyelinating disease, amyotrophic lateral sclerosis,
Neurodegenerative diseases including neuropathy, peripheral neuropathy, and neuralgia; chronic obstructive pulmonary disease, bronchitis, pneumonia, bronchoconstriction, respiratory diseases including asthma, cough; inflammatory bowel disease (IB
D), inflammatory diseases including psoriasis, fibrositis, osteoarthritis, osteoarthritis, and rheumatoid arthritis; allergic diseases including eczema; and rhinitis; hypersensitivity diseases including hypersensitivity diseases to vine plants; conjunctivitis, spring conjunctivitis Ophthalmologic disorders, including catarrh, spring catarrh, blood-aqueous-water barrier destruction, increased intraocular pressure, and miosis associated with various inflammatory eye diseases; contact dermatitis, atopic dermatitis, urticaria, and other eczema Skin diseases including dermatitis-like; addiction including alcoholism; somatic diseases due to stress; reflex sympathetic dystrophy including shoulder-hand syndrome; mood swings; undesired immune reactions and systemic including graft rejection Diseases associated with immune enhancement or immunosuppression, including lupus erythematosus; diseases due to abnormalities in the nerves regulating the internal organs; gastroenteritis, including colitis, ulcerative colitis, Crohn's disease; Vomiting induced by chemotherapeutic agents, poisons, toxins, pregnancy, vestibular disorders, postoperative illness, gastrointestinal obstruction, gastrointestinal motility, visceral pain, migraine, increased intracranial pressure, decreased intracranial pressure, or side effects associated with the administration of various drugs Vomiting, including cystitis, bladder dysfunction including urinary incontinence; Collagen disease, scleroderma, eosinophilia due to fasciola infection; vasodilation or contraction, including angina, migraine, and Raynaud's disease Diseases caused by abnormal blood flow due to;
It is useful as a preventive and therapeutic agent for pain nociceptive pain including migraine, headache, and toothache.

The administration form of the compound (I) of the present invention includes, for example, oral administration by tablets, capsules, granules, powders or syrups, and parenteral administration by injections or suppositories. These preparations may contain excipients (e.g., sugar derivatives such as lactose, sucrose, glucose, mannitol, sorbitol; starch derivatives such as corn starch, potato starch, alpha starch, dextrin, carboxymethyl starch; crystalline cellulose). Cellulose derivatives such as low-substituted hydroxypropylcellulose, hydroxypropylmethylcellulose, carboxymethylcellulose, carboxymethylcellulose calcium, internally crosslinked sodium carboxymethylcellulose; gum arabic; dextran; organic excipients such as pullulan And silicate derivatives such as light anhydrous silicic acid, synthetic aluminum silicate and magnesium metasilicate aluminate; phosphates such as calcium phosphate; carbonates such as calcium carbonate; sulfates such as calcium sulfate. Excipients), lubricants (eg, stearic acid, metal stearate such as calcium stearate, magnesium stearate; talc; colloidal silica; waxes such as veegum, gay wax; boric acid; Adipic acid; sulfates such as sodium sulfate; glycol; fumaric acid; sodium benzoate; DL leucine; fatty acid sodium salts; lauryl sulfates such as sodium lauryl sulfate and magnesium lauryl sulfate; Silicic acids; and the above-mentioned starch derivatives.) A binder (for example, polyvinylpyrrolidone, macrogol, and the same compound as the above-mentioned excipient); a disintegrant (for example, the same compound as the above-mentioned excipient;
And chemically modified starch celluloses such as croscarmellose sodium, sodium carboxymethyl starch, cross-linked polyvinyl pyrrolidone. ), Stabilizers (paraoxybenzoic acid esters such as methylparaben and propylparaben; alcohols such as chlorobutanol, benzyl alcohol and phenylethyl alcohol; benzalkonium chloride;
Phenols such as phenol and cresol; thimerosal; dehydroacetic acid; and sorbic acid. ), Flavoring agents (eg, commonly used,
Sweeteners, acidulants, flavors and the like can be mentioned. ), And manufactured by a known method using additives such as a diluent.

The dosage varies depending on the condition, age, administration method and the like. For example, in the case of oral administration,
As a lower limit, 0.01 mg / kg body weight (preferably 0.1 mg / kg body weight)
mg / kg body weight), and an upper limit of 100 mg / kg body weight (preferably 50 mg / kg body weight).
Per dose, the lower limit is 0.01 mg / kg body weight (preferably 0.05 mg / kg body weight), and the upper limit is 100 mg / kg body weight.
It is desirable to administer the body weight (preferably 50 mg / kg body weight) once or several times a day depending on the symptoms.

Hereinafter, the present invention will be described more specifically with reference to examples.

[0271]

Example 1 1- [2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl] -4-phenylpiperidi
4-Carboxamide

[0272]

Example 1 (a) 3- (3,4-dichlorophenyl) -3-butenoic acid
11.31 g (0.47 mol) of chill ester metal magnesium was added to 300 ml of ether, a small amount of iodine was added, and the mixture was allowed to stand for 1 hour.
02.87 g (0.46 mol) of ether (150 m
l) The solution was slowly added dropwise. After adding 150 ml of ether, 60.33 g (44.3 mmol) of anhydrous zinc chloride was slowly added, followed by stirring for 1 hour. Further, bis (triphenylphosphine) palladium chloride3.
After addition of 10 g (4.42 mmol) diketene 3
4.15 ml (42.8 mmol) of ether (600
ml) solution was added dropwise and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was poured into 1 liter of ice-cooled 1N hydrochloric acid, extracted with ether (500 ml × 3 times), and the collected organic layer was washed with a 1N aqueous sodium hydroxide solution (700 ml ×
3 times). The aqueous layer was acidified with concentrated hydrochloric acid under ice-cooling, extracted with ether (500 ml × 3 times), and the organic layer was dried over magnesium sulfate. The solvent was distilled off under reduced pressure,
The residue was dissolved in methanol (350 ml), concentrated sulfuric acid (10 ml) was added, and the mixture was heated under reflux for 30 minutes. After allowing to cool and neutralizing with a saturated aqueous sodium hydrogen carbonate solution, methanol was distilled off under reduced pressure, and the residue was methylene chloride (200 ml).
× 3 times). After the organic layer was dried over magnesium sulfate, the solvent was concentrated under reduced pressure. The residue was distilled under reduced pressure to give the target compound as a pale yellow oil (69.13 g, 62%).
%)Obtained. Boiling point: 144 to 146 ° C. (5 mmHg) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.51 (1H, d, J = 2.2Hz), 7.40 (1H, d, J = 8.2Hz), 7.25
(1H, dd, J = 8.2,2.2Hz), 5.55 (1H, s), 5.30 (1H, s), 3.67 (3H,
s), 3.49 (2H, s)

[0273]

Example 1 (b) 3- (3,4-dichlorophenyl) -3-butenol
11.76 g (0.28 mol) of lithium aluminum tert- butylsilyl ether aluminum hydride was suspended in 500 ml of anhydrous tetrahydrofuran,
Then, 3- (3,4-dichlorophenyl) -3-butenoic acid methyl ester synthesized in Example 1 (a)
06 g (0.28 mol) of anhydrous tetrahydrofuran (5
00 ml) solution was slowly added dropwise at 0 ° C. over 15 minutes under a nitrogen atmosphere. At the same temperature, the reaction mixture
After stirring for 30 minutes, water (500 ml) and 10% aqueous sodium hydroxide solution (500 ml) were slowly added,
Further, the mixture was stirred at room temperature for 1 hour. After filtering the reaction mixture through celite, the filtrate was ethyl acetate (500 ml × 3 times).
After extracting the organic layer with magnesium sulfate,
The solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure. This was dissolved in 250 ml of anhydrous dimethylformamide, and 47.12 ml (0.34 mol) of triethylamine was added under ice cooling.
-Dimethylaminopyridine 6.88 g (0.06 mol)
And 50.96 g of t-butyldimethylsilyl chloride
(0.34 mol), and the mixture was further stirred for 2 hours under ice cooling. 1 liter of ethyl acetate was added to the reaction mixture,
Next, the mixture was washed with ice-cooled 10% hydrochloric acid and saturated saline in that order, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel flash column chromatography (developing solvent: n-hexane: ethyl acetate = 50: 1).
~ 20: 1) to give 43.52 g (47%) of the target compound as a colorless oil. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.50 (1H, d, J = 2.1Hz), 7.38 (1H, d, J = 8.1Hz), 7.24
(1H, dd, J = 8.1,2.1Hz), 5.35 (1H, s), 5.16 (1H, s), 3.70 (2H,
t, J = 6.9Hz), 2.67 (2H, t, J = 6.9Hz), 0.86 (9H, s), 0.00 (6H,
s).

[0274]

Example 1 (c) 4-t-butyldimethylsilyloxy- (2R)-
(3,4-dichlorophenyl) butane-1,2-dio
Le (DHQD)_Two -PHAL (hydroquinidine 1,4
-Phthalazine diyl diether) 790 mg (1.01
Mmol), K_Three Fe (CN)₆ (Potassium ferricyanide
100.19 g (0.30 mol), potassium carbonate
42.06 g (0.30 mol) and osmium tetroxide
(0.393 M toluene solution) 0.516 ml (0.2
0 mmol) in 500 ml of t-butanol and 50
Dissolved in 0 ml, cooled to 0 ° C., and combined with Example 1 (b).
33.61 g (0.10 mol) of the formed olefin compound was added.
Further, the mixture was further stirred at 0 ° C. for 5 hours. Sodium sulfite
150 g was added and stirred at room temperature for 1 hour.
The mixture was extracted with ethyl acetate (800 ml × 3 times).
The organic layer was dried with magnesium sulfate. The solvent is distilled off under reduced pressure
After that, the residue is subjected to silica gel flash column chromatography.
(Developing solvent: n-hexane: ethyl acetate = 5: 1 to 1
1: 1) to give the target compound as a colorless oil
32.3 g (87%) were obtained. Optical purity: 97% ee [α]_D ^{twenty four} +11.39 (c = 1.01, methano
) Nuclear magnetic resonance spectrum (400 MHz, CDCl_Three )
δ ppm: 7.57 (1H, d, J = 2.1Hz), 7.43 (1H, d, J = 8.1Hz), 7.24
(1H, dd, J = 8.1,2.1Hz), 5.00 (1H, s), 3.80 (1H, ddd, J = 10.4,
3.8,3.8Hz), 3.5 to 3.7 (3H, m), 2.51 (1H, dd, J = 8.0,5.2H
z), 2.37 (1H, ddd, J = 15.0,11.1,4.0Hz), 1.86 (1H, ddd, J = 1
5.0,2.9,2.9Hz), 0.89 (9H, s), 0.04 (3H, s),-0.01 (3H, s)

[0275]

Example 1 (d)1-azido-4-t-butyldimethylsilyloxy-
(2R)-(3,4-dichlorophenyl) -2-butano
Rule 32.07 g of the diol compound synthesized in Example 1 (c) (8
7.8 mmol) and 4-dimethylaminopyridine.
07 g (8.76 mmol) in 320 ml of pyridine
Methanesulfonyl chloride under ice-cooling.
9 ml (0.132 mol) was slowly added dropwise, and a nitrogen atmosphere was added.
The mixture was stirred at the same temperature for 2 hours under an atmosphere. Mix the reaction mixture on ice
Pour into cold 10% hydrochloric acid (1500 ml) and then
Extract with ethyl acetate (200 ml × 3 times) and extract the organic layer.
Was washed with saturated saline and dried over magnesium sulfate
did. The solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure. this
Is dissolved in 300 ml of anhydrous dimethylformamide,
Add 11.41 g (0.18 mol) of sodium azide
Then, it was heated at 120 ° C. for 4 hours under a nitrogen atmosphere. Anti
After the reaction mixture was brought to room temperature, it was added to 1,000 ml of a saturated saline solution.
The mixture was poured and extracted with ethyl acetate (500 ml × 3 times).
After drying the organic layer over magnesium sulfate, the solvent was distilled off under reduced pressure.
And the residue is flash column chromatographed on silica gel.
(Developing solvent: n-hexane: ethyl acetate = 10: 1
~ 5: 1) to purify the target compound as a colorless oil.
This gave 29.3 g (85%). [Α]_D ^{twenty four} -48.56 (c = 1.04, methano
) Nuclear magnetic resonance spectrum (400 MHz, CDCl_Three )
δ ppm: 7.59 (1H, d, J = 2.2 Hz), 7.44 (1H, d, J = 8.3 Hz), 7.24
(1H, dd, J = 8.3,2.2Hz), 5.12 (1H, s), 3.81 (1H, ddd, J = 10.6,
4.1,3.0Hz), 3.51 (1H, ddd, J = 10.6,10.6,2.8Hz), 3.40 (1H,
d, J = 12.5Hz), 3.31 (1H, d, J = 12.5Hz), 2.35 (1H, ddd, J = 15.
8,10.6,4.1Hz), 1.91 (1H, ddd, J = 15.8,3.0,2.8Hz), 0.88 (9
H, s), 0.02 (3H, s),-0.04 (3H, s)

[0276]

Example 1 (e)1-amino-4-t-butyldimethylsilyloxy-
(2R)-(3,4-dichlorophenyl) -2-butano
Rule 10.00 g of the azide compound synthesized in Example 1 (d) (2
5.6 mmol) in 100 ml of tetrahydrofuran
Dissolved in 0.6 ml of water and triphenylphosphine
7.39 g (28.2 mmol) was added, and a nitrogen atmosphere was added.
The mixture was stirred at 80 ° C for 4 hours. The solvent was distilled off under reduced pressure.
After adding n-hexane to the residue and filtering out the precipitated crystals,
The filtrate is concentrated under reduced pressure, and the residue is subjected to silica gel flash column.
Chromatography (developing solvent: methylene chloride: methano
= 30: 1 to 10: 1) and purify the target compound.
The product was obtained as a colorless oil (3.83 g, 41%). [Α]_D ^{twenty four} +3.94 (c = 0.71, methano
) Nuclear magnetic resonance spectrum (400 MHz, CDCl_Three )
δ ppm: 7.56 (1H, d, J = 2.2Hz), 7.42 (1H, d, J = 8.6Hz), 7.22
(1H, dd, J = 8.6,2.2Hz), 4.91 (1H, br.s), 3.73 (1H, ddd, J = 1
0.3,4.6,3.7Hz), 3.53 (1H, ddd, J = 10.3,10.2,3.7Hz), 2.91
(1H, d, J = 13.1Hz), 2.86 (1H, d, J = 13.1Hz), 2.16 (1H, ddd, J =
14.6,10.2,4.6Hz), 1.88 (1H, ddd, J = 14.6,3.7,3.7Hz), 1.4
4 (2H, br.s), 0.87 (9H, s), 0.01 (3H, s),-0.04 (3H, s)

[0277]

Example 1 (f) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
N-5-yl] ethanol t-butyldimethylsilyl
Ether The amino alcohol derivative 1.35 synthesized in Example 1 (e)
g (3.71 mmol) was dissolved in 50 ml of benzene, 167 mg (5.57 mmol) of paraformaldehyde and 13 mg of p-toluenesulfonyl chloride were added, and the mixture was heated to 100 ° C. under a nitrogen atmosphere using a Dean-Stark apparatus. And heated to reflux for 3 hours. After evaporating the solvent under reduced pressure, 100 ml of ethyl acetate was added to the residue, washed with a saturated aqueous solution of sodium hydrogen carbonate, and dried over magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was methylene chloride (50 ml).
And dissolved in 0.62 ml (4.45) of triethylamine.
Mmol) and 45 mg of 4-dimethylaminopyridine
(0.37 mmol), and then added with 3,4,5 under ice-cooling.
1.03 g of trimethoxybenzoyl chloride (4.
(47 mmol) and stirred at 0 ° C. for 1 hour. After adding 100 ml of methylene chloride to the reaction mixture,
% Hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and a saturated saline solution, and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel flash column chromatography (developing solvent: ethyl acetate: n-hexane =
1: 5 to 2: 1) to give 1.27 g (60%) of the target compound as white amorphos. [Α] _D ²⁴ +61.73 (c = 1.39, methanol)

[0278]

Example 1 (g) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
N-5-yl] ethanol methanesulfonate 3.95 g (6.92 mmol) of the t-butyldimethylsilyl ether compound synthesized in Example 1 (f) was added to acetic acid: tetrahydrofuran: water = 3: 3: 1. The mixture was dissolved in 70 ml of a mixed solution and heated at 80 ° C. for 8 hours under a nitrogen atmosphere. After neutralization with a saturated aqueous solution of sodium hydrogen carbonate, the mixture was extracted with ethyl acetate, and the organic layer was dried over magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was dissolved in 30 ml of pyridine, and 70 mg (0.57
Mmol) and methanesulfonyl chloride 0.66 ml
(8.53 mmol) under ice-cooling and under a nitrogen atmosphere.
Stirred at 0 ° C. for 2 hours. The reaction mixture was cooled on ice 10
% Hydrochloric acid, and then ethyl acetate (10%
0 ml × 3 times). The collected organic layer was washed with saturated saline and dried over magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was subjected to silica gel flash column chromatography (developing solvent: n-hexane: ethyl acetate = 5: 1).
１1: 1) to give 3.02 g (82%) of the target compound as white amorphos. [Α] _D ²⁴ +53.1 (c = 1.0, methanol)

[0279]

Example 1 (h) 1- [2-[(5R)-(3,4-dichlorophenyl)
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl] -4-phenylpiperidi
4-carboxylic acid amide 150 mg (0.2 mg) of the mesyl compound synthesized in Example 1 (g)
8 mmol) and 75 mg (0.31 mmol) of 4-phenylpiperidine-4-carboxylic acid amide hydrochloride in 3 ml of anhydrous dimethylformamide, followed by 71 mg (0.85 mmol) of sodium hydrogen carbonate and 70 mg of potassium iodide (0.42 mmol) and heated at 80 ° C. for 6 hours under a nitrogen atmosphere. Saturated saline 5
0 ml was added, and then ethyl acetate (50 ml × 3 times)
, And the collected organic layer was dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel thin-layer chromatography (developing solvent: methylene chloride: methanol = 10: 1) to obtain 127 mg (71%) of the target compound as white amorphous. [Α] _D ²⁴ +25.2 (c = 0.48, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.50 to 7.10 (8H, m), 6.67 (2H, s), 5.30 to 4.85 (2H,
m), 5.18 (2H, s), 4.13 ~ 3.70 (2H, m), 3.87 (3H, s), 3.85 (6H,
s), 2.67 to 1.93 (12H, m) Infrared absorption spectrum ν _max (KBr) cm ^-1 : 29
40,1678,1640,1584,1456,14
16, 1236, 1128 Elemental analysis value (% as C ₃₃ H ₃₇ N ₃ O ₆ Cl ₂ .0.5H ₂ O) Calculated values: C: 60.77, H: 5.83, N: 6.45, Cl: 10.89 Found: C: 60.63, H: 5.94, N: 6.39, Cl: 10.93 Mass spectrometry (FAB) m / z: 642 ((M + H)
⁺ ) By performing the same method as in the above Examples, the following compounds can be produced.

[0280]

Example 2 1- [2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl] -4-phenylpiperidi
4-Carboxylic acid dimethylamide yield: 76% [α] _D ²⁴ +19.2 (c = 1.05, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.60-7.10 (8H, m), 6.71 (2H, br.s), 5.50-4.90
(2H, m), 3.88 (9H, s), 3.40-1.40 (20H, m) Infrared absorption spectrum ν _max (KBr) cm ^-1 : 29
38, 1633, 1584, 1464, 1416, 12
36,1128 Elemental analysis value (% as C ₃₅ H ₄₁ N ₃ O ₆ Cl ₂ .H ₂ O) Calculated value: C: 61.05, H: 6.29, N: 6.10, Cl: 10. 30 actual values: C: 60.66, H: 6.25, N: 5.80, Cl: 10.65

[0281]

Example 3 1- [2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl] -4-phenylpiperidi
4-Carboxylic acid pyrrolidineamide yield: 82% [α] _D ²⁴ +23.2 (c = 0.49, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.52 ~ 7.40 (2H, m), 7.33 ~ 7.00 (6H, m), 6.68 (2H, m
s), 5.30 to 4.85 (2H, m), 4.09 to 3.65 (2H, m), 3.87 (3H, s), 3.
86 (6H, s), 3.56-3.41 (2H, br.s), 2.89-2.60 (4H, m), 2.48
~ 2.29 (4H, m), 2.20 ~ 1.98 (10H, m) Infrared absorption spectrum ν _max (KBr) cm ^-1 : 29
48, 1625, 1584, 1464, 1415, 12
35,1128 Elemental analysis (% as C ₃₇ H ₄₃ N ₃ O ₆ Cl ₂ .0.5H ₂ O) Calculated: C: 62.98, H: 6.28, N: 5.95, Cl: 10.04 Found: C: 63.01, H: 6.43, N: 5.97, Cl: 9.71 Mass spectrometry (FAB) m / z: 696 ((M + H)
⁺ )

[0282]

Example 4 1- [2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl] -4-phenylpiperidi
4-carboxylic acid morpholinamide yield: 63% [α] _D ²⁴ +20.5 (c = 1.04, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.60 to 7.10 (8H, m), 6.70 (2H, s), 5.40 to 4.90 (2H,
m), 3.87 (9H, s), 4.10 to 1.40 (22H, m) Infrared absorption spectrum ν _max (KBr) cm ^-1 : 29
66, 1637, 1584, 1455, 1416, 12
33,1128 Elemental analysis value (% as C ₃₇ H ₄₃ N ₃ O ₇ Cl ₂ .0.5H ₂ O) Calculated value: C: 61.58, H: 6.15, N: 5.82, Cl: 9.83 found: C: 61.47, H: 6.62, N: 5.45, Cl: 9.67 mass spectrometry (FAB) m / z: 712 ((M + H)
⁺ ) In the same manner as in the above Examples, the following compounds of Examples 5 to 40 were synthesized.

[0283]

Embedded image

[0284]

Embedded image

[0285]

Embedded image

[0286]

Working Example 41 1- [3-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] propyl-4-phenylpiperidi
4-Carboxamide

[0287]

Example 41 (a) 4- (3,4-dichlorophenyl) -4-oxobutane
1.00 g (6.80 mmol) of acid methyl ester dichlorobenzene and 0.72 g (7.14 mmol) of succinic anhydride were suspended in 3 ml of dichloroethane, and 1.36 g (10.2 mmol) of aluminum chloride (powder) was suspended. ) At 60 ° C
For 3 hours. The reaction mixture was ice-cooled, 1N hydrochloric acid was added, and the mixture was extracted with methylene chloride. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was dissolved in 30 ml of methanol,
0.20 ml of sulfuric acid was added, and the mixture was heated under reflux for 2 hours. The reaction solution was brought to room temperature, poured into water and extracted with ethyl ether.
The organic phase was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue is subjected to silica gel column chromatography (elution solvent: n
-Hexane: ethyl ether = 17: 3 to 7: 3) to give 0.25 g of the target compound as pale orange crystals
(14%). Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 8.07 (1H, d, J = 2Hz), 7.81 (1H, dd, J = 2,8Hz), 7.56
(1H, d, J = 8Hz), 3.71 (3H, s), 3.27 (2H, t, J = 7Hz), 2.78 (2H,
(t, J = 7Hz)

[0288]

Example 41 (b) 4- (3,4-dichlorophenyl) -4-pentenoic acid
330 mg of methyl ester methyltriphenylphosphonium bromide
(0.92 mmol) and potassium t-butoxide 105
mg (0.94 mmol) in 4 ml of dry benzene
And stirred at room temperature under a nitrogen stream for 4 hours. 4- (3,4-dichlorophenyl) -4-oxobutanoic acid methyl ester 200 m obtained in Example 41 (a)
g was dissolved in 1 ml of benzene and added, followed by stirring for 18 hours. The reaction solution was filtered through celite, washed with ethyl ether, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: n-hexane: ethyl ether = 23: 2) to give 95 mg (64%) of the desired compound as a pale yellow oil. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.48 (1H, d, J = 2Hz), 7.40 (1H, d, J = 8Hz), 7.23 (1H,
(dd, J = 2,8Hz), 5.32 (1H, s), 5.14 (1H.s), 3.67 (3H, s), 2.79
(2H, t, J = 8Hz), 2.48 (2H, t, J = 8Hz)

[0289]

Example 41 (c) 4- (3,4-dichlorophenyl) -4-pentene-1
-All t-butyldimethylsilyl ether Using 4- (3,4-dichlorophenyl) -4-pentenoic acid methyl ester obtained in Example 41 (b),
The target compound was obtained in a yield of 93% in the same manner as in Example 1 (b).
I got it. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.49 (1H, d, J = 2Hz), 7.38 (1H, d, J = 9Hz), 7.24 (1H,
dd, J = 2,9Hz), 5.30 (1H, s), 5.13 (1H, d, J = 1Hz), 3.62 (2H, t,
J = 6Hz), 2.52 (2H, t, J = 8Hz), 1.60-1.68 (2H, m), 0.90 (9H,
s), 0.04 (6H, s)

[0290]

Example 41 (d) (2R) -5- (t-butyldimethylsilyloxy)-
2- (3,4-dichlorophenyl) pentane-1,2-
Diol Using 4- (3,4-dichlorophenyl) -4-penten-1-ol t-butyldimethylsilyl ether obtained in Example 41 (c) in the same manner as in Example 1 (c). The target compound was obtained in a yield of 90%. [Α] _D ²⁴ -2.08 (c = 0.48, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.56 (1H, d, J = 2 Hz), 7.41 (1H, d, J = 8 Hz), 7.23 (1H,
(dd, J = 2,8Hz), 4.96 (1H, s), 3.53-3.70 (4H, m), 1.98-2.14
(3H, m), 1.35-1.57 (2H, m), 0.91 (9H, s), 0.082 (3H, s), 0.0
78 (3H, s)

[0291]

Example 41 (e) (2R) -1-azido-5- (t-butyldimethylsilyl)
Ruoxy) -2- (3,4-dichlorophenyl) -2-
Pentanol Example 1 was prepared using (2R) -5- (t-butyldimethylsilyloxy) -2- (3,4-dichlorophenyl) pentane-1,2-diol obtained in Example 41 (d). The target compound was obtained in a yield of 86% in the same manner as in (d). [Α] _D ²⁴ -48.2 (c = 0.61, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃₎
δ ppm: 7.58 (1H, d, J = 2Hz), 7.42 (1H, d, J = 9Hz), 7.23 (1H,
(dd, J = 2.9Hz), 4.93 (1H, s), 3.67 (1H, m), 3.58 (1H, m), 3.43
(1H, d, J = 12Hz), 3.31 (1H, d, J = 12Hz), 2.13 (1H, m), 2.04 (1
H, m), 1.54 (1H, m), 1.40 (1H, m), 0.91 (9H, s), 0.09 (3H, s),
0.08 (3H, s)

[0292]

Example 41 (f) (f) (2R) -1-amino-5- (t-butyldimethylene)
Lucylyloxy) -2- (3,4-dichlorophenyl)
-2-pentanol (2R) -1-azide-5 obtained in Example 41 (e)
-(T-butyldimethylsilyloxy) -2- (3,4
Using (-dichlorophenyl) -2-pentanol, the target compound was obtained in a yield of 76% in the same manner as in Example 1 (e). [Α] _D ²⁴ -8.13 (c = 0.48, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.54 (1H, d, J = 2Hz), 7.40 (1H, d, J = 9Hz), 7.21 (1H,
dd, J = 2.9 Hz), 4.57 (1H, br.s), 3.50 to 3.62 (2H, m), 2.96 (1
H, d, J = 13Hz), 2.82 (1H, d, J = 13Hz), 1.93 (1H, m), 1.80 (1H,
m), 1.33 ~ 1.60 (2H, m), 0.89 (9H, s), 0.04 (6H, s)

[0293]

Example 41 (g) 3-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
N-5-yl] -1-propanol t-butyl dimethyl
Lucylyl ether (2R) -1-amino-5 obtained in Example 41 (f)
-(T-butyldimethylsilyloxy) -2- (3,4
Using -dichlorophenyl) -2-pentanol, the target compound was obtained in a yield of 48% in the same manner as in Example 1 (f). [Α] _D ²⁴ +37.73 (c = 0.44, methanol)

[0294]

Example 41 (h) 3-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
N-5-yl] -1-propanol methanesulfone
Over preparative Example 41 (g) obtained in 3 - [(5R) -5-
(3,4-dichlorophenyl) -3- (3,4,5-trimethoxybenzoyl) oxazolidin-5-yl]-
Using 1-propanol t-butyldimethylsilyl ether, the target compound was obtained in a yield of 93% in the same manner as in Example 1 (g). [Α] _D ²⁴ +52.90 (c = 0.62, methanol)

[0295]

Example 41 (i) 1- [3-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] propyl-4-phenylpiperidi
Obtained in emission-4-carboxylic acid amide Example 41 (h) 3 - [( 5R) - (3,4
Example 1 using -dichlorophenyl) -3- (3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] -1-propanol methanesulfonate.
The target compound was obtained in a yield of 66% in the same manner as in (h). [Α] _D ²⁴ +35.9 (c = 0.48, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.60 to 7.10 (8H, m), 6.68 (2H, br.s), 5.40 to 4.90
(4H, m), 3.88 (9H, s), 3.87 (9H, s), 4.10 to 1.10 (16H, m) Infrared absorption spectrum ν _max (KBr) cm ^-1 : 34
40, 3353, 2940, 1676, 1641, 15
85 Elemental analysis value (% as C ₃₄ H ₃₉ N ₃ O ₆ Cl ₂ .0.5H ₂ O) Calculated value: C: 61.35, H: 6.06, N: 6.31, Cl: 10. 65 Found: C: 61.81, H: 6.22, N: 6.50, Cl: 10.26 Mass spectrometry (FAB) m / z: 656 ((M + H)
⁺ ) In the same manner as in the above Examples, the following compounds of Examples 41 to 50 were synthesized.

[0296]

Embedded image

[0297]

Example 51 (Exemplified Compounds, Table 2-1969) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] -4-phenylpiperidine-4-ca
Rubonamide

[0298]

Example 51 (a) 3- (3,4-dichlorophenyl) -3-butenoic acid
11.31 g (0.47 mol) of chill ester metal magnesium was added to 300 ml of ether, a small amount of iodine was added, and the mixture was allowed to stand for 1 hour.
02.87 g (0.46 mol) of ether (150 m
l) The solution was slowly added dropwise. After adding 150 ml of ether, 60.33 g (44.3 mmol) of anhydrous zinc chloride was slowly added, followed by stirring for 1 hour. Further, bis (triphenylphosphine) palladium chloride3.
After addition of 10 g (4.42 mmol) diketene 3
4.15 ml (42.8 mmol) of ether (600
ml) solution was added dropwise and the reaction mixture was stirred at room temperature for 30 minutes. The reaction mixture was poured into 1 liter of ice-cooled 1N hydrochloric acid, extracted with ether (500 ml × 3 times), and the collected organic layer was washed with a 1N aqueous sodium hydroxide solution (700 ml ×
3 times). The aqueous layer was acidified with concentrated hydrochloric acid under ice-cooling, extracted with ether (500 ml × 3 times), and the organic layer was dried over magnesium sulfate. The solvent was distilled off under reduced pressure,
The residue was dissolved in methanol (350 ml), concentrated sulfuric acid (10 ml) was added, and the mixture was heated under reflux for 30 minutes. After allowing to cool and neutralizing with a saturated aqueous sodium hydrogen carbonate solution, methanol was distilled off under reduced pressure, and the residue was methylene chloride (200 ml).
× 3 times). After the organic layer was dried over magnesium sulfate, the solvent was concentrated under reduced pressure. The residue was distilled under reduced pressure to give the target compound as a pale yellow oil (69.13 g, 62%).
%)Obtained. Boiling point: 144 to 146 ° C. (5 mmHg) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.51 (1H, d, J = 2.2Hz), 7.40 (1H, d, J = 8.2Hz), 7.25
(1H, dd, J = 8.2,2.2Hz), 5.55 (1H, s), 5.30 (1H, s), 3.67 (3H,
s), 3.49 (2H, s)

[0299]

Working Example 51 (b) 3- (3,4-dichlorophenyl) -3-butenol
11.76 g (0.28 mol) of lithium aluminum tert- butylsilyl ether aluminum hydride was suspended in 500 ml of anhydrous tetrahydrofuran,
Then, 3- (3,4-dichlorophenyl) -3-butenoic acid methyl ester 6 synthesized in Example 51 (a)
A solution of 9.06 g (0.28 mol) in anhydrous tetrahydrofuran (500 ml) was added at 0 ° C. under a nitrogen atmosphere for 15 minutes.
Slowly dropped over a period of minutes. After stirring the reaction mixture at the same temperature for 30 minutes, water (500 ml) and 10%
An aqueous sodium hydroxide solution (500 ml) was slowly added, and the mixture was further stirred at room temperature for 1 hour. After the reaction mixture was filtered through celite, the filtrate was washed with ethyl acetate (500 ml × 3).
), The organic layer was dried over magnesium sulfate, the solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure. After dissolving this in 250 ml of anhydrous dimethylformamide, 47.12 ml (0.34 mol) of triethylamine and 6.88 g (0.04 g) of 4-dimethylaminopyridine under ice cooling.
6 mol) and t-butyldimethylsilyl chloride 50.
96 g (0.34 mol) were added successively, and further,
Stirred for hours. Ethyl acetate (1 liter) was added to the reaction mixture, which was then washed successively with ice-cooled 10% hydrochloric acid and saturated saline, and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel flash column chromatography (developing solvent: n-hexane: ethyl acetate = 5).
0: 1 to 20: 1) to give 43.52 g (47%) of the target compound as a colorless oil. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.50 (1H, d, J = 2.1Hz), 7.38 (1H, d, J = 8.1Hz), 7.24
(1H, dd, J = 8.1,2.1Hz), 5.35 (1H, s), 5.16 (1H, s), 3.70 (2H,
t, J = 6.9Hz), 2.67 (2H, t, J = 6.9Hz), 0.86 (9H, s), 0.00 (6H,
s)

[0300]

Example 51 (c) 3- (3,4-dichlorophenyl) -3,4-epoxy
-1-butanol tert-butyldimethylsilyl ether
Le 3- (3,4-dichlorophenyl) -3-butenol
3.00 g of tert-butyldimethylsilyl ether (9.
Was dissolved in 60 ml of methylene chloride, and 2.52 g (30.0 mmol) of sodium hydrogen carbonate and 3.88 g (15.7 mm) of 3-chloroperbenzoic acid (content 70%) were dissolved.
ol) and stirred at room temperature for 3 hours. The reaction solution was diluted with methylene chloride and washed with a 1 N aqueous sodium hydroxide solution and saturated saline. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (eluent: n-hexane: ethyl ether = 24: 1 to 19: 1) to give 2.70 g of the desired compound. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.47 (1H, d, J = 2Hz), 7.38 (1H, d, J = 8Hz), 7.21 (1H,
(dd, J = 2,8Hz), 3.57 ~ 3.72 (2H, m), 3.01 (1H, d, J = 5Hz), 2.68
(1H, d, J = 5Hz), 2.27 (1H, m), 2.01 (1H, m), 0.84 (9H, s),-0.0
16 (3H, s),-0.024 (3H, s)

[0301]

Embodiment 51 (d)4- (tert-butyldimethylsilyloxy) -2-
(3,4-dichlorophenyl) -1- [N- (tert-butyl
Toxicarbonyl) -N- (2-hydroxyethyl) a
Mino] -2-butanol 3- (3,4-dichloro) obtained in Example 51 (c)
Phenyl) -3,4-ethoxy-1-butanol tert
-Butyldimethylsilyl ether 1.50 g (4.32)
mmol) and 1.84 g (17.3 mmol) of lithium perchlorate.
l) in 30 ml of acetonitrile
The mixture was stirred at room temperature for 10 minutes. Add 2-ami
After adding 2.11 g (34.5 mmol) of ethanol, 5
Heated to reflux for a while. The reaction solution was cooled to room temperature and acetic acid
It was diluted with ethyl and washed with saturated saline. No organic layer
After drying over sodium sulfate, the solvent was distilled off under reduced pressure.
Was. The residue was dissolved in 30 ml of methylene chloride,
0.89 ml (6.42 mmol) of diamine and di-tert-butyl
943 mg (4.32 mmol) of tildicarbonate was added,
Stirred at room temperature for 16 hours. Pour the reaction solution into water and add salt
The mixture was extracted with methylene chloride and washed with saturated saline. Organic layer
Was dried over anhydrous sodium sulfate, and then the solvent was removed under reduced pressure.
Distilled off. The residue is subjected to silica gel column chromatography.
-(Developing solvent: n-hexane: ethyl acetate = 3: 2)
Further purification gave 1.94 g of the target compound. Nuclear magnetic resonance spectrum (400 MHz, CDCl_Three )
δ ppm: 7.30 to 7.75 (3H, m), 5.30 and 5.57 (1H in total, each b
r.s), 3.05-4.00 (9H, m), 2.00-2.40 (2H, m), 1.53 (9H, s),
0.94 (9H, s), 0.09 (3H, s), 0.07 (3H, s) Infrared absorption spectrum ν_max cm^-1(KBr): 329
8, 2955, 2936, 2885, 2857, 1659 Mass spectrum (FAB) m / z: 508 ((M +
H)⁺)

[0302]

Working Example 51 (e) 2- [4-tert-butoxycarbonyl-2- (3,4-
Dichlorophenyl) morpholin-2-yl] ethanol
tert-butyldimethylsilyl ether 4- (tert-butyldimethylsilyloxy) -2- (3,4-dichlorophenyl) -1- [N- (tert-butoxycarbonyl)-obtained in Example 51 (d). N-
(2-hydroxyethyl) amino] -2-butanol 1
0.4 g (20.5 mmol) and 8.03 g (30.6 mmol) of triphenylphosphine were added to dry toluene 18
Then, a solution of 5.33 g (30.6 mmol) of diethyl azodicarboxylate in 20 ml of toluene was added dropwise at room temperature under a nitrogen atmosphere, and the mixture was stirred for 2 hours. The reaction solution is
The mixture was poured into an aqueous ammonium chloride solution, extracted with ethyl acetate, and washed with saturated saline. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue
Purification by silica gel column chromatography (elution solvent: hexane: ethyl acetate = 23: 2 to 9: 1) gave 8.85 g of the target compound. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.56 (1H, br.s), 7.43 (1H, d, J = 9 Hz), 7.28 (1H, dd,
J = 2.9Hz), 4.20 ~ 4.55 (1H, br.s), 3.00 ~ 3.80 (8H, m), 1.80
~ 2.10 (2H, m), 1.35 ~ 1.60 (9H, br.s), 0.85 (9H, s),-0.01
(6H, s) infrared absorption spectrum ν _max cm ^-1 (CHCl ₃ ):
2957, 2931, 2859, 1730, 1687 Mass spectrum (FAB) m / z: 490 ((M +
H) ⁺ )

[0303]

Working Example 51 (f) 2- [2- (3,4-dichlorophenyl) morpholine-
2- [2-yl] ethanol 2- [4-tert-butoxycarbonyl-2- (3,4-dichlorophenyl) morpholin-2-yl] ethanol tert-butyldimethylsilyl ether obtained in Example 51 (e) 7. 80 g (15.9 mmol) was dissolved in 150 ml of methylene chloride, 7.05 g (35.5 mmol) of B-bromocatecholborane was added, and the mixture was stirred at room temperature under a nitrogen stream for 2 hours. 150 ml of water was added to the reaction solution, and the mixture was further stirred for 2 hours. A 1N aqueous sodium hydroxide solution was added to make the mixture alkaline, and the mixture was extracted with methylene chloride and washed with saturated saline. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue
Purification by silica gel column chromatography (elution solvent: methylene chloride: methanol = 19: 1 to 17: 3) gave 4.40 g of the desired compound. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.51 (1H, d, J = 2Hz), 7.48 (1H, d, J = 8Hz), 7.24 (1H
H, dd, J = 2,8Hz), 3.76 (1H, dt, J = 3,12Hz), 3.66 (1H, m), 3.58
(2H, t, J = 6Hz), 3.36 (1H, d, J = 13Hz), 3.11 (1H, d, J = 13Hz),
2.97 (1H, m), 2.79 (1H, dt, J = 3,13Hz), 2.14 (1H, dt, J = 6,15H
z) .1.79 (1H, dt, J = 6,15Hz)

[0304]

Example 51 (g) 2- [2- (3,4-dichlorophenyl) -4- (3,
4,5-trimethoxybenzoyl) morpholin-2-i
Le] obtained in ethanol Example 51 (f), 2- [2- a (3,4-dichlorophenyl) morpholin-2-yl] ethanol 1.28 g (4.63 mmol), was dissolved in methylene chloride 30ml , 2.66 g (26.3 mmol) of triethylamine
l), 1.28 g (5.55 mmol) of 3,4,5-trimethoxybenzoyl chloride and 5 mg of 4-dimethylaminopyridine were added, and the mixture was stirred at room temperature for 6 hours. The reaction solution was poured into an aqueous solution of sodium hydrogen carbonate, extracted with methylene chloride, and washed with saturated saline. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: methylene chloride: acetone = 4: 1 to 7: 3) to obtain 1.72 g of the desired compound. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 6.80 to 7.80 (3H, m), 6.47 (2H, s), 3.40 to 4.80 (8H,
m), 3.84 and 3.86 (total 9H, each s), 1.75 to 2.25 (2H, m) Infrared absorption spectrum ν _max cm ^-1 (KBr): 3429,
2940, 2838, 1630, 1585 Mass spectrum (EI) m / z: 469 (M ⁺ )

[0305]

Example 51 (h) 2- [2- (3,4-dichlorophenyl) -4- (3,
4,5-trimethoxybenzoyl) morpholin-2-i
[Ethanol] methanesulfonate 388 mg of 2- [2- (3,4-dichlorophenyl-4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethanol obtained in Example 51 (g).
(0.83 mmol) was dissolved in 5 ml of methylene chloride, 126 mg (1.25 mmol) of triethylamine and 0.078 ml (1.01 mmol) of methanesulfonyl chloride were added, and the mixture was stirred at room temperature for 2 hours. The reaction solution was diluted with methylene chloride and washed with 1N hydrochloric acid and saturated saline.
After drying the organic layer over anhydrous sodium sulfate,
The solvent was distilled off. The residue was subjected to silica gel column chromatography (elution solvent: hexane: ethyl acetate = 1: 4-
0: 1) to give 424 mg of the desired compound. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 6.90 to 7.80 (3H, m), 6.52 (2H, s), 3.40 to 4.35 (8H,
m), 3.86 and 3.87 (total 9H, each s), 2.93 (3H, s), 2.10 to 2.55
(2H, m) infrared absorption spectrum ν _max cm ^-1 (KBr): 2999,
2966, 2939, 2875, 1634, 1585 Mass spectrum (FAB) m / z: 548 ((M +
H) ⁺ )

[0306]

Working Example 51 (i) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] -4-phenylpiperidine-4-ca
Rubonamide 200 mg of 2- [2- (3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethanolmethanesulfonate obtained in Example 51 (h). (0.36 mmol), 105 mg of 4-phenylpiperidine-4-carboxamide hydrochloride (0.4 mg).
4 mmol), 100 mg of sodium hydrogen carbonate (1.19 mmol)
l) and 100 mg (0.60 mmol) of potassium iodide
Suspend in 2 ml of dimethylformamide and add 8
Stirred at 0 ° C. for 6 hours. The reaction solution was poured into water, extracted with ethyl acetate, and washed sequentially with an aqueous solution of sodium thiosulfate, water and saturated saline. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by thin-layer chromatography (developing solvent: methylene chloride: methanol = 9: 1) and crystallized from hexane to obtain 205 mg of the desired compound (86% yield). Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 6.80-7.75 (8H, m), 6.48 (2H, s), 5.18 (2H, s), 1.8
0 to 4.70 (18H, m), 3.83 and 3.85 (total 9H, each s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 3440,
3356, 2937, 2831, 1679, 1631, 1584 Mass spectrum (FAB) m / z: 656 ((M +
H) ⁺⁾ Elemental analysis as _{(C 34 H 39 N 3 O} 6 Cl 2 · 1/10 H 2 O): Calculated: C: 62.02; H: 6.00 ; N: 6.38; Cl: 10.76 Found: C : 61.54; H: 6.07; N: 6.25; Cl: 11.35 The following compounds of Examples 52 to 69 were synthesized in the same manner as in Example 51 above.

[0307]

Example 52 (Exemplified Compounds, Table 2-1971) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] -4-phenylpiperidine-4-ca
Rubonic acid dimethylamide yield: 84% Mass spectrum (FAB) m / z: 684 ((M +
H) ⁺ ) Elemental analysis (as C ₃₆ H ₄₃ N ₃ O ₆ Cl ₂ ): Calculated: C: 63.16; H: 6.33; N: 6.14; Cl: 10.36 Found: C: 63.28; H: 6.64; N: 5.79; Cl: 9.96

[0308]

Example 53 (Exemplified Compounds, Table 2-1975) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] -4-phenylpiperidine-4-ca
Rubonic acid pyrrolidineamide yield: 76% Mass spectrum (FAB) m / z: 710 ((M +
H) ⁺⁾ Elemental analysis as _{(C 38 H 45 N 3 O} 6 Cl 2 · 1/10 H 2 O): Calculated: C: 64.06; H: 6.39 ; N: 5.90; Cl: 9.95 Found: C : 63.62; H: 6.37; N: 5.75; Cl: 9.96

[0309]

Example 54 (Exemplified Compounds, Table 2-1975) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] -4-phenylpiperidine-4-ca
Rubonic acid morpholinamide yield: 68% Mass spectrum (FAB) m / z: 726 ((M +
H) ⁺⁾ Elemental analysis as _{(C 38 H 45 N 3 O} 7 Cl 2 · 1/10 H 2 O): Calculated: C: 62.65; H: 6.25 ; N: 5.77; Cl: 9.73 Found: C : 62.26; H: 6.18; N: 5.66; Cl: 9.87

[0310]

Example 55 (Exemplified Compounds, Table 2-2006) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] spiro [isobenzofuran-1 (3
H), 4'-piperidine] Yield: 63% Mass spectrum (FAB) m / z: 641 ((M +
H) ⁺⁾ Elemental analysis as _{(C 34 H 38 N 2 O} 6 Cl 2 · 1/10 H 2 O): Calculated: C: 63.47; H: 5.98 ; N: 4.35; Cl: 11.02 Found: C : 63.04; H: 6.10; N: 4.24; Cl: 11.10

[0311]

Example 56 (Exemplified compounds shown in Table 2-2014)1- [2- [2- (3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] -1-methanesulfonyl-spiro
(Indoline-3,4'-piperidine) Yield: 85% Mass spectrum (FAB) m / z: 718 ((M +
H)⁺ ) Elemental analysis value (C₃₅H₄₁N_Three O₇ SCl_Two As): Calculated: C: 58.49; H: 5.75; N: 5.85; Cl: 9.87; S: 4.46 Found: C: 58.26; H: 5.80; N: 5.74; Cl: 10.02; S: 4.33

[0312]

Example 57 (Exemplified Compounds, Table 2-2008) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] spiro [benzo [c] thiophene-
1 (3H), 4'-piperidine] Yield: 78% Mass spectrum (FAB) m / z: 657 ((M +
H) ⁺ ) Elemental analysis (as C ₃₄ H ₃₈ N ₂ O ₅ SCl ₂ .H ₂ O): Calculated: C: 60.44; H: 5.97; N: 4.15; Cl: 10.49; S: 4.74 Found: C: 60.68; H: 5.95; N: 3.92; Cl: 10.60; S: 4.85

[0313]

Example 58 (Exemplified Compounds, Table 2-2010) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] spiro [benzo [c] thiophene-
1 (3H), 4'-piperidine] -2-oxide yield: 60% mass spectrum (FAB) m / z: 673 ((M +
H) ⁺ ) Elemental analysis (as C ₃₄ H ₃₈ N ₂ O ₆ SCl ₂ ): Calculated: C: 60.62; H: 5.69; N: 4.16; Cl: 10.53; S: 4.76 Found: C: 60.50; H: 5.94; N: 4.09; Cl: 10.35; S: 4.71

[0314]

Example 59 (Exemplified Compounds, Table 2-2015)1- [2- [2- (3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethyl] spiro [isoquinoline-1 (2
H), 4'-Piperidine] -3 (4H) -one Yield: 80% Mass spectrum (FAB) m / z: 668 ((M +
H)⁺ ) Elemental analysis value (C₃₅H₃₉N_Three O₆ Cl_Two As): Calculated: C: 62.87; H: 5.88; N: 6.29; Cl: 10.61 Found: C: 62.95; H: 5.98; N: 6.07; Cl: 10.77.

[0315]

Example 60 (Exemplified compounds shown in Table 2-2353) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(2-pyridylcarbonyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid
De Yield: 73% mass spectrum (FAB) m / z: 567 ((M +
H) ⁺⁾ Elemental analysis as _{(C 30 H 32 N 4 O} 3 Cl 2 · 1/2 H 2 O): Calculated: C: 62.50; H: 5.77 ; N: 9.72; Cl: 12.30 Found: C : 62.19; H: 5.88; N: 9.39; Cl: 13.12

[0316]

Example 61 (Exemplified compounds shown in Table 2-2355) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(2-pyridylcarbonyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid di
Methylamide yield: 70% Mass spectrum (FAB) m / z: 595 ((M +
H) ⁺⁾ Elemental analysis as _{(C 32 H 36 N 4 O} 3 Cl 2 · 1/2 H 2 O): Calculated: C: 63.57; H: 6.17 ; N: 9.27; Cl: 11.73 Found: C : 63.34; H: 6.26; N: 9.23; Cl: 11.97.

[0317]

Example 62 (Exemplified Compounds, Table 2-1585) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(2-methoxybenzoyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid
De Yield: 75% mass spectrum (FAB) m / z: 596 ((M +
H) ⁺⁾ Elemental analysis as _{(C 32 H 35 N 3 O} 4 Cl 2 · 1/2 H 2 O): Calculated: C: 63.47; H: 5.99 ; N: 6.94; Cl: 11.71 Found: C : 63.02; H: 6.12; N: 6.74; Cl: 12.97.

[0318]

Example 63 (Exemplified Compounds, Table 2-1587) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(2-methoxybenzoyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid di
Methylamide yield: 77% Mass spectrum (FAB) m / z: 624 ((M +
H) ⁺⁾ Elemental analysis as _{(C 34 H 39 N 3 O} 4 Cl 2 · 1/2 H 2 O): Calculated: C: 64.45; H: 6.36 ; N: 6.63; Cl: 11.19 Found: C : 64.29; H: 6.42; N: 6.68; Cl: 11.57

[0319]

Example 64 (Exemplified Compounds, Table 2-1633) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(3-methoxybenzoyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid
De Yield: 80% mass spectrum (FAB) m / z: 596 ((M +
H) ⁺⁾ Elemental analysis as _{(C 32 H 35 N 3 O} 4 Cl 2 · 1/2 H 2 O): Calculated: C: 63.47; H: 5.99 ; N: 6.94; Cl: 11.71 Found: C : 63.44; H: 5.79; N: 6.79; Cl: 11.47.

[0320]

Example 65 (Exemplified Compounds, Table 2-1635) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(3-methoxybenzoyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid di
Methyl amide yield: 80% Mass spectrum (FAB) m / z: 624 ((M +
H) ⁺⁾ Elemental analysis as _{(C 34 H 39 N 3 O} 4 Cl 2 · 1/5 H 2 O): Calculated: C: 65.01; H: 6.32 ; N: 6.69; Cl: 11.29 Found: C : 64.79; H: 6.47; N: 6.42; Cl: 10.93

[0321]

Example 66 (Exemplified compounds shown in Table 2-1681) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(4-methoxybenzoyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid
De Yield: 94% mass spectrum (FAB) m / z: 596 ((M +
H) ⁺⁾ Elemental analysis as _{(C 32 H 35 N 3 O} 4 Cl 2 · 1/5 H 2 O): Calculated: C: 64.04; H: 5.95 ; N: 7.00; Cl: 11.82 Found: C : 63.67; H: 5.97; N: 6.70; Cl: 12.20

[0322]

Example 67 (Exemplified Compounds, Table 2-1683) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(4-methoxybenzoyl) morpholin-2-yl] d
Tyl] -4-phenylpiperidine-4-carboxylic acid di
Methylamide yield: 78% Mass spectrum (FAB) m / z: 624 ((M +
H) ⁺ ) Elemental analysis (as C ₃₄ H ₃₉ N ₃ O ₄ Cl ₂ ): Calculated: C: 65.38; H: 6.29; N: 6.73; Cl: 11.35 Found: C: 65.32; H: 6.94; N: 6.61; Cl: 10.97

[0323]

Example 68 (Exemplified Compounds, Table 2-2497) 1- [2- [2- (3,4-dichlorophenyl) -4-]
(2-pyrazinylcarbonyl) morpholin-2-yl]
Ethyl] -4-phenylpiperidine-4-carboxylic acid
Mide yield: 31% Mass spectrum (FAB) m / z: 568 ((M +
H) ⁺ ) Elemental analysis (as C ₂₉ H ₃₁ N ₅ O ₃ Cl ₂ .H ₂ O): Calculated: C: 59.39; H: 5.67; N: 11.87; Cl: 12.09 Found: C: 59.58; H: 5.82; N: 11.30; Cl: 12.56

[0324]

Example 69 (Exemplified compounds shown in Table 2-2499) 1- [2- [2- (3,4-Dichlorophenyl) -4-]
(2-pyrazinylcarbonyl) morpholin-2-yl]
Ethyl] -4-phenylpiperidine-4-carboxylic acid
Dimethylamide yield: 33% Mass spectrum (FAB) m / z: 596 ((M +
H) ⁺ ) Elemental analysis (as C ₃₁ H ₃₅ N ₅ O ₃ Cl ₂ .H ₂ O): Calculated: C: 60.58; H: 6.07; N: 11.40; Cl: 11.54 Found: C: 60.57; H: 5.95; N: 9.97; Cl: 12.88

[0325]

Example 70 (Exemplified Compounds, Table 2-1969) 1- [2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Rin-2-yl] ethyl] -4-phenylpiperidine-
4-carboxylic amide

[0326]

Example 70 (a)4-tert-butyldimethylsilyloxy- (2R)-
(3,4-dichlorophenyl) butane-1,2-dio
Le (DHQD)_Two -PHAL (hydroquinidine 1,4
-Phthalazine diyl diether) 790 mg (1.01
Mmol), K_Three Fe (CN)₆ (Potassium ferricyanide
100.19 g (0.30 mol), potassium carbonate
42.06 g (0.30 mol) and osmium tetroxide
(0.393 M toluene solution) 0.516 ml (0.2
0 mmol) in 500 ml of tert-butanol and 5
Example 51 (b) dissolved in 00 ml and cooled to 0 ° C.
33.61 g (0.10 mol) of olefin compound synthesized in
Was added and further stirred at 0 ° C. for 5 hours. Nato sulfite
After adding 150 g of lithium and stirring at room temperature for 1 hour,
Extract the reaction mixture with ethyl acetate (800 ml x 3)
The organic layer was dried over magnesium sulfate. Decompress the solvent
After distillation, the residue is purified by silica gel flash column chromatography.
Raffy (developing solvent: n-hexane: ethyl acetate = 5:
1: 1: 1) to give the target compound as a colorless oil
32.3 g (87%) were obtained. Optical purity: 97% ee [α]_D ^{twenty four} +11.39 (C = 1.01, methano
) Nuclear magnetic resonance spectrum (400 MHz, CDCl_Three )
δ ppm: 7.57 (1H, d, J = 2.1Hz), 7.43 (1H, d, J = 8.1Hz), 7.24
(1H, dd, J = 8.1,2.1Hz), 5.00 (1H, s), 3.80 (1H, ddd, J = 10.4,
3.8,3.8Hz), 3.5 to 3.7 (3H, m), 2.51 (1H, dd, J = 8.0,5.2H
z), 2.37 (1H, ddd, J = 15.0,11.1,4.0Hz), 1.86 (1H, ddd, J = 1
5.0,2.9,2.9Hz), 0.89 (9H, s), 0.04 (3H, s),-0.01 (3H, s)

[0327]

Example 70 (b) 1-azido-4-tert-butyldimethylsilyloxy-
(2R)-(3,4-dichlorophenyl) -2-butano
Diol 32.07g synthesized in Lumpur Example 70 (a)
(87.8 mmol) and 1.07 g (8.76 mmol) of 4-dimethylaminopyridine in 320 m of pyridine
methanesulfonyl chloride 1 under ice-cooling.
0.19 ml (0.132 mol) is slowly dropped,
The mixture was stirred at the same temperature for 2 hours under a nitrogen atmosphere. The reaction mixture was poured into ice-cooled 10% hydrochloric acid (1500 ml), and then extracted with ethyl acetate (200 ml × 3 times).
The organic layer was washed with a saturated saline solution and dried over magnesium sulfate. The solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure.
This was dissolved in 300 ml of anhydrous dimethylformamide, added with 11.41 g (0.18 mol) of sodium azide, and heated at 120 ° C. for 4 hours under a nitrogen atmosphere.
After the reaction mixture was brought to room temperature, it was poured into 1,000 ml of saturated saline and extracted with ethyl acetate (500 ml × 3 times). After the organic layer was dried over magnesium sulfate, the solvent was distilled off under reduced pressure, and the residue was subjected to silica gel flash column chromatography (developing solvent: n-hexane: ethyl acetate = 1).
0: 1 to 5: 1) to give 29.3 g (85%) of the target compound as a colorless oil. [Α] _D ²⁴ -48.56 (C = 1.04, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.59 (1H, d, J = 2.2Hz), 7.44 (1H, d, J = 8.3Hz), 7.24
(1H, dd, J = 8.3,2.2Hz), 5.12 (1H, s), 3.81 (1H, ddd, J = 10.6,
4.1,3.0Hz), 3.51 (1H, ddd, J = 10.6,10.6,2.8Hz), 3.40 (1H,
d, J = 12.5Hz), 3.31 (1H, d, J = 12.5Hz), 2.35 (1H, ddd, J = 15.
8,10.6,4.1Hz), 1.91 (1H, ddd, J = 15.8,3.0,2.8Hz), 0.88 (9
H, s), 0.02 (3H, s),-0.04 (3H, s)

[0328]

Example 70 (c) 1-amino-4-tert-butyldimethylsilyloxy-
(2R)-(3,4-dichlorophenyl) -2-butano
Lumpur Example 70 (b) synthesized in the azide compound 10.00 g (2
(5.6 mmol) was dissolved in 100 ml of tetrahydrofuran and 0.6 ml of water, 7.39 g (28.2 mmol) of triphenylphosphine was added, and the mixture was stirred at 80 ° C. for 4 hours under a nitrogen atmosphere. The solvent was distilled off under reduced pressure, n-hexane was added to the residue, and the precipitated crystals were separated by filtration.
After the filtrate was concentrated under reduced pressure, the residue was purified by silica gel flash column chromatography (developing solvent: methylene chloride: methanol = 30: 1 to 10: 1), and 3.83 g (41%) of the target compound as a colorless oil. )Obtained. [Α] _D ²⁴ +3.94 (C = 0.71, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δ ppm: 7.56 (1H, d, J = 2.2Hz), 7.42 (1H, d, J = 8.6Hz), 7.22
(1H, dd, J = 8.6,2.2Hz), 4.91 (1H, br.s), 3.73 (1H, ddd, J = 1
0.3,4.6,3.7Hz), 3.53 (1H, ddd, J = 10.3,10.2,3.7Hz), 2.91
(1H, d, J = 13.1Hz), 2.86 (1H, d, J = 13.1Hz), 2.16 (1H, ddd, J =
14.6,10.2,4.6Hz), 1.88 (1H, ddd, J = 14.6,3.7,3.7Hz), 1.4
4 (2H, br.s), 0.87 (9H, s), 0.01 (3H, s),-0.04 (3H, s)

[0329]

Example 70 (d) 1- (chloroacetyl) amino-4-tert-butyldimethyl
Tylsilyloxy- (2R)-(3,4-dichlorophene
2. Nyl) -2-butanol Amino alcohol derivative synthesized in Example 70 (c).
60 g (9.88 mmol) and triethylamine 1.
64 ml (11.8 mmol), 121 mg (0.99 mmol) of 4-dimethylaminopyridine were added to methylene chloride 1
Of chloroacetyl chloride under ice cooling, and added dropwise at the same temperature.
Stirred for hours. 100 ml of methylene chloride was added to the reaction mixture, and the mixture was washed successively with ice-cooled 10% hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and saturated saline, and then dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel flash column chromatography (developing solvent: ethyl acetate: n-hexane = 1: 5-1: 2) to give the target compound as a colorless oil. .32g
(76%). Nuclear magnetic resonance spectrum (270 MHz, CDCl ₃ )
δppm: 7.64 (1H, d, J = 2.1Hz), 7.47 (1H, d, J = 8.4Hz), 7.28
(1H, dd, J = 8.4,2.1Hz), 7.03 (1H, br.t), 5.27 (1H, s), 4.04
(2H, ABq, J = 15.1Hz, Δδ = 0.08ppm), 3.81 (1H, dt, J = 10.5,
3.7Hz), 3.72 (1H, dd, J = 13.5,6.2Hz), 3.53 (1H, dd, J = 10.9,
2.3Hz), 3.45 (1H, dd, J = 13.5,5.4Hz), 2.24 (1H, ddd, J = 14.
8,10.9,4.1Hz), 1.93 (1H, dt, J = 14.8,2.8Hz), 0.92 (9H, s),
0.06 (3H, s), 0.00 (3H, s)

[0330]

Working Example 70 (e) 2-[(2R)-(3,4-dichlorophenyl) -5-
Oxomorpholin-2-yl] ethanol tert-butyl
219 mg (5.48 mmol) of sodium dimethylsilyl ether hydride (containing 60%) was suspended in 30 ml of anhydrous tetrahydrofuran, and then 1.61 g of chloroacetyl compound synthesized in Example 70 (d) (3. (.65 mmol) in 30 ml of anhydrous tetrahydrofuran was slowly added dropwise over 30 minutes under ice-cooling, and the mixture was further stirred at the same temperature for 4 hours. The reaction mixture was poured into ice-cooled 10% hydrochloric acid, extracted with ethyl acetate (100 ml × 3 times), and the organic layer was washed with brine and dried over magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was subjected to silica gel flash column chromatography (developing solvent; ethyl acetate:
Purification was performed using n-hexane = 1: 4 to 2: 1) to obtain 700 mg (47%) of the target compound. [Α] _D ²⁴ = + 67.65 (c = 0.81, methanol) Nuclear magnetic resonance spectrum (270 MHz, CDCl ₃ )
δppm: 7.532 (1H, d, J = 2.2Hz), 7.526 (1H, d, J = 8.1Hz), 7.
27 (1H, dd, J = 8.1,2.2Hz), 6.76 (1H, br.s), 4.17 (2H, ABq, J =
17.3Hz, Δδ = 0.24ppm), 3.98 (1H, dd, J = 13.0,3.9Hz), 3.7
6 (1H, dd, J = 13.0,2.0Hz), 3.63 (1H, m), 3.29 (1H, m), 2.12 (2
H, m), 0.91 (9H, s), 0.04 (3H, s), 0.03 (3H, s)

[0331]

Working Example 70 (f) 2-[(2R)-(3,4-dichlorophenyl) morpho
Rin-2-yl] ethanol 2-[(2R)-(3, obtained in Example 70 (e).
4-dichlorophenyl) -5-oxomorpholine-2-
[Ill] ethanol 580 mg (1.43 mmol) of tert-butyldimethylsilyl ether is dissolved in 6 ml of dry tetrahydrofuran, and the mixture is heated to reflux under a stream of nitrogen to obtain 0.60 ml of a borane dimethylsulfide complex (10M).
(6.0 mmol) was added dropwise, and the mixture was stirred for 2 hours. The solvent of the reaction solution was distilled off, 5 ml of 1N hydrochloric acid was added, and the mixture was stirred at 100 ° C. for 1 hour. After allowing the reaction solution to cool, it was made alkaline with a 1N aqueous sodium hydroxide solution, diluted with saturated saline, and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (elution solvent: methylene chloride: methanol =
9: 1 to 17: 3) to purify the target compound 360
mg was obtained. [Α] _D ²⁴ = + 16.22 (c = 0.45, methanol) The nuclear magnetic resonance spectrum, infrared absorption spectrum and mass spectrum were identical to those of the racemic product produced in Example 51 (f).

[0332]

Example 70 (g) 2-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethanol 2-[(2R)-(3, obtained in Example 70 (f).
Using 4-dichlorophenyl) morpholin-2-yl] ethanol in the same manner as in Example 51 (g), the target compound was obtained in a yield of 92%. [Α] _D ²⁴ = + 30.65 (c = 0.56, methanol) The nuclear magnetic resonance spectrum, infrared absorption spectrum and mass spectrum were identical to those of the racemic product prepared in Example 51 (g).

[0333]

Working Example 70 (h) 2-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethanol methanesulfonate 2-[(2R)-(3, obtained in Example 70 (g).
Using 4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethanol in the same manner as in Example 51 (h), the target compound was obtained in a yield of 99%. Was. [Α] _D ²⁴ = + 18.52 (c = 0.61, methanol) The nuclear magnetic resonance spectrum, infrared absorption spectrum and mass spectrum were identical to those of the racemic product prepared in Example 51 (h).

[0334]

Example 70 (i) 1- [ 2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Rin-2-yl] ethyl] -4-phenylpiperidine-
4-carboxylic acid amide 2-[(2R)-(3, obtained in Example 70 (h).
4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethanol
The same procedure as in Example 51 (i) was carried out using methanesulfonate to obtain the desired compound in a yield of 79%. [Α] ^{_{D 24 = + 7.53 (c =}} 0.50, methanol) (as _{C 34 H 39 N 3 O 6} Cl 2 · 1/5 H 2 O) Elemental analysis: Calculated: C: 61.85; H N: 6.36; N: 6.74; Cl: 10.74 Found: C: 61.51; H: 6.18; N: 6.13; Cl: 10.72 The nuclear magnetic resonance spectrum, infrared absorption spectrum, and mass spectrum were prepared in Example 51 (i). Was consistent with that of the racemate.

In the same manner as in Example 70, the following compounds of Examples 71 to 74 were synthesized.

[0336]

Example 71 (Exemplified Compounds, Table 2-1970) 1- [2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Rin-2-yl] ethyl] -4-phenylpiperidine-
4-Carboxylic acid dimethylamide yield: 84% [α] _D ²⁴ = + 7.04 (c = 0.45, methanol) Elemental analysis (as C ₃₆ H ₄₈ N ₃ O ₆ Cl ₂ ): Calculated: C : 62.69; H: 7.02; N: 6.09; Cl: 10.28 Found: C: 62.37; H: 6.42; N: 5.94; Cl: 10.72.

[0337]

Example 72 (Exemplified Compounds, Table 2-2010) 1- [2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphorus-2-yl] ethyl] spiro [benzo [c] thiof
Ene-1 (3H), 4′-piperidine] -2-oxide yield: 66% [α] _D ²⁴ = −2.50 (c = 0.50, methanol) Elemental analysis (C ₃₄ H ₃₈ N) ₂ as O ₆ SCl _2): calculated: C: 60.62; H: 5.69 ; N: 4.16; Cl: 10.53; S: 4.76 Found: C: 60.17; H: 5.68 ; N: 4.00; Cl: 10.47; S ： 4.55

[0338]

Example 73 (Exemplified compounds described later in Table 2-2015)1- [2-[(2R)-(3,4-dichlorophenyl)
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphor-2-yl] ethyl] spiro [isoquinoline-1
(2H), 4'-piperidine] -3 (4H) -one Yield: 75% [α]_D ^{twenty four} = + 2.58 (c = 0.40, methanol) Elemental analysis value (C₃₅H₃₉N_Three O₆ Cl_Two As): Calculated: C: 62.87; H: 5.88; N: 6.29; Cl: 10.61 Found: C: 62.46; H: 6.01; N: 6.08; Cl: 9.63

[0339]

Example 74 (Exemplified Compounds, Table 2-1635) 1- [2-[(2R)-(3,4-dichlorophenyl)]
-4- (3-methoxybenzoyl) morpholin-2-i
[Ethyl] -4-phenylpiperidine-4-carboxyl
Acid dimethylamide Yield: 78% [α] ^{_{D 24 = + 9.67 (c =}} 0.50, methanol) Elemental analysis (as _{C 34 H 39 N 3 O 4} Cl 2 · 1/5 H 2 O): Calculated: C: 65.01; H: 6.32; N: 6.69; Cl: 11.29 Found: C: 64.84; H: 6.46; N: 6.52; Cl: 11.58.

[0340]

Example 75 (Exemplified compounds shown below, Table 1-4097) 1- {2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl {spiro [benzo [c] thi
Offen-1 (3H), 4'-piperidine] -2-oxo
Sid

[0341]

Example 75 (a) 3- (3,4-dichlorophenyl) -3-butenoic acid
11.31 g (0.47 mol) of a chill ester metal magnesium piece was
To 300 ml of ether, a small amount of iodine was added, and the mixture was allowed to stand for 1 hour. Then, 102.87 g (0.46 mol) of 1-bromo-3,4-dichlorobenzene (150 m
l) The solution was slowly added dropwise. After adding 150 ml of ether, 60.33 g (44.3 mmol) of anhydrous zinc chloride was slowly added, followed by stirring for 1 hour. Further, bis (triphenylphosphine) palladium chloride3.
After addition of 10 g (4.42 mmol) diketene 3
4.15 ml (42.8 mmol) of ether (600
ml) solution was added dropwise and the reaction mixture was stirred at room temperature for 30 minutes.

The reaction mixture was poured into 1 liter of ice-cooled 1N hydrochloric acid, and extracted with ether (500 ml × 3 times).
The collected organic layer was washed with 1N aqueous sodium hydroxide solution (700
ml x 3). The aqueous layer was acidified with concentrated hydrochloric acid under ice-cooling, extracted with ether (500 ml × 3 times), and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the residue was dissolved in methanol (350 ml), concentrated sulfuric acid (10 ml) was added, and the mixture was heated under reflux for 30 minutes. After allowing to cool, neutralized with a saturated aqueous sodium hydrogen carbonate solution, methanol was distilled off under reduced pressure, and the residue was extracted with methylene chloride (200 ml × 3 times). After the organic layer was dried over anhydrous magnesium sulfate, the solvent was concentrated under reduced pressure. The residue was distilled under reduced pressure to give the target compound as a pale yellow oil, 6
9.13 g (62%) were obtained.

Boiling point: 144 to 146 ° C. (5 mmHg) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.51 (1H, d, J = 2.2Hz), 7.40 (1H, d, J = 8.2H
z), 7.25 (1H, dd, J = 8.2, 2.2Hz), 5.55 (1H, s), 5.30
(1H, s), 3.67 (3H, s), 3.49 (2H, s).

[0344]

Example 75 (b) 3- (3,4-dichlorophenyl) -3-butene-1-
All tert-butyldimethylsilyl ether lithium aluminum hydride (11.76 g, 0.28 mol) was suspended in anhydrous tetrahydrofuran (500 ml).
Then, 3- (3,4-dichlorophenyl) -3-butenoic acid methyl ester 6 synthesized in Example 75 (a) 6
A solution of 9.06 g (0.28 mol) in anhydrous tetrahydrofuran (500 ml) was added at 0 ° C. under a nitrogen atmosphere for 15 minutes.
Slowly dropped over a period of minutes. After stirring the reaction mixture at the same temperature for 30 minutes, water (500 ml) and 10%
An aqueous sodium hydroxide solution (500 ml) was slowly added, and the mixture was further stirred at room temperature for 1 hour.

After filtering the reaction mixture through celite, the filtrate was extracted with ethyl acetate (500 ml × 3), the organic layer was dried over anhydrous magnesium sulfate, the solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure. This was dissolved in 250 ml of anhydrous dimethylformamide, and then 47.12 ml (0.34 mol) of triethylamine, 6.88 g (0.06 mol) of 4-dimethylaminopyridine and tert-
50.96 g of butyldimethylsilyl chloride (0.34
Mol), and the mixture was further stirred for 2 hours under ice cooling.

To the reaction mixture was added 1 liter of ethyl acetate, and the mixture was washed successively with ice-cooled 10% hydrochloric acid and saturated saline, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel flash column chromatography (elution solvent: n-hexane: ethyl acetate =
Purification was carried out at 50: 1 to 20: 1) to obtain 43.52 g (47%) of the target compound as a colorless oil.

A nuclear magnetic resonance spectrum (400 MHz, C
DCl ₃ ) δ ppm: 7.50 (1H, d, J = 2.1 Hz), 7.38 (1
H, d, J = 8.1Hz), 7.24 (1H, dd, J = 8.1, 2.1Hz), 5.35
(1H, s), 5.16 (1H, s), 3.70 (2H, t, J = 6.9Hz), 2.67
(2H, t, J = 6.9Hz), 0.86 (9H, s), 0.00 (6H, s).

[0348]

Example 75 (c) 4-tert-butyldimethylsilyloxy- (2R)
-(3,4-dichlorophenyl) butane-1,2-dio
Lumpur (DHQD) ₂ -PHAL (Hydro quinidine 1,4
-Phthalazine diyl diether) 790 mg (1.01
Mmol), 100.19 g (0.30 mol) of K ₃ Fe (CN) ₆ (potassium ferricyanide), 42.06 g (0.30 mol) of potassium carbonate and 0.516 ml of osmium tetroxide (0.393 M toluene solution) 0.2
0 mmol) in 2-methyl-2-propanol 500
dissolved in 500 ml of water and 500 ml of water, and cooled to 0 ° C., 33.61 g of the olefin compound synthesized in Example 75 (b).
(0.10 mol), and the mixture was further stirred at 0 ° C. for 5 hours.

After adding 150 g of sodium sulfite and stirring at room temperature for 1 hour, the reaction mixture was diluted with ethyl acetate (80%).
(0 ml × 3 times), and the organic layer was dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was purified by silica gel flash column chromatography (eluent: n-hexane: ethyl acetate = 5: 1 to 1: 1) to obtain 32.3 g of the desired compound as a colorless oil. (87
%)Obtained.

Optical purity: 97% ee [α] _D ²⁴ +11.39 (c = 1.01, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.57 (1H, d, J = 2.1Hz), 7.43 (1H, d, J = 8.1H
z), 7.24 (1H, dd, J = 8.1, 2.1Hz), 5.00 (1H, s), 3.80
(1H, ddd, J = 10.4, 3.8, 3.8Hz), 3.5-3.7 (3H, m), 2.5
1 (1H, dd, J = 8.0, 5.2Hz), 2.37 (1H, ddd, J = 15.0, 1
1.1, 4.0Hz), 1.86 (1H, ddd, J = 15.0, 2.9, 2.9Hz), 0.
89 (9H, s), 0.04 (3H, s), -0.01 (3H, s).

[0351]

Example 75 (d) 1-azido-4-tert-butyldimethylsilyloxy
C- (2R)-(3,4-dichlorophenyl) -2-bu
Synthesized diol 32.07g in ethanol Example 75 (c)
(87.8 mmol) and 1.07 g (8.76 mmol) of 4-dimethylaminopyridine in 320 m of pyridine
methanesulfonyl chloride 1 under ice-cooling.
0.19 ml (0.132 mol) is slowly dropped,
The mixture was stirred at the same temperature for 2 hours under a nitrogen atmosphere.

The reaction mixture was cooled with ice-cooled 10% hydrochloric acid (15%).
00 ml) and then ethyl acetate (200 ml)
× 3), and the organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure.

This was treated with anhydrous dimethylformamide 300
dissolved in sodium chloride and 11.41 g of sodium azide (0.4 g).
18 mol) and heated under a nitrogen atmosphere at 120 ° C. for 4 hours. After the reaction mixture was brought to room temperature, saturated saline 1
The mixture was poured into a liter, and extracted with ethyl acetate (500 ml × 3 times). After the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel flash column chromatography (elution solvent: n-hexane: ethyl acetate = 10: 1 to 5: 1). 29.3 g (85%) of the desired compound was obtained as a colorless oil.

[Α] _D ²⁴ −48.56 (C = 1.04,
Methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.59 (1H, d, J = 2.2Hz), 7.44 (1H, d, J = 8.3H)
z), 7.24 (1H, dd, J = 8.3, 2.2Hz), 5.12 (1H, s), 3.81
(1H, ddd, J = 10.6, 4.1, 3.0Hz), 3.51 (1H, ddd, J = 10.
6, 10.6, 2.8Hz), 3.40 (1H, d, J = 12.5Hz), 3.31 (1H,
d, J = 12.5Hz), 2.35 (1H, ddd, J = 15.8, 10.6, 4.1Hz),
1.91 (1H, ddd, J = 15.8, 3.0, 2.8Hz), 0.88 (9H, s),
0.02 (3H, s), -0.04 (3H, s).

[0355]

Example 75 (e) 1-amino-4-tert-butyldimethylsilyloxy
C- (2R)-(3,4-dichlorophenyl) -2-bu
Pentanol Example 75 (d) synthesized in the azide compound 10.00 g (2
(5.6 mmol) was dissolved in 100 ml of tetrahydrofuran and 0.6 ml of water, 7.39 g (28.2 mmol) of triphenylphosphine was added, and the mixture was stirred at 80 ° C. for 4 hours under a nitrogen atmosphere. The solvent was distilled off under reduced pressure, n-hexane was added to the residue, and the precipitated crystals were separated by filtration.
After the filtrate was concentrated under reduced pressure, the residue was purified by silica gel flash column chromatography (elution solvent: methylene chloride: methanol = 30: 1 to 10: 1) to give 3.83 g (41%) of the target compound as a colorless oil. )Obtained.

[Α] _D ²⁴ +3.94 (C = 0.71, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.56 (1H, d, J = 2.2Hz), 7.42 (1H, d, J = 8.6H
z), 7.22 (1H, dd, J = 8.6, 2.2Hz), 4.91 (1H, br.s),
3.73 (1H, ddd, J = 10.3, 4.6, 3.7Hz), 3.53 (1H, ddd,
J = 10.3, 10.2, 3.7Hz), 2.91 (1H, d, J = 13.1Hz), 2.86
(1H, d, J = 13.1Hz), 2.16 (1H, ddd, J = 14.6, 10.2, 4.6
Hz), 1.88 (1H, ddd, J = 14.6, 3.7, 3.7Hz), 1.44 (2H,
br.s), 0.87 (9H, s), 0.01 (3H, s),-0.04 (3H, s)
.

[0357]

Working Example 75 (f) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
N-5-yl] ethanol tert-butyldimethyl
Silyl ether 1.3 amino alcohol compound synthesized in Example 75 (e)
5 g (3.71 mmol) are dissolved in 50 ml of benzene and 167 mg (5.57 mmol) of paraformaldehyde and 13 mg of p-toluenesulfonyl chloride are dissolved.
Was added and heated to reflux at 100 ° C. for 3 hours under a nitrogen atmosphere using a Dean-Stark apparatus. After the solvent was distilled off under reduced pressure, 100 ml of ethyl acetate was added to the residue, washed with a saturated aqueous solution of sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate.

After distilling off the solvent under reduced pressure, the obtained 2-[(5
R)-(3,4-Dichlorophenyl) oxazolidine-
5-yl) ethanol The residue of tert-butyldimethylether was dissolved in 50 ml of methylene chloride, 0.62 ml (4.45 mmol) of triethylamine and 45 mg (0.37 mmol) of 4-dimethylaminopyridine were added, and then the mixture was cooled on ice. , 3,4,5-trimethoxybenzoyl chloride 1.03 g (4.47 mmol) were added,
The mixture was stirred at 0 ° C. for 1 hour.

To the reaction mixture was added 100 ml of methylene chloride, and the mixture was washed successively with 10% hydrochloric acid, a saturated aqueous solution of sodium hydrogen carbonate and saturated saline, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by flash column chromatography on silica gel (eluent: ethyl acetate: n-hexane = 1: 5-2: 1) to give 1.27 g (60%) of the target compound as white amorphous.
%)Obtained.

[Α] _D ²⁴ +61.73 (C = 1.39,
methanol).

[0361]

Working Example 75 (g) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
N-5-yl] ethanol methanesulfonate 3.95 g (6.92 mmol) of the tert-butyldimethylsilyl ether compound synthesized in Example 75 (f) was obtained.
Mixed solution 7 of acetic acid: tetrahydrofuran: water = 3: 3: 1
It was dissolved in 0 ml and heated at 80 ° C. for 8 hours under a nitrogen atmosphere. After neutralization with a saturated aqueous solution of sodium hydrogen carbonate, the mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was treated with pyridine 3
0 ml, 4-dimethylaminopyridine 70m
g (0.57 mmol) and 0.66 ml (8.53 mmol) of methanesulfonyl chloride under ice-cooling.
The mixture was stirred at 0 ° C for 2 hours under a nitrogen atmosphere. The reaction mixture is poured into 200 ml of ice-cooled 10% hydrochloric acid and then
Extracted with ethyl acetate (100 ml × 3 times). The collected organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was purified by silica gel flash column chromatography (eluent: n-hexane: ethyl acetate = 5: 1 to 1: 1) to obtain 3.02 g of the target compound as a white amorphous substance (3.02 g). 82
%)Obtained.

[Α] _D ²⁴ +53.1 (C = 1.0, methanol).

[0363]

Working Example 75 (h) 1- {2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl {spiro [benzo [c] thi
Offen-1 (3H), 4'-piperidine] -2-oxo
Sid 600 mg of the mesyl compound obtained in Example 75 (g) (1.
12 mmol), and the spiro [benzo [c] thiophene-1 (3H), 4′-piperidine] obtained in Reference Example 4.
318 mg (1.23 mmol) of 2-oxide hydrochloride, 283 mg (3.37 mmol) of sodium hydrogen carbonate, 280 mg (1.69 mmol) of potassium iodide
Was suspended in 10 ml of anhydrous dimethylformamide and heated at 80 ° C. for 8 hours under a nitrogen atmosphere. The reaction solution was poured into 100 ml of saturated saline and extracted with ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The residue was subjected to silica gel column chromatography (elution solvent: methylene chloride: methanol = 40: 1 to 20:
Purification according to 1) and crystallization from diisopropyl ether gave 496 mg of the target compound as white crystals.

The nuclear magnetic resonance spectrum (400 MHz, C
DCl ₃ ) δ ppm: 7.1-7.6 (7H, m), 6.70 and 6.68 (total
2H, each s), 4.9-5.4 (total 2H, m), 4.29 (1H, d, J = 16.8Hz), 4.00
(1H, d, J = 16.8Hz), 3.7-4.2 (2H, m), 3.86, 3.87, 3.88 and
3.89 (9H in total, each s), 1.4-3.1 (12H, m) Infrared absorption spectrum ν _max cm ^-1 (KBr): 294
0, 1642, 1585, 1416, 1236, 112
8 Mass spectrum (FAB) m / z: 659 ((M +
H) ⁺⁾ Elemental analysis _{(C 33 H 36 N 2 O} 6 SCl 2 · 0.5H 2 O as a%) Calculated: C: 59.28, H: 5.58 , N: 4.19, S: 4.79, Cl: 10.60 Found Values: C: 59.57, H: 5.23, N: 4.15, S: 4.75, Cl: 10.30.

[0365]

Working Example 76 (Exemplified Compounds, Table 3-10) 1- {2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl {spiro [benzo [c] thi
Offen-1 (3H), 4'-piperidine]-(2S)
-Oxide

[0366]

Example 76 (a) 3- (3,4-dichlorophenyl) -3-butenoic acid
11.31 g (0.47 mol) of a chill ester metal magnesium piece was
To 300 ml of ether, a small amount of iodine was added, and the mixture was allowed to stand for 1 hour. Then, 102.87 g (0.46 mol) of 1-bromo-3,4-dichlorobenzene (150 m
l) The solution was slowly added dropwise. After adding 150 ml of ether, 60.33 g (44.3 mmol) of anhydrous zinc chloride was slowly added, followed by stirring for 1 hour. Further, bis (triphenylphosphine) palladium chloride3.
After addition of 10 g (4.42 mmol) diketene 3
4.15 ml (42.8 mmol) of ether (600
ml) solution was added dropwise and the reaction mixture was stirred at room temperature for 30 minutes.

The reaction mixture was poured into 1 liter of ice-cooled 1N hydrochloric acid, and extracted with ether (500 ml × 3 times).
The collected organic layer was washed with 1N aqueous sodium hydroxide solution (700
ml x 3). The aqueous layer was acidified with concentrated hydrochloric acid under ice-cooling, extracted with ether (500 ml × 3 times), and the organic layer was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, the residue was dissolved in methanol (350 ml), concentrated sulfuric acid (10 ml) was added, and the mixture was heated under reflux for 30 minutes. After allowing to cool, neutralized with a saturated aqueous sodium hydrogen carbonate solution, methanol was distilled off under reduced pressure, and the residue was extracted with methylene chloride (200 ml × 3 times). After the organic layer was dried over anhydrous magnesium sulfate, the solvent was concentrated under reduced pressure. The residue was distilled under reduced pressure to give the target compound as a pale yellow oil, 6
9.13 g (62%) were obtained.

Boiling point: 144 to 146 ° C. (5 mmHg) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.51 (1H, d, J = 2.2Hz), 7.40 (1H, d, J = 8.2H
z), 7.25 (1H, dd, J = 8.2, 2.2Hz), 5.55 (1H, s), 5.30
(1H, s), 3.67 (3H, s), 3.49 (2H, s).

[0369]

Working Example 76 (b) 3- (3,4-dichlorophenyl) -3-butene-1-
All tert-butyldimethylsilyl ether lithium aluminum hydride (11.76 g, 0.28 mol) was suspended in anhydrous tetrahydrofuran (500 ml).
Next, 3- (3,4-dichlorophenyl) -3-butenoic acid methyl ester 6 synthesized in Example 76 (a)
A solution of 9.06 g (0.28 mol) in anhydrous tetrahydrofuran (500 ml) was added at 0 ° C. under a nitrogen atmosphere for 15 minutes.
Slowly dropped over a period of minutes. After stirring the reaction mixture at the same temperature for 30 minutes, water (500 ml) and 10%
An aqueous sodium hydroxide solution (500 ml) was slowly added, and the mixture was further stirred at room temperature for 1 hour.

After filtering the reaction mixture through celite, the filtrate was extracted with ethyl acetate (500 ml × 3 times), the organic layer was dried over anhydrous magnesium sulfate, the solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure. This was dissolved in 250 ml of anhydrous dimethylformamide, and then 47.12 ml (0.34 mol) of triethylamine, 6.88 g (0.06 mol) of 4-dimethylaminopyridine and 50.96 g of tert-butyldimethylsilyl chloride were added under ice cooling. (0.34 mol), and the mixture was further stirred for 2 hours under ice cooling.

To the reaction mixture was added 1 liter of ethyl acetate, and the mixture was washed successively with ice-cooled 10% hydrochloric acid and saturated saline, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel flash column chromatography (elution solvent: n-hexane: ethyl acetate =
Purification was carried out at 50: 1 to 20: 1) to obtain 43.52 g (47%) of the target compound as a colorless oil.

A nuclear magnetic resonance spectrum (400 MHz, C
DCl ₃ ) δ ppm: 7.50 (1H, d, J = 2.1 Hz), 7.38 (1
H, d, J = 8.1Hz), 7.24 (1H, dd, J = 8.1, 2.1Hz), 5.35
(1H, s), 5.16 (1H, s), 3.70 (2H, t, J = 6.9Hz), 2.67
(2H, t, J = 6.9Hz), 0.86 (9H, s), 0.00 (6H, s).

[0373]

Example 76 (c)4-tert-butyldimethylsilyloxy- (2R)-
(3,4-dichlorophenyl) butane-1,2-dio
Le (DHQD)_Two -PHAL (hydroquinidine 1,4
-Phthalazine diyl diether) 790 mg (1.01
Mmol), K_Three Fe (CN)₆ (Potassium ferricyanide
100.19 g (0.30 mol), potassium carbonate
42.06 g (0.30 mol) and osmium tetroxide
(0.393 M toluene solution) 0.516 ml (0.2
0 mmol) in 2-methyl-2-propanol 500
dissolved in water and 500 ml of water and cooled to 0 ° C.
33.61 g of the olefin compound synthesized in Example 76 (b)
(0.10 mol) and further stirred at 0 ° C. for 5 hours.
did.

After adding 150 g of sodium sulfite and stirring at room temperature for 1 hour, the reaction mixture was diluted with ethyl acetate (80%).
(0 ml × 3 times), and the organic layer was dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was purified by silica gel flash column chromatography (eluent: n-hexane: ethyl acetate = 5: 1 to 1: 1) to obtain 32.3 g of the desired compound as a colorless oil. (87
%)Obtained.

Optical purity: 97% ee [α] _D ²⁴ +11.39 (c = 1.01, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.57 (1H, d, J = 2.1Hz), 7.43 (1H, d, J = 8.1H
z), 7.24 (1H, dd, J = 8.1, 2.1Hz), 5.00 (1H, s), 3.80
(1H, ddd, J = 10.4, 3.8, 3.8Hz), 3.5-3.7 (3H, m), 2.5
1 (1H, dd, J = 8.0, 5.2Hz), 2.37 (1H, ddd, J = 15.0, 1
1.1, 4.0Hz), 1.86 (1H, ddd, J = 15.0, 2.9, 2.9Hz), 0.
89 (9H, s), 0.04 (3H, s), -0.01 (3H, s).

[0376]

Example 76 (d) 1-azido-4-tert-butyldimethylsilyloxy-
(2R)-(3,4-dichlorophenyl) -2-butano
Diol 32.07g synthesized in Lumpur Example 76 (c)
(87.8 mmol) and 1.07 g (8.76 mmol) of 4-dimethylaminopyridine in 320 m of pyridine
methanesulfonyl chloride 1 under ice-cooling.
0.19 ml (0.132 mol) is slowly dropped,
The mixture was stirred at the same temperature for 2 hours under a nitrogen atmosphere.

The reaction mixture was cooled with ice-cooled 10% hydrochloric acid (15%).
00 ml) and then ethyl acetate (200 ml)
× 3), and the organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was concentrated under reduced pressure, and the residue was dried under reduced pressure.

This was treated with anhydrous dimethylformamide 300
dissolved in sodium chloride and 11.41 g of sodium azide (0.4 g).
18 mol) and heated under a nitrogen atmosphere at 120 ° C. for 4 hours. After the reaction mixture was brought to room temperature, saturated saline 1
The mixture was poured into a liter, and extracted with ethyl acetate (500 ml × 3 times). After the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and the residue was purified by silica gel flash column chromatography (elution solvent: n-hexane: ethyl acetate = 10: 1 to 5: 1). 29.3 g (85%) of the desired compound was obtained as a colorless oil.

[Α] _D ²⁴ −48.56 (c = 1.04, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.59 (1H, d, J = 2.2Hz), 7.44 (1H, d, J = 8.3H)
z), 7.24 (1H, dd, J = 8.3, 2.2Hz), 5.12 (1H, s), 3.81
(1H, ddd, J = 10.6, 4.1, 3.0Hz), 3.51 (1H, ddd, J = 10.
6, 10.6, 2.8Hz), 3.40 (1H, d, J = 12.5Hz), 3.31 (1H,
d, J = 12.5Hz), 2.35 (1H, ddd, J = 15.8, 10.6, 4.1Hz),
1.91 (1H, ddd, J = 15.8, 3.0, 2.8Hz), 0.88 (9H, s),
0.02 (3H, s), -0.04 (3H, s).

[0380]

Working Example 76 (e) 1-amino-4-tert-butyldimethylsilyloxy-
(2R)-(3,4-dichlorophenyl) -2-butano
Lumpur Example 76 (d) synthesized in the azide compound 10.00 g (2
(5.6 mmol) was dissolved in 100 ml of tetrahydrofuran and 0.6 ml of water, 7.39 g (28.2 mmol) of triphenylphosphine was added, and the mixture was stirred at 80 ° C. for 4 hours under a nitrogen atmosphere. The solvent was distilled off under reduced pressure, n-hexane was added to the residue, and the precipitated crystals were separated by filtration.
After the filtrate was concentrated under reduced pressure, the residue was purified by silica gel flash column chromatography (elution solvent: methylene chloride: methanol = 30: 1 to 10: 1) to give 3.83 g (41%) of the target compound as a colorless oil. )Obtained.

[Α] _D ²⁴ +3.94 (c = 0.71, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.56 (1H, d, J = 2.2Hz), 7.42 (1H, d, J = 8.6H
z), 7.22 (1H, dd, J = 8.6, 2.2Hz), 4.91 (1H, br.s),
3.73 (1H, ddd, J = 10.3, 4.6, 3.7Hz), 3.53 (1H, ddd,
J = 10.3, 10.2, 3.7Hz), 2.91 (1H, d, J = 13.1Hz), 2.86
(1H, d, J = 13.1Hz), 2.16 (1H, ddd, J = 14.6, 10.2, 4.6
Hz), 1.88 (1H, ddd, J = 14.6, 3.7, 3.7Hz), 1.44 (2H,
br.s), 0.87 (9H, s), 0.01 (3H, s),-0.04 (3H, s)
.

[0382]

Working Example 76 (f) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
N-5-yl] ethanol tert-butyldimethylsilyl
Aminoalcohol compound was synthesized in ether Example 76 (e) 1.3
5 g (3.71 mmol) are dissolved in 50 ml of benzene and 167 mg (5.57 mmol) of paraformaldehyde and 13 mg of p-toluenesulfonyl chloride are dissolved.
Was added and heated to reflux at 100 ° C. for 3 hours under a nitrogen atmosphere using a Dean-Stark apparatus. After the solvent was distilled off under reduced pressure, 100 ml of ethyl acetate was added to the residue, washed with a saturated aqueous solution of sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate.

After distilling off the solvent under reduced pressure, the obtained 2-[(5
R)-(3,4-Dichlorophenyl) oxazolidine-
5-yl) ethanol The residue of tert-butyldimethylether was dissolved in 50 ml of methylene chloride, 0.62 ml (4.45 mmol) of triethylamine and 45 mg (0.37 mmol) of 4-dimethylaminopyridine were added, and then the mixture was cooled on ice. , 3,4,5-trimethoxybenzoyl
1.03 g (4.47 mmol) of chloride was added,
For 1 hour.

After adding 100 ml of methylene chloride to the reaction mixture, the mixture was washed successively with 10% hydrochloric acid, a saturated aqueous solution of sodium hydrogencarbonate and saturated saline, and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by flash column chromatography on silica gel (eluent: ethyl acetate: n-hexane = 1: 5-2: 1) to give 1.27 g (60%) of the target compound as white amorphous.
%)Obtained.

[Α] _D ²⁴ +61.73 (c = 1.39,
methanol).

[0386]

Working Example 76 (g) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4,5-trimethoxybenzoyl) oxazolidi
[N-5-yl] ethanol methanesulfonate 3.95 g (6.92 mmol) of the tert-butyldimethylsilyl ether compound synthesized in Example 76 (f) was treated with acetic acid: tetrahydrofuran: water = 3: 3: 1. Mixed liquid 70
The mixture was dissolved in the same solution and heated at 80 ° C. for 8 hours under a nitrogen atmosphere. After neutralization with saturated aqueous sodium hydrogen carbonate solution,
The mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was treated with pyridine (30 m).
l-dimethylaminopyridine 70 mg
(0.57 mmol) and 0.66 ml (8.53 mmol) of methanesulfonyl chloride were added under ice-cooling, and the mixture was stirred at 0 ° C. under a nitrogen atmosphere for 2 hours. The reaction mixture is
The mixture was poured into 200 ml of ice-cooled 10% hydrochloric acid, and then extracted with ethyl acetate (100 ml × 3 times). The collected organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was purified by silica gel flash column chromatography (eluent: n-hexane: ethyl acetate = 5: 1 to 1: 1) to obtain 3.02 g of the target compound as a white amorphous ( 82%).

[Α] _D ²⁴ +53.1 (c = 1.0, methanol).

[0388]

Working Example 76 (h) 1- {2-[(5R)-(3,4-dichlorophenyl)]
-3- (3,4,5-trimethoxybenzoyl) oxa
Zolidin-5-yl] ethyl {spiro [benzo [c] thi
Offen-1 (3H), 4'-piperidine]-(2S)
-Oxide 600 mg of the mesyl compound obtained in Example 76 (g) (1.
Spiro [benzo [c] thiophene-1 (3H), 4'-piperidine] obtained in Reference Example 9.
318 mg (1.23 mmol) of-(2S) -oxide hydrochloride, 283 mg (3.37 mmol) of sodium hydrogencarbonate and 280 mg (1.69 mmol) of potassium iodide are suspended in 10 ml of anhydrous dimethylformamide, and a nitrogen atmosphere is added. The mixture was heated at 80 ° C. for 8 hours. The reaction solution was poured into 100 ml of saturated saline and extracted with ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The residue is subjected to silica gel column chromatography (elution solvent: methylene chloride: methanol = 40: 1 to 1).
20: 1), and crystallized from diisopropyl ether to give 496 mg of the target compound as white crystals.
Obtained.

[Α] _D ²⁴ +41.0 (c = 1, methanol) High Performance Liquid Chromatography (HPLC) Analysis: Column; YMC-Pack ODS-A (250 ×
4.6 mmφ) Elution solvent; CH ₃ CN: H ₂ O = 40: 60, 0.1%
Ammonium acetate Flow rate: 1.0 ml / min Retention time: 28.6 minutes Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.1-7.6 (7H, m), 6.70 (2H, s), 4.9-5.3 (total
2H, br.s), 4.32 (1H, d, J = 16.7Hz), 4.00 (1H, d, J = 1
6.7Hz), 3.7-4.2 (2H, m), 3.87 and 3.89 (9H in total, each
s), 1.5-3.1 (12H, m) infrared absorption spectrum ν _max cm ^-1 (KBr): 294
0, 1642, 1584, 1416, 1237, 112
8 Mass spectrum (FAB) m / z: 659 ((M +
H) ⁺⁾ Elemental analysis _{(C 33 H 36 N 2 O} 6 SCl 2 · 0.5H 2 O as a%) Calculated: C: 59.28, H: 5.58 , N: 4.19, S: 4.79, Cl: 10.60 Found Values: C: 59.36, H: 5.58, N: 4.12, S: 4.73, Cl: 10.60.

[0390]

Example 77 (Exemplified compounds shown below, Table 3-42) 1- {2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphorus-2-yl] ethyl {spiro [benzo [c] thiof
Ene-1 (3H), 4'-piperidine]-(2S) -o
Oxide

[0391]

Example 77 (a) 4- (tert-butyldimethylsilyloxy)-(2R)
-(3,4-dichlorophenyl) -1- [N- (tert-
Butoxycarbonyl) -N- (2-hydroxyethyl)
Amino] -2-butanol 4-tert-butyldimethylsilyloxy- (2R)-(3,4-dichlorophenyl) butane-1,2-diol 39.9 g (109 mmol) obtained in Example 76 (c) Was dissolved in pyridine (80 ml), p-toluenesulfonyl chloride (31.3 g, 164 mmol) was added, and the mixture was stirred under a nitrogen atmosphere at room temperature for 2 days. The reaction solution was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated saline, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was acetonitrile 600 m
Then, 35.0 g (329 mmol) of lithium perchlorate and 33.4 g (547 mmol) of 2-aminoethanol were added, and the mixture was refluxed for 16 hours. The reaction solution was cooled to room temperature, diluted with ethyl acetate, washed with saturated saline, and then the organic layer was dried over anhydrous sodium sulfate. After evaporating the solvent under reduced pressure, the residue was dissolved in 700 ml of methylene chloride, and 22.8 ml (164 mmol) of triethylamine was dissolved.
And 26.3 g of di-tert-butyl dicarbonate (12
0 mmol) and stirred at room temperature for 12 hours. The reaction solution was poured into water and extracted with methylene chloride. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The residue is subjected to silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 4:
1-7: 3) to give 49.9 g of the desired compound.

[Α] _D ²⁴ +3.92 (c = 0.72, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.30-7.75 (3H, m), 5.30 and 5.57 (1H,
Br.s), 3.05-4.00 (9H, m), 2.00-2.40 (2H, m), 1.53
(9H, s), 0.94 (9H, s), 0.09 (3H, s), 0.07 (3H, s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 342
0, 2957, 2933, 2885, 2861, 168
7 Mass spectrum (FAB) m / z: 508 ((M + H)
⁺ ).

[0393]

Example 77 (b)2- [4-tert-butoxycarbonyl- (2R)-
(3,4-dichlorophenyl) morpholin-2-yl]
Ethanol tert-butyldimethylsilyl ether 4- (tert-butyl dimethyl) obtained in Example 77 (a)
Lucylyloxy)-(2R)-(3,4-dichlorophene)
Nil) -1- [N- (tert-butoxycarbonyl) -N
-(2-hydroxyethyl) amino] -2-butanol
49.9 g (98.1 mmol) and triphenylphos
30.9 g (118 mmol) of fin dried torue
Dissolved in 600 ml of nitrogen at room temperature under a nitrogen atmosphere.
51.3 g of a 40% toluene solution of diethyl dicarboxylate
(118 mmol) was added dropwise and stirred for 2 hours. Solvent
The residue is evaporated under reduced pressure, and the residue is subjected to silica gel column chromatography.
(Eluent: n-hexane: ethyl acetate = 47: 3
~ 23: 2) to give 43.2 g of the desired compound
Was.

[Α] _D ²⁴ +32.67 (c = 0.60, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.56 (1H, br.s), 7.43 (1H, d, J = 9Hz), 7.2
8 (1H, dd, J = 2,9Hz), 3.00-4.55 (8H, m), 1.80-2.10
(2H, m), 1.35-1.60 (9H, br.s), 0.85 (9H, s), -0.01
(6H, s) infrared absorption spectrum ν _max cm ^-1 (CHCl ₃ ): 2
957, 2931, 2859, 1687 Mass spectrum (FAB) m / z: 490 ((M + H)
⁺ ).

[0395]

Example 77 (c) (2R)-(3,4-dichlorophenyl) -2- (2-
(Hydroxyethyl) morpholine hydrochloride 2- [4-tert-butoxycarbonyl- (2R)-(3,4-dichlorophenyl) obtained in Example 77 (b)
Morpholin-2-yl] ethanol 43.1 g (87.9 mmol) of tert-butyldimethylsilyl ether was dissolved in 4N hydrochloric acid in dioxane (600 ml),
Stirred at 60 ° C. for 4 hours. After evaporating the solvent under reduced pressure, diethyl ether was added and the mixture was evaporated under reduced pressure again. The residue was recrystallized from ethanol / ethyl acetate to give 24.1 g of the desired compound.
I got

[Α] _D ²⁴ +48.07 (c = 0.57, methanol) Nuclear magnetic resonance spectrum (400 MHz, DMSO-d
₆ ) δppm: 8.60-9.80 (2H, br.s), 7.72 (1H, s),
7.70 (1H, d, J = 9Hz), 7.44 (1H, dd, J = 2,9Hz), 4.53
(1H, br.s), 3.89 (1H, dt, J = 4, 13Hz), 3.75 (1H, d,
J = 14Hz), 3.68 (1H, m), 3.30-3.45 (2H, m), 2.93-3.13
(3H, m), 2.09 (1H, m), 1.90 (1H, m) Infrared absorption spectrum ν _max cm ^-1 (KBr): 337
8, 2966, 2893, 2812, 2783, 272
4, 2656, 2530, 1598 Mass spectrum (FAB) m / z: 276 ((M + H)
⁺ (Free body)).

[0397]

Working Example 77 (d) 2-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethanol 22.9 g (82.9 mmol) of (2R)-(3,4-dichlorophenyl) -2- (2-hydroxyethyl) morpholine hydrochloride obtained in Example 77 (c) were treated with methylene chloride. Suspended in 500 ml of triethylamine 2
7.6 ml (199 mmol), 3,4,5-trimethoxybenzoyl chloride 21.0 g (91.0 mmol) and 4-dimethylaminopyridine 100 mg were added, and the mixture was stirred at room temperature for 12 hours. The reaction solution was poured into water, extracted with methylene chloride, and the organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: methylene chloride: acetone = 4: 1 to 7: 3) to obtain 30.0 g of the desired compound.

[Α] _D ²⁴ +30.65 (c = 0.56, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 6.80-7.80 (3H, m), 6.47 (2H, s), 3.40-4.80
(8H, m), 3.84 and 3.86 (total 9H, each s), 1.75-2.25
(2H, m) infrared absorption spectrum ν _max cm ^-1 (KBr): 342
9, 2940, 2838, 1630, 1585 Mass spectrum (EI) m / z: 469 (M ^<+> ).

[0399]

Working Example 77 (e) 2-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethanol methanesulfonate 2-[(2R)-(3,4) obtained in Example 77 (d).
-Dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethanol 3
0.0 g (63.8 mmol) of methylene chloride (500
ml), and triethylamine 11.5 under ice-cooling.
ml (83.0 mmol) and 5.93 ml (76.6 mmol) of methanesulfonyl chloride were sequentially added, and the mixture was stirred under a nitrogen atmosphere at room temperature for 2 hours. The reaction solution was diluted with methylene chloride, washed with 1N hydrochloric acid and saturated saline, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 1: 4 to 1: 9) to obtain 34.8 g of the desired compound.

[Α] _D ²⁴ +26.36 (c = 0.66, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 6.90-7.80 (3H, m), 6.52 (2H, s), 3.40-4.35
(8H, m), 3.86 and 3.87 (total 9H, each s), 2.93 (3H,
s), 2.10-2.55 (2H, m) infrared absorption spectrum ν _max cm ^-1 (KBr): 299
9, 2966, 2939, 2875, 1634, 158
5 Mass spectrum (FAB) m / z: 548 ((M + H)
⁺ ).

[0401]

Working Example 77 (f) 2-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethanal oxalyl chloride 0.88 ml (10.1 mmol)
Is dissolved in 10 ml of methylene chloride, and-
0.79 ml of dimethyl sulfoxide at 11.degree.
Mmol) in methylene chloride (5 ml) was added dropwise.
Stir for 30 minutes. 2-obtained in Example 77 (d)
[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] ethanol 950 mg (2.02 mmol)
Was added dropwise and stirred for 4 hours. Furthermore, 2.24 ml of triethylamine (16.2.
Mmol) and stirred at room temperature for 2 hours. The reaction solution was poured into water and extracted with methylene chloride. The organic layer was washed with water and saturated saline, and then dried over anhydrous sodium sulfate.
The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel column chromatography (elution solvent: methylene chloride: acetone = 23:
2-21: 4) to give 878 m of the desired compound.
g was obtained.

[Α] _D ²⁴ +36.15 (c = 0.65, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 9.56 (1H, s), 6.90-7.80 (3H, m), 6.50 (2H,
s), 3.40-4.60 (6H, m), 3.85-3.87 (total 9H, each s), 2.7
0-3.05 (2H, m) infrared absorption spectrum ν _max cm ^-1 (KBr): 296
2, 2930, 2838, 1723, 1636, 158
5 Mass spectrum (FAB) m / z: 468 ((M + H)
⁺ ).

[0403]

Example 77 (g) 1- {2-[(2R)-(3,4-dichlorophenyl)
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphorus-2-yl] ethyl {spiro [benzo [c] thiof
Ene-1 (3H), 4'-piperidine]-(2S) -o
Oxide 15.00 g of the mesyl compound obtained in Example 77 (e) (2
7.4 mmol), and 7.76 g of spiro [benzo [c] thiophene-1 (3H), 4′-piperidine]-(2S) -oxide hydrochloride obtained in Reference Example 9.
1 mmol), 6.89 g of sodium hydrogen carbonate (82.
0 mmol) and 6.81 g (41.0 mmol) of potassium iodide were suspended in 150 ml of anhydrous dimethylformamide and heated at 80 ° C. for 8 hours under a nitrogen atmosphere. The reaction solution was poured into 400 ml of saturated saline and extracted with ethyl acetate. After the organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure. The residue is subjected to silica gel column chromatography (elution solvent: methylene chloride: methanol = 40:
1 to 20: 1), and crystallized from n-hexane to obtain 15.5 g of the target compound as white crystals.

[Α] _D ²⁴ +14.0 (c = 1, methanol) HPLC analysis: Column; YMC-Pack ODS-A (250 ×
4.6 mmφ) Elution solvent; CH ₃ CN: H ₂ O = 40: 60, 0.1%
Ammonium acetate Flow rate: 1.0 ml / min Retention time: 23.7 minutes Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.1-7.8 (7H, m), 6.49 (2H, br.s), 4.31 (1
H, d, J = 16.8Hz), 3.99 (1H, d, J = 16.8Hz), 3.86 and
3.84 (Total 9H, each s), 3.3-4.0 (6H, m), 1.5-3.1 (12H,
m) Infrared absorption spectrum ν _max cm ^-1 (KBr): 293
9, 1636, 1584, 1464, 1426, 132
9, 1237, 1128 Mass spectrum (FAB) m / z: 673 ((M + H)
⁺ ) Elemental analysis (% as C ₃₄ H ₃₈ N ₂ O ₆ SCl ₂ .0.5H ₂ O) Calculated: C: 59.82, H: 5.76, N: 4.10, S: 4.70, Cl: 10.39 Actual: C: 60.20, H: 6.14, N: 4.04, S: 4.54, Cl: 10.38.

[0405]

Working Example 77 (h) 1- {2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphorus-2-yl] ethyl {spiro [benzo [c] thiof
Ene-1 (3H), 4'-piperidine]-(2S) -o
Oxide 2-[(2R)-(3,4) obtained in Example 77 (f).
-Dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethanal 15
0 mg (0.32 mmol) and spiro [benzo [c] thiophene-1 (3H), 4′- obtained in Reference Example 9.
Piperidine]-(2S) -oxide hydrochloride 99mg
(0.38 mmol) was dissolved in 1 ml of methanol, 100 mg of molecular sieves 3A (powder) and 209 mg (3.33 mmol) of sodium cyanoborohydride were added, and the mixture was refluxed for 8 hours under a nitrogen atmosphere. After the reaction solution was filtered through celite, the filtrate was poured into water and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: methylene chloride: methanol = 97: 3 to 19: 1) to obtain 184 mg of the desired compound. The various device data coincided with those synthesized in Example 77 (g).

[0406]

Example 78 (Exemplified compounds shown below, Table 3-811)1- {2-[(2R)-(3,4-dichlorophenyl)
-4-[(3-isopropyloxyphenyl) acetyl
L] morpholin-2-yl] ethyl} spiro [benzo]
[C] thiophene-1 (3H), 4'-piperidine]-
(2S) -oxide

[0407]

Example 78 (a) (2R)-{2- (3,4-dichlorophenyl) -4-
[(3-isopropyloxyphenyl) acetyl] mol
1.03 g of folin-2-yl @ ethanol- 3-isopropyloxyphenylacetic acid (5.
28 mmol) was dissolved in methylene chloride (50 ml), and the mixture was dissolved in ice-cooled WSC.HCl (Water Solub).
le Carbodiimide.HCl) 1.10 g
(5.76 mmol), 780 mg (5.76 mmol) of 1-hydroxybenzotriazole monohydrate, 1.61 ml (11.5 mmol) of triethylamine and (2R)-() synthesized in Example 77 (c). 1.50 g (4.80 mmol) of 3,4-dichlorophenyl) -2- (2-hydroxyethyl) morpholine hydrochloride were sequentially added, and the mixture was further stirred at room temperature for 15 hours under a nitrogen atmosphere. A saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed successively with saturated aqueous sodium hydrogen carbonate and saturated saline, and then dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was subjected to silica gel column chromatography (elution solvent: n-hexane: ethyl acetate =
3: 1 to 2: 1) to give the desired compound 1.81
g was obtained.

[Α] _D ²⁴ -8.2 (c = 0.60, methanol) Nuclear magnetic resonance spectrum (270 MHz, CDCl ₃ ) δ
ppm: 6.45-7.57 (7H, m), 4.74 (1H, d, J = 13.9Hz),
4.37-4.52 (1H, m), 3.22-3.90 (9H, m), 2.10-2.21 (1
H, br.s), 1.87-2.09 (2H, m), 1.30 (3H, s), 1.28 (3
H, s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 369
3, 3622, 3589, 2981, 2934, 164
5, 1608, 1583 Mass spectrum (FAB) m / z: 452 ((M + H)
⁺ ).

[0409]

Example 78 (b) (2R)-{2- (3,4-dichlorophenyl) -4-
[(3-isopropyloxyphenyl) acetyl] mol
Holin-2-yl @ ethanol methanesulfonate 1.81 g of alcohol synthesized in Example 78 (a)
(4.00 mmol) in 5 ml of pyridine and 4
-Dimethylaminopyridine 45 mg (0.40 mmol) and methanesulfonyl chloride 0.46 ml (6.
(00 mmol) under ice-cooling, and the mixture was stirred at 0 ° C. for 2 hours under a nitrogen atmosphere. The reaction mixture was poured into ice-cooled 10% hydrochloric acid and then extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the residue was subjected to silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 1: 1 to 1).
1: 2) to give 2.00 g of the desired compound as a colorless oil.

[Α] _D ²⁴ -6.3 (c = 0.70, methanol) Nuclear magnetic resonance spectrum (270 MHz, CDCl ₃ ) δ
ppm: 6.51-7.59 (7H, m), 4.40-4.63 (2H, m), 3.17
-4.26 (9H, m), 2.93 (3H, s), 2.08-2.32 (2H, m), 1.3
1 (3H, s), 1.29 (3H, s) infrared absorption spectrum ν _max cm ^-1 (KBr): 298
1, 2934, 1645, 1608, 1583 Mass spectrum (FAB) m / z: 530 ((M + H)
⁺ ).

[0411]

Example 78 (c)1- {2-[(2R)-(3,4-dichlorophenyl)
-4-[(3-isopropyloxyphenyl) acetyl
L] morpholin-2-yl] ethyl} spiro [benzo]
[C] thiophene-1 (3H), 4'-piperidine]-
(2S) -oxide 630 mg of the mesyl compound synthesized in Example 78 (b) (1.
19 mmol) and the spiro [ben obtained in Reference Example 9.
Zo [c] thiophene-1 (3H), 4'-piperidine]
-(2S) -oxide hydrochloride 367 mg (1.43
Rimol), 299 mg of sodium hydrogen carbonate (3.56 mi)
296 mg (1.78 mmol) of potassium iodide
Is suspended in 6 ml of anhydrous dimethylformamide,
Heated at 80 ° C. for 6 hours in a nitrogen atmosphere. Saturated reaction solution
The mixture was poured into a saline solution and extracted with ethyl acetate. Organic layer anhydrous
After drying over magnesium sulfate, the solvent was distilled off under reduced pressure. Residue
To silica gel column chromatography (elution solvent: salt
Methylene chloride: methanol = 25: 1), n
-Crystallize with hexane to obtain the target compound as white crystals.
To give 400 mg.

Melting point 85-88 ° C. [α] _D ²⁴ +2.5 (c = 0.51, methanol) HPLC analysis: Column: YMC-Pack ODS-A (250 ×
4.6 mmφ) Elution solvent: CH ₃ CN: H ₂ O = 60: 40, 0.1%
Ammonium acetate Flow rate: 1.0 ml / min Retention time: 23.7 minutes Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 6.55-7.61 (11H, m), 4.71 (1H, d, J = 13.8H
z), 4.40-4.51 (1H, m), 4.31 (1H, d, J = 16.8Hz), 3.99
(1H, d, J = 16.8Hz), 3.25-3.85 (8H, m), 2.56-2.97 (2
H, m), 2.01-2.45 (6H, m), 1.88-2.45 (2H, m), 1.48-
1.59 (1H, m), 1.30 (3H, s), 1.29 (3H, s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 297
5, 2923, 1645, 1607, 1582, 104
7 Mass spectrum (FAB) m / z: 655 ((M + H)
⁺ ) Elemental analysis (% as C ₃₅ H ₄₀ N ₂ O ₄ SCl ₂ .0.5H ₂ O) Calculated: C: 63.25, H: 6.22, N: 4.21, S: 4.82, Cl: 10.67 Actual: C: 62.96, H: 6.38, N: 4.08, S: 4.71, Cl: 10.41.

[0413]

Example 79 (Exemplified compounds shown below in Table 3-74) 1- {2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) -hex
Sahydro-1,4-oxazepin-2-yl] ethyl
Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine]-(2S) -oxide

[0414]

Example 79 (a)4- (tert-butyldimethylsilyloxy)-(2R)
-(3,4-dichlorophenyl) -1- [N- (tert-
Butoxycarbonyl) -N- (3-hydroxypropyl
Ru) amino] -2-butanol 4-tert-butyldimethyl obtained in Example 76 (c)
Silyloxy- (2R)-(3,4-dichlorophenyl)
) Butane-1,2-diol 5.00 g (13.7 mi)
Rimol) as starting material and 3-amino-1-pro
Using 5.15 g (68.6 mmol) of panol,
5. The target compound was prepared in the same manner as in Example 77 (a).
00 g was obtained.

[Α] _D ²⁴ -1.31 (c = 1.22, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.20-7.70 (3H, m), 5.04 and 5.32 (1H,
S), 3.15-3.85 (9H, m), 1.95-2.30 (2H, m), 1.65-1.
85 (2H, m), 1.45 (9H, s), 0.86 (9H, s), -0.08 and
-0.01 (total 6H, each s) Infrared absorption spectrum ν _max cm ^-1 (CHCl ₃ ): 3
432, 2957, 2885, 2861, 1675 Mass spectrum (FAB) m / z: 522 ((M + H)
⁺ ).

[0416]

Example 79 (b)2- [4-tert-butoxycarbonyl- (2R)-
(3,4-dichlorophenyl) hexahydro-1,4-
Oxazepin-2-yl] ethanol tert-butyldi
Methylsilyl ether 4- (tert-butyl dimethyl) obtained in Example 79 (a)
Lucylyloxy)-(2R)-(3,4-dichlorophene)
Nil) -1- [N- (tert-butoxycarbonyl) -N
-(3-hydroxypropyl) amino] -2-butanol
300 mg (0.57 mmol) in pyridine (2 m
1) and then dissolved in p-toluenesulfonyl chloride
196 mg (1.03 mmol) was added and the atmosphere was nitrogen.
The mixture was stirred at room temperature for 16 hours. Pour the reaction solution into water and add acetic acid
Extracted with ethyl. Wash the organic layer with water and saturated saline
Then, it was dried over anhydrous sodium sulfate. The solvent is distilled off under reduced pressure
And the residue was taken up in 2-methyl-2-propanol (3 ml).
After dissolution, potassium tert-butoxide (67 mg, 0.58
Mmol) and heated at 80 ° C. for 8 hours under a nitrogen atmosphere.
did. After returning the reaction solution to room temperature, it was poured into water, and ethyl acetate was added.
Extracted. After washing the organic layer with saturated saline,
Dried with sodium acid. The solvent is distilled off under reduced pressure, and the residue is
Ricagel column chromatography (elution solvent: n-he
Purified by xane: ethyl acetate = 47: 3-23: 2)
Thus, 56 mg of the target compound was obtained.

[Α] _D ²⁴ +14.19 (c = 0.74, methanol) Nuclear magnetic resonance spectrum (270 MHz, CDCl ₃ ) δ
ppm: 7.17-7.65 (3H, m), 3.10-4.10 (8H, m), 1.75
-2.30 (4H, m), 1.37 and 1.44 (total 9H, each s), 0.82
(9H, s), -0.07 and -0.05 (total 6H, each s) Mass spectrum (FAB) m / z: 504 ((M + H)
⁺ ).

[0418]

Working Example 79 (c) 2-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) hexahydro
-1,4-oxazepin-2-yl] ethanolmethane
Sulfonate 2- [4-tert-butoxycarbonyl- (2R)-(3,4-dichlorophenyl) obtained in Example 79 (b)
Hexahydro-1,4-oxazepin-2-yl] ethanol Using tert-butyldimethylsilyl ether, the target compound was obtained in a yield according to the method of Example 77 (c), 77 (d), 77 (e). Obtained at 65%.

[Α] _D ²⁴ +19.41 (c = 0.45, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.20-7.65 (3H, m), 6.62 (2H, s), 0.75-4.90
(12H, m), 3.87 and 3.89 (total 9H, each s), 2.86 (3H, s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 293
5, 1637, 1585 Mass spectrum (FAB): 562 ((M + H) ^<+> ).

[0420]

Working Example 79 (d) 1- {2-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) hexa
Hydro-1,4-oxazepin-2-yl] ethyldiethyl
Pyro [benzo [c] thiophene-1 (3H), 4'-pi
Peridine]-(2S) -oxide 2-[(2R)-(3,4) obtained in Example 79 (c).
-Dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepine-
2-yl] ethanol methanesulfonate,
The target compound was obtained in a yield of 5 according to the method of Example 77 (g).
Obtained at 9%.

[Α] _D ²⁴ +19.33 (c = 0.1, methanol) HPLC analysis: Column; YMC-Pack ODS-A (250 × 4.
6 mm φ) Elution solvent; CH ₃ CN: H ₂ O = 40: 60, 0.1%
Ammonium acetate Flow rate: 1.0 ml / min Retention time: 17.7 minutes Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.15-7.75 (7H, m), 6.62 (2H, br), 0.75-4.8
0 (29H, m), 4.29 (1H, d, J = 17Hz), 3.97 (1H, d, J = 17
Hz) Infrared absorption spectrum ν _max cm ^-1 (KBr): 292
8, 2855, 2836, 1637, 1584. Mass spectrum (FAB) m / z: 687 ((M + H)
⁺ ).

[0422]

Working Example 80 (Exemplified Compounds, Table 3-42) 1- {3-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphorus-2-yl) propyl} spiro [benzo [c] thio
Phen-1 (3H), 4'-piperidine]-(2S)-
Oxide

[0423]

Example 80 (a) 4- (3,4-dichlorophenyl) -4-oxobutane
Acid methyl ester dichlorobenzene 150 ml and succinic anhydride 8.50
g (84.9 mmol) and aluminum bromide 24.8
g (93.0 mmol) were sequentially added, and the mixture was stirred at room temperature for 5 hours. The reaction solution was poured into ice water and extracted with methylene chloride. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure.
The mixture was dissolved in 0 ml, sulfuric acid (1.0 ml) was added, and the mixture was refluxed for 4 hours. The reaction was brought to room temperature, poured into water and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated saline, and then dried over anhydrous sodium sulfate.
The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: n-hexane: diethyl ether = 17: 3 to 7: 3) to obtain 9.10 g of the target compound as pale orange crystals. Was.

A nuclear magnetic resonance spectrum (400 MHz, C
DCl ₃ ) δ ppm: 8.07 (1H, d, J = 2 Hz), 7.81 (1H,
dd, J = 2,8Hz), 7.56 (1H, d, J = 8Hz), 3.71 (3H, s), 3.
27 (2H, t, J = 7 Hz), 2.78 (2H, t, J = 7 Hz) Infrared absorption spectrum ν _max cm ^-1 (KBr): 309
3, 3061, 2954, 1746, 1678, 158
3 Mass spectrum (EI) mz: 260 (M ⁺ ).

[0425]

Working Example 80 (b) 4- (3,4-Dichlorophenyl) -4-pentenoic acid
1.75 g of methyl ester methyltriphenylphosphonium bromide
(49.0 mmol) and potassium t-butoxide 5.5
0 g (49.0 mmol) of dried benzene (200
ml) and stirred for 6 hours at room temperature under a nitrogen atmosphere. 8.50 g of 4- (3,4-dichlorophenyl) -4-oxobutanoic acid methyl ester obtained in Example 80 (a) was dissolved in 40 ml of benzene and added dropwise, followed by stirring for 1 hour. The reaction solution was poured into water and extracted with ethyl acetate. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the residue was subjected to silica gel column chromatography (elution solvent: n-hexane: diethyl ether = 1).
9: 1 to 23: 2) to give 4.20 g of the desired compound as a pale yellow oil.

A nuclear magnetic resonance spectrum (400 MHz, C
DCl ₃ ) δ ppm: 7.48 (1H, d, J = 2 Hz), 7.40 (1H,
d, J = 8Hz), 7.23 (1H, dd, J = 2,8Hz), 5.32 (1H, s),
5.14 (1H, s), 3.67 (3H, s), 2.79 (2H, t, J = 8Hz), 2.
48 (2H, t, J = 8Hz) Infrared absorption spectrum ν _max cm ^-1 (film): 29
52, 1740, 1630, 1550 Mass spectrum (EI) m / z: 258 (M ^<+> ).

[0427]

Working Example 80 (c) 4- (3,4-Dichlorophenyl) -4-pentene-1
-All tert-butyldimethylsilyl ether Using 4- (3,4-dichlorophenyl) -4-pentenoic acid methyl ester obtained in Example 80 (b),
The target compound was obtained in a yield of 93 in the same manner as in Example 76 (b).
%.

A nuclear magnetic resonance spectrum (400 MHz, C
DCl ₃ ) δ ppm: 7.49 (1H, d, J = 2 Hz), 7.38 (1H,
d, J = 9Hz), 7.24 (1H, dd, J = 2,9Hz), 5.30 (1H, s),
5.13 (1H, s), 3.62 (2H, t, J = 6Hz), 2.52 (2H, t, J =
8Hz), 1.60-1.68 (2H, m), 0.90 (9H, s), 0.04 (6H, s) Infrared absorption spectrum ν _max cm ^-1 (film): 29
54, 2929, 2887, 2858, 1627, 15
50 Mass spectrum (FAB) m / z: 345 ((M + H)
⁺ ).

[0429]

Working Example 80 (d) (2R) -5-tert-butyldimethylsilyloxy-2
-(3,4-dichlorophenyl) pentane-1,2-di
All using 4- (3,4-dichlorophenyl) -4-penten-1-ol tert-butyldimethylsilyl ether obtained in Example 80 (c) in the same manner as in Example 76 (c), The compound was obtained with a yield of 94%.

Optical purity: 98% ee [α] _D ²⁴ -2.08 (c = 0.48, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.56 (1H, d, J = 2Hz), 7.41 (1H, d, J = 8Hz),
7.23 (1H, dd, J = 2,8Hz), 4.96 (1H, s), 3.53-3.70 (4
H, m), 1.98-2.14 (3H, m), 1.35-1.57 (2H, m), 0.91
(9H, s), 0.082 (3H, s), 0.078 (3H, s) Infrared absorption spectrum ν _max cm ^-1 (CHCl ₃ ): 3
584, 3311, 2956, 2932, 2861 Mass spectrum (FAB) m / z: 379 (M) ^<+> .

[0431]

Working Example 80 (e) (2R) -5- (tert-butyldimethylsilyloxy)
-2- (3,4-dichlorophenyl) -1- [N- (te
rt-butoxycarbonyl) -N- (2-hydroxyethyl
L) amino] -2-pentanol Using (2R) -5-tert-butyldimethylsilyloxy-2- (3,4-dichlorophenyl) pentane-1,2-diol obtained in Example 80 (d). Example 7
The target compound was obtained in a yield of 95% in the same manner as in 7 (a).

[Α] _D ²⁴ -14.75 (c = 0.61, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.15-7.65 (3H, m), 5.30 and 5.79 (1H,
S), 2.50-3.95 (9H, m), 1.85-2.25 (2H, m), 1.30-1.
60 (2H, m), 1.43 (9H, s), 0.89 (9H, s), 0.04 and
0.05 (total 6H, each s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 335
5, 2955, 2931, 2894, 2858, 166
8 Mass spectrum (FAB) m / z: 522 ((M + H)
⁺ ).

[0433]

Working Example 80 (f) (2R) -2- [4-tert-butoxycarbonyl-2-
(3,4-dichlorophenyl) morpholin-2-yl]
-1-propanol tert-butyldimethylsilyl acrylate
(2R) -5- (tert-butyldimethylsilyloxy) -2- (3,4-dichlorophenyl) -1- [N- (tert-butoxycarbonyl) obtained in Tell Example 80 (e)
Using -N- (2-hydroxyethyl) amino] -2-pentanol, the target compound was obtained in a yield of 92% in the same manner as in Example 77 (b).

[Α] _D ²⁴ +58.15 (c = 0.54, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.40-7.65 (3H, m), 4.14 (1H, d, J = 14Hz),
3.42-3.75 (5H, m), 3.23 (2H, d, J = 14Hz), 1.15-2.00
(4H, m), 1.44 and 1.52 (total 9H, each br.s), 0.85 (9H,
s), 0.00 and 0.01 (total 6H, each s) Infrared absorption spectrum ν _max cm ^-1 (CHCl ₃ ): 2
957, 2931, 2860, 1668 Mass spectrum (FAB) m / z: 504 ((M + H)
⁺ ).

[0435]

Working Example 80 (g) 3-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] -1-propanol 3- [4-tert-butoxycarbonyl- (2R)-(3,4-dichlorophenyl) obtained in Example 80 (f)
Morpholin-2-yl] -1-propanol tert-butyldimethylsilyl ether (3.43 g, 6.80 mmol) was dissolved in methylene chloride (60 ml), and 2.98 g (15.0 mmol) of B-bromocatecholborane was dissolved. Was added and the mixture was stirred at room temperature under a nitrogen atmosphere for 2 hours. 60 ml of water was added to the reaction solution, and the mixture was further stirred for 2 hours. A 1N aqueous sodium hydroxide solution was added to make the mixture alkaline, and the mixture was extracted with methylene chloride. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was dissolved in methylene chloride (40 ml), and 1.23 ml (8.87 mmol) of triethylamine, 1.65 g (7.15 mmol) of 3,4,5-trimethoxybenzoyl chloride and 10 mg of 4-dimethylaminopyridine were added. And stirred at room temperature for 12 hours. The reaction solution was poured into water and extracted with methylene chloride. The organic layer was washed with brine, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: methylene chloride: acetone = 7: 3) to obtain 2.13 g of the target compound.

[Α] _D ²⁴ +30.78 (c = 0.51, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 6.80-7.80 (3H, m), 6.48 (2H, br.s), 3.30-
4.80 (8H, m), 3.84 and 3.86 (total 9H, each s), 1.10-2.
35 (4H, m) infrared absorption spectrum ν _max cm ^-1 (KBr): 342
6, 2942, 2872, 1632, 1584 Mass spectrum (FAB) m / z: 484 ((M + H)
⁺ ).

[0437]

Working Example 80 (h) 3-[(2R)-(3,4-dichlorophenyl) -4-
(3,4,5-trimethoxybenzoyl) morpholine-
2-yl] -1-propanol methanesulfonate 3-[(2R)-(3,4) obtained in Example 80 (g).
-Dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] -1-propanol and the target compound was obtained in a yield of 84% in the same manner as in Example 77 (e). Obtained.

[Α] _D ²⁴ +27.87 (c = 0.54, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 6.80-7.80 (3H, m), 6.50 (2H, s), 3.20-4.50
(8H, m), 3.85 and 3.86 (total 9H, each s), 2.97 (3H,
s), 1.35-2.35 (4H, m) Infrared absorption spectrum ν _max cm ^-1 (KBr): 300
1, 2939, 2875, 2839, 1634, 158
5 Mass spectrum (FAB) m / z: 562 ((M + H)
⁺ ).

[0439]

Working Example 80 (i) 1- {3-[(2R)-(3,4-dichlorophenyl)]
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphorus-2-yl] propyl} spiro [benzo [c] thio
Phen-1 (3H), 4'-piperidine]-(2S)-
Oxide 3-[(2R)-(3,4) obtained in Example 80 (h).
Example 77 (g) using -dichlorophenyl) -4- (3,4,5-trimethoxybenzoylmorpholin) -2-yl] -1-propanol methanesulfonate.
In a similar manner to the above, the target compound was obtained in a yield of 68%.

[Α] _D ²⁴ +26.97 (c = 0.55, methanol) HPLC analysis: Column; YMC-Pack ODS-A (250 × 4.
6 mm φ) Elution solvent; CH ₃ CN: H ₂ O = 40: 60, 0.1%
Ammonium acetate Flow rate: 1.0 ml / min Retention time: 23.4 minutes Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 6.80-7.80 (7H, m), 6.48 (2H, br.s), 0.80-
4.70 (20H, m), 4.32 (1H, d, J = 17Hz), 4.00 (1H, d, J
= 17Hz), 3.84 and 3.86 (total 9H, each s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 294
0, 2872, 2834, 2771, 1636, 158
4 Mass spectrum (FAB) m / z: 687 (M + H)
⁺ ).

[0441]

Example 81 (Exemplified compounds shown in Table 3-2055)1- {2-[(5R)-(3,4-dichlorophenyl)
-3- (3,4-dimethoxybenzenesulfonyl) oxo
Sazolidin-5-yl] ethyl {spiro [benzo [c]
Thiophene-1 (3H), 4'-piperidine]-(2
S) -oxide

[0442]

Example 81 (a) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4-dimethoxybenzenesulfonyl) oxazoly
Zin-5-yl] ethanol tert-butyldimethyl
Lyl ether 2-[(5R) -synthesized in the previous step of Example 76 (f).
(3,4-Dichlorophenyl) oxazolidin-5-yl] ethanol tert-butyldimethylsilyl ether (1.00 g, 2.72 mmol) was added to pyridine (10 m
1), 773 mg (3.27 mmol) of 3,4-dimethoxybenzenesulfonyl chloride was added under ice cooling, and the mixture was stirred under a nitrogen atmosphere for 2 hours. The reaction solution was poured into ice-cooled 10% hydrochloric acid (100 ml) and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 10: 1 to 2: 1).
1.27 g of the target compound was obtained as white crystals.

[Α] _D ²⁴ -5.74 (c = 1.29, methanol) Infrared absorption spectrum ν _max cm ^-1 (KBr): 158
8, 1510, 1468, 1264, 1155, 114
0.

[0444]

Working Example 81 (b) 2-[(5R)-(3,4-dichlorophenyl) -3-
(3,4-dimethoxybenzenesulfonyl) oxazoly
Zin-5-yl] ethanol methanesulfonate 1.19 g (2.06 mmol) of the tert-butyldimethylsilyl ether compound synthesized in Example 81 (a) was treated with acetic acid:
20 ml of a mixture of tetrahydrofuran: water = 3: 3: 1
And heated under a nitrogen atmosphere at 80 ° C. for 2 hours. After neutralization with a saturated aqueous solution of sodium hydrogen carbonate, the mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was dissolved in 10 ml of pyridine, and 23 mg of 4-dimethylaminopyridine (0.1 mg) was added.
9 mmol) and methanesulfonyl chloride 0.22 m
1 (2.84 mmol) under ice-cooling, and under a nitrogen atmosphere,
Stirred at 0 ° C. for 2 hours. The reaction solution was poured into ice-cooled 10% hydrochloric acid (200 ml) and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous magnesium sulfate. After evaporating the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluent: n-hexane: ethyl acetate = 2: 1 to 1: 2) to obtain 992 mg of the desired compound as white crystals.

[Α] _D ²⁴ −3.80 (c = 0.5, methanol) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.33 (1H, d, J = 8.6Hz), 7.30 (1H, dd, J = 8.
6, 2.1Hz), 7.14 (1H, d, J = 2.2Hz), 7.11 (1H, d, J = 2.
1Hz), 6.92 (1H, dd, J = 8.7, 2.2Hz), 6.80 (1H, d, J =
8.7Hz), 5.08 (1H, d, J = 5.7Hz), 4.98 (1H, d, J = 5.7H
z), 4.11 (1H, m), 3.94 (3H, s), 3.86 (3H, s), 3.82
(1H, m), 3.70 (2H, ABq, J = 11.3Hz, Δδ = 0.08ppm),
2.88 (3H, s), 2.16 (2H, m) Mass spectrum (FAB) m / z: 540 (M + H)
⁺ ).

[0446]

Example 81 (c)1- {2-[(5R)-(3,4-dichlorophenyl)
-3- (3,4-dimethoxybenzenesulfonyl) oxo
Sazolidin-5-yl] ethyl {spiro [benzo [c]
Thiophene-1 (3H), 4'-piperidine]-(2
S) -oxide 105 mg of the mesyl compound obtained in Example 81 (b) (0.
19 mmol) and the spiro [ben obtained in Reference Example 9.
Zo [c] thiophene-1 (3H), 4'-piperidine]
-(2S) -oxide hydrochloride 55 mg (0.21 mm
Mol), 49 mg of sodium hydrogen carbonate (0.58 mmol
), Potassium iodide 48 mg (0.29 mmol)
Suspend in 2 ml of anhydrous dimethylformamide,
Heated at 80 ° C. for 8 hours under ambient atmosphere. The reaction solution was saturated saline
Poured into 10 ml of water and extracted with ethyl acetate. Organic layer
After drying over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure.
The residue is purified by silica gel column chromatography (elution
Medium: methylene chloride: methanol = 40: 1 to 20: 1)
And crystallized from diisopropyl ether.
Thus, 82 mg of the target compound was obtained as white crystals.

[Α] _D ²⁴ +2.5 (c = 0.52, methanol) HPLC Analysis: Column; YMC-Pack ODS-A (250 × 4.
6 mm φ) Elution solvent; CH ₃ CN: H ₂ O = 40: 60, 0.1%
Ammonium acetate Flow rate: 1.0 ml / min Retention time: 21.4 minutes Infrared absorption spectrum ν _max cm ^-1 (KBr): 167
4, 1587, 1509, 1469, 1350, 126
4, 1155, 1140, 1039 Mass spectrum (FAB) m / z: 665 (M + H)
⁺ .

[0448]

Example 82 (Iodide of Exemplified Compound Table 3-42)
Methyl salt)1- {2-[(2R)-(3,4-dichlorophenyl)
-4- (3,4,5-trimethoxybenzoyl) morpho
Phosphorus-2-yl] ethyl} -1-methylspiro [benzo
[C] Thiophene-1 (3H), 4′-piperidinium
]-(2S) -oxide iodide salt 1- {2-[(2R)-(3,4) obtained in Example 77
-Dichlorophenyl) -4- (3,4,5-trimethoxy)
Cibenzoyl) morpholin-2-yl] ethyl @ spiro
[Benzo [c] thiophene 1 (3H), 4'-piperidi
]-(2S) -oxide 300 mg (0.45 mmol
Is dissolved in 3 ml of acetonitrile, and methyl iodide is dissolved.
30 μl (0.48 mmol) was added and under a nitrogen atmosphere,
Stirred overnight at room temperature. The solvent was distilled off under reduced pressure, and the residue
Crystallize with propyl ether, and the target compound is pale yellow
312 mg were obtained as crystals.

[Α] _D ²⁴ +42.0 (c = 1, methanol) HPLC analysis: Column; YMC-Pack ODS-A (250 × 4.
6 mm φ) Elution solvent; CH ₃ CN: H ₂ O = 40: 60, 0.1%
Ammonium acetate Flow rate: 1.0 ml / min Retention time: 9.9 minutes Infrared absorption spectrum ν _max cm ^-1 (KBr): 344
4, 1632, 1584, 1464, 1126 Mass spectrum (FAB) m / z: 687 (free form M
⁺ ) Elemental analysis (% as C ₃₅ H ₄₁ N ₂ O ₆ SCl ₂ I) Calculated: C: 51.54, H: 5.07, N: 3.44, S: 3.93, Cl: 8.69, I: 15.56 Actual: C: 51.14, H: 5.39, N: 3.42, S: 4.01, Cl: 8.50, I: 15.96.

The following compounds shown in Table 1 [compounds represented by the following general formula (I-1)], compounds shown in Table 2 [compounds represented by the following general formula (I-2)] and The compound [3] [compound represented by the following general formula (I-3)] is also synthesized in the same manner as in the above Examples.

[0451]

Embedded image

In the following tables, the substituents (denoted by “置” in the table) represent the following groups.

[0453]

Embedded image

[0454]

Embedded image

[0455]

Embedded image

[0456]

Embedded image

(In the formula 84,> S ^* → O represents a sulfoxide group in the S configuration.) D represents an oxygen atom, and G represents a dimethylene group or a trimethylene group.

[0458]

[Table 1] ──────────────────────────────────── Compound number R ¹ R ^Two ABZ────────────────────────────────────1-1 Place 33 3,4-diClPh CH _Two Single bond device 1 1-2 device 33 3,4-diClPh CH _Two Single bond device 2 1-3 device 33 3,4-diClPh CH _Two Single bond unit 3 1-4 unit 33 3,4-diClPh CH _Two Single bond unit 4 1-5 unit 33 3,4-diClPh CH _Two Single bond device 5 1-6 device 33 3,4-diClPh CH _Two Single bond device 6 1-7 device 33 3,4-diClPh CH _Two Single bond device 7 1-8 device 33 3,4-diClPh CH _Two Single bond device 8 1-9 device 33 3,4-diClPh CH _Two Single bond device 9 1-10 device 33 3,4-diClPh CH _Two Single bond device 10 1-11 device 33 3,4-diClPh CH _Two Single bond unit 11 1-12 unit 33 3,4-diClPh CH _Two Single bond unit 12 1-13 unit 33 3,4-diClPh CH _Two Single bond unit 13 1-14 unit 33 3,4-diClPh CH _Two Single bond unit 14 1-15 unit 33 3,4-diClPh CH _Two Single bond unit 15 1-16 unit 33 3,4-diClPh CH _Two Single bond unit 16 1-17 unit 33 3,4-diClPh CH _Two Single bond unit 17 1-18 unit 33 3,4-diClPh CH _Two Single bond unit 18 1-19 unit 33 3,4-diClPh CH _Two Single bond unit 19 1-20 unit 33 3,4-diClPh CH _Two Single bond unit 20 1-21 unit 33 3,4-diClPh CH _Two Single bond unit 21 1-22 unit 33 3,4-diClPh CH _Two Single bond unit 22 1-23 unit 33 3,4-diClPh CH _Two Single bond unit 23 1-24 unit 33 3,4-diClPh CH _Two Single bond unit 24 1-25 unit 33 3,4-diClPh CH _Two Single bond unit 25 1-26 unit 33 3,4-diClPh CH _Two Single bond unit 26 1-27 unit 33 3,4-diClPh CH _Two Single bond unit 27 1-28 unit 33 3,4-diClPh CH _Two Single bond unit 28 1-29 unit 33 3,4-diClPh CH _Two Single bond unit 29 1-30 unit 33 3,4-diClPh CH _Two Single bond unit 30 1-31 unit 33 3,4-diClPh CH _Two Single bond unit 31 1-32 unit 33 3,4-diClPh CH _Two Single bond unit 32 1-33 unit 34 3,4-diClPh CH _Two Single bond unit 1 1-34 unit 34 3,4-diClPh CH _Two Single bond unit 21-35 unit 34 3,4-diClPh CH _Two Single bond position 3 1-36 position 34 3,4-diClPh CH _Two Single bond device 4 1-37 device 34 3,4-diClPh CH _Two Single bond device 5 1-38 device 34 3,4-diClPh CH _Two Single bond unit 6 1-39 unit 34 3,4-diClPh CH _Two Single bond unit 7 1-40 unit 34 3,4-diClPh CH _Two Single bond device 8 1-41 device 34 3,4-diClPh CH _Two Single bond device 9 1-42 device 34 3,4-diClPh CH _Two Single bond device 10 1-43 device 34 3,4-diClPh CH _Two Single bond unit 11 1-44 unit 34 3,4-diClPh CH _Two Single bond unit 12 1-45 unit 34 3,4-diClPh CH _Two Single bond unit 13 1-46 unit 34 3,4-diClPh CH _Two Single bond unit 14 1-47 unit 34 3,4-diClPh CH _Two Single bond unit 15 1-48 unit 34 3,4-diClPh CH _Two Single bond unit 16 1-49 unit 34 3,4-diClPh CH _Two Single bond unit 17 1-50 unit 34 3,4-diClPh CH _Two Single bond unit 18 1-51 unit 34 3,4-diClPh CH _Two Single bond unit 19 1-52 unit 34 3,4-diClPh CH _Two Single bond unit 20 1-53 unit 34 3,4-diClPh CH _Two Single bond unit 21 1-54 unit 34 3,4-diClPh CH _Two Single bond unit 22 1-55 unit 34 3,4-diClPh CH _Two Single bond unit 23 1-56 unit 34 3,4-diClPh CH _Two Single bond unit 24 1-57 unit 34 3,4-diClPh CH _Two Single bond unit 25 1-58 unit 34 3,4-diClPh CH _Two Single bond unit 26 1-59 unit 34 3,4-diClPh CH _Two Single bond unit 27 1-60 unit 34 3,4-diClPh CH _Two Single bond unit 28 1-61 unit 34 3,4-diClPh CH _Two Single bond unit 29 1-62 unit 34 3,4-diClPh CH _Two Single bond unit 30 1-63 unit 34 3,4-diClPh CH _Two Single bond unit 31 1-64 unit 34 3,4-diClPh CH _Two Single bond unit 32 1-65 unit 35 3,4-diClPh CH _Two Single bond device 1 1-66 device 35 3,4-diClPh CH _Two Single bond position 2 1-67 position 35 3,4-diClPh CH _Two Single bond position 3 1-68 position 35 3,4-diClPh CH _Two Single bond unit 4 1-69 unit 35 3,4-diClPh CH _Two Single bond device 5 1-70 device 35 3,4-diClPh CH _Two Single bond device 6 1-71 device 35 3,4-diClPh CH _Two Single bond unit 7 1-72 unit 35 3,4-diClPh CH _Two Single bond device 8 1-73 device 35 3,4-diClPh CH _Two Single bond device 9 1-74 device 35 3,4-diClPh CH _Two Single bond unit 10 1-75 unit 35 3,4-diClPh CH _Two Single bond unit 11 1-76 unit 35 3,4-diClPh CH _Two Single bond unit 12 1-77 unit 35 3,4-diClPh CH _Two Single bond unit 13 1-78 unit 35 3,4-diClPh CH _Two Single bond unit 14 1-79 unit 35 3,4-diClPh CH _Two Single bond unit 15 1-80 unit 35 3,4-diClPh CH _Two Single bond unit 16 1-81 unit 35 3,4-diClPh CH _Two Single bond unit 17 1-82 unit 35 3,4-diClPh CH _Two Single bond unit 18 1-83 unit 35 3,4-diClPh CH _Two Single bond unit 19 1-84 unit 35 3,4-diClPh CH _Two Single bond unit 20 1-85 unit 35 3,4-diClPh CH _Two Single bond unit 21 1-86 unit 35 3,4-diClPh CH _Two Single bond unit 22 1-87 unit 35 3,4-diClPh CH _Two Single bond unit 23 1-88 unit 35 3,4-diClPh CH _Two Single bond unit 24 1-89 unit 35 3,4-diClPh CH _Two Single bond unit 25 1-90 unit 35 3,4-diClPh CH _Two Single bond unit 26 1-91 unit 35 3,4-diClPh CH _Two Single bond unit 27 1-92 unit 35 3,4-diClPh CH _Two Single bond unit 28 1-93 unit 35 3,4-diClPh CH _Two Single bond unit 29 1-94 unit 35 3,4-diClPh CH _Two Single bond unit 30 1-95 unit 35 3,4-diClPh CH _Two Single bond unit 31 1-96 unit 35 3,4-diClPh CH _Two Single bond unit 32 1-97 unit 36 3,4-diClPh CH _Two Single bond unit 1 1-98 unit 36 3,4-diClPh CH _Two Single bond unit 21-99 unit 36 3,4-diClPh CH _Two Single bond device 3 1-100 device 36 3,4-diClPh CH _Two Single bond unit 4 1-101 unit 36 3,4-diClPh CH _Two Single bond device 5 1-102 device 36 3,4-diClPh CH _Two Single bond device 6 1-103 device 36 3,4-diClPh CH _Two Single bond 7 7-104 36 3,4-diClPh CH _Two Single bond device 8 1-105 device 36 3,4-diClPh CH _Two Single bond unit 9 1-106 unit 36 3,4-diClPh CH _Two Single bond unit 10 1-107 unit 36 3,4-diClPh CH _Two Single bond unit 11 1-108 unit 36 3,4-diClPh CH _Two Single bond unit 12 1-109 unit 36 3,4-diClPh CH _Two Single bond unit 13 1-110 unit 36 3,4-diClPh CH _Two Single bond unit 14 1-111 unit 36 3,4-diClPh CH _Two Single bond unit 15 1-112 unit 36 3,4-diClPh CH _Two Single bond unit 16 1-113 unit 36 3,4-diClPh CH _Two Single bond unit 17 1-114 unit 36 3,4-diClPh CH _Two Single bond unit 18 1-115 unit 36 3,4-diClPh CH _Two Single bond unit 19 1-116 unit 36 3,4-diClPh CH _Two Single bond device 20 1-117 device 36 3,4-diClPh CH _Two Single bond unit 21 1-118 unit 36 3,4-diClPh CH _Two Single bond unit 22 1-119 unit 36 3,4-diClPh CH _Two Single bond unit 23 1-120 unit 36 3,4-diClPh CH _Two Single bond unit 24 1-121 unit 36 3,4-diClPh CH _Two Single bond unit 25 1-122 unit 36 3,4-diClPh CH _Two Single bond unit 26 1-123 unit 36 3,4-diClPh CH _Two Single bond unit 27 1-124 unit 36 3,4-diClPh CH _Two Single bond unit 28 1-125 unit 36 3,4-diClPh CH _Two Single bond unit 29 1-126 unit 36 3,4-diClPh CH _Two Single bond device 30 1-127 device 36 3,4-diClPh CH _Two Single bond unit 31 1-128 unit 36 3,4-diClPh CH _Two Single bond unit 32 1-129 unit 37 3,4-diClPh CH _Two Single bond device 1 1-130 device 37 3,4-diClPh CH _Two Single bond unit 21-131 unit 37 3,4-diClPh CH _Two Single bond device 3 1-132 device 37 3,4-diClPh CH _Two Single bond unit 4 1-133 unit 37 3,4-diClPh CH _Two Single bond device 5 1-134 device 37 3,4-diClPh CH _Two Single bond device 6 1-135 device 37 3,4-diClPh CH _Two Single bond device 7 1-136 device 37 3,4-diClPh CH _Two Single bond device 8 1-137 device 37 3,4-diClPh CH _Two Single bond device 9 1-138 device 37 3,4-diClPh CH _Two Single bond device 10 1-139 device 37 3,4-diClPh CH _Two Single bond unit 11 1-140 unit 37 3,4-diClPh CH _Two Single bond unit 12 1-141 unit 37 3,4-diClPh CH _Two Single bond unit 13 1-142 unit 37 3,4-diClPh CH _Two Single bond unit 14 1-143 unit 37 3,4-diClPh CH _Two Single bond unit 15 1-144 unit 37 3,4-diClPh CH _Two Single bond unit 16 1-145 unit 37 3,4-diClPh CH _Two Single bond unit 17 1-146 unit 37 3,4-diClPh CH _Two Single bond unit 18 1-147 unit 37 3,4-diClPh CH _Two Single bond unit 19 1-148 unit 37 3,4-diClPh CH _Two Single bond device 20 1-149 device 37 3,4-diClPh CH _Two Single bond unit 21 1-150 unit 37 3,4-diClPh CH _Two Single bond unit 22 1-151 unit 37 3,4-diClPh CH _Two Single bond unit 23 1-152 unit 37 3,4-diClPh CH _Two Single bond unit 24 1-153 unit 37 3,4-diClPh CH _Two Single bond Unit 25 1-154 Unit 37 3,4-diClPh CH _Two Single bond unit 26 1-155 unit 37 3,4-diClPh CH _Two Single bond unit 27 1-156 unit 37 3,4-diClPh CH _Two Single bond unit 28 1-157 unit 37 3,4-diClPh CH _Two Single bond unit 29 1-158 unit 37 3,4-diClPh CH _Two Single bond device 30 1-159 device 37 3,4-diClPh CH _Two Single bond unit 31 1-160 unit 37 3,4-diClPh CH _Two Single bond unit 32 1-161 unit 38 3,4-diClPh CH _Two Single bond unit 1 1-162 unit 38 3,4-diClPh CH _Two Single bond unit 2 1-163 unit 38 3,4-diClPh CH _Two Single bond unit 3 1-164 unit 38 3,4-diClPh CH _Two Single bond unit 4 1-165 unit 38 3,4-diClPh CH _Two Single bond device 5 1-166 device 38 3,4-diClPh CH _Two Single bond unit 6 1-167 unit 38 3,4-diClPh CH _Two Single bond device 7 1-168 device 38 3,4-diClPh CH _Two Single bond device 8 1-169 device 38 3,4-diClPh CH _Two Single bond device 9 1-170 device 38 3,4-diClPh CH _Two Single bond unit 10 1-171 unit 38 3,4-diClPh CH _Two Single bond unit 11 1-172 unit 38 3,4-diClPh CH _Two Single bond unit 12 1-173 unit 38 3,4-diClPh CH _Two Single bond unit 13 1-174 unit 38 3,4-diClPh CH _Two Single bond unit 14 1-175 unit 38 3,4-diClPh CH _Two Single bond unit 15 1-176 unit 38 3,4-diClPh CH _Two Single bond unit 16 1-177 unit 38 3,4-diClPh CH _Two Single bond unit 17 1-178 unit 38 3,4-diClPh CH _Two Single bond unit 18 1-179 unit 38 3,4-diClPh CH _Two Single bond unit 19 1-180 unit 38 3,4-diClPh CH _Two Single bond unit 20 1-181 unit 38 3,4-diClPh CH _Two Single bond unit 21 1-182 unit 38 3,4-diClPh CH _Two Single bond unit 22 1-183 unit 38 3,4-diClPh CH _Two Single bond unit 23 1-184 unit 38 3,4-diClPh CH _Two Single bond unit 24 1-185 unit 38 3,4-diClPh CH _Two Single bond unit 25 1-186 unit 38 3,4-diClPh CH _Two Single bond unit 26 1-187 unit 38 3,4-diClPh CH _Two Single bond unit 27 1-188 unit 38 3,4-diClPh CH _Two Single bond unit 28 1-189 unit 38 3,4-diClPh CH _Two Single bond unit 29 1-190 unit 38 3,4-diClPh CH _Two Single bond unit 30 1-191 unit 38 3,4-diClPh CH _Two Single bond unit 31 1-192 unit 38 3,4-diClPh CH _Two Single bond unit 32 1-193 unit 39 3,4-diClPh CH _Two Single bond unit 1 1-194 unit 39 3,4-diClPh CH _Two Single bond unit 2 1-195 unit 39 3,4-diClPh CH _Two Single bond position 3 1-196 position 39 3,4-diClPh CH _Two Single bond position 4 1-197 position 39 3,4-diClPh CH _Two Single bond device 5 1-198 device 39 3,4-diClPh CH _Two Single bond device 6 1-199 device 39 3,4-diClPh CH _Two Single bond device 7 1-200 device 39 3,4-diClPh CH _Two Single bond device 8 1-201 device 39 3,4-diClPh CH _Two Single bond unit 9 1-202 unit 39 3,4-diClPh CH _Two Single bond unit 10 1-203 unit 39 3,4-diClPh CH _Two Single bond unit 11 1-204 unit 39 3,4-diClPh CH _Two Single bond unit 12 1-205 unit 39 3,4-diClPh CH _Two Single bond unit 13 1-206 unit 39 3,4-diClPh CH _Two Single bond unit 14 1-207 unit 39 3,4-diClPh CH _Two Single bond unit 15 1-208 unit 39 3,4-diClPh CH _Two Single bond unit 16 1-209 unit 39 3,4-diClPh CH _Two Single bond unit 17 1-210 unit 39 3,4-diClPh CH _Two Single bond unit 18 1-211 unit 39 3,4-diClPh CH _Two Single bond unit 19 1-212 unit 39 3,4-diClPh CH _Two Single bond device 20 1-213 device 39 3,4-diClPh CH _Two Single bond unit 21 1-214 unit 39 3,4-diClPh CH _Two Single bond unit 22 1-215 unit 39 3,4-diClPh CH _Two Single bond unit 23 1-216 unit 39 3,4-diClPh CH _Two Single bond unit 24 1-217 unit 39 3,4-diClPh CH _Two Single bond unit 25 1-218 unit 39 3,4-diClPh CH _Two Single bond unit 26 1-219 unit 39 3,4-diClPh CH _Two Single bond unit 27 1-220 unit 39 3,4-diClPh CH _Two Single bond unit 28 1-221 unit 39 3,4-diClPh CH _Two Single bond unit 29 1-222 unit 39 3,4-diClPh CH _Two Single bond device 30 1-223 device 39 3,4-diClPh CH _Two Single bond unit 31 1-224 unit 39 3,4-diClPh CH _Two Single bond unit 32 1-225 unit 40 3,4-diClPh CH _Two Single bond device 1 1-226 device 40 3,4-diClPh CH _Two Single bond device 2 1-227 device 40 3,4-diClPh CH _Two Single bond device 3 1-228 device 40 3,4-diClPh CH _Two Single bond device 4 1-229 device 40 3,4-diClPh CH _Two Single bond device 5 1-230 device 40 3,4-diClPh CH _Two Single bond device 6 1-231 device 40 3,4-diClPh CH _Two Single bond device 7 1-232 device 40 3,4-diClPh CH _Two Single bond device 8 1-233 device 40 3,4-diClPh CH _Two Single bond device 9 1-234 device 40 3,4-diClPh CH _Two Single bond device 10 1-235 device 40 3,4-diClPh CH _Two Single bond unit 11 1-236 unit 40 3,4-diClPh CH _Two Single bond unit 12 1-237 unit 40 3,4-diClPh CH _Two Single bond unit 13 1-238 unit 40 3,4-diClPh CH _Two Single bond unit 14 1-239 unit 40 3,4-diClPh CH _Two Single bond unit 15 1-240 unit 40 3,4-diClPh CH _Two Single bond unit 16 1-241 unit 40 3,4-diClPh CH _Two Single bond unit 17 1-242 unit 40 3,4-diClPh CH _Two Single bond unit 18 1-243 unit 40 3,4-diClPh CH _Two Single bond unit 19 1-244 unit 40 3,4-diClPh CH _Two Single bond device 20 1-245 device 40 3,4-diClPh CH _Two Single bond unit 21 1-246 unit 40 3,4-diClPh CH _Two Single bond unit 22 1-247 unit 40 3,4-diClPh CH _Two Single bond unit 23 1-248 unit 40 3,4-diClPh CH _Two Single bond unit 24 1-249 unit 40 3,4-diClPh CH _Two Single bond unit 25 1-250 unit 40 3,4-diClPh CH _Two Single bond unit 26 1-251 unit 40 3,4-diClPh CH _Two Single bond unit 27 1-252 unit 40 3,4-diClPh CH _Two Single bond unit 28 1-253 unit 40 3,4-diClPh CH _Two Single bond unit 29 1-254 unit 40 3,4-diClPh CH _Two Single bond device 30 1-255 device 40 3,4-diClPh CH _Two Single bond unit 31 1-256 unit 40 3,4-diClPh CH _Two Single bond unit 32 1-257 unit 41 3,4-diClPh CH _Two Single bond device 1 1-258 device 41 3,4-diClPh CH _Two Single bond device 2 1-259 device 41 3,4-diClPh CH _Two Single bond device 3 1-260 device 41 3,4-diClPh CH _Two Single bond unit 4 1-261 unit 41 3,4-diClPh CH _Two Single bond device 5 1-262 device 41 3,4-diClPh CH _Two Single bond device 6 1-263 device 41 3,4-diClPh CH _Two Single bond device 7 1-264 device 41 3,4-diClPh CH _Two Single bond device 8 1-265 device 41 3,4-diClPh CH _Two Single bond device 9 1-266 device 41 3,4-diClPh CH _Two Single bond device 10 1-267 device 41 3,4-diClPh CH _Two Single bond unit 11 1-268 unit 41 3,4-diClPh CH _Two Single bond unit 12 1-269 unit 41 3,4-diClPh CH _Two Single bond unit 13 1-270 unit 41 3,4-diClPh CH _Two Single bond unit 14 1-271 unit 41 3,4-diClPh CH _Two Single bond unit 15 1-272 unit 41 3,4-diClPh CH _Two Single bond unit 16 1-273 unit 41 3,4-diClPh CH _Two Single bond unit 17 1-274 unit 41 3,4-diClPh CH _Two Single bond unit 18 1-275 unit 41 3,4-diClPh CH _Two Single bond unit 19 1-276 unit 41 3,4-diClPh CH _Two Single bond unit 20 1-277 unit 41 3,4-diClPh CH _Two Single bond unit 21 1-278 unit 41 3,4-diClPh CH _Two Single bond unit 22 1-279 unit 41 3,4-diClPh CH _Two Single bond unit 23 1-280 unit 41 3,4-diClPh CH _Two Single bond unit 24 1-281 unit 41 3,4-diClPh CH _Two Single bond unit 25 1-282 unit 41 3,4-diClPh CH _Two Single bond unit 26 1-283 unit 41 3,4-diClPh CH _Two Single bond unit 27 1-284 unit 41 3,4-diClPh CH _Two Single bond unit 28 1-285 unit 41 3,4-diClPh CH _Two Single bond unit 29 1-286 unit 41 3,4-diClPh CH _Two Single bond device 30 1-287 device 41 3,4-diClPh CH _Two Single bond unit 31 1-288 unit 41 3,4-diClPh CH _Two Single bond unit 32 1-289 unit 42 3,4-diClPh CH _Two Single bond device 1 1-290 device 42 3,4-diClPh CH _Two Single bond unit 21-291 unit 42 3,4-diClPh CH _Two Single bond unit 31-292 unit 42 3,4-diClPh CH _Two Single bond unit 4 1-293 unit 42 3,4-diClPh CH _Two Single bond device 5 1-294 device 42 3,4-diClPh CH _Two Single bond unit 6 1-295 unit 42 3,4-diClPh CH _Two Single bond device 7 1-296 device 42 3,4-diClPh CH _Two Single bond device 8 1-297 device 42 3,4-diClPh CH _Two Single bond device 9 1-298 device 42 3,4-diClPh CH _Two Single bond device 10 1-299 device 42 3,4-diClPh CH _Two Single bond unit 11 1-300 unit 42 3,4-diClPh CH _Two Single bond unit 12 1-301 unit 42 3,4-diClPh CH _Two Single bond unit 13 1-302 unit 42 3,4-diClPh CH _Two Single bond unit 14 1-303 unit 42 3,4-diClPh CH _Two Single bond unit 15 1-304 unit 42 3,4-diClPh CH _Two Single bond unit 16 1-305 unit 42 3,4-diClPh CH _Two Single bond unit 17 1-306 unit 42 3,4-diClPh CH _Two Single bond unit 18 1-307 unit 42 3,4-diClPh CH _Two Single bond unit 19 1-308 unit 42 3,4-diClPh CH _Two Single bond unit 20 1-309 unit 42 3,4-diClPh CH _Two Single bond unit 21 1-310 unit 42 3,4-diClPh CH _Two Single bond unit 22 1-311 unit 42 3,4-diClPh CH _Two Single bond unit 23 1-312 unit 42 3,4-diClPh CH _Two Single bond unit 24 1-313 unit 42 3,4-diClPh CH _Two Single bond unit 25 1-314 unit 42 3,4-diClPh CH _Two Single bond unit 26 1-315 unit 42 3,4-diClPh CH _Two Single bond unit 27 1-316 unit 42 3,4-diClPh CH _Two Single bond unit 28 1-317 unit 42 3,4-diClPh CH _Two Single bond unit 29 1-318 unit 42 3,4-diClPh CH _Two Single bond device 30 1-319 device 42 3,4-diClPh CH _Two Single bond unit 31 1-320 unit 42 3,4-diClPh CH _Two Single bond unit 32 1-321 unit 43 3,4-diClPh CH _Two Single bond device 1 1-322 device 43 3,4-diClPh CH _Two Single bond device 2 1-323 device 43 3,4-diClPh CH _Two Single bond unit 31-324 unit 43 3,4-diClPh CH _Two Single bond device 4 1-325 device 43 3,4-diClPh CH _Two Single bond device 5 1-326 device 43 3,4-diClPh CH _Two Single bond device 6 1-327 device 43 3,4-diClPh CH _Two Single bond device 7 1-328 device 43 3,4-diClPh CH _Two Single bond device 8 1-329 device 43 3,4-diClPh CH _Two Single bond unit 9 1-330 unit 43 3,4-diClPh CH _Two Single bond device 10 1-331 device 43 3,4-diClPh CH _Two Single bond unit 11 1-332 unit 43 3,4-diClPh CH _Two Single bond unit 12 1-333 unit 43 3,4-diClPh CH _Two Single bond unit 13 1-334 unit 43 3,4-diClPh CH _Two Single bond unit 14 1-335 unit 43 3,4-diClPh CH _Two Single bond unit 15 1-336 unit 43 3,4-diClPh CH _Two Single bond Unit 16 1-337 Unit 43 3,4-diClPh CH _Two Single bond unit 17 1-338 unit 43 3,4-diClPh CH _Two Single bond unit 18 1-339 unit 43 3,4-diClPh CH _Two Single bond unit 19 1-340 unit 43 3,4-diClPh CH _Two Single bond unit 20 1-341 unit 43 3,4-diClPh CH _Two Single bond unit 21 1-342 unit 43 3,4-diClPh CH _Two Single bond unit 22 1-343 unit 43 3,4-diClPh CH _Two Single bond unit 23 1-344 unit 43 3,4-diClPh CH _Two Single bond unit 24 1-345 unit 43 3,4-diClPh CH _Two Single bond unit 25 1-346 unit 43 3,4-diClPh CH _Two Single bond unit 26 1-347 unit 43 3,4-diClPh CH _Two Single bond Unit 27 1-348 Unit 43 3,4-diClPh CH _Two Single bond unit 28 1-349 unit 43 3,4-diClPh CH _Two Single bond unit 29 1-350 unit 43 3,4-diClPh CH _Two Single bond unit 30 1-351 unit 43 3,4-diClPh CH _Two Single bond unit 31 1-352 unit 43 3,4-diClPh CH _Two Single bond unit 32 1-353 unit 44 3,4-diClPh CH _Two Single bond unit 1 1-354 unit 44 3,4-diClPh CH _Two Single bond unit 2 1-355 unit 44 3,4-diClPh CH _Two Single bond unit 31-356 unit 44 3,4-diClPh CH _Two Single bond unit 4 1-357 unit 44 3,4-diClPh CH _Two Single bond device 5 1-358 device 44 3,4-diClPh CH _Two Single bond unit 6 1-359 unit 44 3,4-diClPh CH _Two Single bond unit 7 1-360 unit 44 3,4-diClPh CH _Two Single bond unit 8 1-361 unit 44 3,4-diClPh CH _Two Single bond position 9 1-362 position 44 3,4-diClPh CH _Two Single bond unit 10 1-363 unit 44 3,4-diClPh CH _Two Single bond unit 11 1-364 unit 44 3,4-diClPh CH _Two Single bond unit 12 1-365 unit 44 3,4-diClPh CH _Two Single bond unit 13 1-366 unit 44 3,4-diClPh CH _Two Single bond unit 14 1-367 unit 44 3,4-diClPh CH _Two Single bond Unit 15 1-368 Unit 44 3,4-diClPh CH _Two Single bond unit 16 1-369 unit 44 3,4-diClPh CH _Two Single bond Unit 17 1-370 Unit 44 3,4-diClPh CH _Two Single bond unit 18 1-371 unit 44 3,4-diClPh CH _Two Single bond unit 19 1-372 unit 44 3,4-diClPh CH _Two Single bond unit 20 1-373 unit 44 3,4-diClPh CH _Two Single bond unit 21 1-374 unit 44 3,4-diClPh CH _Two Single bond unit 22 1-375 unit 44 3,4-diClPh CH _Two Single bond unit 23 1-376 unit 44 3,4-diClPh CH _Two Single bond unit 24 1-377 unit 44 3,4-diClPh CH _Two Single bond unit 25 1-378 unit 44 3,4-diClPh CH _Two Single bond unit 26 1-379 unit 44 3,4-diClPh CH _Two Single bond unit 27 1-380 unit 44 3,4-diClPh CH _Two Single bond unit 28 1-381 unit 44 3,4-diClPh CH _Two Single bond unit 29 1-382 unit 44 3,4-diClPh CH _Two Single bond unit 30 1-383 unit 44 3,4-diClPh CH _Two Single bond unit 31 1-384 unit 44 3,4-diClPh CH _Two Single bond unit 32 1-385 unit 45 3,4-diClPh CH _Two Single bond unit 1 1-386 unit 45 3,4-diClPh CH _Two Single bond unit 2 1-387 unit 45 3,4-diClPh CH _Two Single bond unit 31-388 unit 45 3,4-diClPh CH _Two Single bond unit 4 1-389 unit 45 3,4-diClPh CH _Two Single bond unit 5 1-390 unit 45 3,4-diClPh CH _Two Single bond unit 6 1-391 unit 45 3,4-diClPh CH _Two Single bond 7 7-392 45 3,4-diClPh CH _Two Single bond unit 8 1-393 unit 45 3,4-diClPh CH _Two Single bond unit 9 1-394 unit 45 3,4-diClPh CH _Two Single bond unit 10 1-395 unit 45 3,4-diClPh CH _Two Single bond unit 11 1-396 unit 45 3,4-diClPh CH _Two Single bond unit 12 1-397 unit 45 3,4-diClPh CH _Two Single bond unit 13 1-398 unit 45 3,4-diClPh CH _Two Single bond unit 14 1-399 unit 45 3,4-diClPh CH _Two Single bond unit 15 1-400 unit 45 3,4-diClPh CH _Two Single bond unit 16 1-401 unit 45 3,4-diClPh CH _Two Single bond unit 17 1-402 unit 45 3,4-diClPh CH _Two Single bond unit 18 1-403 unit 45 3,4-diClPh CH _Two Single bond unit 19 1-404 unit 45 3,4-diClPh CH _Two Single bond unit 20 1-405 unit 45 3,4-diClPh CH _Two Single bond unit 21 1-406 unit 45 3,4-diClPh CH _Two Single bond unit 22 1-407 unit 45 3,4-diClPh CH _Two Single bond unit 23 1-408 unit 45 3,4-diClPh CH _Two Single bond unit 24 1-409 unit 45 3,4-diClPh CH _Two Single bond unit 25 1-410 unit 45 3,4-diClPh CH _Two Single bond unit 26 1-411 unit 45 3,4-diClPh CH _Two Single bond unit 27 1-412 unit 45 3,4-diClPh CH _Two Single bond unit 28 1-413 unit 45 3,4-diClPh CH _Two Single bond unit 29 1-414 unit 45 3,4-diClPh CH _Two Single bond unit 30 1-415 unit 45 3,4-diClPh CH _Two Single bond unit 31 1-416 unit 45 3,4-diClPh CH _Two Single bond unit 32 1-417 unit 46 3,4-diClPh CH _Two Single bond device 1 1-418 device 46 3,4-diClPh CH _Two Single bond device 2 1-419 device 46 3,4-diClPh CH _Two Single bond unit 31-420 unit 46 3,4-diClPh CH _Two Single bond unit 4 1-421 unit 46 3,4-diClPh CH _Two Single bond device 5 1-422 device 46 3,4-diClPh CH _Two Single bond device 6 1-423 device 46 3,4-diClPh CH _Two Single bond device 7 1-424 device 46 3,4-diClPh CH _Two Single bond device 8 1-425 device 46 3,4-diClPh CH _Two Single bond device 9 1-426 device 46 3,4-diClPh CH _Two Single bond device 10 1-427 device 46 3,4-diClPh CH _Two Single bond Unit 11 1-428 Unit 46 3,4-diClPh CH _Two Single bond unit 12 1-429 unit 46 3,4-diClPh CH _Two Single bond unit 13 1-430 unit 46 3,4-diClPh CH _Two Single bond unit 14 1-431 unit 46 3,4-diClPh CH _Two Single bond unit 15 1-432 unit 46 3,4-diClPh CH _Two Single bond unit 16 1-433 unit 46 3,4-diClPh CH _Two Single bond unit 17 1-434 unit 46 3,4-diClPh CH _Two Single bond unit 18 1-435 unit 46 3,4-diClPh CH _Two Single bond unit 19 1-436 unit 46 3,4-diClPh CH _Two Single bond unit 20 1-437 unit 46 3,4-diClPh CH _Two Single bond unit 21 1-438 unit 46 3,4-diClPh CH _Two Single bond unit 22 1-439 unit 46 3,4-diClPh CH _Two Single bond unit 23 1-444 unit 46 3,4-diClPh CH _Two Single bond unit 24 1-441 unit 46 3,4-diClPh CH _Two Single bond unit 25 1-442 unit 46 3,4-diClPh CH _Two Single bond unit 26 1-443 unit 46 3,4-diClPh CH _Two Single bond unit 27 1-444 unit 46 3,4-diClPh CH _Two Single bond unit 28 1-445 unit 46 3,4-diClPh CH _Two Single bond unit 29 1-446 unit 46 3,4-diClPh CH _Two Single bond unit 30 1-447 unit 46 3,4-diClPh CH _Two Single bond unit 31 1-448 unit 46 3,4-diClPh CH _Two Single bond unit 32 1-449 unit 47 3,4-diClPh CH _Two Single bond unit 1 1-450 unit 47 3,4-diClPh CH _Two Single bond unit 21-451 unit 47 3,4-diClPh CH _Two Single bond unit 31-452 unit 47 3,4-diClPh CH _Two Single bond unit 4 1-453 unit 47 3,4-diClPh CH _Two Single bond device 51 1-454 device 47 3,4-diClPh CH _Two Single bond unit 6 1-455 unit 47 3,4-diClPh CH _Two Single bond device 7 1-456 device 47 3,4-diClPh CH _Two Single bond unit 8 1-457 unit 47 3,4-diClPh CH _Two Single bond device 9 1-458 device 47 3,4-diClPh CH _Two Single bond unit 10 1-459 unit 47 3,4-diClPh CH _Two Single bond unit 11 1-460 unit 47 3,4-diClPh CH _Two Single bond unit 12 1-461 unit 47 3,4-diClPh CH _Two Single bond unit 13 1-462 unit 47 3,4-diClPh CH _Two Single bond unit 14 1-463 unit 47 3,4-diClPh CH _Two Single bond unit 15 1-464 unit 47 3,4-diClPh CH _Two Single bond unit 16 1-465 unit 47 3,4-diClPh CH _Two Single bond Unit 17 1-466 Unit 47 3,4-diClPh CH _Two Single bond unit 18 1-467 unit 47 3,4-diClPh CH _Two Single bond unit 19 1-468 unit 47 3,4-diClPh CH _Two Single bond unit 20 1-469 unit 47 3,4-diClPh CH _Two Single bond Unit 21 1-470 Unit 47 3,4-diClPh CH _Two Single bond unit 22 1-471 unit 47 3,4-diClPh CH _Two Single bond unit 23 1-472 unit 47 3,4-diClPh CH _Two Single bond unit 24 1-473 unit 47 3,4-diClPh CH _Two Single bond unit 25 1-474 unit 47 3,4-diClPh CH _Two Single bond unit 26 1-475 unit 47 3,4-diClPh CH _Two Single bond unit 27 1-476 unit 47 3,4-diClPh CH _Two Single bond unit 28 1-477 unit 47 3,4-diClPh CH _Two Single bond unit 29 1-478 unit 47 3,4-diClPh CH _Two Single bond unit 30 1-479 unit 47 3,4-diClPh CH _Two Single bond unit 31 1-480 unit 47 3,4-diClPh CH _Two Single bond unit 32 1-481 unit 48 3,4-diClPh CH _Two Single bond unit 1 1-482 unit 48 3,4-diClPh CH _Two Single bond unit 2-1-483 unit 48 3,4-diClPh CH _Two Single bond unit 31-484 unit 48 3,4-diClPh CH _Two Single bond unit 4 1-485 unit 48 3,4-diClPh CH _Two Single bond device 5 1-486 device 48 3,4-diClPh CH _Two Single bond unit 6 1-487 unit 48 3,4-diClPh CH _Two Single bond unit 7 1-488 unit 48 3,4-diClPh CH _Two Single bond position 8 1-489 position 48 3,4-diClPh CH _Two Single bond unit 9 1-490 unit 48 3,4-diClPh CH _Two Single bond unit 10 1-491 unit 48 3,4-diClPh CH _Two Single bond unit 11 1-492 unit 48 3,4-diClPh CH _Two Single bond unit 12 1-493 unit 48 3,4-diClPh CH _Two Single bond unit 13 1-494 unit 48 3,4-diClPh CH _Two Single bond unit 14 1-495 unit 48 3,4-diClPh CH _Two Single bond unit 15 1-496 unit 48 3,4-diClPh CH _Two Single bond unit 16 1-497 unit 48 3,4-diClPh CH _Two Single bond unit 17 1-498 unit 48 3,4-diClPh CH _Two Single bond unit 18 1-499 unit 48 3,4-diClPh CH _Two Single bond unit 19 1-500 unit 48 3,4-diClPh CH _Two Single bond unit 20 1-501 unit 48 3,4-diClPh CH _Two Single bond unit 21 1-502 unit 48 3,4-diClPh CH _Two Single bond unit 22 1-503 unit 48 3,4-diClPh CH _Two Single bond unit 23 1-504 unit 48 3,4-diClPh CH _Two Single bond unit 24 1-505 unit 48 3,4-diClPh CH _Two Single bond unit 25 1-506 unit 48 3,4-diClPh CH _Two Single bond unit 26 1-507 unit 48 3,4-diClPh CH _Two Single bond unit 27 1-508 unit 48 3,4-diClPh CH _Two Single bond unit 28 1-509 unit 48 3,4-diClPh CH _Two Single bond unit 29 1-510 unit 48 3,4-diClPh CH _Two Single bond unit 30 1-511 unit 48 3,4-diClPh CH _Two Single bond unit 31 1-512 unit 48 3,4-diClPh CH _Two Single bond position 32 ──────────────────────────────────── Compound number R ¹ R ^Two ABZ ──────────────────────────────────── 1-513 Place 49 3,4-diClPh CH _Two Single bond position 1 1-514 position 49 3,4-diClPh CH _Two Single bond unit 21-515 unit 49 3,4-diClPh CH _Two Single bond position 3 1-516 position 49 3,4-diClPh CH _Two Single bond position 4 1-517 position 49 3,4-diClPh CH _Two Single bond unit 5 1-518 unit 49 3,4-diClPh CH _Two Single bond unit 6 1-519 unit 49 3,4-diClPh CH _Two Single bond unit 7 1-520 unit 49 3,4-diClPh CH _Two Single bond unit 8 1-521 unit 49 3,4-diClPh CH _Two Single bond position 9 1-522 position 49 3,4-diClPh CH _Two Single bond unit 10 1-523 unit 49 3,4-diClPh CH _Two Single bond unit 11 1-524 unit 49 3,4-diClPh CH _Two Single bond unit 12 1-525 unit 49 3,4-diClPh CH _Two Single bond unit 13 1-526 unit 49 3,4-diClPh CH _Two Single bond unit 14 1-527 unit 49 3,4-diClPh CH _Two Single bond unit 15 1-528 unit 49 3,4-diClPh CH _Two Single bond unit 16 1-529 unit 49 3,4-diClPh CH _Two Single bond unit 17 1-530 unit 49 3,4-diClPh CH _Two Single bond unit 18 1-531 unit 49 3,4-diClPh CH _Two Single bond unit 19 1-532 unit 49 3,4-diClPh CH _Two Single bond unit 20 1-533 unit 49 3,4-diClPh CH _Two Single bond unit 21 1-534 unit 49 3,4-diClPh CH _Two Single bond unit 22 1-535 unit 49 3,4-diClPh CH _Two Single bond unit 23 1-536 unit 49 3,4-diClPh CH _Two Single bond unit 24 1-537 unit 49 3,4-diClPh CH _Two Single bond unit 25 1-538 unit 49 3,4-diClPh CH _Two Single bond unit 26 1-539 unit 49 3,4-diClPh CH _Two Single bond unit 27 1-540 unit 49 3,4-diClPh CH _Two Single bond unit 28 1-541 unit 49 3,4-diClPh CH _Two Single bond unit 29 1-542 unit 49 3,4-diClPh CH _Two Single bond unit 30 1-543 unit 49 3,4-diClPh CH _Two Single bond unit 31 1-544 unit 49 3,4-diClPh CH _Two Single bond unit 32 1-545 unit 50 3,4-diClPh CH _Two Single bond device 1 1-546 device 50 3,4-diClPh CH _Two Single bond unit 2 1-547 unit 50 3,4-diClPh CH _Two Single bond device 3 1-548 device 50 3,4-diClPh CH _Two Single bond unit 4 1-549 unit 50 3,4-diClPh CH _Two Single bond device 5 1-550 device 50 3,4-diClPh CH _Two Single bond device 6 1-551 device 50 3,4-diClPh CH _Two Single bond device 7 1-552 device 50 3,4-diClPh CH _Two Single bond device 8 1-553 device 50 3,4-diClPh CH _Two Single bond device 9 1-554 device 50 3,4-diClPh CH _Two Single bond device 10 1-555 device 50 3,4-diClPh CH _Two Single bond unit 11 1-556 unit 50 3,4-diClPh CH _Two Single bond unit 12 1-557 unit 50 3,4-diClPh CH _Two Single bond unit 13 1-558 unit 50 3,4-diClPh CH _Two Single bond unit 14 1-559 unit 50 3,4-diClPh CH _Two Single bond unit 15 1-560 unit 50 3,4-diClPh CH _Two Single bond unit 16 1-561 unit 50 3,4-diClPh CH _Two Single bond unit 17 1-562 unit 50 3,4-diClPh CH _Two Single bond unit 18 1-563 unit 50 3,4-diClPh CH _Two Single bond unit 19 1-564 unit 50 3,4-diClPh CH _Two Single bond unit 20 1-565 unit 50 3,4-diClPh CH _Two Single bond unit 21 1-566 unit 50 3,4-diClPh CH _Two Single bond unit 22 1-567 unit 50 3,4-diClPh CH _Two Single bond unit 23 1-568 unit 50 3,4-diClPh CH _Two Single bond unit 24 1-569 unit 50 3,4-diClPh CH _Two Single bond unit 25 1-570 unit 50 3,4-diClPh CH _Two Single bond unit 26 1-571 unit 50 3,4-diClPh CH _Two Single bond unit 27 1-572 unit 50 3,4-diClPh CH _Two Single bond unit 28 1-573 unit 50 3,4-diClPh CH _Two Single bond unit 29 1-574 unit 50 3,4-diClPh CH _Two Single bond unit 30 1-575 unit 50 3,4-diClPh CH _Two Single bond unit 31 1-576 unit 50 3,4-diClPh CH _Two Single bond unit 32 1-577 unit 51 3,4-diClPh CH _Two Single bond unit 1 1-578 unit 51 3,4-diClPh CH _Two Single bond unit 21-579 unit 51 3,4-diClPh CH _Two Single bond unit 31-580 unit 51 3,4-diClPh CH _Two Single bond unit 4 1-581 unit 51 3,4-diClPh CH _Two Single bond device 5 1-582 device 51 3,4-diClPh CH _Two Single bond unit 6 1-583 unit 51 3,4-diClPh CH _Two Single bond unit 7 1-584 unit 51 3,4-diClPh CH _Two Single bond device 8 1-585 device 51 3,4-diClPh CH _Two Single bond device 9 1-586 device 51 3,4-diClPh CH _Two Single bond device 10 1-587 device 51 3,4-diClPh CH _Two Single bond unit 11 1-588 unit 51 3,4-diClPh CH _Two Single bond unit 12 1-589 unit 51 3,4-diClPh CH _Two Single bond unit 13 1-590 unit 51 3,4-diClPh CH _Two Single bond unit 14 1-591 unit 51 3,4-diClPh CH _Two Single bond unit 15 1-592 unit 51 3,4-diClPh CH _Two Single bond unit 16 1-593 unit 51 3,4-diClPh CH _Two Single bond unit 17 1-594 unit 51 3,4-diClPh CH _Two Single bond unit 18 1-595 unit 51 3,4-diClPh CH _Two Single bond unit 19 1-596 unit 51 3,4-diClPh CH _Two Single bond unit 20 1-597 unit 51 3,4-diClPh CH _Two Single bond unit 21 1-598 unit 51 3,4-diClPh CH _Two Single bond unit 22 1-599 unit 51 3,4-diClPh CH _Two Single bond unit 23 1-600 unit 51 3,4-diClPh CH _Two Single bond unit 24 1-601 unit 51 3,4-diClPh CH _Two Single bond unit 25 1-602 unit 51 3,4-diClPh CH _Two Single bond unit 26 1-603 unit 51 3,4-diClPh CH _Two Single bond unit 27 1-604 unit 51 3,4-diClPh CH _Two Single bond unit 28 1-605 unit 51 3,4-diClPh CH _Two Single bond unit 29 1-606 unit 51 3,4-diClPh CH _Two Single bond device 30 1-607 device 51 3,4-diClPh CH _Two Single bond unit 31 1-608 unit 51 3,4-diClPh CH _Two Single bond unit 32 1-609 unit 52 3,4-diClPh CH _Two Single bond device 1 1-610 device 52 3,4-diClPh CH _Two Single bond device 2 1-611 device 52 3,4-diClPh CH _Two Single bond device 3 1-612 device 52 3,4-diClPh CH _Two Single bond unit 4 1-613 unit 52 3,4-diClPh CH _Two Single bond 5 1-614 5 52 3,4-diClPh CH _Two Single bond device 6 1-615 device 52 3,4-diClPh CH _Two Single bond device 7 1-616 device 52 3,4-diClPh CH _Two Single bond device 8 1-617 device 52 3,4-diClPh CH _Two Single bond device 9 1-618 device 52 3,4-diClPh CH _Two Single bond device 10 1-619 device 52 3,4-diClPh CH _Two Single bond unit 11 1-620 unit 52 3,4-diClPh CH _Two Single bond unit 12 1-621 unit 52 3,4-diClPh CH _Two Single bond unit 13 1-622 unit 52 3,4-diClPh CH _Two Single bond unit 14 1-623 unit 52 3,4-diClPh CH _Two Single bond unit 15 1-624 unit 52 3,4-diClPh CH _Two Single bond unit 16 1-625 unit 52 3,4-diClPh CH _Two Single bond unit 17 1-626 unit 52 3,4-diClPh CH _Two Single bond unit 18 1-627 unit 52 3,4-diClPh CH _Two Single bond unit 19 1-628 unit 52 3,4-diClPh CH _Two Single bond unit 20 1-629 unit 52 3,4-diClPh CH _Two Single bond unit 21 1-630 unit 52 3,4-diClPh CH _Two Single bond unit 22 1-631 unit 52 3,4-diClPh CH _Two Single bond unit 23 1-632 unit 52 3,4-diClPh CH _Two Single bond unit 24 1-633 unit 52 3,4-diClPh CH _Two Single bond unit 25 1-634 unit 52 3,4-diClPh CH _Two Single bond unit 26 1-635 unit 52 3,4-diClPh CH _Two Single bond unit 27 1-636 unit 52 3,4-diClPh CH _Two Single bond unit 28 1-637 unit 52 3,4-diClPh CH _Two Single bond unit 29 1-638 unit 52 3,4-diClPh CH _Two Single bond unit 30 1-639 unit 52 3,4-diClPh CH _Two Single bond unit 31 1-640 unit 52 3,4-diClPh CH _Two Single bond unit 32 1-641 unit 53 3,4-diClPh CH _Two Single bond unit 1 1-642 unit 53 3,4-diClPh CH _Two Single bond unit 2 1-643 unit 53 3,4-diClPh CH _Two Single bond position 3 1-644 position 53 3,4-diClPh CH _Two Single bond unit 4 1-645 unit 53 3,4-diClPh CH _Two Single bond 5 1-646 5 3 3,4-diClPh CH _Two Single bond unit 6 1-647 unit 53 3,4-diClPh CH _Two Single bond position 7 1-648 position 53 3,4-diClPh CH _Two Single bond unit 8 1-649 unit 53 3,4-diClPh CH _Two Single bond unit 9 1-650 unit 53 3,4-diClPh CH _Two Single bond unit 10 1-651 unit 53 3,4-diClPh CH _Two Single bond unit 11 1-652 unit 53 3,4-diClPh CH _Two Single bond unit 12 1-653 unit 53 3,4-diClPh CH _Two Single bond unit 13 1-654 unit 53 3,4-diClPh CH _Two Single bond unit 14 1-655 unit 53 3,4-diClPh CH _Two Single bond unit 15 1-656 unit 53 3,4-diClPh CH _Two Single bond unit 16 1-657 unit 53 3,4-diClPh CH _Two Single bond unit 17 1-658 unit 53 3,4-diClPh CH _Two Single bond unit 18 1-659 unit 53 3,4-diClPh CH _Two Single bond unit 19 1-660 unit 53 3,4-diClPh CH _Two Single bond unit 20 1-661 unit 53 3,4-diClPh CH _Two Single bond unit 21 1-662 unit 53 3,4-diClPh CH _Two Single bond unit 22 1-663 unit 53 3,4-diClPh CH _Two Single bond unit 23 1-664 unit 53 3,4-diClPh CH _Two Single bond unit 24 1-665 unit 53 3,4-diClPh CH _Two Single bond unit 25 1-666 unit 53 3,4-diClPh CH _Two Single bond unit 26 1-667 unit 53 3,4-diClPh CH _Two Single bond unit 27 1-668 unit 53 3,4-diClPh CH _Two Single bond unit 28 1-669 unit 53 3,4-diClPh CH _Two Single bond unit 29 1-670 unit 53 3,4-diClPh CH _Two Single bond unit 30 1-671 unit 53 3,4-diClPh CH _Two Single bond unit 31 1-672 unit 53 3,4-diClPh CH _Two Single bond unit 32 1-673 unit 54 3,4-diClPh CH _Two Single bond unit 1 1-674 unit 54 3,4-diClPh CH _Two Single bond unit 21-675 unit 54 3,4-diClPh CH _Two Single bond unit 31-676 unit 54 3,4-diClPh CH _Two Single bond unit 4 1-677 unit 54 3,4-diClPh CH _Two Single bond unit 5 1-678 unit 54 3,4-diClPh CH _Two Single bond device 6 1-679 device 54 3,4-diClPh CH _Two Single bond unit 7 1-680 unit 54 3,4-diClPh CH _Two Single bond unit 8 1-681 unit 54 3,4-diClPh CH _Two Single bond unit 9 1-682 unit 54 3,4-diClPh CH _Two Single bond device 10 1-683 device 54 3,4-diClPh CH _Two Single bond unit 11 1-684 unit 54 3,4-diClPh CH _Two Single bond unit 12 1-685 unit 54 3,4-diClPh CH _Two Single bond unit 13 1-686 unit 54 3,4-diClPh CH _Two Single bond unit 14 1-687 unit 54 3,4-diClPh CH _Two Single bond unit 15 1-688 unit 54 3,4-diClPh CH _Two Single bond unit 16 1-689 unit 54 3,4-diClPh CH _Two Single bond unit 17 1-690 unit 54 3,4-diClPh CH _Two Single bond unit 18 1-691 unit 54 3,4-diClPh CH _Two Single bond unit 19 1-692 unit 54 3,4-diClPh CH _Two Single bond unit 20 1-693 unit 54 3,4-diClPh CH _Two Single bond unit 21 1-694 unit 54 3,4-diClPh CH _Two Single bond unit 22 1-695 unit 54 3,4-diClPh CH _Two Single bond unit 23 1-696 unit 54 3,4-diClPh CH _Two Single bond unit 24 1-697 unit 54 3,4-diClPh CH _Two Single bond unit 25 1-698 unit 54 3,4-diClPh CH _Two Single bond unit 26 1-699 unit 54 3,4-diClPh CH _Two Single bond unit 27 1-700 unit 54 3,4-diClPh CH _Two Single bond unit 28 1-701 unit 54 3,4-diClPh CH _Two Single bond unit 29 1-702 unit 54 3,4-diClPh CH _Two Single bond unit 30 1-703 unit 54 3,4-diClPh CH _Two Single bond unit 31 1-704 unit 54 3,4-diClPh CH _Two Single bond unit 32 1-705 unit 55 3,4-diClPh CH _Two Single bond unit 1 1-706 unit 55 3,4-diClPh CH _Two Single bond unit 21-707 unit 55 3,4-diClPh CH _Two Single bond position 3 1-708 position 55 3,4-diClPh CH _Two Single bond unit 4 1-709 unit 55 3,4-diClPh CH _Two Single bond device 5 1-710 device 55 3,4-diClPh CH _Two Single bond unit 6 1-711 unit 55 3,4-diClPh CH _Two Single bond unit 7 1-712 unit 55 3,4-diClPh CH _Two Single bond unit 8 1-713 unit 55 3,4-diClPh CH _Two Single bond position 9 1-714 position 55 3,4-diClPh CH _Two Single bond unit 10 1-715 unit 55 3,4-diClPh CH _Two Single bond unit 11 1-716 unit 55 3,4-diClPh CH _Two Single bond unit 12 1-717 unit 55 3,4-diClPh CH _Two Single bond unit 13 1-718 unit 55 3,4-diClPh CH _Two Single bond unit 14 1-719 unit 55 3,4-diClPh CH _Two Single bond unit 15 1-720 unit 55 3,4-diClPh CH _Two Single bond unit 16 1-721 unit 55 3,4-diClPh CH _Two Single bond unit 17 1-722 unit 55 3,4-diClPh CH _Two Single bond unit 18 1-723 unit 55 3,4-diClPh CH _Two Single bond unit 19 1-724 unit 55 3,4-diClPh CH _Two Single bond unit 20 1-725 unit 55 3,4-diClPh CH _Two Single bond unit 21 1-726 unit 55 3,4-diClPh CH _Two Single bond unit 22 1-727 unit 55 3,4-diClPh CH _Two Single bond unit 23 1-728 unit 55 3,4-diClPh CH _Two Single bond unit 24 1-729 unit 55 3,4-diClPh CH _Two Single bond unit 25 1-730 unit 55 3,4-diClPh CH _Two Single bond unit 26 1-731 unit 55 3,4-diClPh CH _Two Single bond unit 27 1-732 unit 55 3,4-diClPh CH _Two Single bond unit 28 1-733 unit 55 3,4-diClPh CH _Two Single bond unit 29 1-734 unit 55 3,4-diClPh CH _Two Single bond unit 30 1-735 unit 55 3,4-diClPh CH _Two Single bond unit 31 1-736 unit 55 3,4-diClPh CH _Two Single bond unit 32 1-737 unit 56 3,4-diClPh CH _Two Single bond position 1 1-738 position 56 3,4-diClPh CH _Two Single bond position 2 1-739 position 56 3,4-diClPh CH _Two Single bond unit 31-740 unit 56 3,4-diClPh CH _Two Single bond unit 4 1-741 unit 56 3,4-diClPh CH _Two Single bond unit 5 1-742 unit 56 3,4-diClPh CH _Two Single bond unit 6 1-743 unit 56 3,4-diClPh CH _Two Single bond unit 7 1-744 unit 56 3,4-diClPh CH _Two Single bond device 8 1-745 device 56 3,4-diClPh CH _Two Single bond position 9 1-746 position 56 3,4-diClPh CH _Two Single bond unit 10 1-747 unit 56 3,4-diClPh CH _Two Single bond unit 11 1-748 unit 56 3,4-diClPh CH _Two Single bond unit 12 1-749 unit 56 3,4-diClPh CH _Two Single bond unit 13 1-750 unit 56 3,4-diClPh CH _Two Single bond unit 14 1-751 unit 56 3,4-diClPh CH _Two Single bond unit 15 1-752 unit 56 3,4-diClPh CH _Two Single bond unit 16 1-753 unit 56 3,4-diClPh CH _Two Single bond unit 17 1-754 unit 56 3,4-diClPh CH _Two Single bond unit 18 1-755 unit 56 3,4-diClPh CH _Two Single bond unit 19 1-756 unit 56 3,4-diClPh CH _Two Single bond unit 20 1-757 unit 56 3,4-diClPh CH _Two Single bond unit 21 1-758 unit 56 3,4-diClPh CH _Two Single bond unit 22 1-759 unit 56 3,4-diClPh CH _Two Single bond unit 23 1-760 unit 56 3,4-diClPh CH _Two Single bond unit 24 1-761 unit 56 3,4-diClPh CH _Two Single bond unit 25 1-762 unit 56 3,4-diClPh CH _Two Single bond unit 26 1-763 unit 56 3,4-diClPh CH _Two Single bond unit 27 1-764 unit 56 3,4-diClPh CH _Two Single bond unit 28 1-765 unit 56 3,4-diClPh CH _Two Single bond unit 29 1-766 unit 56 3,4-diClPh CH _Two Single bond unit 30 1-767 unit 56 3,4-diClPh CH _Two Single bond unit 31 1-768 unit 56 3,4-diClPh CH _Two Single bond unit 32 1-769 unit 57 3,4-diClPh CH _Two Single bond unit 1 1-770 unit 57 3,4-diClPh CH _Two Single bond unit 2 1-771 unit 57 3,4-diClPh CH _Two Single bond position 3 1-772 position 57 3,4-diClPh CH _Two Single bond unit 4 1-773 unit 57 3,4-diClPh CH _Two Single bond 5 1-774 557 3,4-diClPh CH _Two Single bond device 6 1-775 device 57 3,4-diClPh CH _Two Single bond unit 7 1-776 unit 57 3,4-diClPh CH _Two Single bond position 8 1-777 position 57 3,4-diClPh CH _Two Single bond position 9 1-778 position 57 3,4-diClPh CH _Two Single bond unit 10 1-779 unit 57 3,4-diClPh CH _Two Single bond unit 11 1-780 unit 57 3,4-diClPh CH _Two Single bond unit 12 1-781 unit 57 3,4-diClPh CH _Two Single bond unit 13 1-782 unit 57 3,4-diClPh CH _Two Single bond unit 14 1-783 unit 57 3,4-diClPh CH _Two Single bond unit 15 1-784 unit 57 3,4-diClPh CH _Two Single bond unit 16 1-785 unit 57 3,4-diClPh CH _Two Single bond unit 17 1-786 unit 57 3,4-diClPh CH _Two Single bond unit 18 1-787 unit 57 3,4-diClPh CH _Two Single bond unit 19 1-788 unit 57 3,4-diClPh CH _Two Single bond unit 20 1-789 unit 57 3,4-diClPh CH _Two Single bond unit 21 1-790 unit 57 3,4-diClPh CH _Two Single bond unit 22 1-791 unit 57 3,4-diClPh CH _Two Single bond unit 23 1-792 unit 57 3,4-diClPh CH _Two Single bond unit 24 1-793 unit 57 3,4-diClPh CH _Two Single bond unit 25 1-794 unit 57 3,4-diClPh CH _Two Single bond unit 26 1-795 unit 57 3,4-diClPh CH _Two Single bond unit 27 1-796 unit 57 3,4-diClPh CH _Two Single bond unit 28 1-797 unit 57 3,4-diClPh CH _Two Single bond unit 29 1-798 unit 57 3,4-diClPh CH _Two Single bond unit 30 1-799 unit 57 3,4-diClPh CH _Two Single bond unit 31 1-800 unit 57 3,4-diClPh CH _Two Single bond unit 32 1-801 unit 58 3,4-diClPh CH _Two Single bond unit 1 1-802 unit 58 3,4-diClPh CH _Two Single bond position 2 1-803 position 58 3,4-diClPh CH _Two Single bond position 3 1-804 position 58 3,4-diClPh CH _Two Single bond unit 4 1-805 unit 58 3,4-diClPh CH _Two Single bond device 5 1-806 device 58 3,4-diClPh CH _Two Single bond device 6 1-807 device 58 3,4-diClPh CH _Two Single bond device 7 1-808 device 58 3,4-diClPh CH _Two Single bond device 8 1-809 device 58 3,4-diClPh CH _Two Single bond device 9 1-810 device 58 3,4-diClPh CH _Two Single bond device 10 1-811 device 58 3,4-diClPh CH _Two Single bond unit 11 1-812 unit 58 3,4-diClPh CH _Two Single bond unit 12 1-813 unit 58 3,4-diClPh CH _Two Single bond unit 13 1-814 unit 58 3,4-diClPh CH _Two Single bond unit 14 1-815 unit 58 3,4-diClPh CH _Two Single bond unit 15 1-816 unit 58 3,4-diClPh CH _Two Single bond unit 16 1-817 unit 58 3,4-diClPh CH _Two Single bond unit 17 1-818 unit 58 3,4-diClPh CH _Two Single bond unit 18 1-819 unit 58 3,4-diClPh CH _Two Single bond unit 19 1-820 unit 58 3,4-diClPh CH _Two Single bond unit 20 1-821 unit 58 3,4-diClPh CH _Two Single bond unit 21 1-822 unit 58 3,4-diClPh CH _Two Single bond unit 22 1-823 unit 58 3,4-diClPh CH _Two Single bond unit 23 1-824 unit 58 3,4-diClPh CH _Two Single bond unit 24 1-825 unit 58 3,4-diClPh CH _Two Single bond unit 25 1-826 unit 58 3,4-diClPh CH _Two Single bond unit 26 1-827 unit 58 3,4-diClPh CH _Two Single bond unit 27 1-828 unit 58 3,4-diClPh CH _Two Single bond unit 28 1-829 unit 58 3,4-diClPh CH _Two Single bond unit 29 1-830 unit 58 3,4-diClPh CH _Two Single bond unit 30 1-831 unit 58 3,4-diClPh CH _Two Single bond unit 31 1-832 unit 58 3,4-diClPh CH _Two Single bond unit 32 1-833 unit 59 3,4-diClPh CH _Two Single bond position 1 1-834 position 59 3,4-diClPh CH _Two Single bond position 2 1-835 position 59 3,4-diClPh CH _Two Single bond position 3 1-836 position 59 3,4-diClPh CH _Two Single bond position 4 1-837 position 59 3,4-diClPh CH _Two Single bond 5 1-838 559 3,4-diClPh CH _Two Single bond device 6 1-839 device 59 3,4-diClPh CH _Two Single bond unit 7 1-840 unit 59 3,4-diClPh CH _Two Single bond unit 8 1-841 unit 59 3,4-diClPh CH _Two Single bond position 9 1-842 position 59 3,4-diClPh CH _Two Single bond unit 10 1-843 unit 59 3,4-diClPh CH _Two Single bond unit 11 1-844 unit 59 3,4-diClPh CH _Two Single bond unit 12 1-845 unit 59 3,4-diClPh CH _Two Single bond unit 13 1-846 unit 59 3,4-diClPh CH _Two Single bond unit 14 1-847 unit 59 3,4-diClPh CH _Two Single bond position 15 1-848 position 59 3,4-diClPh CH _Two Single bond unit 16 1-849 unit 59 3,4-diClPh CH _Two Single bond unit 17 1-850 unit 59 3,4-diClPh CH _Two Single bond unit 18 1-851 unit 59 3,4-diClPh CH _Two Single bond unit 19 1-852 unit 59 3,4-diClPh CH _Two Single bond unit 20 1-853 unit 59 3,4-diClPh CH _Two Single bond unit 21 1-854 unit 59 3,4-diClPh CH _Two Single bond unit 22 1-855 unit 59 3,4-diClPh CH _Two Single bond unit 23 1-856 unit 59 3,4-diClPh CH _Two Single bond unit 24 1-857 unit 59 3,4-diClPh CH _Two Single bond unit 25 1-858 unit 59 3,4-diClPh CH _Two Single bond unit 26 1-859 unit 59 3,4-diClPh CH _Two Single bond unit 27 1-860 unit 59 3,4-diClPh CH _Two Single bond unit 28 1-861 unit 59 3,4-diClPh CH _Two Single bond unit 29 1-862 unit 59 3,4-diClPh CH _Two Single bond unit 30 1-863 unit 59 3,4-diClPh CH _Two Single bond unit 31 1-864 unit 59 3,4-diClPh CH _Two Single bond unit 32 1-865 unit 60 3,4-diClPh CH _Two Single bond device 1 1-866 device 60 3,4-diClPh CH _Two Single bond unit 2 1-867 unit 60 3,4-diClPh CH _Two Single bond device 3 1-868 device 60 3,4-diClPh CH _Two Single bond device 4 1-869 device 60 3,4-diClPh CH _Two Single bond device 5 1-870 device 60 3,4-diClPh CH _Two Single bond unit 6 1-871 unit 60 3,4-diClPh CH _Two Single bond unit 7 1-872 unit 60 3,4-diClPh CH _Two Single bond device 8 1-873 device 60 3,4-diClPh CH _Two Single bond device 9 1-874 device 60 3,4-diClPh CH _Two Single bond device 10 1-875 device 60 3,4-diClPh CH _Two Single bond Unit 11 1-876 Unit 60 3,4-diClPh CH _Two Single bond unit 12 1-877 unit 60 3,4-diClPh CH _Two Single bond unit 13 1-878 unit 60 3,4-diClPh CH _Two Single bond Unit 14 1-879 Unit 60 3,4-diClPh CH _Two Single bond Unit 15 1-880 Unit 60 3,4-diClPh CH _Two Single bond unit 16 1-881 unit 60 3,4-diClPh CH _Two Single bond unit 17 1-882 unit 60 3,4-diClPh CH _Two Single bond unit 18 1-883 unit 60 3,4-diClPh CH _Two Single bond unit 19 1-884 unit 60 3,4-diClPh CH _Two Single bond device 20 1-885 device 60 3,4-diClPh CH _Two Single bond Unit 21 1-886 Unit 60 3,4-diClPh CH _Two Single bond unit 22 1-887 unit 60 3,4-diClPh CH _Two Single bond unit 23 1-888 unit 60 3,4-diClPh CH _Two Single bond unit 24 1-889 unit 60 3,4-diClPh CH _Two Single bond unit 25 1-890 unit 60 3,4-diClPh CH _Two Single bond unit 26 1-891 unit 60 3,4-diClPh CH _Two Single bond unit 27 1-892 unit 60 3,4-diClPh CH _Two Single bond unit 28 1-893 unit 60 3,4-diClPh CH _Two Single bond unit 29 1-894 unit 60 3,4-diClPh CH _Two Single bond device 30 1-895 device 60 3,4-diClPh CH _Two Single bond device 31 1-896 device 60 3,4-diClPh CH _Two Single bond unit 32 1-897 unit 61 3,4-diClPh CH _Two Single bond device 1 1-898 device 61 3,4-diClPh CH _Two Single bond device 21-899 device 61 3,4-diClPh CH _Two Single bond device 3 1-900 device 61 3,4-diClPh CH _Two Single bond unit 4 1-901 unit 61 3,4-diClPh CH _Two Single bond device 5 1-902 device 61 3,4-diClPh CH _Two Single bond device 6 1-903 device 61 3,4-diClPh CH _Two Single bond unit 7 1-904 unit 61 3,4-diClPh CH _Two Single bond device 8 1-905 device 61 3,4-diClPh CH _Two Single bond unit 9 1-906 unit 61 3,4-diClPh CH _Two Single bond device 10 1-907 device 61 3,4-diClPh CH _Two Single bond unit 11 1-908 unit 61 3,4-diClPh CH _Two Single bond unit 12 1-909 unit 61 3,4-diClPh CH _Two Single bond unit 13 1-910 unit 61 3,4-diClPh CH _Two Single bond unit 14 1-911 unit 61 3,4-diClPh CH _Two Single bond unit 15 1-912 unit 61 3,4-diClPh CH _Two Single bond unit 16 1-913 unit 61 3,4-diClPh CH _Two Single bond unit 17 1-914 unit 61 3,4-diClPh CH _Two Single bond unit 18 1-915 unit 61 3,4-diClPh CH _Two Single bond unit 19 1-916 unit 61 3,4-diClPh CH _Two Single bond unit 20 1-917 unit 61 3,4-diClPh CH _Two Single bond unit 21 1-918 unit 61 3,4-diClPh CH _Two Single bond unit 22 1-919 unit 61 3,4-diClPh CH _Two Single bond unit 23 1-920 unit 61 3,4-diClPh CH _Two Single bond unit 24 1-921 unit 61 3,4-diClPh CH _Two Single bond unit 25 1-922 unit 61 3,4-diClPh CH _Two Single bond unit 26 1-923 unit 61 3,4-diClPh CH _Two Single bond unit 27 1-924 unit 61 3,4-diClPh CH _Two Single bond unit 28 1-925 unit 61 3,4-diClPh CH _Two Single bond unit 29 1-926 unit 61 3,4-diClPh CH _Two Single bond device 30 1-927 device 61 3,4-diClPh CH _Two Single bond unit 31 1-928 unit 61 3,4-diClPh CH _Two Single bond unit 32 1-929 unit 33 3,4-diClPh CH _Two CH _Two Unit 1 1-930 Unit 33 3,4-diClPh CH _Two CH _Two Unit 2 1-931 Unit 33 3,4-diClPh CH _Two CH _Two Set 3 1-932 Set 33 3,4-diClPh CH _Two CH _Two Unit 4 1-933 Unit 33 3,4-diClPh CH _Two CH _Two Device 5 1-934 Device 33 3,4-diClPh CH _Two CH _Two Unit 6 1-935 Unit 33 3,4-diClPh CH _Two CH _Two Unit 7 1-936 Unit 33 3,4-diClPh CH _Two CH _Two Unit 8 1-937 Unit 33 3,4-diClPh CH _Two CH _Two Set 9 1-938 Set 33 3,4-diClPh CH _Two CH _Two Device 10 1-939 Device 33 3,4-diClPh CH _Two CH _Two Unit 11 1-940 Unit 33 3,4-diClPh CH _Two CH _Two Unit 12 1-941 Unit 33 3,4-diClPh CH _Two CH _Two Unit 13 1-942 Unit 33 3,4-diClPh CH _Two CH _Two Device 14 1-943 Device 33 3,4-diClPh CH _Two CH _Two Unit 15 1-944 Unit 33 3,4-diClPh CH _Two CH _Two Unit 16 1-945 Unit 33 3,4-diClPh CH _Two CH _Two Unit 17 1-946 Unit 33 3,4-diClPh CH _Two CH _Two Device 18 1-947 Device 33 3,4-diClPh CH _Two CH _Two Unit 19 1-948 Unit 33 3,4-diClPh CH _Two CH _Two Device 20 1-949 device 33 3,4-diClPh CH _Two CH _Two Device 21 1-950 Device 33 3,4-diClPh CH _Two CH _Two Unit 22 1-951 Unit 33 3,4-diClPh CH _Two CH _Two Device 23 1-952 Device 33 3,4-diClPh CH _Two CH _Two Device 24 1-953 Device 33 3,4-diClPh CH _Two CH _Two Unit 25 1-954 Unit 33 3,4-diClPh CH _Two CH _Two Device 26 1-955 Device 33 3,4-diClPh CH _Two CH _Two Set 27 1-956 Set 33 3,4-diClPh CH _Two CH _Two Apparatus 28 1-957 Appearance 33 3,4-diClPh CH _Two CH _Two Unit 29 1-958 Unit 33 3,4-diClPh CH _Two CH _Two Device 30 1-959 Device 33 3,4-diClPh CH _Two CH _Two Unit 31 1-960 Unit 33 3,4-diClPh CH _Two CH _Two Device 32 1-961 Device 33 3,4-diClPh CH _Two CH = CH unit 1 1-962 unit 33 3,4-diClPh CH _Two CH = CH unit 21-963 unit 33 3,4-diClPh CH _Two CH = CH unit 3 1-964 unit 33 3,4-diClPh CH _Two CH = CH unit 4 1-965 unit 33 3,4-diClPh CH _Two CH = CH unit 5 1-966 unit 33 3,4-diClPh CH _Two CH = CH unit 6 1-967 unit 33 3,4-diClPh CH _Two CH = CH unit 7 1-968 unit 33 3,4-diClPh CH _Two CH = CH Place 8 1-969 Place 33 3,4-diClPh CH _Two CH = CH Place 9 1-970 Place 33 3,4-diClPh CH _Two CH = CH unit 10 1-971 unit 33 3,4-diClPh CH _Two CH = CH unit 11 1-972 unit 33 3,4-diClPh CH _Two CH = CH unit 12 1-973 unit 33 3,4-diClPh CH _Two CH = CH unit 13 1-974 unit 33 3,4-diClPh CH _Two CH = CH unit 14 1-975 unit 33 3,4-diClPh CH _Two CH = CH unit 15 1-976 unit 33 3,4-diClPh CH _Two CH = CH unit 16 1-977 unit 33 3,4-diClPh CH _Two CH = CH unit 17 1-978 unit 33 3,4-diClPh CH _Two CH = CH unit 18 1-979 unit 33 3,4-diClPh CH _Two CH = CH unit 19 1-980 unit 33 3,4-diClPh CH _Two CH = CH unit 20 1-981 unit 33 3,4-diClPh CH _Two CH = CH unit 21 1-982 unit 33 3,4-diClPh CH _Two CH = CH unit 22 1-983 unit 33 3,4-diClPh CH _Two CH = CH unit 23 1-984 unit 33 3,4-diClPh CH _Two CH = CH unit 24 1-985 unit 33 3,4-diClPh CH _Two CH = CH unit 25 1-986 unit 33 3,4-diClPh CH _Two CH = CH unit 26 1-987 unit 33 3,4-diClPh CH _Two CH = CH unit 27 1-988 unit 33 3,4-diClPh CH _Two CH = CH unit 28 1-989 unit 33 3,4-diClPh CH _Two CH = CH unit 29 1-990 unit 33 3,4-diClPh CH _Two CH = CH unit 30 1-991 unit 33 3,4-diClPh CH _Two CH = CH unit 31 1-992 unit 33 3,4-diClPh CH _Two CH = CH unit 32 1-993 unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 1 1-994 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two App. 2 1-995 App. 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 3 1-996 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 4 1-997 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 5 1-998 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Device 6 1-999 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 7 1-1000 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 8 1-1001 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 9 1-1002 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Device 10 1-1003 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 11 1-1004 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 12 1-1005 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 13 1-1006 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 14 1-1007 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 15 1-1008 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 16 1-1099 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 17 1-1010 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 18 1-1011 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 19 1-1012 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 20 1-1013 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Device 21 1-1014 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 22 1-1015 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 23 1-1016 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 24 1-1017 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 25 1-1018 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 26 1-1019 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Unit 27 1-1020 Unit 33 3,4-diClPh CH _Two CH _Two CH _Two Device 28 1-1021 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Device 29 1-1022 Device 33 3,4-diClPh CH _Two CH _Two CH _Two Equipment 30 1-1023 Equipment 33 3,4-diClPh CH _Two CH _Two CH _Two Device 31 1-124 Device 33 3,4-diClPh CH _Two CH _Two CH _Two 32 ──────────────────────────────────── Compound number R ¹ R ^Two A B Z １− 1-1025 Place 33 3, 4-diClPh CO single bond 1 1-1026 4-diClPh CO single bond device 2 1-1027 device 33 3, 4-diClPh CO single bond place 3 1-128 place 33 3, 4-diClPh CO single bond unit 4 1-1029 unit 33 3, 4-diClPh CO single bond unit 5 1-1030 unit 33 3, 4-diClPh CO single bond device 6 1-1031 device 33 3, 4-diClPh CO single bond unit 7 1-1032 unit 33 3, 4-diClPh CO single bond device 8 1-1033 device 33 3, 4-diClPh CO single bond unit 9 1-1034 unit 33 3, 4-diClPh CO single bond device 10 1-1035 device 33 3, 4-diClPh CO single bond unit 11 1-1036 unit 33 3, 4-diClPh CO single bond unit 12 1-1037 unit 33 3, 4-diClPh CO single bond unit 13 1-1038 unit 33 3, 4-diClPh CO single bond unit 14 1-1039 unit 33 3, 4-diClPh CO single bond unit 15 1-1040 unit 33 3, 4-diClPh CO single bond unit 16 1-1041 unit 33,3 4-diClPh CO single bond unit 17 1-1042 unit 33 3, 4-diClPh CO single bond unit 18 1-1043 unit 33 3, 4-diClPh CO single bond unit 19 1-1044 unit 33 3, 4-diClPh CO single bond unit 20 1-1045 unit 33 3, 4-diClPh CO single bond unit 21 1-1046 unit 33 3, 4-diClPh CO single bond unit 22 1-1047 unit 33 3, 4-diClPh CO single bond unit 23 1-1048 unit 33 3, 4-diClPh CO single bond unit 24 1-1049 unit 33 3, 4-diClPh CO single bond unit 25 1-1050 unit 33 3, 4-diClPh CO single bond unit 26 1-1051 unit 33 3, 4-diClPh CO single bond unit 27 1-1052 unit 33 3, 4-diClPh CO single bond unit 28 1-1053 unit 33 3, 4-diClPh CO single bond unit 29 1-1054 unit 33 3, 4-diClPh CO single bond unit 30 1-1055 unit 33 3, 4-diClPh CO single bond unit 31 1-1056 unit 33 3, 4-diClPh CO single bond unit 32 1-10757 unit 34 3, 4-diClPh CO single bond 1 1-1058 34 4-diClPh CO single bond unit 2 1-1059 unit 34 3, 4-diClPh CO single bond place 3 1-1060 place 34 3, 4-diClPh CO single bond unit 4 1-1061 unit 34 3, 4-diClPh CO single bond unit 5 1-1062 unit 34 3, 4-diClPh CO single bond unit 6 1-1063 unit 34 3, 4-diClPh CO single bond unit 7 1-1064 unit 34 3, 4-diClPh CO single bond unit 8 1-1065 unit 34 3, 4-diClPh CO single bond unit 9 1-1066 unit 34 3, 4-diClPh CO single bond 10 1067 10 34 4-diClPh CO single bond unit 11 1-1068 unit 34 3, 4-diClPh CO single bond unit 12 1-1069 unit 34 3, 4-diClPh CO single bond unit 13 1-1070 unit 34 3, 4-diClPh CO single bond unit 14 1-1071 unit 34 3, 4-diClPh CO single bond unit 15 1-1072 unit 34 3, 4-diClPh CO single bond unit 16 1-1073 unit 34 3, 4-diClPh CO single bond unit 17 1-1074 unit 34 3, 4-diClPh CO single bond unit 18 1-1075 unit 34 3, 4-diClPh CO single bond unit 19 1-1076 unit 34 3, 4-diClPh CO single bond unit 20 1-1077 unit 34 3, 4-diClPh CO single bond unit 21 1-1078 unit 34 3, 4-diClPh CO single bond 22 1-1079 34 4-diClPh CO single bond unit 23 1-1080 unit 34 3, 4-diClPh CO single bond unit 24 1-1081 unit 34 3, 4-diClPh CO single bond unit 25 1-1082 unit 34 3, 4-diClPh CO single bond unit 26 1-1083 unit 34 3, 4-diClPh CO single bond unit 27 1-1084 unit 34 3, 4-diClPh CO single bond unit 28 1-11085 unit 34 3, 4-diClPh CO single bond unit 29 1-1086 unit 34 3, 4-diClPh CO single bond unit 30 1-1087 unit 34 3, 4-diClPh CO single bond unit 31 1-1088 unit 34 3, 4-diClPh CO single bond unit 32 1-1899 unit 35 3, 4-diClPh CO single bond unit 1-11090 unit 35 3, 4-diClPh CO single bond unit 2 1-11091 unit 35 3, 4-diClPh CO single bond place 3 1-1902 place 35 3, 4-diClPh CO single bond unit 4 1-1093 unit 35 3, 4-diClPh CO single bond 5 1-1094 35 4-diClPh CO single bond unit 6 1-1095 unit 35 3, 4-diClPh CO single bond unit 7 1-1096 unit 35 3, 4-diClPh CO single bond device 8 1-1097 device 35 3, 4-diClPh CO single bond device 9 1-1098 device 35 3, 4-diClPh CO single bond unit 10 1-1099 unit 35 3, 4-diClPh CO single bond device 11 1-1100 device 35 3, 4-diClPh CO single bond unit 12 1-1101 unit 35 3, 4-diClPh CO single bond unit 13 1-1102 unit 35 3, 4-diClPh CO single bond device 14 1-1103 device 35 3, 4-diClPh CO single bond unit 15 1-1104 unit 35 3, 4-diClPh CO single bond unit 16 1-1105 unit 35 3, 4-diClPh CO single bond unit 17 1-1106 unit 35 3, 4-diClPh CO single bond unit 18 1-1107 unit 35 3, 4-diClPh CO single bond unit 19 1-1108 unit 35 3, 4-diClPh CO single bond unit 20 1-1109 unit 35 3, 4-diClPh CO single bond unit 21 1-110 unit 35 3, 4-diClPh CO single bond unit 22 1-1111 unit 35 3, 4-diClPh CO single bond unit 23 1-1112 unit 35 3, 4-diClPh CO single bond unit 24 1-1113 unit 35 3, 4-diClPh CO single bond unit 25 1-1114 unit 35 3, 4-diClPh CO single bond unit 26 1-1115 unit 35 3, 4-diClPh CO single bond unit 27 1-1116 unit 35 3, 4-diClPh CO single bond unit 28 1-1117 unit 35 3, 4-diClPh CO single bond unit 29 1-1118 unit 35 3, 4-diClPh CO single bond unit 30 1-1119 unit 35 3, 4-diClPh CO single bond unit 31 1-1120 unit 35 3, 4-diClPh CO single bond unit 32 1-1121 unit 36 3, 4-diClPh CO single bond device 1 1-1122 device 36 3, 4-diClPh CO single bond unit 2 1-1123 unit 36 3, 4-diClPh CO single bond unit 3 1-1124 unit 36 3, 4-diClPh CO single bond unit 4 1-1125 unit 36 3, 4-diClPh CO single bond device 5 1-1126 device 36 3, 4-diClPh CO single bond unit 6 1-1127 unit 36 3, 4-diClPh CO single bond unit 7 1-1128 unit 36 3, 4-diClPh CO single bond unit 8 1-1129 unit 36 3, 4-diClPh CO single bond device 9 1-1130 device 36 3, 4-diClPh CO single bond device 10 1-1131 device 36 3, 4-diClPh CO single bond unit 11 1-1132 unit 36 3, 4-diClPh CO single bond unit 12 1-1133 unit 36 3, 4-diClPh CO single bond unit 13 1-1134 unit 36 3, 4-diClPh CO single bond unit 14 1-1135 unit 36 3, 4-diClPh CO single bond unit 15 1-1136 unit 36 3, 4-diClPh CO single bond unit 16 1-1137 unit 36 3, 4-diClPh CO single bond unit 17 1-1138 unit 36 3, 4-diClPh CO single bond unit 18 1-1139 unit 36 3, 4-diClPh CO single bond unit 19 1-1140 unit 36 3, 4-diClPh CO single bond unit 20 1-1141 unit 36 3, 4-diClPh CO single bond unit 21 1-1142 unit 36 3, 4-diClPh CO single bond unit 22 1-1143 unit 36 3, 4-diClPh CO single bond unit 23 1-1144 unit 36 3, 4-diClPh CO single bond unit 24 1-1145 unit 36 3, 4-diClPh CO single bond unit 25 1-1146 unit 36 3, 4-diClPh CO single bond unit 26 1-1147 unit 36 3, 4-diClPh CO single bond unit 27 1-1148 unit 36 3, 4-diClPh CO single bond unit 28 1-1149 unit 36 3, 4-diClPh CO single bond unit 29 1-1150 unit 36 3, 4-diClPh CO single bond unit 30 1-1151 unit 36 3, 4-diClPh CO single bond unit 31 1-1152 unit 36 3, 4-diClPh CO single bond unit 32 1-1153 unit 37 3, 4-diClPh CO single bond unit 1 1-1154 unit 37 3, 4-diClPh CO single bond place 2 1-1155 place 37 3, 4-diClPh CO single bond unit 3 1-1156 unit 37 3, 4-diClPh CO single bond unit 4 1-1157 unit 37 3, 4-diClPh CO single bond 5 1-1158 37 4-diClPh CO single bond unit 6 1-1159 unit 37 3, 4-diClPh CO single bond device 7 1-1160 device 37 3, 4-diClPh CO single bond device 8 1-1161 device 37 3, 4-diClPh CO single bond unit 9 1-1162 unit 37 3, 4-diClPh CO single bond unit 10 1-1163 unit 37 3, 4-diClPh CO single bond unit 11 1-1164 unit 37 3, 4-diClPh CO single bond unit 12 1-1165 unit 37 3, 4-diClPh CO single bond unit 13 1-1166 unit 37 3, 4-diClPh CO single bond unit 14 1-1167 unit 37 3, 4-diClPh CO single bond unit 15 1-1168 unit 37 3, 4-diClPh CO single bond unit 16 1-1169 unit 37 3, 4-diClPh CO single bond unit 17 1-1170 unit 37 3, 4-diClPh CO single bond unit 18 1-1171 unit 37 3, 4-diClPh CO single bond unit 19 1-1172 unit 37 3, 4-diClPh CO single bond unit 20 1-1173 unit 37 3, 4-diClPh CO single bond unit 21 1-1174 unit 37 3, 4-diClPh CO single bond unit 22 1-1175 unit 37 3, 4-diClPh CO single bond place 23 1-1176 place 37 3, 4-diClPh CO single bond unit 24 1-1177 unit 37 3, 4-diClPh CO single bond unit 25 1-1178 unit 37 3, 4-diClPh CO single bond unit 26 1-1179 unit 37 3, 4-diClPh CO single bond device 27 1-1180 device 37 3, 4-diClPh CO single bond unit 28 1-1181 unit 37 3, 4-diClPh CO single bond unit 29 1-1182 unit 37 3, 4-diClPh CO single bond unit 30 1-1183 unit 37 3, 4-diClPh CO single bond unit 31 1-1184 unit 37 3, 4-diClPh CO single bond unit 32 1-1185 unit 38 3, 4-diClPh CO single bond unit 1 1-1186 unit 38 3, 4-diClPh CO single bond place 2 1-1187 place 38 3, 4-diClPh CO single bond place 3 1-1188 place 38 3, 4-diClPh CO single bond place 4 1-1189 place 38 3, 4-diClPh CO single bond device 5 1-1190 device 38 3, 4-diClPh CO single bond 6 1-1191 38 4-diClPh CO single bond place 7 1-1192 place 38 3, 4-diClPh CO single bond unit 8 1-1193 unit 38 3, 4-diClPh CO single bond place 9 1-1194 place 38 3, 4-diClPh CO single bond unit 10 1-1195 unit 38 3, 4-diClPh CO single bond unit 11 1-1196 unit 38 3, 4-diClPh CO single bond unit 12 1-1197 unit 38 3, 4-diClPh CO single bond unit 13 1-1198 unit 38 3, 4-diClPh CO single bond unit 14 1-1199 unit 38 3, 4-diClPh CO single bond device 15 1-1200 device 38 3, 4-diClPh CO single bond unit 16 1-1201 unit 38 4-diClPh CO single bond unit 17 1-1202 unit 38 3, 4-diClPh CO single bond unit 18 1-1203 unit 38 3, 4-diClPh CO single bond device 19 1-1204 device 38 3, 4-diClPh CO single bond unit 20 1-1205 unit 38 3, 4-diClPh CO single bond unit 21 1-1206 unit 38 3, 4-diClPh CO single bond unit 22 1-1207 unit 38 3, 4-diClPh CO single bond unit 23 1-1208 unit 38 3, 4-diClPh CO single bond unit 24 1-1209 unit 38 3, 4-diClPh CO single bond unit 25 1-1210 unit 38 3, 4-diClPh CO single bond unit 26 1-1121 unit 38 3, 4-diClPh CO single bond unit 27 1-1212 unit 38 3, 4-diClPh CO single bond unit 28 1-1213 unit 38 3, 4-diClPh CO single bond unit 29 1-1214 unit 38 3, 4-diClPh CO single bond unit 30 1-1215 unit 38 3, 4-diClPh CO single bond place 31 1-1216 place 38 3, 4-diClPh CO single bond place 32 1-1217 place 39 3, 4-diClPh CO single bond unit 1-11218 unit 39 3, 4-diClPh CO single bond place 2 1-1219 place 39 3, 4-diClPh CO single bond unit 3 1-1220 unit 39 3, 4-diClPh CO single bond unit 4 1-1221 unit 39 3, 4-diClPh CO single bond device 5 1-1222 device 39 3, 4-diClPh CO single bond unit 6 1-1223 unit 39 3, 4-diClPh CO single bond place 7 1-1224 place 39 3, 4-diClPh CO single bond device 8 1-125 device 39 3, 4-diClPh CO single bond place 9 1-1226 place 39 3, 4-diClPh CO single bond device 10 1-1227 device 39 3, 4-diClPh CO single bond device 11 1-1228 device 39 3, 4-diClPh CO single bond 12 1-1229 39 4-diClPh CO single bond unit 13 1-1230 unit 39 3, 4-diClPh CO single bond unit 14 1-1231 unit 39 3, 4-diClPh CO single bond unit 15 1-1232 unit 39 3, 4-diClPh CO single bond unit 16 1-1233 unit 39 3, 4-diClPh CO single bond unit 17 1-1234 unit 39 3, 4-diClPh CO single bond unit 18 1-1235 unit 39 3, 4-diClPh CO single bond unit 19 1-1236 unit 39 3, 4-diClPh CO single bond unit 20 1-1237 unit 39 3, 4-diClPh CO single bond unit 21 1-1238 unit 39 3, 4-diClPh CO single bond device 22 1-1239 device 39 3, 4-diClPh CO single bond device 23 1-1240 device 39 3, 4-diClPh CO single bond device 24 1-1241 device 39 3, 4-diClPh CO single bond unit 25 1-1242 unit 39 3, 4-diClPh CO single bond unit 26 1-1243 unit 39 3, 4-diClPh CO single bond unit 27 1-1244 unit 39 3, 4-diClPh CO single bond unit 28 1-1245 unit 39 3, 4-diClPh CO single bond unit 29 1-1246 unit 39 3, 4-diClPh CO single bond unit 30 1-1247 unit 39 3, 4-diClPh CO single bond place 31 1-1248 place 39 3, 4-diClPh CO single bond unit 32 1-1249 unit 40 3, 4-diClPh CO single bond device 1 1-1250 device 40 3, 4-diClPh CO single bond device 2 1-1251 device 40 3, 4-diClPh CO single bond device 3 1-1252 device 40 3, 4-diClPh CO single bond unit 4 1-1253 unit 40 3, 4-diClPh CO single bond device 5 1-1254 device 40 3, 4-diClPh CO single bond unit 6 1-1255 unit 40 3, 4-diClPh CO single bond device 7 1-1256 device 40 3, 4-diClPh CO single bond device 8 1-1257 device 40 3, 4-diClPh CO single bond device 9 1-1258 device 40 3, 4-diClPh CO single bond device 10 1-1259 device 40 3, 4-diClPh CO single bond unit 11 1-1260 unit 40 3, 4-diClPh CO single bond unit 12 1-1261 unit 40 3, 4-diClPh CO single bond unit 13 1-1262 unit 40 3, 4-diClPh CO single bond unit 14 1-1263 unit 40 3, 4-diClPh CO single bond unit 15 1-1264 unit 40 3, 4-diClPh CO single bond unit 16 1-1265 unit 40 3, 4-diClPh CO single bond unit 17 1-1266 unit 40 3, 4-diClPh CO single bond unit 18 1-1267 unit 40 3, 4-diClPh CO single bond device 19 1-1268 device 40 3, 4-diClPh CO single bond device 20 1-1269 device 40 3, 4-diClPh CO single bond unit 21 1-1270 unit 40 3, 4-diClPh CO single bond unit 22 1-1271 unit 40 3, 4-diClPh CO single bond unit 23 1-1272 unit 40 3, 4-diClPh CO single bond unit 24 1-1273 unit 40 3, 4-diClPh CO single bond unit 25 1-1274 unit 40 3, 4-diClPh CO single bond unit 26 1-1275 unit 40 3, 4-diClPh CO single bond unit 27 1-1276 unit 40 3, 4-diClPh CO single bond unit 28 1-1277 unit 40 3, 4-diClPh CO single bond unit 29 1-1278 unit 40 3, 4-diClPh CO single bond unit 30 1-1279 unit 40 3, 4-diClPh CO single bond unit 31 1-1280 unit 40 3, 4-diClPh CO single bond unit 32 1-1281 unit 41 3, 4-diClPh CO single bond unit 1-11-282 unit 41 3, 4-diClPh CO single bond place 2 1-1283 place 41 3, 4-diClPh CO single bond place 3 1-1284 place 41 3, 4-diClPh CO single bond unit 4 1-1285 unit 41 3, 4-diClPh CO single bond device 5 1-1286 device 41 3, 4-diClPh CO single bond device 6 1-1287 device 41 3, 4-diClPh CO single bond place 7 1-1288 place 41 3, 4-diClPh CO single bond device 8 1-1289 device 41 3, 4-diClPh CO single bond place 9 1-1290 place 41 3, 4-diClPh CO single bond device 10 1-1291 device 41 3, 4-diClPh CO single bond unit 11 1-1292 unit 41 3, 4-diClPh CO single bond unit 12 1-1293 unit 41 3, 4-diClPh CO single bond unit 13 1-1294 unit 41 3, 4-diClPh CO single bond unit 14 1-1295 unit 41 3, 4-diClPh CO single bond unit 15 1-1296 unit 41 3, 4-diClPh CO single bond unit 16 1-1297 unit 41 3, 4-diClPh CO single bond unit 17 1-1298 unit 41 3, 4-diClPh CO single bond unit 18 1-1299 unit 41 3, 4-diClPh CO single bond device 19 1-1300 device 41 3, 4-diClPh CO single bond unit 20 1-1301 unit 41 3, 4-diClPh CO single bond device 21 1-1302 device 41 3, 4-diClPh CO single bond device 22 1-1303 device 41 3, 4-diClPh CO single bond device 23 1-1304 device 41 3, 4-diClPh CO single bond unit 24 1-1305 unit 41 3, 4-diClPh CO single bond device 25 1-1306 device 41 3, 4-diClPh CO single bond unit 26 1-1307 unit 41 3, 4-diClPh CO single bond unit 27 1-1308 unit 41 3, 4-diClPh CO single bond unit 28 1-1309 unit 41 3, 4-diClPh CO single bond device 29 1-1310 device 41 3, 4-diClPh CO single bond unit 30 1-11311 unit 41 3, 4-diClPh CO single bond unit 31 1-11312 unit 41 3, 4-diClPh CO single bond unit 32 1-11313 unit 42 3, 4-diClPh CO single bond unit 1-11-1314 unit 42 3, 4-diClPh CO single bond unit 2 1-1315 unit 42 3, 4-diClPh CO single bond place 3 1-1316 place 42 3, 4-diClPh CO single bond unit 4 1-1317 unit 42 3, 4-diClPh CO single bond device 5 1-1318 device 42 3, 4-diClPh CO single bond device 6 1-1319 device 42 3, 4-diClPh CO single bond unit 7 1-1320 unit 42 3, 4-diClPh CO single bond unit 8 1-11321 unit 42 3, 4-diClPh CO single bond device 9 1-1322 device 42 3, 4-diClPh CO single bond device 10 1-1323 device 42 3, 4-diClPh CO single bond unit 11 1-1324 unit 42 3, 4-diClPh CO single bond unit 12 1-1325 unit 42 3, 4-diClPh CO single bond unit 13 1-1326 unit 42 3, 4-diClPh CO single bond unit 14 1-1327 unit 42 3, 4-diClPh CO single bond unit 15 1-1328 unit 42 3, 4-diClPh CO single bond unit 16 1-1329 unit 42 3, 4-diClPh CO single bond unit 17 1-1330 unit 42 3, 4-diClPh CO single bond unit 18 1-1331 unit 42 3, 4-diClPh CO single bond unit 19 1-1332 unit 42 3, 4-diClPh CO single bond unit 20 1-1333 unit 42 3, 4-diClPh CO single bond unit 21 1-1334 unit 42 3, 4-diClPh CO single bond unit 22 1-1335 unit 42 3, 4-diClPh CO single bond unit 23 1-1336 unit 42 3, 4-diClPh CO single bond unit 24 1-1337 unit 42 3, 4-diClPh CO single bond unit 25 1-1338 unit 42 3, 4-diClPh CO single bond device 26 1-1339 device 42 3, 4-diClPh CO single bond unit 27 1-1340 unit 42 3, 4-diClPh CO single bond unit 28 1-11341 unit 42 3, 4-diClPh CO single bond unit 29 1-1342 unit 42 3, 4-diClPh CO single bond unit 30 1-1343 unit 42 3, 4-diClPh CO single bond unit 31 1-1344 unit 42 3, 4-diClPh CO single bond unit 32 1-1345 unit 43 3, 4-diClPh CO single bond device 1 1-1346 device 43 3, 4-diClPh CO single bond place 2 1-1347 place 43 3, 4-diClPh CO single bond place 3 1-1348 place 43 3, 4-diClPh CO single bond unit 4 1-1349 unit 43 3, 4-diClPh CO single bond device 5 1-1350 device 43 3, 4-diClPh CO single bond device 6 1-1351 device 43 3, 4-diClPh CO single bond place 7 1-1352 place 43 3, 4-diClPh CO single bond device 8 1-1353 device 43 3, 4-diClPh CO single bond device 9 1-1354 device 43 3, 4-diClPh CO single bond unit 10 1-1355 unit 43 3, 4-diClPh CO single bond unit 11 1-1356 unit 43 3, 4-diClPh CO single bond unit 12 1-1357 unit 43 3, 4-diClPh CO single bond unit 13 1-1358 unit 43 3, 4-diClPh CO single bond unit 14 1-1359 unit 43 3, 4-diClPh CO single bond unit 15 1-1360 unit 43 3, 4-diClPh CO single bond unit 16 1-1361 unit 43 3, 4-diClPh CO single bond unit 17 1-1362 unit 43 3, 4-diClPh CO single bond unit 18 1-1363 unit 43 3, 4-diClPh CO single bond unit 19 1-1364 unit 43 3, 4-diClPh CO single bond unit 20 1-1365 unit 43 3, 4-diClPh CO single bond unit 21 1-1366 unit 43 3, 4-diClPh CO single bond unit 22 1-1367 unit 43 3, 4-diClPh CO single bond place 23 1-1368 place 43 3, 4-diClPh CO single bond unit 24 1-1369 unit 43 3, 4-diClPh CO single bond unit 25 1-1370 unit 43 3, 4-diClPh CO single bond unit 26 1-1371 unit 43 3, 4-diClPh CO single bond unit 27 1-1372 unit 43 3, 4-diClPh CO single bond unit 28 1-1373 unit 43 3, 4-diClPh CO single bond unit 29 1-1374 unit 43 3, 4-diClPh CO single bond unit 30 1-1375 unit 43 3, 4-diClPh CO single bond unit 31 1-1376 unit 43 3, 4-diClPh CO single bond place 32 1-1377 place 44 3, 4-diClPh CO single bond unit 1-11-1378 unit 44 3, 4-diClPh CO single bond device 2 1-1379 device 44 3, 4-diClPh CO single bond place 3 1-1380 place 44 3, 4-diClPh CO single bond unit 4 1-1381 unit 44 3, 4-diClPh CO single bond unit 5 1-1382 unit 44 3, 4-diClPh CO single bond unit 6 1-1383 unit 44 3, 4-diClPh CO single bond unit 7 1-1384 unit 44 3, 4-diClPh CO single bond device 8 1-1385 device 44 3, 4-diClPh CO single bond unit 9 1-1386 unit 44 3, 4-diClPh CO single bond unit 10 1-1387 unit 443 4-diClPh CO single bond unit 11 1-1388 unit 44 3, 4-diClPh CO single bond unit 12 1-1389 unit 44 3, 4-diClPh CO single bond unit 13 1-1390 unit 44 3, 4-diClPh CO single bond unit 14 1-1391 unit 44 3, 4-diClPh CO single bond unit 15 1-1392 unit 44 3, 4-diClPh CO single bond unit 16 1-1393 unit 44 3, 4-diClPh CO single bond unit 17 1-1394 unit 44 3, 4-diClPh CO single bond unit 18 1-1395 unit 44 3, 4-diClPh CO single bond unit 19 1-1396 unit 44 3, 4-diClPh CO single bond unit 20 1-1397 unit 44 3, 4-diClPh CO single bond unit 21 1-1398 unit 44 3, 4-diClPh CO single bond unit 22 1-1399 unit 44 3, 4-diClPh CO single bond unit 23 1-1400 unit 44 3, 4-diClPh CO single bond unit 24 1-1401 unit 44 3, 4-diClPh CO single bond device 25 1-1402 device 44 3, 4-diClPh CO single bond unit 26 1-1403 unit 44 3, 4-diClPh CO single bond unit 27 1-1404 unit 44 3, 4-diClPh CO single bond unit 28 1-1405 unit 44 3, 4-diClPh CO single bond unit 29 1-1406 unit 44 3, 4-diClPh CO single bond unit 30 1-1407 unit 44 3, 4-diClPh CO single bond unit 31 1-1408 unit 44 3, 4-diClPh CO single bond unit 32 1-1409 unit 45 3, 4-diClPh CO single bond unit 1-11-110 unit 45 3, 4-diClPh CO single bond unit 2 1-1411 unit 45 3, 4-diClPh CO single bond place 3 1-1412 place 45 3, 4-diClPh CO single bond unit 4 1-1413 unit 45 3, 4-diClPh CO single bond unit 5 1-1414 unit 45 3, 4-diClPh CO single bond unit 6 1-1415 unit 45 3, 4-diClPh CO single bond place 7 1-1416 place 45 3, 4-diClPh CO single bond place 8 1-1417 place 45 3, 4-diClPh CO single bond unit 9 1-1418 unit 45 3, 4-diClPh CO single bond unit 10 1-1419 unit 45 3, 4-diClPh CO single bond unit 11 1-1420 unit 45 3, 4-diClPh CO single bond unit 12 1-1421 unit 45 3, 4-diClPh CO single bond unit 13 1-1422 unit 45 3, 4-diClPh CO single bond unit 14 1-1423 unit 45 3, 4-diClPh CO single bond unit 15 1-1424 unit 45 3, 4-diClPh CO single bond unit 16 1-1425 unit 45 3, 4-diClPh CO single bond Unit 17 1-1426 Unit 45 3, 4-diClPh CO single bond unit 18 1-1427 unit 45 3, 4-diClPh CO single bond unit 19 1-1428 unit 45 3, 4-diClPh CO single bond unit 20 1-1429 unit 45 3, 4-diClPh CO single bond unit 21 1-1430 unit 45 3, 4-diClPh CO single bond unit 22 1-1431 unit 45 3, 4-diClPh CO single bond unit 23 1-1432 unit 45 3, 4-diClPh CO single bond unit 24 1-1433 unit 45 3, 4-diClPh CO single bond unit 25 1-1434 unit 45 3, 4-diClPh CO single bond unit 26 1-1435 unit 45 3, 4-diClPh CO single bond unit 27 1-1436 unit 45 3, 4-diClPh CO single bond 28 1-1437 45 3 4-diClPh CO single bond unit 29 1-1438 unit 45 3, 4-diClPh CO single bond unit 30 1-1439 unit 45 3, 4-diClPh CO single bond unit 31 1-1440 unit 45 3, 4-diClPh CO single bond unit 32 1-1441 unit 46 3, 4-diClPh CO single bond unit 1-11-142 unit 46 3, 4-diClPh CO single bond unit 2 1-1443 unit 46 3, 4-diClPh CO single bond device 3 1-1444 device 46 3, 4-diClPh CO single bond unit 4 1-1445 unit 46 3, 4-diClPh CO single bond device 5 1-1446 device 46 3, 4-diClPh CO single bond unit 6 1-1447 unit 46 3, 4-diClPh CO single bond unit 7 1-1448 unit 46 3, 4-diClPh CO single bond device 8 1-1449 device 46 3, 4-diClPh CO single bond unit 9 1-1450 unit 46 3, 4-diClPh CO single bond unit 10 1-1451 unit 463 4-diClPh CO single bond unit 11 1-1452 unit 46 3, 4-diClPh CO single bond unit 12 1-1453 unit 46 3, 4-diClPh CO single bond unit 13 1-1454 unit 46 3, 4-diClPh CO single bond unit 14 1-1455 unit 46 3, 4-diClPh CO single bond unit 15 1-1456 unit 46 3, 4-diClPh CO single bond unit 16 1-1457 unit 46 3, 4-diClPh CO single bond unit 17 1-1458 unit 46 3, 4-diClPh CO single bond unit 18 1-1459 unit 46 3, 4-diClPh CO single bond unit 19 1-1460 unit 46 3, 4-diClPh CO single bond unit 20 1-1461 unit 46 3, 4-diClPh CO single bond unit 21 1-1462 unit 46 3, 4-diClPh CO single bond unit 22 1-1463 unit 46 3, 4-diClPh CO single bond unit 23 1-1146 unit 46 3, 4-diClPh CO single bond unit 24 1-1465 unit 46 3, 4-diClPh CO single bond unit 25 1-1466 unit 46 3, 4-diClPh CO single bond unit 26 1-1467 unit 46 3, 4-diClPh CO single bond unit 27 1-1468 unit 46 3, 4-diClPh CO single bond unit 28 1-1469 unit 46 3, 4-diClPh CO single bond unit 29 1-1470 unit 46 3, 4-diClPh CO single bond unit 30 1-1471 unit 46 3, 4-diClPh CO single bond unit 31 1-1472 unit 46 3, 4-diClPh CO single bond unit 32 1-1473 unit 47 3, 4-diClPh CO single bond unit 1-11-1474 unit 47 3, 4-diClPh CO single bond unit 2 1-1475 unit 47 3, 4-diClPh CO single bond unit 3 1-1476 unit 47 3, 4-diClPh CO single bond unit 4 1-1477 unit 47 3, 4-diClPh CO single bond 5 1-1478 Place 47 3, 4-diClPh CO single bond unit 6 1-1479 unit 47 3, 4-diClPh CO single bond device 7 1-1480 device 47 3, 4-diClPh CO single bond device 8 1-1481 device 47 3, 4-diClPh CO single bond device 9 1-1482 device 47 3, 4-diClPh CO single bond device 10 1-1483 device 47 3, 4-diClPh CO single bond unit 11 1-1484 unit 47 3, 4-diClPh CO single bond unit 12 1-1485 unit 47 3, 4-diClPh CO single bond unit 13 1-1486 unit 47 3, 4-diClPh CO single bond unit 14 1-1487 unit 47 3, 4-diClPh CO single bond unit 15 1-1488 unit 47 3, 4-diClPh CO single bond unit 16 1-1489 unit 47 3, 4-diClPh CO single bond unit 17 1-1490 unit 47 3, 4-diClPh CO single bond unit 18 1-11491 unit 47 3, 4-diClPh CO single bond unit 19 1-1492 unit 47 3, 4-diClPh CO single bond unit 20 1-1493 unit 47 3, 4-diClPh CO single bond unit 21 1-1494 unit 47 3, 4-diClPh CO single bond unit 22 1-1495 unit 47 3, 4-diClPh CO single bond unit 23 1-1496 unit 47 3, 4-diClPh CO single bond unit 24 1-1497 unit 47 3, 4-diClPh CO single bond unit 25 1-1498 unit 47 3, 4-diClPh CO single bond unit 26 1-1499 unit 47 3, 4-diClPh CO single bond device 27 1-1500 device 47 3, 4-diClPh CO single bond unit 28 1-15011 unit 47 3, 4-diClPh CO single bond unit 29 1-1502 unit 47,3 4-diClPh CO single bond unit 30 1-1503 unit 47 4-diClPh CO single bond unit 31 1-1504 unit 47,3 4-diClPh CO single bond unit 32 1-1505 unit 48 3, 4-diClPh CO single bond unit 1-11-1506 unit 48 3, 4-diClPh CO single bond unit 2 1-1507 unit 483 4-diClPh CO single bond unit 3 1-1508 unit 48 3, 4-diClPh CO single bond unit 4 1-1509 unit 48 3, 4-diClPh CO single bond unit 5 1-1510 unit 48 3, 4-diClPh CO single bond 6 1-1511 11 48 4-diClPh CO single bond device 7 1-1512 device 48 3, 4-diClPh CO single bond device 8 1-1513 device 48 3, 4-diClPh CO single bond unit 9 1-1514 unit 48 3, 4-diClPh CO single bond unit 10 1-1515 unit 48 3, 4-diClPh CO single bond unit 11 1-1516 unit 48 3, 4-diClPh CO single bond unit 12 1-1517 unit 48 3, 4-diClPh CO single bond unit 13 1-1518 unit 48 3, 4-diClPh CO single bond unit 14 1-1519 unit 48 3, 4-diClPh CO single bond unit 15 1-1520 unit 48 3, 4-diClPh CO single bond unit 16 1-1521 unit 48 3, 4-diClPh CO single bond unit 17 1-1522 unit 48 3, 4-diClPh CO single bond device 18 1-1523 device 48 3, 4-diClPh CO single bond unit 19 1-1524 unit 48 3, 4-diClPh CO single bond unit 20 1-1525 unit 48 3, 4-diClPh CO single bond unit 21 1-1526 unit 48 3, 4-diClPh CO single bond unit 22 1-1527 unit 48 3, 4-diClPh CO single bond unit 23 1-1528 unit 48 3, 4-diClPh CO single bond unit 24 1-1529 unit 48 3, 4-diClPh CO single bond unit 25 1-1530 unit 48 3, 4-diClPh CO single bond unit 26 1-1531 unit 48 3, 4-diClPh CO single bond unit 27 1-1532 unit 48 3, 4-diClPh CO single bond unit 28 1-1533 unit 48 3, 4-diClPh CO single bond unit 29 1-1534 unit 48 3, 4-diClPh CO single bond unit 30 1-1535 unit 48 3, 4-diClPh CO single bond unit 31 1-1536 unit 48 3, 4-diClPh CO single bond position 32 化合物 Compound number R ¹ R ^Two ABZ ──────────────────────────────────── 1-1537 Place 49 3,4-diClPh CO Single bond unit 1 1-1538 unit 49 3,4-diClPh CO Single bond unit 2 1-15339 unit 49 3,4-diClPh CO Single bond unit 3 1-1540 unit 49 3,4-diClPh CO Single bond unit 4 1 -1541 setting 49 3,4-diClPh CO single bond 5 5 -1542 setting 49 3,4-diClPh CO single bond 6 1-1543 setting 49 3,4-diClPh CO single bond 7 1-1544 setting 49 3 , 4-diClPh CO single bond unit 8 1-1545 unit 49 3,4-diClPh CO single bond unit 9 1-1546 unit 49 3,4-diClPhCO single bond unit 10 1-1547 unit 49 3,4-diClPh CO Single bond unit 11 1-1548 unit 49 3,4-diClPh CO single bond unit 12 1-1549 unit 49 3,4-diClPh CO single bond unit 13 1-1550 unit 4 3,4-diClPh CO single bond unit 14 1-1551 unit 49 3,4-diClPh CO single bond unit 15 1-1552 unit 49 3,4-diClPh CO single bond unit 16 1-1553 unit 49 3,4-diClPh CO single bond unit 17 1-1554 unit 49 3,4-diClPh CO single bond unit 18 1-1555 unit 49 3,4-diClPh CO single bond unit 19 1-1556 unit 49 3,4-diClPh CO single bond unit 20 1-1557 Setting 49 3,4-diClPh CO single bond 21 21-1558 Setting 49 3,4-diClPh CO single bond 22 1-155 9 Setting 49 3,4-diClPh CO single bond 23 1-1560 Setting 49 3,4-diClPh CO single bond unit 24 1-1561 unit 49 3,4-diClPh CO single bond unit 25 1-1562 unit 49 3,4-diClPh CO single bond unit 26 1-1563 unit 49 3,4-diClPh CO single bond unit 27 1-1564 unit 49 3,4-diClPh CO single bond unit 28 1-1565 49 3,4-diClPh CO single bond unit 29 1-1566 unit 49 3,4-diClPh CO single bond unit 30 1-1567 unit 49 3,4-diClPh CO single bond unit 31 1-1568 unit 49 3,4- diClPh CO single bond unit 32 1-1569 unit 50 3,4-diClPh CO single bond unit 1 1-1570 unit 50 3,4-diClPh CO single bond unit 2 1-1571 unit 50 3,4-diClPh CO single bond unit 3 1-1572 unit 50 3,4-diClPh CO single bond unit 4 1-1573 unit 50 3,4-diClPh CO single bond unit 5 1-1574 unit 50 3,4-diClPh CO single bond unit 6 1-1575 unit 50 3,4-diClPh CO single bond unit 7 1-1576 unit 50 3,4-diClPh CO single bond unit 8 1-1577 unit 50 3,4-diClPh CO single bond unit 9 1-1578 unit 50 3,4- diClPh CO single bond device 10 1-1579 device 50 3,4-diClPh CO single bond device 11 1-1580 device 50 3,4-d iClPh CO single bond device 12 1-1581 device 50 3,4-diClPh CO single bond device 13 1-1582 device 50 3,4-diClPh CO single bond device 14 1-1583 device 50 3,4-diClPh CO single bond device 15 1-1584 unit 50 3,4-diClPh CO single bond unit 16 1-1585 unit 50 3,4-diClPh CO single bond unit 17 1-1586 unit 50 3,4-diClPh CO single bond unit 18 1-1587 unit 50 3,4-diClPh CO single bond unit 19 1-1588 unit 50 3,4-diClPh CO single bond unit 20 1-1589 unit 50 3,4-diClPh CO single bond unit 21 1-1590 unit 50 3,4- diClPh CO single bond device 22 1-1591 device 50 3,4-diClPh CO single bond device 23 1-1592 device 50 3,4-diClPh CO single bond device 24 1-1593 device 50 3,4-diClPh CO single bond device 25 1-1594 unit 50 3,4-diClPh CO single bond unit 26 1-1595 unit 50 3,4-diClPh CO single bond unit 27 1-1596 unit 50 3,4-diClPh CO single bond unit 28 1-1597 unit 50 3,4-diClPh CO single bond unit 29 1-1598 unit 50 3,4-diClPh CO single bond device 30 1-1599 device 50 3,4-diClPh CO single bond device 31 1-1600 device 50 3,4-diClPh CO single bond device 32 1-1601 device 51 3,4-diClPh CO single bond device 1 1-1602 device 51 51,4-diClPh CO single bond device 2 1-1603 device 51 3,4-diClPh CO single bond device 3 1-1604 device 51 3,4-diClPh CO single bond device 4 1-1605 device 51 3,4-diClPh CO single bond device 5 1-1606 device 51 3,4-diClPh CO single bond device 6 1-1607 device 51 3,4-diClPh CO single bond device 7 1-1608 device 51 3,4-diClPh CO single bond device 8 1-1609 device 51 3,4-diClPh CO single bond device 9 1-1610 device 51 3,4-diClPh O single bond device 10 1-1611 device 51 3,4-diClPh CO single bond device 11 1-1612 device 51 3,4-diClPh CO single bond device 12 1-1613 device 51 3,4-diClPh CO single bond device 13 1-1416 14 unit 51 3,4-diClPh CO single bond unit 14 1-11615 unit 51 3,4-diClPh CO single bond unit 15 1-1616 unit 51 3,4-diClPh CO single bond unit 16 1-1617 unit 51 3,4-diClPh CO single bond device 17 1-1618 device 51 3,4-diClPh CO single bond device 18 1-11619 device 51 3,4-diClPh CO single bond device 19 1-1620 device 51 3,4-diClPh CO single bond device 20 1-1621 device 51 3,4-diClPh CO single bond device 21 1-1622 device 51 3,4-diClPh CO single bond device 22 1-1623 device 51 3,4-diClPh CO single bond device 23 1-1624 24 51,4-diClPh CO single bond 24 1-1625 51 51,4-diCl Ph CO single bond device 25 1-1626 device 51 3,4-diClPh CO single bond device 26 1-1627 device 51 3,4-diClPh CO single bond device 27 1-1628 device 51 3,4-diClPh CO single bond device 28 1-1629 place 51 3,4-diClPh CO single bond place 29 1-1630 place 51 3,4-diClPh CO single bond place 30 1-1631 place 51 3,4-diClPh CO single bond place 31 1-1632 place 51 3,4-diClPh CO single bond device 32 1-1633 device 52 3,4-diClPh CO single bond device 1 1-1634 device 52 3,4-diClPh CO single bond device 2 1-1635 device 52 3,4- diClPh CO single bond unit 3 1-1636 unit 52 3,4-diClPh CO single bond unit 4 1-1637 unit 52 3,4-diClPh CO single bond unit 5 1-1638 unit 52 3,4-diClPh CO single bond unit 6 1-1639 unit 52 3,4-diClPh CO single bond unit 7 1-1640 unit 52 3,4-diClPh CO Single bond device 8 1-1641 device 52 3,4-diClPh CO single bond device 9 1-1642 device 52 3,4-diClPh CO single bond device 10 1-1643 device 52 3,4-diClPh CO single bond device 11 1 −1644 unit 52 3,4-diClPh CO single bond unit 12 1-1645 unit 52 3,4-diClPh CO single bond unit 13 1-1646 unit 52 3,4-diClPh CO single bond unit 14 1-1647 unit 52 3 , 4-diClPh CO single bond unit 15 1-1648 unit 52 3,4-diClPh CO single bond unit 16 1-16449 unit 52 3,4-diClPh CO single bond unit 17 1-1650 unit 52 3,4-diClPh CO Single bond device 18 1-11651 device 52 3,4-diClPh CO Single bond device 19 1-1652 device 52 3,4-diClPh CO single bond device 20 1-1653 device 52 3,4-diClPh CO single bond device 21 1 −1654 Setting 52 3,4-diClPh CO Single bond Setting 22 1-1655 Setting 52 3,4-diClPh C Single bond unit 23 1-1656 unit 52 3,4-diClPh CO Single bond unit 24 1-1657 unit 52 3,4-diClPh CO single unit unit 25 1-1658 unit 52 3,4-diClPh CO single bond unit 26 1 -1659 unit 52 3,4-diClPh CO single bond unit 27 1-1660 unit 52 3,4-diClPh CO single bond unit 28 1-1661 unit 52 3,4-diClPh CO single bond unit 29 1-1662 unit 52 3 , 4-diClPh CO single bond unit 30 1-1663 unit 52 3,4-diClPh CO single bond unit 31 1-1664 unit 52 3,4-diClPh CO single bond unit 32 1-1665 unit 53 3,4-diClPh CO Single bond device 1 1-1666 device 53 3,4-diClPh CO Single bond device 2 1-1667 device 53 3,4-diClPh CO Single bond device 3 1-1668 device 53 3,4-diClPh CO Single bond device 4 1 -1669 setting 53 3,4-diClPh CO single bond 5 1-1670 setting 53 3,4-diClPh CO single Bonding unit 6 1-1671 unit 53 3,4-diClPh CO single bond unit 7 1-1672 unit 53 3,4-diClPh CO single bond unit 8 1-1673 unit 53 3,4-diClPh CO single bond unit 9 1- 1674 unit 53 3,4-diClPh CO single bond unit 10 1-1675 unit 53 3,4-diClPh CO single bond unit 11 1-1676 unit 53 3,4-diClPh CO single bond unit 12 1-1677 unit 53 3, 4-diClPh CO single bond unit 13 1-1678 unit 53 3,4-diClPh CO single bond unit 14 1-1679 unit 53 3,4-diClPh CO single bond unit 15 1-1680 unit 53 3,4-diClPh CO single unit Bonding unit 16 1-1681 unit 53 3,4-diClPh CO single bond unit 17 1-1682 unit 53 3,4-diClPh CO single bond unit 18 1-1683 unit 53 3,4-diClPh CO single bond unit 19 1- 1684 Place 53 3,4-diClPh CO single bond 20 1-1685 Place 53 3,4-diClPh CO single bond Unit 21 1-1686 Unit 53 3,4-diClPh CO single bond Unit 22 1-1687 Unit 53 3,4-diClPh CO Single bond Unit 23 1-1688 Unit 53 3,4-diClPh CO Single bond Unit 24 1- 1689 placement 53 3,4-diClPh CO single bond 25 1-1690 placement 53 3,4-diClPh CO single bond 26 1-1691 placement 53 3,4-diClPh CO single bond 27 1-1692 placement 53 3, 4-diClPh CO single bond unit 28 1-1693 unit 53 3,4-diClPh CO single bond unit 29 1-1694 unit 53 3,4-diClPh CO single bond unit 30 1-1695 unit 53 3,4-diClPh CO single unit Bonding unit 31 1-1696 unit 53 3,4-diClPh CO single bond unit 32 1-1697 unit 54 3,4-diClPh CO single bond unit 1 1-1698 unit 54 3,4-diClPh CO single bond unit 2 1- 1699 Place 54 3,4-diClPh CO single bond 3 1-1700 Place 54 3,4-diClPh CO single bond Unit 4 1-1701 Unit 54 3,4-diClPh CO single bond Unit 5 1-1702 Unit 54 3,4-diClPh CO single bond Unit 6 1-1703 Unit 54 3,4-diClPh CO single bond Unit 7 1-1704 Unit 54 3,4-diClPh CO single bond unit 8 1-1705 Unit 54 3,4-diClPh CO single bond unit 9 1-1706 Unit 54 3,4-diClPh CO single bond unit 10 1-1707 Unit 54 3,4 -diClPh CO single bond unit 11 1-1708 unit 54 3,4-diClPh CO single bond unit 12 1-1709 unit 54 3,4-diClPh CO single bond unit 13 1-1710 unit 54 3,4-diClPh CO single bond Unit 14 1-1711 Unit 54 3,4-diClPh CO single bond Unit 15 1-1712 Unit 54 3,4-diClPh CO single bond Unit 16 1-1713 Unit 54 3,4-diClPh CO single bond Unit 17 1-1714 Device 54 3,4-diClPh CO single bond device 18 1-1715 Device 54 3,4-diClPh CO single bond device 9 1-1716 unit 54 3,4-diClPh CO single bond unit 20 1-1717 unit 54 3,4-diClPh CO single bond unit 21 1-1718 unit 54 3,4-diClPh CO single bond unit 22 1-1719 unit 54 3,4-diClPh CO single bond unit 23 1-1720 unit 54 3,4-diClPh CO single bond unit 24 1-1721 unit 54 3,4-diClPh CO single bond unit 25 1-1722 unit 54 3,4- diClPh CO single bond unit 26 1-1723 unit 54 3,4-diClPh CO single bond unit 27 1-1724 unit 54 3,4-diClPh CO single bond unit 28 1-1725 unit 54 3,4-diClPh CO single bond unit 29 1-1726 place 54 3,4-diClPh CO single bond place 30 1-1727 place 54 3,4-diClPh CO single bond place 31 1-1728 place 54 3,4-diClPh CO single bond place 32 1-1729 place 55 3,4-diClPh CO single bond 1 1-1730 Place 55 3,4-diClPh CO single bond 2 1-1731 unit 55 3,4-diClPh CO single bond unit 3 1-1732 unit 55 3,4-diClPh CO single bond unit 4 1-1733 unit 55 3,4-diClPh CO single bond unit 5 1-1734 unit 55 3,4-diClPh CO single bond device 6 1-1735 device 55 3,4-diClPh CO single bond device 7 1-1736 device 55 3,4-diClPh CO single bond device 8 1-1737 device 55 3,4- diClPh CO single bond device 9 1-1738 position 55 3,4-diClPh CO single bond device 10 1-1739 position 55 3,4-diClPh CO single bond device 11 1-1740 position 55 3,4-diClPh CO single bond device 12 1-1741 unit 55 3,4-diClPh CO single bond unit 13 1-1742 unit 55 3,4-diClPh CO single bond unit 14 1-1743 unit 55 3,4-diClPh CO single bond unit 15 1-1744 unit 55 3,4-diClPh CO single bond unit 16 1-1745 unit 55 3,4-diClPh CO single bond unit 17 −1746 setting 55 3,4-diClPh CO single bond 18 1-1747 setting 55 3,4-diClPh CO single bond 19 1-1748 setting 55 3,4-diClPh CO single bond 20 1-1749 setting 55 3 , 4-diClPh CO single bond unit 21 1-1750 unit 55 3,4-diClPh CO single bond unit 22 1-1751 unit 55 3,4-diClPh CO single bond unit 23 1-1752 unit 55 3,4-diClPh CO Single bond unit 24 1-1753 unit 55 3,4-diClPh CO Single bond unit 25 1-1754 unit 55 3,4-diClPh CO single bond unit 26 1-1755 unit 55 3,4-diClPh CO single bond unit 27 1 −1756 setting 55 3,4-diClPh CO single bond 28 1-1757 setting 55 3,4-diClPh CO single bond 29 1-1758 setting 55 3,4-diClPh CO single bond 30 1-1759 setting 55 3 , 4-diClPh CO single bond unit 31 1-1760 unit 55 3,4-diClPh CO single bond unit 3 1-1761 unit 56 3,4-diClPh CO single bond unit 1 1-1776 unit 56 3,4-diClPh CO single bond unit 2 1-1763 unit 56 3,4-diClPh CO single bond unit 3 1-1764 unit 56 3,4-diClPh CO single bond unit 4 1-1765 unit 56 3,4-diClPh CO single bond unit 5 1-1766 unit 56 3,4-diClPh CO single bond unit 6 1-1767 unit 56 3,4-diClPh CO single bond device 7 1-1768 device 56 3,4-diClPh CO single bond device 8 1-169 device 56 3,4-diClPh CO single bond device 9 1-1770 device 56 3,4-diClPh CO single bond device 10 1-11771 setting 56 3,4-diClPh CO single bond setting 11 1-11772 setting 56 3,4-diClPh CO single bond setting 12 1-1177 setting 56 3,4-diClPh CO single bond setting 13 1-1774 setting 56 3,4-diClPh CO single bond device 14 1-1775 device 56 3,4-diClPh CO single bond device 15 1-1 76 Unit 56 3,4-diClPh CO single bond unit 16 1-1177 Unit 56 3,4-diClPh CO single bond unit 17 1-1778 unit 56 3,4-diClPh CO single bond unit 18 1-1779 unit 56 3, 4-diClPh CO single bond unit 19 1-1780 unit 56 3,4-diClPh CO single bond unit 20 1-11781 unit 56 3,4-diClPh CO single bond unit 21 1-1782 unit 56 3,4-diClPh CO single unit Bonding unit 22 1-1783 unit 56 3,4-diClPh CO single bond unit 23 1-1784 unit 56 3,4-diClPh CO single bond unit 24 1-1785 unit 56 3,4-diClPh CO single bond unit 25 1- 1786 setting 56 3,4-diClPh CO single bond setting 26 1-1787 setting 56 3,4-diClPh CO single bond setting 27 1-1788 setting 56 3,4-diClPh CO single bond setting 28 1-1789 setting 56 3, 4-diClPh CO single bond device 29 1-1790 device 56 3,4-diClPh CO single bond device 30 1 1791 unit 56 3,4-diClPh CO single bond unit 31 1-1792 unit 56 3,4-diClPh CO single bond unit 32 1-1793 unit 57 3,4-diClPh CO single bond unit 1 1-1794 unit 57 3, 4-diClPh CO single bond unit 2 1-1795 unit 57 3,4-diClPh CO single bond unit 3 1-1796 unit 57 3,4-diClPh CO single bond unit 4 1-1797 unit 57 3,4-diClPh CO single unit Bonding unit 5 1-1798 unit 57 3,4-diClPh CO single bond unit 6 1-1799 unit 57 3,4-diClPh CO single bond unit 7 1-1800 unit 57 3,4-diClPh CO single bond unit 8 1- 1801 unit 57 3,4-diClPh CO single bond unit 9 1-1802 unit 57 3,4-diClPh CO single bond unit 10 1-1803 unit 57 3,4-diClPh CO single bond unit 11 1-1804 unit 57 3, 4-diClPh CO single bond device 12 1-1805 device 57 3,4-diClPh CO single bond device 13 1-1806 Device 57 3,4-diClPh CO single bond device 14 1-1807 device 57 3,4-diClPh CO single bond device 15 1-1808 device 57 3,4-diClPh CO single bond device 16 1-1809 device 57 3,4 -diClPh CO single bond unit 17 1-1810 unit 57 3,4-diClPh CO single bond unit 18 1-1811 unit 57 3,4-diClPh CO single bond unit 19 1-1812 unit 57 3,4-diClPh CO single bond Unit 20 1-1813 Unit 57 3,4-diClPh CO single bond Unit 21 1-1814 Unit 57 3,4-diClPh CO single bond Unit 22 1-1815 Unit 57 3,4-diClPh CO single bond Unit 23 1-1816 Device 57 3,4-diClPh CO single bond device 24 1-1817 Device 57 3,4-diClPh CO single bond Device 25 1-1818 Device 57 3,4-diClPh CO single bond Device 26 1-1819 Device 57 3,4 -diClPh CO single bond unit 27 1-1820 unit 57 3,4-diClPh CO single bond unit 28 1-18 1 unit 57 3,4-diClPh CO single bond unit 29 1-1822 unit 57 3,4-diClPh CO single bond unit 30 1-1823 unit 57 3,4-diClPh CO single bond unit 31 1-1824 unit 57 3, 4-diClPh CO single bond device 32 1-1825 device 58 3,4-diClPh CO single bond device 1 1-1826 device 58 3,4-diClPh CO single bond device 2 1-1827 device 58 3,4-diClPh CO single device Bonding device 3 1-1828 device 58 3,4-diClPh CO single bond device 4 1-1829 device 58 3,4-diClPh CO single bond device 5 1-1830 device 58 3,4-diClPh CO single bond device 6 1- 1831 position 58 3,4-diClPh CO single bond device 7 1-1832 position 58 3,4-diClPh CO single bond device 8 1-1833 position 58 3,4-diClPh CO single bond device 9 1-1834 position 58 3, 4-diClPh CO single bond device 10 1-1835 device 58 3,4-diClPh CO single bond device 11 1-1836 device 5 3,4-diClPh CO single bond 12 1-1837 position 58 3,4-diClPh CO single bond 13 1-1838 position 58 3,4-diClPh CO single bond 14 1-1839 position 58 3,4-diClPh CO single bond unit 15 1-1840 unit 58 3,4-diClPh CO single bond unit 16 1-1841 unit 58 3,4-diClPh CO single bond unit 17 1-1842 unit 58 3,4-diClPh CO single bond unit 18 1-1843 setting 58 3,4-diClPh CO single bond setting 19 1-1844 setting 58 3,4-diClPh CO single bonding setting 20 1-1845 setting 58 3,4-diClPh CO single bonding setting 21 1-1846 setting 58 3,4-diClPh CO single bond unit 22 1-1847 unit 58 3,4-diClPh CO single bond unit 23 1-1848 unit 58 3,4-diClPh CO single bond unit 24 1-1845 unit 58 3,4-diClPh CO single bond device 25 1-1850 device 58 3,4-diClPh CO single bond device 26 1-11851 58 3,4-diClPh CO single bond unit 27 1-1852 unit 58 3,4-diClPh CO single bond unit 28 1-1853 unit 58 3,4-diClPh CO single bond unit 29 1-1854 unit 58 3,4- diClPh CO single bond unit 30 1-1855 unit 58 3,4-diClPh CO single bond unit 31 1-1856 unit 58 3,4-diClPh CO single bond unit 32 1-1857 unit 59 3,4-diClPh CO single bond unit 1 1-1858 unit 59 3,4-diClPh CO single bond unit 2 1-1859 unit 59 3,4-diClPh CO single bond unit 3 1-1860 unit 59 3,4-diClPh CO single bond unit 4 1-1861 unit 59 3,4-diClPh CO single bond unit 5 1-1862 unit 59 3,4-diClPh CO single bond unit 6 1-1863 unit 59 3,4-diClPh CO single bond unit 7 1-1864 unit 59 3,4- diClPh CO single bond unit 8 1-1865 unit 59 3,4-diClPh CO single bond unit 9 1-1866 unit 59 3,4-d iClPh CO single bond device 10 1-1867 device 59 3,4-diClPh CO single bond device 11 1-1868 device 59 3,4-diClPh CO single bond device 12 1-1869 device 59 3,4-diClPh CO single bond device 13 1-1870 setting 59 3,4-diClPh CO single bond setting 14 1-1871 setting 59 3,4-diClPh CO single bond setting 15 1-1872 setting 59 3,4-diClPh CO single bond setting 16 1-1873 setting 59 3,4-diClPh CO single bond unit 17 1-1874 unit 59 3,4-diClPh CO single bond unit 18 1-1875 unit 59 3,4-diClPh CO single bond unit 19 1-1876 unit 59 3,4- diClPh CO single bond device 20 1-1877 position 59 3,4-diClPh CO single bond device 21 1-1877 position 59 3,4-diClPh CO single bond device 22 1-1879 position 59 3,4-diClPh CO single bond device 23 1-1880 position 59 3,4-diClPh CO single bond 24 24-1881 position 59 3,4-diClPh CO single bond device 25 1-1882 device 59 3,4-diClPh CO single bond device 26 1-1883 device 59 3,4-diClPh CO single bond device 27 1-1884 device 59 3,4-diClPh CO single bond unit 28 1-1885 unit 59 3,4-diClPh CO single bond unit 29 1-1886 unit 59 3,4-diClPh CO single bond unit 30 1-1887 unit 59 3,4-diClPh CO single bond unit 31 1-1888 position 59 3,4-diClPh CO single bond 32 1-1889 position 60 3,4-diClPh CO single bond 1 1-1890 position 60 3,4-diClPh CO single bond 2 1-11891 position 60 3,4-diClPh CO single bond device 3 1-1892 device 60 3,4-diClPh CO single bond device 4 1-1893 device 60 3,4-diClPh CO single bond device 5 1-1894 device 60 3,4-diClPh CO single bond device 6 1-1895 device 60 3,4-diClPh CO single bond device 7 1-1896 device 60 3,4-diClPh h CO single bond device 8 1-1897 device 60 3,4-diClPh CO single bond device 9 1-1898 device 60 3,4-diClPh CO single bond device 10 1-1899 device 60 3,4-diClPh CO single bond device 11 1-1900 unit 60 3,4-diClPh CO single bond unit 12 1-1901 unit 60 3,4-diClPh CO single bond unit 13 1-1902 unit 60 3,4-diClPh CO single bond unit 14 1-1903 unit 60 3,4-diClPh CO single bond device 15 1-1904 device 60 3,4-diClPh CO single bond device 16 1-1905 device 60 3,4-diClPh CO single bond device 17 1-1906 device 60 3,4- diClPh CO single bond unit 18 1-1907 unit 60 3,4-diClPh CO single bond unit 19 1-1908 unit 60 3,4-diClPh CO single bond unit 20 1-1909 unit 60 3,4-diClPh CO single bond unit 21 1-1910 unit 60 3,4-diClPh CO single bond unit 22 1-1911 unit 60 3,4-diCl Ph CO single bond device 23 1-1912 device 60 3,4-diClPh CO single bond device 24 1-1913 device 60 3,4-diClPh CO single bond device 25 1-1914 device 60 3,4-diClPh CO single bond device 26 1-1915 unit 60 3,4-diClPh CO single bond unit 27 1-1916 unit 60 3,4-diClPh CO single bond unit 28 1-1917 unit 60 3,4-diClPh CO single bond unit 29 1-1918 unit 60 3,4-diClPh CO single bond device 30 1-1919 device 60 3,4-diClPh CO single bond device 31 1-1920 device 60 3,4-diClPh CO single bond device 32 1-1921 device 61 3,4- diClPh CO single bond device 1-1922 device 61 3,4-diClPh CO single bond device 2-1923 device 61 3,4-diClPh CO single bond device 3-1924 device 61 3,4-diClPh CO single bond device 4 1-1925 unit 61 3,4-diClPh CO single bond unit 5 1-1926 unit 61 3,4-diClPh O single bond unit 6 1-1927 unit 61 3,4-diClPh CO single bond unit 7 1-1928 unit 61 3,4-diClPh CO single bond unit 8 1-1929 unit 61 3,4-diClPh CO single bond unit 9 1-1930 setting 61 3,4-diClPh CO single bond setting 10 1-1931 setting 61 3,4-diClPh CO single bonding setting 11 1-1932 setting 61 3,4-diClPh CO single bonding setting 12 1-1933 setting 61 3,4-diClPh CO single bond unit 13 1-1934 unit 61 3,4-diClPh CO single bond unit 14 1-1935 unit 61 3,4-diClPh CO single bond unit 15 1-1936 unit 61 3,4-diClPh CO single bond unit 16 1-1937 unit 61 3,4-diClPh CO single bond unit 17 1-1938 unit 61 3,4-diClPh CO single bond unit 18 1-1939 unit 61 3,4-diClPh CO single bond unit 19 1-1940 unit 61 3,4-diClPh CO single bond unit 20 1-1940 unit 61 3,4-diClPh C Single bond unit 21 1-1942 unit 61 3,4-diClPh CO Single bond unit 22 1-1943 unit 61 3,4-diClPh CO single bond unit 23 1-1944 unit 61 3,4-diClPh CO single bond unit 24 1 −1945 setting 61 3,4-diClPh CO single bond 25 1 1946 setting 61 3,4-diClPh CO single bond 26 1-1947 setting 61 3,4-diClPh CO single bond 27 1-1948 setting 61 3 , 4-diClPh CO single bond unit 28 1-1949 unit 61 3,4-diClPh CO single bond unit 29 1-1950 unit 61 3,4-diClPh CO single bond unit 30 1-1951 unit 61 3,4-diClPh CO Single bond unit 31 1-1952 unit 61 3,4-diClPh CO Single bond unit 32 1-1953 unit 33 3,4-diClPh CO CH _Two Unit 1 1-1954 Unit 33 3,4-diClPh CO CH _Two App. 2 1-1955 App. 33 3,4-diClPh CO CH _Two Unit 3 1-1956 Unit 33 3,4-diClPh CO CH _Two Unit 4 1-1957 Unit 33 3,4-diClPh CO CH _Two Unit 5 1-1958 Unit 33 3,4-diClPh CO CH _Two Unit 6 1-1959 Unit 33 3,4-diClPh CO CH _Two Unit 7 1-1960 Unit 33 3,4-diClPh CO CH _Two Unit 8 1-1961 Unit 33 3,4-diClPh CO CH _Two Unit 9 1-1962 Unit 33 3,4-diClPh CO CH _Two Device 10 1-1963 Device 33 3,4-diClPh CO CH _Two Unit 11 1-1964 Unit 33 3,4-diClPh CO CH _Two Unit 12 1-1965 Unit 33 3,4-diClPh CO CH _Two Unit 13 1-1966 Unit 33 3,4-diClPh CO CH _Two Unit 14 1-1967 Unit 33 3,4-diClPh CO CH _Two Unit 15 1-1968 Unit 33 3,4-diClPh CO CH _Two Device 16 1-1969 Device 33 3,4-diClPh CO CH _Two Unit 17 1-1970 Unit 33 3,4-diClPh CO CH _Two Equipment 18 1-1971 Equipment 33 3,4-diClPh CO CH _Two Unit 19 1-1972 Unit 33 3,4-diClPh CO CH _Two Device 20 1-173 device 33 3,4-diClPh CO CH _Two Unit 21 1-1974 Unit 33 3,4-diClPh CO CH _Two Unit 22 1-1975 Unit 33 3,4-diClPh CO CH _Two Device 23 1-1976 Device 33 3,4-diClPh CO CH _Two Unit 24 1-1977 Unit 33 3,4-diClPh CO CH _Two Unit 25 1-1978 Unit 33 3,4-diClPh CO CH _Two Unit 26 1-1979 Unit 33 3,4-diClPh CO CH _Two Unit 27 1-1980 Unit 33 3,4-diClPh CO CH _Two Unit 28 1-181 Unit 33 3,4-diClPh CO CH _Two Unit 29 1-182 Unit 33 3,4-diClPh CO CH _Two Unit 30 1-183 Unit 33 3,4-diClPh CO CH _Two Unit 31 1-1984 Unit 33 3,4-diClPh CO CH _Two Unit 32 1-1985 Unit 33 3,4-diClPh CO CH = CH Unit 1 1-186 Unit 33 3,4-diClPh CO CH = CH Unit 21-1987 Unit 33 3,4-diClPh CO CH = CH Unit 3 1-188 unit 33 3,4-diClPh CO CH = CH unit 4 1-189 unit 33 3,4-diClPh CO CH = CH unit 5 1-1990 unit 33 3,4-diClPh CO CH = CH unit 6 1- 1991 setting 33 3,4-diClPh CO CH = CH setting 7 1-1992 setting 33 3,4-diClPh CO CH = CH setting 8 1-1993 setting 33 3,4-diClPh CO CH = CH setting 9 1-1994 setting 33 3,4-diClPh CO CH = CH device 10 1-1995 device 33 3,4-diClPh CO CH = CH device 11 1-1996 device 33 3,4-diClPh CO CH = CH device 12 1-1997 device 33 3 , 4-diClPh CO CH = CH device 13 1-1998 device 33 3,4-diClPh CO CH = CH device 14 1-1999 device 33 3,4-diClPh CO CH = CH device 15 1-2000 device 33 3,4 -diClPh CO CH = CH unit 16 1-2001 device 33 3,4-diClPh CO CH = CH device 17 1-2002 device 33 3,4-diClPh CO CH = CH device 18 1-2003 device 33 3,4-diClPh CO CH = CH device 19 1- 2004 device 33 3,4-diClPh CO CH = CH device 20 1-2005 device 33 3,4-diClPh CO CH = CH device 21 1-2006 device 33 3,4-diClPh CO CH = CH device 22 1-2007 device 33 3,4-diClPh CO CH = CH device 23 1-2008 device 33 3,4-diClPh CO CH = CH device 24 1-2009 device 33 3,4-diClPh CO CH = CH device 25 1-2010 device 33 3 , 4-diClPh CO CH = CH device 26 1-2011 device 33 3,4-diClPh CO CH = CH device 27 1-2012 device 33 3,4-diClPh CO CH = CH device 28 1-2013 device 33 3,4 -diClPh CO CH = CH device 29 1-2014 device 33 3,4-diClPh CO CH = CH device 30 1-2015 device 33 3,4-diClPh CO CH = CH device 31 1-2016 device 33 3,4-diClPh CO CH = CH 32 1-2017 location 33 3,4-diClPh CO CH _Two CH _Two Set 1 1-2018 Set 33 3,4-diClPh CO CH _Two CH _Two Place 2 1-2019 Place 33 3,4-diClPh CO CH _Two CH _Two Place 3 1-2020 Place 33 3,4-diClPh CO CH _Two CH _Two Unit 4 1-2202 Unit 33 3,4-diClPh CO CH _Two CH _Two Set 5 1-2022 Set 33 3,4-diClPh CO CH _Two CH _Two Set 6 1-2023 Set 33 3,4-diClPh CO CH _Two CH _Two Place 7 1-2024 Place 33 3,4-diClPh CO CH _Two CH _Two Set 8 1-2025 Set 33 3,4-diClPh CO CH _Two CH _Two Set 9 1-2026 Set 33 3,4-diClPh CO CH _Two CH _Two Set 10 1-2027 Set 33 3,4-diClPh CO CH _Two CH _Two Place 11 1-2028 Place 33 3,4-diClPh CO CH _Two CH _Two Unit 12 1-2029 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 13 1-2030 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 14 1-2031 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 15 1-2032 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 16 1-2033 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 17 1-2034 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 18 1-2035 Unit 33 3,4-diClPh CO CH _Two CH _Two Storage 19 1-2036 Storage 33 3,4-diClPh CO CH _Two CH _Two Set 20 1-2037 Set 33 3,4-diClPh CO CH _Two CH _Two Unit 21 1-2038 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 22 1-2039 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 23 1-2040 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 24 1-2041 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 25 1-2042 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 26 1-2043 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 27 1-2044 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 28 1-2045 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 29 1-2046 Unit 33 3,4-diClPh CO CH _Two CH _Two 30 30-2047 33 33,4-diClPh CO CH _Two CH _Two Unit 31 1-2048 Unit 33 3,4-diClPh CO CH _Two CH _Two 32 ──────────────────────────────────── Compound number R ¹ R ^Two ABZ ──────────────────────────────────── 1-2049 Place 33 3,4-diClPh SO _Two Single bond unit 1 1-2050 unit 33 3,4-diClPh SO _Two Single bond unit 2 1-2051 unit 33 3,4-diClPh SO _Two Single bond device 3 1-2052 device 33 3,4-diClPh SO _Two Single bond unit 4 1-2053 unit 33 3,4-diClPh SO _Two Single bond device 5 1-2054 device 33 3,4-diClPh SO _Two Single bond 6 1-2055 33 33,4-diClPh SO _Two Single bond device 7 1-2056 device 33 3,4-diClPh SO _Two Single bond device 8 1-2057 device 33 3,4-diClPh SO _Two Single bond device 9 1-2058 device 33 3,4-diClPh SO _Two Single bond device 10 1-2059 device 33 3,4-diClPh SO _Two Single bond unit 11 1-2060 unit 33 3,4-diClPh SO _Two Single bond unit 12 1-2061 unit 33 3,4-diClPh SO _Two Single bond unit 13 1-2062 unit 33 3,4-diClPh SO _Two Single bond unit 14 1-2063 unit 33 3,4-diClPh SO _Two Single bond unit 15 1-2064 unit 33 3,4-diClPh SO _Two Single bond unit 16 1-2065 unit 33 3,4-diClPh SO _Two Single bond unit 17 1-2066 unit 33 3,4-diClPh SO _Two Single bond unit 18 1-2067 unit 33 3,4-diClPh SO _Two Single bond unit 19 1-2068 unit 33 3,4-diClPh SO _Two Single bond unit 20 1-2069 unit 33 3,4-diClPh SO _Two Single bond unit 21 1-2070 unit 33 3,4-diClPh SO _Two Single bond unit 22 1-2071 unit 33 3,4-diClPh SO _Two Single bond unit 23 1-2072 unit 33 3,4-diClPh SO _Two Single bond unit 24 1-2073 unit 33 3,4-diClPh SO _Two Single bond unit 25 1-2074 unit 33 3,4-diClPh SO _Two Single bond unit 26 1-2075 unit 33 3,4-diClPh SO _Two Single bond unit 27 1-2076 unit 33 3,4-diClPh SO _Two Single bond unit 28 1-2077 unit 33 3,4-diClPh SO _Two Single bond unit 29 1-2078 unit 33 3,4-diClPh SO _Two Single bond device 30 1-2079 device 33 3,4-diClPh SO _Two Single bond unit 31 1-2080 unit 33 3,4-diClPh SO _Two Single bond unit 32 1-2082 unit 34 3,4-diClPh SO _Two Single bond unit 2 1-2083 unit 34 3,4-diClPh SO _Two Single bond unit 3 1-2084 unit 34 3,4-diClPh SO _Two Single bond unit 4 1-2085 unit 34 3,4-diClPh SO _Two Single bond 5 1-2086 4 34 3,4-diClPh SO _Two Single bond device 6 1-2087 device 34 3,4-diClPh SO _Two Single bond unit 7 1-2088 unit 34 3,4-diClPh SO _Two Single bond device 8 1-2089 device 34 3,4-diClPh SO _Two Single bond device 9 1-2090 device 34 3,4-diClPh SO _Two Single bond device 10 1-2091 device 34 3,4-diClPh SO _Two Single bond unit 11 1-2092 unit 34 3,4-diClPh SO _Two Single bond unit 12 1-2093 unit 34 3,4-diClPh SO _Two Single bond unit 13 1-2094 unit 34 3,4-diClPh SO _Two Single bond unit 14 1-2095 unit 34 3,4-diClPh SO _Two Single bond unit 15 1-2096 unit 34 3,4-diClPh SO _Two Single bond unit 16 1-2097 unit 34 3,4-diClPh SO _Two Single bond unit 17 1-2098 unit 34 3,4-diClPh SO _Two Single bond unit 18 1-2099 unit 34 3,4-diClPh SO _Two Single bond unit 19 1-2100 unit 34 3,4-diClPh SO _Two Single bond device 20 1-2101 device 34 3,4-diClPh SO _Two Single bond unit 21 1-2102 unit 34 3,4-diClPh SO _Two Single bond unit 22 1-2103 unit 34 3,4-diClPh SO _Two Single bond unit 23 1-2104 unit 34 3,4-diClPh SO _Two Single bond unit 24 1-2105 unit 34 3,4-diClPh SO _Two Single bond unit 25 1-2106 unit 34 3,4-diClPh SO _Two Single bond unit 26 1-2107 unit 34 3,4-diClPh SO _Two Single bond unit 27 1-2108 unit 34 3,4-diClPh SO _Two Single bond unit 28 1-2109 unit 34 3,4-diClPh SO _Two Single bond unit 29 1-2110 unit 34 3,4-diClPh SO _Two Single bond device 30 1-2111 device 34 3,4-diClPh SO _Two Single bond unit 31 1-2112 unit 34 3,4-diClPh SO _Two Single bond unit 32 1-2113 unit 35 3,4-diClPh SO _Two Single bond device 1 1-2114 device 35 3,4-diClPh SO _Two Single bond device 2 1-2115 device 35 3,4-diClPh SO _Two Single bond device 3 1-2116 device 35 3,4-diClPh SO _Two Single bond device 4 1-2117 device 35 3,4-diClPh SO _Two Single bond device 5 1-2118 device 35 3,4-diClPh SO _Two Single bond device 6 1-2119 device 35 3,4-diClPh SO _Two Single bond device 7 1-2120 device 35 3,4-diClPh SO _Two Single bond device 8 1-2121 device 35 3,4-diClPh SO _Two Single bond device 9 1-2122 device 35 3,4-diClPh SO _Two Single bond device 10 1-2123 device 35 3,4-diClPh SO _Two Single bond unit 11 1-2124 unit 35 3,4-diClPh SO _Two Single bond unit 12 1-2125 unit 35 3,4-diClPh SO _Two Single bond unit 13 1-2126 unit 35 3,4-diClPh SO _Two Single bond unit 14 1-2127 unit 35 3,4-diClPh SO _Two Single bond device 15 1-2128 device 35 3,4-diClPh SO _Two Single bond Unit 16 1-2129 Unit 35 3,4-diClPh SO _Two Single bond unit 17 1-2130 unit 35 3,4-diClPh SO _Two Single bond unit 18 1-2131 unit 35 3,4-diClPh SO _Two Single bond unit 19 1-2132 unit 35 3,4-diClPh SO _Two Single bond unit 20 1-2133 unit 35 3,4-diClPh SO _Two Single bond unit 21 1-2134 unit 35 3,4-diClPh SO _Two Single bond unit 22 1-2135 unit 35 3,4-diClPh SO _Two Single bond unit 23 1-2136 unit 35 3,4-diClPh SO _Two Single bond unit 24 1-2137 unit 35 3,4-diClPh SO _Two Single bond unit 25 1-2138 unit 35 3,4-diClPh SO _Two Single bond unit 26 1-2140 unit 35 3,4-diClPh SO _Two Single bond unit 28 1-2141 unit 35 3,4-diClPh SO _Two Single bond unit 29 1-2142 unit 35 3,4-diClPh SO _Two Single bond unit 30 1-2143 unit 35 3,4-diClPh SO _Two Single bond unit 31 1-2144 unit 35 3,4-diClPh SO _Two Single bond unit 32 1-2145 unit 36 3,4-diClPh SO _Two Single bond device 1 1-2146 device 36 3,4-diClPh SO _Two Single bond device 2 1-2147 device 36 3,4-diClPh SO _Two Single bond device 3 1-2148 device 36 3,4-diClPh SO _Two Single bond device 4 1-2149 device 36 3,4-diClPh SO _Two Single bond device 5 1-2150 device 36 3,4-diClPh SO _Two Single bond device 6 1-2151 device 36 3,4-diClPh SO _Two Single bond device 7 1-2152 device 36 3,4-diClPh SO _Two Single bond device 8 1-2153 device 36 3,4-diClPh SO _Two Single bond device 9 1-2154 device 36 3,4-diClPh SO _Two Single bond device 10 1-2155 device 36 3,4-diClPh SO _Two Single bond unit 11 1-2156 unit 36 3,4-diClPh SO _Two Single bond unit 12 1-2157 unit 36 3,4-diClPh SO _Two Single bond unit 13 1-2158 unit 36 3,4-diClPh SO _Two Single bond unit 14 1-2159 unit 36 3,4-diClPh SO _Two Single bond unit 15 1-2160 unit 36 3,4-diClPh SO _Two Single bond unit 16 1-2161 unit 36 3,4-diClPh SO _Two Single bond unit 17 1-2162 unit 36 3,4-diClPh SO _Two Single bond unit 18 1-2163 unit 36 3,4-diClPh SO _Two Single bond unit 19 1-2164 unit 36 3,4-diClPh SO _Two Single bond unit 20 1-2165 unit 36 3,4-diClPh SO _Two Single bond unit 21 1-2166 unit 36 3,4-diClPh SO _Two Single bond unit 22 1-2167 unit 36 3,4-diClPh SO _Two Single bond unit 23 1-2169 unit 36 3,4-diClPh SO _Two Single bond device 25 1-2170 device 36 3,4-diClPh SO _Two Single bond unit 26 1-2171 unit 36 3,4-diClPh SO _Two Single bond unit 27 1-2172 unit 36 3,4-diClPh SO _Two Single bond unit 28 1-2173 unit 36 3,4-diClPh SO _Two Single bond unit 29 1-2174 unit 36 3,4-diClPh SO _Two Single bond device 30 1-2175 device 36 3,4-diClPh SO _Two Single bond unit 31 1-2176 unit 36 3,4-diClPh SO _Two Single bond device 32 1-2177 device 37 3,4-diClPh SO _Two Single bond device 1 1-2178 device 37 3,4-diClPh SO _Two Single bond device 2 1-2179 device 37 3,4-diClPh SO _Two Single bond device 3 1-2180 device 37 3,4-diClPh SO _Two Single bond device 4 1-2181 device 37 3,4-diClPh SO _Two Single bond device 5 1-2182 device 37 3,4-diClPh SO _Two Single bond device 6 1-2183 device 37 3,4-diClPh SO _Two Single bond device 7 1-2184 device 37 3,4-diClPh SO _Two Single bond device 8 1-2185 device 37 3,4-diClPh SO _Two Single bond device 9 1-2186 device 37 3,4-diClPh SO _Two Single bond device 10 1-2187 device 37 3,4-diClPh SO _Two Single bond unit 11 1-2188 unit 37 3,4-diClPh SO _Two Single bond unit 12 1-2189 unit 37 3,4-diClPh SO _Two Single bond unit 13 1-2190 unit 37 3,4-diClPh SO _Two Single bond unit 14 1-2191 unit 37 3,4-diClPh SO _Two Single bond unit 15 1-2192 unit 37 3,4-diClPh SO _Two Single bond unit 16 1-2193 unit 37 3,4-diClPh SO _Two Single bond unit 17 1-2194 unit 37 3,4-diClPh SO _Two Single bond unit 18 1-2195 unit 37 3,4-diClPh SO _Two Single bond unit 19 1-2196 unit 37 3,4-diClPh SO _Two Single bond unit 20 1-2198 unit 37 3,4-diClPh SO _Two Single bond unit 22 1-2199 unit 37 3,4-diClPh SO _Two Single bond device 23 1-2200 device 37 3,4-diClPh SO _Two Single bond unit 24 1-2201 unit 37 3,4-diClPh SO _Two Single bond unit 25 1-2202 unit 37 3,4-diClPh SO _Two Single bond unit 26 1-2203 unit 37 3,4-diClPh SO _Two Single bond unit 27 1-2204 unit 37 3,4-diClPh SO _Two Single bond unit 28 1-2205 unit 37 3,4-diClPh SO _Two Single bond unit 29 1-2206 unit 37 3,4-diClPh SO _Two Single bond device 30 1-2207 device 37 3,4-diClPh SO _Two Single bond unit 31 1-2208 unit 37 3,4-diClPh SO _Two Single bond unit 32 1-2209 unit 38 3,4-diClPh SO _Two Single bond device 1 1-2210 device 38 3,4-diClPh SO _Two Single bond Unit 2 1-2221 Unit 38 3,4-diClPh SO _Two Single bond device 3 1-2212 device 38 3,4-diClPh SO _Two Single bond device 4 1-2213 device 38 3,4-diClPh SO _Two Single bond device 5 1-2214 device 38 3,4-diClPh SO _Two Single bond device 6 1-2215 device 38 3,4-diClPh SO _Two Single bond device 7 1-2216 device 38 3,4-diClPh SO _Two Single bond device 8 1-2217 device 38 3,4-diClPh SO _Two Single bond device 9 1-2218 device 38 3,4-diClPh SO _Two Single bond device 10 1-2219 device 38 3,4-diClPh SO _Two Single bond unit 11 1-2220 unit 38 3,4-diClPh SO _Two Single bond unit 12 1-2221 unit 38 3,4-diClPh SO _Two Single bond unit 13 1-2222 unit 38 3,4-diClPh SO _Two Single bond unit 14 1-2223 unit 38 3,4-diClPh SO _Two Single bond unit 15 1-2224 unit 38 3,4-diClPh SO _Two Single bond unit 16 1-2225 unit 38 3,4-diClPh SO _Two Single bond unit 17 1-2227 unit 38 3,4-diClPh SO _Two Single bond unit 19 1-2228 unit 38 3,4-diClPh SO _Two Single bond device 20 1-2229 device 38 3,4-diClPh SO _Two Single bond unit 21 1-2230 unit 38 3,4-diClPh SO _Two Single bond unit 22 1-2231 unit 38 3,4-diClPh SO _Two Single bond unit 23 1-2232 unit 38 3,4-diClPh SO _Two Single bond unit 24 1-2233 unit 38 3,4-diClPh SO _Two Single bond unit 25 1-2234 unit 38 3,4-diClPh SO _Two Single bond unit 26 1-2235 unit 38 3,4-diClPh SO _Two Single bond unit 27 1-2236 unit 38 3,4-diClPh SO _Two Single bond unit 28 1-2237 unit 38 3,4-diClPh SO _Two Single bond unit 29 1-2238 unit 38 3,4-diClPh SO _Two Single bond device 30 1-2239 device 38 3,4-diClPh SO _Two Single bond unit 31 1-2240 unit 38 3,4-diClPh SO _Two Single bond unit 32 1-2241 unit 39 3,4-diClPh SO _Two Single bond device 1 1-2242 device 39 3,4-diClPh SO _Two Single bond device 2 1-2243 device 39 3,4-diClPh SO _Two Single bond device 3 1-2244 device 39 3,4-diClPh SO _Two Single bond unit 4 1-2245 unit 39 3,4-diClPh SO _Two Single bond device 5 1-2246 device 39 3,4-diClPh SO _Two Single bond device 6 1-2247 device 39 3,4-diClPh SO _Two Single bond device 7 1-2248 device 39 3,4-diClPh SO _Two Single bond device 8 1-2249 device 39 3,4-diClPh SO _Two Single bond device 9 1-2250 device 39 3,4-diClPh SO _Two Single bond device 10 1-2251 device 39 3,4-diClPh SO _Two Single bond unit 11 1-2252 unit 39 3,4-diClPh SO _Two Single bond unit 12 1-2253 unit 39 3,4-diClPh SO _Two Single bond unit 13 1-2254 unit 39 3,4-diClPh SO _Two Single bond unit 14 1-2256 unit 39 3,4-diClPh SO _Two Single bond unit 16 1-2257 unit 39 3,4-diClPh SO _Two Single bond unit 17 1-2258 unit 39 3,4-diClPh SO _Two Single bond unit 18 1-2259 unit 39 3,4-diClPh SO _Two Single bond unit 19 1-2260 unit 39 3,4-diClPh SO _Two Single bond device 20 1-2261 device 39 3,4-diClPh SO _Two Single bond device 21 1-2262 device 39 3,4-diClPh SO _Two Single bond unit 22 1-2263 unit 39 3,4-diClPh SO _Two Single bond unit 23 1-2264 unit 39 3,4-diClPh SO _Two Single bond unit 24 1-2265 unit 39 3,4-diClPh SO _Two Single bond unit 25 1-2266 unit 39 3,4-diClPh SO _Two Single bond unit 26 1-2267 unit 39 3,4-diClPh SO _Two Single bond unit 27 1-2268 unit 39 3,4-diClPh SO _Two Single bond unit 28 1-2269 unit 39 3,4-diClPh SO _Two Single bond unit 29 1-2270 unit 39 3,4-diClPh SO _Two Single bond device 30 1-2271 device 39 3,4-diClPh SO _Two Single bond unit 31 1-2272 unit 39 3,4-diClPh SO _Two Single bond device 32 1-2273 device 40 3,4-diClPh SO _Two Single bond device 1 1-2274 device 40 3,4-diClPh SO _Two Single bond device 2 1-2275 device 40 3,4-diClPh SO _Two Single bond device 3 1-2276 device 40 3,4-diClPh SO _Two Single bond device 4 1-2277 device 40 3,4-diClPh SO _Two Single bond device 5 1-2278 device 40 3,4-diClPh SO _Two Single bond device 6 1-2279 device 40 3,4-diClPh SO _Two Single bond device 7 1-2280 device 40 3,4-diClPh SO _Two Single bond device 8 1-2281 device 40 3,4-diClPh SO _Two Single bond device 9 1-2282 device 40 3,4-diClPh SO _Two Single bond device 10 1-2283 device 40 3,4-diClPh SO _Two Single bond unit 11 1-2285 unit 40 3,4-diClPh SO _Two Single bond unit 13 1-2286 unit 40 3,4-diClPh SO _Two Single bond unit 14 1-2287 unit 40 3,4-diClPh SO _Two Single bond unit 15 1-2288 unit 40 3,4-diClPh SO _Two Single bond Unit 16 1-2289 Unit 40 3,4-diClPh SO _Two Single bond unit 17 1-2290 unit 40 3,4-diClPh SO _Two Single bond unit 18 1-2291 unit 40 3,4-diClPh SO _Two Single bond unit 19 1-2292 unit 40 3,4-diClPh SO _Two Single bond device 20 1-2293 device 40 3,4-diClPh SO _Two Single bond unit 21 1-2294 unit 40 3,4-diClPh SO _Two Single bond unit 22 1-2295 unit 40 3,4-diClPh SO _Two Single bond device 23 1-2296 device 40 3,4-diClPh SO _Two Single bond unit 24 1-2297 unit 40 3,4-diClPh SO _Two Single bond unit 25 1-2298 unit 40 3,4-diClPh SO _Two Single bond unit 26 1-2299 unit 40 3,4-diClPh SO _Two Single bond unit 27 1-2300 unit 40 3,4-diClPh SO _Two Single bond unit 28 1-2301 unit 40 3,4-diClPh SO _Two Single bond unit 29 1-2302 unit 40 3,4-diClPh SO _Two Single bond device 30 1-2303 device 40 3,4-diClPh SO _Two Single bond unit 31 1-2304 unit 40 3,4-diClPh SO _Two Single bond unit 32 1-2305 unit 41 3,4-diClPh SO _Two Single bond device 1 1-2306 device 41 3,4-diClPh SO _Two Single bond unit 2 1-2307 unit 41 3,4-diClPh SO _Two Single bond device 3 1-2308 device 41 3,4-diClPh SO _Two Single bond device 4 1-2309 device 41 3,4-diClPh SO _Two Single bond device 5 1-2310 device 41 3,4-diClPh SO _Two Single bond device 6 1-2311 device 41 3,4-diClPh SO _Two Single bond device 7 1-2312 device 41 3,4-diClPh SO _Two Single bond device 8 1-2314 device 41 3,4-diClPh SO _Two Single bond device 10 1-2315 device 41 3,4-diClPh SO _Two Single bond unit 11 1-2316 unit 41 3,4-diClPh SO _Two Single bond unit 12 1-2317 unit 41 3,4-diClPh SO _Two Single bond unit 13 1-2318 unit 41 3,4-diClPh SO _Two Single bond unit 14 1-2319 unit 41 3,4-diClPh SO _Two Single bond unit 15 1-2320 unit 41 3,4-diClPh SO _Two Single bond Unit 16 1-2321 Unit 41 3,4-diClPh SO _Two Single bond unit 17 1-2322 unit 41 3,4-diClPh SO _Two Single bond unit 18 1-2323 unit 41 3,4-diClPh SO _Two Single bond unit 19 1-2324 unit 41 3,4-diClPh SO _Two Single bond unit 20 1-2325 unit 41 3,4-diClPh SO _Two Single bond device 21 1-2326 device 41 3,4-diClPh SO _Two Single bond unit 22 1-2327 unit 41 3,4-diClPh SO _Two Single bond unit 23 1-2328 unit 41 3,4-diClPh SO _Two Single bond unit 24 1-2329 unit 41 3,4-diClPh SO _Two Single bond unit 25 1-2330 unit 41 3,4-diClPh SO _Two Single bond unit 26 1-2331 unit 41 3,4-diClPh SO _Two Single bond unit 27 1-2332 unit 41 3,4-diClPh SO _Two Single bond unit 28 1-2333 unit 41 3,4-diClPh SO _Two Single bond unit 29 1-2334 unit 41 3,4-diClPh SO _Two Single bond device 30 1-2335 device 41 3,4-diClPh SO _Two Single bond unit 31 1-2336 unit 41 3,4-diClPh SO _Two Single bond unit 32 1-2337 unit 42 3,4-diClPh SO _Two Single bond device 1 1-2338 device 42 3,4-diClPh SO _Two Single bond device 2 1-2339 device 42 3,4-diClPh SO _Two Single bond device 3 1-2340 device 42 3,4-diClPh SO _Two Single bond device 4 1-2341 device 42 3,4-diClPh SO _Two Single bond device 5 1-2343 device 42 3,4-diClPh SO _Two Single bond device 7 1-2344 device 42 3,4-diClPh SO _Two Single bond device 8 1-2345 device 42 3,4-diClPh SO _Two Single bond device 9 1-2346 device 42 3,4-diClPh SO _Two Single bond device 10 1-2347 device 42 3,4-diClPh SO _Two Single bond unit 11 1-2348 unit 42 3,4-diClPh SO _Two Single bond unit 12 1-2349 unit 42 3,4-diClPh SO _Two Single bond unit 13 1-2350 unit 42 3,4-diClPh SO _Two Single bond Unit 14 1-2351 Unit 42 3,4-diClPh SO _Two Single bond unit 15 1-2352 unit 42 3,4-diClPh SO _Two Single bond unit 16 1-2353 unit 42 3,4-diClPh SO _Two Single bond unit 17 1-2354 unit 42 3,4-diClPh SO _Two Single bond unit 18 1-2355 unit 42 3,4-diClPh SO _Two Single bond unit 19 1-2356 unit 42 3,4-diClPh SO _Two Single bond unit 20 1-2357 unit 42 3,4-diClPh SO _Two Single bond unit 21 1-2358 unit 42 3,4-diClPh SO _Two Single bond unit 22 1-2359 unit 42 3,4-diClPh SO _Two Single bond unit 23 1-2360 unit 42 3,4-diClPh SO _Two Single bond device 24 1-2361 device 42 3,4-diClPh SO _Two Single bond unit 25 1-2362 unit 42 3,4-diClPh SO _Two Single bond unit 26 1-2363 unit 42 3,4-diClPh SO _Two Single bond unit 27 1-2364 unit 42 3,4-diClPh SO _Two Single bond unit 28 1-2365 unit 42 3,4-diClPh SO _Two Single bond unit 29 1-2366 unit 42 3,4-diClPh SO _Two Single bond unit 30 1-2367 unit 42 3,4-diClPh SO _Two Single bond unit 31 1-2368 unit 42 3,4-diClPh SO _Two Single bond unit 32 1-2369 unit 43 3,4-diClPh SO _Two Single bond device 1 1-2370 device 43 3,4-diClPh SO _Two Single bond unit 2 1-2372 unit 43 3,4-diClPh SO _Two Single bond unit 4 1-2373 unit 43 3,4-diClPh SO _Two Single bond device 5 1-2374 device 43 3,4-diClPh SO _Two Single bond device 6 1-2375 device 43 3,4-diClPh SO _Two Single bond device 7 1-2376 device 43 3,4-diClPh SO _Two Single bond device 8 1-2377 device 43 3,4-diClPh SO _Two Single bond device 9 1-2378 device 43 3,4-diClPh SO _Two Single bond device 10 1-2379 device 43 3,4-diClPh SO _Two Single bond unit 11 1-2380 unit 43 3,4-diClPh SO _Two Single bond unit 12 1-2381 unit 43 3,4-diClPh SO _Two Single bond unit 13 1-2382 unit 43 3,4-diClPh SO _Two Single bond unit 14 1-2383 unit 43 3,4-diClPh SO _Two Single bond unit 15 1-2384 unit 43 3,4-diClPh SO _Two Single bond unit 16 1-2385 unit 43 3,4-diClPh SO _Two Single bond unit 17 1-2386 unit 43 3,4-diClPh SO _Two Single bond unit 18 1-2387 unit 43 3,4-diClPh SO _Two Single bond unit 19 1-2388 unit 43 3,4-diClPh SO _Two Single bond unit 20 1-2389 unit 43 3,4-diClPh SO _Two Single bond unit 21 1-2390 unit 43 3,4-diClPh SO _Two Single bond unit 22 1-2391 unit 43 3,4-diClPh SO _Two Single bond unit 23 1-2392 unit 43 3,4-diClPh SO _Two Single bond unit 24 1-2393 unit 43 3,4-diClPh SO _Two Single bond unit 25 1-2394 unit 43 3,4-diClPh SO _Two Single bond unit 26 1-2395 unit 43 3,4-diClPh SO _Two Single bond unit 27 1-2396 unit 43 3,4-diClPh SO _Two Single bond unit 28 1-2397 unit 43 3,4-diClPh SO _Two Single bond unit 29 1-2398 unit 43 3,4-diClPh SO _Two Single bond unit 30 1-2399 unit 43 3,4-diClPh SO _Two Single bond unit 31 1-2400 unit 43 3,4-diClPh SO _Two Single bond unit 32 1-2401 unit 44 3,4-diClPh SO _Two Single bond device 1 1-2402 device 44 3,4-diClPh SO _Two Single bond device 2 1-2403 device 44 3,4-diClPh SO _Two Single bond device 3 1-2404 device 44 3,4-diClPh SO _Two Single bond unit 4 1-2405 unit 44 3,4-diClPh SO _Two Single bond device 5 1-2406 device 44 3,4-diClPh SO _Two Single bond unit 6 1-2407 unit 44 3,4-diClPh SO _Two Single bond device 7 1-2408 device 44 3,4-diClPh SO _Two Single bond device 8 1-2409 device 44 3,4-diClPh SO _Two Single bond device 9 1-2410 device 44 3,4-diClPh SO _Two Single bond device 10 1-2411 device 44 3,4-diClPh SO _Two Single bond unit 11 1-212 unit 44 3,4-diClPh SO _Two Single bond unit 12 1-2413 unit 44 3,4-diClPh SO _Two Single bond unit 13 1-2414 unit 44 3,4-diClPh SO _Two Single bond unit 14 1-2415 unit 44 3,4-diClPh SO _Two Single bond unit 15 1-2416 unit 44 3,4-diClPh SO _Two Single bond Unit 16 1-2417 Unit 44 3,4-diClPh SO _Two Single bond unit 17 1-2418 unit 44 3,4-diClPh SO _Two Single bond unit 18 1-2419 unit 44 3,4-diClPh SO _Two Single bond unit 19 1-2420 unit 44 3,4-diClPh SO _Two Single bond device 20 1-2421 device 44 3,4-diClPh SO _Two Single bond unit 21 1-2422 unit 44 3,4-diClPh SO _Two Single bond unit 22 1-2423 unit 44 3,4-diClPh SO _Two Single bond unit 23 1-2424 unit 44 3,4-diClPh SO _Two Single bond unit 24 1-2425 unit 44 3,4-diClPh SO _Two Single bond unit 25 1-2426 unit 44 3,4-diClPh SO _Two Single bond unit 26 1-2427 unit 44 3,4-diClPh SO _Two Single bond unit 27 1-2428 unit 44 3,4-diClPh SO _Two Single bond unit 28 1-2430 unit 44 3,4-diClPh SO _Two Single bond device 30 1-2431 device 44 3,4-diClPh SO _Two Single bond unit 31 1-232 unit 44 3,4-diClPh SO _Two Single bond unit 32 1-2433 unit 45 3,4-diClPh SO _Two Single bond device 1 1-2434 device 45 3,4-diClPh SO _Two Single bond unit 2 1-2435 unit 45 3,4-diClPh SO _Two Single bond device 3 1-2436 device 45 3,4-diClPh SO _Two Single bond unit 4 1-2437 unit 45 3,4-diClPh SO _Two Single bond device 5 1-2438 device 45 3,4-diClPh SO _Two Single bond device 6 1-2439 device 45 3,4-diClPh SO _Two Single bond device 7 1-2440 device 45 3,4-diClPh SO _Two Single bond unit 8 1-2441 unit 45 3,4-diClPh SO _Two Single bond unit 9 1-2442 unit 45 3,4-diClPh SO _Two Single bond device 10 1-2443 device 45 3,4-diClPh SO _Two Single bond unit 11 1-2444 unit 45 3,4-diClPh SO _Two Single bond Unit 12 1-2445 Unit 45 3,4-diClPh SO _Two Single bond unit 13 1-2446 unit 45 3,4-diClPh SO _Two Single bond unit 14 1-247 unit 45 3,4-diClPh SO _Two Single bond unit 15 1-2448 unit 45 3,4-diClPh SO _Two Single bond Unit 16 1-2449 Unit 45 3,4-diClPh SO _Two Single bond unit 17 1-2450 unit 45 3,4-diClPh SO _Two Single bond unit 18 1-2451 unit 45 3,4-diClPh SO _Two Single bond unit 19 1-2452 unit 45 3,4-diClPh SO _Two Single bond unit 20 1-2453 unit 45 3,4-diClPh SO _Two Single bond unit 21 1-2454 unit 45 3,4-diClPh SO _Two Single bond unit 22 1-2455 unit 45 3,4-diClPh SO _Two Single bond unit 23 1-2456 unit 45 3,4-diClPh SO _Two Single bond unit 24 1-2457 unit 45 3,4-diClPh SO _Two Single bond Unit 25 1-259 Unit 45 3,4-diClPh SO _Two Single bond unit 27 1-2460 unit 45 3,4-diClPh SO _Two Single bond unit 28 1-2461 unit 45 3,4-diClPh SO _Two Single bond unit 29 1-2462 unit 45 3,4-diClPh SO _Two Single bond unit 30 1-2463 unit 45 3,4-diClPh SO _Two Single bond unit 31 1-264 unit 45 3,4-diClPh SO _Two Single bond unit 32 1-2465 unit 46 3,4-diClPh SO _Two Single bond device 1 1-2466 device 46 3,4-diClPh SO _Two Single bond unit 2 1-2467 unit 46 3,4-diClPh SO _Two Single bond device 3 1-2468 device 46 3,4-diClPh SO _Two Single bond unit 4 1-2469 unit 46 3,4-diClPh SO _Two Single bond device 5 1-2470 device 46 3,4-diClPh SO _Two Single bond device 6 1-2471 device 46 3,4-diClPh SO _Two Single bond device 7 1-2472 device 46 3,4-diClPh SO _Two Single bond device 8 1-2473 device 46 3,4-diClPh SO _Two Single bond unit 9 1-2474 unit 46 3,4-diClPh SO _Two Single bond device 10 1-2475 device 46 3,4-diClPh SO _Two Single bond unit 11 1-2476 unit 46 3,4-diClPh SO _Two Single bond unit 12 1-2277 unit 46 3,4-diClPh SO _Two Single bond unit 13 1-2478 unit 46 3,4-diClPh SO _Two Single bond unit 14 1-2479 unit 46 3,4-diClPh SO _Two Single bond unit 15 1-2480 unit 46 3,4-diClPh SO _Two Single bond unit 16 1-2481 unit 46 3,4-diClPh SO _Two Single bond unit 17 1-2482 unit 46 3,4-diClPh SO _Two Single bond unit 18 1-2483 unit 46 3,4-diClPh SO _Two Single bond unit 19 1-2484 unit 46 3,4-diClPh SO _Two Single bond unit 20 1-2485 unit 46 3,4-diClPh SO _Two Single bond unit 21 1-2486 unit 46 3,4-diClPh SO _Two Single bond unit 22 1-2488 unit 46 3,4-diClPh SO _Two Single bond unit 24 1-2489 unit 46 3,4-diClPh SO _Two Single bond unit 25 1-2490 unit 46 3,4-diClPh SO _Two Single bond unit 26 1-2491 unit 46 3,4-diClPh SO _Two Single bond unit 27 1-2492 unit 46 3,4-diClPh SO _Two Single bond unit 28 1-2493 unit 46 3,4-diClPh SO _Two Single bond unit 29 1-2494 unit 46 3,4-diClPh SO _Two Single bond unit 30 1-2495 unit 46 3,4-diClPh SO _Two Single bond unit 31 1-2496 unit 46 3,4-diClPh SO _Two Single bond unit 32 1-2497 unit 47 3,4-diClPh SO _Two Single bond device 1 1-2498 device 47 3,4-diClPh SO _Two Single bond unit 2 1-2499 unit 47 3,4-diClPh SO _Two Single bond device 3 1-2500 device 47 3,4-diClPh SO _Two Single bond unit 4 1-2501 unit 47 3,4-diClPh SO _Two Single bond 5 1-2502 47 3,4-diClPh SO _Two Single bond unit 6 1-2503 unit 47 3,4-diClPh SO _Two Single bond unit 7 1-2504 unit 47 3,4-diClPh SO _Two Single bond unit 8 1-2505 unit 47 3,4-diClPh SO _Two Single bond unit 9 1-2506 unit 47 3,4-diClPh SO _Two Single bond unit 10 1-2507 unit 47 3,4-diClPh SO _Two Single bond unit 11 1-2508 unit 47 3,4-diClPh SO _Two Single bond Unit 12 1-2509 Unit 47 3,4-diClPh SO _Two Single bond unit 13 1-2510 unit 47 3,4-diClPh SO _Two Single bond unit 14 1-2511 unit 47 3,4-diClPh SO _Two Single bond unit 15 1-2512 unit 47 3,4-diClPh SO _Two Single bond unit 16 1-2513 unit 47 3,4-diClPh SO _Two Single bond unit 17 1-2514 unit 47 3,4-diClPh SO _Two Single bond unit 18 1-2515 unit 47 3,4-diClPh SO _Two Single bond unit 19 1-2517 unit 47 3,4-diClPh SO _Two Single bond unit 21 1-2518 unit 47 3,4-diClPh SO _Two Single bond unit 22 1-2519 unit 47 3,4-diClPh SO _Two Single bond unit 23 1-2520 unit 47 3,4-diClPh SO _Two Single bond unit 24 1-2521 unit 47 3,4-diClPh SO _Two Single bond unit 25 1-2522 unit 47 3,4-diClPh SO _Two Single bond unit 26 1-2523 unit 47 3,4-diClPh SO _Two Single bond unit 27 1-2524 unit 47 3,4-diClPh SO _Two Single bond unit 28 1-2525 unit 47 3,4-diClPh SO _Two Single bond unit 29 1-2526 unit 47 3,4-diClPh SO _Two Single bond unit 30 1-2527 unit 47 3,4-diClPh SO _Two Single bond unit 31 1-2528 unit 47 3,4-diClPh SO _Two Single bond unit 32 1-2529 unit 48 3,4-diClPh SO _Two Single bond device 1 1-2530 device 48 3,4-diClPh SO _Two Single bond unit 2 1-2531 unit 48 3,4-diClPh SO _Two Single bond device 3 1-2532 device 48 3,4-diClPh SO _Two Single bond unit 4 1-2533 unit 48 3,4-diClPh SO _Two Single bond device 5 1-2534 device 48 3,4-diClPh SO _Two Single bond unit 6 1-2535 unit 48 3,4-diClPh SO _Two Single bond device 7 1-2536 device 48 3,4-diClPh SO _Two Single bond device 8 1-2537 device 48 3,4-diClPh SO _Two Single bond unit 9 1-2538 unit 48 3,4-diClPh SO _Two Single bond device 10 1-2539 device 48 3,4-diClPh SO _Two Single bond unit 11 1-2540 unit 48 3,4-diClPh SO _Two Single bond Unit 12 1-2541 Unit 48 3,4-diClPh SO _Two Single bond unit 13 1-2542 unit 48 3,4-diClPh SO _Two Single bond unit 14 1-2543 unit 48 3,4-diClPh SO _Two Single bond unit 15 1-2544 unit 48 3,4-diClPh SO _Two Single bond unit 16 1-2546 unit 48 3,4-diClPh SO _Two Single bond unit 18 1-2547 unit 48 3,4-diClPh SO _Two Single bond unit 19 1-2548 unit 48 3,4-diClPh SO _Two Single bond unit 20 1-2549 unit 48 3,4-diClPh SO _Two Single bond unit 21 1-2550 unit 48 3,4-diClPh SO _Two Single bond unit 22 1-2551 unit 48 3,4-diClPh SO _Two Single bond unit 23 1-2552 unit 48 3,4-diClPh SO _Two Single bond unit 24 1-2553 unit 48 3,4-diClPh SO _Two Single bond unit 25 1-2554 unit 48 3,4-diClPh SO _Two Single bond unit 26 1-2555 unit 48 3,4-diClPh SO _Two Single bond unit 27 1-2556 unit 48 3,4-diClPh SO _Two Single bond unit 28 1-2557 unit 48 3,4-diClPh SO _Two Single bond unit 29 1-2558 unit 48 3,4-diClPh SO _Two Single bond unit 30 1-2559 unit 48 3,4-diClPh SO _Two Single bond unit 31 1-2560 unit 48 3,4-diClPh SO _Two Single bond position 32 ──────────────────────────────────── Compound number R ¹ R ^Two A B Z １− 1-2561 Place 49 3,4-diClPh SO _Two Single bond unit 1 1-2562 unit 49 3,4-diClPh SO _Two Single bond unit 2 1-2563 unit 49 3,4-diClPh SO _Two Single bond unit 3 1-2564 unit 49 3,4-diClPh SO _Two Single bond unit 4 1-2565 unit 49 3,4-diClPh SO _Two Single bond device 5 1-2566 device 49 3,4-diClPh SO _Two Single bond unit 6 1-2567 unit 49 3,4-diClPh SO _Two Single bond device 7 1-2568 device 49 3,4-diClPh SO _Two Single bond device 8 1-2569 device 49 3,4-diClPh SO _Two Single bond device 9 1-2570 device 49 3,4-diClPh SO _Two Single bond unit 10 1-2571 unit 49 3,4-diClPh SO _Two Single bond Unit 11 1-2572 Unit 49 3,4-diClPh SO _Two Single bond unit 12 1-2573 unit 49 3,4-diClPh SO _Two Single bond unit 13 1-2574 unit 49 3,4-diClPh SO _Two Single bond unit 14 1-2575 unit 49 3,4-diClPh SO _Two Single bond unit 15 1-2576 unit 49 3,4-diClPh SO _Two Single bond unit 16 1-2577 unit 49 3,4-diClPh SO _Two Single bond unit 17 1-2578 unit 49 3,4-diClPh SO _Two Single bond unit 18 1-2579 unit 49 3,4-diClPh SO _Two Single bond unit 19 1-2580 unit 49 3,4-diClPh SO _Two Single bond unit 20 1-2581 unit 49 3,4-diClPh SO _Two Single bond unit 21 1-2582 unit 49 3,4-diClPh SO _Two Single bond unit 22 1-2583 unit 49 3,4-diClPh SO _Two Single bond unit 23 1-2584 unit 49 3,4-diClPh SO _Two Single bond unit 24 1-2585 unit 49 3,4-diClPh SO _Two Single bond unit 25 1-2586 unit 49 3,4-diClPh SO _Two Single bond unit 26 1-2587 unit 49 3,4-diClPh SO _Two Single bond unit 27 1-2588 unit 49 3,4-diClPh SO _Two Single bond unit 28 1-2589 unit 49 3,4-diClPh SO _Two Single bond unit 29 1-2590 unit 49 3,4-diClPh SO _Two Single bond unit 30 1-2591 unit 49 3,4-diClPh SO _Two Single bond unit 31 1-2592 unit 49 3,4-diClPh SO _Two Single bond unit 32 1-2593 unit 50 3,4-diClPh SO _Two Single bond unit 1 1-2594 unit 50 3,4-diClPh SO _Two Single bond unit 2 1-2595 unit 50 3,4-diClPh SO _Two Single bond device 3 1-2596 device 50 3,4-diClPh SO _Two Single bond unit 4 1-2597 unit 50 3,4-diClPh SO _Two Single bond device 5 1-2598 device 50 3,4-diClPh SO _Two Single bond device 6 1-2599 device 50 3,4-diClPh SO _Two Single bond device 7 1-2601 device 50 3,4-diClPh SO _Two Single bond device 9 1-2602 device 50 3,4-diClPh SO _Two Single bond device 10 1-2603 device 50 3,4-diClPh SO _Two Single bond unit 11 1-2604 unit 50 3,4-diClPh SO _Two Single bond unit 12 1-2605 unit 50 3,4-diClPh SO _Two Single bond unit 13 1-2606 unit 50 3,4-diClPh SO _Two Single bond unit 14 1-2607 unit 50 3,4-diClPh SO _Two Single bond unit 15 1-2608 unit 50 3,4-diClPh SO _Two Single bond unit 16 1-2609 unit 50 3,4-diClPh SO _Two Single bond unit 17 1-2610 unit 50 3,4-diClPh SO _Two Single bond unit 18 1-2611 unit 50 3,4-diClPh SO _Two Single bond unit 19 1-2612 unit 50 3,4-diClPh SO _Two Single bond device 20 1-2613 device 50 3,4-diClPh SO _Two Single bond unit 21 1-2614 unit 50 3,4-diClPh SO _Two Single bond unit 22 1-2615 unit 50 3,4-diClPh SO _Two Single bond unit 23 1-2616 unit 50 3,4-diClPh SO _Two Single bond unit 24 1-2617 unit 50 3,4-diClPh SO _Two Single bond unit 25 1-2618 unit 50 3,4-diClPh SO _Two Single bond unit 26 1-2619 unit 50 3,4-diClPh SO _Two Single bond unit 27 1-2620 unit 50 3,4-diClPh SO _Two Single bond unit 28 1-2621 unit 50 3,4-diClPh SO _Two Single bond unit 29 1-2622 unit 50 3,4-diClPh SO _Two Single bond device 30 1-2623 device 50 3,4-diClPh SO _Two Single bond unit 31 1-2624 unit 50 3,4-diClPh SO _Two Single bond unit 32 1-2625 unit 51 3,4-diClPh SO _Two Single bond device 1 1-2626 device 51 3,4-diClPh SO _Two Single bond device 2 1-2627 device 51 3,4-diClPh SO _Two Single bond device 3 1-2628 device 51 3,4-diClPh SO _Two Single bond device 4 1-2630 device 51 3,4-diClPh SO _Two Single bond device 6 1-2631 device 51 3,4-diClPh SO _Two Single bond device 7 1-2632 device 51 3,4-diClPh SO _Two Single bond device 8 1-2633 device 51 3,4-diClPh SO _Two Single bond device 9 1-2634 device 51 3,4-diClPh SO _Two Single bond device 10 1-2635 device 51 3,4-diClPh SO _Two Single bond unit 11 1-2636 unit 51 3,4-diClPh SO _Two Single bond unit 12 1-2637 unit 51 3,4-diClPh SO _Two Single bond unit 13 1-2638 unit 51 3,4-diClPh SO _Two Single bond unit 14 1-2639 unit 51 3,4-diClPh SO _Two Single bond Unit 15 1-2640 Unit 51 3,4-diClPh SO _Two Single bond Unit 16 1-2641 Unit 51 3,4-diClPh SO _Two Single bond Unit 17 1-2642 Unit 51 3,4-diClPh SO _Two Single bond unit 18 1-2643 unit 51 3,4-diClPh SO _Two Single bond unit 19 1-2644 unit 51 3,4-diClPh SO _Two Single bond device 20 1-2645 device 51 3,4-diClPh SO _Two Single bond device 21 1-2646 device 51 3,4-diClPh SO _Two Single bond unit 22 1-2647 unit 51 3,4-diClPh SO _Two Single bond unit 23 1-2648 unit 51 3,4-diClPh SO _Two Single bond unit 24 1-2649 unit 51 3,4-diClPh SO _Two Single bond unit 25 1-2650 unit 51 3,4-diClPh SO _Two Single bond unit 26 1-2651 unit 51 3,4-diClPh SO _Two Single bond Unit 27 1-2652 Unit 51 3,4-diClPh SO _Two Single bond unit 28 1-2653 unit 51 3,4-diClPh SO _Two Single bond unit 29 1-2654 unit 51 3,4-diClPh SO _Two Single bond device 30 1-2655 device 51 3,4-diClPh SO _Two Single bond unit 31 1-2656 unit 51 3,4-diClPh SO _Two Single bond unit 32 1-2657 unit 52 3,4-diClPh SO _Two Single bond device 1 1-2659 device 52 3,4-diClPh SO _Two Single bond device 3 1-2660 device 52 3,4-diClPh SO _Two Single bond unit 4 1-2661 unit 52 3,4-diClPh SO _Two Single bond device 5 1-2662 device 52 3,4-diClPh SO _Two Single bond device 6 1-2663 device 52 3,4-diClPh SO _Two Single bond Unit 7 1-2664 Unit 52 3,4-diClPh SO _Two Single bond device 8 1-2665 device 52 3,4-diClPh SO _Two Single bond device 9 1-2666 device 52 3,4-diClPh SO _Two Single bond device 10 1-2667 device 52 3,4-diClPh SO _Two Single bond unit 11 1-2668 unit 52 3,4-diClPh SO _Two Single bond unit 12 1-2669 unit 52 3,4-diClPh SO _Two Single bond unit 13 1-2670 unit 52 3,4-diClPh SO _Two Single bond unit 14 1-2671 unit 52 3,4-diClPh SO _Two Single bond unit 15 1-2672 unit 52 3,4-diClPh SO _Two Single bond unit 16 1-2673 unit 52 3,4-diClPh SO _Two Single bond unit 17 1-267 unit 52 3,4-diClPh SO _Two Single bond unit 18 1-2675 unit 52 3,4-diClPh SO _Two Single bond unit 19 1-2676 unit 52 3,4-diClPh SO _Two Single bond unit 20 1-2677 unit 52 3,4-diClPh SO _Two Single bond unit 21 1-2678 unit 52 3,4-diClPh SO _Two Single bond unit 22 1-2679 unit 52 3,4-diClPh SO _Two Single bond unit 23 1-2680 unit 52 3,4-diClPh SO _Two Single bond unit 24 1-2681 unit 52 3,4-diClPh SO _Two Single bond unit 25 1-2682 unit 52 3,4-diClPh SO _Two Single bond unit 26 1-2683 unit 52 3,4-diClPh SO _Two Single bond unit 27 1-2684 unit 52 3,4-diClPh SO _Two Single bond unit 28 1-2685 unit 52 3,4-diClPh SO _Two Single bond unit 29 1-2686 unit 52 3,4-diClPh SO _Two Single bond device 30 1-2687 device 52 3,4-diClPh SO _Two Single bond unit 31 1-2688 unit 52 3,4-diClPh SO _Two Single bond unit 32 1-2689 unit 53 3,4-diClPh SO _Two Single bond device 1 1-2690 device 53 3,4-diClPh SO _Two Single bond device 2 1-2691 device 53 3,4-diClPh SO _Two Single bond device 3 1-2692 device 53 3,4-diClPh SO _Two Single bond unit 4 1-2693 unit 53 3,4-diClPh SO _Two Single bond unit 5 1-2694 unit 53 3,4-diClPh SO _Two Single bond device 6 1-2695 device 53 3,4-diClPh SO _Two Single bond device 7 1-2696 device 53 3,4-diClPh SO _Two Single bond device 8 1-2697 device 53 3,4-diClPh SO _Two Single bond device 9 1-2698 device 53 3,4-diClPh SO _Two Single bond device 10 1-2699 device 53 3,4-diClPh SO _Two Single bond unit 11 1-2700 unit 53 3,4-diClPh SO _Two Single bond unit 12 1-2701 unit 53 3,4-diClPh SO _Two Single bond unit 13 1-2702 unit 53 3,4-diClPh SO _Two Single bond unit 14 1-2703 unit 53 3,4-diClPh SO _Two Single bond unit 15 1-2704 unit 53 3,4-diClPh SO _Two Single bond unit 16 1-2705 unit 53 3,4-diClPh SO _Two Single bond unit 17 1-2706 unit 53 3,4-diClPh SO _Two Single bond unit 18 1-2707 unit 53 3,4-diClPh SO _Two Single bond unit 19 1-2708 unit 53 3,4-diClPh SO _Two Single bond device 20 1-2709 device 53 3,4-diClPh SO _Two Single bond unit 21 1-2710 unit 53 3,4-diClPh SO _Two Single bond Unit 22 1-2711 Unit 53 3,4-diClPh SO _Two Single bond unit 23 1-2712 unit 53 3,4-diClPh SO _Two Single bond unit 24 1-2713 unit 53 3,4-diClPh SO _Two Single bond unit 25 1-2714 unit 53 3,4-diClPh SO _Two Single bond unit 26 1-2715 unit 53 3,4-diClPh SO _Two Single bond unit 27 1-2717 unit 53 3,4-diClPh SO _Two Single bond unit 29 1-2718 unit 53 3,4-diClPh SO _Two Single bond device 30 1-2719 device 53 3,4-diClPh SO _Two Single bond unit 31 1-2720 unit 53 3,4-diClPh SO _Two Single bond unit 32 1-2721 unit 54 3,4-diClPh SO _Two Single bond device 1 1-2722 device 54 3,4-diClPh SO _Two Single bond device 2 1-2723 device 54 3,4-diClPh SO _Two Single bond device 3 1-2724 device 54 3,4-diClPh SO _Two Single bond unit 4 1-2725 unit 54 3,4-diClPh SO _Two Single bond device 5 1-2726 device 54 3,4-diClPh SO _Two Single bond device 6 1-2727 device 54 3,4-diClPh SO _Two Single bond device 7 1-2728 device 54 3,4-diClPh SO _Two Single bond device 8 1-2729 device 54 3,4-diClPh SO _Two Single bond device 9 1-2730 device 54 3,4-diClPh SO _Two Single bond device 10 1-2731 device 54 3,4-diClPh SO _Two Single bond unit 11 1-2732 unit 54 3,4-diClPh SO _Two Single bond unit 12 1-2733 unit 54 3,4-diClPh SO _Two Single bond unit 13 1-2734 unit 54 3,4-diClPh SO _Two Single bond unit 14 1-2735 unit 54 3,4-diClPh SO _Two Single bond unit 15 1-2736 unit 54 3,4-diClPh SO _Two Single bond unit 16 1-2737 unit 54 3,4-diClPh SO _Two Single bond unit 17 1-2738 unit 54 3,4-diClPh SO _Two Single bond unit 18 1-2739 unit 54 3,4-diClPh SO _Two Single bond unit 19 1-2740 unit 54 3,4-diClPh SO _Two Single bond unit 20 1-2741 unit 54 3,4-diClPh SO _Two Single bond unit 21 1-2742 unit 54 3,4-diClPh SO _Two Single bond unit 22 1-2743 unit 54 3,4-diClPh SO _Two Single bond unit 23 1-2744 unit 54 3,4-diClPh SO _Two Single bond unit 24 1-2746 unit 54 3,4-diClPh SO _Two Single bond unit 26 1-2747 unit 54 3,4-diClPh SO _Two Single bond unit 27 1-2748 unit 54 3,4-diClPh SO _Two Single bond unit 28 1-2749 unit 54 3,4-diClPh SO _Two Single bond unit 29 1-2750 unit 54 3,4-diClPh SO _Two Single bond device 30 1-2751 device 54 3,4-diClPh SO _Two Single bond unit 31 1-2752 unit 54 3,4-diClPh SO _Two Single bond unit 32 1-2753 unit 55 3,4-diClPh SO _Two Single bond unit 1 1-2754 unit 55 3,4-diClPh SO _Two Single bond unit 2 1-2755 unit 55 3,4-diClPh SO _Two Single bond position 3 1-2756 position 55 3,4-diClPh SO _Two Single bond 4 1-2757 55 3,4-diClPh SO _Two Single bond device 5 1-2758 device 55 3,4-diClPh SO _Two Single bond unit 6 1-2759 unit 55 3,4-diClPh SO _Two Single bond unit 7 1-2760 unit 55 3,4-diClPh SO _Two Single bond device 8 1-2761 device 55 3,4-diClPh SO _Two Single bond device 9 1-2762 device 55 3,4-diClPh SO _Two Single bond device 10 1-2763 device 55 3,4-diClPh SO _Two Single bond unit 11 1-2764 unit 55 3,4-diClPh SO _Two Single bond unit 12 1-2765 unit 55 3,4-diClPh SO _Two Single bond unit 13 1-2766 unit 55 3,4-diClPh SO _Two Single bond unit 14 1-2767 unit 55 3,4-diClPh SO _Two Single bond unit 15 1-2768 unit 55 3,4-diClPh SO _Two Single bond unit 16 1-2769 unit 55 3,4-diClPh SO _Two Single bond unit 17 1-2770 unit 55 3,4-diClPh SO _Two Single bond unit 18 1-27771 unit 55 3,4-diClPh SO _Two Single bond unit 19 1-2772 unit 55 3,4-diClPh SO _Two Single bond unit 20 1-2773 unit 55 3,4-diClPh SO _Two Single bond unit 21 1-2775 unit 55 3,4-diClPh SO _Two Single bond unit 23 1-2776 unit 55 3,4-diClPh SO _Two Single bond unit 24 1-2777 unit 55 3,4-diClPh SO _Two Single bond unit 25 1-2778 unit 55 3,4-diClPh SO _Two Single bond unit 26 1-2779 unit 55 3,4-diClPh SO _Two Single bond unit 27 1-2780 unit 55 3,4-diClPh SO _Two Single bond unit 28 1-2781 unit 55 3,4-diClPh SO _Two Single bond unit 29 1-2782 unit 55 3,4-diClPh SO _Two Single bond device 30 1-2783 device 55 3,4-diClPh SO _Two Single bond unit 31 1-2784 unit 55 3,4-diClPh SO _Two Single bond unit 32 1-2785 unit 56 3,4-diClPh SO _Two Single bond device 1 1-2786 device 56 3,4-diClPh SO _Two Single bond unit 2 1-2787 unit 56 3,4-diClPh SO _Two Single bond device 3 1-2788 device 56 3,4-diClPh SO _Two Single bond unit 4 1-2789 unit 56 3,4-diClPh SO _Two Single bond device 5 1-2790 device 56 3,4-diClPh SO _Two Single bond device 6 1-2791 device 56 3,4-diClPh SO _Two Single bond device 7 1-2792 device 56 3,4-diClPh SO _Two Single bond unit 8 1-2793 unit 56 3,4-diClPh SO _Two Single bond device 9 1-2794 device 56 3,4-diClPh SO _Two Single bond device 10 1-2795 device 56 3,4-diClPh SO _Two Single bond unit 11 1-2796 unit 56 3,4-diClPh SO _Two Single bond unit 12 1-2797 unit 56 3,4-diClPh SO _Two Single bond unit 13 1-2798 unit 56 3,4-diClPh SO _Two Single bond unit 14 1-2799 unit 56 3,4-diClPh SO _Two Single bond unit 15 1-2800 unit 56 3,4-diClPh SO _Two Single bond unit 16 1-2801 unit 56 3,4-diClPh SO _Two Single bond unit 17 1-2802 unit 56 3,4-diClPh SO _Two Single bond unit 18 1-2804 unit 56 3,4-diClPh SO _Two Single bond unit 20 1-2805 unit 56 3,4-diClPh SO _Two Single bond unit 21 1-2806 unit 56 3,4-diClPh SO _Two Single bond unit 22 1-2807 unit 56 3,4-diClPh SO _Two Single bond unit 23 1-2808 unit 56 3,4-diClPh SO _Two Single bond unit 24 1-2809 unit 56 3,4-diClPh SO _Two Single bond unit 25 1-2810 unit 56 3,4-diClPh SO _Two Single bond unit 26 1-28111 unit 56 3,4-diClPh SO _Two Single bond unit 27 1-212 unit 56 3,4-diClPh SO _Two Single bond unit 28 1-2813 unit 56 3,4-diClPh SO _Two Single bond unit 29 1-2814 unit 56 3,4-diClPh SO _Two Single bond device 30 1-2815 device 56 3,4-diClPh SO _Two Single bond unit 31 1-2816 unit 56 3,4-diClPh SO _Two Single bond unit 32 1-2817 unit 57 3,4-diClPh SO _Two Single bond device 1 1-2818 device 57 3,4-diClPh SO _Two Single bond device 2 1-2819 device 57 3,4-diClPh SO _Two Single bond device 3 1-2820 device 57 3,4-diClPh SO _Two Single bond unit 4 1-2821 unit 57 3,4-diClPh SO _Two Single bond device 5 1-2822 device 57 3,4-diClPh SO _Two Single bond device 6 1-2823 device 57 3,4-diClPh SO _Two Single bond device 7 1-2824 device 57 3,4-diClPh SO _Two Single bond device 8 1-2825 device 57 3,4-diClPh SO _Two Single bond device 9 1-2826 device 57 3,4-diClPh SO _Two Single bond unit 10 1-2828 unit 57 3,4-diClPh SO _Two Single bond unit 11 1-2828 unit 57 3,4-diClPh SO _Two Single bond unit 12 1-2829 unit 57 3,4-diClPh SO _Two Single bond unit 13 1-2830 unit 57 3,4-diClPh SO _Two Single bond unit 14 1-2831 unit 57 3,4-diClPh SO _Two Single bond unit 15 1-2833 unit 57 3,4-diClPh SO _Two Single bond unit 17 1-2834 unit 57 3,4-diClPh SO _Two Single bond unit 18 1-2835 unit 57 3,4-diClPh SO _Two Single bond unit 19 1-2836 unit 57 3,4-diClPh SO _Two Single bond device 20 1-2837 device 57 3,4-diClPh SO _Two Single bond unit 21 1-2838 unit 57 3,4-diClPh SO _Two Single bond unit 22 1-2839 unit 57 3,4-diClPh SO _Two Single bond unit 23 1-2840 unit 57 3,4-diClPh SO _Two Single bond unit 24 1-2841 unit 57 3,4-diClPh SO _Two Single bond unit 25 1-2842 unit 57 3,4-diClPh SO _Two Single bond unit 26 1-2843 unit 57 3,4-diClPh SO _Two Single bond unit 27 1-2844 unit 57 3,4-diClPh SO _Two Single bond unit 28 1-2845 unit 57 3,4-diClPh SO _Two Single bond unit 29 1-2846 unit 57 3,4-diClPh SO _Two Single bond device 30 1-2847 device 57 3,4-diClPh SO _Two Single bond unit 31 1-2848 unit 57 3,4-diClPh SO _Two Single bond unit 32 1-2849 unit 58 3,4-diClPh SO _Two Single bond device 1 1-2850 device 58 3,4-diClPh SO _Two Single bond device 2 1-2851 device 58 3,4-diClPh SO _Two Single bond unit 3 1-2852 unit 58 3,4-diClPh SO _Two Single bond unit 4 1-2853 unit 58 3,4-diClPh SO _Two Single bond device 5 1-2854 device 58 3,4-diClPh SO _Two Single bond unit 6 1-2855 unit 58 3,4-diClPh SO _Two Single bond device 7 1-2856 device 58 3,4-diClPh SO _Two Single bond unit 8 1-2857 unit 58 3,4-diClPh SO _Two Single bond unit 9 1-2858 unit 58 3,4-diClPh SO _Two Single bond device 10 1-2859 device 58 3,4-diClPh SO _Two Single bond unit 11 1-2860 unit 58 3,4-diClPh SO _Two Single bond unit 12 1-2862 unit 58 3,4-diClPh SO _Two Single bond unit 14 1-2863 unit 58 3,4-diClPh SO _Two Single bond unit 15 1-2864 unit 58 3,4-diClPh SO _Two Single bond unit 16 1-2865 unit 58 3,4-diClPh SO _Two Single bond unit 17 1-2866 unit 58 3,4-diClPh SO _Two Single bond unit 18 1-2867 unit 58 3,4-diClPh SO _Two Single bond unit 19 1-2868 unit 58 3,4-diClPh SO _Two Single bond unit 20 1-2869 unit 58 3,4-diClPh SO _Two Single bond unit 21 1-2870 unit 58 3,4-diClPh SO _Two Single bond unit 22 1-2871 unit 58 3,4-diClPh SO _Two Single bond unit 23 1-2872 unit 58 3,4-diClPh SO _Two Single bond unit 24 1-2873 unit 58 3,4-diClPh SO _Two Single bond unit 25 1-2874 unit 58 3,4-diClPh SO _Two Single bond unit 26 1-2875 unit 58 3,4-diClPh SO _Two Single bond unit 27 1-2876 unit 58 3,4-diClPh SO _Two Single bond unit 28 1-2877 unit 58 3,4-diClPh SO _Two Single bond unit 29 1-2788 unit 58 3,4-diClPh SO _Two Single bond device 30 1-2879 device 58 3,4-diClPh SO _Two Single bond unit 31 1-2880 unit 58 3,4-diClPh SO _Two Single bond unit 32 1-2881 unit 59 3,4-diClPh SO _Two Single bond device 1 1-2882 device 59 3,4-diClPh SO _Two Single bond unit 2 1-2883 unit 59 3,4-diClPh SO _Two Single bond position 3 1-2884 position 59 3,4-diClPh SO _Two Single bond unit 4 1-2885 unit 59 3,4-diClPh SO _Two Single bond unit 5 1-2886 unit 59 3,4-diClPh SO _Two Single bond device 6 1-2887 device 59 3,4-diClPh SO _Two Single bond device 7 1-2888 device 59 3,4-diClPh SO _Two Single bond device 8 1-2889 device 59 3,4-diClPh SO _Two Single bond device 9 1-2891 device 59 3,4-diClPh SO _Two Single bond unit 11 1-2892 unit 59 3,4-diClPh SO _Two Single bond unit 12 1-2893 unit 59 3,4-diClPh SO _Two Single bond unit 13 1-2894 unit 59 3,4-diClPh SO _Two Single bond unit 14 1-2895 unit 59 3,4-diClPh SO _Two Single bond unit 15 1-2896 unit 59 3,4-diClPh SO _Two Single bond unit 16 1-2897 unit 59 3,4-diClPh SO _Two Single bond unit 17 1-2898 unit 59 3,4-diClPh SO _Two Single bond unit 18 1-2899 unit 59 3,4-diClPh SO _Two Single bond unit 19 1-2900 unit 59 3,4-diClPh SO _Two Single bond unit 20 1-2901 unit 59 3,4-diClPh SO _Two Single bond unit 21 1-2902 unit 59 3,4-diClPh SO _Two Single bond unit 22 1-2903 unit 59 3,4-diClPh SO _Two Single bond unit 23 1-2904 unit 59 3,4-diClPh SO _Two Single bond unit 24 1-2905 unit 59 3,4-diClPh SO _Two Single bond unit 25 1-2906 unit 59 3,4-diClPh SO _Two Single bond unit 26 1-2907 unit 59 3,4-diClPh SO _Two Single bond unit 27 1-2908 unit 59 3,4-diClPh SO _Two Single bond unit 28 1-2909 unit 59 3,4-diClPh SO _Two Single bond unit 29 1-2910 unit 59 3,4-diClPh SO _Two Single bond unit 30 1-2911 unit 59 3,4-diClPh SO _Two Single bond unit 31 1-2912 unit 59 3,4-diClPh SO _Two Single bond device 32 1-2913 device 60 3,4-diClPh SO _Two Single bond device 1 1-2914 device 60 3,4-diClPh SO _Two Single bond device 2 1-2915 device 60 3,4-diClPh SO _Two Single bond device 3 1-2916 device 60 3,4-diClPh SO _Two Single bond device 4 1-2917 device 60 3,4-diClPh SO _Two Single bond device 5 1-2918 device 60 3,4-diClPh SO _Two Single bond device 6 1-2920 device 60 3,4-diClPh SO _Two Single bond device 8 1-2921 device 60 3,4-diClPh SO _Two Single bond device 9 1-2922 device 60 3,4-diClPh SO _Two Single bond device 10 1-2923 device 60 3,4-diClPh SO _Two Single bond unit 11 1-2924 unit 60 3,4-diClPh SO _Two Single bond unit 12 1-2925 unit 60 3,4-diClPh SO _Two Single bond unit 13 1-2926 unit 60 3,4-diClPh SO _Two Single bond Unit 14 1-2927 Unit 60 3,4-diClPh SO _Two Single bond unit 15 1-2928 unit 60 3,4-diClPh SO _Two Single bond device 16 1-2929 device 60 3,4-diClPh SO _Two Single bond unit 17 1-2930 unit 60 3,4-diClPh SO _Two Single bond unit 18 1-2931 unit 60 3,4-diClPh SO _Two Single bond unit 19 1-2932 unit 60 3,4-diClPh SO _Two Single bond device 20 1-2933 device 60 3,4-diClPh SO _Two Single bond unit 21 1-2934 unit 60 3,4-diClPh SO _Two Single bond unit 22 1-2935 unit 60 3,4-diClPh SO _Two Single bond device 23 1-2936 device 60 3,4-diClPh SO _Two Single bond unit 24 1-2937 unit 60 3,4-diClPh SO _Two Single bond unit 25 1-2938 unit 60 3,4-diClPh SO _Two Single bond unit 26 1-2939 unit 60 3,4-diClPh SO _Two Single bond unit 27 1-2940 unit 60 3,4-diClPh SO _Two Single bond unit 28 1-2941 unit 60 3,4-diClPh SO _Two Single bond unit 29 1-2942 unit 60 3,4-diClPh SO _Two Single bond device 30 1-2943 device 60 3,4-diClPh SO _Two Single bond unit 31 1-2944 unit 60 3,4-diClPh SO _Two Single bond unit 32 1-2945 unit 61 3,4-diClPh SO _Two Single bond device 1 1-2946 device 61 3,4-diClPh SO _Two Single bond unit 2 1-2947 unit 61 3,4-diClPh SO _Two Single bond device 3 1-2949 device 61 3,4-diClPh SO _Two Single bond device 5 1-2950 device 61 3,4-diClPh SO _Two Single bond device 6 1-2951 device 61 3,4-diClPh SO _Two Single bond device 7 1-2952 device 61 3,4-diClPh SO _Two Single bond device 8 1-2953 device 61 3,4-diClPh SO _Two Single bond unit 9 1-2954 unit 61 3,4-diClPh SO _Two Single bond device 10 1-2955 device 61 3,4-diClPh SO _Two Single bond unit 11 1-2956 unit 61 3,4-diClPh SO _Two Single bond unit 12 1-2957 unit 61 3,4-diClPh SO _Two Single bond unit 13 1-2958 unit 61 3,4-diClPh SO _Two Single bond unit 14 1-2959 unit 61 3,4-diClPh SO _Two Single bond unit 15 1-2960 unit 61 3,4-diClPh SO _Two Single bond unit 16 1-2961 unit 61 3,4-diClPh SO _Two Single bond Unit 17 1-2962 Unit 61 3,4-diClPh SO _Two Single bond unit 18 1-2963 unit 61 3,4-diClPh SO _Two Single bond unit 19 1-2964 unit 61 3,4-diClPh SO _Two Single bond device 20 1-2965 device 61 3,4-diClPh SO _Two Single bond unit 21 1-2966 unit 61 3,4-diClPh SO _Two Single bond unit 22 1-2976 unit 61 3,4-diClPh SO _Two Single bond unit 23 1-2968 unit 61 3,4-diClPh SO _Two Single bond unit 24 1-2969 unit 61 3,4-diClPh SO _Two Single bond unit 25 1-2970 unit 61 3,4-diClPh SO _Two Single bond unit 26 1-2971 unit 61 3,4-diClPh SO _Two Single bond unit 27 1-2972 unit 61 3,4-diClPh SO _Two Single bond unit 28 1-2973 unit 61 3,4-diClPh SO _Two Single bond unit 29 1-2974 unit 61 3,4-diClPh SO _Two Single bond device 30 1-2975 device 61 3,4-diClPh SO _Two Single bond unit 31 1-2976 unit 61 3,4-diClPh SO _Two Single bond unit 32 1-2977 unit 33 3,4-diClPh SO _Two CH _Two Unit 1 1-2978 Unit 33 3,4-diClPh SO _Two CH _Two Device 2 1-2979 Device 33 3,4-diClPh SO _Two CH _Two Unit 3 1-2980 Unit 33 3,4-diClPh SO _Two CH _Two Unit 4 1-2981 Unit 33 3,4-diClPh SO _Two CH _Two Device 5 1-2982 Device 33 3,4-diClPh SO _Two CH _Two Unit 6 1-2983 Unit 33 3,4-diClPh SO _Two CH _Two Unit 7 1-2984 Unit 33 3,4-diClPh SO _Two CH _Two Unit 8 1-2985 Unit 33 3,4-diClPh SO _Two CH _Two Set 9 1-2986 Set 33 3,4-diClPh SO _Two CH _Two Unit 10 1-2978 Unit 33 3,4-diClPh SO _Two CH _Two Unit 11 1-2988 Unit 33 3,4-diClPh SO _Two CH _Two Unit 12 1-2899 Unit 33 3,4-diClPh SO _Two CH _Two Unit 13 1-2990 Unit 33 3,4-diClPh SO _Two CH _Two Unit 14 1-2991 Unit 33 3,4-diClPh SO _Two CH _Two Unit 15 1-2992 Unit 33 3,4-diClPh SO _Two CH _Two Unit 16 1-2993 Unit 33 3,4-diClPh SO _Two CH _Two Unit 17 1-2994 Unit 33 3,4-diClPh SO _Two CH _Two Device 18 1-2995 Device 33 3,4-diClPh SO _Two CH _Two Unit 19 1-2996 Unit 33 3,4-diClPh SO _Two CH _Two Unit 20 1-2997 Unit 33 3,4-diClPh SO _Two CH _Two Unit 21 1-2998 Unit 33 3,4-diClPh SO _Two CH _Two Unit 22 1-2999 Unit 33 3,4-diClPh SO _Two CH _Two Set 23 1-3000 Set 33 3,4-diClPh SO _Two CH _Two Unit 24 1-3001 Unit 33 3,4-diClPh SO _Two CH _Two Unit 25 1-3002 Unit 33 3,4-diClPh SO _Two CH _Two Device 26 1-3003 Device 33 3,4-diClPh SO _Two CH _Two Unit 27 1-3004 Unit 33 3,4-diClPh SO _Two CH _Two Unit 28 1-3005 Unit 33 3,4-diClPh SO _Two CH _Two Unit 29 1-3006 Unit 33 3,4-diClPh SO _Two CH _Two Set 30 1-307 Set 33 3,4-diClPh SO _Two CH _Two Device 31 1-3008 Device 33 3,4-diClPh SO _Two CH _Two Device 32 1-3099 device 33 3,4-diClPh SO _Two CH = CH unit 1 1-3010 unit 33 3,4-diClPh SO _Two CH = CH unit 2 1-3011 unit 33 3,4-diClPh SO _Two CH = CH unit 3 1-3012 unit 33 3,4-diClPh SO _Two CH = CH unit 4 1-3013 unit 33 3,4-diClPh SO _Two CH = CH unit 5 1-3014 unit 33 3,4-diClPh SO _Two CH = CH unit 6 1-3015 unit 33 3,4-diClPh SO _Two CH = CH Place 7 1-3016 Place 33 3,4-diClPh SO _Two CH = CH unit 8 1-3017 unit 33 3,4-diClPh SO _Two CH = CH Place 9 1-3018 Place 33 3,4-diClPh SO _Two CH = CH device 10 1-3019 device 33 3,4-diClPh SO _Two CH = CH unit 11 1-3020 unit 33 3,4-diClPh SO _Two CH = CH unit 12 1-3021 unit 33 3,4-diClPh SO _Two CH = CH unit 13 1-3022 unit 33 3,4-diClPh SO _Two CH = CH unit 14 1-3023 unit 33 3,4-diClPh SO _Two CH = CH unit 15 1-3024 unit 33 3,4-diClPh SO _Two CH = CH unit 16 1-3025 unit 33 3,4-diClPh SO _Two CH = CH unit 17 1-3026 unit 33 3,4-diClPh SO _Two CH = CH unit 18 1-3027 unit 33 3,4-diClPh SO _Two CH = CH unit 19 1-3028 unit 33 3,4-diClPh SO _Two CH = CH unit 20 1-3029 unit 33 3,4-diClPh SO _Two CH = CH unit 21 1-3030 unit 33 3,4-diClPh SO _Two CH = CH unit 22 1-3031 unit 33 3,4-diClPh SO _Two CH = CH unit 23 1-3032 unit 33 3,4-diClPh SO _Two CH = CH unit 24 1-3033 unit 33 3,4-diClPh SO _Two CH = CH unit 25 1-3034 unit 33 3,4-diClPh SO _Two CH = CH unit 26 1-3035 unit 33 3,4-diClPh SO _Two CH = CH unit 27 1-3036 unit 33 3,4-diClPh SO _Two CH = CH unit 28 1-3037 unit 33 3,4-diClPh SO _Two CH = CH unit 29 1-3038 unit 33 3,4-diClPh SO _Two CH = CH unit 30 1-3039 unit 33 3,4-diClPh SO _Two CH = CH unit 31 1-3040 unit 33 3,4-diClPh SO _Two CH = CH unit 32 1-3041 unit 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 1 1-3042 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Device 2 1-3043 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 3 1-3044 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 4 1-3045 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Device 5 1-3046 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Device 6 1-3047 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 7 1-3048 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 8 1-3049 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Set 9 1-3050 Set 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 10 1-3051 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Set 11 1-3052 Set 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 12 1-3053 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 13 1-3054 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 14 1-3055 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 15 1-3056 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 16 1-3057 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Device 17 1-3058 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Device 18 1-3059 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 19 1-3060 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Device 20 1-3061 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Set 21 1-306 Set 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 22 1-306 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Device 23 1-3064 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 24 1-3065 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two 25 2566 3 33 3,4-diClPh SO _Two CH _Two CH _Two App. 26 1-3067 App. 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 27 1-3068 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Device 28 1-3069 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 29 1-3070 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two Device 30 1-3071 Device 33 3,4-diClPh SO _Two CH _Two CH _Two Unit 31 1-3072 Unit 33 3,4-diClPh SO _Two CH _Two CH _Two 32 ──────────────────────────────────── Compound number R ¹ R ^Two ABZ ──────────────────────────────────── 1-3073 Place 33 3,4-diClPh CO CH _Two Unit 1 1-3074 Unit 33 3,4-diClPh CO CH _Two Unit 2 1-3075 Unit 33 3,4-diClPh CO CH _Two Unit 3 1-3076 Unit 33 3,4-diClPh CO CH _Two Unit 4 1-3077 Unit 33 3,4-diClPh CO CH _Two Device 5 1-3078 Device 33 3,4-diClPh CO CH _Two Unit 6 1-3079 Unit 33 3,4-diClPh CO CH _Two Unit 7 1-3080 Unit 33 3,4-diClPh CO CH _Two Unit 8 1-3081 Unit 33 3,4-diClPh CO CH _Two Unit 9 1-3082 Unit 33 3,4-diClPh CO CH _Two Device 10 1-3083 Device 33 3,4-diClPh CO CH _Two Unit 11 1-3084 Unit 33 3,4-diClPh CO CH _Two Unit 12 1-3085 Unit 33 3,4-diClPh CO CH _Two Unit 13 1-3086 Unit 33 3,4-diClPh CO CH _Two Unit 14 1-3087 Unit 33 3,4-diClPh CO CH _Two Unit 15 1-3088 Unit 33 3,4-diClPh CO CH _Two Unit 16 1-3089 Unit 33 3,4-diClPh CO CH _Two Unit 17 1-3090 Unit 33 3,4-diClPh CO CH _Two Unit 18 1-3091 Unit 33 3,4-diClPh CO CH _Two Unit 19 1-3092 Unit 33 3,4-diClPh CO CH _Two Device 20 1-3093 Device 33 3,4-diClPh CO CH _Two Unit 21 1-3094 Unit 33 3,4-diClPh CO CH _Two Unit 22 1-3095 Unit 33 3,4-diClPh CO CH _Two Device 23 1-3096 Device 33 3,4-diClPh CO CH _Two Unit 24 1-3097 Unit 33 3,4-diClPh CO CH _Two 25 25-3098 33 33,4-diClPh CO CH _Two Unit 26 1-3099 Unit 33 3,4-diClPh CO CH _Two Unit 27 1-3100 Unit 33 3,4-diClPh CO CH _Two Device 28 1-3101 Device 33 3,4-diClPh CO CH _Two Device 29 1-3102 Device 33 3,4-diClPh CO CH _Two Device 30 1-3103 Device 33 3,4-diClPh CO CH _Two Device 31 1-3104 Device 33 3,4-diClPh CO CH _Two Device 32 1-3105 Device 34 3,4-diClPh CO CH _Two Unit 1 1-3106 Unit 34 3,4-diClPh CO CH _Two Unit 2 1-3107 Unit 34 3,4-diClPh CO CH _Two Unit 3 1-3108 Unit 34 3,4-diClPh CO CH _Two Unit 4 1-3109 Unit 34 3,4-diClPh CO CH _Two Unit 5 1-3110 Unit 34 3,4-diClPh CO CH _Two Unit 6 1-3111 Unit 34 3,4-diClPh CO CH _Two Unit 7 1-3112 Unit 34 3,4-diClPh CO CH _Two Unit 8 1-3113 Unit 34 3,4-diClPh CO CH _Two Unit 9 1-3114 Unit 34 3,4-diClPh CO CH _Two Unit 10 1-3115 Unit 34 3,4-diClPh CO CH _Two Unit 11 1-3116 Unit 34 3,4-diClPh CO CH _Two Unit 12 1-3117 Unit 34 3,4-diClPh CO CH _Two Unit 13 1-3118 Unit 34 3,4-diClPh CO CH _Two Unit 14 1-3119 Unit 34 3,4-diClPh CO CH _Two Unit 15 1-3120 Unit 34 3,4-diClPh CO CH _Two Unit 16 1-3121 Unit 34 3,4-diClPh CO CH _Two Unit 17 1-3122 Unit 34 3,4-diClPh CO CH _Two Unit 18 1-3123 Unit 34 3,4-diClPh CO CH _Two Unit 19 1-3124 Unit 34 3,4-diClPh CO CH _Two Unit 20 1-3125 Unit 34 3,4-diClPh CO CH _Two Unit 21 1-3126 Unit 34 3,4-diClPh CO CH _Two Unit 22 1-3127 Unit 34 3,4-diClPh CO CH _Two Unit 23 1-3128 Unit 34 3,4-diClPh CO CH _Two Unit 24 1-3129 Unit 34 3,4-diClPh CO CH _Two Unit 25 1-3130 Unit 34 3,4-diClPh CO CH _Two Unit 26 1-3131 Unit 34 3,4-diClPh CO CH _Two Unit 27 1-3132 Unit 34 3,4-diClPh CO CH _Two Unit 28 1-3133 Unit 34 3,4-diClPh CO CH _Two Unit 29 1-3134 Unit 34 3,4-diClPh CO CH _Two Unit 30 1-3135 Unit 34 3,4-diClPh CO CH _Two Unit 31 1-3136 Unit 34 3,4-diClPh CO CH _Two Device 32 1-3137 Device 35 3,4-diClPh CO CH _Two Unit 1 1-3138 Unit 35 3,4-diClPh CO CH _Two Device 2 1-3139 Device 35 3,4-diClPh CO CH _Two Unit 3 1-3140 Unit 35 3,4-diClPh CO CH _Two Unit 4 1-3314 Unit 35 3,4-diClPh CO CH _Two Unit 5 1-3142 Unit 35 3,4-diClPh CO CH _Two Unit 6 1-3143 Unit 35 3,4-diClPh CO CH _Two Unit 7 1-3144 Unit 35 3,4-diClPh CO CH _Two Unit 8 1-3145 Unit 35 3,4-diClPh CO CH _Two Set 9 1-3146 Set 35 3,4-diClPh CO CH _Two Unit 10 1-3147 Unit 35 3,4-diClPh CO CH _Two Unit 11 1-3148 Unit 35 3,4-diClPh CO CH _Two Unit 12 1-3149 Unit 35 3,4-diClPh CO CH _Two Unit 13 1-3150 Unit 35 3,4-diClPh CO CH _Two Unit 14 1-3151 Unit 35 3,4-diClPh CO CH _Two Unit 15 1-3152 Unit 35 3,4-diClPh CO CH _Two Unit 16 1-3153 Unit 35 3,4-diClPh CO CH _Two Unit 17 1-3154 Unit 35 3,4-diClPh CO CH _Two Unit 18 1-3155 Unit 35 3,4-diClPh CO CH _Two App. 19 1-3156 App. 35 3,4-diClPh CO CH _Two Unit 20 1-3157 Unit 35 3,4-diClPh CO CH _Two Unit 21 1-3158 Unit 35 3,4-diClPh CO CH _Two Unit 22 1-3159 Unit 35 3,4-diClPh CO CH _Two Device 23 1-3160 Device 35 3,4-diClPh CO CH _Two Unit 24 1-3316 Unit 35 3,4-diClPh CO CH _Two Unit 25 1-3162 Unit 35 3,4-diClPh CO CH _Two Unit 26 1-3163 Unit 35 3,4-diClPh CO CH _Two Unit 27 1-3164 Unit 35 3,4-diClPh CO CH _Two Unit 28 1-3165 Unit 35 3,4-diClPh CO CH _Two Unit 29 1-3166 Unit 35 3,4-diClPh CO CH _Two Unit 30 1-3167 Unit 35 3,4-diClPh CO CH _Two Unit 31 1-3168 Unit 35 3,4-diClPh CO CH _Two Device 32 1-3169 Device 36 3,4-diClPh CO CH _Two Unit 1 1-3170 Unit 36 3,4-diClPh CO CH _Two Unit 2 1-3171 Unit 36 3,4-diClPh CO CH _Two Unit 3 1-3172 Unit 36 3,4-diClPh CO CH _Two Unit 4 1-3173 Unit 36 3,4-diClPh CO CH _Two Unit 5 1-3174 Unit 36 3,4-diClPh CO CH _Two Unit 6 1-3175 Unit 36 3,4-diClPh CO CH _Two Unit 7 1-3176 Unit 36 3,4-diClPh CO CH _Two Unit 8 1-3177 Unit 36 3,4-diClPh CO CH _Two Unit 9 1-3178 Unit 36 3,4-diClPh CO CH _Two Unit 10 1-3179 Unit 36 3,4-diClPh CO CH _Two Unit 11 1-3180 Unit 36 3,4-diClPh CO CH _Two Unit 12 1-3181 Unit 36 3,4-diClPh CO CH _Two Unit 13 1-3182 Unit 36 3,4-diClPh CO CH _Two Unit 14 1-3183 Unit 36 3,4-diClPh CO CH _Two Unit 15 1-3184 Unit 36 3,4-diClPh CO CH _Two Unit 16 1-3185 Unit 36 3,4-diClPh CO CH _Two Unit 17 1-3186 Unit 36 3,4-diClPh CO CH _Two Unit 18 1-3187 Unit 36 3,4-diClPh CO CH _Two App. 19 1-3188 App. 36 3,4-diClPh CO CH _Two Unit 20 1-3189 Unit 36 3,4-diClPh CO CH _Two Unit 21 1-3190 Unit 36 3,4-diClPh CO CH _Two Unit 22 1-3191 Unit 36 3,4-diClPh CO CH _Two Device 23 1-3192 Device 36 3,4-diClPh CO CH _Two Unit 24 1-3193 Unit 36 3,4-diClPh CO CH _Two Unit 25 1-3194 Unit 36 3,4-diClPh CO CH _Two Unit 26 1-3195 Unit 36 3,4-diClPh CO CH _Two Unit 27 1-3196 Unit 36 3,4-diClPh CO CH _Two Unit 28 1-3197 Unit 36 3,4-diClPh CO CH _Two Unit 29 1-3198 Unit 36 3,4-diClPh CO CH _Two Unit 30 1-3199 Unit 36 3,4-diClPh CO CH _Two Device 31 1-3200 Device 36 3,4-diClPh CO CH _Two Device 32 1-3201 Device 37 3,4-diClPh CO CH _Two Place 1 1-3202 Place 37 3,4-diClPh CO CH _Two Place 2 1-3203 Place 37 3,4-diClPh CO CH _Two Unit 3 1-3204 Unit 37 3,4-diClPh CO CH _Two Unit 4 1-3205 Unit 37 3,4-diClPh CO CH _Two Unit 5 1-3206 Unit 37 3,4-diClPh CO CH _Two Unit 6 1-3207 Unit 37 3,4-diClPh CO CH _Two Unit 7 1-3208 Unit 37 3,4-diClPh CO CH _Two Unit 8 1-3209 Unit 37 3,4-diClPh CO CH _Two Set 9 1-3210 Set 37 3,4-diClPh CO CH _Two Unit 10 1-321 Unit 37 3,4-diClPh CO CH _Two Unit 11 1-312 Unit 37 3,4-diClPh CO CH _Two Unit 12 1-3213 Unit 37 3,4-diClPh CO CH _Two Unit 13 1-3214 Unit 37 3,4-diClPh CO CH _Two Unit 14 1-3215 Unit 37 3,4-diClPh CO CH _Two Unit 15 1-3216 Unit 37 3,4-diClPh CO CH _Two Unit 16 1-3217 Unit 37 3,4-diClPh CO CH _Two Unit 17 1-3218 Unit 37 3,4-diClPh CO CH _Two Unit 18 1-3219 Unit 37 3,4-diClPh CO CH _Two Unit 19 1-3220 Unit 37 3,4-diClPh CO CH _Two Unit 20 1-3221 Unit 37 3,4-diClPh CO CH _Two Unit 21 1-3222 Unit 37 3,4-diClPh CO CH _Two Set 22 1-3223 Set 37 3,4-diClPh CO CH _Two Device 23 1-3224 Device 37 3,4-diClPh CO CH _Two Unit 24 1-3225 Unit 37 3,4-diClPh CO CH _Two Unit 25 1-3226 Unit 37 3,4-diClPh CO CH _Two Set 26 1-3227 Set 37 3,4-diClPh CO CH _Two Set 27 1-3228 Set 37 3,4-diClPh CO CH _Two Set 28 1-3229 Set 37 3,4-diClPh CO CH _Two Device 29 1-3230 Device 37 3,4-diClPh CO CH _Two Equipment 30 1-3231 Equipment 37 3,4-diClPh CO CH _Two Set 31 1-3232 Set 37 3,4-diClPh CO CH _Two Device 32 1-3233 Device 38 3,4-diClPh CO CH _Two Place 1 1-3234 Place 38 3,4-diClPh CO CH _Two Unit 2 1-3235 Unit 38 3,4-diClPh CO CH _Two Set 3 1-3236 Set 38 3,4-diClPh CO CH _Two Unit 4 1-3237 Unit 38 3,4-diClPh CO CH _Two Unit 5 1-3238 Unit 38 3,4-diClPh CO CH _Two Set 6 1-3239 Set 38 3,4-diClPh CO CH _Two Unit 7 1-3240 Unit 38 3,4-diClPh CO CH _Two Unit 8 1-3241 Unit 38 3,4-diClPh CO CH _Two Unit 9 1-3242 Unit 38 3,4-diClPh CO CH _Two Unit 10 1-3243 Unit 38 3,4-diClPh CO CH _Two Unit 11 1-3244 Unit 38 3,4-diClPh CO CH _Two Unit 12 1-3245 Unit 38 3,4-diClPh CO CH _Two Unit 13 1-3246 Unit 38 3,4-diClPh CO CH _Two Unit 14 1-3247 Unit 38 3,4-diClPh CO CH _Two Unit 15 1-3248 Unit 38 3,4-diClPh CO CH _Two Unit 16 1-3249 Unit 38 3,4-diClPh CO CH _Two Unit 17 1-3250 Unit 38 3,4-diClPh CO CH _Two Unit 18 1-3251 Unit 38 3,4-diClPh CO CH _Two Unit 19 1-3252 Unit 38 3,4-diClPh CO CH _Two Unit 20 1-3253 Unit 38 3,4-diClPh CO CH _Two Unit 21 1-3254 Unit 38 3,4-diClPh CO CH _Two Unit 22 1-3255 Unit 38 3,4-diClPh CO CH _Two Unit 23 1-3256 Unit 38 3,4-diClPh CO CH _Two Unit 24 1-3257 Unit 38 3,4-diClPh CO CH _Two Unit 25 1-3258 Unit 38 3,4-diClPh CO CH _Two Unit 26 1-3259 Unit 38 3,4-diClPh CO CH _Two Unit 27 1-3260 Unit 38 3,4-diClPh CO CH _Two Unit 28 1-3261 Unit 38 3,4-diClPh CO CH _Two Unit 29 1-3262 Unit 38 3,4-diClPh CO CH _Two Unit 30 1-3263 Unit 38 3,4-diClPh CO CH _Two Unit 31 1-3264 Unit 38 3,4-diClPh CO CH _Two Device 32 1-3265 Device 39 3,4-diClPh CO CH _Two Place 1 1-3266 Place 39 3,4-diClPh CO CH _Two App.2 1-3267 App.39 3,4-diClPh CO CH _Two Unit 3 1-3268 Unit 39 3,4-diClPh CO CH _Two Unit 4 1-3269 Unit 39 3,4-diClPh CO CH _Two Device 5 1-3270 Device 39 3,4-diClPh CO CH _Two Unit 6 1-3271 Unit 39 3,4-diClPh CO CH _Two Unit 7 1-3272 Unit 39 3,4-diClPh CO CH _Two Unit 8 1-3273 Unit 39 3,4-diClPh CO CH _Two Set 9 1-3274 Set 39 3,4-diClPh CO CH _Two Device 10 1-3275 Device 39 3,4-diClPh CO CH _Two Unit 11 1-3276 Unit 39 3,4-diClPh CO CH _Two Unit 12 1-3277 Unit 39 3,4-diClPh CO CH _Two Unit 13 1-3278 Unit 39 3,4-diClPh CO CH _Two Unit 14 1-3279 Unit 39 3,4-diClPh CO CH _Two Unit 15 1-3280 Unit 39 3,4-diClPh CO CH _Two Unit 16 1-3281 Unit 39 3,4-diClPh CO CH _Two Unit 17 1-3282 Unit 39 3,4-diClPh CO CH _Two Unit 18 1-3283 Unit 39 3,4-diClPh CO CH _Two Unit 19 1-3284 Unit 39 3,4-diClPh CO CH _Two Unit 20 1-3285 Unit 39 3,4-diClPh CO CH _Two Unit 21 1-3286 Unit 39 3,4-diClPh CO CH _Two Unit 22 1-3287 Unit 39 3,4-diClPh CO CH _Two Device 23 1-3288 Device 39 3,4-diClPh CO CH _Two Unit 24 1-3289 Unit 39 3,4-diClPh CO CH _Two Unit 25 1-3290 Unit 39 3,4-diClPh CO CH _Two Unit 26 1-3129 Unit 39 3,4-diClPh CO CH _Two Unit 27 1-3292 Unit 39 3,4-diClPh CO CH _Two 28- 1293 3 39 3,4-diClPh CO CH _Two Unit 29 1-3294 Unit 39 3,4-diClPh CO CH _Two Device 30 1-3295 Device 39 3,4-diClPh CO CH _Two Device 31 1-3296 Device 39 3,4-diClPh CO CH _Two Device 32 1-3297 Device 40 3,4-diClPh CO CH _Two Unit 1 1-3298 Unit 40 3,4-diClPh CO CH _Two Device 2 1-3299 Device 40 3,4-diClPh CO CH _Two Unit 3 1-3300 Unit 40 3,4-diClPh CO CH _Two Device 4 1-3301 Device 40 3,4-diClPh CO CH _Two Device 5 1-3302 Device 40 3,4-diClPh CO CH _Two Device 6 1-3303 Device 40 3,4-diClPh CO CH _Two Unit 7 1-3304 Unit 40 3,4-diClPh CO CH _Two Unit 8 1-3305 Unit 40 3,4-diClPh CO CH _Two Device 9 1-3306 Device 40 3,4-diClPh CO CH _Two Device 10 1-3307 Device 40 3,4-diClPh CO CH _Two Device 11 1-3308 Device 40 3,4-diClPh CO CH _Two Unit 12 1-3309 Unit 40 3,4-diClPh CO CH _Two Unit 13 1-333 Unit 40 3,4-diClPh CO CH _Two Device 14 1-33311 Device 40 3,4-diClPh CO CH _Two Unit 15 1-333 Unit 40 3,4-diClPh CO CH _Two Device 16 1-3313 Device 40 3,4-diClPh CO CH _Two Unit 17 1-3314 Unit 40 3,4-diClPh CO CH _Two Unit 18 1-3315 Unit 40 3,4-diClPh CO CH _Two Unit 19 1-3316 Unit 40 3,4-diClPh CO CH _Two Device 20 1-3317 Device 40 3,4-diClPh CO CH _Two Device 21 1-3318 Device 40 3,4-diClPh CO CH _Two Unit 22 1-3319 Unit 40 3,4-diClPh CO CH _Two Device 23 1-3320 Device 40 3,4-diClPh CO CH _Two Unit 24 1-3321 Unit 40 3,4-diClPh CO CH _Two Unit 25 1-3322 Unit 40 3,4-diClPh CO CH _Two Device 26 1-3323 Device 40 3,4-diClPh CO CH _Two Unit 27 1-3324 Unit 40 3,4-diClPh CO CH _Two Device 28 1-3325 Device 40 3,4-diClPh CO CH _Two Device 29 1-3326 Device 40 3,4-diClPh CO CH _Two Device 30 1-3327 Device 40 3,4-diClPh CO CH _Two Unit 31 1-3328 Unit 40 3,4-diClPh CO CH _Two Device 32 1-3329 Device 41 3,4-diClPh CO CH _Two Unit 1 1-3330 Unit 41 3,4-diClPh CO CH _Two Unit 2 1-3331 Unit 41 3,4-diClPh CO CH _Two Unit 3 1-3332 Unit 41 3,4-diClPh CO CH _Two Unit 4 1-3333 Unit 41 3,4-diClPh CO CH _Two Device 5 1-3334 Device 41 3,4-diClPh CO CH _Two Unit 6 1-3335 Unit 41 3,4-diClPh CO CH _Two Unit 7 1-3336 Unit 41 3,4-diClPh CO CH _Two Unit 8 1-3337 Unit 41 3,4-diClPh CO CH _Two Unit 9 1-3338 Unit 41 3,4-diClPh CO CH _Two Unit 10 1-3339 Unit 41 3,4-diClPh CO CH _Two Unit 11 1-3340 Unit 41 3,4-diClPh CO CH _Two Unit 12 1-3341 Unit 41 3,4-diClPh CO CH _Two Unit 13 1-3342 Unit 41 3,4-diClPh CO CH _Two Unit 14 1-3343 Unit 41 3,4-diClPh CO CH _Two Unit 15 1-3344 Unit 41 3,4-diClPh CO CH _Two Unit 16 1-3345 Unit 41 3,4-diClPh CO CH _Two Unit 17 1-3346 Unit 41 3,4-diClPh CO CH _Two Unit 18 1-3347 Unit 41 3,4-diClPh CO CH _Two Unit 19 1-3348 Unit 41 3,4-diClPh CO CH _Two Unit 20 1-3349 Unit 41 3,4-diClPh CO CH _Two Unit 21 1-3350 Unit 41 3,4-diClPh CO CH _Two Unit 22 1-3351 Unit 41 3,4-diClPh CO CH _Two Unit 23 1-3352 Unit 41 3,4-diClPh CO CH _Two Unit 24 1-3353 Unit 41 3,4-diClPh CO CH _Two Unit 25 1-3354 Unit 41 3,4-diClPh CO CH _Two Unit 26 1-3355 Unit 41 3,4-diClPh CO CH _Two Unit 27 1-3356 Unit 41 3,4-diClPh CO CH _Two Unit 28 1-3357 Unit 41 3,4-diClPh CO CH _Two Unit 29 1-3358 Unit 41 3,4-diClPh CO CH _Two Unit 30 1-3359 Unit 41 3,4-diClPh CO CH _Two Unit 31 1-3360 Unit 41 3,4-diClPh CO CH _Two Unit 32 1-3361 Unit 42 3,4-diClPh CO CH _Two Unit 1 1-3336 Unit 42 3,4-diClPh CO CH _Two Unit 2 1-3336 Unit 42 3,4-diClPh CO CH _Two Unit 3 1-3364 Unit 42 3,4-diClPh CO CH _Two Unit 4 1-3365 Unit 42 3,4-diClPh CO CH _Two Unit 5 1-3366 Unit 42 3,4-diClPh CO CH _Two Unit 6 1-333 Unit 42 3,4-diClPh CO CH _Two Unit 7 1-3368 Unit 42 3,4-diClPh CO CH _Two Unit 8 1-3369 Unit 42 3,4-diClPh CO CH _Two Set 9 1-3370 Set 42 3,4-diClPh CO CH _Two Unit 10 1-3371 Unit 42 3,4-diClPh CO CH _Two Unit 11 1-3372 Unit 42 3,4-diClPh CO CH _Two Unit 12 1-3373 Unit 42 3,4-diClPh CO CH _Two Unit 13 1-3374 Unit 42 3,4-diClPh CO CH _Two Unit 14 1-3375 Unit 42 3,4-diClPh CO CH _Two Unit 15 1-3376 Unit 42 3,4-diClPh CO CH _Two Unit 16 1-3377 Unit 42 3,4-diClPh CO CH _Two Unit 17 1-3378 Unit 42 3,4-diClPh CO CH _Two Unit 18 1-3379 Unit 42 3,4-diClPh CO CH _Two Unit 19 1-3380 Unit 42 3,4-diClPh CO CH _Two Unit 20 1-3381 Unit 42 3,4-diClPh CO CH _Two Unit 21 1-3382 Unit 42 3,4-diClPh CO CH _Two Unit 22 1-3383 Unit 42 3,4-diClPh CO CH _Two Unit 23 1-3384 Unit 42 3,4-diClPh CO CH _Two Unit 24 1-3385 Unit 42 3,4-diClPh CO CH _Two Unit 25 1-3386 Unit 42 3,4-diClPh CO CH _Two Unit 26 1-3338 Unit 42 3,4-diClPh CO CH _Two Unit 27 1-3388 Unit 42 3,4-diClPh CO CH _Two Unit 28 1-3389 Unit 42 3,4-diClPh CO CH _Two Unit 29 1-3390 Unit 42 3,4-diClPh CO CH _Two Device 30 1-3391 Device 42 3,4-diClPh CO CH _Two Unit 31 1-3392 Unit 42 3,4-diClPh CO CH _Two Device 32 1-3393 device 43 3,4-diClPh CO CH _Two Unit 1 1-3394 Unit 43 3,4-diClPh CO CH _Two Unit 2 1-3395 Unit 43 3,4-diClPh CO CH _Two Unit 3 1-3396 Unit 43 3,4-diClPh CO CH _Two Unit 4 1-33397 Unit 43 3,4-diClPh CO CH _Two Unit 5 1-3398 Unit 43 3,4-diClPh CO CH _Two Unit 6 1-3399 Unit 43 3,4-diClPh CO CH _Two Unit 7 1-3400 Unit 43 3,4-diClPh CO CH _Two Unit 8 1-3401 Unit 43 3,4-diClPh CO CH _Two Unit 9 1-3402 Unit 43 3,4-diClPh CO CH _Two Unit 10 1-3403 Unit 43 3,4-diClPh CO CH _Two Unit 11 1-3404 Unit 43 3,4-diClPh CO CH _Two Unit 12 1-3405 Unit 43 3,4-diClPh CO CH _Two Unit 13 1-3406 Unit 43 3,4-diClPh CO CH _Two Unit 14 1-3407 Unit 43 3,4-diClPh CO CH _Two Unit 15 1-3408 Unit 43 3,4-diClPh CO CH _Two Unit 16 1-3409 Unit 43 3,4-diClPh CO CH _Two Unit 17 1-3410 Unit 43 3,4-diClPh CO CH _Two Unit 18 1-3341 Unit 43 3,4-diClPh CO CH _Two Unit 19 1-312 Unit 43 3,4-diClPh CO CH _Two Unit 20 1-3413 Unit 43 3,4-diClPh CO CH _Two Unit 21 1-3414 Unit 43 3,4-diClPh CO CH _Two Unit 22 1-3415 Unit 43 3,4-diClPh CO CH _Two Unit 23 1-3416 Unit 43 3,4-diClPh CO CH _Two Unit 24 1-3317 Unit 43 3,4-diClPh CO CH _Two Unit 25 1-3418 Unit 43 3,4-diClPh CO CH _Two Unit 26 1-3419 Unit 43 3,4-diClPh CO CH _Two Unit 27 1-3420 Unit 43 3,4-diClPh CO CH _Two Unit 28 1-3421 Unit 43 3,4-diClPh CO CH _Two Unit 29 1-3422 Unit 43 3,4-diClPh CO CH _Two Unit 30 1-3423 Unit 43 3,4-diClPh CO CH _Two Unit 31 1-3424 Unit 43 3,4-diClPh CO CH _Two Device 32 1-3425 Device 44 3,4-diClPh CO CH _Two Place 1 1-3426 Place 44 3,4-diClPh CO CH _Two Unit 2 1-3427 Unit 44 3,4-diClPh CO CH _Two Set 3 1-3428 Set 44 3,4-diClPh CO CH _Two Unit 4 1-3429 Unit 44 3,4-diClPh CO CH _Two Device 5 1-3430 Device 44 3,4-diClPh CO CH _Two Unit 6 1-3343 Unit 44 3,4-diClPh CO CH _Two Unit 7 1-3432 Unit 44 3,4-diClPh CO CH _Two Unit 8 1-3433 Unit 44 3,4-diClPh CO CH _Two Set 9 1-3434 Set 44 3,4-diClPh CO CH _Two Unit 10 1-3435 Unit 44 3,4-diClPh CO CH _Two Unit 11 1-3436 Unit 44 3,4-diClPh CO CH _Two Unit 12 1-334 Unit 44 3,4-diClPh CO CH _Two Unit 13 1-3438 Unit 44 3,4-diClPh CO CH _Two Set 14 1-3439 Set 44 3,4-diClPh CO CH _Two Unit 15 1-3440 Unit 44 3,4-diClPh CO CH _Two Unit 16 1-3441 Unit 44 3,4-diClPh CO CH _Two Unit 17 1-3442 Unit 44 3,4-diClPh CO CH _Two Unit 18 1-3443 Unit 44 3,4-diClPh CO CH _Two Unit 19 1-3444 Unit 44 3,4-diClPh CO CH _Two Unit 20 1-3445 Unit 44 3,4-diClPh CO CH _Two Device 21 1-3446 Device 44 3,4-diClPh CO CH _Two Device 22 1-3447 Device 44 3,4-diClPh CO CH _Two Device 23 1-3448 Device 44 3,4-diClPh CO CH _Two Unit 24 1-3449 Unit 44 3,4-diClPh CO CH _Two Unit 25 1-3450 Unit 44 3,4-diClPh CO CH _Two Unit 26 1-3451 Unit 44 3,4-diClPh CO CH _Two Unit 27 1-3452 Unit 44 3,4-diClPh CO CH _Two Unit 28 1-3453 Unit 44 3,4-diClPh CO CH _Two Unit 29 1-3454 Unit 44 3,4-diClPh CO CH _Two Unit 30 1-3455 Unit 44 3,4-diClPh CO CH _Two Unit 31 1-3456 Unit 44 3,4-diClPh CO CH _Two Unit 32 1-3457 Unit 45 3,4-diClPh CO CH _Two Unit 1 1-3458 Unit 45 3,4-diClPh CO CH _Two Unit 2 1-3459 Unit 45 3,4-diClPh CO CH _Two Unit 3 1-3460 Unit 45 3,4-diClPh CO CH _Two Unit 4 1-3461 Unit 45 3,4-diClPh CO CH _Two Unit 5 1-3462 Unit 45 3,4-diClPh CO CH _Two Unit 6 1-3463 Unit 45 3,4-diClPh CO CH _Two Unit 7 1-3346 Unit 45 3,4-diClPh CO CH _Two Unit 8 1-3465 Unit 45 3,4-diClPh CO CH _Two Unit 9 1-3466 Unit 45 3,4-diClPh CO CH _Two Unit 10 1-3467 Unit 45 3,4-diClPh CO CH _Two Unit 11 1-3468 Unit 45 3,4-diClPh CO CH _Two Unit 12 1-3469 Unit 45 3,4-diClPh CO CH _Two Unit 13 1-3470 Unit 45 3,4-diClPh CO CH _Two Unit 14 1-3471 Unit 45 3,4-diClPh CO CH _Two Unit 15 1-3472 Unit 45 3,4-diClPh CO CH _Two Unit 16 1-3473 Unit 45 3,4-diClPh CO CH _Two Unit 17 1-3474 Unit 45 3,4-diClPh CO CH _Two Unit 18 1-3475 Unit 45 3,4-diClPh CO CH _Two Unit 19 1-3476 Unit 45 3,4-diClPh CO CH _Two Unit 20 1-3347 Unit 45 3,4-diClPh CO CH _Two Unit 21 1-3478 Unit 45 3,4-diClPh CO CH _Two Unit 22 1-3479 Unit 45 3,4-diClPh CO CH _Two Unit 23 1-3480 Unit 45 3,4-diClPh CO CH _Two Unit 24 1-3481 Unit 45 3,4-diClPh CO CH _Two Unit 25 1-3482 Unit 45 3,4-diClPh CO CH _Two Unit 26 1-3483 Unit 45 3,4-diClPh CO CH _Two Unit 27 1-3484 Unit 45 3,4-diClPh CO CH _Two Unit 28 1-3485 Unit 45 3,4-diClPh CO CH _Two Unit 29 1-3486 Unit 45 3,4-diClPh CO CH _Two Unit 30 1-3487 Unit 45 3,4-diClPh CO CH _Two Unit 31 1-3488 Unit 45 3,4-diClPh CO CH _Two Device 32 1-3489 Device 46 3,4-diClPh CO CH _Two Unit 1 1-3490 Unit 46 3,4-diClPh CO CH _Two Unit 2 1-3491 Unit 46 3,4-diClPh CO CH _Two Unit 3 1-3492 Unit 46 3,4-diClPh CO CH _Two Unit 4 1-3493 Unit 46 3,4-diClPh CO CH _Two Unit 5 1-3494 Unit 46 3,4-diClPh CO CH _Two Set 6 1-3495 Set 46 3,4-diClPh CO CH _Two Unit 7 1-3496 Unit 46 3,4-diClPh CO CH _Two Unit 8 1-3497 Unit 46 3,4-diClPh CO CH _Two Set 9 1-3498 Set 46 3,4-diClPh CO CH _Two Unit 10 1-3499 Unit 46 3,4-diClPh CO CH _Two Unit 11 1-3500 Unit 46 3,4-diClPh CO CH _Two Unit 12 1-3501 Unit 46 3,4-diClPh CO CH _Two Unit 13 1-3502 Unit 46 3,4-diClPh CO CH _Two Unit 14 1-3503 Unit 46 3,4-diClPh CO CH _Two Unit 15 1-3504 Unit 46 3,4-diClPh CO CH _Two Unit 16 1-3505 Unit 46 3,4-diClPh CO CH _Two Unit 17 1-3506 Unit 46 3,4-diClPh CO CH _Two Unit 18 1-3507 Unit 46 3,4-diClPh CO CH _Two Unit 19 1-3508 Unit 46 3,4-diClPh CO CH _Two Unit 20 1-3509 Unit 46 3,4-diClPh CO CH _Two Unit 21 1-3510 Unit 46 3,4-diClPh CO CH _Two Unit 22 1-351 Unit 46 3,4-diClPh CO CH _Two Unit 23 1-351 Unit 46 3,4-diClPh CO CH _Two Unit 24 1-3513 Unit 46 3,4-diClPh CO CH _Two Unit 25 1-3514 Unit 46 3,4-diClPh CO CH _Two Unit 26 1-3515 Unit 46 3,4-diClPh CO CH _Two Unit 27 1-3516 Unit 46 3,4-diClPh CO CH _Two Unit 28 1-3517 Unit 46 3,4-diClPh CO CH _Two Unit 29 1-3518 Unit 46 3,4-diClPh CO CH _Two Unit 30 1-3519 Unit 46 3,4-diClPh CO CH _Two Unit 31 1-3520 Unit 46 3,4-diClPh CO CH _Two Device 32 1-3521 Device 47 3,4-diClPh CO CH _Two Unit 1 1-3522 Unit 47 3,4-diClPh CO CH _Two Unit 2 1-3523 Unit 47 3,4-diClPh CO CH _Two Unit 3 1-3524 Unit 47 3,4-diClPh CO CH _Two Unit 4 1-3525 Unit 47 3,4-diClPh CO CH _Two Unit 5 1-3526 Unit 47 3,4-diClPh CO CH _Two Unit 6 1-3527 Unit 47 3,4-diClPh CO CH _Two Unit 7 1-3528 Unit 47 3,4-diClPh CO CH _Two Unit 8 1-3529 Unit 47 3,4-diClPh CO CH _Two Unit 9 1-3530 Unit 47 3,4-diClPh CO CH _Two Unit 10 1-3531 Unit 47 3,4-diClPh CO CH _Two Unit 11 1-3532 Unit 47 3,4-diClPh CO CH _Two Unit 12 1-3533 Unit 47 3,4-diClPh CO CH _Two Unit 13 1-3534 Unit 47 3,4-diClPh CO CH _Two Unit 14 1-3535 Unit 47 3,4-diClPh CO CH _Two Unit 15 1-3536 Unit 47 3,4-diClPh CO CH _Two Unit 16 1-33537 Unit 47 3,4-diClPh CO CH _Two Unit 17 1-3538 Unit 47 3,4-diClPh CO CH _Two Unit 18 1-33539 Unit 47 3,4-diClPh CO CH _Two Unit 19 1-3540 Unit 47 3,4-diClPh CO CH _Two Unit 20 1-3541 Unit 47 3,4-diClPh CO CH _Two Unit 21 1-3542 Unit 47 3,4-diClPh CO CH _Two Unit 22 1-3543 Unit 47 3,4-diClPh CO CH _Two Unit 23 1-3544 Unit 47 3,4-diClPh CO CH _Two Unit 24 1-3545 Unit 47 3,4-diClPh CO CH _Two Unit 25 1-3546 Unit 47 3,4-diClPh CO CH _Two Unit 26 1-3547 Unit 47 3,4-diClPh CO CH _Two Unit 27 1-3548 Unit 47 3,4-diClPh CO CH _Two Unit 28 1-3549 Unit 47 3,4-diClPh CO CH _Two Unit 29 1-3550 Unit 47 3,4-diClPh CO CH _Two Device 30 1-3551 Device 47 3,4-diClPh CO CH _Two Unit 31 1-355 Unit 47 3,4-diClPh CO CH _Two Device 32 1-3553 device 48 3,4-diClPh CO CH _Two Unit 1 1-3554 Unit 48 3,4-diClPh CO CH _Two Unit 2 1-3555 Unit 48 3,4-diClPh CO CH _Two Unit 3 1-3556 Unit 48 3,4-diClPh CO CH _Two Unit 4 1-3557 Unit 48 3,4-diClPh CO CH _Two Unit 5 1-3558 Unit 48 3,4-diClPh CO CH _Two Unit 6 1-3559 Unit 48 3,4-diClPh CO CH _Two Unit 7 1-3560 Unit 48 3,4-diClPh CO CH _Two Unit 8 1-3561 Unit 48 3,4-diClPh CO CH _Two Unit 9 1-3562 Unit 48 3,4-diClPh CO CH _Two Unit 10 1-3563 Unit 48 3,4-diClPh CO CH _Two Unit 11 1-3564 Unit 48 3,4-diClPh CO CH _Two Unit 12 1-3565 Unit 48 3,4-diClPh CO CH _Two Unit 13 1-3566 Unit 48 3,4-diClPh CO CH _Two Unit 14 1-3567 Unit 48 3,4-diClPh CO CH _Two Unit 15 1-3568 Unit 48 3,4-diClPh CO CH _Two Unit 16 1-3569 Unit 48 3,4-diClPh CO CH _Two Unit 17 1-3570 Unit 48 3,4-diClPh CO CH _Two Unit 18 1-3571 Unit 48 3,4-diClPh CO CH _Two Unit 19 1-3572 Unit 48 3,4-diClPh CO CH _Two Unit 20 1-3573 Unit 48 3,4-diClPh CO CH _Two Unit 21 1-3574 Unit 48 3,4-diClPh CO CH _Two Unit 22 1-3575 Unit 48 3,4-diClPh CO CH _Two Unit 23 1-3576 Unit 48 3,4-diClPh CO CH _Two Unit 24 1-3577 Unit 48 3,4-diClPh CO CH _Two Unit 25 1-3578 Unit 48 3,4-diClPh CO CH _Two Unit 26 1-3579 Unit 48 3,4-diClPh CO CH _Two Unit 27 1-3580 Unit 48 3,4-diClPh CO CH _Two Unit 28 1-3581 Unit 48 3,4-diClPh CO CH _Two Unit 29 1-3582 Unit 48 3,4-diClPh CO CH _Two Device 30 1-3583 Device 48 3,4-diClPh CO CH _Two Unit 31 1-3584 Unit 48 3,4-diClPh CO CH _Two 32 ──────────────────────────────────── Compound number R ¹ R ^Two A B Z １− 1-3585 Place 49 3,4-diClPh CO CH _Two Unit 1 1-3586 Unit 49 3,4-diClPh CO CH _Two Unit 2 1-3587 Unit 49 3,4-diClPh CO CH _Two Unit 3 1-3588 Unit 49 3,4-diClPh CO CH _Two Unit 4 1-3589 Unit 49 3,4-diClPh CO CH _Two Unit 5 1-3590 Unit 49 3,4-diClPh CO CH _Two Unit 6 1-3591 Unit 49 3,4-diClPh CO CH _Two Unit 7 1-3592 Unit 49 3,4-diClPh CO CH _Two Unit 8 1-3593 Unit 49 3,4-diClPh CO CH _Two Unit 9 1-3594 Unit 49 3,4-diClPh CO CH _Two Unit 10 1-3595 Unit 49 3,4-diClPh CO CH _Two Unit 11 1-3596 Unit 49 3,4-diClPh CO CH _Two Unit 12 1-3597 Unit 49 3,4-diClPh CO CH _Two Unit 13 1-3598 Unit 49 3,4-diClPh CO CH _Two Unit 14 1-3599 Unit 49 3,4-diClPh CO CH _Two Unit 15 1-3600 Unit 49 3,4-diClPh CO CH _Two Unit 16 1-3601 Unit 49 3,4-diClPh CO CH _Two Unit 17 1-3602 Unit 49 3,4-diClPh CO CH _Two Unit 18 1-3603 Unit 49 3,4-diClPh CO CH _Two Unit 19 1-3604 Unit 49 3,4-diClPh CO CH _Two Unit 20 1-3605 Unit 49 3,4-diClPh CO CH _Two Unit 21 1-3606 Unit 49 3,4-diClPh CO CH _Two Unit 22 1-3607 Unit 49 3,4-diClPh CO CH _Two Unit 23 1-3608 Unit 49 3,4-diClPh CO CH _Two Unit 24 1-3609 Unit 49 3,4-diClPh CO CH _Two Unit 25 1-3610 Unit 49 3,4-diClPh CO CH _Two Unit 26 1-361 Unit 49 3,4-diClPh CO CH _Two Unit 27 1-3612 Unit 49 3,4-diClPh CO CH _Two Unit 28 1-3613 Unit 49 3,4-diClPh CO CH _Two Unit 29 1-3614 Unit 49 3,4-diClPh CO CH _Two Unit 30 1-3615 Unit 49 3,4-diClPh CO CH _Two Unit 31 1-3616 Unit 49 3,4-diClPh CO CH _Two Device 32 1-3617 Device 50 3,4-diClPh CO CH _Two Unit 1 1-3618 Unit 50 3,4-diClPh CO CH _Two Device 2 1-3619 Device 50 3,4-diClPh CO CH _Two Unit 3 1-3620 Unit 50 3,4-diClPh CO CH _Two Unit 4 1-3621 Unit 50 3,4-diClPh CO CH _Two Device 5 1-3622 Device 50 3,4-diClPh CO CH _Two Device 6 1-3623 Device 50 3,4-diClPh CO CH _Two Unit 7 1-3624 Unit 50 3,4-diClPh CO CH _Two Unit 8 1-3625 Unit 50 3,4-diClPh CO CH _Two Device 9 1-3626 Device 50 3,4-diClPh CO CH _Two Device 10 1-3627 Device 50 3,4-diClPh CO CH _Two Unit 11 1-3628 Unit 50 3,4-diClPh CO CH _Two Unit 12 1-3629 Unit 50 3,4-diClPh CO CH _Two Unit 13 1-3630 Unit 50 3,4-diClPh CO CH _Two Unit 14 1-3631 Unit 50 3,4-diClPh CO CH _Two Unit 15 1-3632 Unit 50 3,4-diClPh CO CH _Two Device 16 1-3633 Device 50 3,4-diClPh CO CH _Two Unit 17 1-3634 Unit 50 3,4-diClPh CO CH _Two Unit 18 1-3635 Unit 50 3,4-diClPh CO CH _Two Unit 19 1-3636 Unit 50 3,4-diClPh CO CH _Two Device 20 1-3637 Device 50 3,4-diClPh CO CH _Two Device 21 1-33638 Device 50 3,4-diClPh CO CH _Two Device 22 1-33639 Device 50 3,4-diClPh CO CH _Two Device 23 1-3640 Device 50 3,4-diClPh CO CH _Two Unit 24 1-3641 Unit 50 3,4-diClPh CO CH _Two Unit 25 1-3642 Unit 50 3,4-diClPh CO CH _Two Unit 26 1-3643 Unit 50 3,4-diClPh CO CH _Two Unit 27 1-3644 Unit 50 3,4-diClPh CO CH _Two Device 28 1-3645 Device 50 3,4-diClPh CO CH _Two Device 29 1-3646 Device 50 3,4-diClPh CO CH _Two Device 30 1-3647 Device 50 3,4-diClPh CO CH _Two Device 31 1-3648 Device 50 3,4-diClPh CO CH _Two Unit 32 1-3649 Unit 51 3,4-diClPh CO CH _Two Unit 1 1-3650 Unit 51 3,4-diClPh CO CH _Two Unit 2 1-3651 Unit 51 3,4-diClPh CO CH _Two Unit 3 1-3652 Unit 51 3,4-diClPh CO CH _Two Device 4 1-3653 Device 51 3,4-diClPh CO CH _Two Unit 5 1-3654 Unit 51 3,4-diClPh CO CH _Two Unit 6 1-3655 Unit 51 3,4-diClPh CO CH _Two Unit 7 1-3656 Unit 51 3,4-diClPh CO CH _Two Unit 8 1-3657 Unit 51 3,4-diClPh CO CH _Two Unit 9 1-3658 Unit 51 3,4-diClPh CO CH _Two Device 10 1-3659 Device 51 3,4-diClPh CO CH _Two Unit 11 1-3660 Unit 51 3,4-diClPh CO CH _Two Unit 12 1-366 Unit 51 3,4-diClPh CO CH _Two Unit 13 1-366 Unit 51 3,4-diClPh CO CH _Two Unit 14 1-3663 Unit 51 3,4-diClPh CO CH _Two Unit 15 1-3664 Unit 51 3,4-diClPh CO CH _Two Unit 16 1-3665 Unit 51 3,4-diClPh CO CH _Two Unit 17 1-3666 Unit 51 3,4-diClPh CO CH _Two Unit 18 1-367 Unit 51 3,4-diClPh CO CH _Two Unit 19 1-3668 Unit 51 3,4-diClPh CO CH _Two Device 20 1-3669 Device 51 3,4-diClPh CO CH _Two Unit 21 1-3670 Unit 51 3,4-diClPh CO CH _Two Unit 22 1-3671 Unit 51 3,4-diClPh CO CH _Two Unit 23 1-367 Unit 51 3,4-diClPh CO CH _Two Unit 24 1-367 Unit 51 3,4-diClPh CO CH _Two Unit 25 1-367 Unit 51 3,4-diClPh CO CH _Two Unit 26 1-3675 Unit 51 3,4-diClPh CO CH _Two Unit 27 1-3676 Unit 51 3,4-diClPh CO CH _Two Unit 28 1-3677 Unit 51 3,4-diClPh CO CH _Two Unit 29 1-3678 Unit 51 3,4-diClPh CO CH _Two Unit 30 1-3679 Unit 51 3,4-diClPh CO CH _Two Unit 31 1-3680 Unit 51 3,4-diClPh CO CH _Two Device 32 1-368 Device 52 3,4-diClPh CO CH _Two Place 1 1-3682 Place 52 3,4-diClPh CO CH _Two Unit 2 1-3683 Unit 52 3,4-diClPh CO CH _Two Unit 3 1-3684 Unit 52 3,4-diClPh CO CH _Two Unit 4 1-385 Unit 52 3,4-diClPh CO CH _Two Unit 5 1-3686 Unit 52 3,4-diClPh CO CH _Two Unit 6 1-3687 Unit 52 3,4-diClPh CO CH _Two Unit 7 1-3688 Unit 52 3,4-diClPh CO CH _Two Unit 8 1-3689 Unit 52 3,4-diClPh CO CH _Two Set 9 1-3690 Set 52 3,4-diClPh CO CH _Two Device 10 1-3691 Device 52 3,4-diClPh CO CH _Two Device 11 1-3692 Device 52 3,4-diClPh CO CH _Two Unit 12 1-3693 Unit 52 3,4-diClPh CO CH _Two Unit 13 1-3694 Unit 52 3,4-diClPh CO CH _Two Device 14 1-3695 Device 52 3,4-diClPh CO CH _Two Unit 15 1-3696 Unit 52 3,4-diClPh CO CH _Two Device 16 1-3697 Device 52 3,4-diClPh CO CH _Two Unit 17 1-3698 Unit 52 3,4-diClPh CO CH _Two Unit 18 1-3699 Unit 52 3,4-diClPh CO CH _Two Device 19 1-3700 Device 52 3,4-diClPh CO CH _Two Unit 20 1-3701 Unit 52 3,4-diClPh CO CH _Two Unit 21 1-3702 Unit 52 3,4-diClPh CO CH _Two Unit 22 1-3703 Unit 52 3,4-diClPh CO CH _Two Device 23 1-3704 Device 52 3,4-diClPh CO CH _Two Unit 24 1-3705 Unit 52 3,4-diClPh CO CH _Two Unit 25 1-3706 Unit 52 3,4-diClPh CO CH _Two Unit 26 1-3707 Unit 52 3,4-diClPh CO CH _Two Unit 27 1-3708 Unit 52 3,4-diClPh CO CH _Two Unit 28 1-3709 Unit 52 3,4-diClPh CO CH _Two Unit 29 1-3710 Unit 52 3,4-diClPh CO CH _Two Device 30 1-3711 Device 52 3,4-diClPh CO CH _Two Unit 31 1-3712 Unit 52 3,4-diClPh CO CH _Two Device 32 1-3713 Device 53 3,4-diClPh CO CH _Two Unit 1 1-3714 Unit 53 3,4-diClPh CO CH _Two Unit 2 1-3715 Unit 53 3,4-diClPh CO CH _Two Unit 3 1-3716 Unit 53 3,4-diClPh CO CH _Two Unit 4 1-3717 Unit 53 3,4-diClPh CO CH _Two Set 5 1-3718 Set 53 3,4-diClPh CO CH _Two Set 6 1-3719 Set 53 3,4-diClPh CO CH _Two Unit 7 1-3720 Unit 53 3,4-diClPh CO CH _Two Unit 8 1-3721 Unit 53 3,4-diClPh CO CH _Two Unit 9 1-3722 Unit 53 3,4-diClPh CO CH _Two Device 10 1-3723 Device 53 3,4-diClPh CO CH _Two Unit 11 1-3724 Unit 53 3,4-diClPh CO CH _Two Unit 12 1-3725 Unit 53 3,4-diClPh CO CH _Two Unit 13 1-3726 Unit 53 3,4-diClPh CO CH _Two Unit 14 1-3727 Unit 53 3,4-diClPh CO CH _Two Unit 15 1-3728 Unit 53 3,4-diClPh CO CH _Two Unit 16 1-3729 Unit 53 3,4-diClPh CO CH _Two Unit 17 1-3730 Unit 53 3,4-diClPh CO CH _Two Unit 18 1-3731 Unit 53 3,4-diClPh CO CH _Two Unit 19 1-3732 Unit 53 3,4-diClPh CO CH _Two Device 20 1-3733 Device 53 3,4-diClPh CO CH _Two Device 21 1-3734 Device 53 3,4-diClPh CO CH _Two Unit 22 1-3735 Unit 53 3,4-diClPh CO CH _Two Device 23 1-3736 Device 53 3,4-diClPh CO CH _Two Unit 24 1-3737 Unit 53 3,4-diClPh CO CH _Two Unit 25 1-33738 Unit 53 3,4-diClPh CO CH _Two Unit 26 1-33739 Unit 53 3,4-diClPh CO CH _Two Unit 27 1-3740 Unit 53 3,4-diClPh CO CH _Two Unit 28 1-3741 Unit 53 3,4-diClPh CO CH _Two Unit 29 1-3742 Unit 53 3,4-diClPh CO CH _Two Unit 30 1-3743 Unit 53 3,4-diClPh CO CH _Two Unit 31 1-3744 Unit 53 3,4-diClPh CO CH _Two Device 32 1-3745 Device 54 3,4-diClPh CO CH _Two Unit 1 1-3746 Unit 54 3,4-diClPh CO CH _Two Unit 2 1-3747 Unit 54 3,4-diClPh CO CH _Two Unit 3 1-3748 Unit 54 3,4-diClPh CO CH _Two Unit 4 1-3749 Unit 54 3,4-diClPh CO CH _Two Unit 5 1-3750 Unit 54 3,4-diClPh CO CH _Two Unit 6 1-3751 Unit 54 3,4-diClPh CO CH _Two Unit 7 1-3752 Unit 54 3,4-diClPh CO CH _Two Unit 8 1-3753 Unit 54 3,4-diClPh CO CH _Two Unit 9 1-3754 Unit 54 3,4-diClPh CO CH _Two Unit 10 1-3755 Unit 54 3,4-diClPh CO CH _Two Unit 11 1-3756 Unit 54 3,4-diClPh CO CH _Two Unit 12 1-3757 Unit 54 3,4-diClPh CO CH _Two Unit 13 1-3758 Unit 54 3,4-diClPh CO CH _Two Unit 14 1-3759 Unit 54 3,4-diClPh CO CH _Two Unit 15 1-3760 Unit 54 3,4-diClPh CO CH _Two Unit 16 1-3761 Unit 54 3,4-diClPh CO CH _Two Unit 17 1-3762 Unit 54 3,4-diClPh CO CH _Two Unit 18 1-3763 Unit 54 3,4-diClPh CO CH _Two Unit 19 1-3764 Unit 54 3,4-diClPh CO CH _Two Unit 20 1-3765 Unit 54 3,4-diClPh CO CH _Two Unit 21 1-3766 Unit 54 3,4-diClPh CO CH _Two Unit 22 1-3767 Unit 54 3,4-diClPh CO CH _Two Unit 23 1-3768 Unit 54 3,4-diClPh CO CH _Two Unit 24 1-3767 Unit 54 3,4-diClPh CO CH _Two Unit 25 1-3770 Unit 54 3,4-diClPh CO CH _Two Unit 26 1-3771 Unit 54 3,4-diClPh CO CH _Two Unit 27 1-3772 Unit 54 3,4-diClPh CO CH _Two Unit 28 1-3773 Unit 54 3,4-diClPh CO CH _Two Unit 29 1-3774 Unit 54 3,4-diClPh CO CH _Two Unit 30 1-3775 Unit 54 3,4-diClPh CO CH _Two Unit 31 1-3776 Unit 54 3,4-diClPh CO CH _Two Device 32 1-3777 Device 55 3,4-diClPh CO CH _Two Unit 1 1-3778 Unit 55 3,4-diClPh CO CH _Two Unit 2 1-3779 Unit 55 3,4-diClPh CO CH _Two Unit 3 1-3780 Unit 55 3,4-diClPh CO CH _Two Unit 4 1-3781 Unit 55 3,4-diClPh CO CH _Two Device 5 1-3782 Device 55 3,4-diClPh CO CH _Two Unit 6 1-3783 Unit 55 3,4-diClPh CO CH _Two Unit 7 1-3784 Unit 55 3,4-diClPh CO CH _Two Unit 8 1-3785 Unit 55 3,4-diClPh CO CH _Two Unit 9 1-3786 Unit 55 3,4-diClPh CO CH _Two Unit 10 1-3787 Unit 55 3,4-diClPh CO CH _Two Unit 11 1-3788 Unit 55 3,4-diClPh CO CH _Two Unit 12 1-3789 Unit 55 3,4-diClPh CO CH _Two Unit 13 1-3790 Unit 55 3,4-diClPh CO CH _Two Unit 14 1-3791 Unit 55 3,4-diClPh CO CH _Two Unit 15 1-3792 Unit 55 3,4-diClPh CO CH _Two Device 16 1-3793 Device 55 3,4-diClPh CO CH _Two Unit 17 1-3794 Unit 55 3,4-diClPh CO CH _Two Device 18 1-3795 Device 55 3,4-diClPh CO CH _Two Unit 19 1-3796 Unit 55 3,4-diClPh CO CH _Two Unit 20 1-3797 Unit 55 3,4-diClPh CO CH _Two Unit 21 1-3798 Unit 55 3,4-diClPh CO CH _Two Unit 22 1-3799 Unit 55 3,4-diClPh CO CH _Two Device 23 1-3800 Device 55 3,4-diClPh CO CH _Two Unit 24 1-3801 Unit 55 3,4-diClPh CO CH _Two Unit 25 1-3802 Unit 55 3,4-diClPh CO CH _Two Unit 26 1-3803 Unit 55 3,4-diClPh CO CH _Two Unit 27 1-3804 Unit 55 3,4-diClPh CO CH _Two Unit 28 1-3805 Unit 55 3,4-diClPh CO CH _Two Unit 29 1-3806 Unit 55 3,4-diClPh CO CH _Two Device 30 1-3807 Device 55 3,4-diClPh CO CH _Two Unit 31 1-3808 Unit 55 3,4-diClPh CO CH _Two Device 32 1-3809 device 56 3,4-diClPh CO CH _Two Unit 1 1-3810 Unit 56 3,4-diClPh CO CH _Two Unit 2 1-38111 Unit 56 3,4-diClPh CO CH _Two Unit 3 1-3812 Unit 56 3,4-diClPh CO CH _Two Unit 4 1-3813 Unit 56 3,4-diClPh CO CH _Two Unit 5 1-3814 Unit 56 3,4-diClPh CO CH _Two Unit 6 1-3815 Unit 56 3,4-diClPh CO CH _Two Unit 7 1-3816 Unit 56 3,4-diClPh CO CH _Two Unit 8 1-3817 Unit 56 3,4-diClPh CO CH _Two Set 9 1-3818 Set 56 3,4-diClPh CO CH _Two Unit 10 1-3819 Unit 56 3,4-diClPh CO CH _Two Unit 11 1-3820 Unit 56 3,4-diClPh CO CH _Two Unit 12 1-3821 Unit 56 3,4-diClPh CO CH _Two Unit 13 1-3822 Unit 56 3,4-diClPh CO CH _Two Unit 14 1-3823 Unit 56 3,4-diClPh CO CH _Two Unit 15 1-3824 Unit 56 3,4-diClPh CO CH _Two Unit 16 1-3825 Unit 56 3,4-diClPh CO CH _Two Unit 17 1-3826 Unit 56 3,4-diClPh CO CH _Two Unit 18 1-3827 Unit 56 3,4-diClPh CO CH _Two Unit 19 1-3828 Unit 56 3,4-diClPh CO CH _Two Device 20 1-3829 Device 56 3,4-diClPh CO CH _Two Unit 21 1-3830 Unit 56 3,4-diClPh CO CH _Two Unit 22 1-3831 Unit 56 3,4-diClPh CO CH _Two Unit 23 1-3832 Unit 56 3,4-diClPh CO CH _Two Unit 24 1-3833 Unit 56 3,4-diClPh CO CH _Two Unit 25 1-3834 Unit 56 3,4-diClPh CO CH _Two Unit 26 1-3835 Unit 56 3,4-diClPh CO CH _Two Set 27 1-33836 Set 56 3,4-diClPh CO CH _Two 28 28 1-338 37 56 3,4-diClPh CO CH _Two Unit 29 1-33838 Unit 56 3,4-diClPh CO CH _Two Device 30 1-33839 Device 56 3,4-diClPh CO CH _Two Unit 31 1-3840 Unit 56 3,4-diClPh CO CH _Two Unit 32 1-3841 Unit 57 3,4-diClPh CO CH _Two Unit 1 1-3842 Unit 57 3,4-diClPh CO CH _Two Unit 2 1-3843 Unit 57 3,4-diClPh CO CH _Two Unit 3 1-3844 Unit 57 3,4-diClPh CO CH _Two Unit 4 1-3845 Unit 57 3,4-diClPh CO CH _Two Unit 5 1-3846 Unit 57 3,4-diClPh CO CH _Two Unit 6 1-3847 Unit 57 3,4-diClPh CO CH _Two Unit 7 1-3848 Unit 57 3,4-diClPh CO CH _Two Unit 8 1-3849 Unit 57 3,4-diClPh CO CH _Two Unit 9 1-3850 Unit 57 3,4-diClPh CO CH _Two Unit 10 1-3851 Unit 57 3,4-diClPh CO CH _Two Unit 11 1-3852 Unit 57 3,4-diClPh CO CH _Two Unit 12 1-3853 Unit 57 3,4-diClPh CO CH _Two Unit 13 1-3854 Unit 57 3,4-diClPh CO CH _Two Unit 14 1-3855 Unit 57 3,4-diClPh CO CH _Two Unit 15 1-3856 Unit 57 3,4-diClPh CO CH _Two Unit 16 1-3857 Unit 57 3,4-diClPh CO CH _Two Unit 17 1-3858 Unit 57 3,4-diClPh CO CH _Two Device 18 1-38559 Device 57 3,4-diClPh CO CH _Two Unit 19 1-3860 Unit 57 3,4-diClPh CO CH _Two Device 20 1-3861 Device 57 3,4-diClPh CO CH _Two Unit 21 1-3862 Unit 57 3,4-diClPh CO CH _Two Unit 22 1-3863 Unit 57 3,4-diClPh CO CH _Two Unit 23 1-3864 Unit 57 3,4-diClPh CO CH _Two Unit 24 1-3865 Unit 57 3,4-diClPh CO CH _Two Unit 25 1-3866 Unit 57 3,4-diClPh CO CH _Two Unit 26 1-3867 Unit 57 3,4-diClPh CO CH _Two Unit 27 1-3868 Unit 57 3,4-diClPh CO CH _Two Unit 28 1-3869 Unit 57 3,4-diClPh CO CH _Two Unit 29 1-3870 Unit 57 3,4-diClPh CO CH _Two Unit 30 1-3871 Unit 57 3,4-diClPh CO CH _Two Unit 31 1-3872 Unit 57 3,4-diClPh CO CH _Two Device 32 1-3873 Device 58 3,4-diClPh CO CH _Two Unit 1 1-3874 Unit 58 3,4-diClPh CO CH _Two Unit 2 1-3875 Unit 58 3,4-diClPh CO CH _Two Unit 3 1-3876 Unit 58 3,4-diClPh CO CH _Two Unit 4 1-3877 Unit 58 3,4-diClPh CO CH _Two Unit 5 1-3878 Unit 58 3,4-diClPh CO CH _Two Unit 6 1-3879 Unit 58 3,4-diClPh CO CH _Two Unit 7 1-3880 Unit 58 3,4-diClPh CO CH _Two Unit 8 1-3881 Unit 58 3,4-diClPh CO CH _Two Unit 9 1-3882 Unit 58 3,4-diClPh CO CH _Two Unit 10 1-3883 Unit 58 3,4-diClPh CO CH _Two Unit 11 1-3884 Unit 58 3,4-diClPh CO CH _Two Unit 12 1-3885 Unit 58 3,4-diClPh CO CH _Two Unit 13 1-3886 Unit 58 3,4-diClPh CO CH _Two Unit 14 1-3887 Unit 58 3,4-diClPh CO CH _Two Unit 15 1-3888 Unit 58 3,4-diClPh CO CH _Two Unit 16 1-3889 Unit 58 3,4-diClPh CO CH _Two Unit 17 1-3890 Unit 58 3,4-diClPh CO CH _Two Unit 18 1-3891 Unit 58 3,4-diClPh CO CH _Two Unit 19 1-3892 Unit 58 3,4-diClPh CO CH _Two Unit 20 1-3893 Unit 58 3,4-diClPh CO CH _Two Unit 21 1-3894 Unit 58 3,4-diClPh CO CH _Two Unit 22 1-3895 Unit 58 3,4-diClPh CO CH _Two Unit 23 1-3896 Unit 58 3,4-diClPh CO CH _Two Unit 24 1-3897 Unit 58 3,4-diClPh CO CH _Two Unit 25 1-3898 Unit 58 3,4-diClPh CO CH _Two Unit 26 1-3899 Unit 58 3,4-diClPh CO CH _Two Unit 27 1-3900 Unit 58 3,4-diClPh CO CH _Two Unit 28 1-3901 Unit 58 3,4-diClPh CO CH _Two Unit 29 1-3902 Unit 58 3,4-diClPh CO CH _Two Unit 30 1-3903 Unit 58 3,4-diClPh CO CH _Two Unit 31 1-3904 Unit 58 3,4-diClPh CO CH _Two Set 32 1-3905 Set 59 3,4-diClPh CO CH _Two Unit 1 1-3906 Unit 59 3,4-diClPh CO CH _Two Unit 2 1-3907 Unit 59 3,4-diClPh CO CH _Two Unit 3 1-3908 Unit 59 3,4-diClPh CO CH _Two Unit 4 1-3909 Unit 59 3,4-diClPh CO CH _Two Unit 5 1-3910 Unit 59 3,4-diClPh CO CH _Two Set 6 1-3911 Set 59 3,4-diClPh CO CH _Two Unit 7 1-3912 Unit 59 3,4-diClPh CO CH _Two Unit 8 1-3913 Unit 59 3,4-diClPh CO CH _Two Set 9 1-3914 Set 59 3,4-diClPh CO CH _Two Unit 10 1-3915 Unit 59 3,4-diClPh CO CH _Two Unit 11 1-3916 Unit 59 3,4-diClPh CO CH _Two Unit 12 1-3917 Unit 59 3,4-diClPh CO CH _Two Unit 13 1-3918 Unit 59 3,4-diClPh CO CH _Two Set 14 1-3919 Set 59 3,4-diClPh CO CH _Two Unit 15 1-3920 Unit 59 3,4-diClPh CO CH _Two Unit 16 1-3921 Unit 59 3,4-diClPh CO CH _Two Unit 17 1-3922 Unit 59 3,4-diClPh CO CH _Two Unit 18 1-3923 Unit 59 3,4-diClPh CO CH _Two Unit 19 1-3924 Unit 59 3,4-diClPh CO CH _Two Unit 20 1-3925 Unit 59 3,4-diClPh CO CH _Two Unit 21 1-3926 Unit 59 3,4-diClPh CO CH _Two Unit 22 1-3927 Unit 59 3,4-diClPh CO CH _Two Set 23 1-3928 Set 59 3,4-diClPh CO CH _Two Set 24 1-3929 Set 59 3,4-diClPh CO CH _Two Unit 25 1-3930 Unit 59 3,4-diClPh CO CH _Two Unit 26 1-3931 Unit 59 3,4-diClPh CO CH _Two Set 27 1-393 Set 59 3,4-diClPh CO CH _Two 28 28-3933 3 59 3,4-diClPh CO CH _Two Set 29 1-3934 Set 59 3,4-diClPh CO CH _Two Set 30 1-3935 Set 59 3,4-diClPh CO CH _Two Set 31 1-3936 Set 59 3,4-diClPh CO CH _Two Device 32 1-3937 Device 60 3,4-diClPh CO CH _Two Unit 1 1-3938 Unit 60 3,4-diClPh CO CH _Two Unit 2 1-3939 Unit 60 3,4-diClPh CO CH _Two Unit 3 1-3940 Unit 60 3,4-diClPh CO CH _Two Unit 4 1-3941 Unit 60 3,4-diClPh CO CH _Two Unit 5 1-3942 Unit 60 3,4-diClPh CO CH _Two Unit 6 1-3943 Unit 60 3,4-diClPh CO CH _Two Unit 7 1-3944 Unit 60 3,4-diClPh CO CH _Two Unit 8 1-3945 Unit 60 3,4-diClPh CO CH _Two Set 9 1-3946 Set 60 3,4-diClPh CO CH _Two Unit 10 1-3947 Unit 60 3,4-diClPh CO CH _Two Unit 11 1-3948 Unit 60 3,4-diClPh CO CH _Two Unit 12 1-3949 Unit 60 3,4-diClPh CO CH _Two Unit 13 1-3950 Unit 60 3,4-diClPh CO CH _Two Unit 14 1-3951 Unit 60 3,4-diClPh CO CH _Two Unit 15 1-3952 Unit 60 3,4-diClPh CO CH _Two Device 16 1-3953 Device 60 3,4-diClPh CO CH _Two Unit 17 1-3954 Unit 60 3,4-diClPh CO CH _Two Device 18 1-3955 Device 60 3,4-diClPh CO CH _Two Set 19 1-3956 Set 60 3,4-diClPh CO CH _Two Device 20 1-3957 Device 60 3,4-diClPh CO CH _Two Unit 21 1-3958 Unit 60 3,4-diClPh CO CH _Two Unit 22 1-3959 Unit 60 3,4-diClPh CO CH _Two Set 23 1-3960 Set 60 3,4-diClPh CO CH _Two Unit 24 1-3961 Unit 60 3,4-diClPh CO CH _Two Unit 25 1-3962 Unit 60 3,4-diClPh CO CH _Two Unit 26 1-3963 Unit 60 3,4-diClPh CO CH _Two Unit 27 1-3964 Unit 60 3,4-diClPh CO CH _Two Unit 28 1-3965 Unit 60 3,4-diClPh CO CH _Two Device 29 1-3966 Device 60 3,4-diClPh CO CH _Two Device 30 1-3967 Device 60 3,4-diClPh CO CH _Two Device 31 1-3968 Device 60 3,4-diClPh CO CH _Two Device 32 1-3969 Device 61 3,4-diClPh CO CH _Two Unit 1 1-3970 Unit 61 3,4-diClPh CO CH _Two Unit 2 1-3971 Unit 61 3,4-diClPh CO CH _Two Unit 3 1-3972 Unit 61 3,4-diClPh CO CH _Two Unit 4 1-3973 Unit 61 3,4-diClPh CO CH _Two App 5 1-3974 App 61 3,4-diClPh CO CH _Two Unit 6 1-3975 Unit 61 3,4-diClPh CO CH _Two Unit 7 1-3976 Unit 61 3,4-diClPh CO CH _Two Unit 8 1-3977 Unit 61 3,4-diClPh CO CH _Two Unit 9 1-3978 Unit 61 3,4-diClPh CO CH _Two Unit 10 1-3979 Unit 61 3,4-diClPh CO CH _Two Unit 11 1-3980 Unit 61 3,4-diClPh CO CH _Two Unit 12 1-3981 Unit 61 3,4-diClPh CO CH _Two Unit 13 1-3982 Unit 61 3,4-diClPh CO CH _Two Unit 14 1-3983 Unit 61 3,4-diClPh CO CH _Two Unit 15 1-3984 Unit 61 3,4-diClPh CO CH _Two Unit 16 1-3985 Unit 61 3,4-diClPh CO CH _Two Unit 17 1-3986 Unit 61 3,4-diClPh CO CH _Two Unit 18 1-3987 Unit 61 3,4-diClPh CO CH _Two Set 19 1-3988 Set 61 3,4-diClPh CO CH _Two Set 20 1-3989 Set 61 3,4-diClPh CO CH _Two Unit 21 1-3990 Unit 61 3,4-diClPh CO CH _Two Unit 22 1-3991 Unit 61 3,4-diClPh CO CH _Two Device 23 1-3992 Device 61 3,4-diClPh CO CH _Two Unit 24 1-3993 Unit 61 3,4-diClPh CO CH _Two Unit 25 1-3939 Unit 61 3,4-diClPh CO CH _Two Unit 26 1-3995 Unit 61 3,4-diClPh CO CH _Two Unit 27 1-3996 Unit 61 3,4-diClPh CO CH _Two Unit 28 1-3997 Unit 61 3,4-diClPh CO CH _Two Set 29 1-3998 Set 61 3,4-diClPh CO CH _Two Unit 30 1-3999 Unit 61 3,4-diClPh CO CH _Two Unit 31 1-4000 Unit 61 3,4-diClPh CO CH _Two Device 32 1-4001 device 33 3,4-diClPh CO CH _Two CH _Two Place 1 1-4002 Place 33 3,4-diClPh CO CH _Two CH _Two Set 2 1-403 Set 33 3,4-diClPh CO CH _Two CH _Two Place 3 1-4004 Place 33 3,4-diClPh CO CH _Two CH _Two Unit 4 1-4005 Unit 33 3,4-diClPh CO CH _Two CH _Two Set 5 1-4006 Set 33 3,4-diClPh CO CH _Two CH _Two Place 6 1-407 Place 33 3,4-diClPh CO CH _Two CH _Two Place 7 1-4008 Place 33 3,4-diClPh CO CH _Two CH _Two Set 8 1-409 Set 33 3,4-diClPh CO CH _Two CH _Two Set 9 1-4010 Set 33 3,4-diClPh CO CH _Two CH _Two Set 10 1-4011 Set 33 3,4-diClPh CO CH _Two CH _Two Unit 11 1-4012 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 12 1-4013 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 13 1-4014 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 14 1-4015 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 15 1-4016 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 16 1-4017 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 17 1-4018 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 18 1-4019 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 19 1-4020 Unit 33 3,4-diClPh CO CH _Two CH _Two Storage 20 1-421 Storage 33 3,4-diClPh CO CH _Two CH _Two Unit 21 1-4022 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 22 1-4023 Unit 33 3,4-diClPh CO CH _Two CH _Two Set 23 1-4024 Set 33 3,4-diClPh CO CH _Two CH _Two Unit 24 1-4025 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 25 1-4026 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 26 1-4027 Unit 33 3,4-diClPh CO CH _Two CH _Two Set 27 1-4028 Set 33 3,4-diClPh CO CH _Two CH _Two Set 28 1-4029 Set 33 3,4-diClPh CO CH _Two CH _Two Unit 29 1-4030 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 30 1-401 Unit 33 3,4-diClPh CO CH _Two CH _Two Unit 31 1-4032 Unit 33 3,4-diClPh CO CH _Two CH _Two Set 32 1-4033 Set 33 3,4-diClPh CO CH _Two CH = CH Place 1 1-4034 Place 33 3,4-diClPh CO CH _Two CH = CH unit 2 1-4035 unit 33 3,4-diClPh CO CH _Two CH = CH Place 3 1-4036 Place 33 3,4-diClPh CO CH _Two CH = CH Place 4 1-4037 Place 33 3,4-diClPh CO CH _Two CH = CH device 5 1-4038 device 33 3,4-diClPh CO CH _Two CH = CH unit 6 1-4039 unit 33 3,4-diClPh CO CH _Two CH = CH Place 7 1-4040 Place 33 3,4-diClPh CO CH _Two CH = CH Place 8 1-4041 Place 33 3,4-diClPh CO CH _Two CH = CH Place 9 1-402 Place 33 3,4-diClPh CO CH _Two CH = CH unit 10 1-4043 unit 33 3,4-diClPh CO CH _Two CH = CH unit 11 1-4044 unit 33 3,4-diClPh CO CH _Two CH = CH unit 12 1-4045 unit 33 3,4-diClPh CO CH _Two CH = CH unit 13 1-4046 unit 33 3,4-diClPh CO CH _Two CH = CH unit 14 1-4047 unit 33 3,4-diClPh CO CH _Two CH = CH unit 15 1-4048 unit 33 3,4-diClPh CO CH _Two CH = CH unit 16 1-4049 unit 33 3,4-diClPh CO CH _Two CH = CH unit 17 1-4050 unit 33 3,4-diClPh CO CH _Two CH = CH unit 18 1-4051 unit 33 3,4-diClPh CO CH _Two CH = CH unit 19 1-4052 unit 33 3,4-diClPh CO CH _Two CH = CH unit 20 1-4053 unit 33 3,4-diClPh CO CH _Two CH = CH unit 21 1-4054 unit 33 3,4-diClPh CO CH _Two CH = CH unit 22 1-4055 unit 33 3,4-diClPh CO CH _Two CH = CH unit 23 1-4056 unit 33 3,4-diClPh CO CH _Two CH = CH unit 24 1-4057 unit 33 3,4-diClPh CO CH _Two CH = CH 25 25-4058 33,4-diClPh CO CH _Two CH = CH unit 26 1-4059 unit 33 3,4-diClPh CO CH _Two CH = CH unit 27 1-4060 unit 33 3,4-diClPh CO CH _Two CH = CH unit 28 1-4061 unit 33 3,4-diClPh CO CH _Two CH = CH unit 29 1-4062 unit 33 3,4-diClPh CO CH _Two CH = CH unit 30 1-4063 unit 33 3,4-diClPh CO CH _Two CH = CH unit 31 1-4064 unit 33 3,4-diClPh CO CH _Two CH = CH unit 32 1-4065 unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 1 1-4066 Unit 33 3,4-diClPh CO (CH _Two ) _Three Device 2 1-4067 device 33 3,4-diClPh CO (CH _Two ) _Three Unit 3 1-4068 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 4 1-4069 Unit 33 3,4-diClPh CO (CH _Two ) _Three Device 5 1-4070 Device 33 3,4-diClPh CO (CH _Two ) _Three Unit 6 1-4071 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 7 1-4072 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 8 1-4073 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 9 1-4074 Unit 33 3,4-diClPh CO (CH _Two ) _Three Device 10 1-4075 Device 33 3,4-diClPh CO (CH _Two ) _Three Unit 11 1-4076 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 12 1-4077 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 13 1-4078 Unit 33 3,4-diClPh CO (CH _Two ) _Three Device 14 1-4079 device 33 3,4-diClPh CO (CH _Two ) _Three Unit 15 1-4080 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 16 1-4081 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 17 1 -4082 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 18 1-4083 Unit 33 3,4-diClPh CO (CH _Two ) _Three Unit 19 1-4084 Unit 33 3,4-diClPh CO (CH _Two ) _Three Device 20 1-4085 device 33 3,4-diClPh CO (CH _Two ) _Three Device 21 1-4086 device 33 3,4-diClPh CO (CH _Two ) _Three Device 22 1-4087 device 33 3,4-diClPh CO (CH _Two ) _Three Device 23 1-4088 device 33 3,4-diClPh CO (CH _Two ) _Three Device 24 1-4089 device 33 3,4-diClPh CO (CH _Two ) _Three Unit 25 1-4090 Unit 33 3,4-diClPh CO (CH _Two ) _Three Device 26 1-4091 device 33 3,4-diClPh CO (CH _Two ) _Three Device 27 1-4092 device 33 3,4-diClPh CO (CH _Two ) _Three 28 1-4093 28 33,4-diClPh CO (CH _Two ) _Three Device 29 1-4094 device 33 3,4-diClPh CO (CH _Two ) _Three Device 30 1-4095 device 33 3,4-diClPh CO (CH _Two ) _Three Device 31 1-4096 device 33 3,4-diClPh CO (CH _Two ) _Three Device 32 1-4097 device 42 3,4-diClPh CO single bond device 74 ───────────────────────────────── ───

[0459]

[Table 2] Compound No. R ¹ R ^Two ABZ────────────────────────────────────2-1 Place 33 3,4-diClPh CH _Two Single bond device 1 2-2 device 33 3,4-diClPh CH _Two Single bond device 2 2-3 device 33 3,4-diClPh CH _Two Single bond device 3 2-4 device 33 3,4-diClPh CH _Two Single bond unit 4 2-5 unit 33 3,4-diClPh CH _Two Single bond device 5 2-6 device 33 3,4-diClPh CH _Two Single bond device 6 2-7 device 33 3,4-diClPh CH _Two Single bond unit 7 2-8 unit 33 3,4-diClPh CH _Two Single bond device 8 2-9 device 33 3,4-diClPh CH _Two Single bond device 9 2-10 device 33 3,4-diClPh CH _Two Single bond device 10 2-11 device 33 3,4-diClPh CH _Two Single bond unit 11 2-12 unit 33 3,4-diClPh CH _Two Single bond unit 12 2-13 unit 33 3,4-diClPh CH _Two Single bond unit 13 2-14 unit 33 3,4-diClPh CH _Two Single bond unit 14 2-15 unit 33 3,4-diClPh CH _Two Single bond unit 15 2-16 unit 33 3,4-diClPh CH _Two Single bond unit 16 2-17 unit 33 3,4-diClPh CH _Two Single bond unit 17 2-18 unit 33 3,4-diClPh CH _Two Single bond unit 18 2-19 unit 33 3,4-diClPh CH _Two Single bond unit 19 2-20 unit 33 3,4-diClPh CH _Two Single bond unit 20 2-21 unit 33 3,4-diClPh CH _Two Single bond unit 21 2-22 unit 33 3,4-diClPh CH _Two Single bond unit 22 2-23 unit 33 3,4-diClPh CH _Two Single bond unit 23 2-24 unit 33 3,4-diClPh CH _Two Single bond unit 24 2-25 unit 33 3,4-diClPh CH _Two Single bond unit 25 2-26 unit 33 3,4-diClPh CH _Two Single bond unit 26 2-27 unit 33 3,4-diClPh CH _Two Single bond unit 27 2-28 unit 33 3,4-diClPh CH _Two Single bond unit 28 2-29 unit 33 3,4-diClPh CH _Two Single bond unit 29 2-30 unit 33 3,4-diClPh CH _Two Single bond device 30 2-31 device 33 3,4-diClPh CH _Two Single bond unit 31 2-32 unit 33 3,4-diClPh CH _Two Single bond unit 32 2-33 unit 33 3,4-diClPh CH _Two Single bond device 65 2-34 device 33 3,4-diClPh CH _Two Single bond unit 66 2-35 unit 33 3,4-diClPh CH _Two Single bond unit 67 2-36 unit 33 3,4-diClPh CH _Two Single bond device 68 2-37 device 33 3,4-diClPh CH _Two Single bond unit 69 2-38 unit 33 3,4-diClPh CH _Two Single bond unit 70 2-39 unit 33 3,4-diClPh CH _Two Single bond unit 71 2-40 unit 33 3,4-diClPh CH _Two Single bond unit 72 2-41 unit 33 3,4-diClPh CH _Two Single bond device 73 2-42 device 33 3,4-diClPh CH _Two Single bond unit 74 2-43 unit 33 3,4-diClPh CH _Two Single bond unit 75 2-44 unit 33 3,4-diClPh CH _Two Single bond unit 76 2-45 unit 33 3,4-diClPh CH _Two Single bond unit 77 2-46 unit 33 3,4-diClPh CH _Two Single bond unit 78 2-47 unit 33 3,4-diClPh CH _Two Single bond device 79 2-48 device 33 3,4-diClPh CH _Two Single bond device 80 2-49 device 34 3,4-diClPh CH _Two Single bond device 1 2-50 device 34 3,4-diClPh CH _Two Single bond unit 2 2-51 unit 34 3,4-diClPh CH _Two Single bond device 3 2-52 device 34 3,4-diClPh CH _Two Single bond unit 4 2-53 unit 34 3,4-diClPh CH _Two Single bond unit 5 2-54 unit 34 3,4-diClPh CH _Two Single bond 6 6-55 34 3,4-diClPh CH _Two Single bond unit 7 2-56 unit 34 3,4-diClPh CH _Two Single bond unit 8 2-57 unit 34 3,4-diClPh CH _Two Single bond unit 9 2-58 unit 34 3,4-diClPh CH _Two Single bond unit 10 2-59 unit 34 3,4-diClPh CH _Two Single bond unit 11 2-60 unit 34 3,4-diClPh CH _Two Single bond unit 12 2-61 unit 34 3,4-diClPh CH _Two Single bond unit 13 2-62 unit 34 3,4-diClPh CH _Two Single bond unit 14 2-63 unit 34 3,4-diClPh CH _Two Single bond unit 15 2-64 unit 34 3,4-diClPh CH _Two Single bond unit 16 2-65 unit 34 3,4-diClPh CH _Two Single bond unit 17 2-66 unit 34 3,4-diClPh CH _Two Single bond unit 18 2-67 unit 34 3,4-diClPh CH _Two Single bond unit 19 2-68 unit 34 3,4-diClPh CH _Two Single bond unit 20 2-69 unit 34 3,4-diClPh CH _Two Single bond unit 21 2-70 unit 34 3,4-diClPh CH _Two Single bond unit 22 2-71 unit 34 3,4-diClPh CH _Two Single bond unit 23 2-72 unit 34 3,4-diClPh CH _Two Single bond unit 24 2-73 unit 34 3,4-diClPh CH _Two Single bond unit 25 2-74 unit 34 3,4-diClPh CH _Two Single bond unit 26 2-75 unit 34 3,4-diClPh CH _Two Single bond unit 27 2-76 unit 34 3,4-diClPh CH _Two Single bond unit 28 2-77 unit 34 3,4-diClPh CH _Two Single bond unit 29 2-78 unit 34 3,4-diClPh CH _Two Single bond device 30 2-79 device 34 3,4-diClPh CH _Two Single bond unit 31 2-80 unit 34 3,4-diClPh CH _Two Single bond unit 32 2-81 unit 34 3,4-diClPh CH _Two Single bond device 65 2-82 device 34 3,4-diClPh CH _Two Single bond device 66 2-83 device 34 3,4-diClPh CH _Two Single bond unit 67 2-84 unit 34 3,4-diClPh CH _Two Single bond device 68 2-85 device 34 3,4-diClPh CH _Two Single bond device 69 2-86 device 34 3,4-diClPh CH _Two Single bond unit 70 2-87 unit 34 3,4-diClPh CH _Two Single bond unit 71 2-88 unit 34 3,4-diClPh CH _Two Single bond unit 72 2-89 unit 34 3,4-diClPh CH _Two Single bond unit 73 2-90 unit 34 3,4-diClPh CH _Two Single bond unit 74 2-91 unit 34 3,4-diClPh CH _Two Single bond unit 75 2-92 unit 34 3,4-diClPh CH _Two Single bond unit 76 2-93 unit 34 3,4-diClPh CH _Two Single bond unit 77 2-94 unit 34 3,4-diClPh CH _Two Single bond unit 78 2-95 unit 34 3,4-diClPh CH _Two Single bond device 79 2-96 device 34 3,4-diClPh CH _Two Single bond device 80 2-97 device 35 3,4-diClPh CH _Two Single bond device 1 2-98 device 35 3,4-diClPh CH _Two Single bond unit 22-99 unit 35 3,4-diClPh CH _Two Single bond device 3 2-100 device 35 3,4-diClPh CH _Two Single bond unit 4 2-101 unit 35 3,4-diClPh CH _Two Single bond device 5 2-102 device 35 3,4-diClPh CH _Two Single bond device 6 2-103 device 35 3,4-diClPh CH _Two Single bond device 7 2-104 device 35 3,4-diClPh CH _Two Single bond device 8 2-105 device 35 3,4-diClPh CH _Two Single bond device 9 2-106 device 35 3,4-diClPh CH _Two Single bond device 10 2-107 device 35 3,4-diClPh CH _Two Single bond unit 11 2-108 unit 35 3,4-diClPh CH _Two Single bond unit 12 2-109 unit 35 3,4-diClPh CH _Two Single bond unit 13 2-110 unit 35 3,4-diClPh CH _Two Single bond unit 14 2-111 unit 35 3,4-diClPh CH _Two Single bond unit 15 2-112 unit 35 3,4-diClPh CH _Two Single bond unit 16 2-113 unit 35 3,4-diClPh CH _Two Single bond unit 17 2-114 unit 35 3,4-diClPh CH _Two Single bond unit 18 2-115 unit 35 3,4-diClPh CH _Two Single bond unit 19 2-116 unit 35 3,4-diClPh CH _Two Single bond unit 20 2-117 unit 35 3,4-diClPh CH _Two Single bond unit 21 2-118 unit 35 3,4-diClPh CH _Two Single bond unit 22 2-119 unit 35 3,4-diClPh CH _Two Single bond unit 23 2-120 unit 35 3,4-diClPh CH _Two Single bond unit 24 2-121 unit 35 3,4-diClPh CH _Two Single bond unit 25 2-122 unit 35 3,4-diClPh CH _Two Single bond unit 26 2-123 unit 35 3,4-diClPh CH _Two Single bond unit 27 2-124 unit 35 3,4-diClPh CH _Two Single bond unit 28 2-125 unit 35 3,4-diClPh CH _Two Single bond unit 29 2-126 unit 35 3,4-diClPh CH _Two Single bond unit 30 2-127 unit 35 3,4-diClPh CH _Two Single bond unit 31 2-128 unit 35 3,4-diClPh CH _Two Single bond unit 32 2-129 unit 35 3,4-diClPh CH _Two Single bond device 65 2-130 device 35 3,4-diClPh CH _Two Single bond device 66 2-131 device 35 3,4-diClPh CH _Two Single bond unit 67 2-132 unit 35 3,4-diClPh CH _Two Single bond device 68 2-133 device 35 3,4-diClPh CH _Two Single bond unit 69 2-134 unit 35 3,4-diClPh CH _Two Single bond unit 70 2-135 unit 35 3,4-diClPh CH _Two Single bond unit 71 2-136 unit 35 3,4-diClPh CH _Two Single bond unit 72 2-137 unit 35 3,4-diClPh CH _Two Single bond unit 73 2-138 unit 35 3,4-diClPh CH _Two Single bond unit 74 2-139 unit 35 3,4-diClPh CH _Two Single bond unit 75 2-140 unit 35 3,4-diClPh CH _Two Single bond unit 76 2-141 unit 35 3,4-diClPh CH _Two Single bond unit 77 2-142 unit 35 3,4-diClPh CH _Two Single bond unit 78 2-143 unit 35 3,4-diClPh CH _Two Single bond unit 79 2-144 unit 35 3,4-diClPh CH _Two Single bond device 80 2-145 device 36 3,4-diClPh CH _Two Single bond device 1 2-146 device 36 3,4-diClPh CH _Two Single bond unit 22-147 unit 36 3,4-diClPh CH _Two Single bond position 3 2-148 position 36 3,4-diClPh CH _Two Single bond unit 4 2-149 unit 36 3,4-diClPh CH _Two Single bond device 5 2-150 device 36 3,4-diClPh CH _Two Single bond unit 6 2-151 unit 36 3,4-diClPh CH _Two Single bond unit 7 2-152 unit 36 3,4-diClPh CH _Two Single bond device 8 2-153 device 36 3,4-diClPh CH _Two Single bond unit 9 2-154 unit 36 3,4-diClPh CH _Two Single bond unit 10 2-155 unit 36 3,4-diClPh CH _Two Single bond unit 11 2-156 unit 36 3,4-diClPh CH _Two Single bond unit 12 2-157 unit 36 3,4-diClPh CH _Two Single bond unit 13 2-158 unit 36 3,4-diClPh CH _Two Single bond unit 14 2-159 unit 36 3,4-diClPh CH _Two Single bond unit 15 2-160 unit 36 3,4-diClPh CH _Two Single bond unit 16 2-161 unit 36 3,4-diClPh CH _Two Single bond unit 17 2-162 unit 36 3,4-diClPh CH _Two Single bond unit 18 2-163 unit 36 3,4-diClPh CH _Two Single bond unit 19 2-164 unit 36 3,4-diClPh CH _Two Single bond unit 20 2-165 unit 36 3,4-diClPh CH _Two Single bond unit 21 2-166 unit 36 3,4-diClPh CH _Two Single bond unit 22 2-167 unit 36 3,4-diClPh CH _Two Single bond unit 23 2-168 unit 36 3,4-diClPh CH _Two Single bond unit 24 24-169 unit 36 3,4-diClPh CH _Two Single bond unit 25 2-170 unit 36 3,4-diClPh CH _Two Single bond unit 26 2-171 unit 36 3,4-diClPh CH _Two Single bond unit 27 2-172 unit 36 3,4-diClPh CH _Two Single bond unit 28 2-173 unit 36 3,4-diClPh CH _Two Single bond unit 29 2-174 unit 36 3,4-diClPh CH _Two Single bond unit 30 2-175 unit 36 3,4-diClPh CH _Two Single bond unit 31 2-176 unit 36 3,4-diClPh CH _Two Single bond unit 32 2-177 unit 36 3,4-diClPh CH _Two Single bond unit 65 2-178 unit 36 3,4-diClPh CH _Two Single bond device 66 2-179 device 36 3,4-diClPh CH _Two Single bond unit 67 2-180 unit 36 3,4-diClPh CH _Two Single bond device 68 2-181 device 36 3,4-diClPh CH _Two Single bond device 69 2-182 device 36 3,4-diClPh CH _Two Single bond device 70 2-183 device 36 3,4-diClPh CH _Two Single bond unit 71 2-184 unit 36 3,4-diClPh CH _Two Single bond unit 72 2-185 unit 36 3,4-diClPh CH _Two Single bond unit 73 2-186 unit 36 3,4-diClPh CH _Two Single bond device 74 2-187 device 36 3,4-diClPh CH _Two Single bond unit 75 2-188 unit 36 3,4-diClPh CH _Two Single bond unit 76 2-189 unit 36 3,4-diClPh CH _Two Single bond unit 77 2-190 unit 36 3,4-diClPh CH _Two Single bond unit 78 2-191 unit 36 3,4-diClPh CH _Two Single bond unit 79 2-192 unit 36 3,4-diClPh CH _Two Single bond device 80 2-193 device 37 3,4-diClPh CH _Two Single bond device 1 2-194 device 37 3,4-diClPh CH _Two Single bond device 2 2-195 device 37 3,4-diClPh CH _Two Single bond place 3 2-196 place 37 3,4-diClPh CH _Two Single bond place 4 2-197 place 37 3,4-diClPh CH _Two Single bond device 5 2-198 device 37 3,4-diClPh CH _Two Single bond device 6 2-199 device 37 3,4-diClPh CH _Two Single bond device 7 2-200 device 37 3,4-diClPh CH _Two Single bond device 8 2-201 device 37 3,4-diClPh CH _Two Single bond device 9 2-202 device 37 3,4-diClPh CH _Two Single bond device 10 2-203 device 37 3,4-diClPh CH _Two Single bond unit 11 2-204 unit 37 3,4-diClPh CH _Two Single bond unit 12 2-205 unit 37 3,4-diClPh CH _Two Single bond unit 13 2-206 unit 37 3,4-diClPh CH _Two Single bond unit 14 2-207 unit 37 3,4-diClPh CH _Two Single bond unit 15 2-208 unit 37 3,4-diClPh CH _Two Single bond unit 16 2-209 unit 37 3,4-diClPh CH _Two Single bond Unit 17 2-210 Unit 37 3,4-diClPh CH _Two Single bond unit 18 2-211 unit 37 3,4-diClPh CH _Two Single bond unit 19 2-212 unit 37 3,4-diClPh CH _Two Single bond unit 20 2-213 unit 37 3,4-diClPh CH _Two Single bond unit 21 2-214 unit 37 3,4-diClPh CH _Two Single bond Unit 22 2-215 Unit 37 3,4-diClPh CH _Two Single bond unit 23 2-216 unit 37 3,4-diClPh CH _Two Single bond Unit 24 2-217 Unit 37 3,4-diClPh CH _Two Single bond unit 25 2-218 unit 37 3,4-diClPh CH _Two Single bond unit 26 2-219 unit 37 3,4-diClPh CH _Two Single bond unit 27 2-220 unit 37 3,4-diClPh CH _Two Single bond unit 28 2-221 unit 37 3,4-diClPh CH _Two Single bond unit 29 2-222 unit 37 3,4-diClPh CH _Two Single bond unit 30 2-223 unit 37 3,4-diClPh CH _Two Single bond unit 31 2-224 unit 37 3,4-diClPh CH _Two Single bond unit 32 2-225 unit 37 3,4-diClPh CH _Two Single bond device 65 2-226 device 37 3,4-diClPh CH _Two Single bond unit 66 2-227 unit 37 3,4-diClPh CH _Two Single bond unit 67 2-228 unit 37 3,4-diClPh CH _Two Single bond device 68 2-229 device 37 3,4-diClPh CH _Two Single bond device 69 2-230 device 37 3,4-diClPh CH _Two Single bond unit 70 2-231 unit 37 3,4-diClPh CH _Two Single bond unit 71 2-232 unit 37 3,4-diClPh CH _Two Single bond unit 72 2-233 unit 37 3,4-diClPh CH _Two Single bond device 73 2-234 device 37 3,4-diClPh CH _Two Single bond device 74 2-235 device 37 3,4-diClPh CH _Two Single bond unit 75 2-236 unit 37 3,4-diClPh CH _Two Single bond unit 76 2-237 unit 37 3,4-diClPh CH _Two Single bond unit 77 2-238 unit 37 3,4-diClPh CH _Two Single bond unit 78 2-239 unit 37 3,4-diClPh CH _Two Single bond device 79 2-240 device 37 3,4-diClPh CH _Two Single bond device 80 2-241 device 38 3,4-diClPh CH _Two Single bond device 1 2-242 device 38 3,4-diClPh CH _Two Single bond unit 22-243 unit 38 3,4-diClPh CH _Two Single bond position 3 2-244 position 38 3,4-diClPh CH _Two Single bond unit 4 2-245 unit 38 3,4-diClPh CH _Two Single bond 5 2 246 5 38 3,4-diClPh CH _Two Single bond 6 6-247 38 3,4-diClPh CH _Two Single bond place 7 2-248 place 38 3,4-diClPh CH _Two Single bond 8 8 2-249 38 3,4-diClPh CH _Two Single bond device 9 2-250 device 38 3,4-diClPh CH _Two Single bond unit 10 2-251 unit 38 3,4-diClPh CH _Two Single bond unit 11 2-252 unit 38 3,4-diClPh CH _Two Single bond unit 12 2-253 unit 38 3,4-diClPh CH _Two Single bond unit 13 2-254 unit 38 3,4-diClPh CH _Two Single bond unit 14 2-255 unit 38 3,4-diClPh CH _Two Single bond unit 15 2-256 unit 38 3,4-diClPh CH _Two Single bond unit 16 2-257 unit 38 3,4-diClPh CH _Two Single bond unit 17 2-258 unit 38 3,4-diClPh CH _Two Single bond unit 18 2-259 unit 38 3,4-diClPh CH _Two Single bond unit 19 2-260 unit 38 3,4-diClPh CH _Two Single bond unit 20 2-261 unit 38 3,4-diClPh CH _Two Single bond unit 21 2-262 unit 38 3,4-diClPh CH _Two Single bond unit 22 2-263 unit 38 3,4-diClPh CH _Two Single bond 23 23-264 38 3,4-diClPh CH _Two Single bond unit 24 24-65 unit 38 3,4-diClPh CH _Two Single bond unit 25 2-266 unit 38 3,4-diClPh CH _Two Single bond unit 26 2-267 unit 38 3,4-diClPh CH _Two Single bond unit 27 2-268 unit 38 3,4-diClPh CH _Two Single bond unit 28 2-269 unit 38 3,4-diClPh CH _Two Single bond unit 29 2-270 unit 38 3,4-diClPh CH _Two Single bond device 30 2-271 device 38 3,4-diClPh CH _Two Single bond unit 31 2-272 unit 38 3,4-diClPh CH _Two Single bond unit 32 2-273 unit 38 3,4-diClPh CH _Two Single bond device 65 2-274 device 38 3,4-diClPh CH _Two Single bond device 66 2-275 device 38 3,4-diClPh CH _Two Single bond unit 67 2-276 unit 38 3,4-diClPh CH _Two Single bond device 68 2-277 device 38 3,4-diClPh CH _Two Single bond unit 69 2-278 unit 38 3,4-diClPh CH _Two Single bond unit 70 2-279 unit 38 3,4-diClPh CH _Two Single bond unit 71 2-280 unit 38 3,4-diClPh CH _Two Single bond unit 72 2-281 unit 38 3,4-diClPh CH _Two Single bond unit 73 2-282 unit 38 3,4-diClPh CH _Two Single bond unit 74 2-283 unit 38 3,4-diClPh CH _Two Single bond unit 75 2-284 unit 38 3,4-diClPh CH _Two Single bond unit 76 2-285 unit 38 3,4-diClPh CH _Two Single bond unit 77 2-286 unit 38 3,4-diClPh CH _Two Single bond unit 78 2-287 unit 38 3,4-diClPh CH _Two Single bond unit 79 2-288 unit 38 3,4-diClPh CH _Two Single bond device 80 2-289 device 39 3,4-diClPh CH _Two Single bond position 1 2-290 position 39 3,4-diClPh CH _Two Single bond unit 22-291 unit 39 3,4-diClPh CH _Two Single bond position 3 2-292 position 39 3,4-diClPh CH _Two Single bond unit 4 2-293 unit 39 3,4-diClPh CH _Two Single bond unit 5 2-294 unit 39 3,4-diClPh CH _Two Single bond position 6 2-295 position 39 3,4-diClPh CH _Two Single bond place 7 2-296 place 39 3,4-diClPh CH _Two Single bond position 8 2-297 position 39 3,4-diClPh CH _Two Single bond unit 9 2-298 unit 39 3,4-diClPh CH _Two Single bond device 10 2-299 device 39 3,4-diClPh CH _Two Single bond unit 11 2-300 unit 39 3,4-diClPh CH _Two Single bond unit 12 2-301 unit 39 3,4-diClPh CH _Two Single bond unit 13 2-302 unit 39 3,4-diClPh CH _Two Single bond unit 14 2-303 unit 39 3,4-diClPh CH _Two Single bond unit 15 2-304 unit 39 3,4-diClPh CH _Two Single bond unit 16 2-305 unit 39 3,4-diClPh CH _Two Single bond unit 17 2-306 unit 39 3,4-diClPh CH _Two Single bond unit 18 2-307 unit 39 3,4-diClPh CH _Two Single bond unit 19 2-308 unit 39 3,4-diClPh CH _Two Single bond device 20 2-309 device 39 3,4-diClPh CH _Two Single bond unit 21 2-310 unit 39 3,4-diClPh CH _Two Single bond unit 22 2-311 unit 39 3,4-diClPh CH _Two Single bond unit 23 2-312 unit 39 3,4-diClPh CH _Two Single bond unit 24 2-313 unit 39 3,4-diClPh CH _Two Single bond unit 25 2-314 unit 39 3,4-diClPh CH _Two Single bond unit 26 2-315 unit 39 3,4-diClPh CH _Two Single bond unit 27 2-316 unit 39 3,4-diClPh CH _Two Single bond unit 28 2-317 unit 39 3,4-diClPh CH _Two Single bond unit 29 2-318 unit 39 3,4-diClPh CH _Two Single bond device 30 2-319 device 39 3,4-diClPh CH _Two Single bond unit 31 2-320 unit 39 3,4-diClPh CH _Two Single bond unit 32 2-321 unit 39 3,4-diClPh CH _Two Single bond unit 65 2-322 unit 39 3,4-diClPh CH _Two Single bond unit 66 2-323 unit 39 3,4-diClPh CH _Two Single bond unit 67 2-324 unit 39 3,4-diClPh CH _Two Single bond device 68 2-325 device 39 3,4-diClPh CH _Two Single bond unit 69 2-326 unit 39 3,4-diClPh CH _Two Single bond unit 70 2-327 unit 39 3,4-diClPh CH _Two Single bond unit 71 2-328 unit 39 3,4-diClPh CH _Two Single bond unit 72 2-329 unit 39 3,4-diClPh CH _Two Single bond unit 73 2-330 unit 39 3,4-diClPh CH _Two Single bond unit 74 2-331 unit 39 3,4-diClPh CH _Two Single bond unit 75 2-332 unit 39 3,4-diClPh CH _Two Single bond unit 76 2-333 unit 39 3,4-diClPh CH _Two Single bond unit 77 2-334 unit 39 3,4-diClPh CH _Two Single bond unit 78 2-335 unit 39 3,4-diClPh CH _Two Single bond device 79 2-336 device 39 3,4-diClPh CH _Two Single bond device 80 2-337 device 40 3,4-diClPh CH _Two Single bond device 1 2-338 device 40 3,4-diClPh CH _Two Single bond device 2 2-339 device 40 3,4-diClPh CH _Two Single bond unit 3 2-340 unit 40 3,4-diClPh CH _Two Single bond device 4 2-341 device 40 3,4-diClPh CH _Two Single bond device 5 2-342 device 40 3,4-diClPh CH _Two Single bond device 6 2-343 device 40 3,4-diClPh CH _Two Single bond device 7 2-344 device 40 3,4-diClPh CH _Two Single bond device 8 2-345 device 40 3,4-diClPh CH _Two Single bond device 9 2-346 device 40 3,4-diClPh CH _Two Single bond unit 10 2-347 unit 40 3,4-diClPh CH _Two Single bond unit 11 2-348 unit 40 3,4-diClPh CH _Two Single bond unit 12 2-349 unit 40 3,4-diClPh CH _Two Single bond unit 13 2-350 unit 40 3,4-diClPh CH _Two Single bond unit 14 2-351 unit 40 3,4-diClPh CH _Two Single bond unit 15 2-352 unit 40 3,4-diClPh CH _Two Single bond unit 16 2-353 unit 40 3,4-diClPh CH _Two Single bond unit 17 2-354 unit 40 3,4-diClPh CH _Two Single bond unit 18 2-355 unit 40 3,4-diClPh CH _Two Single bond unit 19 2-356 unit 40 3,4-diClPh CH _Two Single bond unit 20 2-357 unit 40 3,4-diClPh CH _Two Single bond unit 21 2-358 unit 40 3,4-diClPh CH _Two Single bond Unit 22 2-359 Unit 40 3,4-diClPh CH _Two Single bond Unit 23 2-360 Unit 40 3,4-diClPh CH _Two Single bond unit 24 2-361 unit 40 3,4-diClPh CH _Two Single bond unit 25 2-362 unit 40 3,4-diClPh CH _Two Single bond unit 26 2-363 unit 40 3,4-diClPh CH _Two Single bond unit 27 2-364 unit 40 3,4-diClPh CH _Two Single bond unit 28 2-365 unit 40 3,4-diClPh CH _Two Single bond unit 29 2-366 unit 40 3,4-diClPh CH _Two Single bond device 30 2-367 device 40 3,4-diClPh CH _Two Single bond unit 31 2-368 unit 40 3,4-diClPh CH _Two Single bond unit 32 2-369 unit 40 3,4-diClPh CH _Two Single bond unit 65 2-370 unit 40 3,4-diClPh CH _Two Single bond unit 66 2-371 unit 40 3,4-diClPh CH _Two Single bond unit 67 2-372 unit 40 3,4-diClPh CH _Two Single bond device 68 2-373 device 40 3,4-diClPh CH _Two Single bond device 69 2-374 device 40 3,4-diClPh CH _Two Single bond unit 70 2-375 unit 40 3,4-diClPh CH _Two Single bond unit 71 2-376 unit 40 3,4-diClPh CH _Two Single bond unit 72 2-377 unit 40 3,4-diClPh CH _Two Single bond unit 73 2-378 unit 40 3,4-diClPh CH _Two Single bond unit 74 2-379 unit 40 3,4-diClPh CH _Two Single bond unit 75 2-380 unit 40 3,4-diClPh CH _Two Single bond unit 76 2-381 unit 40 3,4-diClPh CH _Two Single bond unit 77 2-382 unit 40 3,4-diClPh CH _Two Single bond unit 78 2-383 unit 40 3,4-diClPh CH _Two Single bond unit 79 2-384 unit 40 3,4-diClPh CH _Two Single bond device 80 2-385 device 41 3,4-diClPh CH _Two Single bond device 1 2-386 device 41 3,4-diClPh CH _Two Single bond unit 2 2-387 unit 41 3,4-diClPh CH _Two Single bond unit 3 2-388 unit 41 3,4-diClPh CH _Two Single bond unit 4 2-389 unit 41 3,4-diClPh CH _Two Single bond device 5 2-390 device 41 3,4-diClPh CH _Two Single bond unit 6 2-391 unit 41 3,4-diClPh CH _Two Single bond unit 7 2-392 unit 41 3,4-diClPh CH _Two Single bond device 8 2-393 device 41 3,4-diClPh CH _Two Single bond unit 9 2-394 unit 41 3,4-diClPh CH _Two Single bond Unit 10 2-395 Unit 41 3,4-diClPh CH _Two Single bond unit 11 2-396 unit 41 3,4-diClPh CH _Two Single bond unit 12 2-397 unit 41 3,4-diClPh CH _Two Single bond unit 13 2-398 unit 41 3,4-diClPh CH _Two Single bond unit 14 2-399 unit 41 3,4-diClPh CH _Two Single bond unit 15 2-400 unit 41 3,4-diClPh CH _Two Single bond Unit 16 2-401 Unit 41 3,4-diClPh CH _Two Single bond unit 17 2-402 unit 41 3,4-diClPh CH _Two Single bond unit 18 2-403 unit 41 3,4-diClPh CH _Two Single bond unit 19 2-404 unit 41 3,4-diClPh CH _Two Single bond unit 20 2-405 unit 41 3,4-diClPh CH _Two Single bond unit 21 2-406 unit 41 3,4-diClPh CH _Two Single bond Unit 22 2-407 Unit 41 3,4-diClPh CH _Two Single bond unit 23 2-408 unit 41 3,4-diClPh CH _Two Single bond unit 24 2-409 unit 41 3,4-diClPh CH _Two Single bond unit 25 2-410 unit 41 3,4-diClPh CH _Two Single bond unit 26 2-411 unit 41 3,4-diClPh CH _Two Single bond unit 27 2-412 unit 41 3,4-diClPh CH _Two Single bond unit 28 2-413 unit 41 3,4-diClPh CH _Two Single bond unit 29 2-414 unit 41 3,4-diClPh CH _Two Single bond unit 30 2-415 unit 41 3,4-diClPh CH _Two Single bond unit 31 2-416 unit 41 3,4-diClPh CH _Two Single bond unit 32 2-417 unit 41 3,4-diClPh CH _Two Single bond device 65 2-418 device 41 3,4-diClPh CH _Two Single bond Unit 66 2-419 Unit 41 3,4-diClPh CH _Two Single bond unit 67 2-420 unit 41 3,4-diClPh CH _Two Single bond device 68 2-421 device 41 3,4-diClPh CH _Two Single bond unit 69 2-422 unit 41 3,4-diClPh CH _Two Single bond unit 70 2-423 unit 41 3,4-diClPh CH _Two Single bond unit 71 2-424 unit 41 3,4-diClPh CH _Two Single bond unit 72 2-425 unit 41 3,4-diClPh CH _Two Single bond unit 73 2-426 unit 41 3,4-diClPh CH _Two Single bond unit 74 2-427 unit 41 3,4-diClPh CH _Two Single bond unit 75 2-428 unit 41 3,4-diClPh CH _Two Single bond unit 76 2-429 unit 41 3,4-diClPh CH _Two Single bond unit 77 2-430 unit 41 3,4-diClPh CH _Two Single bond unit 78 2-431 unit 41 3,4-diClPh CH _Two Single bond unit 79 2-432 unit 41 3,4-diClPh CH _Two Single bond device 80 2-433 device 42 3,4-diClPh CH _Two Single bond unit 1 2-434 unit 42 3,4-diClPh CH _Two Single bond Unit 2 2-435 Unit 42 3,4-diClPh CH _Two Single bond unit 3 2-436 unit 42 3,4-diClPh CH _Two Single bond unit 4 2-437 unit 42 3,4-diClPh CH _Two Single bond unit 5 2-438 unit 42 3,4-diClPh CH _Two Single bond unit 6 2-439 unit 42 3,4-diClPh CH _Two Single bond device 7 2-440 device 42 3,4-diClPh CH _Two Single bond unit 8 2-441 unit 42 3,4-diClPh CH _Two Single bond unit 9 2-442 unit 42 3,4-diClPh CH _Two Single bond unit 10 2-443 unit 42 3,4-diClPh CH _Two Single bond unit 11 2-444 unit 42 3,4-diClPh CH _Two Single bond unit 12 2-445 unit 42 3,4-diClPh CH _Two Single bond unit 13 2-446 unit 42 3,4-diClPh CH _Two Single bond unit 14 2-447 unit 42 3,4-diClPh CH _Two Single bond unit 15 2-448 unit 42 3,4-diClPh CH _Two Single bond Unit 16 2-449 Unit 42 3,4-diClPh CH _Two Single bond unit 17 2-450 unit 42 3,4-diClPh CH _Two Single bond unit 18 2-451 unit 42 3,4-diClPh CH _Two Single bond unit 19 2-452 unit 42 3,4-diClPh CH _Two Single bond unit 20 2-453 unit 42 3,4-diClPh CH _Two Single bond unit 21 2-454 unit 42 3,4-diClPh CH _Two Single bond unit 22 2-455 unit 42 3,4-diClPh CH _Two Single bond unit 23 2-456 unit 42 3,4-diClPh CH _Two Single bond unit 24 2-457 unit 42 3,4-diClPh CH _Two Single bond unit 25 2-458 unit 42 3,4-diClPh CH _Two Single bond unit 26 2-459 unit 42 3,4-diClPh CH _Two Single bond unit 27 2-460 unit 42 3,4-diClPh CH _Two Single bond unit 28 2-461 unit 42 3,4-diClPh CH _Two Single bond unit 29 2-462 unit 42 3,4-diClPh CH _Two Single bond unit 30 2-463 unit 42 3,4-diClPh CH _Two Single bond unit 31 2-464 unit 42 3,4-diClPh CH _Two Single bond unit 32 2-465 unit 42 3,4-diClPh CH _Two Single bond unit 65 2-466 unit 42 3,4-diClPh CH _Two Single bond unit 66 2-467 unit 42 3,4-diClPh CH _Two Single bond unit 67 2-468 unit 42 3,4-diClPh CH _Two Single bond device 68 2-469 device 42 3,4-diClPh CH _Two Single bond unit 69 2-470 unit 42 3,4-diClPh CH _Two Single bond unit 70 2-471 unit 42 3,4-diClPh CH _Two Single bond unit 71 2-472 unit 42 3,4-diClPh CH _Two Single bond unit 72 2-473 unit 42 3,4-diClPh CH _Two Single bond unit 73 2-474 unit 42 3,4-diClPh CH _Two Single bond unit 74 2-475 unit 42 3,4-diClPh CH _Two Single bond Unit 75 2-476 Unit 42 3,4-diClPh CH _Two Single bond unit 76 2-477 unit 42 3,4-diClPh CH _Two Single bond unit 77 2-478 unit 42 3,4-diClPh CH _Two Single bond unit 78 2-479 unit 42 3,4-diClPh CH _Two Single bond device 79 2-480 device 42 3,4-diClPh CH _Two Single bond device 80 2-481 device 43 3,4-diClPh CH _Two Single bond unit 1 2-482 unit 43 3,4-diClPh CH _Two Single bond unit 2 2-483 unit 43 3,4-diClPh CH _Two Single bond position 3 2-484 position 43 3,4-diClPh CH _Two Single bond unit 4 2-485 unit 43 3,4-diClPh CH _Two Single bond device 5 2-486 device 43 3,4-diClPh CH _Two Single bond unit 6 2-487 unit 43 3,4-diClPh CH _Two Single bond place 7 2-488 place 43 3,4-diClPh CH _Two Single bond device 8 2-489 device 43 3,4-diClPh CH _Two Single bond unit 9 2-490 unit 43 3,4-diClPh CH _Two Single bond unit 10 2-491 unit 43 3,4-diClPh CH _Two Single bond unit 11 2-492 unit 43 3,4-diClPh CH _Two Single bond unit 12 2-493 unit 43 3,4-diClPh CH _Two Single bond unit 13 2-494 unit 43 3,4-diClPh CH _Two Single bond unit 14 2-495 unit 43 3,4-diClPh CH _Two Single bond unit 15 2-496 unit 43 3,4-diClPh CH _Two Single bond unit 16 2-497 unit 43 3,4-diClPh CH _Two Single bond unit 17 2-498 unit 43 3,4-diClPh CH _Two Single bond unit 18 2-499 unit 43 3,4-diClPh CH _Two Single bond unit 19 2-500 unit 43 3,4-diClPh CH _Two Single bond unit 20 2-501 unit 43 3,4-diClPh CH _Two Single bond unit 21 2-502 unit 43 3,4-diClPh CH _Two Single bond unit 22 2-503 unit 43 3,4-diClPh CH _Two Single bond unit 23 2-504 unit 43 3,4-diClPh CH _Two Single bond unit 24 2-505 unit 43 3,4-diClPh CH _Two Single bond unit 25 2-506 unit 43 3,4-diClPh CH _Two Single bond unit 26 2-507 unit 43 3,4-diClPh CH _Two Single bond unit 27 2-508 unit 43 3,4-diClPh CH _Two Single bond unit 28 2-509 unit 43 3,4-diClPh CH _Two Single bond unit 29 2-510 unit 43 3,4-diClPh CH _Two Single bond device 30 2-511 device 43 3,4-diClPh CH _Two Single bond unit 31 2-512 unit 43 3,4-diClPh CH _Two Single bond unit 32 2-513 unit 43 3,4-diClPh CH _Two Single bond device 65 2-514 device 43 3,4-diClPh CH _Two Single bond unit 66 2-515 unit 43 3,4-diClPh CH _Two Single bond device 67 2-516 device 43 3,4-diClPh CH _Two Single bond device 68 2-517 device 43 3,4-diClPh CH _Two Single bond device 69 2-518 device 43 3,4-diClPh CH _Two Single bond device 70 2-519 device 43 3,4-diClPh CH _Two Single bond unit 71 2-520 unit 43 3,4-diClPh CH _Two Single bond unit 72 2-521 unit 43 3,4-diClPh CH _Two Single bond unit 73 2-522 unit 43 3,4-diClPh CH _Two Single bond unit 74 2-523 unit 43 3,4-diClPh CH _Two Single bond unit 75 2-524 unit 43 3,4-diClPh CH _Two Single bond unit 76 2-525 unit 43 3,4-diClPh CH _Two Single bond unit 77 2-526 unit 43 3,4-diClPh CH _Two Single bond unit 78 2-527 unit 43 3,4-diClPh CH _Two Single bond device 79 2-528 device 43 3,4-diClPh CH _Two Single bond position 80 化合物 Compound number R ¹ R ^Two A B Z──────────────────────────────────── 2-529 Place 44 3,4-diClPh CH _Two Single bond unit 1 2-530 unit 44 3,4-diClPh CH _Two Single bond unit 2 2-531 unit 44 3,4-diClPh CH _Two Single bond position 3 2-532 position 44 3,4-diClPh CH _Two Single bond unit 4 2-533 unit 44 3,4-diClPh CH _Two Single bond device 5 2-534 device 44 3,4-diClPh CH _Two Single bond unit 6 2-535 unit 44 3,4-diClPh CH _Two Single bond device 7 2-536 device 44 3,4-diClPh CH _Two Single bond device 8 2-537 device 44 3,4-diClPh CH _Two Single bond device 9 2-538 device 44 3,4-diClPh CH _Two Single bond unit 10 2-539 unit 44 3,4-diClPh CH _Two Single bond unit 11 2-540 unit 44 3,4-diClPh CH _Two Single bond unit 12 2-541 unit 44 3,4-diClPh CH _Two Single bond unit 13 2-542 unit 44 3,4-diClPh CH _Two Single bond unit 14 2-543 unit 44 3,4-diClPh CH _Two Single bond unit 15 2-544 unit 44 3,4-diClPh CH _Two Single bond unit 16 2-545 unit 44 3,4-diClPh CH _Two Single bond unit 17 2-546 unit 44 3,4-diClPh CH _Two Single bond unit 18 2-548 unit 44 3,4-diClPh CH _Two Single bond unit 20 2-549 unit 44 3,4-diClPh CH _Two Single bond unit 21 2-550 unit 44 3,4-diClPh CH _Two Single bond unit 22 2-551 unit 44 3,4-diClPh CH _Two Single bond unit 23 2-552 unit 44 3,4-diClPh CH _Two Single bond unit 24 2-553 unit 44 3,4-diClPh CH _Two Single bond unit 25 2-554 unit 44 3,4-diClPh CH _Two Single bond unit 26 2-555 unit 44 3,4-diClPh CH _Two Single bond unit 27 2-556 unit 44 3,4-diClPh CH _Two Single bond unit 28 2-557 unit 44 3,4-diClPh CH _Two Single bond unit 29 2-558 unit 44 3,4-diClPh CH _Two Single bond unit 30 2-559 unit 44 3,4-diClPh CH _Two Single bond unit 31 2-560 unit 44 3,4-diClPh CH _Two Single bond unit 32 2-561 unit 44 3,4-diClPh CH _Two Single bond unit 65 2-562 unit 44 3,4-diClPh CH _Two Single bond unit 66 2-563 unit 44 3,4-diClPh CH _Two Single bond unit 67 2-564 unit 44 3,4-diClPh CH _Two Single bond unit 68 2-565 unit 44 3,4-diClPh CH _Two Single bond device 69 2-566 device 44 3,4-diClPh CH _Two Single bond unit 70 2-567 unit 44 3,4-diClPh CH _Two Single bond unit 71 2-568 unit 44 3,4-diClPh CH _Two Single bond unit 72 2-569 unit 44 3,4-diClPh CH _Two Single bond unit 73 2-570 unit 44 3,4-diClPh CH _Two Single bond unit 74 2-571 unit 44 3,4-diClPh CH _Two Single bond unit 75 2-572 unit 44 3,4-diClPh CH _Two Single bond unit 76 2-573 unit 44 3,4-diClPh CH _Two Single bond unit 77 2-574 unit 44 3,4-diClPh CH _Two Single bond unit 78 2-575 unit 44 3,4-diClPh CH _Two Single bond unit 79 2-576 unit 44 3,4-diClPh CH _Two Single bond unit 80 2-577 unit 45 3,4-diClPh CH _Two Single bond position 1 2-578 position 45 3,4-diClPh CH _Two Single bond unit 22-579 unit 45 3,4-diClPh CH _Two Single bond position 3 2-580 position 45 3,4-diClPh CH _Two Single bond unit 4 2-581 unit 45 3,4-diClPh CH _Two Single bond device 5 2-582 device 45 3,4-diClPh CH _Two Single bond unit 6 2-583 unit 45 3,4-diClPh CH _Two Single bond unit 7 2-584 unit 45 3,4-diClPh CH _Two Single bond unit 8 2-585 unit 45 3,4-diClPh CH _Two Single bond unit 9 2-586 unit 45 3,4-diClPh CH _Two Single bond unit 10 2-587 unit 45 3,4-diClPh CH _Two Single bond unit 11 2-588 unit 45 3,4-diClPh CH _Two Single bond unit 12 2-589 unit 45 3,4-diClPh CH _Two Single bond unit 13 2-590 unit 45 3,4-diClPh CH _Two Single bond unit 14 2-591 unit 45 3,4-diClPh CH _Two Single bond unit 15 2-592 unit 45 3,4-diClPh CH _Two Single bond unit 16 2-593 unit 45 3,4-diClPh CH _Two Single bond unit 17 2-594 unit 45 3,4-diClPh CH _Two Single bond unit 18 2-595 unit 45 3,4-diClPh CH _Two Single bond unit 19 2-596 unit 45 3,4-diClPh CH _Two Single bond unit 20 2-597 unit 45 3,4-diClPh CH _Two Single bond unit 21 2-598 unit 45 3,4-diClPh CH _Two Single bond unit 22 2-599 unit 45 3,4-diClPh CH _Two Single bond unit 23 2-600 unit 45 3,4-diClPh CH _Two Single bond unit 24 2-601 unit 45 3,4-diClPh CH _Two Single bond unit 25 2-602 unit 45 3,4-diClPh CH _Two Single bond unit 26 2-603 unit 45 3,4-diClPh CH _Two Single bond unit 27 2-604 unit 45 3,4-diClPh CH _Two Single bond unit 28 2-605 unit 45 3,4-diClPh CH _Two Single bond unit 29 2-606 unit 45 3,4-diClPh CH _Two Single bond unit 30 2-607 unit 45 3,4-diClPh CH _Two Single bond unit 31 2-608 unit 45 3,4-diClPh CH _Two Single bond unit 32 2-609 unit 45 3,4-diClPh CH _Two Single bond device 65 2-610 device 45 3,4-diClPh CH _Two Single bond unit 66 2-611 unit 45 3,4-diClPh CH _Two Single bond unit 67 2-612 unit 45 3,4-diClPh CH _Two Single bond device 68 2-613 device 45 3,4-diClPh CH _Two Single bond unit 69 2-614 unit 45 3,4-diClPh CH _Two Single bond unit 70 2-615 unit 45 3,4-diClPh CH _Two Single bond Unit 71 2-616 Unit 45 3,4-diClPh CH _Two Single bond unit 72 2-617 unit 45 3,4-diClPh CH _Two Single bond unit 73 2-618 unit 45 3,4-diClPh CH _Two Single bond Unit 74 2-618 Unit 45 3,4-diClPh CH _Two Single bond unit 75 2-620 unit 45 3,4-diClPh CH _Two Single bond unit 76 2-621 unit 45 3,4-diClPh CH _Two Single bond unit 77 2-622 unit 45 3,4-diClPh CH _Two Single bond unit 78 2-623 unit 45 3,4-diClPh CH _Two Single bond unit 79 2-624 unit 45 3,4-diClPh CH _Two Single bond device 80 2-625 device 46 3,4-diClPh CH _Two Single bond device 1 2-626 device 46 3,4-diClPh CH _Two Single bond unit 22-627 unit 46 3,4-diClPh CH _Two Single bond position 3 2-628 position 46 3,4-diClPh CH _Two Single bond position 4 2-629 position 46 3,4-diClPh CH _Two Single bond unit 5 2-630 unit 46 3,4-diClPh CH _Two Single bond device 6 2-631 device 46 3,4-diClPh CH _Two Single bond unit 7 2-632 unit 46 3,4-diClPh CH _Two Single bond device 8 2-633 device 46 3,4-diClPh CH _Two Single bond position 9 2-634 position 46 3,4-diClPh CH _Two Single bond device 10 2-635 device 46 3,4-diClPh CH _Two Single bond unit 11 2-636 unit 46 3,4-diClPh CH _Two Single bond unit 12 2-637 unit 46 3,4-diClPh CH _Two Single bond unit 13 2-638 unit 46 3,4-diClPh CH _Two Single bond unit 14 2-639 unit 46 3,4-diClPh CH _Two Single bond unit 15 2-640 unit 46 3,4-diClPh CH _Two Single bond unit 16 2-641 unit 46 3,4-diClPh CH _Two Single bond unit 17 2-642 unit 46 3,4-diClPh CH _Two Single bond unit 18 2-643 unit 46 3,4-diClPh CH _Two Single bond unit 19 2-644 unit 46 3,4-diClPh CH _Two Single bond unit 20 2-645 unit 46 3,4-diClPh CH _Two Single bond unit 21 2-646 unit 46 3,4-diClPh CH _Two Single bond unit 22 2-647 unit 46 3,4-diClPh CH _Two Single bond unit 23 2-648 unit 46 3,4-diClPh CH _Two Single bond unit 24 2-649 unit 46 3,4-diClPh CH _Two Single bond unit 25 2-650 unit 46 3,4-diClPh CH _Two Single bond unit 26 2-651 unit 46 3,4-diClPh CH _Two Single bond unit 27 2-652 unit 46 3,4-diClPh CH _Two Single bond unit 28 2-653 unit 46 3,4-diClPh CH _Two Single bond unit 29 2-654 unit 46 3,4-diClPh CH _Two Single bond unit 30 2-655 unit 46 3,4-diClPh CH _Two Single bond unit 31 2-656 unit 46 3,4-diClPh CH _Two Single bond unit 32 2-657 unit 46 3,4-diClPh CH _Two Single bond device 65 2-658 device 46 3,4-diClPh CH _Two Single bond unit 66 2-659 unit 46 3,4-diClPh CH _Two Single bond unit 67 2-660 unit 46 3,4-diClPh CH _Two Single bond device 68 2-661 device 46 3,4-diClPh CH _Two Single bond unit 69 2-662 unit 46 3,4-diClPh CH _Two Single bond unit 70 2-663 unit 46 3,4-diClPh CH _Two Single bond unit 71 2-664 unit 46 3,4-diClPh CH _Two Single bond unit 72 2-665 unit 46 3,4-diClPh CH _Two Single bond unit 73 2-666 unit 46 3,4-diClPh CH _Two Single bond unit 74 2-667 unit 46 3,4-diClPh CH _Two Single bond unit 75 2-668 unit 46 3,4-diClPh CH _Two Single bond device 76 2-669 device 46 3,4-diClPh CH _Two Single bond unit 77 2-670 unit 46 3,4-diClPh CH _Two Single bond unit 78 2-671 unit 46 3,4-diClPh CH _Two Single bond unit 79 2-672 unit 46 3,4-diClPh CH _Two Single bond unit 80 2-673 unit 47 3,4-diClPh CH _Two Single bond position 1 2-674 position 47 3,4-diClPh CH _Two Single bond unit 22-675 unit 47 3,4-diClPh CH _Two Single bond position 3 2-676 position 47 3,4-diClPh CH _Two Single bond unit 4 2-677 unit 47 3,4-diClPh CH _Two Single bond unit 5 2-678 unit 47 3,4-diClPh CH _Two Single bond device 6 2-679 device 47 3,4-diClPh CH _Two Single bond unit 7 2-680 unit 47 3,4-diClPh CH _Two Single bond device 8 2-681 device 47 3,4-diClPh CH _Two Single bond unit 9 2-682 unit 47 3,4-diClPh CH _Two Single bond device 10 2-683 device 47 3,4-diClPh CH _Two Single bond unit 11 2-684 unit 47 3,4-diClPh CH _Two Single bond unit 12 2-685 unit 47 3,4-diClPh CH _Two Single bond unit 13 2-686 unit 47 3,4-diClPh CH _Two Single bond unit 14 2-687 unit 47 3,4-diClPh CH _Two Single bond unit 15 2-688 unit 47 3,4-diClPh CH _Two Single bond unit 16 2-689 unit 47 3,4-diClPh CH _Two Single bond unit 17 2-690 unit 47 3,4-diClPh CH _Two Single bond unit 18 2-691 unit 47 3,4-diClPh CH _Two Single bond unit 19 2-692 unit 47 3,4-diClPh CH _Two Single bond unit 20 2-693 unit 47 3,4-diClPh CH _Two Single bond unit 21 2-694 unit 47 3,4-diClPh CH _Two Single bond unit 22 2-695 unit 47 3,4-diClPh CH _Two Single bond unit 23 2-696 unit 47 3,4-diClPh CH _Two Single bond unit 24 2-697 unit 47 3,4-diClPh CH _Two Single bond unit 25 2-698 unit 47 3,4-diClPh CH _Two Single bond unit 26 2-699 unit 47 3,4-diClPh CH _Two Single bond unit 27 2-700 unit 47 3,4-diClPh CH _Two Single bond unit 28 2-701 unit 47 3,4-diClPh CH _Two Single bond unit 29 2-702 unit 47 3,4-diClPh CH _Two Single bond unit 30 2-703 unit 47 3,4-diClPh CH _Two Single bond unit 31 2-704 unit 47 3,4-diClPh CH _Two Single bond unit 32 2-705 unit 47 3,4-diClPh CH _Two Single bond unit 65 2-706 unit 47 3,4-diClPh CH _Two Single bond unit 66 2-707 unit 47 3,4-diClPh CH _Two Single bond unit 67 2-708 unit 47 3,4-diClPh CH _Two Single bond device 68 2-709 device 47 3,4-diClPh CH _Two Single bond unit 69 2-710 unit 47 3,4-diClPh CH _Two Single bond unit 70 2-711 unit 47 3,4-diClPh CH _Two Single bond unit 71 2-712 unit 47 3,4-diClPh CH _Two Single bond unit 72 2-713 unit 47 3,4-diClPh CH _Two Single bond unit 73 2-714 unit 47 3,4-diClPh CH _Two Single bond unit 74 2-715 unit 47 3,4-diClPh CH _Two Single bond unit 75 2-716 unit 47 3,4-diClPh CH _Two Single bond unit 76 2-717 unit 47 3,4-diClPh CH _Two Single bond unit 77 2-718 unit 47 3,4-diClPh CH _Two Single bond unit 78 2-719 unit 47 3,4-diClPh CH _Two Single bond unit 79 2-720 unit 47 3,4-diClPh CH _Two Single bond device 80 2-721 device 81 3,4-diClPh CH _Two Single bond unit 1 2-722 unit 81 3,4-diClPh CH _Two Single bond unit 2 2-723 unit 81 3,4-diClPh CH _Two Single bond position 3 2-724 position 81 3,4-diClPh CH _Two Single bond unit 4 2-725 unit 81 3,4-diClPh CH _Two Single bond device 5 2-726 device 81 3,4-diClPh CH _Two Single bond device 6 2-727 device 81 3,4-diClPh CH _Two Single bond unit 7 2-728 unit 81 3,4-diClPh CH _Two Single bond device 8 2-729 device 81 3,4-diClPh CH _Two Single bond unit 9 2-730 unit 81 3,4-diClPh CH _Two Single bond unit 10 2-731 unit 81 3,4-diClPh CH _Two Single bond unit 11 2-732 unit 81 3,4-diClPh CH _Two Single bond unit 12 2-733 unit 81 3,4-diClPh CH _Two Single bond unit 13 2-734 unit 81 3,4-diClPh CH _Two Single bond unit 14 2-735 unit 81 3,4-diClPh CH _Two Single bond unit 15 2-736 unit 81 3,4-diClPh CH _Two Single bond unit 16 2-737 unit 81 3,4-diClPh CH _Two Single bond unit 17 2-738 unit 81 3,4-diClPh CH _Two Single bond unit 18 2-739 unit 81 3,4-diClPh CH _Two Single bond unit 19 2-740 unit 81 3,4-diClPh CH _Two Single bond unit 20 2-741 unit 81 3,4-diClPh CH _Two Single bond unit 21 2-742 unit 81 3,4-diClPh CH _Two Single bond unit 22 2-743 unit 81 3,4-diClPh CH _Two Single bond unit 23 2-744 unit 81 3,4-diClPh CH _Two Single bond unit 24 2-745 unit 81 3,4-diClPh CH _Two Single bond unit 25 2-746 unit 81 3,4-diClPh CH _Two Single bond unit 26 2-747 unit 81 3,4-diClPh CH _Two Single bond unit 27 2-748 unit 81 3,4-diClPh CH _Two Single bond unit 28 2-749 unit 81 3,4-diClPh CH _Two Single bond unit 29 2-750 unit 81 3,4-diClPh CH _Two Single bond unit 30 2-751 unit 81 3,4-diClPh CH _Two Single bond unit 31 2-752 unit 81 3,4-diClPh CH _Two Single bond unit 32 2-753 unit 81 3,4-diClPh CH _Two Single bond device 65 2-754 device 81 3,4-diClPh CH _Two Single bond unit 66 2-755 unit 81 3,4-diClPh CH _Two Single bond unit 67 2-756 unit 81 3,4-diClPh CH _Two Single bond device 68 2-757 device 81 3,4-diClPh CH _Two Single bond unit 69 2-758 unit 81 3,4-diClPh CH _Two Single bond unit 70 2-759 unit 81 3,4-diClPh CH _Two Single bond unit 71 2-760 unit 81 3,4-diClPh CH _Two Single bond unit 72 2-761 unit 81 3,4-diClPh CH _Two Single bond unit 73 2-762 unit 81 3,4-diClPh CH _Two Single bond unit 74 2-763 unit 81 3,4-diClPh CH _Two Single bond unit 75 2-764 unit 81 3,4-diClPh CH _Two Single bond unit 76 2-765 unit 81 3,4-diClPh CH _Two Single bond unit 77 2-766 unit 81 3,4-diClPh CH _Two Single bond unit 78 2-767 unit 81 3,4-diClPh CH _Two Single bond device 79 2-768 device 81 3,4-diClPh CH _Two Single bond unit 80 2-769 unit 48 3,4-diClPh CH _Two Single bond device 1 2-770 device 48 3,4-diClPh CH _Two Single bond unit 22-771 unit 48 3,4-diClPh CH _Two Single bond position 3 2-772 position 48 3,4-diClPh CH _Two Single bond unit 4 2-773 unit 48 3,4-diClPh CH _Two Single bond unit 5 2-774 unit 48 3,4-diClPh CH _Two Single bond unit 6 2-775 unit 48 3,4-diClPh CH _Two Single bond device 7 2-776 device 48 3,4-diClPh CH _Two Single bond unit 8 2-777 unit 48 3,4-diClPh CH _Two Single bond unit 9 2-778 unit 48 3,4-diClPh CH _Two Single bond unit 10 2-779 unit 48 3,4-diClPh CH _Two Single bond unit 11 2-780 unit 48 3,4-diClPh CH _Two Single bond unit 12 2-781 unit 48 3,4-diClPh CH _Two Single bond unit 13 2-782 unit 48 3,4-diClPh CH _Two Single bond unit 14 2-783 unit 48 3,4-diClPh CH _Two Single bond unit 15 2-784 unit 48 3,4-diClPh CH _Two Single bond unit 16 2-785 unit 48 3,4-diClPh CH _Two Single bond unit 17 2-786 unit 48 3,4-diClPh CH _Two Single bond unit 18 2-787 unit 48 3,4-diClPh CH _Two Single bond unit 19 2-788 unit 48 3,4-diClPh CH _Two Single bond unit 20 2-789 unit 48 3,4-diClPh CH _Two Single bond unit 21 2-790 unit 48 3,4-diClPh CH _Two Single bond unit 22 2-791 unit 48 3,4-diClPh CH _Two Single bond unit 23 2-792 unit 48 3,4-diClPh CH _Two Single bond unit 24 2-793 unit 48 3,4-diClPh CH _Two Single bond unit 25 2-794 unit 48 3,4-diClPh CH _Two Single bond unit 26 2-795 unit 48 3,4-diClPh CH _Two Single bond unit 27 2-796 unit 48 3,4-diClPh CH _Two Single bond unit 28 2-797 unit 48 3,4-diClPh CH _Two Single bond unit 29 2-798 unit 48 3,4-diClPh CH _Two Single bond device 30 2-799 device 48 3,4-diClPh CH _Two Single bond unit 31 2-800 unit 48 3,4-diClPh CH _Two Single bond unit 32 2-801 unit 48 3,4-diClPh CH _Two Single bond device 65 2-802 device 48 3,4-diClPh CH _Two Single bond unit 66 2-803 unit 48 3,4-diClPh CH _Two Single bond unit 67 2-804 unit 48 3,4-diClPh CH _Two Single bond device 68 2-805 device 48 3,4-diClPh CH _Two Single bond device 69 2-806 device 48 3,4-diClPh CH _Two Single bond device 70 2-807 device 48 3,4-diClPh CH _Two Single bond unit 71 2-808 unit 48 3,4-diClPh CH _Two Single bond unit 72 2-809 unit 48 3,4-diClPh CH _Two Single bond unit 73 2-810 unit 48 3,4-diClPh CH _Two Single bond unit 74 2-811 unit 48 3,4-diClPh CH _Two Single bond unit 75 2-812 unit 48 3,4-diClPh CH _Two Single bond unit 76 2-813 unit 48 3,4-diClPh CH _Two Single bond unit 77 2-814 unit 48 3,4-diClPh CH _Two Single bond unit 78 2-815 unit 48 3,4-diClPh CH _Two Single bond device 79 2-816 device 48 3,4-diClPh CH _Two Single bond device 80 2-817 device 49 3,4-diClPh CH _Two Single bond position 1 2-818 position 49 3,4-diClPh CH _Two Single bond unit 22-819 unit 49 3,4-diClPh CH _Two Single bond position 3 2-820 position 49 3,4-diClPh CH _Two Single bond unit 4 2-821 unit 49 3,4-diClPh CH _Two Single bond 5 2-822 49 3,4-diClPh CH _Two Single bond 6 2-823 49,4-diClPh CH _Two Single bond unit 7 2-824 unit 49 3,4-diClPh CH _Two Single bond device 8 2-825 device 49 3,4-diClPh CH _Two Single bond unit 9 2-826 unit 49 3,4-diClPh CH _Two Single bond unit 10 2-827 unit 49 3,4-diClPh CH _Two Single bond unit 11 2-828 unit 49 3,4-diClPh CH _Two Single bond unit 12 2-829 unit 49 3,4-diClPh CH _Two Single bond unit 13 2-830 unit 49 3,4-diClPh CH _Two Single bond unit 14 2-831 unit 49 3,4-diClPh CH _Two Single bond unit 15 2-832 unit 49 3,4-diClPh CH _Two Single bond unit 16 2-833 unit 49 3,4-diClPh CH _Two Single bond unit 17 2-834 unit 49 3,4-diClPh CH _Two Single bond unit 18 2-835 unit 49 3,4-diClPh CH _Two Single bond unit 19 2-836 unit 49 3,4-diClPh CH _Two Single bond unit 20 2-837 unit 49 3,4-diClPh CH _Two Single bond unit 21 2-838 unit 49 3,4-diClPh CH _Two Single bond unit 22 2-839 unit 49 3,4-diClPh CH _Two Single bond unit 23 2-840 unit 49 3,4-diClPh CH _Two Single bond unit 24 2-841 unit 49 3,4-diClPh CH _Two Single bond unit 25 2-842 unit 49 3,4-diClPh CH _Two Single bond unit 26 2-843 unit 49 3,4-diClPh CH _Two Single bond unit 27 2-844 unit 49 3,4-diClPh CH _Two Single bond unit 28 2-845 unit 49 3,4-diClPh CH _Two Single bond unit 29 2-846 unit 49 3,4-diClPh CH _Two Single bond device 30 2-847 device 49 3,4-diClPh CH _Two Single bond unit 31 2-848 unit 49 3,4-diClPh CH _Two Single bond unit 32 2-849 unit 49 3,4-diClPh CH _Two Single bond device 65 2-850 device 49 3,4-diClPh CH _Two Single bond unit 66 2-851 unit 49 3,4-diClPh CH _Two Single bond unit 67 2-852 unit 49 3,4-diClPh CH _Two Single bond unit 68 2-853 unit 49 3,4-diClPh CH _Two Single bond unit 69 2-854 unit 49 3,4-diClPh CH _Two Single bond unit 70 2-855 unit 49 3,4-diClPh CH _Two Single bond unit 71 2-856 unit 49 3,4-diClPh CH _Two Single bond unit 72 2-857 unit 49 3,4-diClPh CH _Two Single bond unit 73 2-858 unit 49 3,4-diClPh CH _Two Single bond unit 74 2-859 unit 49 3,4-diClPh CH _Two Single bond unit 75 2-860 unit 49 3,4-diClPh CH _Two Single bond unit 76 2-861 unit 49 3,4-diClPh CH _Two Single bond unit 77 2-862 unit 49 3,4-diClPh CH _Two Single bond unit 78 2-863 unit 49 3,4-diClPh CH _Two Single bond unit 79 2-864 unit 49 3,4-diClPh CH _Two Single bond device 80 2-865 device 50 3,4-diClPh CH _Two Single bond device 1 2-866 device 50 3,4-diClPh CH _Two Single bond unit 2 2-867 unit 50 3,4-diClPh CH _Two Single bond device 3 2-868 device 50 3,4-diClPh CH _Two Single bond device 4 2-869 device 50 3,4-diClPh CH _Two Single bond device 5 2-870 device 50 3,4-diClPh CH _Two Single bond unit 6 2-871 unit 50 3,4-diClPh CH _Two Single bond device 7 2-872 device 50 3,4-diClPh CH _Two Single bond device 8 2-873 device 50 3,4-diClPh CH _Two Single bond device 9 2-874 device 50 3,4-diClPh CH _Two Single bond device 10 2-875 device 50 3,4-diClPh CH _Two Single bond unit 11 2-876 unit 50 3,4-diClPh CH _Two Single bond unit 12 2-877 unit 50 3,4-diClPh CH _Two Single bond unit 13 2-878 unit 50 3,4-diClPh CH _Two Single bond unit 14 2-879 unit 50 3,4-diClPh CH _Two Single bond unit 15 2-880 unit 50 3,4-diClPh CH _Two Single bond unit 16 2-881 unit 50 3,4-diClPh CH _Two Single bond unit 17 2-882 unit 50 3,4-diClPh CH _Two Single bond unit 18 2-883 unit 50 3,4-diClPh CH _Two Single bond unit 19 2-884 unit 50 3,4-diClPh CH _Two Single bond unit 20 2-885 unit 50 3,4-diClPh CH _Two Single bond unit 21 2-886 unit 50 3,4-diClPh CH _Two Single bond unit 22 2-887 unit 50 3,4-diClPh CH _Two Single bond unit 23 2-888 unit 50 3,4-diClPh CH _Two Single bond unit 24 2-889 unit 50 3,4-diClPh CH _Two Single bond unit 25 2-890 unit 50 3,4-diClPh CH _Two Single bond unit 26 2-891 unit 50 3,4-diClPh CH _Two Single bond unit 27 2-892 unit 50 3,4-diClPh CH _Two Single bond unit 28 2-893 unit 50 3,4-diClPh CH _Two Single bond unit 29 2-894 unit 50 3,4-diClPh CH _Two Single bond device 30 2-895 device 50 3,4-diClPh CH _Two Single bond unit 31 2-896 unit 50 3,4-diClPh CH _Two Single bond unit 32 2-897 unit 50 3,4-diClPh CH _Two Single bond device 65 2-898 device 50 3,4-diClPh CH _Two Single bond device 66 2-899 device 50 3,4-diClPh CH _Two Single bond unit 67 2-900 unit 50 3,4-diClPh CH _Two Single bond device 68 2-901 device 50 3,4-diClPh CH _Two Single bond unit 69 2-902 unit 50 3,4-diClPh CH _Two Single bond device 70 2-903 device 50 3,4-diClPh CH _Two Single bond unit 71 2-904 unit 50 3,4-diClPh CH _Two Single bond unit 72 2-905 unit 50 3,4-diClPh CH _Two Single bond device 73 2-906 device 50 3,4-diClPh CH _Two Single bond unit 74 2-907 unit 50 3,4-diClPh CH _Two Single bond unit 75 2-908 unit 50 3,4-diClPh CH _Two Single bond unit 76 2-909 unit 50 3,4-diClPh CH _Two Single bond unit 77 2-910 unit 50 3,4-diClPh CH _Two Single bond unit 78 2-911 unit 50 3,4-diClPh CH _Two Single bond device 79 2-912 device 50 3,4-diClPh CH _Two Single bond device 80 2-913 device 51 3,4-diClPh CH _Two Single bond device 1 2-914 device 51 3,4-diClPh CH _Two Single bond device 2 2-915 device 51 3,4-diClPh CH _Two Single bond position 3 2-916 position 51 3,4-diClPh CH _Two Single bond unit 4 2-917 unit 51 3,4-diClPh CH _Two Single bond device 5 2-918 device 51 3,4-diClPh CH _Two Single bond device 6 2-919 device 51 3,4-diClPh CH _Two Single bond device 7 2-920 device 51 3,4-diClPh CH _Two Single bond device 8 2-921 device 51 3,4-diClPh CH _Two Single bond device 9 2-922 device 51 3,4-diClPh CH _Two Single bond device 10 2-923 device 51 3,4-diClPh CH _Two Single bond unit 11 2-924 unit 51 3,4-diClPh CH _Two Single bond unit 12 2-925 unit 51 3,4-diClPh CH _Two Single bond unit 13 2-926 unit 51 3,4-diClPh CH _Two Single bond unit 14 2-927 unit 51 3,4-diClPh CH _Two Single bond unit 15 2-928 unit 51 3,4-diClPh CH _Two Single bond unit 16 2-929 unit 51 3,4-diClPh CH _Two Single bond unit 17 2-930 unit 51 3,4-diClPh CH _Two Single bond unit 18 2-931 unit 51 3,4-diClPh CH _Two Single bond unit 19 2-932 unit 51 3,4-diClPh CH _Two Single bond device 20 2-933 device 51 3,4-diClPh CH _Two Single bond unit 21 2-934 unit 51 3,4-diClPh CH _Two Single bond unit 22 2-935 unit 51 3,4-diClPh CH _Two Single bond unit 23 2-936 unit 51 3,4-diClPh CH _Two Single bond unit 24 2-937 unit 51 3,4-diClPh CH _Two Single bond unit 25 2-938 unit 51 3,4-diClPh CH _Two Single bond unit 26 2-939 unit 51 3,4-diClPh CH _Two Single bond unit 27 2-940 unit 51 3,4-diClPh CH _Two Single bond unit 28 2-941 unit 51 3,4-diClPh CH _Two Single bond unit 29 2-942 unit 51 3,4-diClPh CH _Two Single bond device 30 2-943 device 51 3,4-diClPh CH _Two Single bond unit 31 2-944 unit 51 3,4-diClPh CH _Two Single bond unit 32 2-945 unit 51 3,4-diClPh CH _Two Single bond device 65 2-946 device 51 3,4-diClPh CH _Two Single bond device 66 2-947 device 51 3,4-diClPh CH _Two Single bond unit 67 2-948 unit 51 3,4-diClPh CH _Two Single bond device 68 2-949 device 51 3,4-diClPh CH _Two Single bond device 69 2-950 device 51 3,4-diClPh CH _Two Single bond unit 70 2-951 unit 51 3,4-diClPh CH _Two Single bond unit 71 2-952 unit 51 3,4-diClPh CH _Two Single bond unit 72 2-953 unit 51 3,4-diClPh CH _Two Single bond unit 73 2-954 unit 51 3,4-diClPh CH _Two Single bond unit 74 2-955 unit 51 3,4-diClPh CH _Two Single bond unit 75 2-956 unit 51 3,4-diClPh CH _Two Single bond unit 76 2-957 unit 51 3,4-diClPh CH _Two Single bond unit 77 2-958 unit 51 3,4-diClPh CH _Two Single bond unit 78 2-959 unit 51 3,4-diClPh CH _Two Single bond device 79 2-960 device 51 3,4-diClPh CH _Two Single bond device 80 2-961 device 52 3,4-diClPh CH _Two Single bond device 1 2-962 device 52 3,4-diClPh CH _Two Single bond unit 2 2-963 unit 52 3,4-diClPh CH _Two Single bond unit 3 2-964 unit 52 3,4-diClPh CH _Two Single bond unit 4 2-965 unit 52 3,4-diClPh CH _Two Single bond device 5 2-966 device 52 3,4-diClPh CH _Two Single bond 6 6-967 52 3,4-diClPh CH _Two Single bond unit 7 2-968 unit 52 3,4-diClPh CH _Two Single bond device 8 2-969 device 52 3,4-diClPh CH _Two Single bond device 9 2-970 device 52 3,4-diClPh CH _Two Single bond unit 10 2-971 unit 52 3,4-diClPh CH _Two Single bond unit 11 2-972 unit 52 3,4-diClPh CH _Two Single bond unit 12 2-973 unit 52 3,4-diClPh CH _Two Single bond unit 13 2-974 unit 52 3,4-diClPh CH _Two Single bond unit 14 2-975 unit 52 3,4-diClPh CH _Two Single bond unit 15 2-976 unit 52 3,4-diClPh CH _Two Single bond unit 16 2-977 unit 52 3,4-diClPh CH _Two Single bond unit 17 2-978 unit 52 3,4-diClPh CH _Two Single bond unit 18 2-979 unit 52 3,4-diClPh CH _Two Single bond unit 19 2-980 unit 52 3,4-diClPh CH _Two Single bond unit 20 2-981 unit 52 3,4-diClPh CH _Two Single bond unit 21 2-982 unit 52 3,4-diClPh CH _Two Single bond unit 22 2-983 unit 52 3,4-diClPh CH _Two Single bond unit 23 2-984 unit 52 3,4-diClPh CH _Two Single bond unit 24 2-985 unit 52 3,4-diClPh CH _Two Single bond unit 25 2-986 unit 52 3,4-diClPh CH _Two Single bond unit 26 2-987 unit 52 3,4-diClPh CH _Two Single bond unit 27 2-988 unit 52 3,4-diClPh CH _Two Single bond unit 28 2-989 unit 52 3,4-diClPh CH _Two Single bond unit 29 2-990 unit 52 3,4-diClPh CH _Two Single bond device 30 2-991 device 52 3,4-diClPh CH _Two Single bond unit 31 2-992 unit 52 3,4-diClPh CH _Two Single bond unit 32 2-993 unit 52 3,4-diClPh CH _Two Single bond unit 65 2-994 unit 52 3,4-diClPh CH _Two Single bond unit 66 2-995 unit 52 3,4-diClPh CH _Two Single bond unit 67 2-996 unit 52 3,4-diClPh CH _Two Single bond device 68 2-997 device 52 3,4-diClPh CH _Two Single bond device 69 2-998 device 52 3,4-diClPh CH _Two Single bond device 70 2-999 device 52 3,4-diClPh CH _Two Single bond device 71 2-1000 device 52 3,4-diClPh CH _Two Single bond unit 72 2-1001 unit 52 3,4-diClPh CH _Two Single bond device 73 2-1002 device 52 3,4-diClPh CH _Two Single bond unit 74 2-1003 unit 52 3,4-diClPh CH _Two Single bond unit 75 2-1004 unit 52 3,4-diClPh CH _Two Single bond unit 76-2 1005 unit 52 3,4-diClPh CH _Two Single bond unit 77 2-1006 unit 52 3,4-diClPh CH _Two Single bond unit 78 2-1007 unit 52 3,4-diClPh CH _Two Single bond unit 79 2-1008 unit 52 3,4-diClPh CH _Two Single bond device 80 2-1009 device 53 3,4-diClPh CH _Two Single bond device 1 2-1010 device 53 3,4-diClPh CH _Two Single bond unit 2 2-1011 unit 53 3,4-diClPh CH _Two Single bond device 3 2-1012 device 53 3,4-diClPh CH _Two Single bond device 4 2-1013 device 53 3,4-diClPh CH _Two Single bond 5 2-1014 5 53 3,4-diClPh CH _Two Single bond device 6 2-1015 device 53 3,4-diClPh CH _Two Single bond device 7 2-1016 device 53 3,4-diClPh CH _Two Single bond device 8 2-1017 device 53 3,4-diClPh CH _Two Single bond device 9 2-1018 device 53 3,4-diClPh CH _Two Single bond device 10 2-1019 device 53 3,4-diClPh CH _Two Single bond unit 11 2-1020 unit 53 3,4-diClPh CH _Two Single bond unit 12 2-1021 unit 53 3,4-diClPh CH _Two Single bond unit 13 2-1022 unit 53 3,4-diClPh CH _Two Single bond unit 14 2-1023 unit 53 3,4-diClPh CH _Two Single bond unit 15 2-1024 unit 53 3,4-diClPh CH _Two Single bond unit 16 2-1025 unit 53 3,4-diClPh CH _Two Single bond unit 17 2-1026 unit 53 3,4-diClPh CH _Two Single bond unit 18 2-1027 unit 53 3,4-diClPh CH _Two Single bond unit 19 2-1028 unit 53 3,4-diClPh CH _Two Single bond device 20 2-1029 device 53 3,4-diClPh CH _Two Single bond unit 21 2-1030 unit 53 3,4-diClPh CH _Two Single bond unit 22 2-1031 unit 53 3,4-diClPh CH _Two Single bond unit 23 2-1032 unit 53 3,4-diClPh CH _Two Single bond unit 24 2-1033 unit 53 3,4-diClPh CH _Two Single bond unit 25 2-1034 unit 53 3,4-diClPh CH _Two Single bond unit 26 2-1035 unit 53 3,4-diClPh CH _Two Single bond unit 27 2-1036 unit 53 3,4-diClPh CH _Two Single bond unit 28 2-1037 unit 53 3,4-diClPh CH _Two Single bond unit 29 2-1038 unit 53 3,4-diClPh CH _Two Single bond device 30 2-1039 device 53 3,4-diClPh CH _Two Single bond unit 31 2-1040 unit 53 3,4-diClPh CH _Two Single bond unit 32 2-1041 unit 53 3,4-diClPh CH _Two Single bond device 65 2-1042 device 53 3,4-diClPh CH _Two Single bond unit 66 2-1043 unit 53 3,4-diClPh CH _Two Single bond unit 67 2-1044 unit 53 3,4-diClPh CH _Two Single bond unit 68 2-1045 unit 53 3,4-diClPh CH _Two Single bond unit 69 2-1046 unit 53 3,4-diClPh CH _Two Single bond device 70 2-1047 device 53 3,4-diClPh CH _Two Single bond unit 71 2-1048 unit 53 3,4-diClPh CH _Two Single bond unit 72 2-1049 unit 53 3,4-diClPh CH _Two Single bond unit 73 2-1050 unit 53 3,4-diClPh CH _Two Single bond unit 74 2-1051 unit 53 3,4-diClPh CH _Two Single bond unit 75 2-1052 unit 53 3,4-diClPh CH _Two Single bond unit 76 2-1053 unit 53 3,4-diClPh CH _Two Single bond unit 77 2-1054 unit 53 3,4-diClPh CH _Two Single bond unit 78 2-1055 unit 53 3,4-diClPh CH _Two Single bond device 79 2-1056 device 53 3,4-diClPh CH _Two Single bond position 80 化合物 Compound number R ¹ R ^Two ABZ ──────────────────────────────────── 2-1057 Place 54 3,4-diClPh CH _Two Single bond unit 1 2-1058 unit 54 3,4-diClPh CH _Two Single bond unit 2 2-1059 unit 54 3,4-diClPh CH _Two Single bond device 3 2-1060 device 54 3,4-diClPh CH _Two Single bond unit 4 2-1061 unit 54 3,4-diClPh CH _Two Single bond device 5 2-1062 device 54 3,4-diClPh CH _Two Single bond 6 6-1063 54 3,4-diClPh CH _Two Single bond unit 7 2-1064 unit 54 3,4-diClPh CH _Two Single bond unit 8 2-1065 unit 54 3,4-diClPh CH _Two Single bond device 9 2-1066 device 54 3,4-diClPh CH _Two Single bond unit 10 2-1067 unit 54 3,4-diClPh CH _Two Single bond unit 11 2-1068 unit 54 3,4-diClPh CH _Two Single bond unit 12 2-1069 unit 54 3,4-diClPh CH _Two Single bond unit 13 2-1070 unit 54 3,4-diClPh CH _Two Single bond unit 14 2-1071 unit 54 3,4-diClPh CH _Two Single bond unit 15 2-1072 unit 54 3,4-diClPh CH _Two Single bond unit 16 2-1073 unit 54 3,4-diClPh CH _Two Single bond unit 17 2-1074 unit 54 3,4-diClPh CH _Two Single bond unit 18 2-1075 unit 54 3,4-diClPh CH _Two Single bond unit 19 2-1076 unit 54 3,4-diClPh CH _Two Single bond unit 20 2-1077 unit 54 3,4-diClPh CH _Two Single bond unit 21 2-1078 unit 54 3,4-diClPh CH _Two Single bond unit 22 2-1079 unit 54 3,4-diClPh CH _Two Single bond unit 23 2-1080 unit 54 3,4-diClPh CH _Two Single bond unit 24 2-1081 unit 54 3,4-diClPh CH _Two Single bond unit 25 2-1082 unit 54 3,4-diClPh CH _Two Single bond unit 26 2-1083 unit 54 3,4-diClPh CH _Two Single bond unit 27 2-1084 unit 54 3,4-diClPh CH _Two Single bond unit 28 2-1085 unit 54 3,4-diClPh CH _Two Single bond unit 29 2-1086 unit 54 3,4-diClPh CH _Two Single bond device 30 2-1087 device 54 3,4-diClPh CH _Two Single bond unit 31 2-1088 unit 54 3,4-diClPh CH _Two Single bond unit 32 2-1089 unit 54 3,4-diClPh CH _Two Single bond device 65 2-1090 device 54 3,4-diClPh CH _Two Single bond unit 66 2-1091 unit 54 3,4-diClPh CH _Two Single bond unit 67 2-1092 unit 54 3,4-diClPh CH _Two Single bond device 68 2-1093 device 54 3,4-diClPh CH _Two Single bond unit 69 2-1094 unit 54 3,4-diClPh CH _Two Single bond unit 70 2-1095 unit 54 3,4-diClPh CH _Two Single bond unit 71 2-1096 unit 54 3,4-diClPh CH _Two Single bond unit 72 2-1097 unit 54 3,4-diClPh CH _Two Single bond unit 73 2-1098 unit 54 3,4-diClPh CH _Two Single bond unit 74 2-1099 unit 54 3,4-diClPh CH _Two Single bond unit 75 2-1100 unit 54 3,4-diClPh CH _Two Single bond Unit 76 2-101 Unit 54 3,4-diClPh CH _Two Single bond unit 77 2-1102 unit 54 3,4-diClPh CH _Two Single bond unit 78 2-1103 unit 54 3,4-diClPh CH _Two Single bond device 79 2-1104 device 54 3,4-diClPh CH _Two Single bond device 80 2-1105 device 55 3,4-diClPh CH _Two Single bond device 1 2-1106 device 55 3,4-diClPh CH _Two Single bond unit 2 2-1107 unit 55 3,4-diClPh CH _Two Single bond device 3 2-1108 device 55 3,4-diClPh CH _Two Single bond unit 4 2-1109 unit 55 3,4-diClPh CH _Two Single bond device 5 2-1110 device 55 3,4-diClPh CH _Two Single bond device 6 2-1111 device 55 3,4-diClPh CH _Two Single bond device 7 2-1112 device 55 3,4-diClPh CH _Two Single bond device 8 2-1113 device 55 3,4-diClPh CH _Two Single bond device 9 2-1114 device 55 3,4-diClPh CH _Two Single bond unit 10 2-1115 unit 55 3,4-diClPh CH _Two Single bond unit 11 2-1116 unit 55 3,4-diClPh CH _Two Single bond unit 12 2-1117 unit 55 3,4-diClPh CH _Two Single bond unit 13 2-1118 unit 55 3,4-diClPh CH _Two Single bond unit 14 2-1119 unit 55 3,4-diClPh CH _Two Single bond unit 15 2-1120 unit 55 3,4-diClPh CH _Two Single bond unit 16 2-1121 unit 55 3,4-diClPh CH _Two Single bond unit 17 2-1122 unit 55 3,4-diClPh CH _Two Single bond unit 18 2-1123 unit 55 3,4-diClPh CH _Two Single bond unit 19 2-1124 unit 55 3,4-diClPh CH _Two Single bond unit 20 2-1125 unit 55 3,4-diClPh CH _Two Single bond unit 21 2-1126 unit 55 3,4-diClPh CH _Two Single bond unit 22 2-1127 unit 55 3,4-diClPh CH _Two Single bond unit 23 2-1128 unit 55 3,4-diClPh CH _Two Single bond unit 24 2-1129 unit 55 3,4-diClPh CH _Two Single bond unit 25 2-1130 unit 55 3,4-diClPh CH _Two Single bond unit 26 2-1131 unit 55 3,4-diClPh CH _Two Single bond unit 27 2-1132 unit 55 3,4-diClPh CH _Two Single bond unit 28 2-1133 unit 55 3,4-diClPh CH _Two Single bond unit 29 2-1134 unit 55 3,4-diClPh CH _Two Single bond unit 30 2-1135 unit 55 3,4-diClPh CH _Two Single bond unit 31 2-1136 unit 55 3,4-diClPh CH _Two Single bond unit 32 2-1137 unit 55 3,4-diClPh CH _Two Single bond unit 65 2-1138 unit 55 3,4-diClPh CH _Two Single bond unit 66 2-1139 unit 55 3,4-diClPh CH _Two Single bond unit 67 2-1140 unit 55 3,4-diClPh CH _Two Single bond unit 68 2-1141 unit 55 3,4-diClPh CH _Two Single bond unit 69 2-142 unit 55 3,4-diClPh CH _Two Single bond unit 70 2-1143 unit 55 3,4-diClPh CH _Two Single bond unit 71 2-1144 unit 55 3,4-diClPh CH _Two Single bond unit 72 2-1145 unit 55 3,4-diClPh CH _Two Single bond unit 73 2-1146 unit 55 3,4-diClPh CH _Two Single bond unit 74 2-1147 unit 55 3,4-diClPh CH _Two Single bond unit 75 2-1148 unit 55 3,4-diClPh CH _Two Single bond unit 76 2-1149 unit 55 3,4-diClPh CH _Two Single bond unit 77 2-150 unit 55 3,4-diClPh CH _Two Single bond unit 78 2-1151 unit 55 3,4-diClPh CH _Two Single bond unit 79 2-1152 unit 55 3,4-diClPh CH _Two Single bond device 80 2-1153 device 56 3,4-diClPh CH _Two Single bond 1 2 1154 Position 56 3,4-diClPh CH _Two Single bond position 2 2-1155 position 56 3,4-diClPh CH _Two Single bond position 3 2-1156 position 56 3,4-diClPh CH _Two Single bond unit 4 2-1157 unit 56 3,4-diClPh CH _Two Single bond device 5 2-1158 device 56 3,4-diClPh CH _Two Single bond unit 6 2-1159 unit 56 3,4-diClPh CH _Two Single bond device 7 2-1160 device 56 3,4-diClPh CH _Two Single bond unit 8 2-1161 unit 56 3,4-diClPh CH _Two Single bond unit 9 2-1162 unit 56 3,4-diClPh CH _Two Single bond unit 10 2-1163 unit 56 3,4-diClPh CH _Two Single bond unit 11 2-1164 unit 56 3,4-diClPh CH _Two Single bond unit 12 2-1165 unit 56 3,4-diClPh CH _Two Single bond unit 13 2-1166 unit 56 3,4-diClPh CH _Two Single bond unit 14 2-1167 unit 56 3,4-diClPh CH _Two Single bond unit 15 2-1168 unit 56 3,4-diClPh CH _Two Single bond unit 16 2-1169 unit 56 3,4-diClPh CH _Two Single bond unit 17 2-1170 unit 56 3,4-diClPh CH _Two Single bond unit 18 2-1171 unit 56 3,4-diClPh CH _Two Single bond unit 19 2-1172 unit 56 3,4-diClPh CH _Two Single bond unit 20 2-1173 unit 56 3,4-diClPh CH _Two Single bond unit 21 2-1174 unit 56 3,4-diClPh CH _Two Single bond unit 22 2-1175 unit 56 3,4-diClPh CH _Two Single bond unit 23 2-1176 unit 56 3,4-diClPh CH _Two Single bond unit 24 2-1177 unit 56 3,4-diClPh CH _Two Single bond unit 25 2-1178 unit 56 3,4-diClPh CH _Two Single bond Unit 26 2-1179 Unit 56 3,4-diClPh CH _Two Single bond unit 27 2-180 unit 56 3,4-diClPh CH _Two Single bond unit 28 2-1181 unit 56 3,4-diClPh CH _Two Single bond unit 29 2-1182 unit 56 3,4-diClPh CH _Two Single bond unit 30 2-1183 unit 56 3,4-diClPh CH _Two Single bond unit 31 2-1184 unit 56 3,4-diClPh CH _Two Single bond unit 32 2-1185 unit 56 3,4-diClPh CH _Two Single bond device 65 2-1186 device 56 3,4-diClPh CH _Two Single bond unit 66 2-1187 unit 56 3,4-diClPh CH _Two Single bond unit 67 2-1188 unit 56 3,4-diClPh CH _Two Single bond device 68 2-1189 device 56 3,4-diClPh CH _Two Single bond device 69 2-1190 device 56 3,4-diClPh CH _Two Single bond unit 70 2-1191 unit 56 3,4-diClPh CH _Two Single bond unit 71 2-1192 unit 56 3,4-diClPh CH _Two Single bond unit 72 2-1193 unit 56 3,4-diClPh CH _Two Single bond unit 73 2-1194 unit 56 3,4-diClPh CH _Two Single bond unit 74 2-1195 unit 56 3,4-diClPh CH _Two Single bond unit 75 2-1196 unit 56 3,4-diClPh CH _Two Single bond unit 76 2-1197 unit 56 3,4-diClPh CH _Two Single bond unit 77 2-1198 unit 56 3,4-diClPh CH _Two Single bond unit 78 2-1199 unit 56 3,4-diClPh CH _Two Single bond device 79 2-1200 device 56 3,4-diClPh CH _Two Single bond device 80 2-1201 device 57 3,4-diClPh CH _Two Single bond device 1 2-1202 device 57 3,4-diClPh CH _Two Single bond device 2 2-1203 device 57 3,4-diClPh CH _Two Single bond device 3 2-1204 device 57 3,4-diClPh CH _Two Single bond unit 4 2-1205 unit 57 3,4-diClPh CH _Two Single bond device 5 2-1206 device 57 3,4-diClPh CH _Two Single bond device 6 2-1207 device 57 3,4-diClPh CH _Two Single bond device 7 2-1208 device 57 3,4-diClPh CH _Two Single bond device 8 2-1209 device 57 3,4-diClPh CH _Two Single bond device 9 2-1210 device 57 3,4-diClPh CH _Two Single bond unit 10 2-1211 unit 57 3,4-diClPh CH _Two Single bond unit 11 2-1212 unit 57 3,4-diClPh CH _Two Single bond unit 12 2-1213 unit 57 3,4-diClPh CH _Two Single bond unit 13 2-1214 unit 57 3,4-diClPh CH _Two Single bond unit 14 2-1215 unit 57 3,4-diClPh CH _Two Single bond unit 15 2-1216 unit 57 3,4-diClPh CH _Two Single bond unit 16 2-1217 unit 57 3,4-diClPh CH _Two Single bond unit 17 2-1218 unit 57 3,4-diClPh CH _Two Single bond unit 18 2-1219 unit 57 3,4-diClPh CH _Two Single bond unit 19 2-1220 unit 57 3,4-diClPh CH _Two Single bond unit 20 2-1221 unit 57 3,4-diClPh CH _Two Single bond unit 21 2-1222 unit 57 3,4-diClPh CH _Two Single bond unit 22 2-1223 unit 57 3,4-diClPh CH _Two Single bond unit 23 2-1224 unit 57 3,4-diClPh CH _Two Single bond unit 24 2-1225 unit 57 3,4-diClPh CH _Two Single bond unit 25 2-1226 unit 57 3,4-diClPh CH _Two Single bond unit 26 2-1227 unit 57 3,4-diClPh CH _Two Single bond unit 27 2-1228 unit 57 3,4-diClPh CH _Two Single bond unit 28 2-1229 unit 57 3,4-diClPh CH _Two Single bond unit 29 2-1230 unit 57 3,4-diClPh CH _Two Single bond unit 30 2-1231 unit 57 3,4-diClPh CH _Two Single bond unit 31 2-1232 unit 57 3,4-diClPh CH _Two Single bond unit 32 2-1233 unit 57 3,4-diClPh CH _Two Single bond device 65 2-1234 device 57 3,4-diClPh CH _Two Single bond device 66 2-1235 device 57 3,4-diClPh CH _Two Single bond unit 67 2-1236 unit 57 3,4-diClPh CH _Two Single bond device 68 2-1237 device 57 3,4-diClPh CH _Two Single bond device 69 2-1238 device 57 3,4-diClPh CH _Two Single bond device 70 2-1239 device 57 3,4-diClPh CH _Two Single bond unit 71 2-1240 unit 57 3,4-diClPh CH _Two Single bond unit 72 2-1241 unit 57 3,4-diClPh CH _Two Single bond unit 73 2-1242 unit 57 3,4-diClPh CH _Two Single bond unit 74 2-1243 unit 57 3,4-diClPh CH _Two Single bond unit 75 2-1244 unit 57 3,4-diClPh CH _Two Single bond unit 76 2-1245 unit 57 3,4-diClPh CH _Two Single bond unit 77 2-1246 unit 57 3,4-diClPh CH _Two Single bond unit 78 2-1247 unit 57 3,4-diClPh CH _Two Single bond device 79 2-1248 device 57 3,4-diClPh CH _Two Single bond device 80 2-1249 device 58 3,4-diClPh CH _Two Single bond device 1 2-1250 device 58 3,4-diClPh CH _Two Single bond unit 2 2-1251 unit 58 3,4-diClPh CH _Two Single bond position 3 2-1252 position 58 3,4-diClPh CH _Two Single bond unit 4 2-1253 unit 58 3,4-diClPh CH _Two Single bond 5 2 1254 5 58 3,4-diClPh CH _Two Single bond 6 6 1255 5 58 3,4-diClPh CH _Two Single bond device 7 2-1256 device 58 3,4-diClPh CH _Two Single bond device 8 2-1257 device 58 3,4-diClPh CH _Two Single bond device 9 2-1258 device 58 3,4-diClPh CH _Two Single bond unit 10 2-1259 unit 58 3,4-diClPh CH _Two Single bond unit 11 2-1260 unit 58 3,4-diClPh CH _Two Single bond unit 12 2-1261 unit 58 3,4-diClPh CH _Two Single bond unit 13 2-1262 unit 58 3,4-diClPh CH _Two Single bond unit 14 2-1263 unit 58 3,4-diClPh CH _Two Single bond unit 15 2-1264 unit 58 3,4-diClPh CH _Two Single bond unit 16 2-1265 unit 58 3,4-diClPh CH _Two Single bond unit 17 2-1266 unit 58 3,4-diClPh CH _Two Single bond unit 18 2-1267 unit 58 3,4-diClPh CH _Two Single bond unit 19 2-1268 unit 58 3,4-diClPh CH _Two Single bond device 20 2-1269 device 58 3,4-diClPh CH _Two Single bond unit 21 2-1270 unit 58 3,4-diClPh CH _Two Single bond unit 22 2-1271 unit 58 3,4-diClPh CH _Two Single bond unit 23 2-1272 unit 58 3,4-diClPh CH _Two Single bond unit 24 2-1273 unit 58 3,4-diClPh CH _Two Single bond unit 25 2-1274 unit 58 3,4-diClPh CH _Two Single bond unit 26 2-1275 unit 58 3,4-diClPh CH _Two Single bond unit 27 2-1276 unit 58 3,4-diClPh CH _Two Single bond unit 28 2-1277 unit 58 3,4-diClPh CH _Two Single bond unit 29 2-1278 unit 58 3,4-diClPh CH _Two Single bond unit 30 2-1279 unit 58 3,4-diClPh CH _Two Single bond unit 31 2-1280 unit 58 3,4-diClPh CH _Two Single bond unit 32 2-1281 unit 58 3,4-diClPh CH _Two Single bond unit 65 2-1282 unit 58 3,4-diClPh CH _Two Single bond unit 66 2-1283 unit 58 3,4-diClPh CH _Two Single bond unit 67 2-1284 Unit 58 3,4-diClPh CH _Two Single bond unit 68 2-1285 unit 58 3,4-diClPh CH _Two Single bond device 69 2-1286 device 58 3,4-diClPh CH _Two Single bond device 70 2-1287 device 58 3,4-diClPh CH _Two Single bond unit 71 2-1288 unit 58 3,4-diClPh CH _Two Single bond unit 72 2-1289 Unit 58 3,4-diClPh CH _Two Single bond device 73 2-1290 device 58 3,4-diClPh CH _Two Single bond unit 74 2-1291 unit 58 3,4-diClPh CH _Two Single bond unit 75 2-1292 unit 58 3,4-diClPh CH _Two Single bond unit 76 2-1293 unit 58 3,4-diClPh CH _Two Single bond unit 77 2-294 unit 58 3,4-diClPh CH _Two Single bond unit 78 2-1295 unit 58 3,4-diClPh CH _Two Single bond device 79 2-1296 device 58 3,4-diClPh CH _Two Single bond device 80 2-1297 device 59 3,4-diClPh CH _Two Single bond device 1 2-1298 device 59 3,4-diClPh CH _Two Single bond position 2 2-1299 position 59 3,4-diClPh CH _Two Single bond device 3 2-1300 device 59 3,4-diClPh CH _Two Single bond unit 4 2-1301 unit 59 3,4-diClPh CH _Two Single bond device 5 2-1302 device 59 3,4-diClPh CH _Two Single bond unit 6 2-1303 unit 59 3,4-diClPh CH _Two Single bond device 7 2-1304 device 59 3,4-diClPh CH _Two Single bond device 8 2-1305 device 59 3,4-diClPh CH _Two Single bond device 9 2-1306 device 59 3,4-diClPh CH _Two Single bond unit 10 2-1307 unit 59 3,4-diClPh CH _Two Single bond unit 11 2-1308 unit 59 3,4-diClPh CH _Two Single bond unit 12 2-1309 unit 59 3,4-diClPh CH _Two Single bond unit 13 2-1310 unit 59 3,4-diClPh CH _Two Single bond unit 14 2-1311 unit 59 3,4-diClPh CH _Two Single bond unit 15 2-1312 unit 59 3,4-diClPh CH _Two Single bond unit 16 2-1313 unit 59 3,4-diClPh CH _Two Single bond unit 17 2-1314 unit 59 3,4-diClPh CH _Two Single bond unit 18 2-1315 unit 59 3,4-diClPh CH _Two Single bond unit 19 2-1316 unit 59 3,4-diClPh CH _Two Single bond device 20 2-1317 device 59 3,4-diClPh CH _Two Single bond unit 21 2-1318 unit 59 3,4-diClPh CH _Two Single bond unit 22 2-1319 unit 59 3,4-diClPh CH _Two Single bond unit 23 2-1320 unit 59 3,4-diClPh CH _Two Single bond unit 24 2-1321 unit 59 3,4-diClPh CH _Two Single bond unit 25 2-1322 unit 59 3,4-diClPh CH _Two Single bond unit 26 2-1323 unit 59 3,4-diClPh CH _Two Single bond unit 27 2-1324 unit 59 3,4-diClPh CH _Two Single bond unit 28 2-1325 unit 59 3,4-diClPh CH _Two Single bond unit 29 2-1326 unit 59 3,4-diClPh CH _Two Single bond device 30 2-1327 device 59 3,4-diClPh CH _Two Single bond unit 31 2-1328 unit 59 3,4-diClPh CH _Two Single bond unit 32 2-1329 unit 59 3,4-diClPh CH _Two Single bond device 65 2-1330 device 59 3,4-diClPh CH _Two Single bond unit 66 2-1331 unit 59 3,4-diClPh CH _Two Single bond unit 67 2-1332 unit 59 3,4-diClPh CH _Two Single bond device 68 2-1333 device 59 3,4-diClPh CH _Two Single bond device 69 2-1334 device 59 3,4-diClPh CH _Two Single bond device 70 2-1335 device 59 3,4-diClPh CH _Two Single bond unit 71 2-1336 unit 59 3,4-diClPh CH _Two Single bond unit 72 2-1337 unit 59 3,4-diClPh CH _Two Single bond unit 73 2-1338 unit 59 3,4-diClPh CH _Two Single bond unit 74 2-1339 unit 59 3,4-diClPh CH _Two Single bond unit 75 2-1340 unit 59 3,4-diClPh CH _Two Single bond unit 76 2-1341 unit 59 3,4-diClPh CH _Two Single bond unit 77 2-1342 unit 59 3,4-diClPh CH _Two Single bond unit 78 2-1343 unit 59 3,4-diClPh CH _Two Single bond device 79 2-1344 device 59 3,4-diClPh CH _Two Single bond device 80 2-1345 device 82 3,4-diClPh CH _Two Single bond device 1 2-1346 device 82 3,4-diClPh CH _Two Single bond unit 2 2-1347 unit 82 3,4-diClPh CH _Two Single bond device 3 2-1348 device 82 3,4-diClPh CH _Two Single bond unit 4 2-1349 unit 82 3,4-diClPh CH _Two Single bond device 5 2-1350 device 82 3,4-diClPh CH _Two Single bond 6 6 1351 82 3,4-diClPh CH _Two Single bond unit 7 2-1352 unit 82 3,4-diClPh CH _Two Single bond device 8 2-1353 device 82 3,4-diClPh CH _Two Single bond unit 9 2-1354 unit 82 3,4-diClPh CH _Two Single bond unit 10 2-1355 unit 82 3,4-diClPh CH _Two Single bond unit 11 2-1356 unit 82 3,4-diClPh CH _Two Single bond unit 12 2-1357 unit 82 3,4-diClPh CH _Two Single bond unit 13 2-1358 unit 82 3,4-diClPh CH _Two Single bond unit 14 2-1359 unit 82 3,4-diClPh CH _Two Single bond unit 15 2-1360 unit 82 3,4-diClPh CH _Two Single bond unit 16 2-1361 unit 82 3,4-diClPh CH _Two Single bond unit 17 2-1362 unit 82 3,4-diClPh CH _Two Single bond unit 18 2-1363 unit 82 3,4-diClPh CH _Two Single bond unit 19 2-1364 unit 82 3,4-diClPh CH _Two Single bond unit 20 2-1365 unit 82 3,4-diClPh CH _Two Single bond unit 21 2-1366 unit 82 3,4-diClPh CH _Two Single bond unit 22 2-1367 unit 82 3,4-diClPh CH _Two Single bond unit 23 2-1368 unit 82 3,4-diClPh CH _Two Single bond unit 24 2-1369 unit 82 3,4-diClPh CH _Two Single bond unit 25 2-1370 unit 82 3,4-diClPh CH _Two Single bond unit 26 2-1371 unit 82 3,4-diClPh CH _Two Single bond unit 27 2-1372 unit 82 3,4-diClPh CH _Two Single bond unit 28 2-1373 unit 82 3,4-diClPh CH _Two Single bond unit 29 2-1374 unit 82 3,4-diClPh CH _Two Single bond unit 30 2-1375 unit 82 3,4-diClPh CH _Two Single bond unit 31 2-1376 unit 82 3,4-diClPh CH _Two Single bond unit 32 2-1377 unit 82 3,4-diClPh CH _Two Single bond device 65 2-1378 device 82 3,4-diClPh CH _Two Single bond device 66 2-1379 device 82 3,4-diClPh CH _Two Single bond unit 67 2-1380 unit 82 3,4-diClPh CH _Two Single bond device 68 2-1381 device 82 3,4-diClPh CH _Two Single bond device 69 2-1382 device 82 3,4-diClPh CH _Two Single bond unit 70 2-1383 unit 82 3,4-diClPh CH _Two Single bond unit 71 2-1384 unit 82 3,4-diClPh CH _Two Single bond unit 72 2-1385 unit 82 3,4-diClPh CH _Two Single bond unit 73 2-1386 unit 82 3,4-diClPh CH _Two Single bond unit 74 2-1387 unit 82 3,4-diClPh CH _Two Single bond unit 75 2-1388 unit 82 3,4-diClPh CH _Two Single bond unit 76 2-1389 unit 82 3,4-diClPh CH _Two Single bond unit 77 2-1390 unit 82 3,4-diClPh CH _Two Single bond unit 78 2-1391 unit 82 3,4-diClPh CH _Two Single bond device 79 2-1392 device 82 3,4-diClPh CH _Two Single bond unit 80 2-1393 unit 83 3,4-diClPh CH _Two Single bond device 1 2-1394 device 83 3,4-diClPh CH _Two Single bond unit 2 2-1395 unit 83 3,4-diClPh CH _Two Single bond unit 3 2-1396 unit 83 3,4-diClPh CH _Two Single bond unit 4 2-1397 unit 83 3,4-diClPh CH _Two Single bond device 5 2-1398 device 83 3,4-diClPh CH _Two Single bond device 6 2-1399 device 83 3,4-diClPh CH _Two Single bond device 7 2-1400 device 83 3,4-diClPh CH _Two Single bond device 8 2-1401 device 83 3,4-diClPh CH _Two Single bond device 9 2-1402 device 83 3,4-diClPh CH _Two Single bond unit 10 2-1403 unit 83 3,4-diClPh CH _Two Single bond unit 11 2-1404 unit 83 3,4-diClPh CH _Two Single bond unit 12 2-1405 unit 83 3,4-diClPh CH _Two Single bond unit 13 2-1406 unit 83 3,4-diClPh CH _Two Single bond unit 14 2-1407 unit 83 3,4-diClPh CH _Two Single bond unit 15 2-1408 unit 83 3,4-diClPh CH _Two Single bond unit 16 2-1409 unit 83 3,4-diClPh CH _Two Single bond unit 17 2-1410 unit 83 3,4-diClPh CH _Two Single bond unit 18 2-1411 unit 83 3,4-diClPh CH _Two Single bond unit 19 2-1412 unit 83 3,4-diClPh CH _Two Single bond unit 20 2-1413 unit 83 3,4-diClPh CH _Two Single bond unit 21 2-1414 unit 83 3,4-diClPh CH _Two Single bond Unit 22 2-1415 Unit 83 3,4-diClPh CH _Two Single bond unit 23 2-1416 unit 83 3,4-diClPh CH _Two Single bond unit 24 2-1417 unit 83 3,4-diClPh CH _Two Single bond unit 25 2-1418 unit 83 3,4-diClPh CH _Two Single bond unit 26 2-1419 unit 83 3,4-diClPh CH _Two Single bond unit 27 2-1420 unit 83 3,4-diClPh CH _Two Single bond unit 28 2-1421 unit 83 3,4-diClPh CH _Two Single bond unit 29 2-1422 unit 83 3,4-diClPh CH _Two Single bond device 30 2-1423 device 83 3,4-diClPh CH _Two Single bond unit 31 2-1424 unit 83 3,4-diClPh CH _Two Single bond Unit 32 2-1425 Unit 83 3,4-diClPh CH _Two Single bond device 65 2-1426 device 83 3,4-diClPh CH _Two Single bond Unit 66 2-1427 Unit 83 3,4-diClPh CH _Two Single bond unit 67 2-1428 unit 83 3,4-diClPh CH _Two Single bond device 68 2-1429 device 83 3,4-diClPh CH _Two Single bond device 69 2-1430 device 83 3,4-diClPh CH _Two Single bond unit 70 2-1431 unit 83 3,4-diClPh CH _Two Single bond unit 71 2-1432 unit 83 3,4-diClPh CH _Two Single bond unit 72 2-1433 unit 83 3,4-diClPh CH _Two Single bond unit 73 2-1434 unit 83 3,4-diClPh CH _Two Single bond unit 74 2-1435 unit 83 3,4-diClPh CH _Two Single bond unit 75 2-1436 unit 83 3,4-diClPh CH _Two Single bond device 76 2-1437 device 83 3,4-diClPh CH _Two Single bond unit 77 2-1438 unit 83 3,4-diClPh CH _Two Single bond unit 78 2-1439 unit 83 3,4-diClPh CH _Two Single bond device 79 2-1440 device 83 3,4-diClPh CH _Two Single bond device 80 2-1441 device 61 3,4-diClPh CH _Two Single bond 1 2 1442 1 61 3,4-diClPh CH _Two Single bond unit 2 2-1443 unit 61 3,4-diClPh CH _Two Single bond unit 3 2-1444 unit 61 3,4-diClPh CH _Two Single bond unit 4 2-1445 unit 61 3,4-diClPh CH _Two Single bond device 5 2-1446 device 61 3,4-diClPh CH _Two Single bond unit 6 2-1447 unit 61 3,4-diClPh CH _Two Single bond device 7 2-1448 device 61 3,4-diClPh CH _Two Single bond device 8 2-1449 device 61 3,4-diClPh CH _Two Single bond device 9 2-1450 device 61 3,4-diClPh CH _Two Single bond unit 10 2-1451 unit 61 3,4-diClPh CH _Two Single bond unit 11 2-1452 unit 61 3,4-diClPh CH _Two Single bond unit 12 2-1453 unit 61 3,4-diClPh CH _Two Single bond unit 13 2-1454 unit 61 3,4-diClPh CH _Two Single bond unit 14 2-1455 unit 61 3,4-diClPh CH _Two Single bond unit 15 2-1456 unit 61 3,4-diClPh CH _Two Single bond unit 16 2-1457 unit 61 3,4-diClPh CH _Two Single bond unit 17 2-1458 unit 61 3,4-diClPh CH _Two Single bond unit 18 2-1459 unit 61 3,4-diClPh CH _Two Single bond unit 19 2-1460 unit 61 3,4-diClPh CH _Two Single bond unit 20 2-1461 unit 61 3,4-diClPh CH _Two Single bond unit 21 2-1462 unit 61 3,4-diClPh CH _Two Single bond unit 22 2-1463 unit 61 3,4-diClPh CH _Two Single bond unit 23 2-1464 unit 61 3,4-diClPh CH _Two Single bond unit 24 2-1465 unit 61 3,4-diClPh CH _Two Single bond unit 25 2-1466 unit 61 3,4-diClPh CH _Two Single bond unit 26 2-1467 unit 61 3,4-diClPh CH _Two Single bond unit 27 2-1468 unit 61 3,4-diClPh CH _Two Single bond unit 28 2-1469 unit 61 3,4-diClPh CH _Two Single bond unit 29 2-1470 unit 61 3,4-diClPh CH _Two Single bond unit 30 2-1471 unit 61 3,4-diClPh CH _Two Single bond unit 31 2-1472 unit 61 3,4-diClPh CH _Two Single bond unit 32 2-1473 unit 61 3,4-diClPh CH _Two Single bond device 65 2-1474 device 61 3,4-diClPh CH _Two Single bond unit 66 2-1475 unit 61 3,4-diClPh CH _Two Single bond unit 67 2-1476 unit 61 3,4-diClPh CH _Two Single bond device 68 2-1477 device 61 3,4-diClPh CH _Two Single bond unit 69 2-1478 unit 61 3,4-diClPh CH _Two Single bond device 70 2-1479 device 61 3,4-diClPh CH _Two Single bond unit 71 2-1480 unit 61 3,4-diClPh CH _Two Single bond unit 72 2-1481 unit 61 3,4-diClPh CH _Two Single bond device 73 2-1482 device 61 3,4-diClPh CH _Two Single bond device 74 2-1483 device 61 3,4-diClPh CH _Two Single bond unit 75 2-1484 unit 61 3,4-diClPh CH _Two Single bond unit 76 2-1485 unit 61 3,4-diClPh CH _Two Single bond unit 77 2-1486 unit 61 3,4-diClPh CH _Two Single bond unit 78 2-1487 unit 61 3,4-diClPh CH _Two Single bond device 79 2-1488 device 61 3,4-diClPh CH _Two Single bond device 80 2-1489 device 60 3,4-diClPh CH _Two Single bond device 1 2-1490 device 60 3,4-diClPh CH _Two Single bond device 2 2-1491 device 60 3,4-diClPh CH _Two Single bond device 3 2-1492 device 60 3,4-diClPh CH _Two Single bond unit 4 2-1493 unit 60 3,4-diClPh CH _Two Single bond device 5 2-1494 device 60 3,4-diClPh CH _Two Single bond device 6 2-1495 device 60 3,4-diClPh CH _Two Single bond device 7 2-1496 device 60 3,4-diClPh CH _Two Single bond device 8 2-1497 device 60 3,4-diClPh CH _Two Single bond device 9 2-1498 device 60 3,4-diClPh CH _Two Single bond device 10 2-1499 device 60 3,4-diClPh CH _Two Single bond unit 11 2-1500 unit 60 3,4-diClPh CH _Two Single bond unit 12 2-1501 unit 60 3,4-diClPh CH _Two Single bond unit 13 2-1502 unit 60 3,4-diClPh CH _Two Single bond unit 14 2-1503 unit 60 3,4-diClPh CH _Two Single bond unit 15 2-1504 unit 60 3,4-diClPh CH _Two Single bond unit 16 2-1505 unit 60 3,4-diClPh CH _Two Single bond unit 17 2-1506 unit 60 3,4-diClPh CH _Two Single bond unit 18 2-1507 unit 60 3,4-diClPh CH _Two Single bond unit 19 2-1508 unit 60 3,4-diClPh CH _Two Single bond device 20 2-1509 device 60 3,4-diClPh CH _Two Single bond unit 21 2-1510 unit 60 3,4-diClPh CH _Two Single bond Unit 22 2-1511 Unit 60 3,4-diClPh CH _Two Single bond unit 23 2-1512 unit 60 3,4-diClPh CH _Two Single bond unit 24 2-1513 unit 60 3,4-diClPh CH _Two Single bond unit 25 2-1514 unit 60 3,4-diClPh CH _Two Single bond unit 26 2-1515 unit 60 3,4-diClPh CH _Two Single bond unit 27 2-1516 unit 60 3,4-diClPh CH _Two Single bond unit 28 2-1517 unit 60 3,4-diClPh CH _Two Single bond unit 29 2-1518 unit 60 3,4-diClPh CH _Two Single bond device 30 2-1519 device 60 3,4-diClPh CH _Two Single bond unit 31 2-1520 unit 60 3,4-diClPh CH _Two Single bond device 32 2-1521 device 60 3,4-diClPh CH _Two Single bond device 65 2-1522 device 60 3,4-diClPh CH _Two Single bond device 66 2-1523 device 60 3,4-diClPh CH _Two Single bond unit 67 2-1524 unit 60 3,4-diClPh CH _Two Single bond device 68 2-1525 device 60 3,4-diClPh CH _Two Single bond device 69 2-1526 device 60 3,4-diClPh CH _Two Single bond device 70 2-1527 device 60 3,4-diClPh CH _Two Single bond unit 71 2-1528 unit 60 3,4-diClPh CH _Two Single bond unit 72 2-1529 unit 60 3,4-diClPh CH _Two Single bond unit 73 2-1530 unit 60 3,4-diClPh CH _Two Single bond unit 74 2-1531 unit 60 3,4-diClPh CH _Two Single bond unit 75 2-1532 unit 60 3,4-diClPh CH _Two Single bond unit 76 2-1533 unit 60 3,4-diClPh CH _Two Single bond unit 77 2-1534 unit 60 3,4-diClPh CH _Two Single bond unit 78 2-1535 unit 60 3,4-diClPh CH _Two Single bond device 79 2-1536 device 60 3,4-diClPh CH _Two Single bond position 80 化合物 Compound number R ¹ R ^Two A B Z group a group b group ──────────────────────────────────── 2-1537 placement 33 3, 4-diClPh CO single bond or CH _Two Unit 1 2-1538 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 2 2-1539 unit 33 3,4-diClPh CO single bond or CH _Two Unit 3 2-1540 unit 33 3,4-diClPh CO single bond or CH _Two Unit 4 2-1541 unit 33 3,4-diClPh CO single bond or CH _Two App 5 2-1542 App 33 3,4-diClPh CO Single bond or CH _Two App. 6 2-1543 App. 33 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1544 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1545 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 9 2-1546 Unit 33 3,4-diClPh CO Single bond or CH _Two Device 10 2-1547 device 33 3,4-diClPh CO single bond or CH _Two Unit 11 2-1548 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1549 unit 33 3,4-diClPh CO single bond or CH _Two Unit 13 2-1550 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1551 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1552 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1553 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1554 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1555 Unit 33 3,4-diClPh CO Single bond or CH _Two App 19 2-1556 App. 33 3,4-diClPh CO Single bond or CH _Two Unit 20 2-1557 unit 33 3,4-diClPh CO single bond or CH _Two Unit 21 2-1558 unit 33 3,4-diClPh CO single bond or CH _Two Unit 22 2-1559 unit 33 3,4-diClPh CO single bond or CH _Two Unit 23 2-1560 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1561 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1562 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1563 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1564 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1565 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1566 unit 33 3,4-diClPh CO single bond or CH _Two Unit 30 2-1567 unit 33 3,4-diClPh CO single bond or CH _Two Unit 31 2-1568 unit 33 3,4-diClPh CO single bond or CH _Two Device 32 2-1569 device 33 3,4-diClPh CO single bond or CH _Two App. 65 2-1570 App. 33 3,4-diClPh CO Single bond or CH _Two Device 66 2-1571 device 33 3,4-diClPh CO single bond or CH _Two App. 67 2-1572 App. 33 3,4-diClPh CO Single bond or CH _Two App. 68 2-1573 App. 33 3,4-diClPh CO Single bond or CH _Two Device 69 2-1574 device 33 3,4-diClPh CO single bond or CH _Two Unit 70 2-1575 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 71 2-1576 unit 33 3,4-diClPh CO single bond or CH _Two Unit 72 2-1577 unit 33 3,4-diClPh CO single bond or CH _Two Unit 73 2-1578 Unit 33 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1579 Unit 33 3,4-diClPh CO Single bond or CH _Two App. 75 2-1580 App. 33 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1581 Unit 33 3,4-diClPh CO Single bond or CH _Two App. 77 2-1582 App. 33 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1583 unit 33 3,4-diClPh CO single bond or CH _Two Unit 79 2-1584 unit 33 3,4-diClPh CO single bond or CH _Two Unit 80 2-1585 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 1 2-1586 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 2 2-1587 unit 34 3,4-diClPh CO single bond or CH _Two Unit 3 2-1588 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 4 2-1589 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 5 2-1590 Unit 34 3,4-diClPh CO Single bond or CH _Two App. 6 2-1591 App. 34 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1592 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1593 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 9 2-1594 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 10 2-1595 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 11 2-1596 unit 34 3,4-diClPh CO single bond or CH _Two Unit 12 2-1597 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 13 2-1598 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1599 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1600 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1601 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1602 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1603 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 19 2-1604 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 20 2-1605 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 21 2-1606 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 22 2-1607 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 23 2-1608 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1609 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1610 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1611 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1612 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1613 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1614 unit 34 3,4-diClPh CO single bond or CH _Two Unit 30 2-1615 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 31 2-1616 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 32 2-1617 Unit 34 3,4-diClPh CO Single bond or CH _Two Set 65 2-1618 Set 34 3,4-diClPh CO Single bond or CH _Two Unit 66 2-1619 Unit 34 3,4-diClPh CO Single bond or CH _Two App. 67 2-1620 App. 34 3,4-diClPh CO Single bond or CH _Two App. 68 2-1621 App. 34 3,4-diClPh CO Single bond or CH _Two Device 69 2-1622 device 34 3,4-diClPh CO single bond or CH _Two Unit 70 2-1623 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 71 2-1624 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 72 2-1625 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 73 2-1626 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1627 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 75 2-1628 Unit 34 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1629 Unit 34 3,4-diClPh CO Single bond or CH _Two App. 77 2-1630 App. 34 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1631 Unit 34 3,4-diClPh CO Single bond or CH _Two Device 79 2-1632 device 34 3,4-diClPh CO single bond or CH _Two Device 80 2-1633 device 35 3,4-diClPh CO single bond or CH _Two Unit 1 2-1634 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 2 2-1635 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 3 2-1636 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 4 2-1637 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 5 2-1638 Unit 35 3,4-diClPh CO Single bond or CH _Two App. 6 2-1639 App. 35 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1640 Unit 35 3,4-diClPh CO Single bond or CH _Two App. 8 2-1641 App. 35 3,4-diClPh CO Single bond or CH _Two Unit 9 2-1642 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 10 2-1643 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 11 2-1644 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1645 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 13 2-1646 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1647 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1648 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1649 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1650 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1651 Unit 35 3,4-diClPh CO Single bond or CH _Two 19 2-1652 35 35,4-diClPh CO Single bond or CH _Two Unit 20 2-1653 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 21 2-1654 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 22 2-1655 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 23 2-1656 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1657 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1658 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1659 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1660 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1661 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1662 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 30 2-1663 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 31 2-1664 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 32 2-1665 Unit 35 3,4-diClPh CO Single bond or CH _Two App. 65 2-1666 App. 35 3,4-diClPh CO Single bond or CH _Two Unit 66 2-1667 Unit 35 3,4-diClPh CO Single bond or CH _Two App. 67 2-1668 App. 35 3,4-diClPh CO Single bond or CH _Two Unit 68 2-1669 Unit 35 3,4-diClPh CO Single bond or CH _Two Device 69 2-1670 device 35 3,4-diClPh CO single bond or CH _Two Unit 70 2-1671 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 71 2-1672 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 72 2-1673 Unit 35 3,4-diClPh CO Single bond or CH _Two 73 2-1674 35 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1675 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 75 2-1676 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1677 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 77 2-1678 Unit 35 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1679 Unit 35 3,4-diClPh CO Single bond or CH _Two Device 79 2-1680 device 35 3,4-diClPh CO single bond or CH _Two Device 80 2-1681 device 36 3,4-diClPh CO single bond or CH _Two Unit 1 2-1682 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 22-1683 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 3 2-1684 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 4 2-1685 Unit 36 3,4-diClPh CO Single bond or CH _Two 5 2 1686 5 36 3,4-diClPh CO Single bond or CH _Two Unit 6 2-1687 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1688 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1689 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 9 2-1690 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 10 2-1691 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 11 2-1692 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1693 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 13 2-1694 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1695 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1696 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1697 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1698 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1699 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 19 2-1700 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 20 2-1701 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 21 2-1702 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 22 2-1703 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 23 2-1704 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1705 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1706 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1707 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1708 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1709 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1710 unit 36 3,4-diClPh CO single bond or CH _Two Unit 30 2-1711 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 31 2-1712 Unit 36 3,4-diClPh CO Single bond or CH _Two Device 32 2-1713 device 36 3,4-diClPh CO single bond or CH _Two Set 65 2-1714 Set 36 3,4-diClPh CO Single bond or CH _Two Unit 66 2-1715 Unit 36 3,4-diClPh CO Single bond or CH _Two App. 67 2-1716 App. 36 3,4-diClPh CO Single bond or CH _Two Unit 68 2-1717 Unit 36 3,4-diClPh CO Single bond or CH _Two Device 69 2-1718 device 36 3,4-diClPh CO single bond or CH _Two Unit 70 2-1719 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 71 2-1720 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 72 2-1721 unit 36 3,4-diClPh CO single bond or CH _Two Unit 73 2-1722 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1723 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 75 2-1724 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1725 Unit 36 3,4-diClPh CO Single bond or CH _Two App. 77 2-1726 App. 36 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1727 Unit 36 3,4-diClPh CO Single bond or CH _Two Unit 79 2-1728 Unit 36 3,4-diClPh CO Single bond or CH _Two Device 80 2-1729 device 37 3,4-diClPh CO single bond or CH _Two Unit 1 2-1730 Unit 37 3,4-diClPh CO Single bond or CH _Two App.2 2-1731 App.37 3,4-diClPh CO Single bond or CH _Two App. 3 2-1732 App. 37 3,4-diClPh CO Single bond or CH _Two Unit 4 2-1733 Unit 37 3,4-diClPh CO Single bond or CH _Two 5 2 1734 5 37 3,4-diClPh CO Single bond or CH _Two Unit 6 2-1735 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1736 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1737 Unit 37 3,4-diClPh CO Single bond or CH _Two App. 9 2-1738 App. 37 3,4-diClPh CO Single bond or CH _Two Unit 10 2-1739 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 11 2-1740 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1741 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 13 2-1742 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1743 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1744 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1745 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1746 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1747 Unit 37 3,4-diClPh CO Single bond or CH _Two 19-2 1748 30 37,4-diClPh CO Single bond or CH _Two Unit 20 2-1749 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 21 2-1750 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 22 2-1751 unit 37 3,4-diClPh CO single bond or CH _Two Unit 23 2-1752 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1753 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1754 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1755 Unit 37 3,4-diClPh CO Single bond or CH _Two Set 27 2-1756 Set 37 3,4-diClPh CO Single bond or CH _Two 28 1-1757 2 37 3,4-diClPh CO Single bond or CH _Two Set 29 2-1758 Set 37 3,4-diClPh CO Single bond or CH _Two Unit 30 2-1759 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 31 2-1760 Unit 37 3,4-diClPh CO Single bond or CH _Two Device 32 2-1761 device 37 3,4-diClPh CO single bond or CH _Two App. 65 2-1762 App. 37 3,4-diClPh CO Single bond or CH _Two Unit 66 2-1763 Unit 37 3,4-diClPh CO Single bond or CH _Two App. 67 2-1764 App. 37 3,4-diClPh CO Single bond or CH _Two Unit 68 2-1765 Unit 37 3,4-diClPh CO Single bond or CH _Two Device 69 2-1766 device 37 3,4-diClPh CO single bond or CH _Two Unit 70 2-1767 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 71 2-1768 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 72 2-1769 Unit 37 3,4-diClPh CO Single bond or CH _Two App. 73 2-1770 App. 37 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1771 Unit 37 3,4-diClPh CO Single bond or CH _Two App. 75 2-1772 App. 37 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1773 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 77 2-1774 Unit 37 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1775 unit 37 3,4-diClPh CO single bond or CH _Two Device 79 2-1776 device 37 3,4-diClPh CO single bond or CH _Two Device 80 2-1777 device 38 3,4-diClPh CO single bond or CH _Two Unit 1 2-1778 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 2 2-1779 unit 38 3,4-diClPh CO single bond or CH _Two Unit 3 2-1780 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 4 2-1781 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 5 2-1782 Unit 38 3,4-diClPh CO Single bond or CH _Two App. 6 2-1783 App. 38 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1784 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1785 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 9 2-1786 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 10 2-1787 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 11 2-1788 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1789 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 13 2-1790 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1791 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1792 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1793 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1794 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1795 Unit 38 3,4-diClPh CO Single bond or CH _Two App 19 2-1796 App 38 38,4-diClPh CO Single bond or CH _Two Unit 20 2-1797 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 21 2-1798 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 22 2-1799 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 23 2-1800 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1801 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1802 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1803 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1804 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1805 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1806 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 30 2-1807 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 31 2-1808 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 32 2-1809 Unit 38 3,4-diClPh CO Single bond or CH _Two Set 65 2-1810 Set 38 3,4-diClPh CO Single bond or CH _Two Set 66 2-1811 Set 38 3,4-diClPh CO Single bond or CH _Two Unit 67 2-1812 Unit 38 3,4-diClPh CO Single bond or CH _Two App. 68 2-1813 App. 38 3,4-diClPh CO Single bond or CH _Two App. 69 2-1814 App. 38 3,4-diClPh CO Single bond or CH _Two Unit 70 2-1815 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 71 2-1816 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 72 2-1817 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 73 2-1818 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1819 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 75 2-1820 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1821 Unit 38 3,4-diClPh CO Single bond or CH _Two App. 77 2-1822 App. 38 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1823 Unit 38 3,4-diClPh CO Single bond or CH _Two Unit 79 2-1824 Unit 38 3,4-diClPh CO Single bond or CH _Two Device 80 2-1825 device 39 3,4-diClPh CO single bond or CH _Two Unit 1 2-1826 Unit 39 3,4-diClPh CO Single bond or CH _Two 2 2-1827 2 39 4,4-diClPh CO Single bond or CH _Two Unit 3 2-1828 Unit 39 3,4-diClPh CO Single bond or CH _Two App. 4 2-1829 App. 39 3,4-diClPh CO Single bond or CH _Two 5 2 1830 5 39 4,4-diClPh CO Single bond or CH _Two 6 6-1831 3 39 4,4-diClPh CO Single bond or CH _Two 7 2-1832 7 39,4-diClPh CO Single bond or CH _Two Unit 8 2-1833 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 9 2-1834 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 10 2-1835 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 11 2-1836 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1837 unit 39 3,4-diClPh CO single bond or CH _Two Unit 13 2-1838 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1839 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1840 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1841 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1842 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1845 Unit 39 3,4-diClPh CO Single bond or CH _Two 19 2-1844 39 39,4-diClPh CO Single bond or CH _Two Device 20 2-1845 device 39 3,4-diClPh CO single bond or CH _Two Unit 21 2-1846 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 22 2-1847 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 23 2-1848 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1849 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1850 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1851 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1852 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1835 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1854 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 30 2-1855 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 31 2-1856 unit 39 3,4-diClPh CO single bond or CH _Two Device 32 2-1857 device 39 3,4-diClPh CO single bond or CH _Two Set 65 2-1858 Set 39 3,4-diClPh CO Single bond or CH _Two Unit 66 2-1859 Unit 39 3,4-diClPh CO Single bond or CH _Two App. 67 2-1860 App. 39 3,4-diClPh CO Single bond or CH _Two Device 68 2-1861 device 39 3,4-diClPh CO single bond or CH _Two App. 69 2-1862 App. 39 3,4-diClPh CO Single bond or CH _Two Unit 70 2-1863 Unit 39 3,4-diClPh CO Single bond or CH _Two Unit 71 2-1864 unit 39 3,4-diClPh CO single bond or CH _Two Unit 72 2-1865 unit 39 3,4-diClPh CO single bond or CH _Two 73 73 1866 3 39 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1867 Unit 39 3,4-diClPh CO Single bond or CH _Two 75 75 1868 3 39 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1869 Unit 39 3,4-diClPh CO Single bond or CH _Two App. 77 2-1870 App. 39 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1871 unit 39 3,4-diClPh CO single bond or CH _Two Device 79 2-1872 device 39 3,4-diClPh CO single bond or CH _Two Device 80 2-1873 device 40 3,4-diClPh CO single bond or CH _Two Unit 1 2-1874 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 2 2-1875 Unit 40 3,4-diClPh CO Single bond or CH _Two Device 3 2-1876 device 40 3,4-diClPh CO single bond or CH _Two Device 4 2-1877 device 40 3,4-diClPh CO single bond or CH _Two 5 2 1878 5 40 3,4-diClPh CO Single bond or CH _Two Device 6 2-1879 device 40 3,4-diClPh CO single bond or CH _Two Unit 7 2-1880 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1881 Unit 40 3,4-diClPh CO Single bond or CH _Two Device 9 2-1882 device 40 3,4-diClPh CO single bond or CH _Two Device 10 2-1883 device 40 3,4-diClPh CO single bond or CH _Two Unit 11 2-1884 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1885 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 13 2-1886 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1887 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1888 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1889 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1890 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1891 Unit 40 3,4-diClPh CO Single bond or CH _Two 19 2-1892 40 40,4-diClPh CO Single bond or CH _Two Device 20 2-1893 device 40 3,4-diClPh CO single bond or CH _Two Device 21 2- 1894 device 40 3,4-diClPh CO single bond or CH _Two Unit 22 2-1895 Unit 40 3,4-diClPh CO Single bond or CH _Two Device 23 2-1896 device 40 3,4-diClPh CO single bond or CH _Two Device 24 2-1897 device 40 3,4-diClPh CO single bond or CH _Two Unit 25 2-1798 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1899 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1900 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1901 Unit 40 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1902 Unit 40 3,4-diClPh CO Single bond or CH _Two Device 30 2-1903 device 40 3,4-diClPh CO single bond or CH _Two Unit 31 2-1904 Unit 40 3,4-diClPh CO Single bond or CH _Two Device 32 2-1905 device 40 3,4-diClPh CO single bond or CH _Two Device 65 2-1906 device 40 3,4-diClPh CO single bond or CH _Two Device 66 2-1907 device 40 3,4-diClPh CO single bond or CH _Two App. 67 2-1908 App. 40 3,4-diClPh CO Single bond or CH _Two Device 68 2-1909 device 40 3,4-diClPh CO single bond or CH _Two Device 69 2-1910 device 40 3,4-diClPh CO single bond or CH _Two Device 70 2-1911 device 40 3,4-diClPh CO single bond or CH _Two Unit 71 2-1912 unit 40 3,4-diClPh CO single bond or CH _Two Unit 72 2-1913 Unit 40 3,4-diClPh CO Single bond or CH _Two 73 73-1914 40 40 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1915 Unit 40 3,4-diClPh CO Single bond or CH _Two App. 75 2-1916 App. 40 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1917 unit 40 3,4-diClPh CO single bond or CH _Two App. 77 2-1918 App. 40 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1919 unit 40 3,4-diClPh CO single bond or CH _Two Device 79 2-1920 device 40 3,4-diClPh CO single bond or CH _Two Device 80 2-1921 device 41 3,4-diClPh CO single bond or CH _Two Unit 1 2-1922 Unit 41 3,4-diClPh CO Single bond or CH _Two App.2 2-1923 App.41 3,4-diClPh CO Single bond or CH _Two Unit 3 2-1924 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 4 2-1925 Unit 41 3,4-diClPh CO Single bond or CH _Two 5 2 1926 5 41 3,4-diClPh CO Single bond or CH _Two App. 6 2-1927 App. 41 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1928 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1929 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 9 2-1930 Unit 41 3,4-diClPh CO Single bond or CH _Two Device 10 2-1931 device 41 3,4-diClPh CO single bond or CH _Two Unit 11 2-1932 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1933 unit 41 3,4-diClPh CO single bond or CH _Two Unit 13 2-1934 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1935 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1936 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1937 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1938 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 18 2-1939 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 19 2-1940 Unit 41 3,4-diClPh CO Single bond or CH _Two Device 20 2-1941 device 41 3,4-diClPh CO single bond or CH _Two Unit 21 2-1942 unit 41 3,4-diClPh CO single bond or CH _Two Unit 22 2-1943 unit 41 3,4-diClPh CO single bond or CH _Two Unit 23 2-1944 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1945 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1946 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1947 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 27 2-1948 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1949 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1950 Unit 41 3,4-diClPh CO Single bond or CH _Two Device 30 2-1951 device 41 3,4-diClPh CO single bond or CH _Two Unit 31 2-1952 unit 41 3,4-diClPh CO single bond or CH _Two Device 32 2-1953 device 41 3,4-diClPh CO single bond or CH _Two Device 65 2-1954 device 41 3,4-diClPh CO single bond or CH _Two Unit 66 2-1955 Unit 41 3,4-diClPh CO Single bond or CH _Two App. 67 2-1956 App. 41 3,4-diClPh CO Single bond or CH _Two Unit 68 2-1957 Unit 41 3,4-diClPh CO Single bond or CH _Two Device 69 2-1958 device 41 3,4-diClPh CO single bond or CH _Two Device 70 2-1959 device 41 3,4-diClPh CO single bond or CH _Two Unit 71 2-1960 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 72 2-1961 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 73 2-1962 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 74 2-1963 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 75 2-1964 Unit 41 3,4-diClPh CO Single bond or CH _Two Unit 76 2-1965 Unit 41 3,4-diClPh CO Single bond or CH _Two App. 77 2-1966 App. 41 3,4-diClPh CO Single bond or CH _Two Unit 78 2-1967 unit 41 3,4-diClPh CO single bond or CH _Two Device 79 2-1968 device 41 3,4-diClPh CO single bond or CH _Two Device 80 2-1969 device 42 3,4-diClPh CO single bond or CH _Two Unit 1 2-1970 Unit 42 3,4-diClPh CO Single bond or CH _Two App.2 2-1971 App.42 3,4-diClPh CO Single bond or CH _Two App. 3 2-1972 App. 42 3,4-diClPh CO Single bond or CH _Two App. 4 2-1973 App. 42 3,4-diClPh CO Single bond or CH _Two Unit 5 2-1974 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 6 2-1975 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 7 2-1976 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 8 2-1977 Unit 42 3,4-diClPh CO Single bond or CH _Two App. 9 2-1978 App. 42 3,4-diClPh CO Single bond or CH _Two Unit 10 2-1979 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 11 2-1980 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 12 2-1981 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 13 2-1982 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 14 2-1983 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 15 2-1984 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 16 2-1985 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 17 2-1986 Unit 42 3,4-diClPh CO Single bond or CH _Two App. 18 2-1987 App. 42 3,4-diClPh CO Single bond or CH _Two App 19 2-1988 App 42 3,4-diClPh CO Single bond or CH _Two Unit 20 2-1989 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 21 2-1990 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 22 2-1991 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 23 2-1992 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 24 2-1993 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 25 2-1994 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 26 2-1995 Unit 42 3,4-diClPh CO Single bond or CH _Two App. 27 2-1996 App. 42 3,4-diClPh CO Single bond or CH _Two Unit 28 2-1997 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 29 2-1998 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 30 2-1999 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 31 2-2000 Unit 42 3,4-diClPh CO Single bond or CH _Two Device 32 2-2001 device 42 3,4-diClPh CO single bond or CH _Two App. 65 2-2002 App. 42 3,4-diClPh CO Single bond or CH _Two Unit 66 2-2003 Unit 42 3,4-diClPh CO Single bond or CH _Two App. 67 2-2004 App. 42 3,4-diClPh CO Single bond or CH _Two App. 68 2-2005 App. 42 3,4-diClPh CO Single bond or CH _Two App. 69 2-2006 App. 42 3,4-diClPh CO Single bond or CH _Two Unit 70 2-2007 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2008 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2009 Unit 42 3,4-diClPh CO Single bond or CH _Two App. 73 2-2010 App. 42 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2011 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2012 Unit 42 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2013 Unit 42 3,4-diClPh CO Single bond or CH _Two App. 77 2-2014 App. 42 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2015 Unit 42 3,4-diClPh CO Single bond or CH _Two App. 79 2-2016 App. 42 3,4-diClPh CO Single bond or CH _Two Device 80 2-2017 device 43 3,4-diClPh CO single bond or CH _Two Place 1 2-2018 Place 43 3,4-diClPh CO Single bond or CH _Two App.2 2-2019 App.43 3,4-diClPh CO Single bond or CH _Two Device 3 2-2020 device 43 3,4-diClPh CO single bond or CH _Two Unit 4 2-2202 Unit 43 3,4-diClPh CO Single bond or CH _Two App 5 2-2022 Apparatus 43 3,4-diClPh CO Single bond or CH _Two Device 6 2-2023 device 43 3,4-diClPh CO single bond or CH _Two Unit 7 2-2024 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2025 Unit 43 3,4-diClPh CO Single bond or CH _Two App. 9 2-2026 App. 43 3,4-diClPh CO Single bond or CH _Two Device 10 2-2027 device 43 3,4-diClPh CO single bond or CH _Two Unit 11 2-2028 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2029 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2030 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2031 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2032 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2033 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2034 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2035 Unit 43 3,4-diClPh CO Single bond or CH _Two App 19 2-2036 App 43 43,4-diClPh CO Single bond or CH _Two Device 20 2-2037 device 43 3,4-diClPh CO single bond or CH _Two Unit 21 2-2038 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2039 unit 43 3,4-diClPh CO single bond or CH _Two Unit 23 2-2040 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2041 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2042 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2043 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2044 Unit 43 3,4-diClPh CO Single bond or CH _Two App. 28 2-2045 App. 43 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2046 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 30 2-2047 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 31 2-2048 unit 43 3,4-diClPh CO single bond or CH _Two Device 32 2-2049 device 43 3,4-diClPh CO single bond or CH _Two Device 65 2-2050 device 43 3,4-diClPh CO single bond or CH _Two Unit 66 2-2051 Unit 43 3,4-diClPh CO Single bond or CH _Two App. 67 2-2052 App. 43 3,4-diClPh CO Single bond or CH _Two Unit 68 2-2053 Unit 43 3,4-diClPh CO Single bond or CH _Two App. 69 2-2054 App. 43 3,4-diClPh CO Single bond or CH _Two Device 70 2-2055 device 43 3,4-diClPh CO single bond or CH _Two Unit 71 2-2056 unit 43 3,4-diClPh CO single bond or CH _Two Unit 72 2-2057 Unit 43 3,4-diClPh CO Single bond or CH _Two App. 73 2-2058 App. 43 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2059 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2060 Unit 43 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2061 Unit 43 3,4-diClPh CO Single bond or CH _Two App. 77 2-2062 App. 43 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2063 unit 43 3,4-diClPh CO single bond or CH _Two App. 79 2-2064 App. 43 3,4-diClPh CO Single bond or CH _Two No. 80 化合物 Compound number R ¹ R ^Two ABZ group b group ──────────────────────────────────── 2-2065 placement 443 4-diClPh CO single bond or CH _Two Unit 1 2-2066 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 22-2067 unit 44 3,4-diClPh CO single bond or CH _Two Device 3 2-2068 device 44 3,4-diClPh CO single bond or CH _Two Unit 4 2-2069 Unit 44 3,4-diClPh CO Single bond or CH _Two Device 5 2-2070 device 44 3,4-diClPh CO single bond or CH _Two Unit 6 2-2071 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2072 unit 44 3,4-diClPh CO single bond or CH _Two Unit 8 2-2073 unit 44 3,4-diClPh CO single bond or CH _Two Unit 9 2-2074 Unit 44 3,4-diClPh CO Single bond or CH _Two Device 10 2-2075 device 44 3,4-diClPh CO single bond or CH _Two Unit 11 2-2076 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2077 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2078 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2079 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2080 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2081 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2082 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2083 Unit 44 3,4-diClPh CO Single bond or CH _Two App. 19 2-2084 App. 44 3,4-diClPh CO Single bond or CH _Two Unit 20 2-2085 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 21 2-2086 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2087 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2088 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2089 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2090 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2091 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2092 unit 44 3,4-diClPh CO single bond or CH _Two Unit 28 2-2093 unit 44 3,4-diClPh CO single bond or CH _Two Unit 29 2-2094 unit 44 3,4-diClPh CO single bond or CH _Two Device 30 2-2095 device 44 3,4-diClPh CO single bond or CH _Two Unit 31 2-2096 unit 44 3,4-diClPh CO single bond or CH _Two Device 32 2-2097 device 44 3,4-diClPh CO single bond or CH _Two Device 65 2-2098 device 44 3,4-diClPh CO single bond or CH _Two Unit 66 2-2099 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 67 2-2100 Unit 44 3,4-diClPh CO Single bond or CH _Two Device 68 2-2101 device 44 3,4-diClPh CO single bond or CH _Two Device 69 2-2102 device 44 3,4-diClPh CO single bond or CH _Two Device 70 2-2103 device 44 3,4-diClPh CO single bond or CH _Two Unit 71 2-2104 unit 44 3,4-diClPh CO single bond or CH _Two Unit 72 2-2105 unit 44 3,4-diClPh CO single bond or CH _Two Unit 73 2-2106 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2107 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2108 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2109 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 77 2-2110 Unit 44 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2111 unit 44 3,4-diClPh CO single bond or CH _Two Device 79 2-2112 device 44 3,4-diClPh CO single bond or CH _Two Device 80 2-2113 device 45 3,4-diClPh CO single bond or CH _Two Unit 1 2-2114 unit 45 3,4-diClPh CO single bond or CH _Two Unit 2 2-2115 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2116 Unit 45 3,4-diClPh CO Single bond or CH _Two App. 4 2-2117 App. 45 3,4-diClPh CO Single bond or CH _Two Unit 5 2-2118 Unit 45 3,4-diClPh CO Single bond or CH _Two App. 6 2-2119 App. 45 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2120 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2121 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2122 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2123 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2124 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2125 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2126 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2127 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2128 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2129 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2130 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2131 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 19 2-2132 Unit 45 3,4-diClPh CO Single bond or CH _Two Device 20 2-2133 device 45 3,4-diClPh CO single bond or CH _Two Unit 21 2-2134 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2135 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2136 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2137 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2138 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2139 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2140 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 28 2-2141 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2142 Unit 45 3,4-diClPh CO Single bond or CH _Two Device 30 2-2143 device 45 3,4-diClPh CO single bond or CH _Two Unit 31 2-2144 unit 45 3,4-diClPh CO single bond or CH _Two Device 32 2-2145 device 45 3,4-diClPh CO single bond or CH _Two App. 65 2-2146 App. 45 3,4-diClPh CO Single bond or CH _Two Unit 66 2-2147 Unit 45 3,4-diClPh CO Single bond or CH _Two App. 67 2-2148 App. 45 3,4-diClPh CO Single bond or CH _Two App. 68 2-2149 App. 45 3,4-diClPh CO Single bond or CH _Two Device 69 2-2150 device 45 3,4-diClPh CO single bond or CH _Two Device 70 2-2151 device 45 3,4-diClPh CO single bond or CH _Two Unit 71 2-2152 Unit 45 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2153 unit 45 3,4-diClPh CO single bond or CH _Two App. 73 2-2154 App. 45 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2155 Unit 45 3,4-diClPh CO Single bond or CH _Two App. 75 2-2156 App. 45 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2157 Unit 45 3,4-diClPh CO Single bond or CH _Two App. 77 2-2158 App. 45 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2159 unit 45 3,4-diClPh CO single bond or CH _Two Device 79 2-2160 device 45 3,4-diClPh CO single bond or CH _Two Device 80 2-2161 device 46 3,4-diClPh CO single bond or CH _Two App 1 2-2162 App. 46 3,4-diClPh CO Single bond or CH _Two Unit 22-2163 unit 46 3,4-diClPh CO single bond or CH _Two Unit 3 2-2164 Unit 46 3,4-diClPh CO Single bond or CH _Two Device 4 2-2165 device 46 3,4-diClPh CO single bond or CH _Two Device 5 2-2166 device 46 3,4-diClPh CO single bond or CH _Two App. 6 2-2167 App. 46 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2168 Unit 46 3,4-diClPh CO Single bond or CH _Two App. 8 2-2169 App. 46 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2170 Unit 46 3,4-diClPh CO Single bond or CH _Two Device 10 2-2171 device 46 3,4-diClPh CO single bond or CH _Two Unit 11 2-2172 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2173 unit 46 3,4-diClPh CO single bond or CH _Two Unit 13 2-2174 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2175 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2176 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2177 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2178 unit 46 3,4-diClPh CO single bond or CH _Two Unit 18 2-2179 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 19 2-2180 Unit 46 3,4-diClPh CO Single bond or CH _Two Device 20 2-2181 device 46 3,4-diClPh CO single bond or CH _Two Unit 21 2-2182 unit 46 3,4-diClPh CO single bond or CH _Two Unit 22 2-2183 unit 46 3,4-diClPh CO single bond or CH _Two Unit 23 2-2184 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2185 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2186 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2187 Unit 46 3,4-diClPh CO Single bond or CH _Two App. 27 2-2188 App. 46 3,4-diClPh CO Single bond or CH _Two App. 28 2-2189 App. 46 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2190 Unit 46 3,4-diClPh CO Single bond or CH _Two Device 30 2-2191 device 46 3,4-diClPh CO single bond or CH _Two Unit 31 2-2192 unit 46 3,4-diClPh CO single bond or CH _Two Device 32 2-2193 device 46 3,4-diClPh CO single bond or CH _Two App. 65 2-2194 App. 46 3,4-diClPh CO Single bond or CH _Two Device 66 2-2195 device 46 3,4-diClPh CO single bond or CH _Two App. 67 2-2196 App. 46 3,4-diClPh CO Single bond or CH _Two App. 68 2-2197 App. 46 3,4-diClPh CO Single bond or CH _Two Device 69 2-2198 device 46 3,4-diClPh CO single bond or CH _Two Device 70 2-2199 device 46 3,4-diClPh CO single bond or CH _Two Unit 71 2-2200 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2201 Unit 46 3,4-diClPh CO Single bond or CH _Two 73 73 2-2202 Position 46 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2203 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2204 Unit 46 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2205 Unit 46 3,4-diClPh CO Single bond or CH _Two App. 77 2-2206 App. 46 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2207 unit 46 3,4-diClPh CO single bond or CH _Two Device 79 2-2208 device 46 3,4-diClPh CO single bond or CH _Two Device 80 2-2209 device 47 3,4-diClPh CO single bond or CH _Two Unit 1 2-2210 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 22-2221 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2212 Unit 47 3,4-diClPh CO Single bond or CH _Two Device 4 2-2213 device 47 3,4-diClPh CO single bond or CH _Two Device 5 2-2214 device 47 3,4-diClPh CO single bond or CH _Two Unit 6 2-2215 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2216 Unit 47 3,4-diClPh CO Single bond or CH _Two App. 8 2-2217 App. 47 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2218 Unit 47 3,4-diClPh CO Single bond or CH _Two Device 10 2-2219 device 47 3,4-diClPh CO single bond or CH _Two Unit 11 2-2220 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2221 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2222 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2223 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2224 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2225 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2226 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2227 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 19 2-2228 Unit 47 3,4-diClPh CO Single bond or CH _Two Device 20 2-2229 device 47 3,4-diClPh CO single bond or CH _Two Unit 21 2-2230 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2231 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2232 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2233 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2234 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2235 Unit 47 3,4-diClPh CO Single bond or CH _Two App. 27 2-2236 App. 47 3,4-diClPh CO Single bond or CH _Two App. 28 2-2237 App. 47 3,4-diClPh CO Single bond or CH _Two App. 29 2-2238 App. 47 3,4-diClPh CO Single bond or CH _Two Device 30 2-2239 device 47 3,4-diClPh CO single bond or CH _Two Unit 31 2-2240 Unit 47 3,4-diClPh CO Single bond or CH _Two Device 32 2-2241 device 47 3,4-diClPh CO single bond or CH _Two App. 65 2-2242 App. 47 3,4-diClPh CO Single bond or CH _Two Device 66 2-2243 device 47 3,4-diClPh CO single bond or CH _Two App. 67 2-2244 App. 47 3,4-diClPh CO Single bond or CH _Two Device 68 2-2245 device 47 3,4-diClPh CO single bond or CH _Two Device 69 2-2246 device 47 3,4-diClPh CO single bond or CH _Two Device 70 2-2247 device 47 3,4-diClPh CO single bond or CH _Two Unit 71 2-2248 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2249 unit 47 3,4-diClPh CO single bond or CH _Two Unit 73 2-2250 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2251 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2252 Unit 47 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2253 unit 47 3,4-diClPh CO single bond or CH _Two App. 77 2-2254 App. 47 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2255 unit 47 3,4-diClPh CO single bond or CH _Two Device 79 2-2256 device 47 3,4-diClPh CO single bond or CH _Two Device 80 2-2257 device 81 3,4-diClPh CO single bond or CH _Two Unit 1 2-2258 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 2 2-2259 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2260 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 4 2-2261 Unit 81 3,4-diClPh CO Single bond or CH _Two Device 5 2-2262 device 81 3,4-diClPh CO single bond or CH _Two Unit 6 2-2263 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2264 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2265 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2266 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2267 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2268 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2269 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2270 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2271 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2272 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2273 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2274 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2275 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 19 2-2276 Unit 81 3,4-diClPh CO Single bond or CH _Two Device 20 2-2277 device 81 3,4-diClPh CO single bond or CH _Two Unit 21 2-2278 unit 81 3,4-diClPh CO single bond or CH _Two Unit 22 2-2279 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2280 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2281 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2282 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2283 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2284 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 28 2-2285 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2286 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 30 2-2287 unit 81 3,4-diClPh CO single bond or CH _Two Unit 31 2-2288 unit 81 3,4-diClPh CO single bond or CH _Two Device 32 2-2289 device 81 3,4-diClPh CO single bond or CH _Two App. 65 2-2290 App. 81 3,4-diClPh CO Single bond or CH _Two Unit 66 2-2291 Unit 81 3,4-diClPh CO Single bond or CH _Two App. 67 2-2292 App. 81 3,4-diClPh CO Single bond or CH _Two App. 68 2-2293 App. 81 3,4-diClPh CO Single bond or CH _Two Device 69 2-2294 device 81 3,4-diClPh CO single bond or CH _Two Unit 70 2-2295 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2296 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2297 unit 81 3,4-diClPh CO single bond or CH _Two 73-2 2298 781 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2299 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2300 Unit 81 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2301 Unit 81 3,4-diClPh CO Single bond or CH _Two App. 77 2-2302 App. 81 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2303 unit 81 3,4-diClPh CO single bond or CH _Two Device 79 2-2304 device 81 3,4-diClPh CO single bond or CH _Two Device 80 2-2305 device 48 3,4-diClPh CO single bond or CH _Two Unit 1 2-2306 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 22-2307 unit 48 3,4-diClPh CO single bond or CH _Two Unit 3 2-2308 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 4 2-2309 unit 48 3,4-diClPh CO single bond or CH _Two Device 5 2-2310 device 48 3,4-diClPh CO single bond or CH _Two Device 6 2-2311 device 48 3,4-diClPh CO single bond or CH _Two Unit 7 2-2312 Unit 48 3,4-diClPh CO Single bond or CH _Two App. 8 2-2313 App. 48 3,4-diClPh CO Single bond or CH _Two App. 9 2-2314 App. 48 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2315 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2316 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2317 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2318 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2319 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2320 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2321 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2322 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2323 Unit 48 3,4-diClPh CO Single bond or CH _Two App 19 2-2324 App 48 48,4-diClPh CO Single bond or CH _Two Device 20 2-2325 device 48 3,4-diClPh CO single bond or CH _Two Unit 21 2-2326 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2327 unit 48 3,4-diClPh CO single bond or CH _Two Unit 23 2-2328 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2329 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2330 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2331 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2332 Unit 48 3,4-diClPh CO Single bond or CH _Two Device 28 2-2333 device 48 3,4-diClPh CO single bond or CH _Two Unit 29 2-2334 unit 48 3,4-diClPh CO single bond or CH _Two Device 30 2-2335 device 48 3,4-diClPh CO single bond or CH _Two Unit 31 2-2336 unit 48 3,4-diClPh CO single bond or CH _Two Device 32 2-2337 device 48 3,4-diClPh CO single bond or CH _Two App. 65 2-2338 App. 48 3,4-diClPh CO Single bond or CH _Two Device 66 2-2339 device 48 3,4-diClPh CO single bond or CH _Two App. 67 2-2340 App. 48 3,4-diClPh CO Single bond or CH _Two App. 68 2-2341 App. 48 3,4-diClPh CO Single bond or CH _Two Device 69 2-2342 device 48 3,4-diClPh CO single bond or CH _Two Device 70 2-2343 device 48 3,4-diClPh CO single bond or CH _Two Unit 71 2-2344 unit 48 3,4-diClPh CO single bond or CH _Two Unit 72 2-2345 unit 48 3,4-diClPh CO single bond or CH _Two 73 73 2346 3 48 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2347 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2348 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2349 Unit 48 3,4-diClPh CO Single bond or CH _Two Unit 77 2-2350 Unit 48 3,4-diClPh CO Single bond or CH _Two App.78 2-2351 App.48 3,4-diClPh CO Single bond or CH _Two Device 79 2-2352 device 48 3,4-diClPh CO single bond or CH _Two Device 80 2-2353 device 49 3,4-diClPh CO single bond or CH _Two Unit 1 2-2354 Unit 49 3,4-diClPh CO Single bond or CH _Two App.2 2-2355 App.49 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2356 Unit 49 3,4-diClPh CO Single bond or CH _Two App. 4 2-2357 App. 49 3,4-diClPh CO Single bond or CH _Two 5 2 2358 5 49 3,4-diClPh CO Single bond or CH _Two Unit 6 2-2359 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2360 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2361 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2362 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2363 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2364 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2365 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2366 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2367 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2368 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2369 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2370 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2371 Unit 49 3,4-diClPh CO Single bond or CH _Two 19 19 2372 2 49 4,4-diClPh CO Single bond or CH _Two Device 20 2-2373 device 49 3,4-diClPh CO single bond or CH _Two Unit 21 2-2374 unit 49 3,4-diClPh CO single bond or CH _Two Unit 22 2-2375 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2376 unit 49 3,4-diClPh CO single bond or CH _Two Unit 24 2-2377 unit 49 3,4-diClPh CO single bond or CH _Two Unit 25 2-2378 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2379 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2380 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 28 2-2381 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2382 unit 49 3,4-diClPh CO single bond or CH _Two Device 30 2-2383 device 49 3,4-diClPh CO single bond or CH _Two Unit 31 2-2384 unit 49 3,4-diClPh CO single bond or CH _Two Device 32 2-2385 device 49 3,4-diClPh CO single bond or CH _Two App. 65 2-2386 App. 49 3,4-diClPh CO Single bond or CH _Two Device 66 2-287 device 49 3,4-diClPh CO single bond or CH _Two App. 67 2-2388 App. 49 3,4-diClPh CO Single bond or CH _Two Device 68 2-2389 device 49 3,4-diClPh CO single bond or CH _Two App. 69 2-2390 App. 49 3,4-diClPh CO Single bond or CH _Two App. 70 2-2391 App. 49 3,4-diClPh CO Single bond or CH _Two Unit 71 2-392 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2393 unit 49 3,4-diClPh CO single bond or CH _Two Unit 73 2-2394 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2395 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2396 Unit 49 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2397 Unit 49 3,4-diClPh CO Single bond or CH _Two App. 77 2-2398 App. 49 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2399 Unit 49 3,4-diClPh CO Single bond or CH _Two Device 79 2-2400 device 49 3,4-diClPh CO single bond or CH _Two Device 80 2-2401 Device 50 3,4-diClPh CO Single bond or CH _Two Device 1 2-2402 device 50 3,4-diClPh CO single bond or CH _Two Device 2 2-2403 device 50 3,4-diClPh CO single bond or CH _Two Device 3 2-2404 device 50 3,4-diClPh CO single bond or CH _Two Device 4 2-2405 device 50 3,4-diClPh CO single bond or CH _Two Device 5 2-2406 device 50 3,4-diClPh CO single bond or CH _Two Device 6 2-2407 device 50 3,4-diClPh CO single bond or CH _Two Unit 7 2-2408 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2409 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2410 Unit 50 3,4-diClPh CO Single bond or CH _Two Device 10 2-2411 device 50 3,4-diClPh CO single bond or CH _Two Unit 11 2-2412 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2413 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2414 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2415 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2416 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2417 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2418 Unit 50 3,4-diClPh CO Single bond or CH _Two Device 18 2-2419 device 50 3,4-diClPh CO single bond or CH _Two Unit 19 2-2420 Unit 50 3,4-diClPh CO Single bond or CH _Two Device 20 2-2421 device 50 3,4-diClPh CO single bond or CH _Two Device 21 2-2422 device 50 3,4-diClPh CO single bond or CH _Two Unit 22 2-2423 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2424 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2425 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2426 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2427 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2428 Unit 50 3,4-diClPh CO Single bond or CH _Two Device 28 2-2429 device 50 3,4-diClPh CO single bond or CH _Two Device 29 2-2430 device 50 3,4-diClPh CO single bond or CH _Two Device 30 2-2431 device 50 3,4-diClPh CO single bond or CH _Two Unit 31 2-2432 Unit 50 3,4-diClPh CO Single bond or CH _Two Device 32 2-2433 device 50 3,4-diClPh CO single bond or CH _Two Device 65 2-2434 Device 50 3,4-diClPh CO Single bond or CH _Two Device 66 2-2435 device 50 3,4-diClPh CO single bond or CH _Two App. 67 2-2436 App. 50 3,4-diClPh CO Single bond or CH _Two Device 68 2-2437 device 50 3,4-diClPh CO single bond or CH _Two Device 69 2-2438 device 50 3,4-diClPh CO single bond or CH _Two Device 70 2-2439 device 50 3,4-diClPh CO single bond or CH _Two Unit 71 2-2440 Unit 50 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2441 unit 50 3,4-diClPh CO single bond or CH _Two 73 73 2442 50 50 3,4-diClPh CO Single bond or CH _Two Device 74 2-2443 device 50 3,4-diClPh CO single bond or CH _Two 75 75 2244 4 50 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2445 Unit 50 3,4-diClPh CO Single bond or CH _Two App. 77 2-2446 App. 50 3,4-diClPh CO Single bond or CH _Two App. 78 2-2447 App. 50 3,4-diClPh CO Single bond or CH _Two Device 79 2-2448 device 50 3,4-diClPh CO single bond or CH _Two Device 80 2-2449 device 51 3,4-diClPh CO single bond or CH _Two Device 1 2-2450 device 51 3,4-diClPh CO single bond or CH _Two Unit 22-2451 Unit 51 3,4-diClPh CO Single bond or CH _Two Device 3 2-2452 device 51 3,4-diClPh CO single bond or CH _Two Device 4 2-2453 device 51 3,4-diClPh CO single bond or CH _Two Device 5 2-2454 device 51 3,4-diClPh CO single bond or CH _Two Unit 6 2-2455 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2456 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2457 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2458 Unit 51 3,4-diClPh CO Single bond or CH _Two Device 10 2-2459 device 51 3,4-diClPh CO single bond or CH _Two Unit 11 2-2460 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2461 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2462 Unit 51 3,4-diClPh CO Single bond or CH _Two Device 14 2-2463 device 51 3,4-diClPh CO single bond or CH _Two Unit 15 2-2464 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2465 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2466 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2467 Unit 51 3,4-diClPh CO Single bond or CH _Two App 19 2-2468 App 51 51,4-diClPh CO Single bond or CH _Two Device 20 2-2469 device 51 3,4-diClPh CO single bond or CH _Two Device 21 2-2470 device 51 3,4-diClPh CO single bond or CH _Two Unit 22 2-2471 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2472 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2473 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2474 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2475 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2476 Unit 51 3,4-diClPh CO Single bond or CH _Two Device 28 2-2577 device 51 3,4-diClPh CO single bond or CH _Two Unit 29 2-2478 unit 51 3,4-diClPh CO single bond or CH _Two Device 30 2-2479 device 51 3,4-diClPh CO single bond or CH _Two Device 31 2-2480 device 51 3,4-diClPh CO single bond or CH _Two Device 32 2-2481 device 51 3,4-diClPh CO single bond or CH _Two App. 65 2-2482 App. 51 3,4-diClPh CO Single bond or CH _Two Device 66 2-2483 device 51 3,4-diClPh CO single bond or CH _Two App. 67 2-2484 App. 51 3,4-diClPh CO Single bond or CH _Two Unit 68 2-2485 Unit 51 3,4-diClPh CO Single bond or CH _Two Device 69 2-2486 device 51 3,4-diClPh CO single bond or CH _Two Unit 70 2-2487 Unit 51 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2488 unit 51 3,4-diClPh CO single bond or CH _Two Unit 72 2-2489 Unit 51 3,4-diClPh CO Single bond or CH _Two 73 73 2490 5 51 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2491 Unit 51 3,4-diClPh CO Single bond or CH _Two 75 75 2492 5 51 3,4-diClPh CO Single bond or CH _Two Unit 76 2493 Unit 51 3,4-diClPh CO Single bond or CH _Two App. 77 2-2494 App. 51 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2495 unit 51 3,4-diClPh CO single bond or CH _Two Device 79 2-2496 device 51 3,4-diClPh CO single bond or CH _Two Device 80 2-2497 device 52 3,4-diClPh CO single bond or CH _Two Unit 1 2-2498 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 2 2-2499 unit 52 3,4-diClPh CO single bond or CH _Two Unit 3 2-2500 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 4 2-2501 Unit 52 3,4-diClPh CO Single bond or CH _Two Device 5 2-2502 device 52 3,4-diClPh CO single bond or CH _Two Unit 6 2-2503 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2504 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2505 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2506 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2507 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2508 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2509 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2510 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2511 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2512 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2513 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2514 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2515 Unit 52 3,4-diClPh CO Single bond or CH _Two App 19 2-2516 App 52 52,4-diClPh CO Single bond or CH _Two Device 20 2-2517 device 52 3,4-diClPh CO single bond or CH _Two Unit 21 2-2518 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2519 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2520 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2521 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2522 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2523 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2524 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 28 2-2525 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2526 Unit 52 3,4-diClPh CO Single bond or CH _Two Device 30 2-2527 device 52 3,4-diClPh CO single bond or CH _Two Device 31 2-2528 device 52 3,4-diClPh CO single bond or CH _Two Device 32 2-2529 device 52 3,4-diClPh CO single bond or CH _Two Set 65 2-2530 Set 52 3,4-diClPh CO Single bond or CH _Two Device 66 2-2531 device 52 3,4-diClPh CO single bond or CH _Two App. 67 2-2532 App. 52 3,4-diClPh CO Single bond or CH _Two Device 68 2-2533 device 52 3,4-diClPh CO single bond or CH _Two Device 69 2-2534 device 52 3,4-diClPh CO single bond or CH _Two Unit 70 2-2535 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2536 unit 52 3,4-diClPh CO single bond or CH _Two Unit 72 2-2537 Unit 52 3,4-diClPh CO Single bond or CH _Two App. 73 2-2538 App. 52 3,4-diClPh CO Single bond or CH _Two Device 74 2-2539 device 52 3,4-diClPh CO single bond or CH _Two Unit 75 2-2540 Unit 52 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2541 Unit 52 3,4-diClPh CO Single bond or CH _Two App. 77 2-2542 App. 52 3,4-diClPh CO Single bond or CH _Two App. 78 2-2543 App. 52 3,4-diClPh CO Single bond or CH _Two Device 79 2-2544 device 52 3,4-diClPh CO single bond or CH _Two Device 80 2-2545 device 53 3,4-diClPh CO single bond or CH _Two App 1 2-2546 App.53 3,4-diClPh CO Single bond or CH _Two App.2 2-2547 App.53 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2548 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 4 2-2549 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 5 2-2550 Unit 53 3,4-diClPh CO Single bond or CH _Two App. 6 2-2551 App. 53 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2552 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2553 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2554 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2555 Unit 53 3,4-diClPh CO Single bond or CH _Two Device 11 2-2556 device 53 3,4-diClPh CO single bond or CH _Two Unit 12 2-2557 unit 53 3,4-diClPh CO single bond or CH _Two Unit 13 2-2558 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2559 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2560 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2561 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2562 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2563 Unit 53 3,4-diClPh CO Single bond or CH _Two App 192-2564 App.53 3,4-diClPh CO Single bond or CH _Two Device 20 2-2565 device 53 3,4-diClPh CO single bond or CH _Two Unit 21 2-2566 unit 53 3,4-diClPh CO single bond or CH _Two Unit 22 2-2567 unit 53 3,4-diClPh CO single bond or CH _Two Unit 23 2-2568 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2569 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2570 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2571 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2572 Unit 53 3,4-diClPh CO Single bond or CH _Two Device 28 2-2573 device 53 3,4-diClPh CO single bond or CH _Two Unit 29 2-2574 unit 53 3,4-diClPh CO single bond or CH _Two Unit 30 2-2575 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 31 2-2576 unit 53 3,4-diClPh CO single bond or CH _Two Device 32 2-2577 device 53 3,4-diClPh CO single bond or CH _Two App. 65 2-2578 App. 53 3,4-diClPh CO Single bond or CH _Two Device 66 2-2579 device 53 3,4-diClPh CO single bond or CH _Two App. 67 2-2580 App. 53 3,4-diClPh CO Single bond or CH _Two Device 68 2-2581 device 53 3,4-diClPh CO single bond or CH _Two App. 69 2-2582 App. 53 3,4-diClPh CO Single bond or CH _Two App. 70 2-2583 App. 53 3,4-diClPh CO Single bond or CH _Two Unit 71 2-258 Unit 53 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2585 unit 53 3,4-diClPh CO single bond or CH _Two App. 73 2-2586 App. 53 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2587 Unit 53 3,4-diClPh CO Single bond or CH _Two App. 75 2-2588 App. 53 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2589 Unit 53 3,4-diClPh CO Single bond or CH _Two App. 77 2-2590 App. 53 3,4-diClPh CO Single bond or CH _Two App.78 2-2591 App.53 3,4-diClPh CO Single bond or CH _Two Device 79 2-2592 device 53 3,4-diClPh CO single bond or CH _Two No. 80 化合物 Compound number R ¹ R ^Two ABZ group a group b ｂ 2-2593 4-diClPh CO single bond or CH _Two Unit 1 2-2594 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 2 2-2595 Unit 54 3,4-diClPh CO Single bond or CH _Two App 3 2-2596 App. 54 3,4-diClPh CO Single bond or CH _Two Device 4 2-2597 device 54 3,4-diClPh CO single bond or CH _Two Device 5 2-2598 device 54 3,4-diClPh CO single bond or CH _Two Unit 6 2-2599 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2600 Unit 54 3,4-diClPh CO Single bond or CH _Two App. 8 2-2601 App. 54 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2602 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2603 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2604 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2605 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2606 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2607 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2608 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2609 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2610 Unit 54 3,4-diClPh CO Single bond or CH _Two App. 18 2-2611 App. 54 3,4-diClPh CO Single bond or CH _Two App 19 2-2612 App. 54 3,4-diClPh CO Single bond or CH _Two Device 20 2-2613 device 54 3,4-diClPh CO single bond or CH _Two Unit 21 2-2614 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2615 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2616 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2617 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2618 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2619 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2620 Unit 54 3,4-diClPh CO Single bond or CH _Two App. 28 2-2621 App. 54 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2622 Unit 54 3,4-diClPh CO Single bond or CH _Two Device 30 2-2623 device 54 3,4-diClPh CO single bond or CH _Two Unit 31 2-2624 unit 54 3,4-diClPh CO single bond or CH _Two Device 32 2-2625 device 54 3,4-diClPh CO single bond or CH _Two Set 65 2-2626 Set 54 3,4-diClPh CO Single bond or CH _Two Device 66 2-2627 device 54 3,4-diClPh CO single bond or CH _Two App. 67 2-2628 App. 54 3,4-diClPh CO Single bond or CH _Two Device 68 2-2629 device 54 3,4-diClPh CO single bond or CH _Two Device 69 2-2630 Device 54 3,4-diClPh CO Single bond or CH _Two Unit 70 2-2631 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2632 unit 54 3,4-diClPh CO single bond or CH _Two Unit 72 2-2633 Unit 54 3,4-diClPh CO Single bond or CH _Two App. 73 2-2634 App. 54 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2635 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2636 Unit 54 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2637 Unit 54 3,4-diClPh CO Single bond or CH _Two App. 77 2-2638 App. 54 3,4-diClPh CO Single bond or CH _Two App.78 2-2639 App.54 3,4-diClPh CO Single bond or CH _Two Device 79 2-2640 device 54 3,4-diClPh CO single bond or CH _Two Device 80 2-2641 device 55 3,4-diClPh CO single bond or CH _Two Unit 1 2-2642 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 22-2643 Unit 55 3,4-diClPh CO Single bond or CH _Two App.3 2-2644 App.55 3,4-diClPh CO Single bond or CH _Two Unit 4 2-2645 Unit 55 3,4-diClPh CO Single bond or CH _Two 5 2 2646 5 55 3,4-diClPh CO Single bond or CH _Two App. 6 2-2647 App. 55 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2648 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2649 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2650 Unit 55 3,4-diClPh CO Single bond or CH _Two Device 10 2-2651 device 55 3,4-diClPh CO single bond or CH _Two Unit 11 2-2652 Unit 55 3,4-diClPh CO Single bond or CH _Two Device 12 2-2653 device 55 3,4-diClPh CO single bond or CH _Two Unit 13 2-2654 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2655 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2656 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2657 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2658 Unit 55 3,4-diClPh CO Single bond or CH _Two App. 18 2-2659 App. 55 3,4-diClPh CO Single bond or CH _Two App 19 2-2660 App. 55 3,4-diClPh CO Single bond or CH _Two Device 20 2-2661 device 55 3,4-diClPh CO single bond or CH _Two Unit 21 2-2662 unit 55 3,4-diClPh CO single bond or CH _Two Unit 22 2-2663 Unit 55 3,4-diClPh CO Single bond or CH _Two 23 to 2664 64 to 55 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2665 Unit 55 3,4-diClPh CO Single bond or CH _Two 25-2 2666 555 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2667 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2668 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 28 2-2669 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2670 unit 55 3,4-diClPh CO single bond or CH _Two Device 30 2-2671 device 55 3,4-diClPh CO single bond or CH _Two App. 31 2-2672 App. 55 3,4-diClPh CO Single bond or CH _Two Device 32 2-2673 device 55 3,4-diClPh CO single bond or CH _Two App. 65 2-2674 App. 55 3,4-diClPh CO Single bond or CH _Two Device 66 2-2675 device 55 3,4-diClPh CO single bond or CH _Two App. 67 2-2676 App. 55 3,4-diClPh CO Single bond or CH _Two Unit 68 2-2677 Unit 55 3,4-diClPh CO Single bond or CH _Two Device 69 2-2678 device 55 3,4-diClPh CO single bond or CH _Two Device 70 2-2679 device 55 3,4-diClPh CO single bond or CH _Two Unit 71 2-2680 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2681 Unit 55 3,4-diClPh CO Single bond or CH _Two 73 2-2682 55 55 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2683 Unit 55 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2684 Unit 55 3,4-diClPh CO Single bond or CH _Two App. 76 2-2685 App. 55 3,4-diClPh CO Single bond or CH _Two App. 77 2-2686 App. 55 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2687 Unit 55 3,4-diClPh CO Single bond or CH _Two Device 79 2-2688 device 55 3,4-diClPh CO single bond or CH _Two Device 80 2-2689 device 56 3,4-diClPh CO single bond or CH _Two Unit 1 2-2690 Unit 56 3,4-diClPh CO Single bond or CH _Two App.2 2-2691 App.56 3,4-diClPh CO Single bond or CH _Two App.3 2-2692 App.56 3,4-diClPh CO Single bond or CH _Two Device 4 2-2693 device 56 3,4-diClPh CO single bond or CH _Two App. 5 2-2694 App. 56 3,4-diClPh CO Single bond or CH _Two App. 6 2-2695 App. 56 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2696 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2697 Unit 56 3,4-diClPh CO Single bond or CH _Two App. 9 2-2698 App. 56 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2699 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2700 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2701 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2702 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2703 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2704 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2705 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2706 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2707 Unit 56 3,4-diClPh CO Single bond or CH _Two App. 19 2-2708 App. 56 3,4-diClPh CO Single bond or CH _Two Device 20 2-2709 device 56 3,4-diClPh CO single bond or CH _Two Unit 21 2-2710 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2711 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2712 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2713 Unit 56 3,4-diClPh CO Single bond or CH _Two 25 252-1714 56 3,4-diClPhCO Single bond or CH _Two Unit 26 2-2715 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2716 Unit 56 3,4-diClPh CO Single bond or CH _Two App. 28 2-2717 App. 56 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2718 unit 56 3,4-diClPh CO single bond or CH _Two Device 30 2-2719 device 56 3,4-diClPh CO single bond or CH _Two Unit 31 2-2720 unit 56 3,4-diClPh CO single bond or CH _Two Device 32 2-2721 device 56 3,4-diClPh CO single bond or CH _Two Set 65 2-2722 Set 56 3,4-diClPh CO Single bond or CH _Two App. 66 2-2723 App. 56 3,4-diClPh CO Single bond or CH _Two App. 67 2-2724 App. 56 3,4-diClPh CO Single bond or CH _Two Set 68 2-2725 Set 56 3,4-diClPh CO Single bond or CH _Two Device 69 2-2726 device 56 3,4-diClPh CO single bond or CH _Two Unit 70 2-2727 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2728 Unit 56 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2729 Unit 56 3,4-diClPh CO Single bond or CH _Two App. 73 2-2730 App. 56 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2731 Unit 56 3,4-diClPh CO Single bond or CH _Two App. 75 2-2732 App. 56 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2733 unit 56 3,4-diClPh CO single bond or CH _Two App.77 2-2734 App.56 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2735 unit 56 3,4-diClPh CO single bond or CH _Two Device 79 2-2736 device 56 3,4-diClPh CO single bond or CH _Two Device 80 2-2737 device 57 3,4-diClPh CO single bond or CH _Two App. 1-22738 App. 57 3,4-diClPh CO Single bond or CH _Two App.2 2-2739 App.57 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2740 Unit 57 3,4-diClPh CO Single bond or CH _Two Device 4 2-2741 device 57 3,4-diClPh CO single bond or CH _Two 5 2 2742 5 57 3,4-diClPh CO Single bond or CH _Two App. 6 2-2743 App. 57 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2744 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2745 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2746 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2747 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2748 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2749 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2750 Unit 57 3,4-diClPh CO Single bond or CH _Two Device 14 2-2751 device 57 3,4-diClPh CO single bond or CH _Two Unit 15 2-2752 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2753 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2754 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2755 Unit 57 3,4-diClPh CO Single bond or CH _Two App 19 2-2756 App 57 3,4-diClPh CO Single bond or CH _Two Unit 20 2-2775 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 21 2-2758 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2759 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2760 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2761 Unit 57 3,4-diClPh CO Single bond or CH _Two 25-22762 57 57,4-diClPhCO Single bond or CH _Two Unit 26 2-2763 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2765 Unit 57 3,4-diClPh CO Single bond or CH _Two Device 28 2-2765 device 57 3,4-diClPh CO single bond or CH _Two Unit 29 2-2766 unit 57 3,4-diClPh CO single bond or CH _Two Unit 30 2-2767 unit 57 3,4-diClPh CO single bond or CH _Two Unit 31 2-2768 unit 57 3,4-diClPh CO single bond or CH _Two Device 32 2-269 device 57 3,4-diClPh CO single bond or CH _Two App. 65 2-2770 App. 57 3,4-diClPh CO Single bond or CH _Two Device 66 2-2771 device 57 3,4-diClPh CO single bond or CH _Two App. 67 2-2772 App. 57 3,4-diClPh CO Single bond or CH _Two Device 68 2-2773 device 57 3,4-diClPh CO single bond or CH _Two Device 69 2-2774 device 57 3,4-diClPh CO single bond or CH _Two Device 70 2-2775 device 57 3,4-diClPh CO single bond or CH _Two Unit 71 2-2776 unit 57 3,4-diClPh CO single bond or CH _Two Unit 72 2-2777 unit 57 3,4-diClPh CO single bond or CH _Two App. 73 2-2778 App. 57 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2779 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2780 Unit 57 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2781 Unit 57 3,4-diClPh CO Single bond or CH _Two App. 77 2-2782 App. 57 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2783 unit 57 3,4-diClPh CO single bond or CH _Two Device 79 2-2784 device 57 3,4-diClPh CO single bond or CH _Two Device 80 2-2785 device 58 3,4-diClPh CO single bond or CH _Two Unit 1 2-2786 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 22-2787 unit 58 3,4-diClPh CO single bond or CH _Two Unit 3 2-2788 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 4 2-2789 Unit 58 3,4-diClPh CO Single bond or CH _Two Device 5 2-2790 device 58 3,4-diClPh CO single bond or CH _Two Device 6 2-2791 device 58 3,4-diClPh CO single bond or CH _Two Unit 7 2-2792 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2793 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2794 Unit 58 3,4-diClPh CO Single bond or CH _Two Device 10 2-2795 device 58 3,4-diClPh CO single bond or CH _Two Unit 11 2-2796 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2797 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2798 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2799 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2800 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2801 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2802 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2803 Unit 58 3,4-diClPh CO Single bond or CH _Two App 19 2-2804 App 58 58,4-diClPh CO Single bond or CH _Two Device 20 2-2805 device 58 3,4-diClPh CO single bond or CH _Two Unit 21 2-2806 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2807 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2808 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2809 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2810 Unit 58 3,4-diClPh CO Single bond or CH _Two App. 26 2-2811 App. 58 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2812 Unit 58 3,4-diClPh CO Single bond or CH _Two App. 28 2-2813 App. 58 3,4-diClPh CO Single bond or CH _Two App. 29 2-2814 App. 58 3,4-diClPh CO Single bond or CH _Two Unit 30 2-2815 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 31 2-2816 Unit 58 3,4-diClPh CO Single bond or CH _Two Device 32 2-2817 device 58 3,4-diClPh CO single bond or CH _Two Device 65 2-2818 device 58 3,4-diClPh CO single bond or CH _Two Set 66 2-2819 Set 58 3,4-diClPh CO Single bond or CH _Two App. 67 2-2820 App. 58 3,4-diClPh CO Single bond or CH _Two App. 68 2-2821 App. 58 3,4-diClPh CO Single bond or CH _Two Device 69 2-2822 device 58 3,4-diClPh CO single bond or CH _Two Unit 70 2-2823 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2824 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2825 Unit 58 3,4-diClPh CO Single bond or CH _Two 73 73 2826 558 3,4-diClPh CO Single bond or CH _Two Unit 74 2-2827 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2828 Unit 58 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2829 Unit 58 3,4-diClPh CO Single bond or CH _Two App. 77 2-2830 App. 58 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2831 unit 58 3,4-diClPh CO single bond or CH _Two Device 79 2-2832 device 58 3,4-diClPh CO single bond or CH _Two Device 80 2-2833 device 59 3,4-diClPh CO single bond or CH _Two App. 1-22-234 App. 59 3,4-diClPh CO Single bond or CH _Two App.2 2-2835 App.59 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2836 Unit 59 3,4-diClPh CO Single bond or CH _Two App. 4 2-2837 App. 59 3,4-diClPh CO Single bond or CH _Two Unit 5 2-2838 Unit 59 3,4-diClPh CO Single bond or CH _Two App. 6 2-2839 App. 59 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2840 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2841 Unit 59 3,4-diClPh CO Single bond or CH _Two App. 9 2-2842 App. 59 3,4-diClPh CO Single bond or CH _Two Device 10 2-2843 device 59 3,4-diClPh CO single bond or CH _Two Unit 11 2-2844 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2845 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2846 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2847 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2848 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2849 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2850 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2851 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 19 2-2852 Unit 59 3,4-diClPh CO Single bond or CH _Two Device 20 2-2853 device 59 3,4-diClPh CO single bond or CH _Two Unit 21 2-2854 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2855 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2856 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2857 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 25 2-2858 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2859 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2860 Unit 59 3,4-diClPh CO Single bond or CH _Two App. 28 2-2861 App. 59 3,4-diClPh CO Single bond or CH _Two App. 29 2-2862 App. 59 3,4-diClPh CO Single bond or CH _Two Device 30 2-2863 device 59 3,4-diClPh CO single bond or CH _Two Unit 31 2-2864 unit 59 3,4-diClPh CO single bond or CH _Two Device 32 2-2865 device 59 3,4-diClPh CO single bond or CH _Two Set 65 2-2866 Set 59 3,4-diClPh CO Single bond or CH _Two Device 66 2-2867 device 59 3,4-diClPh CO single bond or CH _Two App. 67 2-2868 App. 59 3,4-diClPh CO Single bond or CH _Two Device 68 2-2869 device 59 3,4-diClPh CO single bond or CH _Two Device 69 2-2870 device 59 3,4-diClPh CO single bond or CH _Two Unit 70 2-2871 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2872 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 72 2-2873 Unit 59 3,4-diClPh CO Single bond or CH _Two 73-2 2874 559 3,4-diClPhCO Single bond or CH _Two Unit 74 2-2875 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2876 Unit 59 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2877 Unit 59 3,4-diClPh CO Single bond or CH _Two App.77 2-2878 App.59 3,4-diClPh CO Single bond or CH _Two Unit 78 2-2879 unit 59 3,4-diClPh CO single bond or CH _Two Device 79 2-2880 device 59 3,4-diClPh CO single bond or CH _Two Device 80 2-2881 device 82 3,4-diClPh CO single bond or CH _Two Unit 1 2-2882 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 2 2-2883 unit 82 3,4-diClPh CO single bond or CH _Two Unit 3 2-2884 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 4 2-2885 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 5 2-2886 Unit 82 3,4-diClPh CO Single bond or CH _Two Device 6 2-2887 device 82 3,4-diClPh CO single bond or CH _Two Unit 7 2-2888 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2889 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 9 2-2890 Unit 82 3,4-diClPh CO Single bond or CH _Two Device 10 2-2891 device 82 3,4-diClPh CO single bond or CH _Two Unit 11 2-2892 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2893 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2894 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2895 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2896 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2897 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2898 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2899 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 19 2-2900 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 20 2-2901 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 21 2-2902 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2903 unit 82 3,4-diClPh CO single bond or CH _Two Unit 23 2-2904 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2905 unit 82 3,4-diClPh CO single bond or CH _Two Unit 25 2-2906 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 26 2-2907 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 27 2-2908 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 28 2-2909 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 29 2-2910 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 30 2-2911 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 31 2-2912 unit 82 3,4-diClPh CO single bond or CH _Two Device 32 2-2913 device 82 3,4-diClPh CO single bond or CH _Two App. 65 2-2914 App. 82 3,4-diClPh CO Single bond or CH _Two Device 66 2-2915 device 82 3,4-diClPh CO single bond or CH _Two App. 67 2-2916 App. 82 3,4-diClPh CO Single bond or CH _Two Device 68 2-2917 device 82 3,4-diClPh CO single bond or CH _Two Device 69 2-2918 device 82 3,4-diClPh CO single bond or CH _Two App. 70 2-2919 App. 82 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2920 unit 82 3,4-diClPh CO single bond or CH _Two Unit 72 2-2921 Unit 82 3,4-diClPh CO Single bond or CH _Two 73 73 2922 82 3,4-diClPhCO single bond or CH _Two Unit 74 2-2923 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 75 2-2924 Unit 82 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2925 Unit 82 3,4-diClPh CO Single bond or CH _Two App.77 2-2926 App.82 3,4-diClPh CO Single bond or CH _Two Unit 78 2-927 unit 82 3,4-diClPh CO single bond or CH _Two App. 79 2-2928 App. 82 3,4-diClPh CO Single bond or CH _Two Device 80 2-2929 device 83 3,4-diClPh CO single bond or CH _Two Unit 1 2-2930 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 22-2931 unit 83 3,4-diClPh CO single bond or CH _Two Unit 3 2-2932 unit 83 3,4-diClPh CO single bond or CH _Two App. 4 2-2933 App. 83 3,4-diClPh CO Single bond or CH _Two App 5 2-2934 App.83 3,4-diClPh CO Single bond or CH _Two App. 6 2-2935 App. 83 3,4-diClPh CO Single bond or CH _Two Unit 7 2-2936 Unit 83 3,4-diClPh CO Single bond or CH _Two App. 8 2-2937 App. 83 3,4-diClPh CO Single bond or CH _Two App. 9 2-2938 App. 83 3,4-diClPh CO Single bond or CH _Two Unit 10 2-2939 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 11 2-2940 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2941 unit 83 3,4-diClPh CO single bond or CH _Two Unit 13 2-2942 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2943 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2944 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2945 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2946 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 18 2-2947 Unit 83 3,4-diClPh CO Single bond or CH _Two 19 22-2948 8 3 4 3,4-diClPh CO Single bond or CH _Two Device 20 2-2949 device 83 3,4-diClPh CO single bond or CH _Two Unit 21 2-2950 unit 83 3,4-diClPh CO single bond or CH _Two Unit 22 2-2951 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 23 2-2952 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 24 2-2953 unit 83 3,4-diClPh CO single bond or CH _Two Unit 25 2-2954 Unit 83 3,4-diClPh CO Single bond or CH _Two App. 26 2-2955 App. 83 3,4-diClPh CO Single bond or CH _Two App. 27 2-2956 App. 83 3,4-diClPh CO Single bond or CH _Two Unit 28 2-2957 unit 83 3,4-diClPh CO single bond or CH _Two App. 29 2-2958 App. 83 3,4-diClPh CO Single bond or CH _Two Device 30 2-2959 device 83 3,4-diClPh CO single bond or CH _Two Unit 31 2-2960 Unit 83 3,4-diClPh CO Single bond or CH _Two Device 32 2-2961 device 83 3,4-diClPh CO single bond or CH _Two App. 65 2-2962 App. 83 3,4-diClPh CO Single bond or CH _Two Device 66 2-2963 device 83 3,4-diClPh CO single bond or CH _Two App. 67 2-2964 App. 83 3,4-diClPh CO Single bond or CH _Two App. 68 2-2965 App. 83 3,4-diClPh CO Single bond or CH _Two App. 69 2-2966 App. 83 3,4-diClPh CO Single bond or CH _Two App. 70 2-2967 App. 83 3,4-diClPh CO Single bond or CH _Two Unit 71 2-2968 unit 83 3,4-diClPh CO single bond or CH _Two Unit 72 2-2969 unit 83 3,4-diClPh CO single bond or CH _Two 73 73 2970 73 83,4-diClPh CO Single bond or CH _Two Unit 74 2-2971 Unit 83 3,4-diClPh CO Single bond or CH _Two App. 75 2-2972 App. 83 3,4-diClPh CO Single bond or CH _Two Unit 76 2-2973 Unit 83 3,4-diClPh CO Single bond or CH _Two Unit 77 2-2974 unit 83 3,4-diClPh CO single bond or CH _Two Unit 78 2-2975 unit 83 3,4-diClPh CO single bond or CH _Two Device 79 2-2976 device 83 3,4-diClPh CO single bond or CH _Two Device 80 2-2977 device 61 3,4-diClPh CO single bond or CH _Two Unit 1 2-2978 Unit 61 3,4-diClPh CO Single bond or CH _Two App.2 2-2979 App.61 3,4-diClPh CO Single bond or CH _Two Unit 3 2-2980 Unit 61 3,4-diClPh CO Single bond or CH _Two Device 4 2-2981 device 61 3,4-diClPh CO single bond or CH _Two App. 5 2-2982 App. 61 3,4-diClPh CO Single bond or CH _Two Device 6 2-2983 device 61 3,4-diClPh CO single bond or CH _Two Unit 7 2-2984 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 8 2-2985 Unit 61 3,4-diClPh CO Single bond or CH _Two App. 9 2-2986 App. 61 3,4-diClPh CO Single bond or CH _Two Device 10 2-2987 device 61 3,4-diClPh CO single bond or CH _Two Unit 11 2-2988 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 12 2-2989 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 13 2-2990 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 14 2-2991 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 15 2-2992 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 16 2-2993 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 17 2-2994 Unit 61 3,4-diClPh CO Single bond or CH _Two App. 18 2-2995 App. 61 3,4-diClPh CO Single bond or CH _Two App 19 2-2996 App 61 3,4-diClPh CO Single bond or CH _Two Device 20 2-2997 device 61 3,4-diClPh CO single bond or CH _Two Unit 21 2-2998 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 22 2-2999 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 23 2-3000 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 24 2-3001 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 25 2-3002 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 26 2-3003 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 27 2-3004 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 28 2-305 Unit 61 3,4-diClPh CO Single bond or CH _Two App. 29 2-3006 App. 61 3,4-diClPh CO Single bond or CH _Two Device 30 2-307 device 61 3,4-diClPh CO single bond or CH _Two Unit 31 2-308 Unit 61 3,4-diClPh CO Single bond or CH _Two Device 32 2-309 device 61 3,4-diClPh CO single bond or CH _Two Device 65 2-3010 device 61 3,4-diClPh CO single bond or CH _Two Device 66 2-3011 device 61 3,4-diClPh CO single bond or CH _Two App. 67 2-3012 App. 61 3,4-diClPh CO Single bond or CH _Two Device 68 2-3013 device 61 3,4-diClPh CO single bond or CH _Two Device 69 2-3014 device 61 3,4-diClPh CO single bond or CH _Two Unit 70 2-301 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 71 2-3016 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 72 2-3017 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 73 2-3018 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 74 2-3019 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 75 2-3020 Unit 61 3,4-diClPh CO Single bond or CH _Two Unit 76 2-302 Unit 61 3,4-diClPh CO Single bond or CH _Two App. 77 2-3022 App. 61 3,4-diClPh CO Single bond or CH _Two Unit 78 2-3023 unit 61 3,4-diClPh CO single bond or CH _Two Device 79 2-3024 device 61 3,4-diClPh CO single bond or CH _Two Device 80 2-3025 Device 60 3,4-diClPh CO Single bond or CH _Two Device 1 2-3026 device 60 3,4-diClPh CO single bond or CH _Two Device 2 2-3027 device 60 3,4-diClPh CO single bond or CH _Two Device 3 2-3028 device 60 3,4-diClPh CO single bond or CH _Two Device 4 2-3029 device 60 3,4-diClPh CO single bond or CH _Two Device 5 2-3030 device 60 3,4-diClPh CO single bond or CH _Two App. 6 2-3030 App. 60 3,4-diClPh CO Single bond or CH _Two Unit 7 2-3032 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 8 2-3033 device 60 3,4-diClPh CO single bond or CH _Two Device 9 2-3034 Device 60 3,4-diClPh CO Single bond or CH _Two Device 10 2-3035 device 60 3,4-diClPh CO single bond or CH _Two Device 11 2-3036 device 60 3,4-diClPh CO single bond or CH _Two Unit 12 2-3037 Unit 60 3,4-diClPh CO Single bond or CH _Two Unit 13 2-3038 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 14 2-3039 device 60 3,4-diClPh CO single bond or CH _Two Unit 15 2-3040 Unit 60 3,4-diClPh CO Single bond or CH _Two Unit 16 2-3041 Unit 60 3,4-diClPh CO Single bond or CH _Two Unit 17 2-3042 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 18 2-304 device 60 3,4-diClPh CO single bond or CH _Two 19 2 3044 20 60 3,4-diClPh CO Single bond or CH _Two Device 20 2-3045 device 60 3,4-diClPh CO single bond or CH _Two Unit 21 2-3046 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 22 2-3047 device 60 3,4-diClPh CO single bond or CH _Two Device 23 2-3048 device 60 3,4-diClPh CO single bond or CH _Two Device 24 2-3049 device 60 3,4-diClPh CO single bond or CH _Two Unit 25 2-3050 Unit 60 3,4-diClPh CO Single bond or CH _Two Unit 26 2-3051 Unit 60 3,4-diClPh CO Single bond or CH _Two Unit 27 2-3052 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 28 2-305 device 60 3,4-diClPh CO single bond or CH _Two Unit 29 2-3054 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 30 2-3055 device 60 3,4-diClPh CO single bond or CH _Two Device 31 2-3056 device 60 3,4-diClPh CO single bond or CH _Two Device 32 2-3057 device 60 3,4-diClPh CO single bond or CH _Two Set 65 2-3058 Set 60 3,4-diClPh CO Single bond or CH _Two Device 66 2-3059 device 60 3,4-diClPh CO single bond or CH _Two App. 67 2-3060 App. 60 3,4-diClPh CO Single bond or CH _Two App. 68 2-306 App. 60 3,4-diClPh CO Single bond or CH _Two App. 69 2-306 App. 60 3,4-diClPh CO Single bond or CH _Two Unit 70 2-306 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 71 2-3064 device 60 3,4-diClPh CO single bond or CH _Two Unit 72 2-3065 Unit 60 3,4-diClPh CO Single bond or CH _Two 73-2 3066 Fig. 60 3,4-diClPh CO Single bond or CH _Two Unit 74 2-306 Unit 60 3,4-diClPh CO Single bond or CH _Two Unit 75 2-3068 Unit 60 3,4-diClPh CO Single bond or CH _Two Unit 76 2-3069 Unit 60 3,4-diClPh CO Single bond or CH _Two App. 77 2-3070 App. 60 3,4-diClPh CO Single bond or CH _Two Unit 78 2-3071 Unit 60 3,4-diClPh CO Single bond or CH _Two Device 79 2-3072 device 60 3,4-diClPh CO single bond or CH _Two No. 80 化合物 Compound number R ¹ R ^Two A B Z ──────────────────────────────────── 2-3073 Place 33 3,4-diClPh SO _Two Single bond device 1 2-3074 device 33 3,4-diClPh SO _Two Single bond device 2 2-3075 device 33 3,4-diClPh SO _Two Single bond device 3 2-3076 device 33 3,4-diClPh SO _Two Single bond unit 4 2-3077 unit 33 3,4-diClPh SO _Two Single bond device 5 2-3078 device 33 3,4-diClPh SO _Two Single bond device 6 2-3079 device 33 3,4-diClPh SO _Two Single bond device 7 2-3080 device 33 3,4-diClPh SO _Two Single bond unit 8 2-3081 unit 33 3,4-diClPh SO _Two Single bond device 9 2-3082 device 33 3,4-diClPh SO _Two Single bond unit 10 2-3083 unit 33 3,4-diClPh SO _Two Single bond unit 11 2-3084 unit 33 3,4-diClPh SO _Two Single bond unit 12 2-3085 unit 33 3,4-diClPh SO _Two Single bond unit 13 2-3086 unit 33 3,4-diClPh SO _Two Single bond unit 14 2-3087 unit 33 3,4-diClPh SO _Two Single bond unit 15 2-3088 unit 33 3,4-diClPh SO _Two Single bond unit 16 2-3089 unit 33 3,4-diClPh SO _Two Single bond unit 17 2-3090 unit 33 3,4-diClPh SO _Two Single bond unit 18 2-3091 unit 33 3,4-diClPh SO _Two Single bond unit 19 2-3092 unit 33 3,4-diClPh SO _Two Single bond unit 20 2-3093 unit 33 3,4-diClPh SO _Two Single bond unit 21 2-3094 unit 33 3,4-diClPh SO _Two Single bond unit 22 2-3095 unit 33 3,4-diClPh SO _Two Single bond unit 23 2-3096 unit 33 3,4-diClPh SO _Two Single bond unit 24 2-3097 unit 33 3,4-diClPh SO _Two Single bond unit 25 2-3098 unit 33 3,4-diClPh SO _Two Single bond unit 26 2-3099 unit 33 3,4-diClPh SO _Two Single bond unit 27 2-3100 unit 33 3,4-diClPh SO _Two Single bond unit 28 2-3101 unit 33 3,4-diClPh SO _Two Single bond unit 29 2-3102 unit 33 3,4-diClPh SO _Two Single bond device 30 2-3103 device 33 3,4-diClPh SO _Two Single bond unit 31 2-3104 unit 33 3,4-diClPh SO _Two Single bond unit 32 2-3105 unit 33 3,4-diClPh SO _Two Single bond unit 65 2-3106 unit 33 3,4-diClPh SO _Two Single bond unit 66 2-3107 unit 33 3,4-diClPh SO _Two Single bond device 67 2-3108 device 33 3,4-diClPh SO _Two Single bond unit 68 2-3109 unit 33 3,4-diClPh SO _Two Single bond unit 69 2-3110 unit 33 3,4-diClPh SO _Two Single bond device 70 2-3111 device 33 3,4-diClPh SO _Two Single bond unit 71 2-3112 unit 33 3,4-diClPh SO _Two Single bond unit 72 2-3113 unit 33 3,4-diClPh SO _Two Single bond device 73 2-3114 device 33 3,4-diClPh SO _Two Single bond unit 74 2-3115 unit 33 3,4-diClPh SO _Two Single bond unit 75 2-3116 unit 33 3,4-diClPh SO _Two Single bond unit 76 2-3117 unit 33 3,4-diClPh SO _Two Single bond unit 77 2-3118 unit 33 3,4-diClPh SO _Two Single bond unit 78 2-3119 unit 33 3,4-diClPh SO _Two Single bond device 79 2-3120 device 33 3,4-diClPh SO _Two Single bond device 80 2-3121 device 34 3,4-diClPh SO _Two Single bond device 1 2-312 device 34 3,4-diClPh SO _Two Single bond device 2 2-3123 device 34 3,4-diClPh SO _Two Single bond device 3 2-3124 device 34 3,4-diClPh SO _Two Single bond unit 4 2-3125 unit 34 3,4-diClPh SO _Two Single bond device 5 2-3126 device 34 3,4-diClPh SO _Two Single bond device 6 2-3127 device 34 3,4-diClPh SO _Two Single bond device 7 2-3128 device 34 3,4-diClPh SO _Two Single bond device 8 2-3129 device 34 3,4-diClPh SO _Two Single bond device 9 2-3130 device 34 3,4-diClPh SO _Two Single bond unit 10 2-3131 unit 34 3,4-diClPh SO _Two Single bond unit 11 2-3132 unit 34 3,4-diClPh SO _Two Single bond unit 12 2-3133 unit 34 3,4-diClPh SO _Two Single bond unit 13 2-3134 unit 34 3,4-diClPh SO _Two Single bond Unit 14 2-3135 Unit 34 3,4-diClPh SO _Two Single bond unit 15 2-3136 unit 34 3,4-diClPh SO _Two Single bond unit 16 2-3137 unit 34 3,4-diClPh SO _Two Single bond unit 17 2-3138 unit 34 3,4-diClPh SO _Two Single bond unit 18 2-3139 unit 34 3,4-diClPh SO _Two Single bond unit 19 2-3140 unit 34 3,4-diClPh SO _Two Single bond device 20 2-3314 device 34 3,4-diClPh SO _Two Single bond unit 21 2-3142 unit 34 3,4-diClPh SO _Two Single bond unit 22 2-3143 unit 34 3,4-diClPh SO _Two Single bond unit 23 2-3144 unit 34 3,4-diClPh SO _Two Single bond unit 24 2-3145 unit 34 3,4-diClPh SO _Two Single bond unit 25 2-3146 unit 34 3,4-diClPh SO _Two Single bond unit 26 2-3147 unit 34 3,4-diClPh SO _Two Single bond unit 27 2-3148 unit 34 3,4-diClPh SO _Two Single bond unit 28 2-3149 unit 34 3,4-diClPh SO _Two Single bond unit 29 2-3150 unit 34 3,4-diClPh SO _Two Single bond device 30 2-3151 device 34 3,4-diClPh SO _Two Single bond unit 31 2-3152 unit 34 3,4-diClPh SO _Two Single bond unit 32 2-3153 unit 34 3,4-diClPh SO _Two Single bond device 65 2-3154 device 34 3,4-diClPh SO _Two Single bond unit 66 2-3155 unit 34 3,4-diClPh SO _Two Single bond unit 67 2-3156 unit 34 3,4-diClPh SO _Two Single bond device 68 2-3157 device 34 3,4-diClPh SO _Two Single bond unit 69 2-3158 unit 34 3,4-diClPh SO _Two Single bond unit 70 2-3159 unit 34 3,4-diClPh SO _Two Single bond unit 71 2-3160 unit 34 3,4-diClPh SO _Two Single bond unit 72 2-3161 unit 34 3,4-diClPh SO _Two Single bond unit 73 2-3162 unit 34 3,4-diClPh SO _Two Single bond unit 74 2-3163 unit 34 3,4-diClPh SO _Two Single bond unit 75 2-3164 unit 34 3,4-diClPh SO _Two Single bond unit 76 2-3165 unit 34 3,4-diClPh SO _Two Single bond unit 77 2-3166 unit 34 3,4-diClPh SO _Two Single bond unit 78 2-3167 unit 34 3,4-diClPh SO _Two Single bond device 79 2-3168 device 34 3,4-diClPh SO _Two Single bond device 80 2-3169 device 35 3,4-diClPh SO _Two Single bond device 1 2-3170 device 35 3,4-diClPh SO _Two Single bond unit 2 2-3171 unit 35 3,4-diClPh SO _Two Single bond unit 32-2-3172 unit 35 3,4-diClPh SO _Two Single bond unit 4 2-3173 unit 35 3,4-diClPh SO _Two Single bond 5 2 3174 35 3,4-diClPh SO _Two Single bond device 6 2-3175 device 35 3,4-diClPh SO _Two Single bond unit 7 2-3176 unit 35 3,4-diClPh SO _Two Single bond device 8 2-3177 device 35 3,4-diClPh SO _Two Single bond device 9 2-3178 device 35 3,4-diClPh SO _Two Single bond unit 10 2-3179 unit 35 3,4-diClPh SO _Two Single bond unit 11 2-3180 unit 35 3,4-diClPh SO _Two Single bond unit 12 2-3218 unit 35 3,4-diClPh SO _Two Single bond unit 13 2-3182 unit 35 3,4-diClPh SO _Two Single bond Unit 14 2-3183 Unit 35 3,4-diClPh SO _Two Single bond Unit 15 2-3184 Unit 35 3,4-diClPh SO _Two Single bond Unit 16 2-3185 Unit 35 3,4-diClPh SO _Two Single bond unit 17 2-3186 unit 35 3,4-diClPh SO _Two Single bond unit 18 2-3187 unit 35 3,4-diClPh SO _Two Single bond unit 19 2-3188 unit 35 3,4-diClPh SO _Two Single bond unit 20 2-3189 unit 35 3,4-diClPh SO _Two Single bond unit 21 2-3190 unit 35 3,4-diClPh SO _Two Single bond Unit 22 2-3191 Unit 35 3,4-diClPh SO _Two Single bond unit 23 2-3192 unit 35 3,4-diClPh SO _Two Single bond unit 24 2-3193 unit 35 3,4-diClPh SO _Two Single bond unit 25 2-3194 unit 35 3,4-diClPh SO _Two Single bond unit 26 2-3195 unit 35 3,4-diClPh SO _Two Single bond unit 27 2-3196 unit 35 3,4-diClPh SO _Two Single bond unit 28 2-3197 unit 35 3,4-diClPh SO _Two Single bond unit 29 2-3198 unit 35 3,4-diClPh SO _Two Single bond unit 30 2-3199 unit 35 3,4-diClPh SO _Two Single bond unit 31 2-3200 unit 35 3,4-diClPh SO _Two Single bond unit 32 2-3201 unit 35 3,4-diClPh SO _Two Single bond device 65 2-3202 device 35 3,4-diClPh SO _Two Single bond unit 66 2-3203 unit 35 3,4-diClPh SO _Two Single bond unit 67 2-3204 unit 35 3,4-diClPh SO _Two Single bond unit 68 2-3205 unit 35 3,4-diClPh SO _Two Single bond unit 69 2-3206 unit 35 3,4-diClPh SO _Two Single bond unit 70 2-3207 unit 35 3,4-diClPh SO _Two Single bond unit 71 2-3208 unit 35 3,4-diClPh SO _Two Single bond unit 72 2-3209 unit 35 3,4-diClPh SO _Two Single bond unit 73 2-3210 unit 35 3,4-diClPh SO _Two Single bond unit 74 2-3211 unit 35 3,4-diClPh SO _Two Single bond unit 75 2-312 unit 35 3,4-diClPh SO _Two Single bond unit 76 2-3213 unit 35 3,4-diClPh SO _Two Single bond unit 77 2-3214 unit 35 3,4-diClPh SO _Two Single bond unit 78 2-3215 unit 35 3,4-diClPh SO _Two Single bond device 79 2-3216 device 35 3,4-diClPh SO _Two Single bond device 80 2-3217 device 36 3,4-diClPh SO _Two Single bond device 1 2-3218 device 36 3,4-diClPh SO _Two Single bond device 2 2-3219 device 36 3,4-diClPh SO _Two Single bond unit 3 2-3220 unit 36 3,4-diClPh SO _Two Single bond unit 4 2-3322 unit 36 3,4-diClPh SO _Two Single bond device 5 2-3322 device 36 3,4-diClPh SO _Two Single bond device 6 2-3223 device 36 3,4-diClPh SO _Two Single bond device 7 2-32224 device 36 3,4-diClPh SO _Two Single bond device 8 2-3225 device 36 3,4-diClPh SO _Two Single bond unit 9 2-3226 unit 36 3,4-diClPh SO _Two Single bond device 10 2-3227 device 36 3,4-diClPh SO _Two Single bond unit 11 2-3228 unit 36 3,4-diClPh SO _Two Single bond unit 12 2-3229 unit 36 3,4-diClPh SO _Two Single bond unit 13 2-332 unit 36 3,4-diClPh SO _Two Single bond unit 14 2-3231 unit 36 3,4-diClPh SO _Two Single bond unit 15 2-3232 unit 36 3,4-diClPh SO _Two Single bond unit 16 2-3233 unit 36 3,4-diClPh SO _Two Single bond unit 17 2-3234 unit 36 3,4-diClPh SO _Two Single bond unit 18 2-3235 unit 36 3,4-diClPh SO _Two Single bond unit 19 2-3236 unit 36 3,4-diClPh SO _Two Single bond device 20 2-3237 device 36 3,4-diClPh SO _Two Single bond unit 21 2-3238 unit 36 3,4-diClPh SO _Two Single bond device 22 2-3239 device 36 3,4-diClPh SO _Two Single bond unit 23 2-3240 unit 36 3,4-diClPh SO _Two Single bond unit 24 2-3241 unit 36 3,4-diClPh SO _Two Single bond unit 25 2-3242 unit 36 3,4-diClPh SO _Two Single bond unit 26 2-3243 unit 36 3,4-diClPh SO _Two Single bond unit 27 2-3244 unit 36 3,4-diClPh SO _Two Single bond unit 28 2-3245 unit 36 3,4-diClPh SO _Two Single bond unit 29 2-3246 unit 36 3,4-diClPh SO _Two Single bond device 30 2-3247 device 36 3,4-diClPh SO _Two Single bond unit 31 2-3248 unit 36 3,4-diClPh SO _Two Single bond unit 32 2-3249 unit 36 3,4-diClPh SO _Two Single bond unit 65 2-3250 unit 36 3,4-diClPh SO _Two Single bond unit 66 2-3251 unit 36 3,4-diClPh SO _Two Single bond unit 67 2-3252 unit 36 3,4-diClPh SO _Two Single bond device 68 2-3253 device 36 3,4-diClPh SO _Two Single bond device 69 2-3254 device 36 3,4-diClPh SO _Two Single bond unit 70 2-3255 unit 36 3,4-diClPh SO _Two Single bond device 71 2-3256 device 36 3,4-diClPh SO _Two Single bond unit 72 2-3257 unit 36 3,4-diClPh SO _Two Single bond unit 73 2-3258 unit 36 3,4-diClPh SO _Two Single bond unit 74 2-32259 unit 36 3,4-diClPh SO _Two Single bond device 75 2-3260 device 36 3,4-diClPh SO _Two Single bond unit 76 2-3261 unit 36 3,4-diClPh SO _Two Single bond unit 77 2-3262 unit 36 3,4-diClPh SO _Two Single bond unit 78 2-3263 unit 36 3,4-diClPh SO _Two Single bond device 79 2-3264 device 36 3,4-diClPh SO _Two Single bond device 80 2-3265 device 37 3,4-diClPh SO _Two Single bond device 1 2-3266 device 37 3,4-diClPh SO _Two Single bond device 2 2-3267 device 37 3,4-diClPh SO _Two Single bond place 3 2-3268 place 37 3,4-diClPh SO _Two Single bond unit 4 2-3269 unit 37 3,4-diClPh SO _Two Single bond device 5 2-3270 device 37 3,4-diClPh SO _Two Single bond 6 2-3271 37 3,4-diClPh SO _Two Single bond device 7 2-3272 device 37 3,4-diClPh SO _Two Single bond unit 8 2-3273 unit 37 3,4-diClPh SO _Two Single bond position 9 2-3274 position 37 3,4-diClPh SO _Two Single bond device 10 2-3275 device 37 3,4-diClPh SO _Two Single bond unit 11 2-3276 unit 37 3,4-diClPh SO _Two Single bond unit 12 2-3277 unit 37 3,4-diClPh SO _Two Single bond unit 13 2-3278 unit 37 3,4-diClPh SO _Two Single bond unit 14 2-3279 unit 37 3,4-diClPh SO _Two Single bond unit 15 2-3280 unit 37 3,4-diClPh SO _Two Single bond unit 16 2-3281 unit 37 3,4-diClPh SO _Two Single bond unit 17 2-3282 unit 37 3,4-diClPh SO _Two Single bond unit 18 2-3283 unit 37 3,4-diClPh SO _Two Single bond unit 19 2-3284 unit 37 3,4-diClPh SO _Two Single bond unit 20 2-3285 unit 37 3,4-diClPh SO _Two Single bond unit 21 2-3286 unit 37 3,4-diClPh SO _Two Single bond unit 22 2-3287 unit 37 3,4-diClPh SO _Two Single bond 23 23288 337 3,4-diClPh SO _Two Single bond unit 24 2-3289 unit 37 3,4-diClPh SO _Two Single bond unit 25 2-3290 unit 37 3,4-diClPh SO _Two Single bond unit 26 2-3291 unit 37 3,4-diClPh SO _Two Single bond unit 27 2-3292 unit 37 3,4-diClPh SO _Two Single bond unit 28 2-3293 unit 37 3,4-diClPh SO _Two Single bond unit 29 2-3294 unit 37 3,4-diClPh SO _Two Single bond device 30 2-3295 device 37 3,4-diClPh SO _Two Single bond device 31 2-3296 device 37 3,4-diClPh SO _Two Single bond unit 32 2-3297 unit 37 3,4-diClPh SO _Two Single bond device 65 2-3298 device 37 3,4-diClPh SO _Two Single bond unit 66 2-3299 unit 37 3,4-diClPh SO _Two Single bond unit 67 2-3300 unit 37 3,4-diClPh SO _Two Single bond device 68 2-3301 device 37 3,4-diClPh SO _Two Single bond device 69 2-3302 device 37 3,4-diClPh SO _Two Single bond unit 70 2-3303 unit 37 3,4-diClPh SO _Two Single bond unit 71 2-3304 unit 37 3,4-diClPh SO _Two Single bond unit 72 2-3305 unit 37 3,4-diClPh SO _Two Single bond unit 73 2-3306 unit 37 3,4-diClPh SO _Two Single bond unit 74 2-3307 unit 37 3,4-diClPh SO _Two Single bond device 75 2-3308 device 37 3,4-diClPh SO _Two Single bond unit 76 2-3309 unit 37 3,4-diClPh SO _Two Single bond unit 77 2-330 unit 37 3,4-diClPh SO _Two Single bond unit 78 2-3311 unit 37 3,4-diClPh SO _Two Single bond device 79 2-3312 device 37 3,4-diClPh SO _Two Single bond device 80 2-3313 device 38 3,4-diClPh SO _Two Single bond device 1 2-3314 device 38 3,4-diClPh SO _Two Single bond device 2 2-3315 device 38 3,4-diClPh SO _Two Single bond unit 3 2-3316 unit 38 3,4-diClPh SO _Two Single bond unit 4 2-33 setting 38 3,4-diClPh SO _Two Single bond unit 5 2-3318 unit 38 3,4-diClPh SO _Two Single bond unit 6 2-3319 unit 38 3,4-diClPh SO _Two Single bond device 7 2-3320 device 38 3,4-diClPh SO _Two Single bond unit 8 2-3332 unit 38 3,4-diClPh SO _Two Single bond device 9 2-3322 device 38 3,4-diClPh SO _Two Single bond device 10 2-3323 device 38 3,4-diClPh SO _Two Single bond unit 11 2-3324 unit 38 3,4-diClPh SO _Two Single bond unit 12 2-3325 unit 38 3,4-diClPh SO _Two Single bond unit 13 2-33326 unit 38 3,4-diClPh SO _Two Single bond unit 14 2-3327 unit 38 3,4-diClPh SO _Two Single bond unit 15 2-3328 unit 38 3,4-diClPh SO _Two Single bond unit 16 2-3329 unit 38 3,4-diClPh SO _Two Single bond unit 17 2-333 unit 38 3,4-diClPh SO _Two Single bond unit 18 2-333 unit 38 3,4-diClPh SO _Two Single bond unit 19 2-3332 unit 38 3,4-diClPh SO _Two Single bond unit 20 2-3333 unit 38 3,4-diClPh SO _Two Single bond unit 21 2-3334 unit 38 3,4-diClPh SO _Two Single bond unit 22 2-3335 unit 38 3,4-diClPh SO _Two Single bond unit 23 2-3336 unit 38 3,4-diClPh SO _Two Single bond unit 24 2-33337 unit 38 3,4-diClPh SO _Two Single bond unit 25 2-3338 unit 38 3,4-diClPh SO _Two Single bond unit 26 2-3339 unit 38 3,4-diClPh SO _Two Single bond unit 27 2-3340 unit 38 3,4-diClPh SO _Two Single bond unit 28 2-3341 unit 38 3,4-diClPh SO _Two Single bond unit 29 2-3342 unit 38 3,4-diClPh SO _Two Single bond unit 30 2-3334 unit 38 3,4-diClPh SO _Two Single bond unit 31 2-3334 unit 38 3,4-diClPh SO _Two Single bond unit 32 2-3345 unit 38 3,4-diClPh SO _Two Single bond device 65 2-3346 device 38 3,4-diClPh SO _Two Single bond unit 66 2-33347 unit 38 3,4-diClPh SO _Two Single bond unit 67 2-3348 unit 38 3,4-diClPh SO _Two Single bond device 68 2-3349 device 38 3,4-diClPh SO _Two Single bond unit 69 2-3350 unit 38 3,4-diClPh SO _Two Single bond unit 70 2-3351 unit 38 3,4-diClPh SO _Two Single bond unit 71 2-3352 unit 38 3,4-diClPh SO _Two Single bond unit 72 2-3335 unit 38 3,4-diClPh SO _Two Single bond device 73 2-3354 device 38 3,4-diClPh SO _Two Single bond unit 74 2-3335 unit 38 3,4-diClPh SO _Two Single bond unit 75 2-3356 unit 38 3,4-diClPh SO _Two Single bond Unit 76 2-3335 Unit 38 3,4-diClPh SO _Two Single bond unit 77 2-3358 unit 38 3,4-diClPh SO _Two Single bond unit 78 2-3359 unit 38 3,4-diClPh SO _Two Single bond device 79 2-3360 device 38 3,4-diClPh SO _Two Single bond device 80 2-3361 device 39 3,4-diClPh SO _Two Single bond unit 1 2-3336 unit 39 3,4-diClPh SO _Two Single bond unit 2 2-3336 unit 39 3,4-diClPh SO _Two Single bond unit 32-3-364 unit 39 3,4-diClPh SO _Two Single bond 4 4 3365 5 39 3,4-diClPh SO _Two Single bond 5 2 3366 Position 39 3,4-diClPh SO _Two Single bond 6 6-3367 3 39 3,4-diClPh SO _Two Single bond 7 7 3368 7 39,4-diClPh SO _Two Single bond device 8 2-3369 device 39 3,4-diClPh SO _Two Single bond device 9 2-3370 device 39 3,4-diClPh SO _Two Single bond unit 10 2-3337 unit 39 3,4-diClPh SO _Two Single bond unit 11 2-3337 unit 39 3,4-diClPh SO _Two Single bond unit 12 2-3373 unit 39 3,4-diClPh SO _Two Single bond unit 13 2-3374 unit 39 3,4-diClPh SO _Two Single bond unit 14 2-3375 unit 39 3,4-diClPh SO _Two Single bond unit 15 2-3376 unit 39 3,4-diClPh SO _Two Single bond unit 16 2-33377 unit 39 3,4-diClPh SO _Two Single bond unit 17 2-33378 unit 39 3,4-diClPh SO _Two Single bond unit 18 2-3379 unit 39 3,4-diClPh SO _Two Single bond unit 19 2-3380 unit 39 3,4-diClPh SO _Two Single bond unit 20 2-338 unit 39 3,4-diClPh SO _Two Single bond unit 21 2-3382 unit 39 3,4-diClPh SO _Two Single bond unit 22 2-3383 unit 39 3,4-diClPh SO _Two Single bond unit 23 2-3384 unit 39 3,4-diClPh SO _Two Single bond Unit 24 2-3385 Unit 39 3,4-diClPh SO _Two Single bond Unit 25 2-3386 Unit 39 3,4-diClPh SO _Two Single bond unit 26 2-3338 unit 39 3,4-diClPh SO _Two Single bond unit 27 2-3388 unit 39 3,4-diClPh SO _Two Single bond unit 28 2-3389 unit 39 3,4-diClPh SO _Two Single bond unit 29 2-3390 unit 39 3,4-diClPh SO _Two Single bond device 30 2-3391 device 39 3,4-diClPh SO _Two Single bond unit 31 2-3392 unit 39 3,4-diClPh SO _Two Single bond unit 32 2-3393 unit 39 3,4-diClPh SO _Two Single bond unit 65 2-3394 unit 39 3,4-diClPh SO _Two Single bond unit 66 2-3395 unit 39 3,4-diClPh SO _Two Single bond unit 67 2-3396 unit 39 3,4-diClPh SO _Two Single bond device 68 2-3397 device 39 3,4-diClPh SO _Two Single bond unit 69 2-3398 unit 39 3,4-diClPh SO _Two Single bond unit 70 2-3399 unit 39 3,4-diClPh SO _Two Single bond unit 71 2-3400 unit 39 3,4-diClPh SO _Two Single bond unit 72 2-3401 unit 39 3,4-diClPh SO _Two Single bond unit 73 2-3402 unit 39 3,4-diClPh SO _Two Single bond unit 74 2-3403 unit 39 3,4-diClPh SO _Two Single bond Unit 75 2-3404 Unit 39 3,4-diClPh SO _Two Single bond unit 76 2-3405 unit 39 3,4-diClPh SO _Two Single bond unit 77 2-3406 unit 39 3,4-diClPh SO _Two Single bond unit 78 2-3407 unit 39 3,4-diClPh SO _Two Single bond unit 79 2-3408 unit 39 3,4-diClPh SO _Two Single bond device 80 2-3409 device 40 3,4-diClPh SO _Two Single bond device 1 2-33410 device 40 3,4-diClPh SO _Two Single bond device 2 2-3341 device 40 3,4-diClPh SO _Two Single bond device 3 2-3341 device 40 3,4-diClPh SO _Two Single bond device 4 2-3341 device 40 3,4-diClPh SO _Two Single bond device 5 2-3414 device 40 3,4-diClPh SO _Two Single bond device 6 2-3415 device 40 3,4-diClPh SO _Two Single bond device 7 2-3416 device 40 3,4-diClPh SO _Two Single bond device 8 2-3417 device 40 3,4-diClPh SO _Two Single bond device 9 2-3418 device 40 3,4-diClPh SO _Two Single bond device 10 2-3419 device 40 3,4-diClPh SO _Two Single bond unit 11 2-3420 unit 40 3,4-diClPh SO _Two Single bond unit 12 2-3421 unit 40 3,4-diClPh SO _Two Single bond unit 13 2-3422 unit 40 3,4-diClPh SO _Two Single bond unit 14 2-3423 unit 40 3,4-diClPh SO _Two Single bond device 15 2-3424 device 40 3,4-diClPh SO _Two Single bond Unit 16 2-3425 Unit 40 3,4-diClPh SO _Two Single bond unit 17 2-3426 unit 40 3,4-diClPh SO _Two Single bond device 18 2-3427 device 40 3,4-diClPh SO _Two Single bond device 19 2-3428 device 40 3,4-diClPh SO _Two Single bond device 20 2-3429 device 40 3,4-diClPh SO _Two Single bond unit 21 2-3430 unit 40 3,4-diClPh SO _Two Single bond unit 22 2-3343 unit 40 3,4-diClPh SO _Two Single bond device 23 2-3432 device 40 3,4-diClPh SO _Two Single bond device 24 2-3433 device 40 3,4-diClPh SO _Two Single bond unit 25 2-3434 unit 40 3,4-diClPh SO _Two Single bond unit 26 2-3435 unit 40 3,4-diClPh SO _Two Single bond unit 27 2-3436 unit 40 3,4-diClPh SO _Two Single bond unit 28 2-3437 unit 40 3,4-diClPh SO _Two Single bond unit 29 2-3438 unit 40 3,4-diClPh SO _Two Single bond device 30 2-3339 device 40 3,4-diClPh SO _Two Single bond unit 31 2-3440 unit 40 3,4-diClPh SO _Two Single bond unit 32 2-3441 unit 40 3,4-diClPh SO _Two Single bond unit 65 2-3442 unit 40 3,4-diClPh SO _Two Single bond device 66 2-3443 device 40 3,4-diClPh SO _Two Single bond device 67 2-3344 device 40 3,4-diClPh SO _Two Single bond device 68 2-3445 device 40 3,4-diClPh SO _Two Single bond device 69 2-3446 device 40 3,4-diClPh SO _Two Single bond device 70 2-3447 device 40 3,4-diClPh SO _Two Single bond unit 71 2-3448 unit 40 3,4-diClPh SO _Two Single bond unit 72 2-3449 unit 40 3,4-diClPh SO _Two Single bond unit 73 2-3450 unit 40 3,4-diClPh SO _Two Single bond unit 74 2-3451 unit 40 3,4-diClPh SO _Two Single bond unit 75 2-3452 unit 40 3,4-diClPh SO _Two Single bond unit 76 2-3453 unit 40 3,4-diClPh SO _Two Single bond unit 77 2-3454 unit 40 3,4-diClPh SO _Two Single bond unit 78 2-3455 unit 40 3,4-diClPh SO _Two Single bond device 79 2-3456 device 40 3,4-diClPh SO _Two Single bond unit 80 2-3457 unit 41 3,4-diClPh SO _Two Single bond device 1 2-3458 device 41 3,4-diClPh SO _Two Single bond device 2 2-3459 device 41 3,4-diClPh SO _Two Single bond device 3 2-3460 device 41 3,4-diClPh SO _Two Single bond unit 4 2-3346 unit 41 3,4-diClPh SO _Two Single bond device 5 2-3346 device 41 3,4-diClPh SO _Two Single bond device 6 2-3346 device 41 3,4-diClPh SO _Two Single bond device 7 2-3346 device 41 3,4-diClPh SO _Two Single bond device 8 2-3465 device 41 3,4-diClPh SO _Two Single bond device 9 2-3466 device 41 3,4-diClPh SO _Two Single bond device 10 2-3467 device 41 3,4-diClPh SO _Two Single bond unit 11 2-3468 unit 41 3,4-diClPh SO _Two Single bond unit 12 2-3469 unit 41 3,4-diClPh SO _Two Single bond unit 13 2-3470 unit 41 3,4-diClPh SO _Two Single bond unit 14 2-3347 unit 41 3,4-diClPh SO _Two Single bond unit 15 2-3347 unit 41 3,4-diClPh SO _Two Single bond unit 16 2-3347 unit 41 3,4-diClPh SO _Two Single bond Unit 17 2-3347 Unit 41 3,4-diClPh SO _Two Single bond unit 18 2-3475 unit 41 3,4-diClPh SO _Two Single bond unit 19 2-3476 unit 41 3,4-diClPh SO _Two Single bond unit 20 2-3347 unit 41 3,4-diClPh SO _Two Single bond unit 21 2-3478 unit 41 3,4-diClPh SO _Two Single bond Unit 22 2-3479 Unit 41 3,4-diClPh SO _Two Single bond unit 23 2-3480 unit 41 3,4-diClPh SO _Two Single bond unit 24 2-3481 unit 41 3,4-diClPh SO _Two Single bond unit 25 2-3482 unit 41 3,4-diClPh SO _Two Single bond unit 26 2-3348 unit 41 3,4-diClPh SO _Two Single bond unit 27 2-3484 unit 41 3,4-diClPh SO _Two Single bond unit 28 2-3485 unit 41 3,4-diClPh SO _Two Single bond unit 29 2-3486 unit 41 3,4-diClPh SO _Two Single bond device 30 2-3487 device 41 3,4-diClPh SO _Two Single bond unit 31 2-3488 unit 41 3,4-diClPh SO _Two Single bond device 32 2-3489 device 41 3,4-diClPh SO _Two Single bond unit 65 2-3490 unit 41 3,4-diClPh SO _Two Single bond unit 66 2-3491 unit 41 3,4-diClPh SO _Two Single bond unit 67 2-3492 unit 41 3,4-diClPh SO _Two Single bond unit 68 2-3493 unit 41 3,4-diClPh SO _Two Single bond unit 69 2-3494 unit 41 3,4-diClPh SO _Two Single bond unit 70 2-3495 unit 41 3,4-diClPh SO _Two Single bond unit 71 2-3496 unit 41 3,4-diClPh SO _Two Single bond unit 72 2-3497 unit 41 3,4-diClPh SO _Two Single bond device 73 2-3498 device 41 3,4-diClPh SO _Two Single bond unit 74 2-3499 unit 41 3,4-diClPh SO _Two Single bond unit 75 2-3500 unit 41 3,4-diClPh SO _Two Single bond unit 76 2-301 unit 41 3,4-diClPh SO _Two Single bond unit 77 2-3502 unit 41 3,4-diClPh SO _Two Single bond unit 78 2-3503 unit 41 3,4-diClPh SO _Two Single bond device 79 2-3504 device 41 3,4-diClPh SO _Two Single bond device 80 2-3505 device 42 3,4-diClPh SO _Two Single bond device 1 2-3506 device 42 3,4-diClPh SO _Two Single bond unit 2 2-3507 unit 42 3,4-diClPh SO _Two Single bond device 3 2-3508 device 42 3,4-diClPh SO _Two Single bond unit 4 2-3509 unit 42 3,4-diClPh SO _Two Single bond device 5 2-3510 device 42 3,4-diClPh SO _Two Single bond device 6 2-35111 device 42 3,4-diClPh SO _Two Single bond device 7 2-351 device 42 3,4-diClPh SO _Two Single bond device 8 2-3513 device 42 3,4-diClPh SO _Two Single bond device 9 2-3514 device 42 3,4-diClPh SO _Two Single bond unit 10 2-3515 unit 42 3,4-diClPh SO _Two Single bond device 11 2-3516 device 42 3,4-diClPh SO _Two Single bond unit 12 2-3517 unit 42 3,4-diClPh SO _Two Single bond unit 13 2-3518 unit 42 3,4-diClPh SO _Two Single bond unit 14 2-3519 unit 42 3,4-diClPh SO _Two Single bond unit 15 2-3520 unit 42 3,4-diClPh SO _Two Single bond unit 16 2-3352 unit 42 3,4-diClPh SO _Two Single bond unit 17 2-3352 unit 42 3,4-diClPh SO _Two Single bond unit 18 2-33523 unit 42 3,4-diClPh SO _Two Single bond unit 19 2-3524 unit 42 3,4-diClPh SO _Two Single bond device 20 2-3525 device 42 3,4-diClPh SO _Two Single bond unit 21 2-3526 unit 42 3,4-diClPh SO _Two Single bond unit 22 2-3527 unit 42 3,4-diClPh SO _Two Single bond unit 23 2-3528 unit 42 3,4-diClPh SO _Two Single bond unit 24 2-3529 unit 42 3,4-diClPh SO _Two Single bond unit 25 2-3530 unit 42 3,4-diClPh SO _Two Single bond unit 26 2-3531 unit 42 3,4-diClPh SO _Two Single bond unit 27 2-3532 unit 42 3,4-diClPh SO _Two Single bond unit 28 2-3353 unit 42 3,4-diClPh SO _Two Single bond unit 29 2-3534 unit 42 3,4-diClPh SO _Two Single bond unit 30 2-335 unit 42 3,4-diClPh SO _Two Single bond unit 31 2-3536 unit 42 3,4-diClPh SO _Two Single bond unit 32 2-3537 unit 42 3,4-diClPh SO _Two Single bond device 65 2-3538 device 42 3,4-diClPh SO _Two Single bond unit 66 2-33539 unit 42 3,4-diClPh SO _Two Single bond unit 67 2-3540 unit 42 3,4-diClPh SO _Two Single bond device 68 2-3541 device 42 3,4-diClPh SO _Two Single bond unit 69 2-3542 unit 42 3,4-diClPh SO _Two Single bond unit 70 2-3543 unit 42 3,4-diClPh SO _Two Single bond unit 71 2-3544 unit 42 3,4-diClPh SO _Two Single bond unit 72 2-3545 unit 42 3,4-diClPh SO _Two Single bond unit 73 2-3546 unit 42 3,4-diClPh SO _Two Single bond unit 74 2-3547 unit 42 3,4-diClPh SO _Two Single bond unit 75 2-3548 unit 42 3,4-diClPh SO _Two Single bond unit 76 2-3549 unit 42 3,4-diClPh SO _Two Single bond unit 77 2-3550 unit 42 3,4-diClPh SO _Two Single bond unit 78 2-3551 unit 42 3,4-diClPh SO _Two Single bond unit 79 2-3552 unit 42 3,4-diClPh SO _Two Single bond unit 80 2-355 unit 43 3,4-diClPh SO _Two Single bond Unit 1 2-3554 Unit 43 3,4-diClPh SO _Two Single bond unit 2 2-3555 unit 43 3,4-diClPh SO _Two Single bond device 3 2-3556 device 43 3,4-diClPh SO _Two Single bond unit 4 2-3557 unit 43 3,4-diClPh SO _Two Single bond device 5 2-3558 device 43 3,4-diClPh SO _Two Single bond unit 6 2-3559 unit 43 3,4-diClPh SO _Two Single bond device 7 2-3560 device 43 3,4-diClPh SO _Two Single bond unit 8 2-356 unit 43 3,4-diClPh SO _Two Single bond device 9 2-3562 device 43 3,4-diClPh SO _Two Single bond unit 10 2-3563 unit 43 3,4-diClPh SO _Two Single bond unit 11 2-356 unit 43 3,4-diClPh SO _Two Single bond unit 12 2-3565 unit 43 3,4-diClPh SO _Two Single bond unit 13 2-3566 unit 43 3,4-diClPh SO _Two Single bond unit 14 2-3567 unit 43 3,4-diClPh SO _Two Single bond unit 15 2-3568 unit 43 3,4-diClPh SO _Two Single bond Unit 16 2-3569 Unit 43 3,4-diClPh SO _Two Single bond unit 17 2-3570 unit 43 3,4-diClPh SO _Two Single bond unit 18 2-3571 unit 43 3,4-diClPh SO _Two Single bond unit 19 2-3572 unit 43 3,4-diClPh SO _Two Single bond unit 20 2-3573 unit 43 3,4-diClPh SO _Two Single bond unit 21 2-3574 unit 43 3,4-diClPh SO _Two Single bond unit 22 2-3575 unit 43 3,4-diClPh SO _Two Single bond unit 23 2-3576 unit 43 3,4-diClPh SO _Two Single bond unit 24 2-3577 unit 43 3,4-diClPh SO _Two Single bond unit 25 2-3578 unit 43 3,4-diClPh SO _Two Single bond unit 26 2-3579 unit 43 3,4-diClPh SO _Two Single bond unit 27 2-3580 unit 43 3,4-diClPh SO _Two Single bond unit 28 2-3581 unit 43 3,4-diClPh SO _Two Single bond unit 29 2-3582 unit 43 3,4-diClPh SO _Two Single bond device 30 2-3583 device 43 3,4-diClPh SO _Two Single bond unit 31 2-3584 unit 43 3,4-diClPh SO _Two Single bond unit 32 2-3585 unit 43 3,4-diClPh SO _Two Single bond device 65 2-3586 device 43 3,4-diClPh SO _Two Single bond unit 66 2-3587 unit 43 3,4-diClPh SO _Two Single bond unit 67 2-3588 unit 43 3,4-diClPh SO _Two Single bond device 68 2-3589 device 43 3,4-diClPh SO _Two Single bond unit 69 2-3590 unit 43 3,4-diClPh SO _Two Single bond device 70 2-3591 device 43 3,4-diClPh SO _Two Single bond unit 71 2-3592 unit 43 3,4-diClPh SO _Two Single bond unit 72 2-3593 unit 43 3,4-diClPh SO _Two Single bond unit 73 2-3594 unit 43 3,4-diClPh SO _Two Single bond unit 74 2-3595 unit 43 3,4-diClPh SO _Two Single bond unit 75 2-3596 unit 43 3,4-diClPh SO _Two Single bond unit 76 2-3597 unit 43 3,4-diClPh SO _Two Single bond unit 77 2-3598 unit 43 3,4-diClPh SO _Two Single bond unit 78 2-3599 unit 43 3,4-diClPh SO _Two Single bond unit 79 2-3600 unit 43 3,4-diClPh SO _Two Single bond position 80 化合物 Compound number R ¹ R ^Two A B Z ２− 2-360 Place 44 3,4-diClPh SO _Two Single bond device 1 2-3602 device 44 3,4-diClPh SO _Two Single bond unit 2 2-3603 unit 44 3,4-diClPh SO _Two Single bond unit 3 2-3604 unit 44 3,4-diClPh SO _Two Single bond unit 4 2-3605 unit 44 3,4-diClPh SO _Two Single bond device 5 2-3606 device 44 3,4-diClPh SO _Two Single bond unit 6 2-3607 unit 44 3,4-diClPh SO _Two Single bond device 7 2-3608 device 44 3,4-diClPh SO _Two Single bond device 8 2-3609 device 44 3,4-diClPh SO _Two Single bond device 9 2-3610 device 44 3,4-diClPh SO _Two Single bond device 10 2-361 device 44 3,4-diClPh SO _Two Single bond unit 11 2-336 unit 44 3,4-diClPh SO _Two Single bond unit 12 2-3613 unit 44 3,4-diClPh SO _Two Single bond unit 13 2-3614 unit 44 3,4-diClPh SO _Two Single bond unit 14 2-3615 unit 44 3,4-diClPh SO _Two Single bond unit 15 2-3616 unit 44 3,4-diClPh SO _Two Single bond unit 16 2-3617 unit 44 3,4-diClPh SO _Two Single bond unit 17 2-3618 unit 44 3,4-diClPh SO _Two Single bond unit 18 2-3619 unit 44 3,4-diClPh SO _Two Single bond unit 19 2-3620 unit 44 3,4-diClPh SO _Two Single bond device 20 2-3621 device 44 3,4-diClPh SO _Two Single bond unit 21 2-3622 unit 44 3,4-diClPh SO _Two Single bond unit 22 2-3623 unit 44 3,4-diClPh SO _Two Single bond unit 23 2-3624 unit 44 3,4-diClPh SO _Two Single bond unit 24 2-3625 unit 44 3,4-diClPh SO _Two Single bond unit 25 2-3626 unit 44 3,4-diClPh SO _Two Single bond unit 26 2-3627 unit 44 3,4-diClPh SO _Two Single bond unit 27 2-3628 unit 44 3,4-diClPh SO _Two Single bond unit 28 2-3629 unit 44 3,4-diClPh SO _Two Single bond unit 29 2-3630 unit 44 3,4-diClPh SO _Two Single bond device 30 2-3631 device 44 3,4-diClPh SO _Two Single bond unit 31 2-336 unit 44 3,4-diClPh SO _Two Single bond device 32 2-3633 device 44 3,4-diClPh SO _Two Single bond device 65 2-3634 device 44 3,4-diClPh SO _Two Single bond unit 66 2-3635 unit 44 3,4-diClPh SO _Two Single bond unit 67 2-336 unit 44 3,4-diClPh SO _Two Single bond device 68 2-3637 device 44 3,4-diClPh SO _Two Single bond device 69 2-33638 device 44 3,4-diClPh SO _Two Single bond device 70 2-3639 device 44 3,4-diClPh SO _Two Single bond unit 71 2-3640 unit 44 3,4-diClPh SO _Two Single bond unit 72 2-3641 unit 44 3,4-diClPh SO _Two Single bond unit 73 2-3642 unit 44 3,4-diClPh SO _Two Single bond unit 74 2-3643 unit 44 3,4-diClPh SO _Two Single bond Unit 75 2-3644 Unit 44 3,4-diClPh SO _Two Single bond unit 76 2-364 unit 44 3,4-diClPh SO _Two Single bond unit 77 2-3646 unit 44 3,4-diClPh SO _Two Single bond unit 78 2-3647 unit 44 3,4-diClPh SO _Two Single bond device 79 2-3648 device 44 3,4-diClPh SO _Two Single bond device 80 2-3649 device 45 3,4-diClPh SO _Two Single bond unit 1 2-3650 unit 45 3,4-diClPh SO _Two Single bond unit 22-3651 unit 45 3,4-diClPh SO _Two Single bond device 3 2-3652 device 45 3,4-diClPh SO _Two Single bond unit 4 2-3653 unit 45 3,4-diClPh SO _Two Single bond unit 5 2-3654 unit 45 3,4-diClPh SO _Two Single bond unit 6 2-3655 unit 45 3,4-diClPh SO _Two Single bond unit 7 2-3656 unit 45 3,4-diClPh SO _Two Single bond unit 8 2-3657 unit 45 3,4-diClPh SO _Two Single bond unit 9 2-3658 unit 45 3,4-diClPh SO _Two Single bond device 10 2-3659 device 45 3,4-diClPh SO _Two Single bond unit 11 2-3660 unit 45 3,4-diClPh SO _Two Single bond unit 12 2-3661 unit 45 3,4-diClPh SO _Two Single bond unit 13 2-3662 unit 45 3,4-diClPh SO _Two Single bond unit 14 2-3663 unit 45 3,4-diClPh SO _Two Single bond unit 15 2-366 unit 45 3,4-diClPh SO _Two Single bond unit 16 2-365 unit 45 3,4-diClPh SO _Two Single bond Unit 17 2-3666 Unit 45 3,4-diClPh SO _Two Single bond unit 18 2-3667 unit 45 3,4-diClPh SO _Two Single bond Unit 19 2-3668 Unit 45 3,4-diClPh SO _Two Single bond unit 20 2-369 unit 45 3,4-diClPh SO _Two Single bond unit 21 2-3670 unit 45 3,4-diClPh SO _Two Single bond Unit 22 2-367 Unit 45 3,4-diClPh SO _Two Single bond unit 23 2-3672 unit 45 3,4-diClPh SO _Two Single bond unit 24 2-3673 unit 45 3,4-diClPh SO _Two Single bond unit 25 2-3674 unit 45 3,4-diClPh SO _Two Single bond unit 26 2-3675 unit 45 3,4-diClPh SO _Two Single bond Unit 27 2-3676 Unit 45 3,4-diClPh SO _Two Single bond unit 28 2-3677 unit 45 3,4-diClPh SO _Two Single bond unit 29 2-3678 unit 45 3,4-diClPh SO _Two Single bond unit 30 2-3679 unit 45 3,4-diClPh SO _Two Single bond unit 31 2-3680 unit 45 3,4-diClPh SO _Two Single bond unit 32 2-3681 unit 45 3,4-diClPh SO _Two Single bond unit 65 2-3682 unit 45 3,4-diClPh SO _Two Single bond unit 66 2-3683 unit 45 3,4-diClPh SO _Two Single bond unit 67 2-3684 unit 45 3,4-diClPh SO _Two Single bond unit 68 2-3685 unit 45 3,4-diClPh SO _Two Single bond unit 69 2-3686 unit 45 3,4-diClPh SO _Two Single bond unit 70 2-368 unit 45 3,4-diClPh SO _Two Single bond unit 71 2-3688 unit 45 3,4-diClPh SO _Two Single bond Unit 72 2-3689 Unit 45 3,4-diClPh SO _Two Single bond Unit 73 2-3690 Unit 45 3,4-diClPh SO _Two Single bond unit 74 2-3691 unit 45 3,4-diClPh SO _Two Single bond unit 75 2-3692 unit 45 3,4-diClPh SO _Two Single bond unit 76 2-3693 unit 45 3,4-diClPh SO _Two Single bond unit 77 2-369 unit 45 3,4-diClPh SO _Two Single bond unit 78 2-3695 unit 45 3,4-diClPh SO _Two Single bond unit 79 2-3696 unit 45 3,4-diClPh SO _Two Single bond device 80 2-3697 device 46 3,4-diClPh SO _Two Single bond device 1 2-33698 device 46 3,4-diClPh SO _Two Single bond device 2 2-3699 device 46 3,4-diClPh SO _Two Single bond device 3 2-3700 device 46 3,4-diClPh SO _Two Single bond unit 4 2-3701 unit 46 3,4-diClPh SO _Two Single bond unit 5 2-3700 unit 46 3,4-diClPh SO _Two Single bond unit 6 2-3703 unit 46 3,4-diClPh SO _Two Single bond unit 7 2-3704 unit 46 3,4-diClPh SO _Two Single bond unit 8 2-3705 unit 46 3,4-diClPh SO _Two Single bond unit 9 2-3706 unit 46 3,4-diClPh SO _Two Single bond unit 10 2-3707 unit 46 3,4-diClPh SO _Two Single bond unit 11 2-3708 unit 46 3,4-diClPh SO _Two Single bond unit 12 2-3709 unit 46 3,4-diClPh SO _Two Single bond unit 13 2-33710 unit 46 3,4-diClPh SO _Two Single bond unit 14 2-33711 unit 46 3,4-diClPh SO _Two Single bond unit 15 2-33712 unit 46 3,4-diClPh SO _Two Single bond unit 16 2-3713 unit 46 3,4-diClPh SO _Two Single bond unit 17 2-3714 unit 46 3,4-diClPh SO _Two Single bond unit 18 2-3715 unit 46 3,4-diClPh SO _Two Single bond Unit 19 2-3716 Unit 46 3,4-diClPh SO _Two Single bond device 20 2-3717 device 46 3,4-diClPh SO _Two Single bond unit 21 2-3718 unit 46 3,4-diClPh SO _Two Single bond Unit 22 2-3719 Unit 46 3,4-diClPh SO _Two Single bond unit 23 2-3720 unit 46 3,4-diClPh SO _Two Single bond unit 24 2-3721 unit 46 3,4-diClPh SO _Two Single bond unit 25 2-3722 unit 46 3,4-diClPh SO _Two Single bond unit 26 2-3723 unit 46 3,4-diClPh SO _Two Single bond Unit 27 2-3724 Unit 46 3,4-diClPh SO _Two Single bond Unit 28 2-337 Unit 46 3,4-diClPh SO _Two Single bond unit 29 2-3726 unit 46 3,4-diClPh SO _Two Single bond unit 30 2-3727 unit 46 3,4-diClPh SO _Two Single bond unit 31 2-3728 unit 46 3,4-diClPh SO _Two Single bond unit 32 2-3729 unit 46 3,4-diClPh SO _Two Single bond device 65 2-3730 device 46 3,4-diClPh SO _Two Single bond unit 66 2-3731 unit 46 3,4-diClPh SO _Two Single bond unit 67 2-3732 unit 46 3,4-diClPh SO _Two Single bond device 68 2-3733 device 46 3,4-diClPh SO _Two Single bond device 69 2-3734 device 46 3,4-diClPh SO _Two Single bond unit 70 2-3735 unit 46 3,4-diClPh SO _Two Single bond unit 71 2-3736 unit 46 3,4-diClPh SO _Two Single bond unit 72 2-337 unit 46 3,4-diClPh SO _Two Single bond unit 73 2-3738 unit 46 3,4-diClPh SO _Two Single bond unit 74 2-3739 unit 46 3,4-diClPh SO _Two Single bond unit 75 2-3740 unit 46 3,4-diClPh SO _Two Single bond unit 76 2-3741 unit 46 3,4-diClPh SO _Two Single bond unit 77 2-3742 unit 46 3,4-diClPh SO _Two Single bond unit 78 2-3743 unit 46 3,4-diClPh SO _Two Single bond unit 79 2-3744 unit 46 3,4-diClPh SO _Two Single bond device 80 2-3745 device 47 3,4-diClPh SO _Two Single bond device 1 2-3746 device 47 3,4-diClPh SO _Two Single bond unit 22-3747 unit 47 3,4-diClPh SO _Two Single bond position 3 2-3748 position 47 3,4-diClPh SO _Two Single bond device 4 2-33749 device 47 3,4-diClPh SO _Two Single bond unit 5 2-33750 unit 47 3,4-diClPh SO _Two Single bond device 6 2-3751 device 47 3,4-diClPh SO _Two Single bond device 7 2-3752 device 47 3,4-diClPh SO _Two Single bond device 8 2-3753 device 47 3,4-diClPh SO _Two Single bond unit 9 2-3754 unit 47 3,4-diClPh SO _Two Single bond unit 10 2-3375 unit 47 3,4-diClPh SO _Two Single bond unit 11 2-3756 unit 47 3,4-diClPh SO _Two Single bond Unit 12 2-3375 Position 47 3,4-diClPh SO _Two Single bond unit 13 2-3758 unit 47 3,4-diClPh SO _Two Single bond unit 14 2-3759 unit 47 3,4-diClPh SO _Two Single bond unit 15 2-3760 unit 47 3,4-diClPh SO _Two Single bond unit 16 2-3761 unit 47 3,4-diClPh SO _Two Single bond unit 17 2-3762 unit 47 3,4-diClPh SO _Two Single bond unit 18 2-3763 unit 47 3,4-diClPh SO _Two Single bond unit 19 2-3764 unit 47 3,4-diClPh SO _Two Single bond unit 20 2-3765 unit 47 3,4-diClPh SO _Two Single bond unit 21 2-3766 unit 47 3,4-diClPh SO _Two Single bond unit 22 2-3767 unit 47 3,4-diClPh SO _Two Single bond unit 23 2-3768 unit 47 3,4-diClPh SO _Two Single bond unit 24 2-3769 unit 47 3,4-diClPh SO _Two Single bond unit 25 2-3770 unit 47 3,4-diClPh SO _Two Single bond unit 26 2-3771 unit 47 3,4-diClPh SO _Two Single bond unit 27 2-3772 unit 47 3,4-diClPh SO _Two Single bond unit 28 2-3773 unit 47 3,4-diClPh SO _Two Single bond unit 29 2-3774 unit 47 3,4-diClPh SO _Two Single bond device 30 2-3775 device 47 3,4-diClPh SO _Two Single bond unit 31 2-3776 unit 47 3,4-diClPh SO _Two Single bond unit 32 2-3777 unit 47 3,4-diClPh SO _Two Single bond unit 65 2-3778 unit 47 3,4-diClPh SO _Two Single bond Unit 66 2-3779 Unit 47 3,4-diClPh SO _Two Single bond unit 67 2-3780 unit 47 3,4-diClPh SO _Two Single bond device 68 2-3781 device 47 3,4-diClPh SO _Two Single bond device 69 2-3782 device 47 3,4-diClPh SO _Two Single bond unit 70 2-3783 unit 47 3,4-diClPh SO _Two Single bond unit 71 2-3784 unit 47 3,4-diClPh SO _Two Single bond unit 72 2-3785 unit 47 3,4-diClPh SO _Two Single bond unit 73 2-3780 unit 47 3,4-diClPh SO _Two Single bond unit 74 2-3787 unit 47 3,4-diClPh SO _Two Single bond unit 75 2-3788 unit 47 3,4-diClPh SO _Two Single bond unit 76 2-3789 unit 47 3,4-diClPh SO _Two Single bond unit 77 2-3790 unit 47 3,4-diClPh SO _Two Single bond unit 78 2-3791 unit 47 3,4-diClPh SO _Two Single bond unit 79 2-3792 unit 47 3,4-diClPh SO _Two Single bond device 80 2-3793 device 81 3,4-diClPh SO _Two Single bond device 1 2-3794 device 81 3,4-diClPh SO _Two Single bond device 2 2-3795 device 81 3,4-diClPh SO _Two Single bond unit 32-3796 unit 81 3,4-diClPh SO _Two Single bond unit 4 2-3797 unit 81 3,4-diClPh SO _Two Single bond 5 2 3798 Position 81 3,4-diClPh SO _Two Single bond unit 6 2-3799 unit 81 3,4-diClPh SO _Two Single bond device 7 2-3800 device 81 3,4-diClPh SO _Two Single bond device 8 2-3801 device 81 3,4-diClPh SO _Two Single bond device 9 2-3802 device 81 3,4-diClPh SO _Two Single bond unit 10 2-3803 unit 81 3,4-diClPh SO _Two Single bond unit 11 2-3804 unit 81 3,4-diClPh SO _Two Single bond unit 12 2-3805 unit 81 3,4-diClPh SO _Two Single bond unit 13 2-3806 unit 81 3,4-diClPh SO _Two Single bond unit 14 2-3807 unit 81 3,4-diClPh SO _Two Single bond unit 15 2-3808 unit 81 3,4-diClPh SO _Two Single bond unit 16 2-3809 unit 81 3,4-diClPh SO _Two Single bond unit 17 2-3810 unit 81 3,4-diClPh SO _Two Single bond unit 18 2-3811 unit 81 3,4-diClPh SO _Two Single bond unit 19 2-3812 unit 81 3,4-diClPh SO _Two Single bond unit 20 2-3813 unit 81 3,4-diClPh SO _Two Single bond unit 21 2-3814 unit 81 3,4-diClPh SO _Two Single bond unit 22 2-3815 unit 81 3,4-diClPh SO _Two Single bond unit 23 2-3816 unit 81 3,4-diClPh SO _Two Single bond unit 24 2-3817 unit 81 3,4-diClPh SO _Two Single bond unit 25 2-3818 unit 81 3,4-diClPh SO _Two Single bond unit 26 2-3819 unit 81 3,4-diClPh SO _Two Single bond unit 27 2-3820 unit 81 3,4-diClPh SO _Two Single bond unit 28 2-3821 unit 81 3,4-diClPh SO _Two Single bond unit 29 2-3822 unit 81 3,4-diClPh SO _Two Single bond device 30 2-3823 device 81 3,4-diClPh SO _Two Single bond unit 31 2-3824 unit 81 3,4-diClPh SO _Two Single bond unit 32 2-3825 unit 81 3,4-diClPh SO _Two Single bond unit 65 2-3826 unit 81 3,4-diClPh SO _Two Single bond device 66 2-3827 device 81 3,4-diClPh SO _Two Single bond unit 67 2-3828 unit 81 3,4-diClPh SO _Two Single bond device 68 2-3829 device 81 3,4-diClPh SO _Two Single bond device 69 2-3830 device 81 3,4-diClPh SO _Two Single bond device 70 2-3831 device 81 3,4-diClPh SO _Two Single bond unit 71 2-3832 unit 81 3,4-diClPh SO _Two Single bond unit 72 2-3833 unit 81 3,4-diClPh SO _Two Single bond device 73 2-3834 device 81 3,4-diClPh SO _Two Single bond unit 74 2-33835 unit 81 3,4-diClPh SO _Two Single bond unit 75 2-3836 unit 81 3,4-diClPh SO _Two Single bond device 76 2-3837 device 81 3,4-diClPh SO _Two Single bond unit 77 2-3838 unit 81 3,4-diClPh SO _Two Single bond unit 78 2-3839 unit 81 3,4-diClPh SO _Two Single bond device 79 2-3840 device 81 3,4-diClPh SO _Two Single bond device 80 2-3841 device 48 3,4-diClPh SO _Two Single bond unit 1 2-3842 unit 48 3,4-diClPh SO _Two Single bond unit 2 2-3843 unit 48 3,4-diClPh SO _Two Single bond device 3 2-3844 device 48 3,4-diClPh SO _Two Single bond unit 4 2-3845 unit 48 3,4-diClPh SO _Two Single bond unit 5 2-3846 unit 48 3,4-diClPh SO _Two Single bond unit 6 2-3847 unit 48 3,4-diClPh SO _Two Single bond unit 7 2-3848 unit 48 3,4-diClPh SO _Two Single bond device 8 2-3849 device 48 3,4-diClPh SO _Two Single bond device 9 2-3850 device 48 3,4-diClPh SO _Two Single bond device 10 2-3851 device 48 3,4-diClPh SO _Two Single bond unit 11 2-3852 unit 48 3,4-diClPh SO _Two Single bond unit 12 2-3853 unit 48 3,4-diClPh SO _Two Single bond unit 13 2-3854 unit 48 3,4-diClPh SO _Two Single bond unit 14 2-3855 unit 48 3,4-diClPh SO _Two Single bond Unit 15 2-3856 Unit 48 3,4-diClPh SO _Two Single bond unit 16 2-33857 unit 48 3,4-diClPh SO _Two Single bond Unit 17 2-3858 Unit 48 3,4-diClPh SO _Two Single bond unit 18 2-3859 unit 48 3,4-diClPh SO _Two Single bond unit 19 2-3860 unit 48 3,4-diClPh SO _Two Single bond unit 20 2-3861 unit 48 3,4-diClPh SO _Two Single bond unit 21 2-3862 unit 48 3,4-diClPh SO _Two Single bond unit 22 2-3863 unit 48 3,4-diClPh SO _Two Single bond unit 23 2-3864 unit 48 3,4-diClPh SO _Two Single bond unit 24 2-3865 unit 48 3,4-diClPh SO _Two Single bond unit 25 2-3866 unit 48 3,4-diClPh SO _Two Single bond unit 26 2-3867 unit 48 3,4-diClPh SO _Two Single bond unit 27 2-3868 unit 48 3,4-diClPh SO _Two Single bond unit 28 2-3869 unit 48 3,4-diClPh SO _Two Single bond unit 29 2-3870 unit 48 3,4-diClPh SO _Two Single bond device 30 2-3871 device 48 3,4-diClPh SO _Two Single bond unit 31 2-3872 unit 48 3,4-diClPh SO _Two Single bond unit 32 2-3873 unit 48 3,4-diClPh SO _Two Single bond unit 65 2-3874 unit 48 3,4-diClPh SO _Two Single bond unit 66 2-3875 unit 48 3,4-diClPh SO _Two Single bond unit 67 2-3876 unit 48 3,4-diClPh SO _Two Single bond unit 68 2-3877 unit 48 3,4-diClPh SO _Two Single bond device 69 2-3878 device 48 3,4-diClPh SO _Two Single bond device 70 2-3879 device 48 3,4-diClPh SO _Two Single bond unit 71 2-3880 unit 48 3,4-diClPh SO _Two Single bond unit 72 2-3881 unit 48 3,4-diClPh SO _Two Single bond unit 73 2-3882 unit 48 3,4-diClPh SO _Two Single bond unit 74 2-3883 unit 48 3,4-diClPh SO _Two Single bond unit 75 2-3884 unit 48 3,4-diClPh SO _Two Single bond unit 76 2-3885 unit 48 3,4-diClPh SO _Two Single bond unit 77 2-3886 unit 48 3,4-diClPh SO _Two Single bond unit 78 2-3887 unit 48 3,4-diClPh SO _Two Single bond unit 79 2-3888 unit 48 3,4-diClPh SO _Two Single bond unit 80 2-3889 unit 49 3,4-diClPh SO _Two Single bond unit 1 2-3890 unit 49 3,4-diClPh SO _Two Single bond unit 2 2-3891 unit 49 3,4-diClPh SO _Two Single bond unit 32-2-3892 unit 49 3,4-diClPh SO _Two Single bond unit 4 2-3893 unit 49 3,4-diClPh SO _Two Single bond 5 2 3894 5 49 3,4-diClPh SO _Two Single bond device 6 2-3895 device 49 3,4-diClPh SO _Two Single bond unit 7 2-3896 unit 49 3,4-diClPh SO _Two Single bond device 8 2-3897 device 49 3,4-diClPh SO _Two Single bond device 9 2-3898 device 49 3,4-diClPh SO _Two Single bond device 10 2-3899 device 49 3,4-diClPh SO _Two Single bond unit 11 2-3900 unit 49 3,4-diClPh SO _Two Single bond unit 12 2-3901 unit 49 3,4-diClPh SO _Two Single bond unit 13 2-3902 unit 49 3,4-diClPh SO _Two Single bond unit 14 2-3903 unit 49 3,4-diClPh SO _Two Single bond unit 15 2-3904 unit 49 3,4-diClPh SO _Two Single bond unit 16 2-3905 unit 49 3,4-diClPh SO _Two Single bond unit 17 2-3906 unit 49 3,4-diClPh SO _Two Single bond unit 18 2-3907 unit 49 3,4-diClPh SO _Two Single bond unit 19 2-3908 unit 49 3,4-diClPh SO _Two Single bond unit 20 2-3909 unit 49 3,4-diClPh SO _Two Single bond unit 21 2-3910 unit 49 3,4-diClPh SO _Two Single bond unit 22 2-39111 unit 49 3,4-diClPh SO _Two Single bond unit 23 2-3912 unit 49 3,4-diClPh SO _Two Single bond unit 24 2-3913 unit 49 3,4-diClPh SO _Two Single bond unit 25 2-3914 unit 49 3,4-diClPh SO _Two Single bond unit 26 2-3915 unit 49 3,4-diClPh SO _Two Single bond unit 27 2-3916 unit 49 3,4-diClPh SO _Two Single bond unit 28 2-3917 unit 49 3,4-diClPh SO _Two Single bond unit 29 2-3918 unit 49 3,4-diClPh SO _Two Single bond unit 30 2-3919 unit 49 3,4-diClPh SO _Two Single bond unit 31 2-3920 unit 49 3,4-diClPh SO _Two Single bond unit 32 2-3921 unit 49 3,4-diClPh SO _Two Single bond unit 65 2-3922 unit 49 3,4-diClPh SO _Two Single bond unit 66 2-3923 unit 49 3,4-diClPh SO _Two Single bond unit 67 2-3924 unit 49 3,4-diClPh SO _Two Single bond Unit 68 2-3925 Unit 49 3,4-diClPh SO _Two Single bond unit 69 2-3926 unit 49 3,4-diClPh SO _Two Single bond unit 70 2-3927 unit 49 3,4-diClPh SO _Two Single bond unit 71 2-3928 unit 49 3,4-diClPh SO _Two Single bond unit 72 2-3929 unit 49 3,4-diClPh SO _Two Single bond unit 73 2-3930 unit 49 3,4-diClPh SO _Two Single bond unit 74 2-3931 unit 49 3,4-diClPh SO _Two Single bond unit 75 2-3932 unit 49 3,4-diClPh SO _Two Single bond unit 76 2-3933 unit 49 3,4-diClPh SO _Two Single bond unit 77 2-3934 unit 49 3,4-diClPh SO _Two Single bond unit 78 2-3935 unit 49 3,4-diClPh SO _Two Single bond unit 79 2-3936 unit 49 3,4-diClPh SO _Two Single bond device 80 2-3937 device 50 3,4-diClPh SO _Two Single bond device 1 2-3938 device 50 3,4-diClPh SO _Two Single bond device 2 2-3939 device 50 3,4-diClPh SO _Two Single bond device 3 2-3940 device 50 3,4-diClPh SO _Two Single bond unit 4 2-3941 unit 50 3,4-diClPh SO _Two Single bond unit 5 2-33942 unit 50 3,4-diClPh SO _Two Single bond 6 2-3943 50 50 3,4-diClPh SO _Two Single bond device 7 2-3944 device 50 3,4-diClPh SO _Two Single bond unit 8 2-3945 unit 50 3,4-diClPh SO _Two Single bond device 9 2-3946 device 50 3,4-diClPh SO _Two Single bond unit 10 2-3939 unit 50 3,4-diClPh SO _Two Single bond unit 11 2-3948 unit 50 3,4-diClPh SO _Two Single bond unit 12 2-3939 unit 50 3,4-diClPh SO _Two Single bond unit 13 2-3950 unit 50 3,4-diClPh SO _Two Single bond unit 14 2-3951 unit 50 3,4-diClPh SO _Two Single bond unit 15 2-3952 unit 50 3,4-diClPh SO _Two Single bond unit 16 2-3953 unit 50 3,4-diClPh SO _Two Single bond unit 17 2-3954 unit 50 3,4-diClPh SO _Two Single bond unit 18 2-3955 unit 50 3,4-diClPh SO _Two Single bond unit 19 2-3956 unit 50 3,4-diClPh SO _Two Single bond device 20 2-3975 device 50 3,4-diClPh SO _Two Single bond unit 21 2-3958 unit 50 3,4-diClPh SO _Two Single bond unit 22 2-3959 unit 50 3,4-diClPh SO _Two Single bond unit 23 2-3960 unit 50 3,4-diClPh SO _Two Single bond unit 24 2-3961 unit 50 3,4-diClPh SO _Two Single bond unit 25 2-3962 unit 50 3,4-diClPh SO _Two Single bond unit 26 2-3963 unit 50 3,4-diClPh SO _Two Single bond unit 27 2-3964 unit 50 3,4-diClPh SO _Two Single bond unit 28 2-3965 unit 50 3,4-diClPh SO _Two Single bond unit 29 2-3966 unit 50 3,4-diClPh SO _Two Single bond device 30 2-3967 device 50 3,4-diClPh SO _Two Single bond unit 31 2-3968 unit 50 3,4-diClPh SO _Two Single bond unit 32 2-3969 unit 50 3,4-diClPh SO _Two Single bond device 65 2-3970 device 50 3,4-diClPh SO _Two Single bond device 66 2-3971 device 50 3,4-diClPh SO _Two Single bond unit 67 2-3972 unit 50 3,4-diClPh SO _Two Single bond device 68 2-3973 device 50 3,4-diClPh SO _Two Single bond unit 69 2-3974 unit 50 3,4-diClPh SO _Two Single bond Apparatus 70 2-397 Apparatus 50 3,4-diClPh SO _Two Single bond unit 71 2-3976 unit 50 3,4-diClPh SO _Two Single bond unit 72 2-3977 unit 50 3,4-diClPh SO _Two Single bond unit 73 2-3978 unit 50 3,4-diClPh SO _Two Single bond unit 74 2-3979 unit 50 3,4-diClPh SO _Two Single bond unit 75 2-3980 unit 50 3,4-diClPh SO _Two Single bond unit 76 2-3981 unit 50 3,4-diClPh SO _Two Single bond unit 77 2-3982 unit 50 3,4-diClPh SO _Two Single bond unit 78 2-3983 unit 50 3,4-diClPh SO _Two Single bond device 79 2-3984 device 50 3,4-diClPh SO _Two Single bond device 80 2-3985 device 51 3,4-diClPh SO _Two Single bond device 1 2-3986 device 51 3,4-diClPh SO _Two Single bond device 2 2-3987 device 51 3,4-diClPh SO _Two Single bond unit 3 2-3988 unit 51 3,4-diClPh SO _Two Single bond unit 4 2-3989 unit 51 3,4-diClPh SO _Two Single bond unit 5 2-3990 unit 51 3,4-diClPh SO _Two Single bond device 6 2-3991 device 51 3,4-diClPh SO _Two Single bond device 7 2-3992 device 51 3,4-diClPh SO _Two Single bond device 8 2-3993 device 51 3,4-diClPh SO _Two Single bond device 9 2-3994 device 51 3,4-diClPh SO _Two Single bond device 10 2-3995 device 51 3,4-diClPh SO _Two Single bond unit 11 2-3996 unit 51 3,4-diClPh SO _Two Single bond unit 12 2-3997 unit 51 3,4-diClPh SO _Two Single bond unit 13 2-3998 unit 51 3,4-diClPh SO _Two Single bond unit 14 2-3999 unit 51 3,4-diClPh SO _Two Single bond unit 15 2-4000 unit 51 3,4-diClPh SO _Two Single bond unit 16 2-4001 unit 51 3,4-diClPh SO _Two Single bond unit 17 2-4002 unit 51 3,4-diClPh SO _Two Single bond unit 18 2-4003 unit 51 3,4-diClPh SO _Two Single bond unit 19 2-4004 unit 51 3,4-diClPh SO _Two Single bond 20-20400 5 51 3,4-diClPh SO _Two Single bond unit 21-2-4006 unit 51 3,4-diClPh SO _Two Single bond unit 22-4007 unit 51 3,4-diClPh SO _Two Single bond device 23 2-3008 device 51 3,4-diClPh SO _Two Single bond unit 24-2 4009 unit 51 3,4-diClPh SO _Two Single bond unit 25 2-4010 unit 51 3,4-diClPh SO _Two Single bond unit 26 2-4011 unit 51 3,4-diClPh SO _Two Single bond unit 27 2-4012 unit 51 3,4-diClPh SO _Two Single bond unit 28 2-4013 unit 51 3,4-diClPh SO _Two Single bond unit 29 2-4014 unit 51 3,4-diClPh SO _Two Single bond device 30 2-4015 device 51 3,4-diClPh SO _Two Single bond unit 31 2-4016 unit 51 3,4-diClPh SO _Two Single bond unit 32 2-4017 unit 51 3,4-diClPh SO _Two Single bond device 65 2-4018 device 51 3,4-diClPh SO _Two Single bond device 66 2-4019 device 51 3,4-diClPh SO _Two Single bond device 67 2-4020 device 51 3,4-diClPh SO _Two Single bond device 68 2-4021 device 51 3,4-diClPh SO _Two Single bond device 69 2-4022 device 51 3,4-diClPh SO _Two Single bond device 70 2-4023 device 51 3,4-diClPh SO _Two Single bond unit 71 2-4024 unit 51 3,4-diClPh SO _Two Single bond unit 72 2-4025 unit 51 3,4-diClPh SO _Two Single bond device 73 2-4026 device 51 3,4-diClPh SO _Two Single bond device 74 2-4027 device 51 3,4-diClPh SO _Two Single bond device 75 2-4028 device 51 3,4-diClPh SO _Two Single bond device 76 2-4029 device 51 3,4-diClPh SO _Two Single bond unit 77 2-4030 unit 51 3,4-diClPh SO _Two Single bond unit 78 2-4031 unit 51 3,4-diClPh SO _Two Single bond device 79 2-4032 device 51 3,4-diClPh SO _Two Single bond device 80 2-4033 device 52 3,4-diClPh SO _Two Single bond device 1 2-4034 device 52 3,4-diClPh SO _Two Single bond device 2 2-4035 device 52 3,4-diClPh SO _Two Single bond device 3 2-4036 device 52 3,4-diClPh SO _Two Single bond unit 4 2-4037 unit 52 3,4-diClPh SO _Two Single bond device 5 2-4038 device 52 3,4-diClPh SO _Two Single bond device 6 2-4039 device 52 3,4-diClPh SO _Two Single bond device 7 2-4040 device 52 3,4-diClPh SO _Two Single bond device 8 2-4041 device 52 3,4-diClPh SO _Two Single bond device 9 2-4042 device 52 3,4-diClPh SO _Two Single bond device 10 2-4043 device 52 3,4-diClPh SO _Two Single bond unit 11 2-4044 unit 52 3,4-diClPh SO _Two Single bond unit 12 2-4045 unit 52 3,4-diClPh SO _Two Single bond unit 13 2-4046 unit 52 3,4-diClPh SO _Two Single bond unit 14 2-4047 unit 52 3,4-diClPh SO _Two Single bond unit 15 2-4048 unit 52 3,4-diClPh SO _Two Single bond unit 16 2-4049 unit 52 3,4-diClPh SO _Two Single bond unit 17 2-4050 unit 52 3,4-diClPh SO _Two Single bond unit 18 2-4051 unit 52 3,4-diClPh SO _Two Single bond unit 19 2-4052 unit 52 3,4-diClPh SO _Two Single bond unit 20 2-4053 unit 52 3,4-diClPh SO _Two Single bond unit 21 2-4054 unit 52 3,4-diClPh SO _Two Single bond Unit 22 2-4055 Unit 52 3,4-diClPh SO _Two Single bond unit 23 2-4056 unit 52 3,4-diClPh SO _Two Single bond unit 24 2-4057 unit 52 3,4-diClPh SO _Two Single bond unit 25 2-4058 unit 52 3,4-diClPh SO _Two Single bond unit 26 2-4059 unit 52 3,4-diClPh SO _Two Single bond unit 27 2-4060 unit 52 3,4-diClPh SO _Two Single bond unit 28 2-4061 unit 52 3,4-diClPh SO _Two Single bond unit 29 2-4062 unit 52 3,4-diClPh SO _Two Single bond device 30 2-4063 device 52 3,4-diClPh SO _Two Single bond unit 31 2-4064 unit 52 3,4-diClPh SO _Two Single bond unit 32 2-4065 unit 52 3,4-diClPh SO _Two Single bond device 65 2-4066 device 52 3,4-diClPh SO _Two Single bond device 66 2-4067 device 52 3,4-diClPh SO _Two Single bond unit 67 2-4068 unit 52 3,4-diClPh SO _Two Single bond device 68 2-4069 device 52 3,4-diClPh SO _Two Single bond device 69 2-4070 device 52 3,4-diClPh SO _Two Single bond device 70 2-4071 device 52 3,4-diClPh SO _Two Single bond unit 71 2-4072 unit 52 3,4-diClPh SO _Two Single bond unit 72 2-4073 unit 52 3,4-diClPh SO _Two Single bond device 73 2-4074 device 52 3,4-diClPh SO _Two Single bond unit 74 2-4075 unit 52 3,4-diClPh SO _Two Single bond unit 75 2-4076 unit 52 3,4-diClPh SO _Two Single bond unit 76 2-4077 unit 52 3,4-diClPh SO _Two Single bond unit 77 2-4078 unit 52 3,4-diClPh SO _Two Single bond unit 78 2-4079 unit 52 3,4-diClPh SO _Two Single bond device 79 2-4080 device 52 3,4-diClPh SO _Two Single bond device 80 2-4081 device 53 3,4-diClPh SO _Two Single bond device 1 2 -4082 device 53 3,4-diClPh SO _Two Single bond device 2 2-4083 device 53 3,4-diClPh SO _Two Single bond device 3 2-4084 device 53 3,4-diClPh SO _Two Single bond unit 4 2-4085 unit 53 3,4-diClPh SO _Two Single bond device 5 2-4086 device 53 3,4-diClPh SO _Two Single bond device 6 2-4087 device 53 3,4-diClPh SO _Two Single bond device 7 2-4088 device 53 3,4-diClPh SO _Two Single bond device 8 2-4089 device 53 3,4-diClPh SO _Two Single bond device 9 2-4090 device 53 3,4-diClPh SO _Two Single bond device 10 2-4091 device 53 3,4-diClPh SO _Two Single bond unit 11 2-4092 unit 53 3,4-diClPh SO _Two Single bond unit 12 2-4093 unit 53 3,4-diClPh SO _Two Single bond unit 13 2-4094 unit 53 3,4-diClPh SO _Two Single bond unit 14 2-4095 unit 53 3,4-diClPh SO _Two Single bond unit 15 2-4096 unit 53 3,4-diClPh SO _Two Single bond unit 16 2-4097 unit 53 3,4-diClPh SO _Two Single bond unit 17 2-4098 unit 53 3,4-diClPh SO _Two Single bond unit 18 2-4099 unit 53 3,4-diClPh SO _Two Single bond unit 19 2-4100 unit 53 3,4-diClPh SO _Two Single bond unit 20 2-4101 unit 53 3,4-diClPh SO _Two Single bond unit 21 2-4102 unit 53 3,4-diClPh SO _Two Single bond unit 22 2-4103 unit 53 3,4-diClPh SO _Two Single bond unit 23 2-4104 unit 53 3,4-diClPh SO _Two Single bond unit 24 2-4105 unit 53 3,4-diClPh SO _Two Single bond unit 25 2-4106 unit 53 3,4-diClPh SO _Two Single bond unit 26 2-4107 unit 53 3,4-diClPh SO _Two Single bond unit 27 2-4108 unit 53 3,4-diClPh SO _Two Single bond unit 28 2-4109 unit 53 3,4-diClPh SO _Two Single bond unit 29 2-4110 unit 53 3,4-diClPh SO _Two Single bond unit 30 2-4111 unit 53 3,4-diClPh SO _Two Single bond unit 31 2-4112 unit 53 3,4-diClPh SO _Two Single bond unit 32 2-4113 unit 53 3,4-diClPh SO _Two Single bond device 65 2-4114 device 53 3,4-diClPh SO _Two Single bond unit 66 2-4115 unit 53 3,4-diClPh SO _Two Single bond unit 67 2-4116 unit 53 3,4-diClPh SO _Two Single bond device 68 2-4117 device 53 3,4-diClPh SO _Two Single bond unit 69 2-4118 unit 53 3,4-diClPh SO _Two Single bond device 70 2-4119 device 53 3,4-diClPh SO _Two Single bond unit 71 2-4120 unit 53 3,4-diClPh SO _Two Single bond unit 72 2-4121 unit 53 3,4-diClPh SO _Two Single bond unit 73 2-4122 unit 53 3,4-diClPh SO _Two Single bond unit 74 2-4123 unit 53 3,4-diClPh SO _Two Single bond unit 75 2-4124 unit 53 3,4-diClPh SO _Two Single bond unit 76 2-4125 unit 53 3,4-diClPh SO _Two Single bond unit 77 2-4126 unit 53 3,4-diClPh SO _Two Single bond unit 78 2-4127 unit 53 3,4-diClPh SO _Two Single bond device 79 2-4128 device 53 3,4-diClPh SO _Two Single bond position 80 化合物 Compound number R ¹ R ^Two ABZＺ2-4129 Place 54 3,4-diClPh SO _Two Single bond device 1 2-4130 device 54 3,4-diClPh SO _Two Single bond device 2 2-4131 device 54 3,4-diClPh SO _Two Single bond device 3 2-4132 device 54 3,4-diClPh SO _Two Single bond unit 4 2-4133 unit 54 3,4-diClPh SO _Two Single bond device 5 2-4134 device 54 3,4-diClPh SO _Two Single bond device 6 2-4135 device 54 3,4-diClPh SO _Two Single bond device 7 2-4136 device 54 3,4-diClPh SO _Two Single bond device 8 2-4137 device 54 3,4-diClPh SO _Two Single bond device 9 2-4138 device 54 3,4-diClPh SO _Two Single bond device 10 2-4139 device 54 3,4-diClPh SO _Two Single bond unit 11 2-4140 unit 54 3,4-diClPh SO _Two Single bond unit 12 2-4141 unit 54 3,4-diClPh SO _Two Single bond unit 13 2-4142 unit 54 3,4-diClPh SO _Two Single bond unit 14 2-4143 unit 54 3,4-diClPh SO _Two Single bond unit 15 2-4144 unit 54 3,4-diClPh SO _Two Single bond unit 16 2-4145 unit 54 3,4-diClPh SO _Two Single bond unit 17 2-4146 unit 54 3,4-diClPh SO _Two Single bond unit 18 2-4147 unit 54 3,4-diClPh SO _Two Single bond unit 19 2-4148 unit 54 3,4-diClPh SO _Two Single bond unit 20 2-4149 unit 54 3,4-diClPh SO _Two Single bond unit 21 2-4150 unit 54 3,4-diClPh SO _Two Single bond unit 22 2-4151 unit 54 3,4-diClPh SO _Two Single bond unit 23 2-4152 unit 54 3,4-diClPh SO _Two Single bond unit 24 2-4153 unit 54 3,4-diClPh SO _Two Single bond unit 25 2-4154 unit 54 3,4-diClPh SO _Two Single bond unit 26 2-4155 unit 54 3,4-diClPh SO _Two Single bond unit 27 2-4156 unit 54 3,4-diClPh SO _Two Single bond unit 28 2-4157 unit 54 3,4-diClPh SO _Two Single bond unit 29 2-4158 unit 54 3,4-diClPh SO _Two Single bond device 30 2-4159 device 54 3,4-diClPh SO _Two Single bond unit 31 2-4160 unit 54 3,4-diClPh SO _Two Single bond unit 32 2-4161 unit 54 3,4-diClPh SO _Two Single bond device 65 2-4162 device 54 3,4-diClPh SO _Two Single bond device 66 2-4163 device 54 3,4-diClPh SO _Two Single bond unit 67 2-4164 unit 54 3,4-diClPh SO _Two Single bond device 68 2-4165 device 54 3,4-diClPh SO _Two Single bond device 69 2-4166 device 54 3,4-diClPh SO _Two Single bond device 70 2-4167 device 54 3,4-diClPh SO _Two Single bond device 71 2-4168 device 54 3,4-diClPh SO _Two Single bond unit 72 2-4169 unit 54 3,4-diClPh SO _Two Single bond unit 73 2-4170 unit 54 3,4-diClPh SO _Two Single bond unit 74 2-4171 unit 54 3,4-diClPh SO _Two Single bond unit 75 2-4172 unit 54 3,4-diClPh SO _Two Single bond unit 76 2-4173 unit 54 3,4-diClPh SO _Two Single bond device 77 2-4174 device 54 3,4-diClPh SO _Two Single bond unit 78 2-4175 unit 54 3,4-diClPh SO _Two Single bond device 79 2-4176 device 54 3,4-diClPh SO _Two Single bond device 80 2-4177 device 55 3,4-diClPh SO _Two Single bond device 1 2-4178 device 55 3,4-diClPh SO _Two Single bond device 2 2-4179 device 55 3,4-diClPh SO _Two Single bond device 3 2-4180 device 55 3,4-diClPh SO _Two Single bond unit 4 2-4181 unit 55 3,4-diClPh SO _Two Single bond device 5 2-4182 device 55 3,4-diClPh SO _Two Single bond device 6 2-4183 device 55 3,4-diClPh SO _Two Single bond device 7 2-4184 device 55 3,4-diClPh SO _Two Single bond device 8 2-4185 device 55 3,4-diClPh SO _Two Single bond device 9 2-4186 device 55 3,4-diClPh SO _Two Single bond device 10 2-4187 device 55 3,4-diClPh SO _Two Single bond unit 11 2-4188 unit 55 3,4-diClPh SO _Two Single bond unit 12 2-4189 unit 55 3,4-diClPh SO _Two Single bond unit 13 2-4190 unit 55 3,4-diClPh SO _Two Single bond unit 14 2-4191 unit 55 3,4-diClPh SO _Two Single bond unit 15 2-4192 unit 55 3,4-diClPh SO _Two Single bond unit 16 2-4193 unit 55 3,4-diClPh SO _Two Single bond unit 17 2-4194 unit 55 3,4-diClPh SO _Two Single bond unit 18 2-4195 unit 55 3,4-diClPh SO _Two Single bond unit 19 2-4196 unit 55 3,4-diClPh SO _Two Single bond device 20 2-4197 device 55 3,4-diClPh SO _Two Single bond unit 21 2-4198 unit 55 3,4-diClPh SO _Two Single bond unit 22 2-4199 unit 55 3,4-diClPh SO _Two Single bond unit 23 2-4200 unit 55 3,4-diClPh SO _Two Single bond unit 24 2-4201 unit 55 3,4-diClPh SO _Two Single bond unit 25 2-4202 unit 55 3,4-diClPh SO _Two Single bond unit 26 2-4203 unit 55 3,4-diClPh SO _Two Single bond unit 27 2-4204 unit 55 3,4-diClPh SO _Two Single bond unit 28 2-4205 unit 55 3,4-diClPh SO _Two Single bond unit 29 2-4206 unit 55 3,4-diClPh SO _Two Single bond unit 30 2-4207 unit 55 3,4-diClPh SO _Two Single bond unit 31 2-4208 unit 55 3,4-diClPh SO _Two Single bond unit 32 2-4209 unit 55 3,4-diClPh SO _Two Single bond device 65 2-4210 device 55 3,4-diClPh SO _Two Single bond unit 66 2-4211 unit 55 3,4-diClPh SO _Two Single bond unit 67 2-4122 unit 55 3,4-diClPh SO _Two Single bond device 68 2-4213 device 55 3,4-diClPh SO _Two Single bond device 69 2-4214 device 55 3,4-diClPh SO _Two Single bond device 70 2-4215 device 55 3,4-diClPh SO _Two Single bond device 71 2-4216 device 55 3,4-diClPh SO _Two Single bond unit 72 2-4217 unit 55 3,4-diClPh SO _Two Single bond device 73 2-3218 device 55 3,4-diClPh SO _Two Single bond unit 74 2-4219 unit 55 3,4-diClPh SO _Two Single bond unit 75 2-4220 unit 55 3,4-diClPh SO _Two Single bond unit 76 2-4221 unit 55 3,4-diClPh SO _Two Single bond unit 77 2-4222 unit 55 3,4-diClPh SO _Two Single bond unit 78 2-4223 unit 55 3,4-diClPh SO _Two Single bond device 79 2-4224 device 55 3,4-diClPh SO _Two Single bond device 80 2-4225 device 56 3,4-diClPh SO _Two Single bond device 1 2-4226 device 56 3,4-diClPh SO _Two Single bond device 2 2-4227 device 56 3,4-diClPh SO _Two Single bond device 32-4228 device 56 3,4-diClPh SO _Two Single bond device 4 2-4229 device 56 3,4-diClPh SO _Two Single bond device 5 2-4230 device 56 3,4-diClPh SO _Two Single bond device 6 2-4231 device 56 3,4-diClPh SO _Two Single bond device 7 2-4232 device 56 3,4-diClPh SO _Two Single bond device 8 2-4233 device 56 3,4-diClPh SO _Two Single bond device 9 2-4234 device 56 3,4-diClPh SO _Two Single bond device 10 2-4235 device 56 3,4-diClPh SO _Two Single bond device 11 2-4236 device 56 3,4-diClPh SO _Two Single bond unit 12 2-4237 unit 56 3,4-diClPh SO _Two Single bond unit 13 2-4238 unit 56 3,4-diClPh SO _Two Single bond unit 14 2-4239 unit 56 3,4-diClPh SO _Two Single bond unit 15 2-4240 unit 56 3,4-diClPh SO _Two Single bond unit 16 2-4241 unit 56 3,4-diClPh SO _Two Single bond unit 17 2-4242 unit 56 3,4-diClPh SO _Two Single bond unit 18 2-4243 unit 56 3,4-diClPh SO _Two Single bond unit 19 2-4244 unit 56 3,4-diClPh SO _Two Single bond unit 20 2-4245 unit 56 3,4-diClPh SO _Two Single bond unit 21 2-4246 unit 56 3,4-diClPh SO _Two Single bond unit 22-4247 unit 56 3,4-diClPh SO _Two Single bond unit 23 2-4248 unit 56 3,4-diClPh SO _Two Single bond unit 24 2-4249 unit 56 3,4-diClPh SO _Two Single bond unit 25 2-4250 unit 56 3,4-diClPh SO _Two Single bond unit 26 2-4251 unit 56 3,4-diClPh SO _Two Single bond unit 27 2-4252 unit 56 3,4-diClPh SO _Two Single bond unit 28 2-4253 unit 56 3,4-diClPh SO _Two Single bond unit 29 2-4254 unit 56 3,4-diClPh SO _Two Single bond device 30 2-4255 device 56 3,4-diClPh SO _Two Single bond unit 31 2-4256 unit 56 3,4-diClPh SO _Two Single bond unit 32 2-4257 unit 56 3,4-diClPh SO _Two Single bond device 65 2-4258 device 56 3,4-diClPh SO _Two Single bond device 66 2-4259 device 56 3,4-diClPh SO _Two Single bond unit 67 2-4260 unit 56 3,4-diClPh SO _Two Single bond device 68 2-4261 device 56 3,4-diClPh SO _Two Single bond unit 69 2-4262 unit 56 3,4-diClPh SO _Two Single bond device 70 2-4263 device 56 3,4-diClPh SO _Two Single bond unit 71 2-4264 unit 56 3,4-diClPh SO _Two Single bond unit 72 2-4265 unit 56 3,4-diClPh SO _Two Single bond unit 73 2-4266 unit 56 3,4-diClPh SO _Two Single bond unit 74 2-4267 unit 56 3,4-diClPh SO _Two Single bond unit 75 2-4268 unit 56 3,4-diClPh SO _Two Single bond device 76 2-4269 device 56 3,4-diClPh SO _Two Single bond unit 77 2-4270 unit 56 3,4-diClPh SO _Two Single bond unit 78 2-4271 unit 56 3,4-diClPh SO _Two Single bond device 79 2-4272 device 56 3,4-diClPh SO _Two Single bond device 80 2-4273 device 57 3,4-diClPh SO _Two Single bond device 1 2-4274 device 57 3,4-diClPh SO _Two Single bond device 22-4275 device 57 3,4-diClPh SO _Two Single bond device 3 2-4276 device 57 3,4-diClPh SO _Two Single bond device 4 2-4277 device 57 3,4-diClPh SO _Two Single bond device 5 2-4278 device 57 3,4-diClPh SO _Two Single bond device 6 2-4279 device 57 3,4-diClPh SO _Two Single bond device 7 2-4280 device 57 3,4-diClPh SO _Two Single bond device 8 2-4281 device 57 3,4-diClPh SO _Two Single bond device 9 2-4282 device 57 3,4-diClPh SO _Two Single bond unit 10 2-4283 unit 57 3,4-diClPh SO _Two Single bond unit 11 2-4284 unit 57 3,4-diClPh SO _Two Single bond unit 12 2-4285 unit 57 3,4-diClPh SO _Two Single bond unit 13 2-4286 unit 57 3,4-diClPh SO _Two Single bond unit 14 2-4287 unit 57 3,4-diClPh SO _Two Single bond unit 15 2-4288 unit 57 3,4-diClPh SO _Two Single bond Unit 16 2-4289 Unit 57 3,4-diClPh SO _Two Single bond unit 17 2-4290 unit 57 3,4-diClPh SO _Two Single bond unit 18 2-4291 unit 57 3,4-diClPh SO _Two Single bond unit 19 2-4292 unit 57 3,4-diClPh SO _Two Single bond unit 20 2-4293 unit 57 3,4-diClPh SO _Two Single bond unit 21 2-4294 unit 57 3,4-diClPh SO _Two Single bond unit 22 2-4295 unit 57 3,4-diClPh SO _Two Single bond unit 23 2-4296 unit 57 3,4-diClPh SO _Two Single bond unit 24 2-4297 unit 57 3,4-diClPh SO _Two Single bond unit 25 2-4298 unit 57 3,4-diClPh SO _Two Single bond unit 26 2-4299 unit 57 3,4-diClPh SO _Two Single bond unit 27 2-4300 unit 57 3,4-diClPh SO _Two Single bond unit 28 2-4301 unit 57 3,4-diClPh SO _Two Single bond unit 29 2-4302 unit 57 3,4-diClPh SO _Two Single bond unit 30 2-4303 unit 57 3,4-diClPh SO _Two Single bond unit 31 2-4304 unit 57 3,4-diClPh SO _Two Single bond unit 32 2-4305 unit 57 3,4-diClPh SO _Two Single bond device 65 2-4306 device 57 3,4-diClPh SO _Two Single bond unit 66 2-4307 unit 57 3,4-diClPh SO _Two Single bond unit 67 2-4308 unit 57 3,4-diClPh SO _Two Single bond device 68 2-4309 device 57 3,4-diClPh SO _Two Single bond device 69 2-4310 device 57 3,4-diClPh SO _Two Single bond device 70 2-4311 device 57 3,4-diClPh SO _Two Single bond device 71 2-4312 device 57 3,4-diClPh SO _Two Single bond device 72 2-313 device 57 3,4-diClPh SO _Two Single bond device 73 2-4314 device 57 3,4-diClPh SO _Two Single bond device 74 2-4315 device 57 3,4-diClPh SO _Two Single bond unit 75 2-4316 unit 57 3,4-diClPh SO _Two Single bond device 76 2-4317 device 57 3,4-diClPh SO _Two Single bond unit 77 2-4318 unit 57 3,4-diClPh SO _Two Single bond device 78 2-4319 device 57 3,4-diClPh SO _Two Single bond device 79 2-4320 device 57 3,4-diClPh SO _Two Single bond device 80 2-4321 device 58 3,4-diClPh SO _Two Single bond device 1 2-4322 device 58 3,4-diClPh SO _Two Single bond device 2 2-4323 device 58 3,4-diClPh SO _Two Single bond device 3 2-4324 device 58 3,4-diClPh SO _Two Single bond device 4 2-4325 device 58 3,4-diClPh SO _Two Single bond 5 2-4326 5 58 3,4-diClPh SO _Two Single bond device 6 2-4327 device 58 3,4-diClPh SO _Two Single bond device 7 2-4328 device 58 3,4-diClPh SO _Two Single bond device 8 2-4329 device 58 3,4-diClPh SO _Two Single bond device 9 2-4330 device 58 3,4-diClPh SO _Two Single bond unit 10 2-4331 unit 58 3,4-diClPh SO _Two Single bond unit 11 2-4332 unit 58 3,4-diClPh SO _Two Single bond unit 12 2-4333 unit 58 3,4-diClPh SO _Two Single bond unit 13 2-4334 unit 58 3,4-diClPh SO _Two Single bond unit 14 2-4335 unit 58 3,4-diClPh SO _Two Single bond unit 15 2-4336 unit 58 3,4-diClPh SO _Two Single bond unit 16 2-4337 unit 58 3,4-diClPh SO _Two Single bond unit 17 2-4338 unit 58 3,4-diClPh SO _Two Single bond unit 18 2-4339 unit 58 3,4-diClPh SO _Two Single bond unit 19 2-4340 unit 58 3,4-diClPh SO _Two Single bond unit 20 2-4341 unit 58 3,4-diClPh SO _Two Single bond unit 21 2-4342 unit 58 3,4-diClPh SO _Two Single bond unit 22 2-4343 unit 58 3,4-diClPh SO _Two Single bond unit 23 2-4344 unit 58 3,4-diClPh SO _Two Single bond unit 24 2-4345 unit 58 3,4-diClPh SO _Two Single bond device 25 2-4346 device 58 3,4-diClPh SO _Two Single bond unit 26 2-4347 unit 58 3,4-diClPh SO _Two Single bond unit 27 2-4348 unit 58 3,4-diClPh SO _Two Single bond unit 28 2-4349 unit 58 3,4-diClPh SO _Two Single bond unit 29 2-4350 unit 58 3,4-diClPh SO _Two Single bond device 30 2-4351 device 58 3,4-diClPh SO _Two Single bond unit 31 2-4352 unit 58 3,4-diClPh SO _Two Single bond unit 32 2-4353 unit 58 3,4-diClPh SO _Two Single bond device 65 2-4354 device 58 3,4-diClPh SO _Two Single bond device 66 2-4355 device 58 3,4-diClPh SO _Two Single bond unit 67 2-4356 unit 58 3,4-diClPh SO _Two Single bond device 68 2-4357 device 58 3,4-diClPh SO _Two Single bond device 69 2-4358 device 58 3,4-diClPh SO _Two Single bond device 70 2-4359 device 58 3,4-diClPh SO _Two Single bond unit 71 2-4360 unit 58 3,4-diClPh SO _Two Single bond unit 72 2-4361 unit 58 3,4-diClPh SO _Two Single bond device 73 2-4362 device 58 3,4-diClPh SO _Two Single bond unit 74 2-4363 unit 58 3,4-diClPh SO _Two Single bond unit 75 2-4364 unit 58 3,4-diClPh SO _Two Single bond unit 76 2-4365 unit 58 3,4-diClPh SO _Two Single bond unit 77 2-4366 unit 58 3,4-diClPh SO _Two Single bond unit 78 2-4367 unit 58 3,4-diClPh SO _Two Single bond device 79 2-4368 device 58 3,4-diClPh SO _Two Single bond device 80 2-4369 device 59 3,4-diClPh SO _Two Single bond device 1 2-4370 device 59 3,4-diClPh SO _Two Single bond unit 2 2-4371 unit 59 3,4-diClPh SO _Two Single bond unit 3 2-4372 unit 59 3,4-diClPh SO _Two Single bond unit 4 2-4373 unit 59 3,4-diClPh SO _Two Single bond device 5 2-4374 device 59 3,4-diClPh SO _Two Single bond unit 6 2-4375 unit 59 3,4-diClPh SO _Two Single bond device 7 2-4376 device 59 3,4-diClPh SO _Two Single bond device 8 2-4377 device 59 3,4-diClPh SO _Two Single bond device 9 2-4378 device 59 3,4-diClPh SO _Two Single bond device 10 2-4379 device 59 3,4-diClPh SO _Two Single bond unit 11 2-4380 unit 59 3,4-diClPh SO _Two Single bond unit 12 2-4381 unit 59 3,4-diClPh SO _Two Single bond unit 13 2-4382 unit 59 3,4-diClPh SO _Two Single bond unit 14 2-4383 unit 59 3,4-diClPh SO _Two Single bond unit 15 2-4384 unit 59 3,4-diClPh SO _Two Single bond unit 16 2-4385 unit 59 3,4-diClPh SO _Two Single bond unit 17 2-4386 unit 59 3,4-diClPh SO _Two Single bond unit 18 2-4387 unit 59 3,4-diClPh SO _Two Single bond unit 19 2-4388 unit 59 3,4-diClPh SO _Two Single bond unit 20 2-4389 unit 59 3,4-diClPh SO _Two Single bond unit 21 2-4390 unit 59 3,4-diClPh SO _Two Single bond unit 22 2-4391 unit 59 3,4-diClPh SO _Two Single bond unit 23 2-3392 unit 59 3,4-diClPh SO _Two Single bond unit 24 2-4393 unit 59 3,4-diClPh SO _Two Single bond unit 25 2-4394 unit 59 3,4-diClPh SO _Two Single bond unit 26 2-4395 unit 59 3,4-diClPh SO _Two Single bond unit 27 2-4396 unit 59 3,4-diClPh SO _Two Single bond unit 28 2-4397 unit 59 3,4-diClPh SO _Two Single bond unit 29 2-4398 unit 59 3,4-diClPh SO _Two Single bond device 30 2-4399 device 59 3,4-diClPh SO _Two Single bond unit 31 2-4400 unit 59 3,4-diClPh SO _Two Single bond unit 32 2-4401 unit 59 3,4-diClPh SO _Two Single bond device 65 2-4402 device 59 3,4-diClPh SO _Two Single bond unit 66 2-4403 unit 59 3,4-diClPh SO _Two Single bond unit 67 2-4404 unit 59 3,4-diClPh SO _Two Single bond device 68 2-4405 device 59 3,4-diClPh SO _Two Single bond device 69 2-4406 device 59 3,4-diClPh SO _Two Single bond unit 70 2-4407 unit 59 3,4-diClPh SO _Two Single bond unit 71 2-4408 unit 59 3,4-diClPh SO _Two Single bond unit 72 2-4409 unit 59 3,4-diClPh SO _Two Single bond unit 73 2-34410 unit 59 3,4-diClPh SO _Two Single bond device 74 2-4411 device 59 3,4-diClPh SO _Two Single bond unit 75 2-4412 unit 59 3,4-diClPh SO _Two Single bond unit 76 2-4413 unit 59 3,4-diClPh SO _Two Single bond device 77 2-4414 device 59 3,4-diClPh SO _Two Single bond unit 78 2-4415 unit 59 3,4-diClPh SO _Two Single bond device 79 2-4416 device 59 3,4-diClPh SO _Two Single bond device 80 2-4417 device 82 3,4-diClPh SO _Two Single bond device 1 2-4418 device 82 3,4-diClPh SO _Two Single bond device 2 2-4419 device 82 3,4-diClPh SO _Two Single bond device 3 2-4420 device 82 3,4-diClPh SO _Two Single bond device 4 2-4421 device 82 3,4-diClPh SO _Two Single bond device 5 2-4422 device 82 3,4-diClPh SO _Two Single bond device 6 2-4423 device 82 3,4-diClPh SO _Two Single bond device 7 2-4424 device 82 3,4-diClPh SO _Two Single bond device 8 2-4425 device 82 3,4-diClPh SO _Two Single bond device 9 2-4426 device 82 3,4-diClPh SO _Two Single bond device 10 2-4427 device 82 3,4-diClPh SO _Two Single bond unit 11 2-4428 unit 82 3,4-diClPh SO _Two Single bond unit 12 2-4429 unit 82 3,4-diClPh SO _Two Single bond unit 13 2-4430 unit 82 3,4-diClPh SO _Two Single bond unit 14 2-4431 unit 82 3,4-diClPh SO _Two Single bond unit 15 2-4432 unit 82 3,4-diClPh SO _Two Single bond unit 16 2-4433 unit 82 3,4-diClPh SO _Two Single bond unit 17 2-4434 unit 82 3,4-diClPh SO _Two Single bond unit 18 2-4435 unit 82 3,4-diClPh SO _Two Single bond unit 19 2-4436 unit 82 3,4-diClPh SO _Two Single bond unit 20 2-4437 unit 82 3,4-diClPh SO _Two Single bond unit 21 2-4438 unit 82 3,4-diClPh SO _Two Single bond unit 22 2-4439 unit 82 3,4-diClPh SO _Two Single bond unit 23 2-4440 unit 82 3,4-diClPh SO _Two Single bond unit 24 2-4441 unit 82 3,4-diClPh SO _Two Single bond unit 25 2-4442 unit 82 3,4-diClPh SO _Two Single bond unit 26 2-4443 unit 82 3,4-diClPh SO _Two Single bond unit 27 2-4444 unit 82 3,4-diClPh SO _Two Single bond unit 28 2-4445 unit 82 3,4-diClPh SO _Two Single bond unit 29 2-4446 unit 82 3,4-diClPh SO _Two Single bond device 30 2-4447 device 82 3,4-diClPh SO _Two Single bond unit 31 2-4448 unit 82 3,4-diClPh SO _Two Single bond unit 32 2-3449 unit 82 3,4-diClPh SO _Two Single bond device 65 2-4450 device 82 3,4-diClPh SO _Two Single bond device 66 2-4451 device 82 3,4-diClPh SO _Two Single bond unit 67 2-4452 unit 82 3,4-diClPh SO _Two Single bond device 68 2-4453 device 82 3,4-diClPh SO _Two Single bond device 69 2-4454 device 82 3,4-diClPh SO _Two Single bond device 70 2-4455 device 82 3,4-diClPh SO _Two Single bond device 71 2-4456 device 82 3,4-diClPh SO _Two Single bond unit 72 2-4457 unit 82 3,4-diClPh SO _Two Single bond unit 73 2-3458 unit 82 3,4-diClPh SO _Two Single bond unit 74 2-4459 unit 82 3,4-diClPh SO _Two Single bond unit 75 2-4460 unit 82 3,4-diClPh SO _Two Single bond unit 76 2-4461 unit 82 3,4-diClPh SO _Two Single bond unit 77 2-4462 unit 82 3,4-diClPh SO _Two Single bond unit 78 2-4463 unit 82 3,4-diClPh SO _Two Single bond device 79 2-4464 device 82 3,4-diClPh SO _Two Single bond device 80 2-4465 device 83 3,4-diClPh SO _Two Single bond device 1 2-4466 device 83 3,4-diClPh SO _Two Single bond device 2 2-4467 device 83 3,4-diClPh SO _Two Single bond device 3 2-4468 device 83 3,4-diClPh SO _Two Single bond device 4 2-4469 device 83 3,4-diClPh SO _Two Single bond device 5 2-4470 device 83 3,4-diClPh SO _Two Single bond device 6 2-4491 device 83 3,4-diClPh SO _Two Single bond device 7 2-4472 device 83 3,4-diClPh SO _Two Single bond device 8 2-4473 device 83 3,4-diClPh SO _Two Single bond unit 9 2-4474 unit 83 3,4-diClPh SO _Two Single bond device 10 2-4475 device 83 3,4-diClPh SO _Two Single bond unit 11 2-4476 unit 83 3,4-diClPh SO _Two Single bond unit 12 2-4777 unit 83 3,4-diClPh SO _Two Single bond unit 13 2-4478 unit 83 3,4-diClPh SO _Two Single bond unit 14 2-4479 unit 83 3,4-diClPh SO _Two Single bond unit 15 2-4480 unit 83 3,4-diClPh SO _Two Single bond unit 16 2-4481 unit 83 3,4-diClPh SO _Two Single bond unit 17 2-4482 unit 83 3,4-diClPh SO _Two Single bond unit 18 2-4483 unit 83 3,4-diClPh SO _Two Single bond unit 19 2-4484 unit 83 3,4-diClPh SO _Two Single bond device 20 2-4485 device 83 3,4-diClPh SO _Two Single bond unit 21 2-4486 unit 83 3,4-diClPh SO _Two Single bond unit 22-4487 unit 83 3,4-diClPh SO _Two Single bond unit 23 2-3488 unit 83 3,4-diClPh SO _Two Single bond unit 24 2-4489 unit 83 3,4-diClPh SO _Two Single bond unit 25 2-4490 unit 83 3,4-diClPh SO _Two Single bond unit 26 2-4491 unit 83 3,4-diClPh SO _Two Single bond unit 27 2-4492 unit 83 3,4-diClPh SO _Two Single bond unit 28 2-4493 unit 83 3,4-diClPh SO _Two Single bond unit 29 2-4494 unit 83 3,4-diClPh SO _Two Single bond device 30 2-4495 device 83 3,4-diClPh SO _Two Single bond device 31 2-4496 device 83 3,4-diClPh SO _Two Single bond unit 32 2-4497 unit 83 3,4-diClPh SO _Two Single bond device 65 2-4498 device 83 3,4-diClPh SO _Two Single bond device 66 2-4499 device 83 3,4-diClPh SO _Two Single bond unit 67 2-4500 unit 83 3,4-diClPh SO _Two Single bond device 68 2-4501 device 83 3,4-diClPh SO _Two Single bond unit 69 2-4502 unit 83 3,4-diClPh SO _Two Single bond unit 70 2-4503 unit 83 3,4-diClPh SO _Two Single bond unit 71 2-4504 unit 83 3,4-diClPh SO _Two Single bond unit 72 2-4505 unit 83 3,4-diClPh SO _Two Single bond unit 73 2-3506 Unit 83 3,4-diClPh SO _Two Single bond device 74 2-4507 device 83 3,4-diClPh SO _Two Single bond unit 75 2-4508 unit 83 3,4-diClPh SO _Two Single bond unit 76 2-4509 unit 83 3,4-diClPh SO _Two Single bond unit 77 2-4510 unit 83 3,4-diClPh SO _Two Single bond unit 78 2-4511 unit 83 3,4-diClPh SO _Two Single bond device 79 2-4512 device 83 3,4-diClPh SO _Two Single bond device 80 2-4513 device 61 3,4-diClPh SO _Two Single bond device 1 2-4514 device 61 3,4-diClPh SO _Two Single bond unit 22-4515 unit 61 3,4-diClPh SO _Two Single bond device 3 2-4516 device 61 3,4-diClPh SO _Two Single bond device 4 2-4517 device 61 3,4-diClPh SO _Two Single bond device 5 2-4518 device 61 3,4-diClPh SO _Two Single bond device 6 2-4519 device 61 3,4-diClPh SO _Two Single bond device 7 2-4520 device 61 3,4-diClPh SO _Two Single bond device 8 2-4521 device 61 3,4-diClPh SO _Two Single bond device 9 2-4522 device 61 3,4-diClPh SO _Two Single bond device 10 2-4523 device 61 3,4-diClPh SO _Two Single bond unit 11 2-4524 unit 61 3,4-diClPh SO _Two Single bond Unit 12 2-4525 Unit 61 3,4-diClPh SO _Two Single bond unit 13 2-4526 unit 61 3,4-diClPh SO _Two Single bond unit 14 2-4527 unit 61 3,4-diClPh SO _Two Single bond device 15 2-4528 device 61 3,4-diClPh SO _Two Single bond Unit 16 2-4529 Unit 61 3,4-diClPh SO _Two Single bond unit 17 2-4530 unit 61 3,4-diClPh SO _Two Single bond unit 18 2-4531 unit 61 3,4-diClPh SO _Two Single bond unit 19 2-4532 unit 61 3,4-diClPh SO _Two Single bond unit 20 2-4533 unit 61 3,4-diClPh SO _Two Single bond unit 21 2-4534 unit 61 3,4-diClPh SO _Two Single bond unit 22 2-4353 unit 61 3,4-diClPh SO _Two Single bond unit 23 2-4536 unit 61 3,4-diClPh SO _Two Single bond unit 24 2-4537 unit 61 3,4-diClPh SO _Two Single bond unit 25 2-4538 unit 61 3,4-diClPh SO _Two Single bond unit 26 2-4539 unit 61 3,4-diClPh SO _Two Single bond unit 27 2-4540 unit 61 3,4-diClPh SO _Two Single bond unit 28 2-4541 unit 61 3,4-diClPh SO _Two Single bond unit 29 2-4542 unit 61 3,4-diClPh SO _Two Single bond device 30 2-4543 device 61 3,4-diClPh SO _Two Single bond unit 31 2-4544 unit 61 3,4-diClPh SO _Two Single bond unit 32 2-4545 unit 61 3,4-diClPh SO _Two Single bond device 65 2-4546 device 61 3,4-diClPh SO _Two Single bond device 66 2-4547 device 61 3,4-diClPh SO _Two Single bond device 67 2-4548 device 61 3,4-diClPh SO _Two Single bond device 68 2-4549 device 61 3,4-diClPh SO _Two Single bond device 69 2-4550 device 61 3,4-diClPh SO _Two Single bond unit 70 2-4551 unit 61 3,4-diClPh SO _Two Single bond unit 71 2-4552 unit 61 3,4-diClPh SO _Two Single bond unit 72 2-4553 unit 61 3,4-diClPh SO _Two Single bond unit 73 2-4554 unit 61 3,4-diClPh SO _Two Single bond unit 74 2-4555 unit 61 3,4-diClPh SO _Two Single bond device 75 2-4556 device 61 3,4-diClPh SO _Two Single bond unit 76 2-4557 unit 61 3,4-diClPh SO _Two Single bond device 77 2-4558 device 61 3,4-diClPh SO _Two Single bond unit 78 2-4559 unit 61 3,4-diClPh SO _Two Single bond device 79 2-4560 device 61 3,4-diClPh SO _Two Single bond device 80 2-4561 device 60 3,4-diClPh SO _Two Single bond device 1 2-4562 device 60 3,4-diClPh SO _Two Single bond device 2 2-4563 device 60 3,4-diClPh SO _Two Single bond device 3 2-4564 device 60 3,4-diClPh SO _Two Single bond unit 4 2-4565 unit 60 3,4-diClPh SO _Two Single bond device 5 2-4566 device 60 3,4-diClPh SO _Two Single bond device 6 2-4567 device 60 3,4-diClPh SO _Two Single bond device 7 2-4568 device 60 3,4-diClPh SO _Two Single bond device 8 2-4569 device 60 3,4-diClPh SO _Two Single bond device 9 2-4570 device 60 3,4-diClPh SO _Two Single bond device 10 2-4571 device 60 3,4-diClPh SO _Two Single bond unit 11 2-4572 unit 60 3,4-diClPh SO _Two Single bond unit 12 2-4573 unit 60 3,4-diClPh SO _Two Single bond unit 13 2-4574 unit 60 3,4-diClPh SO _Two Single bond unit 14 2-4575 unit 60 3,4-diClPh SO _Two Single bond unit 15 2-4576 unit 60 3,4-diClPh SO _Two Single bond unit 16 2-4577 unit 60 3,4-diClPh SO _Two Single bond Unit 17 2-4578 Unit 60 3,4-diClPh SO _Two Single bond Unit 18 2-4579 Unit 60 3,4-diClPh SO _Two Single bond unit 19 2-4580 unit 60 3,4-diClPh SO _Two Single bond unit 20 2-4581 unit 60 3,4-diClPh SO _Two Single bond unit 21 2-4582 unit 60 3,4-diClPh SO _Two Single bond unit 22 2-4583 unit 60 3,4-diClPh SO _Two Single bond unit 23 2-4584 unit 60 3,4-diClPh SO _Two Single bond unit 24 2-4585 unit 60 3,4-diClPh SO _Two Single bond unit 25 2-4586 unit 60 3,4-diClPh SO _Two Single bond unit 26 2-4587 unit 60 3,4-diClPh SO _Two Single bond Unit 27 2-4588 Unit 60 3,4-diClPh SO _Two Single bond unit 28 2-4589 unit 60 3,4-diClPh SO _Two Single bond unit 29 2-4590 unit 60 3,4-diClPh SO _Two Single bond device 30 2-4591 device 60 3,4-diClPh SO _Two Single bond unit 31 2-4592 unit 60 3,4-diClPh SO _Two Single bond unit 32 2-4593 unit 60 3,4-diClPh SO _Two Single bond device 65 2-4594 device 60 3,4-diClPh SO _Two Single bond device 66 2-4595 device 60 3,4-diClPh SO _Two Single bond device 67 2-4596 device 60 3,4-diClPh SO _Two Single bond device 68 2-4597 device 60 3,4-diClPh SO _Two Single bond device 69 2-4598 device 60 3,4-diClPh SO _Two Single bond device 70 2-4599 device 60 3,4-diClPh SO _Two Single bond unit 71 2-4600 unit 60 3,4-diClPh SO _Two Single bond unit 72 2-4601 unit 60 3,4-diClPh SO _Two Single bond device 73 2-4602 device 60 3,4-diClPh SO _Two Single bond unit 74 2-4603 unit 60 3,4-diClPh SO _Two Single bond unit 75 2-4604 unit 60 3,4-diClPh SO _Two Single bond unit 76-2 4605 unit 60 3,4-diClPh SO _Two Single bond unit 77 2-4606 unit 60 3,4-diClPh SO _Two Single bond unit 78 2-4607 unit 60 3,4-diClPh SO _Two Single bond device 79 79 4608 device 60 3,4-diClPh SO _Two Single bond device 80 ────────────────────────────────────

[0460]

[Table 3] ──────────────────────────────────── Compound No. R ¹ R ^Two ABEZ 3-1 Place 33 3,4-diClPh -CO- single bond -CH _Two -App. 84 3-2 App. 34 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-3 App. 35 3,4-diClPh -CO- Single bond -CH _Two -App.84 3-4 App.36 3,4-diClPh -CO- Single bond -CH _Two -App.84 3-5 App.37 3,4-diClPh -CO- Single bond -CH _Two -App.84 3-6 App.38 3,4-diClPh -CO- Single bond -CH _Two -App.84 3-7 App.39 3,4-diClPh -CO- Single bond -CH _Two -App.84 3-8 App.40 3,4-diClPh -CO- Single bond -CH _Two -App 84 3-9 App 41 3,4-diClPh -CO- Single bond -CH _Two -App 84 3-10 App 42 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-11 App. 60 3,4-diClPh -CO- Single bond -CH _Two -Fig. 84 3-12 Fig. 43 3,4-diClPh -CO- Single bond -CH _Two -App 84 3-13 App 44 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-14 App. 45 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-15 App. 46 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-16 App. 47 3,4-diClPh -CO- Single bond -CH _Two -App 84 3-17 App 81 3,4-diClPh -CO- Single bond -CH _Two -App.84 3-18 App.48 3,4-diClPh -CO- Single bond -CH _Two -Fig. 84 3-19 Fig. 49 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-20 App. 50 3,4-diClPh -CO- Single bond -CH _Two -Fig. 84 3-21 Fig. 51 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-22 App. 52 3,4-diClPh -CO- Single bond -CH _Two -Fig. 84 3-23 Fig. 53 3,4-diClPh -CO- Single bond -CH _Two -App.84 3-24 App.54 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-25 App. 56 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-26 App. 57 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-27 App. 58 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-28 App. 59 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-29 App. 82 3,4-diClPh -CO- Single bond -CH _Two -Fig. 84 3-30 Fig. 83 3,4-diClPh -CO- Single bond -CH _Two -App 84 3-31 App 61 3,4-diClPh -CO- Single bond -CH _Two -App. 84 3-32 App. 55 3,4-diClPh -CO- Single bond -CH _Two -Fig. 84 3-33 Fig. 33 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-34 App. 34 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-35 App. 35 3,4-diClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-36 Fig. 36 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-37 App. 37 3,4-diClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-38 Fig. 38 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-39 App. 39 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-40 App. 40 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-41 App. 41 3,4-diClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-42 Fig. 42 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-43 App. 60 3,4-diClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-44 Fig. 43 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-45 App. 44 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-46 App. 45 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-47 App. 46 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-48 App. 47 3,4-diClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-49 Fig. 81 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App.84 3-50 App.48 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-51 App. 49 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-52 App. 50 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-53 App. 51 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-54 App. 52 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-55 App. 53 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-56 App. 54 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-57 App. 56 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-58 App. 57 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-59 App. 58 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-60 App. 59 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-61 App. 82 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-62 App. 83 3,4-diClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-63 Fig. 61 3,4-diClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-64 App. 55 3,4-diClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-65 Fig. 33 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-66 Fig. 34 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-67 Fig. 35 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-68 Fig. 36 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-69 Fig. 37 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-70 Fig. 38 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-71 App. 39 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-72 App. 40 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-73 Fig. 41 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-74 Fig. 42 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-75 App. 60 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-76 Fig. 43 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-77 Fig. 44 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-78 App. 45 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-79 App. 46 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-80 App. 47 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-81 Fig. 81 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-82 Fig. 48 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-83 Fig. 49 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-84 Fig. 50 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-85 Fig. 51 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-86 Fig. 52 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-87 Fig. 53 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-88 Fig. 54 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-89 Fig. 56 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-90 Fig. 57 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-91 Fig. 58 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-92 App. 59 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-93 Fig. 82 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-94 Fig. 83 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-95 App. 61 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-96 App. 55 3,4-diClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-97 App. 33 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-98 App. 34 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-99 App. 35 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-100 App. 36 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-101 App. 37 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-102 App. 38 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-103 Fig. 39 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-104 App. 40 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-105 App. 41 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-106 App. 42 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-107 App. 60 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-108 App. 43 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-109 App. 44 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-110 App. 45 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-111 App. 46 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-112 App. 47 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-113 Fig. 81 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-114 App. 48 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-115 App. 49 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-116 App. 50 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-117 App. 51 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-118 App. 52 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-119 Fig. 53 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-120 App. 54 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-121 App. 56 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-122 App. 57 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-123 Fig. 58 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-124 App. 59 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-125 Fig. 82 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-126 Fig. 83 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-127 App. 61 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-128 App. 55 3,4-diClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-129 App. 33 3,4-diClPh -CO- Single bond -CH _Two - c Pr-place 84 3-130 place 34 3,4-diClPh -CO- single bond -CH _Two - c Pr-84 84 3-131 35 3,4-diClPh -CO- Single bond -CH _Two - c Pr-84 84 132 132 36 3,4-diClPh -CO- Single bond -CH _Two - c Pr-84 84-133 37 3,4-diClPh -CO- Single bond -CH _Two - c Pr-configuration 84 3-134 configuration 38 3,4-diClPh -CO- single bond -CH _Two - c Pr-84 84-135 39 39,4-diClPh -CO- Single bond -CH _Two - c Pr-84 84 3-136 40 3,4-diClPh -CO- Single bond -CH _Two - c Pr-84 84-137 41 41 3,4-diClPh -CO- Single bond -CH _Two - c Pr-position 84 3-138 Setting 42 3,4-diClPh -CO- Single bond -CH _Two - c Pr-84 84 3-139 60 3,4-diClPh -CO- Single bond -CH _Two - c Pr-84 84-140 43 3,4-diClPh -CO- Single bond -CH _Two - c Pr-configuration 84 3-141 configuration 44 3,4-diClPh -CO- single bond -CH _Two - c Pr- 84 84 142 142 45 3,4-diClPh -CO- single bond -CH _Two - c Pr-84 84-143 46 3,4-diClPh -CO- Single bond -CH _Two - c Pr-position 84 3-144 Position 47 3,4-diClPh -CO- Single bond -CH _Two - c Pr-configuration 84 3-145 configuration 81 3,4-diClPh -CO- single bond -CH _Two - c Pr-84 84-146 48 3,4-diClPh -CO- Single bond -CH _Two - c Pr-position 84 3-147 Position 49 3,4-diClPh -CO- Single bond -CH _Two - c Pr-place 84 3-148 place 50 3,4-diClPh -CO- single bond -CH _Two - c Pr-configuration 84 3-149 configuration 51 3,4-diClPh -CO- single bond -CH _Two - c Pr-position 84 3-150 Position 52 3,4-diClPh -CO- Single bond -CH _Two - c Pr-configuration 84 3-151 configuration 53 3,4-diClPh -CO- single bond -CH _Two - c Pr-position 84 3-152 Position 54 3,4-diClPh -CO- Single bond -CH _Two - c Pr-84 84 3-153 56 3,4-diClPh -CO- Single bond -CH _Two - c Pr-position 84 3-154 setting 57 3,4-diClPh -CO- single bond -CH _Two - c Pr-place 84 3-155 place 58 3,4-diClPh -CO- single bond -CH _Two - c Pr-place 84 3-156 place 59 3,4-diClPh -CO- single bond -CH _Two - c Pr-84 84 3-157 82 3,4-diClPh -CO- Single bond -CH _Two - c Pr-configuration 84 3-158 configuration 83 3,4-diClPh -CO- single bond -CH _Two - c Pr-place 84 3-159 place 61 3,4-diClPh -CO- single bond -CH _Two - c Pr-place 84 3-160 place 55 3,4-diClPh -CO- single bond -CH _Two - c Pr-configuration 84 3-161 configuration 33 3,4-diClPh -CO- single bond -CH _Two - c Bu-84 84 3-162 34 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-163 35 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-164 36 36,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-165 37 37,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-166 38 38,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-167 39 39,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-168 40 40,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-169 41 41 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-170 42 42,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-171 60 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-172 43 43,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-173 44 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-174 45 45,4-diClPh -CO- Single bond -CH _Two - c Bu-84-175 3-46 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-176 47 47,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-177 81 81 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-178 48 48,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-179 49 494-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-180 50 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-181 51 51,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-182 52 52,4-diClPh -CO- Single bond -CH _Two - c Bu-84-183 3-53 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-184 54 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-185 56 56 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84-186 3-57 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84-187 3-58 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84-188 3-59 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-189 82 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 190 19083 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84-191 61 61 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84-192 3-55 3,4-diClPh -CO- Single bond -CH _Two - c Bu-84 84 3-193 33 3,4-diClPh -CO- Single bond -CH _Two - c Pn- unit 84 3-194 unit 34 3,4-diClPh -CO- single bond -CH _Two - c Pn- device 84 3-195 device 35 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-196 unit 36 3,4-diClPh -CO- single bond -CH _Two - c Pn- device 84 3-197 device 37 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-198 unit 38 3,4-diClPh -CO- single bond -CH _Two - c Pn- device 84 3-199 device 39 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-200 unit 40 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-201 unit 41 3,4-diClPh -CO- single bond -CH _Two - c Pn- device 84 3-202 device 42 3,4-diClPh -CO- single bond -CH _Two - c Pn- device 84 3-203 device 60 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-204 unit 43 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-205 unit 44 3,4-diClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-206 configuration 45 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-207 unit 46 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-208 unit 47 3,4-diClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-209 configuration 81 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-210 unit 48 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-211 unit 49 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-212 unit 50 3,4-diClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-213 configuration 51 3,4-diClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-214 configuration 52 3,4-diClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-215 configuration 53 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-216 unit 54 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-217 unit 56 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-218 unit 57 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-219 unit 58 3,4-diClPh -CO- single bond -CH _Two - c Pn- device 84 3-220 device 59 3,4-diClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-221 configuration 82 3,4-diClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-222 configuration 83 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-223 unit 61 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-224 unit 55 3,4-diClPh -CO- single bond -CH _Two - c Pn- unit 84 3-225 unit 33 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-226 unit 34 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-227 unit 35 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-228 unit 36 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-230 unit 38 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-231 unit 39 3,4-diClPh -CO- single bond -CH _Two - c Hx- device 84 3-232 device 40 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-233 unit 41 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-234 unit 42 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-235 unit 60 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-236 unit 43 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-237 unit 44 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-238 unit 45 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-239 unit 46 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-240 unit 47 3,4-diClPh -CO- single bond -CH _Two - c Hx- configuration 84 3-241 configuration 81 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-242 unit 48 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-243 unit 49 3,4-diClPh -CO- single bond -CH _Two - c Hx- device 84 3-244 device 50 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-245 unit 51 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-246 unit 52 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-247 unit 53 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-248 unit 54 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-249 unit 56 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-250 unit 57 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-251 unit 58 3,4-diClPh -CO- single bond -CH _Two - c Hx- device 84 3-252 device 59 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-253 unit 82 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-254 unit 83 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-255 unit 61 3,4-diClPh -CO- single bond -CH _Two - c Hx- unit 84 3-256 unit 55 3,4-diClPh -CO- single bond -CH _Two - c Hx- configuration 84 3-257 configuration 33 4-ClPh -CO- single bond -CH _Two -App. 84 3-258 App. 34 4-ClPh -CO- Single bond -CH _Two -App. 84 3-259 App. 35 4-ClPh -CO- Single bond -CH _Two -App. 84 3-260 App. 36 4-ClPh -CO- Single bond -CH _Two -App. 84 3-261 App. 37 4-ClPh -CO- Single bond -CH _Two -App. 84 3-262 App. 38 4-ClPh -CO- Single bond -CH _Two -Fig. 84 3-263 Fig. 39 4-ClPh -CO- Single bond -CH _Two -App. 84 3-264 App. 40 4-ClPh -CO- Single bond -CH _Two -App. 84 3-265 App. 41 4-ClPh -CO- Single bond -CH _Two -App. 84 3-266 App. 42 4-ClPh -CO- Single bond -CH _Two -App. 84 3-267 App. 60 4-ClPh -CO- Single bond -CH _Two -App. 84 3-268 App. 43 4-ClPh -CO- Single bond -CH _Two -App. 84 3-269 App. 44 4-ClPh -CO- Single bond -CH _Two -App. 84 3-270 App. 45 4-ClPh -CO- Single bond -CH _Two -App. 84 3-271 App. 46 4-ClPh -CO- Single bond -CH _Two -App. 84 3-272 App. 47 4-ClPh -CO- Single bond -CH _Two -Fig. 84 3-273 Fig. 81 4-ClPh -CO- Single bond -CH _Two -App. 84 3-274 App. 48 4-ClPh -CO- Single bond -CH _Two -App. 84 3-275 App. 49 4-ClPh -CO- Single bond -CH _Two -App. 84 3-276 App. 50 4-ClPh -CO- Single bond -CH _Two -App. 84 3-277 App. 51 4-ClPh -CO- Single bond -CH _Two -App. 84 3-278 App. 52 4-ClPh -CO- Single bond -CH _Two -App. 84 3-279 App. 53 4-ClPh -CO- Single bond -CH _Two -App. 84 3-280 App. 54 4-ClPh -CO- Single bond -CH _Two -App. 84 3-281 App. 56 4-ClPh -CO- Single bond -CH _Two -App. 84 3-282 App. 57 4-ClPh -CO- Single bond -CH _Two -App. 84 3-283 App. 58 4-ClPh -CO- Single bond -CH _Two -App. 84 3-284 App. 59 4-ClPh -CO- Single bond -CH _Two -App. 84 3-285 App. 82 4-ClPh -CO- Single bond -CH _Two -App. 84 3-286 App. 83 4-ClPh -CO- Single bond -CH _Two -Fig. 84 3-287 Fig. 61 4-ClPh -CO- Single bond -CH _Two -App. 84 3-288 App. 55 4-ClPh -CO- Single bond -CH _Two -App. 84 3-289 App. 33 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-290 App. 34 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-291 App. 35 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-292 App. 36 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-293 App. 37 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-294 App. 38 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-295 App. 39 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-296 App. 40 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-297 App. 41 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-298 App. 42 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-299 App. 60 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-300 App. 43 4-ClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-301 Fig. 44 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-302 App. 45 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-303 App. 46 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-304 App. 47 4-ClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-305 Fig. 81 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-306 App. 48 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-307 App. 49 4-ClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-308 Fig. 50 4-ClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-309 Fig. 51 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-310 App. 52 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-311 App. 53 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-312 App. 54 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-313 App. 56 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-314 App. 57 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-315 App. 58 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-316 App. 59 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-317 App. 82 4-ClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-318 Fig. 83 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-319 App. 61 4-ClPh -CO- Single bond -CH _Two CH _Two -App. 84 3-320 App. 55 4-ClPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-321 Fig. 33 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-322 Fig. 34 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-323 Fig. 35 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-324 Fig. 36 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-325 Fig. 37 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-326 Fig. 38 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-327 Fig. 39 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-328 Fig. 40 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-329 Fig. 41 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-330 Fig. 42 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-331 Fig. 60 4-ClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-332 App. 43 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-333 Fig. 44 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-334 Fig. 45 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-335 Fig. 46 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-336 Fig. 47 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-337 Fig. 81 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-338 Fig. 48 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-339 Fig. 49 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-340 Fig. 50 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-341 Fig. 51 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-342 Fig. 52 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-343 Fig. 53 4-ClPh -CO- Single bond-(CH _Two ) _Three -App.84 3-344 App.54 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-345 Fig. 56 4-ClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-346 App. 57 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-347 Fig. 58 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-348 Fig. 59 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-349 Fig. 82 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-350 Fig. 83 4-ClPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-351 Fig. 61 4-ClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-352 App. 55 4-ClPh -CO- Single bond-(CH _Two ) _Three -App. 84 3-353 App. 33 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-354 App. 34 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-355 App. 35 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-356 App. 36 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-357 Fig. 37 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-358 Fig. 38 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-359 App. 39 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-360 App. 40 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-361 App. 41 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-362 Fig. 42 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-363 Fig. 60 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-364 App. 43 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-365 Fig. 44 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-366 App. 45 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-367 App. 46 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-368 App. 47 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-369 Fig. 81 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-370 App. 48 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-371 App. 49 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-372 App. 50 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-373 Fig. 51 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-374 App. 52 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-375 App. 53 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-376 App. 54 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-377 App. 56 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-378 App. 57 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-379 Fig. 58 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-380 App. 59 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-381 Fig. 82 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-382 Fig. 83 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-383 Fig. 61 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-384 App. 55 4-ClPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-385 App. 33 4-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-386 place 34 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-387 place 35 4-ClPh -CO- single bond -CH _Two - c Pr-84 84-388 36-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-389 place 37 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-390 place 38 4-ClPh -CO- single bond -CH _Two - c Pr-84 84-391 39-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-392 place 40 4-ClPh -CO- single bond -CH _Two - c Pr-84 84 3-393 41-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-394 place 42 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-395 place 60 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-396 place 43 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-397 place 44 4-ClPh -CO- single bond -CH _Two - c Pr-84 84-398 45-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-399 place 46 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-400 place 47 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-401 place 81 4-ClPh -CO- single bond -CH _Two - c Pr-84 84-402 48-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-403 place 49 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-404 place 50 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-405 place 51 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-406 place 52 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-407 place 53 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-408 place 54 4-ClPh -CO- single bond -CH _Two - c Pr-84 84-409 56-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-410 place 57 4-ClPh -CO- single bond -CH _Two - c Pr-84 84 3-411 58-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-412 place 59 4-ClPh -CO- single bond -CH _Two - c Pr-84 84 3-413 82-ClPh -CO- Single bond -CH _Two - c Pr-position 84 3-414 Setting 83 4-ClPh -CO- Single bond -CH _Two - c Pr-place 84 3-415 place 61 4-ClPh -CO- single bond -CH _Two - c Pr-place 84 3-416 place 55 4-ClPh -CO- single bond -CH _Two - c Pr-84 84-417 33-ClPh -CO- Single bond -CH _Two - c Bu-84 84-418 34-ClPh -CO- Single bond -CH _Two - c Bu-84 84-419 35-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-420 36-ClPh -CO- Single bond -CH _Two - c Bu-84 84-421 37-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-422 38-ClPh -CO- Single bond -CH _Two - c Bu-84 84-423 39-ClPh -CO- Single bond -CH _Two - c Bu-84 84-424 40-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-425 41-ClPh -CO- Single bond -CH _Two - c Bu-84 84-426 42-ClPh -CO- Single bond -CH _Two - c Bu-84 84-427 60-ClPh -CO- Single bond -CH _Two - c Bu-84-428 3-43 4-ClPh -CO- Single bond -CH _Two - c Bu-84 84-429 44-ClPh -CO- Single bond -CH _Two - c Bu-84 84-430 45-ClPh -CO- Single bond -CH _Two - c Bu-84-431 3-46 4-ClPh -CO- Single bond -CH _Two - c Bu-84 84-432 47-ClPh -CO- Single bond -CH _Two - c Bu-84 84-433 81-ClPh -CO- Single bond -CH _Two - c Bu-84 84-434 48-ClPh -CO- Single bond -CH _Two - c Bu-84 84-435 49-ClPh -CO- Single bond -CH _Two - c Bu-84 84-436 50-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-437 51-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-438 52-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-439 53-ClPh -CO- Single bond -CH _Two - c Bu-84 84-440 54-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-441 56 4-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-442 57-ClPh -CO- Single bond -CH _Two - c Bu-84 84-443 58-ClPh -CO- Single bond -CH _Two - c Bu-84 84-444 59-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-445 82-ClPh -CO- Single bond -CH _Two - c Bu-84 84 3-446 83-ClPh -CO- Single bond -CH _Two - c Bu-84 84-447 61 4-ClPh -CO- Single bond -CH _Two - c Bu-84 84-448 55-ClPh -CO- Single bond -CH _Two - c Bu-84 84-449 33-ClPh -CO- Single bond -CH _Two - c Pn- position 84 3-450 position 34 4-ClPh -CO- single bond -CH _Two - c Pn- unit 84 3-451 unit 35 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-452 configuration 36 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-453 configuration 37 4-ClPh -CO- single bond -CH _Two - c Pn- Fig. 84 3-454 Fig. 38 4-ClPh -CO- Single bond -CH _Two - c Pn- unit 84 3-455 unit 39 4-ClPh -CO- single bond -CH _Two - c Pn-84 84-456 40-ClPh -CO- Single bond -CH _Two - c Pn- configuration 84 3-457 configuration 41 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-458 configuration 42 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-459 position 60 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-460 position 43 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-461 configuration 44 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-462 configuration 45 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-463 configuration 46 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-464 position 47 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-465 position 81 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-466 position 48 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-467 position 49 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-468 position 50 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-469 configuration 51 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-470 position 52 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-471 position 53 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-472 position 54 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-473 configuration 56 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-474 position 57 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-475 position 58 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-476 position 59 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-477 position 82 4-ClPh -CO- single bond -CH _Two - c Pn- position 84 3-478 position 83 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-479 configuration 61 4-ClPh -CO- single bond -CH _Two - c Pn- unit 84 3-480 unit 55 4-ClPh -CO- single bond -CH _Two - c Pn- configuration 84 3-481 configuration 33 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-482 unit 34 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-483 unit 35 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-484 place 36 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-485 unit 37 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-486 unit 38 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-487 unit 39 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-488 unit 40 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-489 unit 41 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-490 place 42 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-491 place 60 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-492 Place 43 4-ClPh -CO- Single bond -CH _Two - c Hx- unit 84 3-493 unit 44 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-494 unit 45 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-495 unit 46 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-496 place 47 4-ClPh -CO- single bond -CH _Two - c Hx- configuration 84 3-497 configuration 81 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-498 place 48 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-499 place 49 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-500 unit 50 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-501 unit 51 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-502 place 52 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-503 place 53 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-504 unit 54 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-505 place 56 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-506 place 57 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 3-507 place 58 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-508 unit 59 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-509 unit 82 4-ClPh -CO- single bond -CH _Two - c Hx- configuration 84 3-510 configuration 83 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-511 unit 61 4-ClPh -CO- single bond -CH _Two - c Hx- unit 84 3-512 unit 55 4-ClPh -CO- single bond -CH _Two - c Hx-place 84 化合物 Compound number R ¹ R ^Two ABEZ ──────────────────────────────────── 3-513 Place 33 4-FPh -CO -Single bond -CH _Two -Fig. 84 3-514 Fig. 34 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-515 Fig. 35 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-516 Fig. 36 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-517 Fig. 37 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-518 Fig. 38 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-519 Fig. 39 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-520 Fig. 40 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-521 Fig. 41 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-522 Fig. 42 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-523 Fig. 60 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-524 Fig. 43 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-525 Fig. 44 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-526 Fig. 45 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-527 Fig. 46 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-528 Fig. 47 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-529 Fig. 81 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-530 Fig. 48 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-531 Fig. 49 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-532 Fig. 50 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-533 Fig. 51 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-534 Fig. 52 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-535 Fig. 53 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-536 Fig. 54 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-537 Fig. 56 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-538 Fig. 57 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-539 Fig. 58 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-540 Fig. 59 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-541 Fig. 82 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-542 Fig. 83 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-543 Fig. 61 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-544 Fig. 55 4-FPh -CO- Single bond -CH _Two -Fig. 84 3-545 Fig. 33 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-546 Fig. 34 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-547 Fig. 35 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-548 Fig. 36 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-549 Fig. 37 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-550 Fig. 38 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-551 Fig. 39 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-552 Fig. 40 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-553 Fig. 41 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-554 Fig. 42 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-555 Fig. 60 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-556 Fig. 43 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-557 Fig. 44 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-558 Fig. 45 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-559 Fig. 46 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-560 Fig. 47 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-561 Fig. 81 4-FPh -CO- Single bond -CH _Two CH _Two -App. 84 3-562 App. 48 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-563 Fig. 49 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-564 Fig. 50 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-565 Fig. 51 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-566 Fig. 52 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-567 Fig. 53 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-568 Fig. 54 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-569 Fig. 56 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-570 Fig. 57 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-571 Fig. 58 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-572 Fig. 59 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-573 Fig. 82 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-574 Fig. 83 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-575 Fig. 61 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-576 Fig. 55 4-FPh -CO- Single bond -CH _Two CH _Two -Fig. 84 3-577 Fig. 33 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-578 Fig. 34 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-579 Fig. 35 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-580 Fig. 36 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-581 Fig. 37 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-582 Fig. 38 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-583 Fig. 39 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-584 Fig. 40 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-585 Fig. 41 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-586 Fig. 42 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-587 Fig. 60 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-588 Fig. 43 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-589 Fig. 44 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-590 Fig. 45 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-591 Fig. 46 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-592 Fig. 47 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-593 Fig. 81 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-594 Fig. 48 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-595 Fig. 49 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-596 Fig. 50 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-597 Fig. 51 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-598 Fig. 52 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-599 Fig. 53 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-600 Fig. 54 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-601 Fig. 56 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-602 Fig. 57 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-603 Fig. 58 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-604 Fig. 59 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-605 Fig. 82 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-606 Fig. 83 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-607 Fig. 61 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-608 Fig. 55 4-FPh -CO- Single bond-(CH _Two ) _Three -Fig. 84 3-609 Fig. 33 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-610 Fig. 34 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-611 Fig. 35 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-612 Fig. 36 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-613 Fig. 37 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-614 Fig. 38 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-615 Fig. 39 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-616 Fig. 40 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-617 Fig. 41 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-618 Fig. 42 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-619 Fig. 60 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-620 Fig. 43 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-621 Fig. 44 4-FPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-622 App. 45 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-623 Fig. 46 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-624 Fig. 47 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-625 Fig. 81 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-626 Fig. 48 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-627 Fig. 49 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-628 Fig. 50 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-629 Fig. 51 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-630 Fig. 52 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-631 Fig. 53 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-632 Fig. 54 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-633 Fig. 56 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-634 Fig. 57 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-635 Fig. 58 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-636 Fig. 59 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-637 Fig. 82 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-638 Fig. 83 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-639 Fig. 61 4-FPh -CO- Single bond -CH _Two C (Me) _Two -App. 84 3-640 App. 55 4-FPh -CO- Single bond -CH _Two C (Me) _Two -Fig. 84 3-641 Fig. 33 4-FPh -CO- Single bond -CH _Two - c Pr-place 84 3-642 place 34 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-643 place 35 4-FPh -CO- single bond -CH _Two - c Pr- position 84 3-644 position 36 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-645 place 37 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-646 place 38 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-647 place 39 4-FPh -CO- single bond -CH _Two - c Pr-84 84-648 40-FPh -CO- Single bond -CH _Two - c Pr-place 84 3-649 place 41 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-650 place 42 4-FPh -CO- single bond -CH _Two - c Pr- position 84 3-651 position 60 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-652 place 43 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-653 place 44 4-FPh -CO- single bond -CH _Two - c Pr- position 84 3-654 position 45 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-655 place 46 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-656 place 47 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-657 place 81 4-FPh -CO- single bond -CH _Two - c Pr- position 84 3-658 position 48 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-659 place 49 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-660 place 50 4-FPh -CO- single bond -CH _Two - c Pr- position 84 3-661 position 51 4-FPh -CO- single bond -CH _Two - c Pr-84 84-662 52-FPh -CO- Single bond -CH _Two - c Pr-place 84 3-663 place 53 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-664 place 54 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-665 place 56 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-666 place 57 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-667 place 58 4-FPh -CO- single bond -CH _Two - c Pr-place 84 3-668 place 59 4-FPh -CO- single bond -CH _Two - c Pr-84 84 3-669 82-FPh -CO- Single bond -CH _Two - c Pr-place 84 3-670 place 83 4-FPh -CO- single bond -CH _Two - c Pr- position 84 3-671 position 61 4-FPh -CO- single bond -CH _Two - c Pr-84 84 3-672 55-FPh -CO- Single bond -CH _Two - c Pr-place 84 3-673 place 33 4-FPh -CO- single bond -CH _Two - c Bu-84 84 3-674 34-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-675 35-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-676 36-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-677 place 37 4-FPh -CO- single bond -CH _Two - c Bu-84 84-678 38-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-679 place 39 4-FPh -CO- single bond -CH _Two - c Bu-84 84 3-680 40-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-681 41-FPh -CO- Single bond -CH _Two - c Bu-84 84-682 42-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-683 place 60 4-FPh -CO- single bond -CH _Two - c Bu-84 84-684 43-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-685 44-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-686 45-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-687 46-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-688 place 47 4-FPh -CO- single bond -CH _Two - c Bu-84 84 3-689 81-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-690 place 48 4-FPh -CO- single bond -CH _Two - c Bu-84 84 3-691 49-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-692 50-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-693 51-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-694 52-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-695 53-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-696 place 54 4-FPh -CO- single bond -CH _Two - c Bu-84 84 6-697 56 4-FPh -CO- Single bond -CH _Two - c Bu-84 84 6-698 57 4-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-699 place 58 4-FPh -CO- single bond -CH _Two - c Bu-84 84-700 59-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-701 82-FPh -CO- Single bond -CH _Two - c Bu-84 84 3-702 83-FPh -CO- Single bond -CH _Two - c Bu-84 84-703 61-FPh -CO- Single bond -CH _Two - c Bu-place 84 3-704 place 55 4-FPh -CO- single bond -CH _Two - c Bu-84 84-705 33-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-706 Fig. 34 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-707 Fig. 35 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-708 Fig. 36 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-709 Fig. 37 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-710 Fig. 38 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-711 Fig. 39 4-FPh -CO- Single bond -CH _Two - c Pn- unit 84 3-712 unit 40 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-713 position 41 4-FPh -CO- single bond -CH _Two - c Pn- Fig. 84 3-714 Fig. 42 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-715 Fig. 60 4-FPh -CO- Single bond -CH _Two - c Pn- position 84 3-716 position 43 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-717 position 44 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-718 position 45 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-719 position 46 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-720 position 47 4-FPh -CO- single bond -CH _Two - c Pn- configuration 84 3-721 configuration 81 4-FPh -CO- single bond -CH _Two - c Pn- Fig. 84 3-722 Fig. 48 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-723 Fig. 49 4-FPh -CO- Single bond -CH _Two - c Pn- position 84 3-724 position 50 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-725 position 51 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-726 position 52 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-727 position 53 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-728 position 54 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-729 position 56 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-730 position 57 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-731 position 58 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-732 position 59 4-FPh -CO- single bond -CH _Two - c Pn- configuration 84 3-733 configuration 82 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-734 position 83 4-FPh -CO- single bond -CH _Two - c Pn- position 84 3-735 position 61 4-FPh -CO- single bond -CH _Two - c Pn- Fig. 84 3-736 Fig. 55 4-FPh -CO- Single bond -CH _Two - c Pn- Fig. 84 3-737 Fig. 33 4-FPh -CO- Single bond -CH _Two - c Hx-place 84 3-738 place 34 4-FPh -CO- single bond -CH _Two - c Hx- Fig. 84 3-739 Fig. 35 4-FPh -CO- Single bond -CH _Two - c Hx- unit 84 3-740 unit 36 4-FPh -CO- single bond -CH _Two - c Hx-place 84 3-741 place 37 4-FPh -CO- single bond -CH _Two - c Hx- Fig. 84 3-742 Fig. 38 4-FPh -CO- Single bond -CH _Two - c Hx-place 84 3-743 place 39 4-FPh -CO- single bond -CH _Two - c Hx- unit 84 3-744 unit 40 4-FPh -CO- single bond -CH _Two - c Hx- unit 84 3-745 unit 41 4-FPh -CO- single bond -CH _Two - c Hx- Fig. 84 3-746 Fig. 42 4-FPh -CO- Single bond -CH _Two - c Hx- Fig. 84 3-747 Fig. 60 4-FPh -CO- Single bond -CH _Two - c Hx- Fig. 84 3-748 Fig. 43 4-FPh -CO- Single bond -CH _Two - c Hx-place 84 3-749 place 44 4-FPh -CO- single bond -CH _Two - c Hx- unit 84 3-750 unit 45 4-FPh -CO- single bond -CH _Two - c Hx-place 84 3-751 place 46 4-FPh -CO- single bond -CH _Two - c Hx-place 84 3-752 place 47 4-FPh -CO- single bond -CH _Two - c Hx-place 84 3-753 place 81 4-FPh -CO- single bond -CH _Two - c Hx-place 84 3-754 place 48 4-FPh -CO- single bond -CH _Two - c Hx- Fig. 84 3-755 Fig. 49 4-FPh -CO- Single bond -CH _Two - c Hx- Fig. 84 3-756 Fig. 50 4-FPh -CO- Single bond -CH _Two - c Hx- unit 84 3-757 unit 51 4-FPh -CO- single bond -CH _Two - c Hx- Fig. 84 3-758 Fig. 52 4-FPh -CO- Single bond -CH _Two - c Hx- Fig. 84 3-759 Fig. 53 4-FPh -CO- Single bond -CH _Two - c Hx-place 84 3-760 place 54 4-FPh -CO- single bond -CH _Two - c Hx-place 84 3-761 place 56 4-FPh -CO- single bond -CH _Two - c Hx- unit 84 3-762 unit 57 4-FPh -CO- single bond -CH _Two - c Hx-place 84 3-763 place 58 4-FPh -CO- single bond -CH _Two - c Hx- unit 84 3-764 unit 59 4-FPh -CO- single bond -CH _Two - c Hx- Fig. 84 3-765 Fig. 82 4-FPh -CO- Single bond -CH _Two - c Hx- unit 84 3-766 unit 83 4-FPh -CO- single bond -CH _Two - c Hx- Fig. 84 3-767 Fig. 61 4-FPh -CO- Single bond -CH _Two - c Hx- unit 84 3-768 unit 55 4-FPh -CO- single bond -CH _Two - c Hx- device 84 3-769 device 33 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-770 App. 34 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-771 App. 35 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-772 App. 36 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-773 App. 37 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-774 App. 38 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-775 App. 39 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-776 App. 40 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-777 App. 41 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-778 App. 42 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-779 App. 60 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-780 App. 43 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-781 App. 44 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-782 App. 45 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-783 App. 46 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-784 App. 47 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-785 App. 81 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-786 App. 48 3,4-diClPh -CO- -CH _Two --CH _Two -Storage 84 3-787 Storage 49 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-788 App. 50 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-789 App. 51 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-790 App. 52 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-791 App. 53 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-792 App. 54 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-793 App. 56 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-794 App. 57 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-795 App. 58 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-796 App. 59 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-797 App. 82 3,4-diClPh -CO- -CH _Two --CH _Two -Storage 84 3-798 Storage 83 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-799 App. 61 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-800 App. 55 3,4-diClPh -CO- -CH _Two --CH _Two -App. 84 3-801 App. 33 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-802 App. 34 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-803 App. 35 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-804 App. 36 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-805 App. 37 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-806 App. 38 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-807 App. 39 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-808 App. 40 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-809 App. 41 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-810 App. 42 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-811 App. 60 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-812 App. 43 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-813 App. 44 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-814 App. 45 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-815 App. 46 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-816 App. 47 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-817 Storage 81 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-818 App. 48 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-819 App. 49 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-820 App. 50 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-821 App. 51 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-822 App. 52 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-823 App. 53 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-824 App. 54 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-825 App. 56 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-826 App. 57 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-827 App. 58 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-828 App. 59 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-829 App. 82 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-830 App. 83 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-831 App. 61 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-832 App. 55 3,4-diClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-833 App. 33 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-834 App. 34 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-835 Storage 35 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-836 App. 36 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-837 App. 37 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-838 App. 38 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-839 App. 39 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-840 App. 40 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-841 App. 41 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-842 App. 42 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-843 App. 60 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-844 App. 43 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-845 App. 44 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-846 App. 45 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-847 App. 46 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-848 App. 47 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-849 App. 81 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-850 App. 48 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-851 App. 49 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-852 App. 50 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-853 App. 51 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-854 App. 52 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-855 App. 53 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-856 App. 54 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-857 App. 56 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-858 App. 57 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-859 App. 58 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-860 App. 59 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-861 App. 82 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-862 App. 83 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-863 App. 61 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-864 App. 55 3,4-diClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-865 App. 33 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-866 App. 34 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-867 App. 35 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-868 App. 36 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-869 App. 37 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-870 App. 38 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-871 App. 39 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-872 App. 40 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-873 App. 41 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-874 App. 42 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-875 App. 60 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-876 App. 43 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-877 App. 44 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-878 App. 45 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-879 App. 46 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-880 App. 47 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-881 App. 81 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-882 App. 48 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-883 App. 49 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-884 App.50 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-885 App. 51 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-886 App. 52 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-887 App. 53 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-888 App. 54 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-889 Storage 56 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-890 App. 57 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-891 App. 58 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-892 App. 59 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-893 App. 82 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-894 App. 83 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-895 Storage 61 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-896 App. 55 3,4-diClPh -CO- -CH _Two --CH _Two C (Me) _Two -App. 84 3-897 App. 33 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-84 84-898 34 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-899 place 35 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-900 place 36 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-901 place 37 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-902 place 38 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-903 place 39 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-904 40 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-905 place 41 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-84 84-906 42 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-907 place 60 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-908 place 43 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-909 place 44 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-unit 84 3-910 Unit 45 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-911 46 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-912 place 47 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-913 place 81 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-914 48 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-915 place 49 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-916 50 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-917 place 51 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-918 place 52 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-919 place 53 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-unit 84 3-920 Unit 54 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-921 56 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-922 place 57 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-923 place 58 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-924 place 59 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-925 place 82 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-926 Place 83 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-927 Place 61 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-928 place 55 3,4-diClPh -CO- -CH _Two --CH _Two - c Pr-unit 84 3-929 unit 33 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-930 34 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-931 35 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-932 36 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-933 37 37,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-934 38 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-935 39 39,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-936 40 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-937 41 41,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-938 42 42,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-939 60 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-940 43 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 843-941 44 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-942 45 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-943 46 46 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-944 47 47,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-945 81 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-946 48 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-947 49 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-948 50 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-949 51 51 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-950 52 52 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-951 53 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-952 54 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-953 56 56 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-954 57 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 955 55 58 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 956 56 59 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-957 82 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-958 83 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84-959 61 61 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-place 84 3-960 place 55 3,4-diClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-961 33 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-962 device 34 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-963 device 35 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-964 device 36 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-965 device 37 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-966 device 38 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-967 device 39 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-968 device 40 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-969 device 41 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-970 device 42 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-971 device 60 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-972 device 43 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-973 device 44 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-974 device 45 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-975 device 46 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-976 device 47 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-977 device 81 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-978 device 48 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-979 device 49 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-980 device 50 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-981 device 51 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-982 device 52 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-983 device 53 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-984 device 54 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-985 device 56 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-986 device 57 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-987 device 58 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-988 device 59 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-989 device 82 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-990 device 83 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-991 device 61 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-992 device 55 3,4-diClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-993 device 33 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-994 device 34 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-995 device 35 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-996 device 36 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-997 device 37 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-998 device 38 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-999 device 39 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1000 device 40 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1001 device 41 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1002 device 42 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1003 device 60 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1004 device 43 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1005 device 44 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1006 device 45 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1007 device 46 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1008 device 47 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1009 device 81 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1010 device 48 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1011 device 49 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1012 device 50 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1013 device 51 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1014 device 52 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1015 device 53 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1016 device 54 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1017 device 56 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1018 device 57 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1019 device 58 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1020 device 59 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1021 device 82 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1022 device 83 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1023 device 61 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1024 device 55 3,4-diClPh -CO- -CH _Two --CH _Two - c Hx-place 84 化合物 Compound number R ¹ R ^Two ABEZ ──────────────────────────────────── 3-1025 Place 33 4-ClPh -CO --CH _Two --CH _Two -App. 84 3-1026 App. 34 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1027 App. 35 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1028 App. 36 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1029 App. 37 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1030 App. 38 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1031 App. 39 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1032 App. 40 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1033 App. 41 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1034 Set 42 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1035 Set 60 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1036 Set 43 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1037 Set 44 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1038 Set 45 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1039 App. 46 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1040 App. 47 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1041 Set 81 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1042 Set 48 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1043 App. 49 4-ClPh -CO- -CH _Two --CH _Two -App.84 3-1044 App.50 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1045 App. 51 4-ClPh -CO- -CH _Two --CH _Two -App.84 3-1046 App.52 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1047 App. 53 4-ClPh -CO- -CH _Two --CH _Two -App.84 3-1048 App.54 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1049 App. 56 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1050 App. 57 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1051 Set 58 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1052 App. 59 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1053 Set 82 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1054 Set 83 4-ClPh -CO- -CH _Two --CH _Two -Set 84 3-1055 Set 61 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1056 App. 55 4-ClPh -CO- -CH _Two --CH _Two -App. 84 3-1057 App. 33 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1058 App. 34 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1059 App. 35 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1060 App. 36 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1061 App. 37 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1062 App. 38 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1063 App. 39 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1064 App. 40 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1065 App. 41 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App.84 3-1066 App.42 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1067 Set 60 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1068 Storage 43 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1069 Set 44 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1070 Storage 45 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1071 App. 46 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1072 App. 47 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1073 Set 81 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1074 Set 48 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1075 App. 49 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App.84 3-1076 App.50 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1077 Set 51 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1078 App. 52 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1079 Set 53 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Place 84 3-1080 Place 54 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1081 App. 56 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1082 App. 57 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1083 Set 58 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1084 Set 59 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1085 Set 82 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1086 Set 83 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1087 Set 61 4-ClPh -CO- -CH _Two --CH _Two CH _Two -Set 84 3-1088 Set 55 4-ClPh -CO- -CH _Two --CH _Two CH _Two -App. 84 3-1089 App. 33 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1090 App. 34 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1091 App. 35 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1092 App. 36 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1093 App. 37 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1094 App. 38 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1095 App. 39 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1096 App. 40 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App. 84 3-1097 App. 41 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -Set 84 3-1098 Set 42 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -Set 84 3-1099 Set 60 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1100 App.43 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1101 App.44 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1102 App.45 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1103 App.46 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1104 App.47 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1105 App.81 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1106 App.48 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1107 App.49 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1108 App.50 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1109 App.51 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1110 App.52 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1111 App.53 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1112 App.54 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1113 App.56 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1114 App.57 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1115 App.58 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1116 App.59 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1117 Storage 82 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1118 App.83 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1119 App.61 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1120 App.55 4-ClPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1121 App.33 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1122 App.34 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1123 App.35 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1124 App.36 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1125 App.37 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1126 App.38 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1127 App.39 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1128 App.40 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1129 App.41 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1130 App.42 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1131 App.60 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1132 App.43 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1133 App.44 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1134 App.45 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1135 App.46 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1136 App.47 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1137 App.81 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1138 App.48 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1139 App.49 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1140 App.50 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1141 App.51 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1142 App.52 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1143 App.53 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1144 App.54 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1145 App.56 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1146 App.57 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1147 App.58 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1148 App.59 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1149 App.82 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -Set 84 3-1150 Set 83 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1151 App.61 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1152 App.55 4-ClPh -CO- -CH _Two --CH _Two C (Me) _Two -App.84 3-1153 App.33 4-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1154 34-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1155 place 35 4-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1156 36-ClPh -CO- -CH _Two --CH _Two - c Pr- 84 84 3-1157 37-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1158 place 38 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1159 place 39 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1160 place 40 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1161 place 41 4-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1162 42-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1163 60-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1164 Place 43 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1165 place 44 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1166 place 45 4-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1167 46-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1168 47-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1169 place 81 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1170 Place 48 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1171 place 49 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1172 place 50 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1173 place 51 4-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1174 52-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1175 53-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1176 place 54 4-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1177 56-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1178 57-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1179 place 58 4-ClPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1180 place 59 4-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1181 82-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1182 83-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1183 61-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1184 55-ClPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1185 33-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1186 34-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1187 35-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1188 36-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1189 37 37 4-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1190 38-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1191 39 39 4-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1192 40-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1193 41-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1194 42-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1195 60-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1196 43-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1197 44-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1198 45-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1199 46-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 1200 1200 47 4-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1201 81-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1202 48-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1203 49-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1204 50-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1205 51 51 4-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1206 52-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1207 53-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1208 54 54 4-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1209 56-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1210 57-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1211 58-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1212 59-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1213 82-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1214 83-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1215 61-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1216 55-ClPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1217 33 33 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1218 device 34 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1219 device 35 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1220 device 36 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1221 device 37 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1222 device 38 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1223 device 39 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1224 device 40 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1225 device 41 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1226 device 42 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1227 device 60 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1228 device 43 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1229 device 44 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1230 device 45 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1231 device 46 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1232 device 47 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1233 device 81 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1234 device 48 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1235 device 49 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1236 device 50 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1237 device 51 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1238 device 52 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1239 device 53 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1240 device 54 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1241 device 56 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1242 device 57 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1243 device 58 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1244 device 59 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1245 device 82 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1246 device 83 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1247 device 61 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1248 device 55 4-ClPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1249 device 33 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1250 device 34 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1251 device 35 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1252 device 36 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1253 device 37 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1254 device 38 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1255 device 39 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1256 device 40 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1257 device 41 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1258 device 42 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1259 device 60 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1260 device 43 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1261 device 44 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1262 device 45 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1263 device 46 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1264 device 47 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1265 device 81 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1266 device 48 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1267 device 49 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1268 device 50 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1269 device 51 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1270 device 52 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1271 device 53 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1272 device 54 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1273 device 56 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1274 device 57 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1275 device 58 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1276 device 59 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1277 device 82 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1278 device 83 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1279 device 61 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1280 device 55 4-ClPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1281 device 33 4-FPh -CO- -CH _Two --CH _Two -Place 84 3-1282 Place 34 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1283 Storage 35 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1284 Storage 36 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1285 Installation 37 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1286 Storage 38 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1287 Storage 39 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1288 Installation 40 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1289 Storage 41 4-FPh -CO- -CH _Two --CH _Two -Place 84 3-1290 Place 42 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1291 Installation 60 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1292 Storage 43 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1293 Storage 44 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1294 Storage 45 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1295 Installation 46 4-FPh -CO- -CH _Two --CH _Two -Place 84 3-1296 Place 47 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1297 Storage 81 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1298 Storage 48 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1299 Storage 49 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1300 Storage 50 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1301 Installation 51 4-FPh -CO- -CH _Two --CH _Two -Place 84 3-1302 Place 52 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1303 Storage 53 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1304 Installation 54 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1305 Installation 56 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1306 Installation 57 4-FPh -CO- -CH _Two --CH _Two -Installation 84 3-1307 Installation 58 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1308 Storage 59 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1309 Storage 82 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1310 Storage 83 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1311 Storage 61 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1312 Storage 55 4-FPh -CO- -CH _Two --CH _Two -Storage 84 3-1313 Storage 33 4-FPh -CO- -CH _Two --CH _Two CH _Two -Place 84 3-1314 Place 34 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1315 Storage 35 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1316 Installation 36 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1317 Storage 37 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1318 Storage 38 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1319 Storage 39 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1320 Installation 40 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1321 Installation 41 4-FPh -CO- -CH _Two --CH _Two CH _Two -Place 84 3-1322 Place 42 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1323 Installation 60 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1324 Installation 43 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1325 Storage 44 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1326 Storage 45 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1327 Storage 46 4-FPh -CO- -CH _Two --CH _Two CH _Two -App.84 3-1328 App.47 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1329 Storage 81 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1330 Installation 48 4-FPh -CO- -CH _Two --CH _Two CH _Two -App.84 3-1331 App.49 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1332 Installation 50 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1333 Installation 51 4-FPh -CO- -CH _Two --CH _Two CH _Two -App.84 3-1334 App.52 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1335 Storage 53 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1336 Storage 54 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1337 Installation 56 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1338 Installation 57 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1339 Installation 58 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1340 Installation 59 4-FPh -CO- -CH _Two --CH _Two CH _Two -Place 84 3-1341 Place 82 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1342 Storage 83 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1343 Installation 61 4-FPh -CO- -CH _Two --CH _Two CH _Two -Installation 84 3-1344 Installation 55 4-FPh -CO- -CH _Two --CH _Two CH _Two -Storage 84 3-1345 Storage 33 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1346 Installation 34 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1347 Installation 35 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1348 Storage 36 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1349 Storage 37 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1350 Storage 38 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1351 Storage 39 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1352 Installation 40 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1353 Installation 41 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1354 Storage 42 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1355 Installation 60 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1356 Installation 43 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1357 Installation 44 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1358 Storage 45 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1359 Installation 46 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Place 84 3-1360 Place 47 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1361 Storage 81 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1362 Installation 48 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1363 Storage 49 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1364 Installation 50 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1365 Installation 51 4-FPh -CO- -CH _Two --(CH _Two ) _Three -App.84 3-1366 App.52 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Place 84 3-1367 Place 53 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1368 Installation 54 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1369 Installation 56 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1370 Installation 57 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1371 Installation 58 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1372 Installation 59 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1373 Storage 82 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1374 Storage 83 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1375 Installation 61 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Installation 84 3-1376 Installation 55 4-FPh -CO- -CH _Two --(CH _Two ) _Three -Storage 84 3-1377 Storage 33 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1378 Installation 34 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1379 Storage 35 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1380 Place 36 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1381 Installation 37 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1382 Storage 38 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1383 Storage 39 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1384 Installation 40 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1385 Place 41 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1386 Storage 42 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1387 Place 60 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1388 Installation 43 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1389 Storage 44 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1390 Storage 45 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1391 Installation 46 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1392 Place 47 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1393 Installation 81 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1394 Place 48 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1395 Storage 49 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1396 Installation 50 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1397 Storage 51 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1398 Place 52 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Fig. 84 3-1399 Fig. 53 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1400 Storage 54 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1401 Installation 56 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1402 Installation 57 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1403 Installation 58 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1404 Place 59 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1405 Storage 82 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1406 Storage 83 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Installation 84 3-1407 Installation 61 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Place 84 3-1408 Place 55 4-FPh -CO- -CH _Two --CH _Two C (Me) _Two -Storage 84 3-1409 Storage 33 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1410 Place 34 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84-1414 35 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1412 36-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1413 place 37 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1414 Place 38 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1415 39-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1416 Place 40 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1417 Place 41 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1418 42-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1419 60-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1420 Place 43 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1421 Place 44 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1422 place 45 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1423 46-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1424 place 47 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1425 81-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1426 48-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1427 49-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1428 50-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1429 Place 51 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1430 Place 52 4-FPh -CO- -CH _Two --CH _Two - c Pr- 84 84 3-1431 53 53 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1432 Place 54 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1433 56-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1434 place 57 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1435 Place 58 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1436 59-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1437 place 82 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1438 place 83 4-FPh -CO- -CH _Two --CH _Two - c Pr-place 84 3-1439 Place 61 4-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1440 55-FPh -CO- -CH _Two --CH _Two - c Pr-84 84 3-1441 33-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1442 34-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1443 35-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1444 36-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1445 37-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1446 38-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1447 39-FPh -CO- -CH _Two --CH _Two - c Bu-place 84 3-1448 Place 40 4-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1449 41-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1450 42-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1451 60-FPh -CO- -CH _Two --CH _Two - c Bu-place 84 3-1452 Place 43 4-FPh -CO- -CH _Two --CH _Two - c Bu-place 84 3-1453 place 44 4-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1454 45-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1455 46-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1456 47-FPh -CO- -CH _Two --CH _Two - c Bu-Place 84 3-1457 Place 81 4-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1458 48-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1459 49-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1460 50-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1461 51-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1462 52-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1463 53 53 4-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1464 54-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1465 56-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1466 57-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1467 58-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1468 59-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1469 82-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1470 83-FPh -CO- -CH _Two --CH _Two - c Bu-place 84 3-1471 place 61 4-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1472 55-FPh -CO- -CH _Two --CH _Two - c Bu-84 84 3-1473 33-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1474 device 34 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1475 device 35 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1476 device 36 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1477 device 37 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1478 device 38 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1479 device 39 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1480 device 40 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1481 device 41 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1482 device 42 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1483 device 60 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1484 device 43 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1485 device 44 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1486 device 45 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1487 device 46 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1488 device 47 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1489 device 81 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1490 device 48 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1491 device 49 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1492 device 50 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1493 device 51 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1494 device 52 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1495 device 53 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1496 device 54 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1497 device 56 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1498 device 57 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1499 device 58 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1500 device 59 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1501 device 82 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1502 device 83 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1503 device 61 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1504 device 55 4-FPh -CO- -CH _Two --CH _Two - c Pn- device 84 3-1505 device 33 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1506 device 34 4-FPh -CO- -CH _Two --CH _Two - c Hx- installation 84 3-1507 installation 35 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1508 device 36 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1509 device 37 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1510 device 38 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1511 device 39 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1512 device 40 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1513 device 41 4-FPh -CO- -CH _Two --CH _Two - c Hx- installation 84 3-1514 installation 42 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1515 device 60 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1516 device 43 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1517 device 44 4-FPh -CO- -CH _Two --CH _Two - c Hx- installation 84 3-1518 installation 45 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1519 device 46 4-FPh -CO- -CH _Two --CH _Two - c Hx- installation 84 3-1520 installation 47 4-FPh -CO- -CH _Two --CH _Two - c Hx- installation 84 3-1521 installation 81 4-FPh -CO- -CH _Two --CH _Two - c Hx- installation 84 3-1522 installation 48 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1523 device 49 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1524 device 50 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1525 device 51 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1526 device 52 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1527 device 53 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1528 device 54 4-FPh -CO- -CH _Two --CH _Two - c Hx- installation 84 3-1529 installation 56 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1530 device 57 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1531 device 58 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1532 device 59 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1533 device 82 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1534 device 83 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1535 device 61 4-FPh -CO- -CH _Two --CH _Two - c Hx- device 84 3-1536 device 55 4-FPh -CO- -CH _Two --CH _Two - c Hx-place 84 化合物 Compound number R ¹ R ^Two ABEZ 3-1537 Place 33 3,4-diClPh -CO- single bond -C (Me) _Two -App.84 3-1538 App.34 3,4-diClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1539 Fig. 35 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1540 App.36 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1541 App.37 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1542 App.38 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1543 App.39 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1544 App.40 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1545 App.41 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1546 App.42 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1547 App.60 3,4-diClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1548 Fig. 43 3,4-diClPh -CO- Single bond-C (Me) _Two -App.84 3-1549 App.44 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1550 App.45 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1551 App.46 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1552 App.47 3,4-diClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1553 Fig. 81 3,4-diClPh -CO- Single bond-C (Me) _Two -App.84 3-1554 App.48 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1555 App.49 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1556 App.50 3,4-diClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1557 Fig. 51 3,4-diClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1558 Fig. 52 3,4-diClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1559 Fig. 53 3,4-diClPh -CO- Single bond-C (Me) _Two -App.84 3-1560 App.54 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1561 App.56 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1562 App.57 3,4-diClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1563 Fig. 58 3,4-diClPh -CO- Single bond-C (Me) _Two -App.84 3-1564 App.59 3,4-diClPh -CO- Single bond -C (Me) _Two -App 84 3-1565 App 82 3,4-diClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1566 Fig. 83 3,4-diClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1567 Fig. 61 3,4-diClPh -CO- Single bond-C (Me) _Two -App.84 3-1568 App.55 3,4-diClPh -CO- Single bond -C (Me) _Two -App.84 3-1569 App.33 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1570 App.34 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1571 Storage 35 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1572 Storage 36 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1573 App.37 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1574 Storage 38 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1575 Storage 39 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1576 App.40 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1577 App.41 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1578 App.42 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1579 Storage 60 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1580 Storage 43 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1581 App.44 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1582 App. 45 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1583 App. 46 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1584 App.47 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1585 Storage 81 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1586 Storage 48 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1587 Storage 49 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1588 App.50 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1589 Storage 51 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1590 Storage 52 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1591 App. 53 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1592 App.54 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1593 App.56 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1594 App.57 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1595 Storage 58 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1596 Storage 59 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1597 Storage 82 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1598 Storage 83 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1599 Storage 61 3,4-diClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1600 App. 55 3,4-diClPh -CO- -CH _Two --C (Me) _Two -Fig. 84 3-1601 Fig. 33 4-ClPh -CO- Single bond-C (Me) _Two -App.84 3-1602 App.34 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1603 App.35 4-ClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1604 Fig. 36 4-ClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1605 Fig. 37 4-ClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1606 Fig. 38 4-ClPh -CO- Single bond-C (Me) _Two -App.84 3-1607 App.39 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1608 App.40 4-ClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1609 Fig. 41 4-ClPh -CO- Single bond-C (Me) _Two -App. 84 3-1610 App. 42 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1611 App.60 4-ClPh -CO- Single bond -C (Me) _Two -App. 84 3-1612 App. 43 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1613 App.44 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1614 App.45 4-ClPh -CO- Single bond -C (Me) _Two -App. 84 3-1615 App. 46 4-ClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1616 Fig. 47 4-ClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1617 Fig. 81 4-ClPh -CO- Single bond-C (Me) _Two -App.84 3-1618 App.48 4-ClPh -CO- Single bond -C (Me) _Two -App. 84 3-1619 App. 49 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1620 App.50 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1621 App.51 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1622 App.52 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1623 App.53 4-ClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1624 Fig. 54 4-ClPh -CO- Single bond-C (Me) _Two -App.84 3-1625 App.56 4-ClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1626 Fig. 57 4-ClPh -CO- Single bond-C (Me) _Two -App.84 3-1627 App.58 4-ClPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1628 Fig. 59 4-ClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1629 Fig. 82 4-ClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1630 Fig. 83 4-ClPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1631 Fig. 61 4-ClPh -CO- Single bond-C (Me) _Two -App.84 3-1632 App.55 4-ClPh -CO- Single bond -C (Me) _Two -App.84 3-1633 App.33 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1634 App.34 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1635 App.35 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1636 App.36 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1637 App.37 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1638 App.38 4-ClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1639 App. 39 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1640 App.40 4-ClPh -CO- -CH _Two --C (Me) _Two -Set 84 3-1641 Set 41 4-ClPh -CO- -CH _Two --C (Me) _Two -Set 84 3-1642 Set 42 4-ClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1643 App. 60 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1644 App.43 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1645 App.44 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1646 App.45 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1647 App.46 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1648 App.47 4-ClPh -CO- -CH _Two --C (Me) _Two -Fig. 84 3-1649 Fig. 81 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1650 App.48 4-ClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1651 App. 49 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1652 App.50 4-ClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1653 App. 51 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1654 App.52 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1655 App.53 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1656 App.54 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1657 App.56 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1658 App.57 4-ClPh -CO- -CH _Two --C (Me) _Two -App. 84 3-1659 App. 58 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1660 App.59 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1661 App.82 4-ClPh -CO- -CH _Two --C (Me) _Two -Fig. 84 3-1662 Fig. 83 4-ClPh -CO- -CH _Two --C (Me) _Two -Set 84 3-1663 Set 61 4-ClPh -CO- -CH _Two --C (Me) _Two -App.84 3-1664 App.55 4-ClPh -CO- -CH _Two --C (Me) _Two -Fig. 84 3-1665 Fig. 33 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1666 Fig. 34 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1667 Fig. 35 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1668 Fig. 36 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1669 Fig. 37 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1670 Fig. 38 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1671 Fig. 39 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1672 Fig. 40 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1673 Fig. 41 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1674 Fig. 42 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1675 Fig. 60 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1676 Fig. 43 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1677 Fig. 44 4-FPh -CO- Single bond-C (Me) _Two -App.84 3-1678 App.45 4-FPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1679 Fig. 46 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1680 Fig. 47 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1681 Fig. 81 4-FPh -CO- Single bond-C (Me) _Two -App.84 3-1682 App.48 4-FPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1683 Fig. 49 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1684 Fig. 50 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1685 Fig. 51 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1686 Fig. 52 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1687 Fig. 53 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1688 Fig. 54 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1689 Fig. 56 4-FPh -CO- Single bond -C (Me) _Two -Fig. 84 3-1690 Fig. 57 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1691 Fig. 58 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1692 Fig. 59 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1693 Fig. 82 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1694 Fig. 83 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1695 Fig. 61 4-FPh -CO- Single bond-C (Me) _Two -Fig. 84 3-1696 Fig. 55 4-FPh -CO- Single bond-C (Me) _Two -Set 84 3-1697 Set 33 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1698 Storage 34 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1699 Storage 35 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1700 Storage 36 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1701 Installation 37 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1702 Place 38 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1703 Place 39 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1704 Installation 40 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1705 Place 41 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1706 Place 42 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1707 Installation 60 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1708 Place 43 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1709 Place 44 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1710 Storage 45 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1711 Installation 46 4-FPh -CO- -CH _Two --C (Me) _Two -Set 84 3-1712 Set 47 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1713 Storage 81 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1714 Installation 48 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1715 Storage 49 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1716 Installation 50 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1717 Installation 51 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1718 Place 52 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1719 Storage 53 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1720 Installation 54 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1721 Storage 56 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1722 Storage 57 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1723 Place 58 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1724 Place 59 4-FPh -CO- -CH _Two --C (Me) _Two -Storage 84 3-1726 Storage 83 4-FPh -CO- -CH _Two --C (Me) _Two -Installation 84 3-1727 Installation 61 4-FPh -CO- -CH _Two --C (Me) _Two -Place 84 3-1728 Place 55 4-FPh -CO- -CH _Two --C (Me) _Two -App.84 3-1729 App.37 3,4-diClPh -CH _Two -Single bond -CH _Two -Storage 84 3-1730 Storage 38 3,4-diClPh -CH _Two -Single bond -CH _Two -App. 84 3-1731 App. 39 3,4-diClPh -CH _Two -Single bond -CH _Two -App.84 3-1732 App.40 3,4-diClPh -CH _Two -Single bond -CH _Two -App.84 3-1733 App.41 3,4-diClPh -CH _Two -Single bond -CH _Two -App.84 3-1734 App.42 3,4-diClPh -CH _Two -Single bond -CH _Two -App.84 3-1735 App.60 3,4-diClPh -CH _Two -Single bond -CH _Two -Storage 84 3-1736 Storage 81 3,4-diClPh -CH _Two -Single bond -CH _Two -Storage 84 3-1737 Storage 48 3,4-diClPh -CH _Two -Single bond -CH _Two -App. 84 3-1738 App. 37 4-ClPh -CH _Two -Single bond -CH _Two -Storage 84 3-1739 Storage 38 4-ClPh -CH _Two -Single bond -CH _Two -Installation 84 3-1740 Installation 39 4-ClPh -CH _Two -Single bond -CH _Two -App. 84 3-1741 App. 40 4-ClPh -CH _Two -Single bond -CH _Two -Installation 84 3-1742 Installation 41 4-ClPh -CH _Two -Single bond -CH _Two -App.84 3-1743 App.42 4-ClPh -CH _Two -Single bond -CH _Two -App.84 3-1744 App.60 4-ClPh -CH _Two -Single bond -CH _Two -Storage 84 3-1745 Storage 81 4-ClPh -CH _Two -Single bond -CH _Two -App.84 3-1746 App.48 4-ClPh -CH _Two -Single bond -CH _Two -Storage 84 3-1747 Storage 37 4-FPh -CH _Two -Single bond -CH _Two -Storage 84 3-1748 Storage 38 4-FPh -CH _Two -Single bond -CH _Two -Storage 84 3-1749 Storage 39 4-FPh -CH _Two -Single bond -CH _Two -Installation 84 3-1750 Installation 40 4-FPh -CH _Two -Single bond -CH _Two -Place 84 3-1751 Place 41 4-FPh -CH _Two -Single bond -CH _Two -Place 84 3-1752 Place 42 4-FPh -CH _Two -Single bond -CH _Two -Storage 84 3-1753 Storage 60 4-FPh -CH _Two -Single bond -CH _Two -Storage 84 3-1754 Storage 81 4-FPh -CH _Two -Single bond -CH _Two -Installation 84 3-1755 Installation 48 4-FPh -CH _Two -Single bond -CH _Two -App.84 3-1756 App.37 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -Storage 84 3-1757 Storage 38 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1758 App.39 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1759 App.40 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1760 App.41 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -App. 84 3-1761 App. 42 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1762 App.60 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -Storage 84 3-1763 storage 81 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -App. 84 3-1764 App. 48 3,4-diClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1765 App.37 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1766 App.38 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1767 App.39 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App. 84 3-1768 App. 40 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App. 84 3-1769 App. 41 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1770 App.42 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App. 84 3-1771 App. 60 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1772 App.81 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -App.84 3-1773 App.48 4-ClPh -CH _Two -Single bond -CH _Two CH _Two -Storage 84 3-1774 Storage 37 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Storage 84 3-1775 storage 38 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Storage 84 3-1776 Storage 39 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Storage 84 3-1777 Storage 40 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Storage 84 3-1778 Storage 41 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Place 84 3-1779 Place 42 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Place 84 3-1780 Place 60 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Installation 84 3-1781 Installation 81 4-FPh -CH _Two -Single bond -CH _Two CH _Two -Place 84 3-1782 Place 48 4-FPh -CH _Two -Single bond -CH _Two CH _Two -App. 84 3-1783 App. 37 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1784 App.38 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1785 App.39 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1786 App.40 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -Storage 84 3-1787 Storage 41 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1788 App.42 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1789 App.60 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -Storage 84 3-1790 Storage 81 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -App. 84 3-1791 App. 48 3,4-diClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1792 App.37 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1793 App.38 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -Storage 84 3-1794 Storage 39 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1795 App.40 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1796 App.41 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1797 App.42 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1798 App.60 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -Storage 84 3-1799 Storage 81 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -App.84 3-1800 App.48 4-ClPh -CH _Two -Single bond-(CH _Two ) _Three -Storage 84 3-1801 storage 37 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Storage 84 3-1802 storage 38 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Storage 84 3-1803 storage 39 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Installation 84 3-1804 Installation 40 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Installation 84 3-1805 Installation 41 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Place 84 3-1806 Place 42 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Installation 84 3-1807 Installation 60 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Installation 84 3-1808 Installation 81 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -Place 84 3-1809 Place 48 4-FPh -CH _Two -Single bond-(CH _Two ) _Three -App. 84 3-1810 App. 37 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1811 Storage 38 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-1812 App. 39 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-1813 App. 40 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App.84 3-1814 App.41 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1815 Storage 42 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App.84 3-1816 App.60 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1817 Storage 81 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1818 Storage 48 3,4-diClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-1819 App. 37 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Installation 84 3-1820 Installation 38 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App.84 3-1821 App.39 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App.84 3-1822 App.40 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App.84 3-1823 App.41 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App.84 3-1824 App.42 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -App.84 3-1825 App.60 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1826 Storage 81 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1827 Storage 48 4-ClPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1828 Storage 37 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1829 Storage 38 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1830 Storage 39 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1831 Storage 40 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1832 Storage 41 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1833 Storage 42 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Installation 84 3-1834 Installation 60 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Installation 84 3-1835 Installation 81 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-1836 Storage 48 4-FPh -CH _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-1837 App. 37 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-84 84-18 1838 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-84 84-18 1839 39 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-unit 84 3-1840 unit 40 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1841 41 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-place 84 3-1842 place 42 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-84 84-1843 60 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1844 81 81 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr- 84 84 3-1845 48 3,4-diClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1846 37-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1847 38-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1848 39-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84-1849 40 4-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1850 41-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1851 42-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1852 60-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1853 81-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1854 48-ClPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1855 37-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1856 38-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1857 39-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1858 40-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1859 41-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1860 42-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 1861 60 4-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 1862 81 4-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84-1863 48-FPh -CH _Two -Single bond -CH _Two - c Pr-84 84 3-1864 37 37,4-diClPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1865 Storage 38 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -App.84 3-1866 App.39 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -App. 84 3-1867 App. 40 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -App.84 3-1868 App.41 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1869 Storage 42 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -App.84 3-1870 App.60 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -App. 84 3-1871 App. 81 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -App. 84 3-1872 App. 48 3,4-diClPh -CH _Two -Single bond -C (Me) _Two -App.84 3-1873 App.37 4-ClPh -CH _Two -Single bond -C (Me) _Two -Fig. 84 3-1874 Fig. 38 4-ClPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1875 Storage 39 4-ClPh -CH _Two -Single bond -C (Me) _Two -App.84 3-1876 App.40 4-ClPh -CH _Two -Single bond -C (Me) _Two -App.84 3-1877 App.41 4-ClPh -CH _Two -Single bond -C (Me) _Two -App. 84 3-1878 App. 42 4-ClPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1879 Storage 60 4-ClPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1880 Storage 81 4-ClPh -CH _Two -Single bond -C (Me) _Two -App. 84 3-1881 App. 48 4-ClPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1882 Storage 37 4-FPh -CH _Two -Single bond -C (Me) _Two -Installation 84 3-1883 Installation 38 4-FPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1884 Storage 39 4-FPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1885 Storage 40 4-FPh -CH _Two -Single bond -C (Me) _Two -Installation 84 3-1886 Installation 41 4-FPh -CH _Two -Single bond -C (Me) _Two -Place 84 3-1887 Place 42 4-FPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1888 Storage 60 4-FPh -CH _Two -Single bond -C (Me) _Two -Storage 84 3-1889 Storage 81 4-FPh -CH _Two -Single bond -C (Me) _Two -Installation 84 3-1890 Installation 48 4-FPh -CH _Two -Single bond -C (Me) _Two -App. 84 3-1891 App. 37 3,4-diClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1892 Storage 38 3,4-diClPh -CH _Two --CH _Two --CH _Two -App. 84 3-1893 App. 39 3,4-diClPh -CH _Two --CH _Two --CH _Two -App.84 3-1894 App.40 3,4-diClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1895 Storage 41 3,4-diClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1896 Storage 42 3,4-diClPh -CH _Two --CH _Two --CH _Two -App. 84 3-1897 App. 60 3,4-diClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1898 storage 81 3,4-diClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1899 Storage 48 3,4-diClPh -CH _Two --CH _Two --CH _Two -App.84 3-1900 App.37 4-ClPh -CH _Two --CH _Two --CH _Two -Installation 84 3-1901 Installation 38 4-ClPh -CH _Two --CH _Two --CH _Two -App.84 3-1902 App.39 4-ClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1903 Storage 40 4-ClPh -CH _Two --CH _Two --CH _Two -App.84 3-1904 App.41 4-ClPh -CH _Two --CH _Two --CH _Two -App.84 3-1905 App.42 4-ClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1906 Storage 60 4-ClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1907 Storage 81 4-ClPh -CH _Two --CH _Two --CH _Two -App.84 3-1908 App.48 4-ClPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1909 Storage 37 4-FPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1910 Storage 38 4-FPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1911 Storage 39 4-FPh -CH _Two --CH _Two --CH _Two -Installation 84 3-1912 Installation 40 4-FPh -CH _Two --CH _Two --CH _Two -Storage 84 3-1913 Storage 41 4-FPh -CH _Two --CH _Two --CH _Two -Place 84 3-1914 Place 42 4-FPh -CH _Two --CH _Two --CH _Two -Installation 84 3-1915 Installation 60 4-FPh -CH _Two --CH _Two --CH _Two -Installation 84 3-1916 Installation 81 4-FPh -CH _Two --CH _Two --CH _Two -Installation 84 3-1917 Installation 48 4-FPh -CH _Two --CH _Two --CH _Two -App.84 3-1918 App.37 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1919 Storage 38 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -App. 84 3-1920 App. 39 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -App.84 3-1921 App.40 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1922 Storage 41 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1923 Storage 42 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -App.84 3-1924 App.60 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1925 Storage 81 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1926 Storage 48 3,4-diClPh -CH _Two --CH _Two --CH _Two CH _Two -App.84 3-1927 App.37 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1928 Storage 38 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1929 Storage 39 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -App.84 3-1930 App.40 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1931 Storage 41 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -Set 84 3-1932 Set 42 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -App.84 3-1933 App.60 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -App.84 3-1934 App.81 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -App.84 3-1935 App.48 4-ClPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1936 Storage 37 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Installation 84 3-1937 Installation 38 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Place 84 3-1938 Place 39 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1939 Storage 40 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Installation 84 3-1940 Installation 41 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Place 84 3-1941 Place 42 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Installation 84 3-1942 Installation 60 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Installation 84 3-1943 Installation 81 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1944 Storage 48 4-FPh -CH _Two --CH _Two --CH _Two CH _Two -Storage 84 3-1945 Storage 37 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1946 App.38 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1947 App.39 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1948 App.40 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1949 App.41 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1950 Storage 42 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1951 Storage 60 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -App. 84 3-1952 App. 81 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1953 Storage 48 3,4-diClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1954 App.37 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1955 Storage 38 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1956 Storage 39 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1957 App.40 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1958 Installation 41 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1959 Storage 42 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1960 App.60 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1961 Installation 81 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -App.84 3-1962 App.48 4-ClPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1963 Installation 37 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1964 Installation 38 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1965 Installation 39 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1966 Installation 40 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1967 Storage 41 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1968 Storage 42 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-1969 Storage 60 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1970 Installation 81 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -Installation 84 3-1971 Installation 48 4-FPh -CH _Two --CH _Two --(CH _Two ) _Three -App. 84 3-1972 App. 37 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1973 Storage 38 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1974 Storage 39 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App.84 3-1975 App.40 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App.84 3-1976 App.41 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App.84 3-1977 App.42 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App.84 3-1978 App.60 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1979 Storage 81 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1980 Storage 48 3,4-diClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-1981 App. 37 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1982 Storage 38 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1983 Storage 39 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App.84 3-1984 App.40 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-1985 App. 41 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-1986 App. 42 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1987 Storage 60 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1988 Storage 81 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App.84 3-1989 App.48 4-ClPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1990 Storage 37 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1991 Storage 38 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1992 Storage 39 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1993 Storage 40 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1994 Storage 41 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1995 Storage 42 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1996 Storage 60 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1997 Storage 81 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-1998 Storage 48 4-FPh -CH _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-1999 App. 37 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 3-2000 38 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2001 place 39 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2002 2002 40 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2003 2003 41 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-unit 84 3-2004 Unit 42 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 3-2005 60 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2006 Place 81 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2007 Place 48 3,4-diClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2008 2008 37 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2009 Place 38 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2010 2010 39 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2011 Place 40 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2012 Place 41 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2013 2013 42 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2014 2014 60 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2015 Place 81 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2016 Place 48 4-ClPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2017 2017 37 4-FPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2018 Place 38 4-FPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2019 place 39 4-FPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 2020 40-FPh -CH _Two --CH _Two --CH _Two - c Pr-84 84-2021 41-FPh -CH _Two --CH _Two --CH _Two - c Pr-84 84-2022 42-FPh -CH _Two --CH _Two --CH _Two - c Pr-place 84 3-2023 place 60 4-FPh -CH _Two --CH _Two --CH _Two - c Pr-84 84 3-2024 81-FPh -CH _Two --CH _Two --CH _Two - c Pr-84 84-2025 48-FPh -CH _Two --CH _Two --CH _Two - c Pr-84 84-2026 37 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2027 App. 38 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2028 App. 39 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2029 App. 40 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2030 App. 41 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2031 App. 42 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2032 App. 60 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2033 App. 81 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2034 App. 48 3,4-diClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2035 App. 37 4-ClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2036 App. 38 4-ClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2037 App. 39 4-ClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2038 App. 40 4-ClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2039 App. 41 4-ClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2040 App. 42 4-ClPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2041 App. 60 4-ClPh -CH _Two --CH _Two --C (Me) _Two -Set 84 3-2042 Set 81 4-ClPh -CH _Two --CH _Two --C (Me) _Two -App.84 3-2043 App.48 4-ClPh -CH _Two --CH _Two --C (Me) _Two -Storage 84 3-2044 Storage 37 4-FPh -CH _Two --CH _Two --C (Me) _Two -Place 84 3-2045 Place 38 4-FPh -CH _Two --CH _Two --C (Me) _Two -Storage 84 3-2046 Storage 39 4-FPh -CH _Two --CH _Two --C (Me) _Two -App. 84 3-2047 App. 40 4-FPh -CH _Two --CH _Two --C (Me) _Two -Installation 84 3-2048 Installation 41 4-FPh -CH _Two --CH _Two --C (Me) _Two -Place 84 3-2049 Place 42 4-FPh -CH _Two --CH _Two --C (Me) _Two -Place 84 3-2050 Place 60 4-FPh -CH _Two --CH _Two --C (Me) _Two -Installation 84 3-2051 Installation 81 4-FPh -CH _Two --CH _Two --C (Me) _Two -Storage 84 3-2052 Storage 48 4-FPh -CH _Two --CH _Two --C (Me) _Two -Place 84 化合物 Compound number R ¹ R ^Two ABEZ 3-2053 Place 37 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2054 App. 38 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2055 App. 39 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2056 App. 40 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2057 App. 41 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2058 App. 42 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2059 App. 60 3,4-diClPh -SO _Two -Single bond -CH _Two -Set 84 3-2060 Set 81 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2061 App. 48 3,4-diClPh -SO _Two -Single bond -CH _Two -App. 84 3-2062 App. 37 4-ClPh -SO _Two -Single bond -CH _Two -Set 84 3-2063 Set 38 4-ClPh -SO _Two -Single bond -CH _Two -Storage 84 3-2064 Storage 39 4-ClPh -SO _Two -Single bond -CH _Two -App. 84 3-2065 App. 40 4-ClPh -SO _Two -Single bond -CH _Two -Set 84 3-2066 Set 41 4-ClPh -SO _Two -Single bond -CH _Two -Set 84 3-2067 Set 42 4-ClPh -SO _Two -Single bond -CH _Two -Set 84 3-2068 Set 60 4-ClPh -SO _Two -Single bond -CH _Two -Set 84 3-2069 Set 81 4-ClPh -SO _Two -Single bond -CH _Two -App.84 3-2070 App.48 4-ClPh -SO _Two -Single bond -CH _Two -Storage 84 3-2071 Storage 37 4-FPh -SO _Two -Single bond -CH _Two -Storage 84 3-2072 Storage 38 4-FPh -SO _Two -Single bond -CH _Two -Storage 84 3-2073 Storage 39 4-FPh -SO _Two -Single bond -CH _Two -Storage 84 3-2074 Storage 40 4-FPh -SO _Two -Single bond -CH _Two -Storage 84 3-2075 Storage 41 4-FPh -SO _Two -Single bond -CH _Two -Storage 84 3-2076 Storage 42 4-FPh -SO _Two -Single bond -CH _Two -Storage 84 3-2077 Storage 60 4-FPh -SO _Two -Single bond -CH _Two -Installation 84 3-2078 Installation 81 4-FPh -SO _Two -Single bond -CH _Two -Storage 84 3-2079 Storage 48 4-FPh -SO _Two -Single bond -CH _Two -App. 84 3-2080 App. 37 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2081 Storage 38 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -App. 84 3-2082 App. 39 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -App. 84 3-2083 App. 40 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2084 Storage 41 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -App.84 3-2085 App.42 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -App.84 3-2086 App.60 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -Set 84 3-2087 Set 81 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -App.84 3-2088 App.48 3,4-diClPh -SO _Two -Single bond -CH _Two CH _Two -App. 84 3-2089 App. 37 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2090 Storage 38 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -App. 84 3-2091 App. 39 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -Set 84 3-2092 Set 40 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -App.84 3-2093 App.41 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -App. 84 3-2094 App. 42 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2095 Storage 60 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -Set 84 3-2096 Set 81 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2097 Storage 48 4-ClPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2098 Storage 37 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2099 Storage 38 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2100 Storage 39 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2101 Storage 40 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Installation 84 3-2102 Installation 41 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2103 Storage 42 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Storage 84 3-2104 Storage 60 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Installation 84 3-2105 Installation 81 4-FPh -SO _Two -Single bond -CH _Two CH _Two -Place 84 3-2106 Place 48 4-FPh -SO _Two -Single bond -CH _Two CH _Two -App. 84 3-2107 App. 37 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2108 App. 38 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2109 App. 39 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2110 Storage 40 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2111 Storage 41 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2112 Storage 42 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2113 Storage 60 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2114 Storage 81 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2115 App. 48 3,4-diClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2116 App. 37 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2117 Storage 38 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2118 Storage 39 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2119 App. 40 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2120 App. 41 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2121 App. 42 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2122 App. 60 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -Set 84 3-2123 Set 81 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2124 App. 48 4-ClPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2125 Storage 37 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2126 Storage 38 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2127 Storage 39 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2128 Storage 40 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2129 Storage 41 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2130 Storage 42 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2131 Storage 60 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2132 Storage 81 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -Storage 84 3-2133 Storage 48 4-FPh -SO _Two -Single bond-(CH _Two ) _Three -App. 84 3-2134 App. 37 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2135 Storage 38 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2136 Storage 39 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2137 App. 40 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2138 App. 41 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2139 Storage 42 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2140 App. 60 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2141 App. 81 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2142 App. 48 3,4-diClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2143 App. 37 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2144 Storage 38 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2145 App. 39 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2146 App. 40 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2147 App. 41 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App.84 3-2148 App.42 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2149 App. 60 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2150 Storage 81 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2151 App. 48 4-ClPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2152 Storage 37 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2153 Storage 38 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2154 Storage 39 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Installation 84 3-2155 Installation 40 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Installation 84 3-2156 Installation 41 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2157 Storage 42 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2158 Storage 60 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Storage 84 3-2159 Storage 81 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -Place 84 3-2160 Place 48 4-FPh -SO _Two -Single bond -CH _Two C (Me) _Two -App. 84 3-2161 App. 37 3,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-place 84 3-2162 place 38 3,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 2-2163 39 39,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-unit 84 3-2164 Unit 40 3,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2165 41 41,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-unit 84 3-2166 Unit 42 3,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2167 60 3,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2168 81 81 3,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-device 84 3-2169 device 48 3,4-diClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2170 37-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2171 38-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2172 39-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2173 40 4-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2174 41-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2175 42-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2176 60-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2177 81-ClPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2178 48-ClPh -SO _Two -Single bond -CH _Two - c Pr-place 84 3-2179 place 37 4-FPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2180 38-FPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2181 39-FPh -SO _Two -Single bond -CH _Two - c Pr-place 84 3-2182 place 40 4-FPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2183 41-FPh -SO _Two -Single bond -CH _Two - c Pr-place 84 3-2184 place 42 4-FPh -SO _Two -Single bond -CH _Two - c Pr-place 84 3-2185 Place 60 4-FPh -SO _Two -Single bond -CH _Two - c Pr-84 84 3-2186 81-FPh -SO _Two -Single bond -CH _Two - c Pr-place 84 3-2187 place 48 4-FPh -SO _Two -Single bond -CH _Two - c Pr-84 84-2 2188 37 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2189 Storage 38 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -App. 84 3-2190 App. 39 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2191 Storage 40 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -App. 84 3-2192 App. 41 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2193 Storage 42 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -App. 84 3-2194 App. 60 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2195 Storage 81 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2196 Storage 48 3,4-diClPh -SO _Two -Single bond -C (Me) _Two -App. 84 3-2197 App. 37 4-ClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2198 Storage 38 4-ClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2199 Storage 39 4-ClPh -SO _Two -Single bond -C (Me) _Two -App. 84 3-2200 App. 40 4-ClPh -SO _Two -Single bond -C (Me) _Two -App. 84 3-2201 App. 41 4-ClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2202 Storage 42 4-ClPh -SO _Two -Single bond -C (Me) _Two -App.84 3-2203 App.60 4-ClPh -SO _Two -Single bond -C (Me) _Two -Set 84 3-2204 Set 81 4-ClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2205 Storage 48 4-ClPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2206 Storage 37 4-FPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2207 Storage 38 4-FPh -SO _Two -Single bond -C (Me) _Two -Installation 84 3-2208 Installation 39 4-FPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2209 Storage 40 4-FPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2210 Storage 41 4-FPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2211 Storage 42 4-FPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2212 Storage 60 4-FPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2213 Storage 81 4-FPh -SO _Two -Single bond -C (Me) _Two -Storage 84 3-2214 Storage 48 4-FPh -SO _Two -Single bond -C (Me) _Two -App. 84 3-2215 App. 37 3,4-diClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2216 App. 38 3,4-diClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2217 App. 39 3,4-diClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2218 App. 40 3,4-diClPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2219 Storage 41 3,4-diClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2220 App. 42 3,4-diClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2221 App. 60 3,4-diClPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2222 Storage 81 3,4-diClPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2223 Storage 48 3,4-diClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2224 App. 37 4-ClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2225 App. 38 4-ClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2226 App. 39 4-ClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2227 App. 40 4-ClPh -SO _Two --CH _Two --CH _Two -Set 84 3-2228 Set 41 4-ClPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2229 Storage 42 4-ClPh -SO _Two --CH _Two --CH _Two -Set 84 3-2230 Set 60 4-ClPh -SO _Two --CH _Two --CH _Two -Set 84 3-2231 Set 81 4-ClPh -SO _Two --CH _Two --CH _Two -App. 84 3-2232 App. 48 4-ClPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2233 Storage 37 4-FPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2234 Storage 38 4-FPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2235 Storage 39 4-FPh -SO _Two --CH _Two --CH _Two -Installation 84 3-2236 Installation 40 4-FPh -SO _Two --CH _Two --CH _Two -Installation 84 3-2237 Installation 41 4-FPh -SO _Two --CH _Two --CH _Two -Place 84 3-2238 Place 42 4-FPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2239 Storage 60 4-FPh -SO _Two --CH _Two --CH _Two -Installation 84 3-2240 Installation 81 4-FPh -SO _Two --CH _Two --CH _Two -Storage 84 3-2241 Storage 48 4-FPh -SO _Two --CH _Two --CH _Two -App. 84 3-2242 App. 37 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2244 Storage 39 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2245 App. 40 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2246 App. 41 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2247 App. 42 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2248 App. 60 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2249 Storage 81 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -App.84 3-2250 App.48 3,4-diClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2251 App. 37 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2252 App. 38 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2253 App. 39 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2254 App. 40 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2255 App. 41 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2256 App. 42 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2257 Storage 60 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -Set 84 3-2258 Set 81 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2259 Storage 48 4-ClPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2260 Storage 37 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2261 Storage 38 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2262 Storage 39 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2263 Storage 40 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Installation 84 3-2264 Installation 41 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2265 Storage 42 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Installation 84 3-2266 Installation 60 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Installation 84 3-2267 Installation 81 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -Storage 84 3-2268 Storage 48 4-FPh -SO _Two --CH _Two --CH _Two CH _Two -App. 84 3-2269 App. 37 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2270 App. 38 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2271 App. 39 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2272 App. 40 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2273 Storage 41 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2274 App. 42 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2275 Storage 60 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2276 Storage 81 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2277 Storage 48 3,4-diClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2278 App. 37 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2279 Storage 38 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2280 App. 39 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2281 App. 40 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2282 App. 41 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2283 App. 42 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2284 App. 60 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -Set 84 3-2285 Set 81 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2286 Storage 48 4-ClPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2287 Storage 37 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2288 Storage 38 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2289 Storage 39 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Place 84 3-2290 Place 40 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2291 Storage 41 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2292 Storage 42 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2293 Storage 60 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2294 Storage 81 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -Storage 84 3-2295 Storage 48 4-FPh -SO _Two --CH _Two --(CH _Two ) _Three -App. 84 3-2296 App. 37 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2297 Storage 38 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2298 App. 39 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2299 App. 40 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2300 Storage 41 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2301 Storage 42 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2302 App. 60 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2303 Storage 81 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2304 App. 48 3,4-diClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2305 App. 37 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2306 Storage 38 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2307 App. 39 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2308 Storage 40 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2309 Storage 41 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2310 App. 42 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2311 Storage 60 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2312 App. 81 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2313 Storage 48 4-ClPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2314 Storage 37 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2315 Storage 38 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Installation 84 3-2316 Installation 39 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Installation 84 3-2317 Installation 40 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Installation 84 3-2318 Installation 41 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2319 Storage 42 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Place 84 3-2320 Place 60 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2321 Storage 81 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -Storage 84 3-2322 Storage 48 4-FPh -SO _Two --CH _Two --CH _Two C (Me) _Two -App. 84 3-2323 App. 37 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-unit 84 3-2324 Unit 38 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-device 84 3-2325 device 39 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2326 40 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2327 41 41 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-unit 84 3-2328 Unit 42 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-unit 84 3-2329 Unit 60 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-unit 84 3-2330 Unit 81 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2331 48 3,4-diClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2332 37-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2333 38-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2334 39-ClPh -SO _Two --CH _Two --CH _Two - c Pr- 84 84 3-2335 40 4-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2336 41-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2337 42-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2338 60 60-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2339 81-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2340 48-ClPh -SO _Two --CH _Two --CH _Two - c Pr-84 843-2341 37-FPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2342 38 38-FPh -SO _Two --CH _Two --CH _Two - c Pr-location 84 3-2343 location 39 4-FPh -SO _Two --CH _Two --CH _Two - c Pr-place 84 3-2344 place 40 4-FPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2345 Station 41 4-FPh -SO _Two --CH _Two --CH _Two - c Pr-place 84 3-2346 Place 42 4-FPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 3-2347 60-FPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 2-2348 81 4-FPh -SO _Two --CH _Two --CH _Two - c Pr-place 84 3-2349 place 48 4-FPh -SO _Two --CH _Two --CH _Two - c Pr-84 84 2-2350 37 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2351 Storage 38 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2352 Storage 39 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -App. 84 3-2353 App. 40 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2354 Storage 41 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -App. 84 3-2355 App. 42 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -App. 84 3-2356 App. 60 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2357 Storage 81 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2358 Storage 48 3,4-diClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2359 Storage 37 4-ClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2360 Storage 38 4-ClPh -SO _Two --CH _Two --C (Me) _Two -App. 84 3-2361 App. 39 4-ClPh -SO _Two --CH _Two --C (Me) _Two -App. 84 3-2362 App. 40 4-ClPh -SO _Two --CH _Two --C (Me) _Two -Set 84 3-2363 Set 41 4-ClPh -SO _Two --CH _Two --C (Me) _Two -Set 84 3-2364 Set 42 4-ClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2365 Storage 60 4-ClPh -SO _Two --CH _Two --C (Me) _Two -Set 84 3-2366 Set 81 4-ClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2367 Storage 48 4-ClPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2368 Storage 37 4-FPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2369 Storage 38 4-FPh -SO _Two --CH _Two --C (Me) _Two -Place 84 3-2370 Place 39 4-FPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2371 Storage 40 4-FPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2372 Storage 41 4-FPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2373 Storage 42 4-FPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2374 Storage 60 4-FPh -SO _Two --CH _Two --C (Me) _Two -Installation 84 3-2375 Installation 81 4-FPh -SO _Two --CH _Two --C (Me) _Two -Storage 84 3-2376 Storage 48 4-FPh -SO _Two --CH _Two --C (Me) _Two -置 84 ──────────────────────────────────── In the table, “Me” is methyl, “iPr "Is isopropyl," A
"c" is acetyl, "Ph" is a phenyl group, " c Pr "
Lopropane-1,1-diyl, " c "Bu" is cyclobutane
-1,1-diyl, " c "Pn" is cyclopentane-1,1
-Jeir, " c "Hx" is cyclohexane-1,1-diyl
And the equation S ^* → O is as defined above.

Among the compounds shown in Table 1 above, preferred compounds are Compound Nos. 1-1025 to 1
-1536 and compound No. 1-4097. Further, preferred compounds include compounds of Compound Nos. 1-1089 to 1-1120, and Compounds Nos. 1-1217 to 1-128.
0, Compound Nos. 1-1313 to 1
Compound No.-1344, Compound Nos. 1-1505 to 1-1536 and Compound No.1-409
7 can be mentioned. The most preferred compounds include
Compounds Nos. 1-1108 to 1-1120, Compound Nos. 1-1313 to 1-11-1
344 and Compound No. 1-4097.

Preferred compounds among the compounds in Table 2 above are Compound Nos. 2-1537 to 2
Compound No. -1728, Compound No. 2-1825 to Compound No. 2-1920, Compound No. 2-1969
To Compound No. 2-2016, Compound No. 2-
2113 to compound No. 2-2160, and
Compounds Nos. 2-2257 to 2-2352 can be mentioned. Further, preferred compounds include Compound Nos. 2-1825 to 2-1.
Compound No. 920, Compound Nos. 2-1969 to 2-2016, and Compound No. 2-225
7 to Compound No. 2-2352. The most preferred compound is Compound No. 2-1.
969 to Compound No. 2-2016.

Among the compounds shown in Table 3 above, preferred compounds are Compound Nos. 3-1 to 3-64 and 3-
97 to 3-160.

Further preferred compounds include compound No. 3
-5 to 3-11, 3-17, 3-18, 3-37 to 3-43, 3-49, 3-50, 3-101 to 3-1
07, 3-113, 3-114, 3-133 to 3-1
39, 3-145, and 3-146.

Most preferably, Compound Nos. 3-7 and 3-
8, 3-10, 3-11, 3-39, 3-40, 3-4
2, 3-43, 3-103, 3-104, 3-106,
The compounds of 3-107, 3-135, 3-136, 3-138 and 3-139 can be mentioned.

Hereinafter, a specific example will be described with reference to a reference example.

[0467]

Reference Example 1 N-tert-butoxycarbonyl-4-phenylpiperidi
4-Carboxylic acid dimethylamide N-tert-butoxycarbonyl-4-phenylpiperidine-4-carboxylic acid 1.0 g (3.27 mmol)
It was dissolved in 20 ml of anhydrous methylene chloride, and 690 mg of WSC (water-soluble carbodiimide: 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide hydrochloride) (3.
HOBT (1-hydroxybenzotriazole) 490 mg (3.6 mmol) and diisopropylethylamine 1.3 ml (7.53 mmol),
295 mg (3.93 mmol) of dimethylamine hydrochloride
Was added and stirred at room temperature under a nitrogen atmosphere for 15 hours.
The reaction solution was diluted with methylene chloride, washed with water and saturated saline, and then dried over sodium sulfate. After the solvent was concentrated under reduced pressure, the residue was subjected to silica gel chromatography (developing solvent;
Purification was performed using ethyl acetate: n-hexane = 10: 1 to 7: 1) to obtain 925 mg of the target compound as white crystals.
(85%). Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δppm: 7.34 (2H, dt, J = 6.7,1.9Hz), 7.26-7.21 (3H, m),
3.96 (2H, br.s), 3.21 (2H, br.s), 2.85 (3H, br.s), 2.60 (3H,
br.s), 2.31 (2H, d, J = 12.05Hz), 1.87 (2H, br.s), 1.45 (9H,
s) Mass spec value m / z 332 (M ⁺ )

[0468]

[Reference Example 2] 4-Phenylpiperidine-4-carboxylic acid dimethylamine
The de hydrochloride [Reference Example 1] synthesized amide 900 mg (2.7 mmol) was dissolved in ethyl acetate 10 ml, 4N hydrochloric acid-dioxane 5 ml, under ice-cooling, the mixture was stirred for 1 hour at 0 ℃ . The precipitated crystals were collected by filtration to obtain 690 mg (95%) of the target compound as white crystals. Nuclear magnetic resonance spectrum (400 MHz, DMSO-d
₆ ) δppm: 9.02 (1H, br.s), 7.43 (2H, t, J = 7.6Hz),
7.31 (1H, d, J = 7.2Hz), 7.23 (2H, d, J = 7.1Hz), 3.25 (2H, d, J =
13.1Hz), 3.03 (2H, t, J = 12.1Hz), 2.79 (3H, br.s), 2.54 (3H,
br.s), 2.37 (2H, d, J = 12.9 Hz), 2.11 (2H, dt, J = 13.4, 3.3 Hz) Mass spec. m / z 232 (free M ⁺ )

[0469]

Reference Example 3 Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] hydrochloride

[0470]

Reference Example 3 (a) 1′-cyanospiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] 2.34 g (22.1 mmol) of bromine cyanide are dissolved in 20 ml of anhydrous chloroform, and the mixture is refluxed with J. Org. Chem., 4
1, 2 '(2.276 g, 10 mmol) of 1'-methyl-spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] synthesized according to the method described in page 2628 (1976). Chloroform solution under nitrogen atmosphere, 2
It was added dropwise over 0 minutes. After refluxing for 9 hours, the mixture was cooled, poured into ice-cooled 1N hydrochloric acid, then the chloroform layer was washed with water and dried over anhydrous sodium sulfate. Solvent
The residue was purified by silica gel column chromatography (developing solvent: ethyl acetate: n-hexane = 1: 9) to obtain 1.3 g (56%) of the target compound as white crystals. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δppm: 7.38-7.27 (3H, m), 7.21 (1H, dd, J = 1.9,6.4Hz), 4.
20 (2H, s), 3.51 (2H, m), 3.37 (2H, dt, J = 2.2,12.9Hz), 2.29
(2H, dt, J = 4.6,12.9Hz), 1.91 (2H, m) Mass spectrum: 231 ((M + H) ⁺ )

[0471]

Reference Example 3 (b) 1′-tert-butoxycarbonylspiro [benzo [c]
Thiophene-1 (3H), 4′-piperidine] 1′-cyanospiro [benzo [c] thiophen-1 (3H), 4′-piperidine] synthesized in Reference Example 3 (a).
1.3 g (5.64 mmol) was dissolved in 20% aqueous hydrochloric acid and refluxed for 20 hours. After the reaction solution was cooled and washed with ethyl acetate, the aqueous layer was made alkaline with 10% aqueous sodium hydroxide and extracted three times with chloroform. After evaporating the solvent under reduced pressure, the residue was dissolved in anhydrous methylene chloride, 1.15 ml (8.18 mmol) of triethylamine was added, and 1.45 g of di-tert-butyl dicarbonate (6.
64 mmol) and stirred at room temperature for 2 hours. The reaction solution was diluted with methylene chloride and washed sequentially with water and saturated saline. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (developing solvent: ethyl acetate: n-hexane = 3: 97) to obtain 1.65 of the target compound as white crystals.
g (96%). Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δppm: 7.28-7.24 (3H, m), 7.17-7.15 (1H, m), 4.23 (2H, b
rs), 4.19 (2H, s), 3.02 (2H, br.s), 2.07 (2H, dt, J = 4.4,13H
z), 1.88 (2H, m), 1.49 (9H, s) Mass spectrum: 305 (M ⁺ )

[0472]

Reference Example 3 (c) Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] was synthesized Hydrochloride Reference Example 3 (b), 1'-tert- butoxycarbonyl-spiro [benzo [c] thiophene -1 (3H),
4′-piperidine] 150 mg (0.49 mmol)
The residue was dissolved in 3 ml of anhydrous methylene chloride, 1 ml of 4N hydrochloric acid-dioxane was added, and the mixture was stirred at room temperature for 1 hour.
%). Nuclear magnetic resonance spectrum (400 MHz, DMSO-d
₆ ) δppm: 9.77 (2H, br.s), 7.37-7.25 (4H, m), 4.24 (2H
H, s), 3.67 (2H, d, J = 12.6Hz), 3.26 (2H, dt, J = 12.6,2.5Hz),
2.74 (2H, dt, J = 3.8,14.0Hz), 2.09 (2H, d, J = 14.0Hz) Mass spectrum: 206 ((M + H) ⁺ ) (free form)

[0473]

Reference Example 4 Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] -2-oxide hydrochloride

[0474]

Reference Example 4 (a) 1′-tert-butoxycarbonylspiro [benzo [c]
Thiophene-1 (3H), 4'-piperidine-2-oxo
1′-tert-butoxycarbonylspiro [benzo [c] thiophene-1 (3H), synthesized in Sid Reference Example 3 (b),
4'-piperidine] 485 mg (1.59 mmol)
Dissolve in 5 ml of anhydrous methylene chloride and add sodium hydrogen carbonate 1
48 mg (1.76 mmol) were added. Under ice-cooling, 325 mg (1.88 mmol, 85% content) of metachloroperbenzoic acid was added. After stirring for 30 minutes under ice-cooling, the mixture was diluted with methylene chloride and washed with water and saturated saline in this order. After drying over anhydrous sodium sulfate, the solvent is distilled off under reduced pressure, and the residue is subjected to thin layer chromatography (developing solvent:
Purification by ethyl acetate: n-hexane = 2: 1) gave 498 mg (98%) of the target compound as white crystals. Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δppm: 7.37-7.32 (3H, m), 7.25-7.23 (1H, m), 4.37 (1H, d,
J = 16.7Hz), 4.13 (2H, br.s), 4.05 (2H, d, J = 16.7Hz), 3.21 (2H
H, br.s), 2.43 (1H, m), 2.21 (1H, m), 1.70 (1H, m), 1.61 (1H, m
m), 1.50 (9H, s) Mass spectrum: 322 ((M + H) ⁺ )

[0475]

Reference Example 4 (b) Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] -2-oxide hydrochloride 1′-tert-butoxycarbonylspiro [benzo [c] thiophene-1 (3H), synthesized in Reference Example 4 (a),
4'-piperidine] -2-oxide (295 mg, 0.92
Mmol) was dissolved in 3 ml of methylene chloride, and cooled under ice-cooling.
1 ml of normal hydrochloric acid-dioxane was added. 1 hour under ice cooling
After stirring, the precipitated crystals were collected by filtration to obtain 173 mg (75%) of the target compound as white crystals. Nuclear magnetic resonance spectrum (400 MHz, DMSO-d
₆ ) δppm: 9.13 (2H, br.s), 7.44-7.36 (3H, m), 7.33-
7.31 (1H, m), 4.66 (1H, d, J = 17Hz), 4.08 (1H, d, J = 17Hz), 3.4
9-3.37 (2H, m), 3.15-3.00 (2H, m), 2.66-2.57 (1H, m), 2.27-
2.23 (1H, m), 2.18-2.10 (1H, m), 1.97-1.93 (1H, m) Mass spectrum: 222 ((M + H) ⁺ ) (free form)

[0476]

Reference Example 5 Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] -2-oxide

[0477]

Reference Example 5 (a) 1′-tert-butoxycarbonyl-spiro [benzo
[C] Thiophene-1 (3H), 4'-piperidine] 81.0 g (0.40 mol) of 2-bromobenzylthiol was dissolved in 800 ml of tetrahydrofuran, and -7
At 8 ° C., 516 ml (0.84 mol) of n-butyllithium (1.6 mol, hexane solution) was added dropwise over 6 hours. After stirring at the same temperature for 1.5 hours, 79.5 g of N-tert-butoxycarbonyl-4-piperidone (0.4 g) was added.
(0 mol) in 800 ml of tetrahydrofuran was added dropwise over 3 hours. After further stirring for 1 hour, a saturated aqueous solution of ammonium chloride was added, followed by extraction with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, 2 L of 4N sulfuric acid was added to the residue, and the mixture was refluxed for 14 hours. Then under ice cooling,
The mixture was made alkaline with 350 g (8.75 mol) of sodium hydroxide and 102 g of di-tert-butyl dicarbonate.
(0.47 mol) was added and stirred for 1 hour. After extraction with methylene chloride, the organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 97: 3) to obtain 56 g of the desired compound as white crystals.

131.0-132.5 ° C. (n-hexane-ethyl acetate) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.28-7.24 (3H, m), 7.17-7.15 (1H, m), 4.23 (2H, b
rs), 4.19 (2H, s), 3.02 (2H, br.s), 2.07 (2H, dt, J = 4.4,13H
z), 1.88 (2H, m), 1.49 (9H, s) Infrared absorption spectrum ν _max cm ^-1 (KBr): 297
0, 1680, 1428, 1234, 1163 Mass spectrum (FAB) m / z: 306 ((M + H)
⁺ ).

[0479]

Reference Example 5 (b) 1′-tert-butoxycarbonyl-spiro [benzo
[C] thiophene-1 (3H), 4'-piperidine]-
2-Oxide 1'-tert-butoxycarbonyl-spiro [benzo [c] thiophene-1 (3) obtained in Reference Example 5 (a)
H), 4'-piperidine] 42.0 g (0.14 mol)
Was dissolved in 420 ml of chloroform, 12.7 g (0.15 mol) of sodium hydrogencarbonate was added, and m was added under ice-cooling.
28.0 g of chloroperbenzoic acid (containing 85%, 0.14
Mol) was added in small portions. After further stirring for 30 minutes under ice cooling, 10 g of potassium iodide was added, and the mixture was stirred at room temperature for 30 minutes. After washing with water and saturated saline, it was dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 1: 1) to obtain 42 g of the desired compound as white crystals.

103-107 ° C. (diisopropyl ether) Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ ) δ
ppm: 7.37-7.32 (3H, m), 7.25-7.23 (1H, m), 4.37 (1H, d,
J = 16.7Hz), 4.13 (2H, br.s), 4.05 (2H, d, J = 16.7Hz), 3.21 (2H
H, br.s), 2.43 (1H, m), 2.21 (1H, m), 1.70 (1H, m), 1.61 (1H, m
m), 1.50 (9H, s) infrared absorption spectrum ν _max cm ^-1 (KBr): 298
5, 1686, 1429, 1368, 1286, 116
7 Mass spectrum (FAB) m / z: 322 ((M + H)
⁺ ).

[0481]

Reference Example 5 (c) Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] -2-oxide 1′-tert-butoxycarbonyl-spiro [benzo [c] thiophene-1 (3) obtained in Reference Example 5 (b)
H), 4'-Piperidine] -2-oxide 42.0 g
(0.13 mol) was dissolved in 2-propanol (420 ml), and 4N hydrochloric acid in dioxane (150 m
l) was added and stirred for 4 hours. Diethyl ether (20
0 ml) and left for 1 hour under ice-cooling. The precipitated crystals were collected by filtration, and the obtained crystals were washed with 5% aqueous sodium hydroxide (20%).
0 ml). After extraction with methylene chloride, the organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain 21.7 g of the target compound as white amorphous.

[0482]

Reference Example 6 Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] -2,2-dioxide hydrochloride

[0483]

Reference Example 6 (a) 1′-tert-butoxycarbonylspiro [benzo [c]
Thiophene-1 (3H), 4'-piperidine] -2,2
1′-tert-butoxycarbonylspiro [benzo [c] thiophene-1 (3H), synthesized in -Dioxide Reference Example 4 (a),
4'-piperidine] -2-oxide 190 mg (0.59
Of Oxone ^™
270 mg (1.77 mmol) of a 10 ml aqueous solution were added. After stirring at room temperature for 5 days, the mixture was poured into water and extracted twice with chloroform. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The residue was purified by thin-layer chromatography (developing solvent: ethyl acetate: n-hexane = 1: 1) to give 175 mg of the target compound as white crystals.
(88%). Nuclear magnetic resonance spectrum (400 MHz, CDCl ₃ )
δppm: 7.52-7.27 (3H, m), 7.23-7.20 (1H, m), 4.36 (2H, m
s), 4.10 (2H, br.s), 3.44 (2H, br.s), 2.38 (2H, m), 2.00 (2H,
m), 1.50 (9H, s) Mass spectrum: 337 (M ⁺ )

[0484]

Reference Example 6 (b) Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine] -2,2-dioxide hydrochloride 1′-tert-butoxycarbonylspiro [benzo [c] thiophene-1 (3H), synthesized in Reference Example 6 (a),
4'-Piperidine] -2,2-dioxide 170 mg
(0.5 mmol) was dissolved in 3 ml of methylene chloride, and 1 ml of 4N hydrochloric acid-dioxane was added under ice cooling. below freezing,
After stirring for 1 hour, the precipitated crystals were collected by filtration to obtain 131 mg (95%) of the target compound as white crystals. Nuclear magnetic resonance spectrum (400 MHz, DMSO-d
₆ ) δppm: 9.32 (2H, br.s), 7.51-7.35 (4H, m), 4.74 (2H
H, s), 3.45-3.67 (2H, m), 3.24-3.12 (2H, m), 2.47-2.43 (4H,
m) Mass spectrum: 238 ((M + H) ⁺ ) (free form)

[0485]

Reference Example 7 3- (3,4-dichlorophenyl) -3-butene-1-
All tert-butyldimethylsilyl ether

[0486]

Reference Example 7 (a) 3- (3,4-dichlorophenyl) -3-oxo-1-
119 g (0.46 mol) of propanolethyl 3- (3,4-dichlorophenyl) -3-oxopropionate are dissolved in 2.4 liters of ethanol, and ethyl orthoformate 115 is dissolved.
ml (0.68 mol) and p-toluenesulfonic acid4.
4 g (22.8 mmol) was added, and the mixture was heated under reflux for 8 hours. The reaction solution was poured into 1 liter of saturated aqueous sodium hydrogen carbonate and extracted with ethyl acetate (700 ml × 3 times). The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. After evaporating the solvent under reduced pressure, the residue was treated with tetrahydrofuran 8
Dissolved in lithium aluminum hydride.
To a suspension of 4 g of tetrahydrofuran of 9 g (0.68 mol) was added dropwise over 1 hour under ice cooling. After stirring at 0 ° C. for 2 hours, water (250 ml) and 10% aqueous sodium hydroxide (125 ml) were added, and the mixture was further stirred at room temperature for 1 hour. The mixture was filtered through celite, the filtrate was poured into 1 liter of saturated saline, and extracted with ethyl acetate. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure.
Dissolved in 0 ml. Under ice-cooling, 500 ml of 50% trifluoroacetic acid was added dropwise over 30 minutes, and the mixture was further stirred for 30 minutes. The reaction solution was diluted with 300 ml of methylene chloride, and the organic layer was washed with water and saturated aqueous sodium hydrogen carbonate, and then dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 9: 1) to obtain 46 g of the desired compound as white crystals.

Nuclear magnetic resonance spectrum (270 MHz, C
DCl ₃ ) δ ppm: 8.05 (1H, d, J = 2.0 Hz), 7.79 (1H, dd,
J = 2.0,8.1Hz), 7.57 (1H, d, J = 8.1Hz), 4.04 (2H, m), 3.19 (2
H, t, J = 5.3Hz) , 2.44 (1H, t, J = 6.6Hz, D 2 O disappeared).

[0488]

Reference Example 7 (b) 3- (3,4-dichlorophenyl) -3-oxo-1-
Propanol tert-butyldimethylsilyl ether
Obtained in Le Reference Example 7 (a) 3- (3,4- dichlorophenyl) -3-oxo-1-propanol 46.0g
(0.21 mol) was dissolved in 460 ml of dimethylformamide, and under ice-cooling, 35 ml of triethylamine (0.2 ml) was dissolved.
5 mol) and tert-butyldimethylchlorosilane 3
8.0 g (0.25 mol) was added, and the mixture was stirred at 0 ° C. for 2 hours. Pour the reaction solution into water, extract with ethyl acetate,
The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: n-hexane: ethyl acetate = 96: 4) to obtain 66.1 g of the desired compound as white crystals.

The nuclear magnetic resonance spectrum (270 MHz, C
DCl ₃ ) δ ppm: 8.06 (1H, d, J = 2.0 Hz), 7.80 (1H, dd,
J = 2.0,8.3Hz), 7.55 (1H, d, J = 8.3Hz), 4.04 (2H, t, J = 6.3H
z), 3.13 (2H, t, J = 6.3 Hz), 0.85 (9H, s), 0.04 (6H, s).

[0490]

Reference Example 7 (c) 3- (3,4-dichlorophenyl) -3-butene-1-
All tert-butyldimethylsilyl ether methyltriphenylphosphonium bromide 215 g
(0.60 mol) and 54 g of potassium t-butoxide
(0.48 mol) was added to 2 liters of dry benzene and stirred at room temperature for 9 hours. 3- (3,4-dichlorophenyl) -3-oxo-1- obtained in Reference Example 7 (b)
40 g (0.12 mol) of propanol tert-butyldimethylsilyl ether was dissolved in 800 ml of benzene, and slowly added dropwise over 2.5 hours. One liter of water was added to the reaction solution, and the mixture was stirred under ice cooling for 30 minutes. The organic layer was separated, washed with water and saturated saline, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel chromatography (elution solvent: n-hexane) to obtain 23.5 g of the desired compound.

Nuclear magnetic resonance spectrum (400 MHz, C
DCl ₃ ) δ ppm: 7.50 (1H, d, J = 2.1 Hz), 7.38 (1H,
d, J = 8.1Hz), 7.24 (1H, dd, J = 8.1,2.1Hz), 5.35 (1H, s), 5.16
(1H, s), 3.70 (2H, t, J = 6.9Hz), 2.67 (2H, t, J = 6.9Hz), 0.86
(9H, s), 0.00 (6H, s).

[0492]

Reference Example 8 3- (3,4-dichlorophenyl) -3-butene-1-
129 mg (5.31 mmol) of all tert-butyldimethylsilyl ether metal magnesium was added to 2 ml of diethyl ether, and a small amount of iodine was added. 1.01 g of 3,4-dichlorobromobenzene (4.
(47 mmol) in diethyl ether (1 ml) was added dropwise, and the mixture was stirred under a nitrogen atmosphere at room temperature for 1 hour. 3-Iodo-3-buten-1-ol 500 mg (1.60 mmol) of tert-butyldimethylsilyl ether and 34 mg (0.048 mmol) of bistriphenylphosphinepalladium (II) chloride were dissolved in 5 ml of dry tetrahydrofuran. The Grignard reagent prepared above was added dropwise at room temperature under a nitrogen atmosphere. Diethyl ether was distilled off while raising the temperature of the reaction solution, and then 60 ° C.
For 1 hour. The reaction solution was poured into an aqueous ammonium chloride solution and extracted with ethyl acetate. The organic layer was washed with saturated saline and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel column chromatography (elution solvent: n-hexane) to obtain the target compound (42).
2 mg were obtained. Various instrument data were consistent with those obtained in Reference Example 7 (c).

[0493]

Reference Example 9 Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine]-(2S) -oxide hydrochloride

[0494]

Reference Example 9 (a) Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine]-(2S) -oxide (S)-(+)-
Spiro obtained in mandelate Reference Example 5 [benzo [c] thiophene -
1 (3H), 4'-piperidine] -2-oxide33.
51 g (0.15 mol) of 3350 ml of acetonitrile
Dissolved in heat and then (S)-(+)-mandelic acid 1
1.52 g (75.7 mmol) were dissolved and left at room temperature overnight. The precipitated crystals were collected by filtration to give the desired compound as 19.
62 g were obtained as white crystals. The mother liquor was concentrated under reduced pressure, the residue was dissolved in 5% aqueous sodium hydroxide, and extracted with methylene chloride. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure, and the residue was 22.01 g (99.5 mmol).
I got The residue was dissolved by heating in 2200 ml of acetonitrile, and 7.22 g of (R)-(-)-mandelic acid was obtained.
(47.5 mmol) was dissolved and left at room temperature overnight.
The precipitated crystals were collected by filtration, and 15.91 g of spiro [benzo [c] thiophene-1 (3H), 4′-piperidine]-(2R) -oxide (R)-(−)-mandelic acid salt was obtained as white crystals. Obtained. Further, the mother liquor was concentrated under reduced pressure, and
% Aqueous sodium hydroxide and extracted with methylene oxide. After the organic layer was dried over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure to obtain 11.51 g (52.0 mmol) of a residue. The residue was heated and dissolved in 1100 ml of acetonitrile, and then 3.95 g of (S)-(+)-mandelic acid (2
6.0 mmol) was dissolved and left at room temperature overnight. The precipitated crystals were collected by filtration to obtain 4.73 g of the desired compound as white crystals. 24.0 out of a total of the obtained target compound.
0 g was dissolved again in 9.6 liters of acetonitrile by heating, and left overnight at room temperature. 20.13 g of precipitated crystals were obtained. This optical purity is 1'-tert-butoxycarbonylspiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine]-(2S) -oxide, which was confirmed to be 99.8% ee by HPLC analysis.

Melting point: 197 to 200 ° C. [α] _D ²⁴ +78.3 (C = 1, methanol) Infrared absorption spectrum ν _max cm ⁻¹ (KBr): 338
8, 3029, 1629, 1332, 1017 Mass spectrum (EI) m / z: 221 (free form M
⁺ ).

[0496]

[Reference Example 9 (b)]1'-tert-butoxycarbonyl-spiro [benzo
[C] thiophene-1 (3H), 4'-piperidine]-
(2S) -oxide (S)-(+)-mandelic acid synthesized in Reference Example 9 (a)
19.88 g (53.2 mmol) of salt was added to 5% sodium hydroxide.
Dissolved in water (200 ml) and methylene chloride (20 ml).
0 ml × 3 times). The organic layer is treated with anhydrous magnesium sulfate.
Then, the solvent was distilled off under reduced pressure. The obtained residue 1
Dissolve 1.80 g in methylene chloride (300 ml) and cool on ice
Below, 11.2 ml of triethylamine (79.8 mM
1), di-tert-butyl dicarbonate 17.4 g (7
9.8 mmol), and the mixture was further stirred at room temperature overnight.
Was. Dilute the reaction solution with 200 ml of methylene chloride and add 10%
After washing with aqueous citric acid and saturated aqueous sodium hydrogen carbonate, anhydrous
Dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the residue was removed.
With silica gel column chromatography (elution solvent; n)
-Hexane: ethyl acetate = 4: 6 to 3: 7)
And recrystallized from diisopropyl ether,
13.1 g of the compound was obtained as white crystals.

Melting point: 129.0 to 130.5 ° C. (diisopropyl ether) [α] _D ²⁴ +57.1 (C = 1, methanol) HPLC analysis; Column: Chiral Cel OD (250 × 4.6)
mmφ) Elution solvent: n-hexane: 2-propanol = 80: 2
0 Flow rate; 0.8 ml / min Retention time: 18.1 min The nuclear magnetic resonance spectrum, infrared absorption spectrum and mass spectrum were identical to those of the racemic form produced in Reference Example 5 (b).

[0498]

Reference Example 9 (c) Spiro [benzo [c] thiophene-1 (3H), 4'-
Piperidine]-(2S) -oxide hydrochloride 1′-tert-butoxycarbonyl-spiro [benzo [c] thiophene 1 (3H) obtained in Reference Example 5 (b),
4'-piperidine]-(2S) -oxide 13.0 g
(40.4 mmol) in 2-propanol (130 m
l) under ice cooling and 4N dioxane hydrochloride (50m
l) was added, and the mixture was stirred for 1 hour and further stirred at room temperature for 6 hours. The mixture was concentrated under reduced pressure, diethyl ether (200 ml) was added, and the mixture was distilled under reduced pressure again (three times). The obtained residue was mixed with a mixed solution of methanol: diethyl ether = 1: 2 (300 m
l) The recrystallization was carried out, and the target compound was obtained as white crystals.
9.10 g were obtained.

209.5-210.5 ° C. [α] _D ²⁴ +63.8 (C = 1, methanol).

[0500]

[Reference Example 10]1'-tert-butoxycarbonylspiro [benzo [c]
Thiophene-1 (3H), 4'-piperidine] -2
(S) -oxide 1'-tert-butoxycarbonylspiro [benzo [c]
Thiophene-1 (3H), 4'-piperidine] 250
mg (0.82 mmol) in 5 ml of methylene chloride
Dissolved; A. Davis et al. (J. Am. Chem. So
c.,114, 1428 (1992)).
R)-(-)-N- (phenylsulfonyl) (3,3-
Dichlorocampforyl) oxaziridine 308mg
(0.82 mmol) and stirred at room temperature overnight. Change
Was added with potassium iodide (500 mg), and the mixture was added at room temperature for 30 minutes.
After stirring for a while, the mixture was washed successively with water and saturated saline,
Dried over sodium. The solvent was distilled off under reduced pressure to give a residue.
To silica gel column chromatography (n-hexa
And ethyl acetate = 1: 2) to give the desired compound 2
45 mg were obtained.

Optical purity: 94% ee.

The following is a specific description with reference to Formulation Examples.

[0503]

Formulation Example 1 Powder A powder is obtained by mixing 5 g of the compound of Example 75, 895 g of lactose, and 100 g of corn starch with a blender.

[0504]

Formulation Example 2 Granules 5 g of the compound of Example 72, 865 g of lactose and 100 g of low-substituted hydroxypropylcellulose were mixed, and then a 10% aqueous solution of hydroxypropylcellulose 3
Add 00 g and knead. This is granulated using an extrusion granulator and dried to obtain a granule.

[0505]

Formulation Example 3 Capsule 5 g of the compound of Example 72, 115 g of lactose, 58 g of corn starch and 2 g of magnesium stearate are mixed using a V-type mixer, and then filled into a No. 3 capsule by 180 mg to obtain a capsule. . The capsules contain the compound 5 of Example 72 per capsule.
mg.

[0506]

Formulation Example 4 Tablets 5 g of the compound of Example 72, 90 g of lactose, 34 g of corn starch, 20 g of crystalline cellulose and 1 g of magnesium stearate are mixed in a blender, and the mixture is compressed with a tablet machine to give tablets.

[0507]

【The invention's effect】

It was prepared Somaku specimens from lung Preparation Male Hartley guinea pigs [NK ₁ receptor binding assay] (a) Sohaimaku specimen. That is, under chloroform anesthesia, the blood was killed by exsanguination from the abdominal vena cava, and the pulmonary airway tissue was immediately removed. The isolated lung was perfused with a buffer (50 mM Tris-HCl, pH 7.4), cut into small pieces, and homogenized in a buffer (a buffer containing 120 mM sodium chloride and 5 mM potassium chloride) using a polytron. The tissue mass was removed from the homogenate by filtration with a nylon mesh (50 μm) and centrifuged (30,000 × g, 30 minutes, 4 minutes).
° C). The pellet is placed in ice-cold buffer (10 mM EDTA).
And a buffer solution containing 300 mM potassium chloride), left at 4 ° C. for 60 minutes, and then washed twice by centrifugation (3.
000 × g, 15 minutes, 4 ° C.). Crude membrane specimens were stored at -80 ° C until use. (B) Receptor binding test Test drug and [ ³ H] -substance P (final concentration 1 n
M) 250 μl (50 mM Tris-HCl, pH
7.4, 6 mM manganese chloride, 800 μg / ml BS
A, 8 μg / ml chymostatin, 8 μg / ml leupeptin, 80 μg / ml bacitracin, 20 μg / ml phosphoramidone), 250 μl of crude lung membrane specimen was added, and incubated at room temperature for 30 minutes. After the reaction, the membrane components were collected on a GF / B glass fiber filter (Whatman) using an automatic filtration device (Brandel). In addition, the glass filter is 0.1% to keep non-specific binding low.
It was pretreated with a polyethyleneimine solution for about 4 hours before use.
Transfer the membrane component collection filter to a mini plastic vial containing 4 ml of Picoflow,
Radioactivity was measured with a counter (Leck 3SC, Beckman). The NK ₁ receptor binding effect was shown at a 50% binding dose (IC ₅₀ ).

[0508]

Table 4 {Test Drug IC ₅₀ (ng / ml)} {Example 75 6.7} Compound A 38 Compound C 6.5} ───────────────────── compounds of the present invention, the NK ₁ receptor binding test in vitro, the compounds of the prior art, the compound C activity equivalent to Indicated.

[NK ₂ Receptor Binding Test] (a) Preparation of Crude Ileum Membrane Specimens Coarse membrane specimens were prepared from the ileum of male Hartley guinea pigs. That is, under chloroform anesthesia, the blood was killed by exsanguination from the abdominal vena cava, and the ileum was immediately removed. The isolated ileum uses a glass slide to scrape the contents of the lumen, secretions, epithelium,
Peel off, buffer (50 mM Tris-HCl, pH 7.
After shredding in 4), homogenization was further performed using a polytron in a buffer solution (a buffer solution containing 120 mM sodium chloride and 5 mM potassium chloride). The tissue mass was removed from the homogenate by filtration with a nylon mesh (50 μm) and centrifuged (30,000 × g, 30 minutes, 4 minutes).
° C). The pellet is placed in ice-cold buffer (10 mM EDTA).
And a buffer solution containing 300 mM potassium chloride), left at 4 ° C. for 60 minutes, and then washed twice by centrifugation (3.
000 × g, 15 minutes, 4 ° C.). Crude membrane specimens were stored at -80 ° C until use. (B) Receptor binding test 250 μl (50 mM Tris-HCl, pH 7.4, 6 mM manganese chloride, 800 mM) of a mixture of the test drug and [ ³ H] -SR-48968 (Amersham, 1 nM final concentration)
μg / ml BSA, 8 μg / ml chymostatin, 8 μ
g / ml leupeptin, 80 μg / ml bacitracin,
20 μg / ml phosphoramidone) and crude ileal membrane sample solution 2
50 μl was added and incubated at room temperature for 30 minutes.
After the reaction, GF / GF was detected using an automatic filtration device (Brandel).
The membrane components were collected on a B glass fiber filter (Whatman). The glass filter was pretreated with a 0.1% polyethyleneimine solution for about 4 hours in order to suppress nonspecific binding. The membrane component recovery filter was transferred to a mini plastic vial containing 4 ml of Picoflow, and a liquid scintillation counter (Beckman, LSC)
3500). The NK ₂ receptor binding effect was shown at a 50% binding dose (IC ₅₀ ).

[0510]

Table 5 {Test Drug IC ₅₀ (ng / ml)} Example 75 7.5 Compound A 18 Compound C 31化合物 The compound of the present invention showed superior activity in the NK ₂ receptor binding test in vitro to the compound of the prior art.

[0511] [angiostatic effect of permeabilization] healthy guinea pigs (body weight 400g longitudinal, Hartley male guinea pigs) is used, NK ₁ receptor agonist Substance P
The effect of (SP) on suppressing vascular hyperpermeability was examined using the amount of leaked dye as an index. Pentobarbital (25m
g / kg, i. p. ), The dye (Evans blue: 20 mg / kg) was injected into the femoral vein of the guinea pig anesthetized with the test drug, and SP (1 μg / kg) was immediately injected intravenously to induce vascular permeability enhancement. Fifteen minutes later, the guinea pig was killed under chloroform anesthesia, and the amount of the dye leaked to the main trachea was determined by the Harada method (J. Pharm.
Pharmacol. 23 , 218 (1971)). The inhibitory action was determined from the amount of the leaked pigment in the guinea pigs of the test drug administration group and the non-administration group, and expressed as a 50% inhibitory drug dose.

[0512]

Table 6 Test Drug ID ₅₀ (mg / ml) {Example 76 0.025 Example 78 0.047} Compound A 8 compound C 0.019 ─────────────────────── compounds of the invention, the NK ₁ receptor antagonist test in vivo, compounds of the prior art Showed an activity equivalent to that of compound C.

[0513] Healthy guinea pigs (body weight 500g longitudinal, Hartley male guinea pigs) [inhibitory effect of bronchoconstriction] using a high NK ₂ receptor agonist having specificity for NK ₂ receptors than neurokinin A (NKA) [Nle ¹⁰ ]
-The inhibitory effect of the test drug on airway constriction by NKA [4-10] was determined by Konzet-Roessler (Naun
yn-Schmiedebergs Arch.Exp. Pathol. pharmakol . 195,
71 (1940)), and airway pressure was used as an index. That is, pentobarbital (30 mg / kg,
s. c. ), A tracheal cannula was attached to a guinea pig anesthetized with gallamine (galamine 20 mg / k).
g, i. v. ), Immediately after treatment with 8 ml / kg,
60 breaths / min positive pressure breath (Ugo-Basile, 702
5) was applied. The airway pressure of the artificial respiration is measured by a pressure transducer attached to the side branch of the tracheal cannula (Nihon Kohden, T
P-200T) via amplification and sensing (Nihon Kohden, AP-
601G) and a recorder (Nihon Kohden, WT-685)
G). Atropine (1 mg / kg, i.p.
v. ) And propranolol (1 mg / kg, i.
v. ), The test drug was intravenously administered, and 5 minutes later, 4 μg / kg of [Nle ¹⁰ ] -NKA [4-10]
Was administered to induce airway constriction, and the airway pressure was measured for 10 minutes. The inhibitory effect was determined from the airway contraction intensity of guinea pigs in the test drug-administered group and the non-administered group, and the 50% inhibitory dose (ID
₅₀ ).

[0514]

[Table 7] Table 7 ─────────────────────── Study drug ID ₅₀ (mg / ml) ──────────── ─────────── Example 76 0.074 Example 77 0.047 化合物 Compound A 10 or more Compound C 1.7 化合物 The compound of the present invention is superior to the compound of the prior art in the in vivo NK ₂ receptor antagonism test. Also showed remarkably excellent activity.

As is clear from Tables 4 to 7, the compounds of the present invention exhibited excellent antagonism to both NK ₁ receptor and NK ₂ receptor. More specifically, the compounds of the invention show antagonism of the prior art about the same strength NK ₁ receptors, further shows the antagonism of excellent NK ₂ receptors than the prior art.

────────────────────────────────────────────────── ─── Continued on the front page (51) Int.Cl. ⁷ Identification code FI A61K 31/54 A61K 31/54 31/55 31/55 A61P 11/00 A61P 11/00 13/02 13/02 25/00 25 / 00 29/00 29/00 37/08 37/08 43/00 111 43/00 111 C07D 263/06 C07D 263/06 263/52 263/52 263/56 263/56 265/30 265/30 267 / 08 267/08 277/04 277/04 413/06 413/06 413/12 413/12 413/14 413/14 417/12 417/12 471/10 101 471/10 101 103 103 103 491/10 491/10 495/10 495/10 498/10 498/10 521/00 521/00 C07M 7:00 C07M 7:00 (72) Inventor Toshi Kurata 1-258 Hiromachi, Shinagawa-ku, Tokyo Sankyo Co., Ltd. (72) Inventor Kimiki Ishibashi 1-58, Hiromachi, Shinagawa-ku, Tokyo Sankyo Co., Ltd. (72) Inventor Katsuyoshi Nakajima 1-2-58, Hiromachi, Shinagawa-ku, Tokyo Sankyo Co., Ltd. (72) Person Takeshi Yamaguchi 1-258 Hiromachi, Shinagawa-ku, Tokyo Sankyo Co., Ltd. (72) Inventor Kazuhiro Ito 1-258 Hiromachi Shinagawa-ku, Tokyo Sankyo Co., Ltd. (56) Reference Patent 3088672 (JP, B2) Patent 3017147 (JP, B2) WO 96/23787 (WO, A1) WO 95/28389 (WO, A1) WO 98/4561 (WO, A1) (58) Fields investigated (Int) .Cl. ⁷ , DB name) REGISTRY (STN) CAPlus (STN)

Claims (44)

(57) [Claims] 1. A compound of the general formula (I): In the formula, R ¹ and R ² are the same or different and each is a group selected from an aryl group, a heteroaryl group, and a substituent group A, and is 1 to 3
A substituted aryl group or a heteroaryl group substituted by 1 to 3 groups selected from a substituent group A; A represents a methylene group, a carbonyl group or a sulfonyl group; bond represents the number 1 to 4 carbon alkylene group or a carbon number 2 to 4 carbon alkenylene group having a carbon, D is, indicates SansoHara child, E is from 1 to carbon atoms which may be substituted with a halogen atom 6 G represents an alkylene group having 3 to 8 carbon atoms including a cycloalkane ring having 3 to 6 carbon atoms, and G represents an alkylene group having 1 to 4 carbon atoms or an alkylene group having 2 to 4 carbon atoms. indicates alkenylene group, L represents the general formula ^{-C (R 4) (R 5} ) - group [wherein with, taken together R ⁴ and R ^5, including the carbon atoms to which they are attached A 5- to 8-membered saturated heterocyclic ring (the heterocyclic ring is a substituent group B Ri may be 1 or 2 substituted by a group selected, aryl ring, or a group selected from Substituent group A may be condensed with 1 to 3 substituted aryl ring.) R ⁷ represents a lower alkyl group. A prophylactic or therapeutic agent for tachykinin-mediated diseases, comprising the compound represented by｝ or a pharmacologically acceptable salt thereof. [Substituent group A] halogen atom, lower alkyl group, halogeno lower alkyl group, lower alkoxy group, lower alkoxycarbonyl group,
A carboxy group, a hydroxyl group, a lower aliphatic acyl group, a lower aliphatic acylamino group, an amino group, and a cyano group [Substituent group B] an oxo group; Lower alkyl, aryl and aralkyl groups, lower aliphatic acyl groups and lower alkanesulfonyl groups which may be substituted; 2. The compound according to claim 1, wherein R ¹ is an aryl group, a heteroaryl group, or an aryl group substituted by 1 to 3 groups selected from the following substituent group A, or a pharmaceutically acceptable compound thereof. A preventive or therapeutic agent for tachykinin-mediated diseases comprising a salt. 3. The compound according to claim 1, wherein R ¹ is an aryl group or an aryl group substituted by 1 to 3 groups selected from the following substituent group A ¹ , or a pharmaceutically acceptable salt thereof. Or a prophylactic or therapeutic agent for tachykinin-mediated diseases. [Substituent group A ¹ ] Lower alkyl group, halogeno lower alkyl group, lower alkoxy group 4. The method according to claim 1, wherein R ² is an aryl group or an aryl group substituted by 1 to 3 groups with a group selected from the group of substituents A. An agent for preventing or treating tachykinin-mediated diseases comprising a compound or a pharmacologically acceptable salt thereof. 5. The compound according to claim 1, wherein R ² is an aryl group or an aryl group substituted with 1 to 3 halogen atoms, or a pharmacologically active compound thereof. An agent for preventing or treating tachykinin-mediated diseases comprising an acceptable salt. 6. The preventive or therapeutic agent for tachykinin-mediated diseases according to claim 1, wherein A is a carbonyl group or a pharmacologically acceptable salt thereof. . 7. The preventive or therapeutic agent for tachykinin-mediated diseases according to any one of claims 1 to 6, wherein B is a compound having a single bond or a pharmacologically acceptable salt thereof. . 8. A any one selected from claims 1 to 7, E is an alkylene group having 1 to 4 carbon atoms, or 3 carbon atoms
An agent for preventing or treating tachykinin-mediated diseases, comprising a compound having 3 to 8 carbon atoms and an alkylene group containing 3 to 6 cycloalkane rings or a pharmaceutically acceptable salt thereof. 9. A any one selected from claims 1 to 7, E is a methylene group, an ethylene group, dimethylmethylene group,
1,1-dimethylethylene group, 2,2-dimethylethylene group, cyclopropane-1,1-diyl group, cyclobutane-1,1-diyl group, cyclopentane-1,1-diyl group, cyclohexane-1,1 -Diyl group, cyclopropane-1,1-diylmethyl group, cyclobutane-1,1
A preventive or therapeutic agent for tachykinin-mediated diseases comprising a compound having a diylmethyl group, a cyclopentane-1,1-diylmethyl group or a cyclohexane-1,1-diylmethyl group, or a pharmacologically acceptable salt thereof. 10. A tachykinin-mediated compound comprising a compound in which G is an alkylene group having 1 to 4 carbon atoms or a pharmacologically acceptable salt thereof, according to any one of claims 1 to 9 , An agent for preventing or treating a disease. 11. A tachykinin-mediated compound comprising a compound in which G is an alkylene group having 2 or 3 carbon atoms or a pharmacologically acceptable salt thereof according to any one of claims 1 to 9 . An agent for preventing or treating a disease. 12. The any one selected from claims 1 to 11, L is represented by the following formula (I _L): ## STR2 ## (Wherein, J represents an alkylene group having 1 to 6 carbon atoms, the ring Ar represents an aryl ring, or one to four substituted aryl ring group selected from Substituent group A.) A prophylactic or therapeutic agent for tachykinin-mediated diseases, comprising a compound having the formula: or a pharmacologically acceptable salt thereof. [Substituent group A] halogen atom, lower alkyl group, halogeno lower alkyl group, lower alkoxy group, lower alkoxycarbonyl group,
Carboxy group, hydroxyl group, lower aliphatic acyl group, lower aliphatic acylamino group, amino group, and cyano group 13. The prophylactic or therapeutic agent for tachykinin-mediated diseases according to claim 12, wherein J is a compound having 1 to 4 carbon atoms of an alkylene group or a pharmaceutically acceptable salt thereof. 14. The preventive or therapeutic agent for tachykinin-mediated diseases according to claim 12, wherein J is a compound in which J is a methylene group or an ethylene group or a pharmaceutically acceptable salt thereof. 15. The oxygen atom of the sulfoxide group of the group having the formula (I _L ) according to any one of the claims 12 to 14 , wherein
An agent for preventing or treating tachykinin-mediated diseases, comprising a compound bonded to a sulfur atom in the S configuration or a pharmacologically acceptable salt thereof. 16. The preventive or therapeutic agent for tachykinin-mediated diseases according to claim 14 , comprising a compound selected from the following and a pharmacologically acceptable salt thereof. 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidine-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] -2-oxide 1- {2- [2 -(3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [isobenzofuran-1
(3H), 4'-piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] 1- {2- [2- (3 4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine] -2-oxide 1- {2- [2 -(3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [isoquinoline-1 (2
H), 4'-Piperidine] -3 (4H) -one 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl @ spiro [isobenzofuran-1 (3H), 4 '
-Piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] -2-oxide 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [isoquinolin-1 (2H), 4'-piperidin] -3 (4H) -one 17. The preventive or therapeutic agent for tachykinin-mediated diseases according to claim 15 , comprising any one compound selected from the following or a pharmacologically acceptable salt thereof. 1- {2-[(5R)-(3,4-dichlorophenyl) -3- (3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} spiro [benzo [c] thiophene-1 ( 3H), 4'-piperidine]-
(2S) -oxide 1- {2-[(5R)-(4-chlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide 1- {2- [(5R)-(4-fluorophenyl)-
3- (3,4,5-trimethoxybenzoyl) oxazolidine-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)
-Oxide 1- {2-[(2R)-(4-chlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide .1- {2- [(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) morpholin-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S) -oxide-1- {2 -[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl} spiro [benzo [c] thiophene-1 (3H),
4′-piperidine]-(2S) -oxide 1- {2-[(2R)-(4-chlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S) -oxide 1- {2-[(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)- Oxide 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl} spiro [benzo [c] thiophene-1 (3H ), 4'-Piperidine]-
(2S) -oxide 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide 1- {2-[(2R)-(4-fluorophenyl)-
4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)
-Oxide 1- {2-[(2R)-(3,4-dichlorophenyl) -5,5-dimethyl-4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [ Benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide. 18. is a NK ₁ receptor and / or NK ₂ receptor inhibitors, prophylactic or therapeutic agent of tachykinin-mediated diseases according to 1, wherein one selected from claims 1 to 17. 19. The preventive or therapeutic agent for tachykinin-mediated diseases according to any one of claims 1 to 17 , which is a preventive or therapeutic agent for asthma and / or bronchitis. 20. The preventive or therapeutic agent for tachykinin-mediated diseases according to any one of claims 1 to 17 , which is a preventive or therapeutic agent for rhinitis. 21. A preventive or therapeutic agent for allergy.
The prophylactic or therapeutic agent for tachykinin-mediated diseases according to any one of claims 1 to 17 . 22. The preventive or therapeutic agent for tachykinin-mediated diseases according to any one of claims 1 to 17 , which is a preventive or therapeutic agent for urinary incontinence. 23. A compound of the general formula (I) as an active ingredient for producing a prophylactic or therapeutic agent for tachykinin-mediated diseases. In the formula, R ¹ and R ² are the same or different and each is a group selected from an aryl group, a heteroaryl group, and a substituent group A, and is 1 to 3
A substituted aryl group or a heteroaryl group substituted by 1 to 3 groups selected from a substituent group A; A represents a methylene group, a carbonyl group or a sulfonyl group; bond represents the number 1 to 4 carbon alkylene group or a carbon number 2 to 4 carbon alkenylene group having a carbon, D is, indicates SansoHara child, E is from 1 to carbon atoms which may be substituted with a halogen atom 6 G represents an alkylene group having 3 to 8 carbon atoms including a cycloalkane ring having 3 to 6 carbon atoms, and G represents an alkylene group having 1 to 4 carbon atoms or an alkylene group having 2 to 4 carbon atoms. indicates alkenylene group, L represents the general formula ^{-C (R 4) (R 5} ) - group [wherein with, taken together R ⁴ and R ^5, including the carbon atoms to which they are attached A 5- to 8-membered saturated heterocyclic ring (the heterocyclic ring is a substituent group B Ri may be 1 or 2 substituted by a group selected, aryl ring, or a group selected from Substituent group A may be condensed with 1 to 3 substituted aryl ring.) R ⁷ represents a lower alkyl group. Use of the compound represented by｝ or a pharmacologically acceptable salt thereof. [Substituent group A] halogen atom, lower alkyl group, halogeno lower alkyl group, lower alkoxy group, lower alkoxycarbonyl group,
A carboxy group, a hydroxyl group, a lower aliphatic acyl group, a lower aliphatic acylamino group, an amino group, and a cyano group [Substituent group B] an oxo group; Optionally, lower alkyl, aryl and aralkyl groups, lower aliphatic acyl groups, lower alkanesulfonyl groups 24. The compound according to claim 23, wherein R ¹ is an aryl group, a heteroaryl group or an aryl group substituted by 1 to 3 groups selected from the following substituent group A, or a pharmaceutically acceptable compound thereof. Use of salt. 25. The compound according to claim 23, wherein R ¹ is an aryl group or an aryl group substituted by 1 to 3 groups selected from the following substituent group A ¹ , or a pharmaceutically acceptable salt thereof. Use of. [Substituent group A ¹ ] Lower alkyl group, halogeno lower alkyl group, lower alkoxy group 26. The method according to any one of claims 23 to 25 , wherein R ² is an aryl group or an aryl group substituted by 1 to 3 groups selected from the group of substituents A. Use of the compound or a pharmacologically acceptable salt thereof. 27. The compound according to any one of claims 23 to 25 , wherein R ² is an aryl group or an aryl group substituted with 1 to 3 halogen atoms, or a pharmacologically active compound thereof. Use of acceptable salts. 28. The compound according to any one of claims 23 to 27 , wherein A is a carbonyl group, or a pharmacologically acceptable salt thereof. 29. The use according to any one of claims 23 to 28 , wherein B is a single bond or a pharmacologically acceptable salt thereof. 30. The method according to any one of claims 23 to 29 , wherein E is an alkylene group having 1 to 4 carbon atoms or 3 carbon atoms.
Use of a compound which is an alkylene group having 3 to 8 carbon atoms containing from 6 to 6 cycloalkane rings or a pharmacologically acceptable salt thereof. 31. The method according to any one of claims 23 to 29 , wherein E is a methylene group, an ethylene group, a dimethylmethylene group,
1,1-dimethylethylene group, 2,2-dimethylethylene group, cyclopropane-1,1-diyl group, cyclobutane-1,1-diyl group, cyclopentane-1,1-diyl group, cyclohexane-1,1 -Diyl group, cyclopropane-1,1-diylmethyl group, cyclobutane-1,1
-Use of a compound which is a diylmethyl group, a cyclopentane-1,1-diylmethyl group or a cyclohexane-1,1-diylmethyl group or a pharmacologically acceptable salt thereof. 32. The compound according to any one of claims 23 to 31 , wherein G is an alkylene group having 1 to 4 carbon atoms, or a pharmacologically acceptable salt thereof. 33. The use according to any one of claims 23 to 31 , wherein G is an alkylene group having 2 or 3 carbon atoms, or a pharmaceutically acceptable salt thereof. 34. In any one of claims 23 to 33 , L is the following formula (I _L ): (Wherein, J represents an alkylene group having 1 to 6 carbon atoms, the ring Ar represents an aryl ring, or one to four substituted aryl ring group selected from Substituent group A.) Or a pharmacologically acceptable salt thereof. [Substituent group A] halogen atom, lower alkyl group, halogeno lower alkyl group, lower alkoxy group, lower alkoxycarbonyl group,
Carboxy group, hydroxyl group, lower aliphatic acyl group, lower aliphatic acylamino group, amino group, and cyano group 35. The use according to claim 34, wherein J is an alkylene group having 1 to 4 carbon atoms, or a pharmacologically acceptable salt thereof. 36. The use according to claim 34, wherein J is a methylene group or an ethylene group, or a pharmaceutically acceptable salt thereof. 37.] claims 34 to any one selected from claims 36, an oxygen atom of the sulfoxide group of radicals having the formula (I _L),
Use of a compound bonded to a sulfur atom in the S configuration or a pharmacologically acceptable salt thereof. 38. The use according to claim 23, wherein any one compound selected from the following or a pharmacologically acceptable salt thereof is used. 1- {2- [5- (3,4-dichlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidine-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] -2-oxide 1- {2- [2 -(3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [isobenzofuran-1
(3H), 4'-piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine] 1- {2- [2- (3 4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine] -2-oxide 1- {2- [2 -(3,4-dichlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [isoquinoline-1 (2
H), 4'-Piperidine] -3 (4H) -one 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl @ spiro [isobenzofuran-1 (3H), 4 '
-Piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [benzo [c] thiophene-1 (3
H), 4'-Piperidine] -2-oxide 1- {2- [2- (3,4-dichlorophenyl) -4]
-(3-methoxybenzoyl) morpholin-2-yl]
Ethyl dispiro [isoquinolin-1 (2H), 4'-piperidin] -3 (4H) -one 39. The use according to claim 37, wherein any one of the following compounds or a pharmacologically acceptable salt thereof is used. 1- {2-[(5R)-(3,4-dichlorophenyl) -3- (3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl} spiro [benzo [c] thiophene-1 ( 3H), 4'-piperidine]-
(2S) -oxide 1- {2-[(5R)-(4-chlorophenyl) -3]
-(3,4,5-trimethoxybenzoyl) oxazolidin-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S) -oxide 1- {2- [(5R)-(4-fluorophenyl)-
3- (3,4,5-trimethoxybenzoyl) oxazolidine-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)
-Oxide 1- {2-[(2R)-(4-chlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl {spiro [benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide .1- {2- [(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) morpholin-5-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S) -oxide-1- {2 -[(2R)-(3,4-dichlorophenyl) -4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl} spiro [benzo [c] thiophene-1 (3H),
4′-piperidine]-(2S) -oxide 1- {2-[(2R)-(4-chlorophenyl) -4
-(3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S) -oxide 1- {2-[(2R)-(4-fluorophenyl)-
4- (3,4,5-trimethoxybenzoyl) hexahydro-1,4-oxazepin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)- Oxide 1- {2-[(2R)-(3,4-dichlorophenyl) -4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl} spiro [benzo [c] thiophene-1 (3H ), 4'-Piperidine]-
(2S) -oxide 1- {2-[(2R)-(4-chlorophenyl) -4]
-(3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)-
Oxide 1- {2-[(2R)-(4-fluorophenyl)-
4- (3-isopropyloxyphenyl) acetyl] morpholin-2-yl] ethyl {spiro [benzo [c] thiophen-1 (3H), 4'-piperidine]-(2S)
-Oxide 1- {2-[(2R)-(3,4-dichlorophenyl) -5,5-dimethyl-4- (3,4,5-trimethoxybenzoyl) morpholin-2-yl] ethyl} spiro [ Benzo [c] thiophene-1 (3H), 4'-piperidine]-(2S) -oxide. 40. The use according to any one of claims 23 to 39, wherein the medicament is an NK ₁ receptor and / or NK ₂ receptor inhibitor. 41. The use according to any one of claims 23 to 39, wherein the medicament is a prophylactic or therapeutic agent for asthma and / or bronchitis. 42. The use according to any one of claims 23 to 39, wherein the medicament is a prophylactic or therapeutic agent for rhinitis. 43. The use according to any one of claims 23 to 39, wherein the medicament is a prophylactic or therapeutic agent for allergy. 44. The use according to any one of claims 23 to 39, wherein the medicament is a prophylactic or therapeutic agent for urinary incontinence.