US20130303535A1

US20130303535A1 - Novel bicyclic heterocyclic compound

Info

Publication number: US20130303535A1
Application number: US13/895,089
Authority: US
Inventors: Katsunori Tsuboi; Yusuke Yamai; Hitoshi Watanabe; Hironori KINOSHITA
Original assignee: Dainippon Sumitomo Pharma Co., Ltd.
Current assignee: Sumitomo Pharma Co Ltd
Priority date: 2008-12-26
Filing date: 2013-05-15
Publication date: 2013-11-14
Also published as: PL2380881T3; PT2380881T; JP5143916B2; JPWO2010074193A1; AU2009331179B2; RU2011131048A; WO2010074193A1; SI2380881T1; US8471038B2; CA2748251C; BRPI0924126A2; LT2380881T; ES2620446T3; CN102264707B; EP2380881A1; AU2009331179A1; RU2518073C2; BRPI0924126B1; CY1118862T1; IL213690A0

Abstract

The invention provides a compound for the treatment or prophylaxis of pathology involving SNS, specifically diseases such as neuropathic pain, nociceptive pain, dysuria, multiple sclerosis and the like. The compound is represented by formula (1) or a pharmaceutically acceptable salt thereof wherein R¹is a hydrogen atom or the like, L is a single bond, —O— or the like, R²is a phenyl group or the like, X is a carbon atom or a nitrogen atom, and R³, R⁴, R^5a, R^5b, R⁶and R⁷are each independently a substituted or unsubstituted alkyl group or the like:

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of copending U.S. patent application Ser. No. 13/141,301, filed on Aug. 17, 2011, which is the U.S. national phase of International Patent Application No. PCT/JP2009/071529, filed on Dec. 25, 2009, which claims priority to Japanese Patent Application No. 2008-332796, filed on Dec. 26, 2008.

TECHNICAL FIELD

The present invention relates to a drug for the treatment or prophylaxis of pathology in general in which SNS (sensory neuron specific sodium channel) is involved, which comprises a novel compound having a benzimidazole or imidazopyridine skeleton as a bicyclic heterocycle or a pharmaceutically acceptable salt thereof as an active ingredient. Specifically, the present invention relates to a drug for the treatment or prophylaxis of diseases such as neuropathic pain, nociceptive pain, dysuria, multiple sclerosis and the like.

BACKGROUND ART

In 1952, Hodgkin and Huxley showed that the main body of neural activity is an Na channel, after which Na channel blockers have been developed as antiarrhythmic or topical anesthetics. In 1961, lidocain, which is one of the Na channel blockers, was found to provide an analgesic effect, and clinical application thereof as an analgesic was started. However, since Na channel is also present in normeural tissues such as muscle, heart and the like, side effects by systemic administration remained as a problem.
With the advance of molecular biology, subtypes of Na channel have been elucidated one after another, and Na channel α subunit that forms pore is known to include 10 kinds at present. A sensory neuron specific sodium channel (sensory nerve-specific Na channel), i.e., SNS, is one of such Na channel α subunits, is a tetrodotoxin (TTX)-resistant Na channel localized in the small diameter cell (C fiber) of dorsal root ganglion involved in nerval perception, and is also called SCN10A, PN3 or NaV1.8 (non-patent documents 1, 2). It has been reported that SNS knockout mouse is insensitive to mechanical stimulations, and administration of antisense to SNS to neuropathic pain or inflammatory pain models attenuates hypersensitivity and abnormal perception.
Therefore, an SNS inhibitor is considered to provide a therapeutic or prophylactic drug showing an analgesic effect for diseases such as neuropathic pain, nociceptive pain and the like, which accompany pain, numbness, burning sensation, dull pain and the like, each involving C fiber. Moreover, since SNS is not expressed in normeural tissues and central nervous system, a medicament that selectively inhibits SNS is considered to be a medicament free of side effects derived from normeural tissues or central nervous system.
In dysuria, moreover, it has been clarified that frequent urination, its main symptom, is caused by overactivity of the C fiber; in other words, dysfunction of afferent sensory nervous pathway from the lower urinary tract is involved in overactive bladder and cystalgia, and suppression of C fiber sensory nerve from the bladder is effective thereon (non-patent document 3). Therefore, a medicament that inhibits SNS mainly causing the neural activity of C fiber is expected to be a therapeutic or prophylactic drug for dysuria, which has a novel point of action.
On the other hand, a recent report has documented that SNS found only in C fiber is ectopically expressed in cerebellar Purkinje cell of multiple sclerosis patients, and is involved in the occurrence of an abnormal firing pattern in the cerebellum (non-patent document 4). As such, an SNS inhibitor is expected to be a first therapeutic or prophylactic drug toward the induction of symptoms caused by abnormal firing associated with SNS expression in the cerebellar neuron, such as ataxia and the like in multiple sclerosis.
The following shows the actual treatment state of the aforementioned diseases in clinical practice.

(1) Neuropathic Pain

Neuropathic pain refers to a pain including spontaneous pain and chronic pain developed by nerve damage or nerve stimulation even when trauma is absent and tissue inflammation is absent after complete recovery. Examples thereof include neuralgia after lumbar operation, diabetic neuropathy, neuralgia after herpes zoster, reflex sympathetic dystrophy, phantom limb pain, spinal cord damage, late stage carcinomatous pain, and prolonged postoperative pain. NSAIDS (non-steroidal anti-inflammatory drugs) such as aspirin and the like are completely ineffective for neuropathic pain, and opioids such as morphine and the like are problematic in drug resistance and induction of psychological symptom.
At present, a sole medicament in the market, which is allegedly effective for neuropathic pain, is mexiletine applicable to diabetic neuropathy. Since mexiletine does not have selectivity to Na channel, though it provides an analgesis effect, side effects are feared and administration at a high dose has been reported to be unavailable. Some other medicaments are clinically applied as aids. Examples thereof include antidepressant (sulpiride, trazodone, fluvoxatine, milnacipran), adrenaline agonist (clonidine, dexmedetomidine), NMDA receptor antagonists (ketamine hydrochloride, dextromethorphan), antianxiety drug (diazepam, lorazepam, etizolam, hydroxyzine hydrochloride), anticonvulsant (carbamazepine, phenyloin, sodium valproate, zonisamide), calcium antagonist (nifedipine, verapamil hydrochloride, lomerizine hydrochloride) and the like, all of which are used as aids. From the above, a therapeutic drug free of side effects derived from normeural tissue or central nervous system and specifically effective for pain is desired.

(2) Nociceptive Pain

Nociceptive pain refers to a pain caused by the activation of nociceptor (Aδ, C fiber) by mechanical, hyperthermic or chemical noxious stimulation due to tissue injury and the like. Nociceptor is sensitized by endogenous chemical stimulation (algetic substance) such as serotonin, substance P, bradykinin, prostaglandin and histamine. Examples of the nociceptive pain include lumbago, abdominal pain, and pain due to rheumatoid arthritis or osteoarthritis. In clinical practice, NSAIDS (acetylsalicylic acid, acetaminophen, diclofenac sodium, indomethacin, mofezolac, flurbiprofen, loxoprofen sodium, ampiroxicam), steroid drugs (prednisolone, methylprednisolone, dexamethasone, betamethasone), PGE₁(prostaglandin E1) (alprostadil, lipo alprostadil, limaprost alprostadil) and PGI₂(beraprost sodium) are used.

(3) Dysuria (Urinary Disturbance)

Dysuria is a disease mainly showing urinary frequency, urorrhea, feeling of residual urine and urodynia as main symptoms. At present, the main drug treatment of overactive bladder uses a muscarinic receptor inhibitor that suppresses the bladder parasympathetic nerve pathway. However, its limitation has also been clarified. Capsaicin and resinifera toxin, which are vanilloid receptor stimulants, have been reported to specifically act on C fiber to suppress its function. However, a medicament that acts on SNS localized in C fiber has not been found.

(4) Multiple Sclerosis

Multiple sclerosis is one kind of demyelination diseases, which shows scattered foci of demyelination in the white matter of the central nervous system, with various old and new lesions. The lesions appear more commonly in the white matter of lateral cerebral ventricle periphery, optic nerve, brain stem, spinal cord and the like. Histologically, myelin sheath is destroyed and axon and nerve cell are not damaged. As clinical symptoms, symptoms such as optic neuritis, double vision, eyeball motion impairments such as nystagmus, convulsive paralysis, painful tonic convulsive attack, Lhermitte's syndrome, ataxia, logopathy, bladder rectal disorder and the like appear in various combinations. The etiology thereof is unknown, though autoimmune disease theory, infection theory and the like are proposed. At present, an effective prophylactic or therapeutic drug for multiple sclerosis is highly desired.
Patent document 1 to be mentioned later relates to a selective modulator of CRF1 receptor and specifically describes a compound represented by the following formula (A) (Example 5, k). The compounds encompassed in the patent document characteristically have an amide bond in methylene on the imidazole ring, and are different from the compound of the present invention having an amino group in methylene on the imidazole ring. In addition, patent document 1 does not at all contain a description suggesting the present invention.
Patent document 2 to be mentioned later relates to a Rho kinase inhibitor, and specifically describes a compound represented by the following formula (B) (Example 321). The compounds encompassed in the patent document do not have a substituent on the nitrogen atom of imidazole ring, and are different from the compound of the present invention essential having the substituent. In addition, patent document 2 does not at all contain a description suggesting the present invention.

DOCUMENT LIST

Patent Document

Patent Document 1: WO 02/28839
Patent Document 2: WO 2009/79011

Non-Patent Document

non-Patent Document 1: Nature 379: 257, 1996
non-Patent Document 2: Pain 78: 107, 1998
non-Patent Document 3: Urology 57: 116, 2001
non-Patent Document 4: Brain Research 959: 235, 2003

SUMMARY OF THE INVENTION

Problems to be Solved by the Invention

The problem of the present invention is to provide a drug for the prophylaxis or treatment of pathology in general in which SNS is involved, specifically, diseases such as neuropathic pain, nociceptive pain, dysuria, multiple sclerosis and the like.

Means of Solving the Problems

The present inventors have conducted intensive studies in an attempt to solve the aforementioned problem and found that a bicyclic compound having an imidazole ring or a pharmaceutically acceptable salt thereof inhibits TTX resistant Na channel in human SNS gene expressing cell, namely, has an SNS inhibitory activity, and is useful as a therapeutic or prophylactic drug for diseases such as a neuropathic pain, a nociceptive pain, dysuria, multiple sclerosis and the like, which resulted in the completion of the present invention.
Accordingly, the present invention provides the following.

[1] a compound represented by the following formula (1) or a pharmaceutically acceptable salt thereof (hereinafter sometimes referred to as “the compound of the present invention”):
a compound represented by

wherein
R¹is a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms or a haloalkoxy group having 1 to 6 carbon atoms (R¹can substitute the benzene ring or pyridine ring at any substitutable position thereon),
L is a single bond, —O— or —CH₂O— (L can substitute the benzene ring or pyridine ring at any substitutable position thereon),
R²is a substituted or unsubstituted 6- to 10-membered aryl group, or a substituted or unsubstituted 5- to 10-membered aromatic heterocyclic group,
X is a carbon atom or a nitrogen atom,
R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 6 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered cycloalkenyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group,
R⁴is a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted 3- to 8-membered cycloalkyl group,
R^5aand R^5bare each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or R⁴and R^5aare optionally bonded to form, together with the nitrogen atom that R⁴is bonded to, a 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle (in this case, R^5bis a hydrogen atom),
R⁶and R⁷are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 6 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered cycloalkenyl group, a substituted or unsubstituted O-5 to 8-membered saturated aliphatic heterocyclic group, a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, a substituted or unsubstituted 6- to 10-membered aryl group, or a substituted or unsubstituted 5- to 10-membered aromatic heterocyclic group, or R⁶and R⁷are optionally bonded to form, together with the nitrogen atom that they are bond to, a substituted or unsubstituted 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle, or a substituted or unsubstituted 5- to 10-membered unsaturated nitrogen-containing aliphatic heterocycle (the saturated or unsaturated nitrogen-containing aliphatic heterocycle contains 0 to 2 oxygen atoms, 0 to 2 sulfur atoms and 1 to 3 nitrogen atoms) (hereinafter sometimes referred to as “compound (1)”) or a pharmaceutically acceptable salt thereof;

[2] the compound of [1], which is represented by the following formula (2):

wherein R¹, R², R³, R⁴, R^5a, R^5b, R⁶, R⁷, L and X are as defined in [1] (hereinafter sometimes referred to as “compound (2)”) or a pharmaceutically acceptable salt thereof;
[3] the compound of [1], which is represented by the following formula (3):
wherein R¹, R², R³, R⁴, R^5a, R^5b, R⁶, R⁷, L and X are as defined in [1] (hereinafter sometimes referred to as “compound (3)”) or a pharmaceutically acceptable salt thereof;
[4] the compound of any one of [1] to [3], wherein R²is a substituted or unsubstituted phenyl group, or a pharmaceutically acceptable salt thereof;

[5] the compound of any one of [1] to [4], wherein R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, or a pharmaceutically acceptable salt thereof;
[6] the compound of any one of [1] to [5], wherein R⁶and R⁷are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, or R⁶and R⁷are optionally bonded to form, together with the nitrogen atom that they are bond to, a substituted or unsubstituted 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle, or a substituted or unsubstituted 5- to 10-membered unsaturated nitrogen-containing aliphatic heterocycle (the saturated or unsaturated nitrogen-containing aliphatic heterocycle contains 0 to 2 oxygen atoms, 0 to 2 sulfur atoms and 1 to 3 nitrogen atoms), or a pharmaceutically acceptable salt thereof;
[7] the compound of any one of [1] to [6], wherein R⁴is a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a pharmaceutically acceptable salt thereof;
[8] the compound of any one of [1] to [7], wherein R^5aand R^5bare each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a pharmaceutically acceptable salt thereof;
[9] the compound of any one of [1] to [8], wherein X is a carbon atom, or a pharmaceutically acceptable salt thereof;
[10] the compound of any one of [1] to [9], wherein R¹is a hydrogen atom or a halogen atom, or a pharmaceutically acceptable salt thereof;
[11] the compound of any one of [1] to [10], wherein L is a single bond, or a pharmaceutically acceptable salt thereof;
[12] the compound of any one of [1] to [10], wherein L is —O—, or a pharmaceutically acceptable salt thereof;
[13] the compound of any one of [1] to [10], wherein L is —CH₂O—, or a pharmaceutically acceptable salt thereof;
[14] N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}glycinamide,
N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-2-methylalaninamide,
N²-{[1-cyclopropyl-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-cyclobutyl-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-chlorophenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-fluorophenoxy)-1-(2-hydroxy-2-methylpropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-fluorophenoxy)-1-(3-methoxypropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(2-chloro-4-fluorophenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-ethyl-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(2,4-difluorophenoxy)-1-(2-hydroxy-2-methylpropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-(2-ethoxyethyl)-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-ethyl-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-(3-methoxypropyl)-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-methylphenoxy)-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[5-chloro-1-(2-ethoxyethyl)-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, or
N²-{[5-chloro-6-(3,4-difluorophenyl)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
or a pharmaceutically acceptable salt thereof;
[15] a medicament comprising the compound of any one of [1] to
[14] or a pharmaceutically acceptable salt thereof as an active ingredient;
[16] the medicament of [15], which is an agent for the prophylaxis or treatment of neuropathic pain, nociceptive pain, dysuria or multiple sclerosis;
[17] a SNS inhibitor comprising the compound of any one of [1] to [14] or a pharmaceutically acceptable salt thereof as an active ingredient;
[18] a pharmaceutical composition comprising the compound of any one of [1] to [14] or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

Effect of the Invention

The present invention provides an SNS inhibitor comprising a novel bicyclic compound or a pharmaceutically acceptable salt thereof. The SNS inhibitor of the present invention is useful as a drug for the treatment or prophylaxis of pathology in general in which SNS is involved, and is specifically applicable to patients with neuropathic pain, nociceptive pain, dysuria, multiple sclerosis and the like.

DESCRIPTION OF EMBODIMENTS

In the present specification, examples of the “halogen atom” include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.
The “alkyl group” means a straight chain or branched alkyl group having 1 to 6 carbon atoms, and specific examples thereof include methyl group, ethyl group, propyl group (1-propyl group), isopropyl group (2-propyl group), butyl group (1-butyl group), sec-butyl group (2-butyl group), isobutyl group (2-methyl-1-propyl group), tert-butyl group (2-methyl-2-propyl group), pentyl group (1-pentyl group), hexyl group (1-hexyl group) and the like. The alkyl group is preferably an alkyl group having 1 to 4 carbon atoms.
The “haloalkyl group” means a straight chain or branched alkyl group having 1 to 6 carbon atoms, which is substituted by the same or different 1 to 5 halogen atoms, and specific examples thereof include trifluoromethyl group, 2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, 2-chloroethyl group, pentafluoroethyl group, 3,3,3-trifluoropropyl group and the like. The haloalkyl group is preferably a haloalkyl group alkyl group having 1 to 4 carbon atoms.
The “alkenyl group” means a straight chain or branched alkenyl group having 2 to 6 carbon atoms, and specific examples thereof include vinyl group, 1-propenyl group, 2-propenyl group, 1-methylvinyl group, 1-butenyl group, 1-ethylvinyl group, 1-methyl-2-propenyl group, 2-butenyl group, 3-butenyl group, 2-methyl-1-propenyl group, 2-methyl-2-propenyl group, 1-pentenyl group, 1-hexenyl group and the like. The alkenyl group is preferably an alkenyl group having 2 to 4 carbon atoms.
The “alkynyl group” means a straight chain or branched alkynyl group having 2 to 6 carbon atoms, and specific examples thereof include ethynyl group, 1-propynyl group, 2-propynyl group, 1-butynyl group, 1-methyl-2-propynyl group, 3-butynyl group, 1-pentynyl group, 1-hexynyl group and the like. The alkynyl group is preferably an alkynyl group having 2 to 4 carbon atoms.
The “alkoxy group” means a straight chain or branched alkoxy group having 1 to 6 carbon atoms, and specific examples thereof include methoxy group, ethoxy group, propoxy group, 1-methylethoxy group, butoxy group, 1-methylpropoxy group, 2-methylpropoxy group, 1,1-dimethylethoxy group, pentyloxy group, hexyloxy group and the like. The alkoxy group is preferably an alkoxy group having 1 to 4 carbon atoms.
The “haloalkoxy group” means a straight chain or branched alkoxy group having 1 to 6 carbon atoms, which is substituted by the same or different 1 to 5 halogen atoms, and specific examples thereof include trifluoromethoxy group, 2,2-difluoroethoxy group, 2,2,2-trifluoroethoxy group, 2-chloroethoxy group, pentafluoroethoxy group, 3,3,3-trifluoropropoxy group and the like. The haloalkoxy group is preferably a haloalkoxy group having 1 to 4 carbon atoms.
The “cycloalkyl group” means a 3- to 8-membered monocyclic or bicyclic cycloalkyl group, and specific examples thereof include cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group and the like. The cycloalkyl group is preferably a 4- to 6-membered cycloalkyl group.
The “cycloalkenyl group” means a 4- to 8-membered monocyclic or bicyclic cycloalkenyl group, and specific examples thereof include cyclobutenyl group, cyclopentenyl group, cyclohexenyl group, cycloheptenyl group and cyclooctenyl group. The position of double bond on the ring is not particularly limited. The cycloalkenyl group is preferably a 5- or 6-membered cycloalkenyl group.
The “saturated aliphatic heterocyclic group” means a O-5 to 8-membered monocyclic or bicyclic saturated aliphatic heterocyclic group containing 1 to 3 hetero atoms selected from a nitrogen atom, an oxygen atom and a sulfur atom (provided that the numbers of the oxygen atom and sulfur atom contained in the saturated aliphatic heterocycle are each up to 2). The position of the hetero atom is not particularly limited as long as the saturated aliphatic heterocyclic group is chemically stable. Specific examples thereof include azetidinyl group, pyrrolidinyl group, piperidyl group, piperidino group, piperazinyl group, azepanyl group, azocanyl group, tetrahydrofuryl group, tetrahydrothienyl group, tetrahydropyranyl group, morpholinyl group, morpholino group, thiomorpholinyl group, 1,4-dioxanyl group, 1,2,5-thiadiazinyl group, 1,4-oxazepanyl group, 1,4-diazepanyl group and the like.
The “unsaturated aliphatic heterocyclic group” means a 5- to 10-membered monocyclic or bicyclic unsaturated aliphatic heterocyclic group containing 1 to 3 double bonds and 1 to 3 hetero atoms selected from a nitrogen atom, an oxygen atom and a sulfur atom (provided that the numbers of the oxygen atom and sulfur atom contained in the unsaturated aliphatic heterocycle are each up to 2). The positions of the hetero atom and double bond are not particularly limited as long as the unsaturated aliphatic heterocyclic group is chemically stable. Specific examples thereof include pyrrolinyl group, imidazolinyl group, tetrahydroisoquinolyl group and the like, and 2-pyrrolinyl group and 2-imidazolinyl group are preferable.
The “saturated nitrogen-containing aliphatic heterocycle” means a 4- to 8-membered monocyclic or bicyclic saturated aliphatic heterocycle containing at least one nitrogen atom and optionally further containing 1 to 3 hetero atoms selected from a nitrogen atom, an oxygen atom and a sulfur atom (provided that the numbers of the oxygen atom and sulfur atom contained in the saturated aliphatic heterocycle are each up to 2). The position of the hetero atom is not particularly limited as long as the saturated nitrogen-containing aliphatic heterocycle is chemically stable. Specific examples thereof include azetidine ring, pyrrolidine ring, imidazolidine ring, pyrazolidine ring, piperidine ring, piperazine ring, azepane ring, azocane ring, morpholine ring, thiomorpholine ring, oxazolidine ring, thiazolidine ring and the like.
The “unsaturated nitrogen-containing aliphatic heterocycle” means a 4- to 8-membered monocyclic or bicyclic unsaturated aliphatic heterocycle containing at least one nitrogen atom and optionally further containing 1 to 3 hetero atoms selected from a nitrogen atom, an oxygen atom and a sulfur atom (provided that the numbers of the oxygen atom and sulfur atom contained in the unsaturated aliphatic heterocycle are each up to 2). The position of the hetero atom is not particularly limited as long as the unsaturated nitrogen-containing aliphatic heterocycle is chemically stable. Specific examples thereof include pyrroline ring, piperidine ring, imidazoline ring, pyrazoline ring, oxazoline ring, thiazoline ring, tetrahydroquinoline ring, tetrahydroisoquinoline ring and the like.
The “aryl group” means a 6- to 10-membered monocyclic or bicyclic aryl group, and specific examples thereof include phenyl group, 1-naphthyl group, 2-naphthyl group and the like.
The “aromatic heterocyclic group” means a 5- to 10-membered monocyclic or bicyclic aromatic heterocyclic group containing 1 to 4 hetero atoms selected from a nitrogen atom, an oxygen atom and a sulfur atom (provided that the numbers of the oxygen atom and sulfur atom contained in the aromatic heterocyclic group are each up to 2). The position of the hetero atom is not particularly limited as long as the aromatic heterocyclic group is chemically stable. Specific examples thereof include furyl group, thienyl group, pyrrolyl group, oxazolyl group, isoxazolyl group, triazolyl group, isothiazolyl group, imidazolyl group, pyrazolyl group, furazanyl group, oxadiazolyl group, triazolyl group, pyridyl group, pyrimidinyl group, pyrazinyl group, indolyl group, quinolyl group, isoquinolyl group, quinazolinyl group, imidazo[2,1-b][1,3]thiazolyl group and the like.
The “alkylthio group” means a straight chain or branched alkylthio group having 1 to 6 carbon atoms, and specific examples thereof include methylthio group, ethylthio group, propylthio group, 1-methylethylthio group, butylthio group, 1-methylpropylthio group, 2-methylpropylthio group, 1,1-dimethylethylthio group, pentylthio group, hexylthio group and the like. The alkylthio group is preferably an alkylthio group having 1 to 4 carbon atoms.
Examples of the alkyl of the “alkylcarbonyl group” include those similar to the aforementioned alkyl group. Preferable examples of the alkylcarbonyl group include acetyl group, propionyl group, butyryl group and the like.
The “alkylcarbonyloxy group” means a group wherein the oxygen atom is bonded to the carbonyl carbon of the aforementioned “alkylcarbonyl group”.
Examples of the alkyl of the “alkylsulfonyl group” include those similar to the aforementioned “alkyl group”. Preferable examples of the alkylsulfonyl group include methylsulfonyl group, ethylsulfonyl group, propylsulfonyl group and the like.
Examples of the alkoxy of the “alkoxycarbonyl group” include those similar to the aforementioned “alkoxy group”. Preferable examples of the alkoxycarbonyl group include methoxycarbonyl group, ethoxycarbonyl group, propoxycarbonyl group, butoxycarbonyl group, tert-butoxycarbonyl group and the like.
Examples of the alkyl group of the “amino group optionally substituted by one alkyl group or the same or different two alkyl groups”, “carbamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups” and “sulfamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups” include those similar to the aforementioned “alkyl group”.
Preferable examples of the “amino group optionally substituted by one alkyl group or the same or different two alkyl groups” include methylamino group, ethylamino group, propylamino group, dimethylamino group, diethylamino group, methylethylamino group and the like.
Preferable examples of the “carbamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups” include methylcarbamoyl group, ethylcarbamoyl group, propylcarbamoyl group, isopropylcarbamoyl group, dimethylcarbamoyl group, diethylcarbamoyl group, methylethylcarbamoyl group and the like.
Preferable examples of the “sulfamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups” include methylsulfamoyl group, ethylsulfamoyl group, propylsulfamoyl group, dimethylsulfamoyl group, diethylsulfamoyl group, methylethylsulfamoyl group and the like.
Examples of the “alkoxycarbonyl group” of the “amidino group optionally substituted by one alkoxycarbonyl group or the same or different two alkoxycarbonyl groups” include those similar to the aforementioned “alkoxycarbonyl group”. Preferable examples of the “amidino group optionally substituted by one alkoxycarbonyl group or the same or different two alkoxycarbonyl groups” include methoxycarbonylamidino group, ethoxycarbonylamidino group, propoxycarbonylamidino group and the like.
The aryl group of the “aryloxy group”, “arylcarbonyl group” and “arylsulfonyl group” is as defined for the aforementioned “aryl group”.
The aromatic heterocyclic group of the “aromatic heterocyclyloxy group”, “aromatic heterocyclylcarbonyl group” and “aromatic heterocyclylsulfonyl group” is as defined for the aforementioned “aromatic heterocyclic group”.
The substituent for the “alkyl group”, “alkenyl group” and “alkynyl group” is selected from the group consisting of the following (i) to (v), and the same or different plural substituents may be present:
(i) a halogen atom, a hydroxyl group, a carboxyl group and a cyano group;
(ii) a substituted or unsubstituted amino group, a substituted or unsubstituted carbamoyl group, and a substituted or unsubstituted sulfamoyl group;
(iii) an alkoxy group, a haloalkoxy group, an alkylcarbonyl group, an alkylcarbonyloxy group, an alkoxycarbonyl group, an alkylthio group and an alkylsulfonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group];
(iv) a cycloalkyl group, a cycloalkenyl group, and a saturated or unsaturated aliphatic heterocyclic group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an oxo group, a thioxo group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, a carbamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups, an alkoxy group, a haloalkoxy group, an optionally substituted alkoxycarbonyl group, an optionally substituted alkylcarbonyl group, an optionally substituted alkylsulfonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkoxycarbonyl group, alkylcarbonyl group, alkylsulfonyl group and alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group, a haloalkoxy group and a carbamoyl group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group];
(v) an aryl group, an aromatic heterocyclic group, an aryloxy group, an aromatic heterocyclyloxy group, an arylcarbonyl group, an aromatic heterocyclylcarbonyl group, an arylsulfonyl group and an aromatic heterocyclylsulfonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, a substituted or unsubstituted amino group, a substituted or unsubstituted carbamoyl group, a substituted or unsubstituted sulfamoyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group].
The substituent for the “cycloalkyl group”, “cycloalkenyl group”, “saturated aliphatic heterocyclic group”, “unsaturated aliphatic heterocyclic group”, “saturated nitrogen-containing aliphatic heterocycle” and “unsaturated nitrogen-containing aliphatic heterocycle” is one substituent or the same or different two or more substituents, which are selected from the group consisting of the following (vi) to (x):
(vi) a halogen atom, a hydroxyl group, a carboxyl group, a cyano group, an oxo group, a thioxo group, and an amidino group optionally substituted by one alkoxycarbonyl group or the same or different two alkoxycarbonyl groups;
(vii) a substituted or unsubstituted amino group, a substituted or unsubstituted carbamoyl group, and a substituted or unsubstituted sulfamoyl group;
(viii) an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkylcarbonyl group, an alkylcarbonyloxy group, an alkoxycarbonyl group, an alkylthio group and an alkylsulfonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, a carbamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups, an alkoxy group optionally substituted by alkoxy group(s) and/or a carbamoyl group(s), a haloalkoxy group, an alkylthio group, an alkoxycarbonyl group, an optionally substituted aryloxy group, an optionally substituted aromatic heterocyclyloxy group, an optionally substituted aryl group, an optionally substituted aromatic heterocyclic group and optionally substituted amino group. Examples of the substituent for the aryloxy group, aromatic heterocyclyloxy group, aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group. Examples of the substituent for the amino group include an optionally substituted alkyl group, an optionally substituted alkylcarbonyl group, an optionally substituted alkylsulfonyl group, and a carbamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups. Examples of the substituent for the alkyl group of the alkyl group, alkylcarbonyl group, alkylsulfonyl group and carbamoyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group, a haloalkoxy group and a carbamoyl group];
(ix) a cycloalkyl group, a cycloalkenyl group, and a saturated or unsaturated aliphatic heterocyclic group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an oxo group, a thioxo group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group];
(x) an aryl group, an aromatic heterocyclic group, an aryloxy group, an aromatic heterocyclyloxy group, an arylcarbonyl group, an aromatic heterocyclylcarbonyl group, an arylsulfonyl group and an aromatic heterocyclylsulfonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, a cyano group, a substituted or unsubstituted amino group, a substituted or unsubstituted carbamoyl group, a substituted or unsubstituted sulfamoyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group].
The substituent for the “phenyl group”, “aryl group” and “aromatic heterocyclic group” is 1 to 5 substituents selected from the group consisting of the following (xi) to (xv):
(xi) a halogen atom, a hydroxyl group, a carboxyl group, a cyano group, a nitro group, a methylenedioxy group, an ethylenedioxy group and —(CH₂)_n— (n is an integer of 3 to 5);
(xii) a substituted or unsubstituted amino group, a substituted or unsubstituted carbamoyl group, and a substituted or unsubstituted sulfamoyl group;
(xiii) an alkyl group, a haloalkyl group, an alkenyl group, an alkynyl group, an alkoxy group, a haloalkoxy group, an alkylcarbonyl group, an alkylcarbonyloxy group, an alkoxycarbonyl group, an alkylthio group and an alkylsulfonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, an optionally substituted alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkoxy group, aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group];
(xiv) a cycloalkyl group, a cycloalkenyl group, and a saturated or unsaturated aliphatic heterocyclic group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an oxo group, a thioxo group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group];
(xv) an aryl group, an aromatic heterocyclic group, an aryloxy group, an aromatic heterocyclyloxy group, an arylcarbonyl group, an aromatic heterocyclylcarbonyl group, an arylsulfonyl group and an aromatic heterocyclylsulfonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, a substituted or unsubstituted amino group, a substituted or unsubstituted carbamoyl group, a substituted or unsubstituted sulfamoyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group].
The substituent for the “amino group”, “carbamoyl group” and “sulfamoyl group” is one substituent or the same or different two substituents, which are selected from the group consisting of the following (xvi)-(xviii):
(xvi) an alkyl group, a haloalkyl group, an alkenyl group, an alkynyl group, an alkylcarbonyl group, an alkylsulfonyl group and an alkoxycarbonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, a carbamoyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a saturated or unsaturated aliphatic heterocyclic group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group];
(xvii) a cycloalkyl group, a cycloalkenyl group, and a saturated or unsaturated aliphatic heterocyclic group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an oxo group, a thioxo group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group];
(xviii) an aryl group, an aromatic heterocyclic group, an arylcarbonyl group, an aromatic heterocyclylcarbonyl group, an arylsulfonyl group and an aromatic heterocyclylsulfonyl group
[these groups are optionally substituted by one or more substituents selected from a halogen atom, a hydroxyl group, a carboxyl group, an amino group optionally substituted by one alkyl group or the same or different two alkyl groups, a carbamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups, a sulfamoyl group optionally substituted by one alkyl group or the same or different two alkyl groups, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, an optionally substituted alkyl group, an optionally substituted aryl group and an optionally substituted aromatic heterocyclic group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the aryl group and aromatic heterocyclic group include a halogen atom, a hydroxyl group, a carboxyl group, an alkyl group, a haloalkyl group, an alkoxy group, a haloalkoxy group, an alkoxycarbonyl group, a nitro group, a cyano group and a carbamoyl group].
In addition, the two substituents for the “amino group”, “carbamoyl group” or “sulfamoyl group” are optionally bonded to form, together with the adjacent nitrogen atom, a 5- to 10-membered nitrogen-containing aliphatic heterocycle.
Examples of the nitrogen-containing aliphatic heterocycle include pyrrolidine ring, piperidine ring, an azepane ring, an azocane ring, a piperazine ring, a morpholine ring, a thiomorpholine ring and a tetrahydroisoquinoline ring. In addition, the nitrogen-containing aliphatic heterocycle is optionally substituted by one or more substituents selected from halogen, a hydroxyl group, a carboxyl group, an optionally substituted alkyl group, a haloalkyl group, an alkoxy group and a haloalkoxy group. Examples of the substituent for the alkyl group include a halogen atom, a hydroxyl group, a carboxyl group, an alkoxy group, a haloalkoxy group and a carbamoyl group.
In the compound of the present invention represented by the formula (1), each of the groups is preferably as follows.
R¹is a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms or a haloalkoxy group having 1 to 6 carbon atoms, preferably a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms or a haloalkyl group having 1 to 6 carbon atoms, more preferably a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms, more preferably a hydrogen atom or a halogen atom, particularly preferably a hydrogen atom. R¹can be present on the benzene ring or pyridine ring at any substitutable position.
Specific examples of R¹include a hydrogen atom, a fluorine atom, a chlorine atom, a methyl group, an ethyl group, a propyl group, a trifluoromethyl group and the like. Among them, a hydrogen atom, a fluorine atom and a chlorine atom are preferable, and a hydrogen atom is more preferable.
L is a single bond, —O— or —CH₂O—, preferably, a single bond or —O—, more preferably —O—. L can be present on the benzene ring or pyridine ring at any substitutable position. When L is —CH₂O—, the oxygen atom of —CH₂O— is bonded to the benzene ring or pyridine ring, and the methylene chain is bonded to R².
R²is a substituted or unsubstituted 6- to 10-membered aryl group, or a substituted or unsubstituted 5- to 10-membered aromatic heterocyclic group, preferably a substituted or unsubstituted 6- to 10-membered aryl group, more preferably a substituted or unsubstituted phenyl group.
Preferable examples of the substituent of the aryl group or aromatic heterocyclic group for R²include a halogen atom, a substituted or unsubstituted alkyl group (preferably an unsubstituted alkyl group having 1 to 6 carbon atoms), a haloalkyl group (preferably a haloalkyl group having 1 to 6 carbon atoms), an alkoxy group (preferably an alkoxy group having 1 to 6 carbon atoms), a haloalkoxy group (preferably a haloalkoxy group having 1 to 6 carbon atoms), a cyano group and the like, specifically, a fluorine atom, a chlorine atom, a methyl group, an ethyl group, an isopropyl group, a tert-butyl group, a trifluoromethyl group, a trifluoromethoxy group, a methoxy group, an ethoxy group, a cyano group and the like. Among them, a fluorine atom, a methyl group and a trifluoromethoxy group are preferable.
Specific examples of the substituted or unsubstituted aryl group for R²include a phenyl group and a phenyl group substituted by preferable substituent(s) for the aforementioned aryl group, and the like.
Specific examples of the aromatic heterocyclic group for R²include a pyridyl group, a furyl group, a thienyl group, a pyrimidinyl group, a pyrazinyl group and the like. Among them, a pyridyl group and a furyl group are preferable.
R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 6 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered cycloalkenyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, preferably a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, more preferably a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, or a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, still more preferably a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted 3- to 8-membered cycloalkyl group.
Preferable examples of the substituent for the alkyl group for R³include a hydroxyl group, an alkoxy group (preferably an alkoxy group having 1 to 6 carbon atoms), a O-5 to 8-membered saturated aliphatic heterocyclic group and the like, specifically, a hydroxyl group, a methoxy group, an ethoxy group, an isopropoxy group, a tetrahydrofuryl group, a tetrahydropyranyl group and the like.
Preferable examples of the substituent for the saturated aliphatic heterocyclic group for R³include an alkylcarbonyl group, an alkoxycarbonyl group, an alkylsulfonyl group, a mono-alkylcarbamoyl group (the alkyl moiety has preferably 1 to 6 carbon atoms) and the like, specifically, an acetyl group, a tert-butoxycarbonyl group, a methylsulfonyl group, an isopropylcarbamoyl group and the like.
Specific examples of R³include an ethyl group, an isopropyl group, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a methoxyethyl group, an ethoxyethyl group, an isopropoxyethyl group, a hydroxyethyl group, a methoxypropyl group, an ethoxypropyl group, a hydroxypropyl group, a tetrahydropyranyl group, a tetrahydrofuryl group, a 2,2-dimethyl-2-hydroxyethyl group, a tetrahydropyranylmethyl group, a tetrahydrofurylmethyl group, a 4-piperidyl group, a 1-(tert-butoxycarbonyl)piperidin-4-yl group, a 1-isopropylcarbamoylpiperidin-4-yl group, a 1-acetylpiperidin-4-yl group, a 1-methylsulfonylpiperidin-4-yl group and the like. R³is more preferable a cyclobutyl group, a 2-ethoxyethyl group or an ethyl group.
R⁴is a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted 3- to 8-membered cycloalkyl group, preferably a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, more preferably a hydrogen atom.
Preferable examples of the substituent for the alkyl group and cycloalkyl group for R⁴include a halogen atom, a hydroxyl group, an alkoxy group (preferably an alkoxy group having 1 to 6 carbon atoms), a 4- to 8-membered saturated aliphatic heterocyclic group and the like, specifically, a fluorine atom, a chlorine atom, a hydroxyl group, a methoxy group, an ethoxy group, a tetrahydrofuryl group, a tetrahydropyranyl group and the like.
Specific examples of R⁴include a hydrogen atom, a methyl group, cyclopropyl group and the like. Among them, a hydrogen atom and a methyl group are preferable, and a hydrogen atom is more preferable.
R^5aand R^5bare each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or R⁴and R^5aare optionally bonded to form, together with the nitrogen atom that R⁴is bonded to, a 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle (in this case, R^5bis a hydrogen atom), preferably independently each a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms. Preferable examples of the substituent for the alkyl group for R^5aor R^5binclude a halogen atom, a hydroxyl group, an alkoxy group (preferably an alkoxy group having 1 to 6 carbon atoms), a 4- to 8-membered saturated aliphatic heterocyclic group and the like, specifically, a fluorine atom, a chlorine atom, a hydroxyl group, a methoxy group, an ethoxy group, tetrahydrofuryl group, tetrahydropyranyl group and the like.
Specific examples of R^5aand R^5binclude independently each a hydrogen atom, a methyl group, an ethyl group and an isopropyl group (preferably R^5ais a hydrogen atom, a methyl group, an ethyl group or an isopropyl group, and R^5bis a methyl group, an ethyl group or an isopropyl group). Among them, a hydrogen atom and a methyl group are preferable (preferably R^5ais a hydrogen atom, and R^5bis a methyl group).
When R^5aand R^5bare different from each other, the carbon atom that they are bonded to is an asymmetric carbon atom, and the steric configuration is preferably S-configuration from the aspects of easy availability of the starting materials.
Specific examples of the 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle formed by R⁴and R^5awhich are bonded to each other, together with the nitrogen atom that R⁴is bonded to, include an azetidine ring, a pyrrolidine ring, a piperidine ring and the like. Among them, pyrrolidine ring is preferable.
R⁶and R⁷are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 6 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered cycloalkenyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, a substituted or unsubstituted 6- to 10-membered aryl group, or a substituted or unsubstituted 5- to 10-membered aromatic heterocyclic group, or R⁶and R⁷are optionally bonded to form, together with the nitrogen atom that they are bond to, a substituted or unsubstituted 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle, or a substituted or unsubstituted 5- to 10-membered unsaturated nitrogen-containing aliphatic heterocycle (the saturated or unsaturated nitrogen-containing aliphatic heterocycle contains 0 to 2 oxygen atoms, 0 to 2 sulfur atoms and 1 to 3 nitrogen atoms), preferably independently each a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, more preferably independently each a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, more preferably a hydrogen atom.
Preferable examples of the substituent for the alkyl group for R⁶or R⁷include a hydroxyl group, an alkoxy group (preferably an alkoxy group having 1 to 6 carbon atoms), a 4- to 8-membered saturated aliphatic heterocyclic group and the like, specifically, a hydroxyl group, a methoxy group, an ethoxy group, a tetrahydrofuryl group, a tetrahydropyranyl group, a pyrrolidinyl group, a piperidyl group, a piperidino group, a piperazinyl group, a morpholino group and the like. Specific examples of the substituted alkyl group for R⁶or R⁷include a methoxyethyl group, a 2,2-dimethyl-2-hydroxyethyl group, a morpholinoethyl group and the like.
Preferable specific examples of R⁶or R⁷include a hydrogen atom, a methyl group, an ethyl group, an isopropyl group and the like. Among them, a hydrogen atom and a methyl group are preferable, and a hydrogen atom is more preferable.
Specific examples of the substituted or unsubstituted 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle and substituted or unsubstituted 5- to 10-membered unsaturated nitrogen-containing aliphatic heterocycle, which are formed by R⁶and R⁷which are bonded to each other, together with the nitrogen atom that they are bond to, include a morpholine ring, a pyrrolidine ring, a piperidine ring, a piperazine ring and the like. Among them, a morpholine ring and a piperazine ring are preferable.
Preferable examples of the substituent for the above-mentioned saturated nitrogen-containing aliphatic heterocycle and unsaturated nitrogen-containing aliphatic heterocycle include an oxo group, a cyano group, a haloalkyl group (preferably a haloalkyl group having 1 to 6 carbon atoms) and the like. Among them, an oxo group, a cyano group and a trifluoromethyl group are preferable.
Preferable examples of compound (1) include the following compounds and a pharmaceutically acceptable salt thereof.
Preferable embodiments thereof include a compound wherein
R¹is a hydrogen atom or a halogen atom,
L is a single bond or —O—,
R²is a substituted or unsubstituted phenyl group,
X is a carbon atom,
R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group,
R⁴is a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms,
R^5aand R^5bare each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, and
R⁶and R⁷are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, or
R⁶and R⁷are optionally bonded to form, together with the nitrogen atom that they are bond to, a substituted or unsubstituted 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle, or a substituted or unsubstituted 5- to 10-membered unsaturated nitrogen-containing aliphatic heterocycle (the saturated or unsaturated nitrogen-containing aliphatic heterocycle contains 0 to 2 oxygen atoms, 0 to 2 sulfur atoms and 1 to 3 nitrogen atoms).
Other preferable embodiments thereof include a compound wherein
R¹is a hydrogen atom, a halogen atom or an alkyl group having 1 to 6 carbon atoms,
L is a single bond or —O—,
R²is a substituted or unsubstituted 6- to 10-membered aryl group (the substituent is preferably a halogen atom, an alkyl group having 1 to 6 carbon atoms or a haloalkoxy group having 1 to 6 carbon atoms, more preferably a fluorine atom, a methyl group or a trifluoromethoxy group),
X is a carbon atom,
R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms (the substituent is preferably a hydroxyl group, an alkoxy group having 1 to 6 carbon atoms or a 4- to 8-membered saturated aliphatic heterocyclic group, more preferably a hydroxyl group, a methoxy group, an ethoxy group, an isopropoxy group, a tetrahydrofuryl group or a tetrahydropyranyl group), a substituted or unsubstituted 3- to 8-membered cycloalkyl group (preferably an unsubstituted 3- to 8-membered cycloalkyl group), a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group (preferably an unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group), or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group (preferably an unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group),
R⁴is a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms (preferably an unsubstituted alkyl group having 1 to 6 carbon atoms),
R^5aand R^5bare each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms (preferably an unsubstituted alkyl group having 1 to 6 carbon atoms), and
R⁶and R⁷are each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms (preferably an unsubstituted alkyl group having 1 to 6 carbon atoms).
Among them, a compound wherein
R¹is a hydrogen atom or a halogen atom,
L is a single bond or —O—,
R²is a substituted or unsubstituted phenyl group (the substituent is preferably a halogen atom, an alkyl group having 1 to 6 carbon atoms or a haloalkoxy group having 1 to 6 carbon atoms, more preferably a fluorine atom, a methyl group or a trifluoromethoxy group),
X is a carbon atom,
R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms (the substituent is preferably a hydroxyl group, an alkoxy group having 1 to 6 carbon atoms or a 4- to 8-membered saturated aliphatic heterocyclic group, more preferably a hydroxyl group, a methoxy group, an ethoxy group, an isopropoxy group, a tetrahydrofuryl group or a tetrahydropyranyl group), or a substituted or unsubstituted 3- to 8-membered cycloalkyl group (preferably an unsubstituted 3- to 8-membered cycloalkyl group),
R⁴is a hydrogen atom or a methyl group,
R^5aand R^5bare each independently a hydrogen atom, a methyl group, an ethyl group or an isopropyl group (preferably R^5ais a hydrogen atom, a methyl group, an ethyl group or an isopropyl group, and R^5bis a methyl group, an ethyl group or an isopropyl group), and
R⁶and R⁷is a hydrogen atom,
is preferable, and
a compound wherein
R¹is a hydrogen atom,

L is —O—,

R²is a substituted or unsubstituted phenyl group (the substituent is preferably a halogen atom, an alkyl group having 1 to 6 carbon atoms or a haloalkoxy group having 1 to 6 carbon atoms, more preferably a fluorine atom, a methyl group or a trifluoromethoxy group),
X is a carbon atom,
R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms (the substituent is preferably a hydroxyl group, an alkoxy group having 1 to 6 carbon atoms or a 4- to 8-membered saturated aliphatic heterocyclic group, more preferably a hydroxyl group, a methoxy group, an ethoxy group, an isopropoxy group, a tetrahydrofuryl group or a tetrahydropyranyl group), or a substituted or unsubstituted 3- to 8-membered cycloalkyl group (preferably an unsubstituted 3- to 8-membered cycloalkyl group),
R⁴is a hydrogen atom or a methyl group,
R^5aand R^5bare each independently a hydrogen atom or a methyl group (preferably R^5ais a hydrogen atom, and R^5bis a methyl group), and
R⁶and R⁷is a hydrogen atom,
is more preferable.
The compound of the present invention is preferably compound (2) or compound (3) or a pharmaceutically acceptable salt thereof, more preferably compound (2) or a pharmaceutically acceptable salt thereof.
Preferable specific examples thereof include the following compounds and a pharmaceutically acceptable salt thereof.
Specific examples thereof include a compound wherein

R¹is

(1) a hydrogen atom,
(2) a halogen atom (preferably a fluorine atom, a chlorine atom),
(3) a C_1-6alkyl group (preferably methyl) or
(4) a C_1-6haloalkyl group (preferably trifluoromethyl),

L is

(1) a single bond,

(2) —O— or

(3) —CH₂O—,

R²is

(1) a C_6-10aryl group (the C_6-10aryl group is optionally condensed with a C_3-6cycloalkane) (preferably phenyl, indanyl, more preferably phenyl) optionally substituted by 1 to 3 substituents selected from

- (a) a halogen atom (preferably a fluorine atom, a chlorine atom),
- (b) a C_1-6alkyl group (preferably methyl, ethyl, isopropyl, tert-butyl),
- (c) a C_1-6haloalkyl group (preferably trifluoromethyl),
- (d) a C_1-6alkoxy group (preferably methoxy, ethoxy),
- (e) a C_1-6haloalkoxy group (preferably trifluoromethoxy) and
- (f) a cyano group, or
  (2) a 5- to 10-membered aromatic heterocyclic group (preferably a 5- or 6-membered aromatic heterocyclic group, more preferably pyridyl, furyl),
  X is a carbon atom or a nitrogen atom,

R³is

(1) a C_1-6alkyl group (preferably methyl, ethyl, propyl, isopropyl, isobutyl) optionally substituted by 1 to 3 substituents selected from

- (a) a C_1-6alkoxy group (preferably methoxy, ethoxy, isopropoxy),
- (b) a 4- to 8-membered saturated aliphatic heterocyclic group (preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably tetrahydropyranyl, tetrahydrofuryl), and
- (c) a hydroxyl group,
  (2) a C_3-8cycloalkyl group (preferably cyclopropyl, cyclobutyl, cyclopentyl), or
  (3) a 4- to 8-membered saturated aliphatic heterocyclic group preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably tetrahydropyranyl, piperidyl) optionally substituted by 1 to 3 substituents selected from
- (a) a C_1-6alkyl-carbonyl group (preferably acetyl),
- (b) a C_1-6alkoxy-carbonyl group (preferably tert-butoxycarbonyl),
- (c) a C_1-6alkylsulfonyl group (preferably methylsulfonyl), and
- (d) a carbamoyl group optionally mono- or di-substituted by C_1-6alkyl group(s) (preferably isopropyl),

R⁴is

(1) a hydrogen atom, or
(2) a C_1-6alkyl group (preferably methyl),
R^5aand R^5bare each independently
(1) a hydrogen atom, or
(2) a C_1-6alkyl group (preferably methyl, ethyl, isopropyl), or
R⁴and R^5aare optionally bonded to form, together with the nitrogen atom that R⁴is bonded to, a 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle (preferably a 5- or 6-membered saturated nitrogen-containing aliphatic heterocycle, more preferably pyrrolidine) (in this case, R^5bis a hydrogen atom), and
R⁶and R⁷are each independently
(1) a hydrogen atom, or
(2) a C_1-6alkyl group (preferably ethyl, isobutyl) optionally substituted by 1 to 3 substituents selected from

- (a) a hydroxyl group,
- (b) a C_1-6alkoxy group (preferably methoxy), and
- (c) a 4- to 8-membered saturated aliphatic heterocyclic group (preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably morpholinyl), or
  R⁶and R⁷are optionally bonded to form, together with the nitrogen atom that they are bond to, a 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle (preferably a 5- or 6-membered saturated nitrogen-containing aliphatic heterocycle, more preferably morpholine, piperazine) optionally substituted by 1 to 3 substituents selected from
- (a) an oxo group,
- (b) a cyano group, and
- (c) a C_1-6haloalkyl group (preferably trifluoromethyl).

Preferable specific examples thereof include a compound herein

R¹is

(1) a hydrogen atom, or
(2) a halogen atom (preferably a fluorine atom, a chlorine atom),

L is

(1) a single bond, or

(2) —O—,

R²is a phenyl group optionally substituted by 1 to 3 substituents selected from

- (a) a halogen atom (preferably a fluorine atom, a chlorine atom),
- (b) a C_1-6alkyl group (preferably methyl, ethyl, isopropyl, tert-butyl),
- (c) a C_1-6haloalkyl group (preferably trifluoromethyl),
- (d) a C_1-6alkoxy group (preferably methoxy, ethoxy),
- (e) a C_1-6haloalkoxy group (preferably trifluoromethoxy), and
- (f) a cyano group,
  X is a carbon atom,

R³is

- (a) a C_1-6alkoxy group (preferably methoxy, ethoxy, isopropoxy),
- (b) a 4- to 8-membered saturated aliphatic heterocyclic group (preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably tetrahydropyranyl, tetrahydrofuryl), and
- (c) a hydroxyl group,
  (2) a C_3-8cycloalkyl group (preferably cyclopropyl, cyclobutyl, cyclopentyl), or
  (3) a 4- to 8-membered saturated aliphatic heterocyclic group (preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably tetrahydropyranyl, piperidyl) optionally substituted by 1 to 3 substituents selected from
- (a) a C_1-6alkyl-carbonyl group (preferably acetyl),
- (b) a C_1-6alkoxy-carbonyl group (preferably tert-butoxycarbonyl),
- (c) a C_1-6alkylsulfonyl group (preferably methylsulfonyl), and
- (d) a carbamoyl group optionally mono- or di-substituted by C_1-6alkyl group(s) (preferably isopropyl),

R⁴is

(1) a hydrogen atom, or
(2) a C_1-6alkyl group (preferably methyl),
R^5aand R^5bare each independently
(1) a hydrogen atom, or
(2) a C_1-6alkyl group (preferably methyl, ethyl, isopropyl), and
R⁶and R⁷are each independently
(1) a hydrogen atom, or
(2) a C_1-6alkyl group (preferably ethyl, isobutyl) optionally substituted by 1 to 3 substituents selected from

Other preferable specific examples thereof include a compound wherein

R¹is

(1) a hydrogen atom,
(2) a halogen atom (preferably a fluorine atom, a chlorine atom), or
(3) a C_1-6alkyl group (preferably methyl),

L is

(1) a single bond, or

(2) —O—,

R²is a C_6-10aryl group (the C_6-10aryl group is optionally condensed with a C_3-6cycloalkane) (preferably phenyl, indanyl, more preferably phenyl) optionally substituted by 1 to 3 substituents selected from

R³is

R⁴is

- (a) a hydroxyl group,
- (b) a C_1-6alkoxy group (preferably methoxy), and
- (c) a 4- to 8-membered saturated aliphatic heterocyclic group (preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably morpholinyl).

Among them, a compound wherein

R¹is

L is

(1) a single bond, or

(2) —O—,

R³is

- (a) a C_1-6alkoxy group (preferably methoxy, ethoxy, isopropoxy),
- (b) a 4- to 8-membered saturated aliphatic heterocyclic group (preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably tetrahydropyranyl, tetrahydrofuryl), and
- (c) a hydroxyl group, or
  (2) a C_3-8cycloalkyl group (preferably cyclopropyl, cyclobutyl, cyclopentyl),
  R⁴is a hydrogen atom or a methyl group,
  R^5aand R^5bare each independently a hydrogen atom, a methyl group, an ethyl group or an isopropyl group (preferably R^5ais a hydrogen atom, a methyl group, an ethyl group or an isopropyl group, and R^5bis a methyl group, an ethyl group or an isopropyl group), and
  R⁶and R⁷is a hydrogen atom,
  is preferable, and
  a compound wherein
  R¹is a hydrogen atom,

L is —O—,

R³is

- (a) a C_1-6alkoxy group (preferably methoxy, ethoxy, isopropoxy),
- (b) a 4- to 8-membered saturated aliphatic heterocyclic group (preferably a 5- or 6-membered saturated aliphatic heterocyclic group, more preferably tetrahydropyranyl, tetrahydrofuryl), and
- (c) a hydroxyl group, or
  (2) a C_3-8cycloalkyl group (preferably cyclopropyl, cyclobutyl, cyclopentyl),
  R⁴is a hydrogen atom or a methyl group, and
  R^5aand R^5bare each independently a hydrogen atom or a methyl group (preferably R^5ais a hydrogen atom, and R^5bis a methyl group), and
  R⁶and R⁷is a hydrogen atom,
  is more preferable.

Other preferable specific examples thereof include

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}glycinamide,
N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-2-methylalaninamide,
N²-{[1-cyclopropyl-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-cyclobutyl-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-chlorophenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-fluorophenoxy)-1-(2-hydroxy-2-methylpropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-fluorophenoxy)-1-(3-methoxypropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(2-chloro-4-fluorophenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-ethyl-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(2,4-difluorophenoxy)-1-(2-hydroxy-2-methylpropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-(2-ethoxyethyl)-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-ethyl-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[1-(3-methoxypropyl)-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[6-(4-methylphenoxy)-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,
N²-{[5-chloro-1-(2-ethoxyethyl)-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, and
N²-{[5-chloro-6-(3,4-difluorophenyl)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, and
pharmaceutically acceptable salts thereof.

Compound (1) can be prepared, for example, according to the method shown below.
wherein R¹, R², R³, R⁴, R^5a, R^5b, R⁶, R⁷, L and X are as defined above.
Compound (1) can be prepared by subjecting compound (1-1) to a reductive amination with the corresponding amine compound. As the solvent, ether solvents such as tetrahydrofuran, 1,4-dioxane and the like, halogenated solvents such as dichloromethane, chloroform, 1,2-dichloroethane and the like, alcohol solvents such as methanol, ethanol and the like, ethyl acetate, N,N-dimethylformamide, acetonitrile and the like can be used. Among them, tetrahydrofuran, dichloromethane and methanol are preferable. As the reducing agent, sodium borohydride, sodium triacetoxyborohydride, sodium cyanoborohydride and the like can be used. The reaction temperature is −20° C.—the refluxing temperature of the reaction solvent, and particularly preferably 0° C.—near room temperature. Molecular sieves or sodium sulfate may be added as a dehydrating agent. Acetic acid or hydrochloric acid may be added as an additive.
Compound (1A), which is compound (1) wherein R⁴and R^5aare not bonded, can also be prepared from compound (1-1) according to the method shown in Reaction Scheme-2 below.
wherein R¹, R², R³, R⁴, R^5a, R^5b, R⁶, R⁷, L and X are as defined above except that R⁴and R^5aare not bonded, and Y is a leaving group such as a halogen atom, a mesyloxy group, a tosyloxy group and the like.
Compound (1-1) is subjected to a reductive amination with compound (1-2) to give compound (1-3), and compound (1-3) is reacted with compound (1-4) in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, 1,4-dioxane and the like), halogenated solvent (e.g., dichloromethane, chloroform, 1,2-dichloroethane and the like), ethyl acetate, N,N-dimethylformamide, acetonitrile and the like, at 0° C.—the refluxing temperature of the reaction solvent to give compound (1A). While the base is not particularly limited, inorganic bases such as potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like, and organic bases such as triethylamine, diisopropylethylamine and the like can be used.
In addition, compound (1) can also be prepared according to the method shown in Reaction Scheme-3 below.
wherein R¹, R², R³, R⁴, R^5a, R^5b, R⁶, R⁷, L, Y and X are as defined above.
Compound (1) can be prepared by reacting compound (1-5) with the corresponding amine compound in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, 1,4-dioxane and the like), halogenated solvent (e.g., dichloromethane, chloroform, 1,2-dichloroethane and the like), ethyl acetate, N,N-dimethylformamide, acetonitrile and the like, at 0° C.—the refluxing temperature of the reaction solvent. While the base is not particularly limited, inorganic bases such as potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like, and organic bases such as triethylamine, diisopropylethylamine and the like can be used.
Compound (1B), which is compound (1) wherein R⁴is a hydrogen atom, can be prepared, for example, by the method shown in Reaction Scheme-4 below.
wherein R¹, R², R³, R^5a, R^5b, R⁶, R⁷, L, Y and X are as defined above.
Compound (1B) can be prepared by reacting compound (1-7), which is obtained from compound (1-5) and compound (1-6) in the same manner as in Reaction Scheme-3, in an acidic solvent such as trifluoroacetic acid, trifluoromethanesulfonic acid, hydrochloric acid, sulfuric acid and the like, at room temperature—the refluxing temperature of the reaction solvent. The reaction is more preferably performed in trifluoroacetic acid at around 50° C.
The above-mentioned compounds (1-1) and (1-5) can be prepared by the method shown below and a method analogous thereto.
Of the above-mentioned compound (1-1), compound (2-1) can be prepared, for example, by the method shown in Reaction Scheme-5 below.
wherein R²and R³are as defined above.
Compound (2-3) can be prepared by reacting 2,4-Difluoronitrobenzene with compound (2-2) in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like), N,N-dimethylformamide, acetonitrile and the like, at room temperature—the refluxing temperature of the reaction solvent. As the base, potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like can be used, and potassium carbonate is preferably used. As the solvent, 1,4-dioxane is preferable.
Compound (2-5) can be prepared by reacting compound (2-3) with compound (2-4) in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like), N,N-dimethylformamide, acetonitrile and the like, at room temperature—the refluxing temperature of the reaction solvent. As the base, potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like can be used, and cesium carbonate is preferably used. As the solvent, 1,4-dioxane is preferable.
Compound (2-6) can be prepared by reducing the nitro group of compound (2-5) to an amino group. The reduction to be used in this reaction may be performed under conventional reduction conditions. Preferred are catalytic reduction by palladium-carbon and the like, reduction using a metal such as iron and the like, and the like. The solvent to be used for the reduction is preferably selected according to the reduction conditions. For example, for catalytic reduction, methanol, ethanol, tetrahydrofuran, ethyl acetate and the like are preferably selected and, for reduction using a metal such as iron and the like, tetrahydrofuran, acetic acid, methanol, ethanol, water and the like are selected. The catalytic reduction is preferably performed at room temperature, and the reduction using a metal such as iron and the like is preferably performed at 50° C.—the refluxing temperature of the reaction solvent.
Compound (2-1) can be prepared by mixing compound (2-6) with glycolic acid and heating them from 100° C. to 150° C., and by oxidizing the hydroxyl group of the obtained corresponding cyclic compound. The oxidation to be used for this reaction may be performed under conventional oxidation conditions. Examples thereof include oxidation with manganese dioxide, chrome and the like, and oxidation with organic oxidant represented by dimethyl sulfoxide. The oxidation with manganese dioxide and Swern oxidation are preferable. Of these, oxidation with manganese dioxide is particularly preferable. The solvent to be used for the oxidation is preferably selected according to the oxidation conditions. For example, for oxidation with a metal, halogenated solvents such as dichloromethane, chloroform and the like, and ether solvents such as tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like are preferably selected. For oxidation with an organic oxidant, halogenated solvents such as dichloromethane, chloroform and the like are preferable. The oxidation with metal is preferably performed at room temperature, and the oxidation with an organic oxidant is preferably performed at −78° C.—room temperature.
In the above-mentioned compound (1-1), compound (3-1) can also be prepared, for example, by the method shown in Reaction Scheme-6 below.
wherein R²and R³are as defined above.
Compound (3-4) can be prepared by reacting compound (3-2) with compound (3-3) in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like), N,N-dimethylformamide, acetonitrile and the like, at room temperature—the refluxing temperature of the reaction solvent. As the base, potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like can be used, and potassium carbonate is preferably used. As the solvent, 1,4-dioxane is preferable.
Compound (3-5) can be prepared by reducing the nitro group of compound (3-4) to an amino group. The reduction to be used in this reaction is preferably a reduction using a metal such as iron, tin etc., and the like. A solvent to be used for the reduction is preferably tetrahydrofuran, acetic acid, methanol, ethanol, water and the like. The reduction using a metal is preferably performed at 50° C.—the refluxing temperature of the reaction solvent.
Compound (3-6) can be prepared by mixing compound (3-5) with glycolic acid and heating them from 100° C. to 150° C. Compound (3-7) can be prepared by oxidizing the hydroxyl group of compound (3-6). The oxidation to be used for this reaction may be performed under conventional oxidation conditions. Examples thereof include oxidation with manganese dioxide, chrome and the like, and oxidation with an organic oxidant represented by dimethyl sulfoxide. The oxidation with manganese dioxide and Swern oxidation are preferable. Of these, oxidation with manganese dioxide is particularly preferable. The solvent to be used for the oxidation is preferably selected according to the oxidation conditions. For example, for oxidation with a metal, halogenated solvent such as dichloromethane, chloroform and the like, ether solvent such as tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like are preferable and, for oxidation with an organic oxidant, halogenated solvent such as dichloromethane, chloroform and the like are preferable. The oxidation with a metal is preferably performed at room temperature, and the oxidation with an organic oxidant is preferably performed at −78° C. to room temperature.
Compound (3-1) can be prepared by reacting compound (3-7) with the corresponding boranic acid compound by using a palladium catalyst, a ligand and a base, in a solvent such as dimethoxyethane, 1,4-dioxane, toluene, ethanol and the like, at room temperature—the refluxing temperature of the solvent. Examples of the palladium catalyst include, but are not particularly limited to, palladium acetate, tetrakistriphenylphosphine palladium, trisbenzylideneacetone dipalladium and the like. While the ligand is not particularly limited, examples thereof include triphenylphosphine, tri-o-tolylphosphine, tri-tert-butylphosphine and the like. While the base is not particularly limited, examples thereof include sodium carbonate, potassium carbonate, cesium carbonate and the like.
In the above-mentioned compound (1-1), compound (4-1) can be prepared, for example, according to the method shown in Reaction Scheme-7 below.
wherein R²and R³are as defined above.
Compound (4-3) can be prepared by reacting compound (3-6) with compound (4-2) by using a copper catalyst, a ligand and a base, in a solvent such as N-methylpyrrolidinone, 1,4-dioxane, dimethyl sulfoxide, N,N-dimethylformamide and the like, at room temperature—the refluxing temperature of the solvent. While the copper catalyst is not particularly limited, examples thereof include copper iodide, copper bromide, copper chloride and the like. While the ligand is not particularly limited, examples thereof include 2,2,6,6-tetramethylheptane-3,5-dione, N,N-dimethylglycine and the like. While the base is not particularly limited, examples thereof include sodium carbonate, potassium carbonate, cesium carbonate and the like.
Compound (4-1) can be prepared by oxidizing the hydroxyl group of compound (4-3). The oxidation to be used for this reaction may be performed under conventional oxidation conditions. Examples thereof include oxidation with manganese dioxide, chrome and the like, and oxidation with organic oxidant represented by dimethyl sulfoxide. The oxidation with manganese dioxide and Swern oxidation are preferable. Of these, oxidation with manganese dioxide is particularly preferable.
The solvent to be used for the oxidation is preferably selected according to the oxidation conditions. For example, for oxidation with a metal, halogenated solvents such as dichloromethane, chloroform and the like, and ether solvents such as tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like are preferably selected. For oxidation with an organic oxidant, halogenated solvents such as dichloromethane, chloroform and the like are preferable. The oxidation with metal is preferably performed at room temperature, and the oxidation with an organic oxidant is preferably performed at −78° C.—room temperature.
In the above-mentioned compound (1-1), compound (5-1) can be prepared, for example, by the method shown in Reaction Scheme-8 below.
wherein R², R³and Y are as defined above.
Compound (5-4) can be prepared by reacting compound (5-2) with compound (5-3) in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like), N,N-dimethylformamide and the like, at room temperature—the refluxing temperature of the reaction solvent. As the base, potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like can be used, and potassium carbonate is preferably used. As the solvent, N,N-dimethylformamide is preferable.
Compound (5-1) can be obtained from compound (5-4) in the same manner as in Reaction Scheme-5.
In the above-mentioned compound (1-1), compound (6-1) can be prepared, for example, according to Reaction Scheme-9 below.
wherein R²and R³are as defined above.
Compound (6-3) can be prepared by reacting 2,6-Dichloro-3-nitropyridine with compound (6-2) in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like), N,N-dimethylformamide, acetonitrile and the like, at room temperature—the refluxing temperature of the reaction solvent. As the base, potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like can be used, and potassium carbonate is preferably used. As the solvent, 1,4-dioxane is preferable.
Compound (6-5) can be prepared by reacting compound (6-3) with compound (6-4) in the presence of a base, in a solvent such as ether solvent (e.g., tetrahydrofuran, dimethoxyethane, 1,4-dioxane and the like), N,N-dimethylformamide, acetonitrile and the like, at room temperature—the refluxing temperature of the reaction solvent. As the base, potassium carbonate, cesium carbonate, sodium hydroxide, sodium hydride, potassium hydride, potassium tert-butoxide and the like can be used, and cesium carbonate is preferably used. As the solvent, 1,4-dioxane is preferable.
Compound (6-1) can be obtained from compound (6-5) in the same manner as in Reaction Scheme-5.
In the above-mentioned compound (1-1), compound (7-1) can be prepared, for example, by the method shown in Reaction Scheme-10 below.
wherein R²and R³are as defined above.
Compound (7-2) can be obtained from compound (6-3) in the same manner as in Reaction Scheme-6.
Compound (7-1) can be prepared by reacting compound (7-2) with the corresponding boranic acid compound by using a palladium catalyst, a ligand and a base, in a solvent such as dimethoxyethane, 1,4-dioxane, toluene, ethanol and the like, at room temperature—the refluxing temperature of the solvent. Examples of the palladium catalyst include, but are not particularly limited to, palladium acetate, tetrakistriphenylphosphine palladium, trisbenzylideneacetone dipalladium and the like. While the ligand is not particularly limited, examples thereof include triphenylphosphine, tri-o-tolylphosphine, tri-tert-butylphosphine and the like. While the base is not particularly limited, examples thereof include sodium carbonate, potassium carbonate, cesium carbonate and the like.
The above-mentioned compound (1-5) can be prepared from compound (8-1), for example, by the method shown in Reaction Scheme-11 below.
wherein R¹, R², R³, L, X and Y are as defined above.
As a conversion step to a leaving group, when the leaving group Y is a mesyloxy group or a tosyloxy group, corresponding chloride (mesyl chloride, tosyl chloride) is reacted in the presence of a base such as triethylamine, pyridine and the like to give corresponding mesyl or tosyl form. When the leaving group Y is a halogen atom, the methods described in Comprehensive Organic Transformation [R. C. Larock, VCH Publishers Inc. (1989)], 4th Edition Jikken Kagaku Kouza (Maruzen), Shinjikken Kagaku Koza (Courses in Experimental Chemistry) (Maruzen) and the like can be employed. For example, corresponding bromide can be obtained by adding phosphorus tribromide in tetrahydrofuran.
Each of the aforementioned reactions can be performed according to the methods described in the Examples of the present specification, Comprehensive Organic Transformation [R. C. Larock, VCH Publishers Inc. (1989)], 4th Edition Jikken Kagaku Kouza (Maruzen), Shinjikken Kagaku Koza (Courses in Experimental Chemistry) (Maruzen).
In addition, the starting material compounds to be used in the aforementioned production methods can be appropriately prepared by using a commercially available product or according to a method known to those of ordinary skill in the art.
Furthermore, when the compound of the present invention or a pharmaceutically acceptable salt thereof is prepared, a functional group such as a hydroxyl group, a carboxyl group, an amino group and the like can be protected or deprotected in any step where necessary. The kind of the protecting group and the method of protection and deprotection may be those well known to those of ordinary skill in the art. For example, “Protective Groups in Organic Synthesis (T. W. Greene et al., John Wiley & Sons, Inc. published in 1991)” and the like may be referred to.
When compound (1) has a group capable of forming a salt in the structure, it can be converted as necessary to an acid addition salt with inorganic acid or organic acid, or an alkali addition salt, which is acceptable as a medicament. Examples of the pharmaceutically acceptable acid addition salt include inorganic acid salts such as hydrochloride, hydrobromide, sulfate, phosphate and the like, salts with organic carboxylic acid such as formate, acetate, fumarate, maleate, oxalate, citrate, malate, tartrate, aspartate, glutamate and the like, salts with sulfonic acid such as methanesulfonate, benzenesulfonate, p-toluenesulfonate, hydroxybenzenesulfonate, dihydroxybenzenesulfonate and the like, and examples of the pharmaceutically acceptable alkali addition salt include ammonium salt, lithium salt, sodium salt, potassium salt, calcium salt, magnesium salt and the like.
In addition, the present invention also encompasses a hydrate, and a solvate such as ethanolate and the like, of compound (1) or a pharmaceutically acceptable salt thereof. Furthermore, the present invention encompasses any tautomer and stereoisomer such as optical isomer and the like, and any crystalline form, of compound (1). These can be appropriately purified by a method well known to those of ordinary skill in the art, such as silica gel column chromatography, HPLC, ion exchange chromatography, recrystallization and the like.
To obtain the aforementioned optical isomer in a pure form, an optical resolution method known to those of ordinary skill in the art may be used. To be specific, when the compound of the present invention or an intermediate thereof has a basic functional group, it can form a salt with an optically active acid (e.g., monocarboxylic acids such as mandelic acid, N-benzyloxyalanine, lactic acid and the like, dicarboxylic acids such as tartaric acid, o-diisopropylidenetartaric acid, malic acid and the like, sulfonic acids such as camphorsulfonic acid, bromocamphorsulfonic acid and the like) in an inert solvent. In addition, when the compound of the present invention or an intermediate thereof has an acidic functional group, it can also form a salt with optically active amine (e.g., organic amines such as α-phenethylamine, kinin, quinidine, cinchonidine, cinchonine, strychnine and the like). The temperature for the formation of the salt is from room temperature to the boiling point of the solvent.
The novel compound having a bicyclic heterocycle of the present invention or a pharmaceutically acceptable salt thereof has an SNS inhibitory activity and can be used as a therapeutic or prophylactic drug for neuropathic pain and nociceptive pain. Examples of the neuropathic pain here include neuralgia after lumbar operation, diabetic neuropathy, neuralgia after herpes zoster, reflex sympathetic dystrophy, phantom limb pain, spinal cord injury, late stage carcinomatous pain and prolonged postoperative pain. Examples of the nociceptive pain include lumbago, abdominal pain, rheumatoid arthritis, pain due to osteoarthritis and the like. In addition, the compound of the present invention or a pharmaceutically acceptable salt thereof can also be used as a therapeutic or prophylactic drug for dysuria. Examples of the dysuria here include frequent urination, cystalgia due to benign prostatic hyperplasia and the like. Furthermore, it can also be used as a therapeutic or prophylactic drug for suppressing abnormal nervous firing in the cerebellum in multiple sclerosis. As a medicament free of side effects derived from normeural tissue or central nervous system, a compound having an SNS-selective inhibitory activity is more preferable.
The therapeutic or prophylactic drug of the present invention for neuropathic pain, nociceptive pain, dysuria or multiple sclerosis can contain various additional components for preparation such as conventional carrier, binder, stabilizer, excipient, diluent, pH buffering agent, disintegrant, solubilizer, dissolution aid, isotonic agent and the like, which are pharmaceutically acceptable. In addition, these therapeutic or prophylactic drugs can be orally or parenterally administered. That is, for oral administration, the drug can be orally administered in the form generally employed, for example, in dosage forms such as tablet, pill, powder, granule, capsule, syrup, emulsion, suspension and the like. For parenteral administration, the drug can be formulated as a preparation in the form of, for example, intravenous injection (drip infusion), intramuscular injection, subcutaneous injection, embrocation, eye drop, ophthalmic ointment and the like.
A solid preparation such as tablet is prepared by mixing the active ingredient with generally pharmacologically acceptable carrier or excipient such as lactose, sucrose, cornstarch and the like, binder such as crystalline cellulose, hydroxypropylcellulose, polyvinylpyrrolidone, hydroxypropylmethylcellulose and the like, disintegrant such as carboxymethylcellulose sodium, starch sodium glycolate and the like, lubricant such as stearic acid, magnesium stearate and the like, preservative and the like.
For parenteral administration, the active ingredient may be dissolved or suspended in physiologically acceptable carrier such as water, saline, oil, aqueous glucose solution and the like, and may be added with emulsifier, stabilizer, salt for adjusting osmotic pressure or buffering agent as aids, where necessary.
The preparation of the compound of the present invention can be prepared according to a conventional method. For example, a tablet can be prepared by mixing the compound of Example 1 (20 mg), lactose (100 mg), crystalline cellulose (25 mg) and magnesium stearate (1 mg), and tableting the obtained mixture.
While the dose and frequency of administration vary depending on the administration method, and age, body weight, the disease state and the like of patients, a method of topical administration to a disease-injury lesion part is preferable. It is also preferable to administer the drug once or twice or more per day. When administering twice or more, consecutive administration or repeat administration at suitable intervals is desirable.
The dose is 10 μg-2 g, preferably 1 mg-1 g, more preferably 10-100 mg, in the amount of the active ingredient for an adult patient per single administration, which can be administered at once or in several portions a day. For parenteral administration, the dose can be 0.1-100 mg/day, more preferably 0.3-50 mg/day, for an adult patient, which can be administered at once or in several portions a day. To reduce administration frequency, a sustained-release preparation can also be used.
In addition, the therapeutic or prophylactic drug of the present invention for neuropathic pain, nociceptive pain, dysuria or multiple sclerosis can also be utilized as an animal drug.

EXAMPLES

The present invention is explained in more detail in the following by referring to Reference Examples and Examples; however, the technical scope of the present invention is not limited to such Examples and the like. The compounds were identified by hydrogen nuclear magnetic resonance absorption spectrum (¹H-NMR) and the like.
In the following, abbreviations shown below may be used sometimes to simplify the description of the present specification.
Me: methyl, Et: ethyl, Pr: propyl, iPr: isopropyl, Ph: phenyl, Ac: acetyl, Boc: tert-butoxycarbonyl, Bn: benzyl, TBDMS: tert-butyldimethylsilyl, PyBOP: benzotriazol-1-yl-oxy-tris(pyrrolidino)phosphonium hexafluorophosphate, J: binding constant, s: singlet, d: doublet, dd: double doublet, ddd: 4 doublets, td: 3 doublets, t: triplet, dt: double triplet, q: quartet, quint: quintet, br: broad, m: multiplet.
Unless otherwise specified, the starting material compounds, reaction reagents and solvents used were commercially available products.

Reference Example 1

To a solution of 2,4-difluoronitrobenzene (15 g, 94 mmol) in dioxane (300 mL) were added potassium carbonate (14.4 g, 104 mmol) and 2-ethoxyethylamine (8.4 g, 104 mmol), and the mixture was stirred at room temperature overnight. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure to give the object product (21 g, 98%).
¹H-NMR (CDCl₃) δ 1.25 (t, J=7.1 Hz, 3H), 3.43 (q, J=5.2 Hz, 2H), 3.58 (q, J=7.1 Hz, 2H), 3.72 (t, J=5.2 Hz, 2H), 6.37 (ddd, J=9.5, 7.3, 2.5 Hz, 1H), 6.51 (dd, J=11.5, 2.5 Hz, 1H), 8.22 (dd, J=9.5, 6.1 Hz, 1H), 8.38 (br, 1H).

Reference Example 2

To a solution (60 mL) of the compound (3.0 g, 13.2 mmol) obtained in Reference Example 1 in dioxane were added cesium carbonate (6.4 g, 19.7 mmol) and phenol (1.5 g, 15.8 mmol), and the mixture was heated to 80° C. After stirring for 7 hr, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure to give the object product (4.1 g, 100%).
¹H-NMR (CDCl₃) δ 1.23 (t, J=7.0 Hz, 3H), 3.34 (q, J=5.2 Hz, 2H), 3.55 (q, J=7.0 Hz, 2H), 3.67 (t, J=5.2 Hz, 2H), 6.22 (dd, J=9.4, 2.5 Hz, 1H), 6.29 (d, J=2.5 Hz, 1H), 7.07-7.12 (m, 2H), 7.23 (m, 1H), 7.35-7.45 (m, 2H), 8.16 (d, J=9.4 Hz, 1H), 8.39 (br, 1H).

Reference Example 3-1

To a solution (50 mL) of the compound (1.8 g, 6.0 mmol) obtained in Reference Example 2 in ethanol was added 10% palladium-carbon (1 g), and the mixture was stirred at room temperature for 4 hr under a hydrogen atmosphere. The reaction mixture was filtered through celite, and the filtrate was concentrated and dried under reduced pressure to give the object product (1.4 g, 86%).
¹H-NMR (CDCl₃) δ 1.22 (t, J=7.0 Hz, 3H), 3.21 (t, J=5.2 Hz, 2H), 3.23 (br, 2H), 3.53 (q, J=7.0 Hz, 2H), 3.67 (t, J=5.2 Hz, 2H), 6.34 (dd, J=8.3, 2.6 Hz, 1H), 6.40 (d, J=2.6 Hz, 1H), 6.67 (d, J=8.3 Hz, 1H), 6.92-7.04 (m, 3H), 7.24-7.30 (m, 2H).

Reference Example 3-2

The above-mentioned object product can also be prepared by the following method.
To a suspension (3:2:1, 120 mL) of iron (13.9 g, 0.25 mol) and ammonium chloride (6.6 g, 0.12 mol) in tetrahydrofuran-methanol-water was added dropwise a solution (60 mL) of the compound (9.8 g, 32 mmol) obtained in Reference Example 2 in a mixed solvent (3:2:1) of tetrahydrofuran-methanol-water while refluxing under heating. After stirring for 2 hr, the reaction mixture was allowed to cool, and filtered through celite. Water was added to the filtrate, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure to give the object product (8.7 g, 100%).

Reference Example 4

To the compound (5.0 g, 18.4 mmol) obtained in Reference
Example 3 was added glycolic acid (8 g), and the mixture was stirred at 120° C. for 30 min. After cooling, water and chloroform were added to the reaction mixture, and the mixture was neutralized with 30% aqueous sodium hydroxide solution under ice-cooling. The organic layer was extracted, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (chloroform:methanol=50:1-30:1) to give the object crude product (4.1 g).

Reference Example 5

To a solution of the compound (4.1 g) obtained in Reference Example 4 in dichloromethane (100 mL) was added manganese dioxide (8 g), and the mixture was stirred at room temperature. After stirring for 2 hr, the reaction mixture was filtered through celite, and the filtrate was concentrated. The residue was purified by silica gel column (ethyl acetate:hexane=1:2) to give the object product (3.5 g, 61%, 2 steps).
¹H-NMR (CDCl₃) δ 1.03 (t, J=7.0 Hz, 3H), 3.37 (q, J=7.0 Hz, 2H), 3.73 (t, J=5.3 Hz, 2H), 4.66 (t, J=5.3 Hz, 2H), 7.04-7.20 (m, 5H), 7.34-7.41 (m, 2H), 7.86 (d, J=8.8 Hz, 1H), 10.05 (s, 1H).

Reference Example 6

The object crude product obtained from 2,4-difluoronitrobenzene (20.0 g, 126 mmol) and 4-fluorophenol in the same manner as in Reference Examples 1-4 was recrystallized from chloroform/hexane and further recrystallized from acetonitrile to give the object product (23.3 g, 56%, 4 steps).
¹H-NMR (CDCl₃) δ 1.05 (t, J=7.0 Hz, 3H), 3.37 (q, J=7.0 Hz, 2H), 3.70 (t, J=5.1 Hz, 2H), 4.34 (t, J=5.1 Hz, 2H), 4.89 (s, 2H), 6.89-7.03 (m, 6H), 7.58 (m, 1H).

Reference Example 7

The object product was obtained in the same manner as in Reference Example 5 from the compound obtained in Reference Example 6.
¹H-NMR (CDCl₃) δ 0.99 (t, J=7.0 Hz, 3H), 3.33 (q, J=7.0 Hz, 2H), 3.69 (t, J=5.1 Hz, 2H), 4.62 (t, J=5.1 Hz, 2H), 6.92-7.09 (m, 6H), 7.81 (m, 1H), 10.00 (s, 1H).

Example 1

N²-{[1-(2-ethoxyethyl)-6-phenoxy-1H-benzimidazol-2-yl]methyl}-L-alaninamide

To a solution of the compound (2.0 g, 6.5 mmol) obtained in Reference Example 5 in dichloromethane (50 mL) was added (L)-alaninamide hydrochloride (0.96 g, 7.7 mmol), and the mixture was stirred at room temperature. After stirring for 1 hr, sodium triacetoxyborohydride (1.6 g, 7.7 mmol) was added thereto, and the mixture was stirred for 2 hr. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was extracted, washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (chloroform:methanol=50:1-10:1) to give the object product (0.59 g, 24%).
¹H-NMR (CDCl₃) δ 1.08 (t, J=7.1 Hz, 3H), 1.41 (d, J=7.0 Hz, 3H), 3.33 (q, J=7.0 Hz, 1H), 3.38 (q, J=7.1 Hz, 2H), 3.68 (t, J=5.1 Hz, 2H), 4.04 (d, J=14.7 Hz, 1H), 4.12 (d, J=14.7 Hz, 1H), 4.17-4.32 (m, 2H), 5.50 (brs, 1H), 6.98-7.02 (m, 4H), 7.09 (m, 1H), 7.28-7.36 (m, 3H), 7.68 (m, 1H).
The above-mentioned compound can also be prepared by the following method.
To a solution of the compound (0.15 g, 0.48 mmol) obtained in Reference Example 5 in tetrahydrofuran (10 mL) were added (L)-alaninamide hydrochloride (0.18 g, 1.45 mmol), sodium sulfate (3 g) and triethylamine (0.20 mL), and the mixture was stirred at room temperature. After stirring for 30 min, sodium cyanoborohydride (45 mg, 0.72 mmol) was added thereto, and the mixture was stirred for 2 hr. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was extracted, washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (chloroform:methanol=50:1-10:1) to give the object product (0.09 g, 49%).

Example 2

N²-{[1-(2-ethoxyethyl)-6-phenoxy-1H-benzimidazol-2-yl]methyl}glycinamide

To a solution of the compound (44 mg, 0.14 mmol) obtained in Reference Example 5 in methanol (3 mL) was added glycinamide hydrochloride (31 mg, 0.28 mmol), and the mixture was stirred at room temperature. After stirring for 1 hr, sodium cyanoborohydride (18 mg, 0.28 mmol) was added thereto, and the mixture was stirred overnight. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was extracted, washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (chloroform:methanol=50:1-10:1) to give the object product (23 mg, 43%).
¹H-NMR (CDCl₃) δ 1.08 (t, J=7.0 Hz, 3H), 3.38 (q, J=7.0 Hz, 2H), 3.42 (s, 2H), 3.68 (t, J=5.1 Hz, 2H), 4.10 (s, 2H), 4.26 (t, J=5.1 Hz, 2H), 5.72 (brs, 1H), 6.96-7.02 (m, 4H), 7.08 (m, 1H), 7.21 (brs, 1H), 7.28-7.36 (m, 2H), 7.68 (m, 1H).

Example 3

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}glycinamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 7.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 3.39 (q, J=7.0 Hz, 2H), 3.42 (s, 2H), 3.69 (t, J=5.0 Hz, 2H), 4.10 (s, 2H), 4.26 (t, J=5.0 Hz, 2H), 5.54 (brs, 1H), 6.93-7.05 (m, 6H), 7.18 (brs, 1H), 7.67 (m, 1H).

Example 4

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-valinamide

The object product was obtained in the same manner as in Example 1 from the compound obtained in Reference Example 7 and (L)-valinamide hydrochloride.
¹H-NMR (CDCl₃) δ 0.99 (d, J=7.0 Hz, 3H), 1.02 (d, J=7.0 Hz, 3H), 1.08 (t, J=7.0 Hz, 3H), 2.08 (m, 1H), 2.97 (d, J=5.5 Hz, 1H), 3.38 (q, J=7.0 Hz, 2H), 3.68 (t, J=5.1 Hz, 2H), 3.98 (d, J=14.5 Hz, 1H), 4.15 (d, J=14.5 Hz, 1H), 4.17-4.40 (m, 2H), 5.56 (brs, 1H), 6.93-7.01 (m, 7H), 7.67 (m, 1H).

Example 5

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-2-methylalaninamide

The object product was obtained in the same manner as in Example 1 from the compound obtained in Reference Example 7 and 2-methylalaninamide which is a known compound.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.46 (s, 6H), 3.38 (q, J=7.0 Hz, 2H), 3.69 (t, J=5.1 Hz, 2H), 4.02 (s, 2H), 4.24 (t, J=5.1 Hz, 2H), 5.43 (brs, 1H), 6.93-7.05 (m, 6H), 7.48 (brs, 1H), 7.68 (m, 1H).

Examples 6-58

The compounds of Examples 6-58 shown in Table 1-Table 9 were prepared in the same manner as in Reference Examples 1-7, Example 1 or Example 2 from 2,4-difluoronitrobenzene and using commercially available or known compounds.

TABLE 1

Example	structural formula	¹H-NMR (CDCl₃) δ

6		1.40 (d, J = 7.0 Hz, 3H), 1.79-1.88 (m, 2H), 2.42- 2.58 (m, 2H), 3.28 (q, J = 7.0 Hz, 1H), 3.51- 3.58 (m, 2H), 4.03 (d, J = 14.8 Hz, 1H), 4.11 (d, J = 14.8 Hz, 1H), 4.13-4.19 (m, 2H), 4.48 (m, 1H), 5.45 (brs, 1H), 6.91-7.05 (m, 6H), 7.26 (brs, 1H), 7.67 (d, J = 8.8 Hz, 1H).

7		0.98-1.05 (m, 2H), 1.15- 1.27 (m, 2H), 1.44 (d, J = 7.0 Hz, 3H), 3.18 (m, 1H), 3.35 (q, J = 7.0 Hz, 1H), 4.09 (d, J = 15.6 Hz, 1H), 4.17 (d, J = 15.6 Hz, 1H), 5.35 (brs, 1H), 6.91-7.05 (m, 5H), 7.14 (d, J = 2.4 Hz, 1H), 7.25 (brs, 1H), 7.63 (d, J = 8.8 Hz, 1H).

8		1.47 (s, 6H), 1.80-1.86 (m, 2H), 2.44-2.58 (m, 2H), 3.50-3.59 (m, 2H), 4.01 (s, 2H), 4.14-4.19 (m, 2H), 4.43 (m, 1H), 5.84 (brs, 1H), 6.90-7.04 (m, 5H), 7.16 (brs, 1H), 7.26 (d, J = 2.0 Hz, 1H), 7.66 (d, J = 8.8 Hz, 1H).

9		1.40 (d, J = 7.0 Hz, 3H), 1.58 (d, J = 7.0 Hz, 6H), 3.30 (q, J = 7.0 Hz, 1H), 4.01 (d, J = 14.7 Hz, 1H), 4.08 (d, J = 14.7 Hz, 1H), 4.69 (m, 1H), 6.10 (brs, 1H), 6.92-7.02 (m, 3H), 7.07 (m, 1H), 7.15 (brs, 1H), 7.21 (m, 1H), 7.27-7.37 (m, 2H), 7.65 (d, J = 8.6 Hz, 1H).

10		1.58 (d, J = 7.0 Hz, 6H), 3.43 (s, 2H), 4.07 (s, 2H), 4.69 (m, 1H), 6.15 (brs, 1H), 6.91-7.01 (m, 4H), 7.04 (m, 1H), 7.11 (brs, 1H), 7.20 (d, J = 1.9 Hz, 1H), 7.29-7.36 (m, 2H), 7.64 (d, J = 8.8 Hz, 1H).

11		1.42 (d, J = 7.0 Hz, 3H), 1.82- 2.04 (m, 2H), 2.44-2.58 (m, 2H), 2.76-2.91 (m, 2H), 3.30 (q, J = 7.0 Hz, 1H), 3.99 (d, J = 14.1 Hz, 1H), 4.06 (d, J = 14.1 Hz, 1H), 4.87 (m, 1H), 5.52 (brs, 1H), 6.94-7.11 (m, 4H), 7.13 (brs, 1H), 7.30-7.37 (m, 3H), 7.66 (d, J = 8.8 Hz, 1H).

TABLE 2

Example	structural formula	¹H-NMR (CDCl₃) δ

12		1.88-2.04 (m, 2H), 2.46-2.59 (m, 2H), 2.76-2.92 (m, 2H), 3.44 (s, 2H), 4.05 (s, 2H), 4.88 (m, 1H), 5.50 (brs, 1H), 6.95-7.12 (m, 5H), 7.30-7.36 (m, 3H), 7.66 (d, J = 8.8 Hz, 1H).

13		1.30-1.54 (m, 4H), 1.43 (d, J = 6.8 Hz, 3H), 2.06 (m, 1H), 3.22-3.37 (m, 3H), 3.86-4.10 (m, 6H), 5.51 (brs, 1H), 6.96-7.13 (m, 6H), 7.29-7.35 (m, 2H), 7.67 (m, 1H).

14		1.32-1.54 (m, 4H), 2.06 (m, 1H), 3.30 (td, J = 11.5, 2.6 Hz, 2H), 3.45 (s, 2H), 3.92-4.00 (m, 4H), 4.06 (s, 2H), 5.57 (brs, 1H), 6.96- 7.12 (m, 6H), 7.30-7.37 (m, 2H), 7.67 (m, 1H).

15		1.08 (t, J = 7.0 Hz, 3H), 1.78-2.05 (m, 3H), 2.29 (m, 1H), 2.60 (m, 1H), 3.16 (m, 1H), 3.28-3.42 (m, 3H), 3.70 (t, J = 5.2 Hz, 2H), 3.94 (d, J = 14.3 Hz, 1H), 4.21 (d, J = 14.3 Hz, 1H), 4.27-4.38 (m, 2H), 5.39 (brs, 1H), 6.93- 7.06 (m, 6H), 7.64 (brs, 1H), 7.68 (d, J = 9.4 Hz, 1H).

16		1.32-1.52 (m, 4H), 1.80-2.35 (m, 5H), 2.59 (q, J = 8.4 Hz, 1H), 3.20-3.36 (m, 4H), 3.88-4.18 (m, 6H), 5.50 (brs, 1H), 6.96-7.12 (m, 5H), 7.28-7.38 (m, 2H), 7.44 (brs, 1H), 7.68 (m, 1H).

17		1.42 (d, J = 6.8 Hz, 3H), 1.86- 2.04 (m, 2H), 2.47-2.57 (m, 2H), 2.78-2.88 (m, 2H), 3.30 (q, J = 6.8 Hz, 1H), 3.99 (d, J = 15.0 Hz, 1H), 4.06 (d, J = 15.0 Hz, 1H), 4.87 (m, 1H), 5.45 (brs, 1H), 6.90-7.06 (m, 5H), 7.12 (brs, 1H), 7.27 (d, J = 2.2 Hz, 1H), 7.66 (d, J = 8.8 Hz, 1H).

TABLE 3

Example	structural formula	¹H-NMR (CDCl₃) δ

18		1.86-2.06 (m, 2H), 2.30-2.58 (m, 2H), 2.75-2.90 (m, 2H), 3.43 (s, 2H), 4.05 (s, 2H), 4.87 (m, 1H), 5.59 (brs, 1H), 6.90-7.10 (m, 6H), 7.27 (m, 1H), 7.65 (d, J = 8.8 Hz, 1H).

19		1.56 (m, 1H), 1.80-2.06 (m, 6H), 2.29 (m, 1H), 2.58 (q, J = 8.5 Hz, 1H), 3.18 (m, 1H), 3.32 (dd, J = 9.8, 5.4 Hz, 1H), 3.67-3.82 (m, 2H), 3.95 (d, J = 14.4 Hz, 1H), 4.11- 4.34 (m, 4H), 5.28 (brs, 1H), 6.96-7.10 (m, 5H), 7.29-7.35 (m, 2H), 7.67 (brs, 1H), 7.68 (d, J = 8.5 Hz, 1H).

20		1.41 (d, J = 7.1 Hz, 3H), 1.55 (m, 1H), 1.80-1.93 (m, 2H), 2.10 (m, 1H), 3.35 (q, J = 7.1 Hz, 1H), 3.67-3.83 (m, 2H), 4.00-4.30 (m, 5H), 5.41 (brs, 1H), 6.85-7.10 (m, 5H), 7.25-7.35 (m, 3H), 7.67 (d, J = 8.5 Hz, 1H).

21		1.55 (m, 1H), 1.80-2.08 (m, 6H), 2.28 (m, 1H), 2.61 (q, J = 8.6 Hz, 1H), 3.22 (m, 1H), 3.33 (dd, J = 9.7, 5.4 Hz, 1H), 3.67-3.81 (m, 2H), 3.98 (d, J = 14.6 Hz, 1H), 4.15- 4.24 (m, 4H), 5.33 (brs, 1H), 6.96-7.10 (m, 5H), 7.29-7.35 (m, 2H), 7.55 (brs, 1H), 7.68 (d, J = 8.5 Hz, 1H).

22		1.41 (d, J = 6.8 Hz, 3H), 1.56 (m, 1H), 1.85-1.95 (m, 2H), 2.05 (m, 1H), 3.32 (q, J = 6.8 Hz, 1H), 3.67-3.84 (m, 2H), 4.03-4.22 (m, 5H), 5.36 (brs, 1H), 6.80-7.10 (m, 5H), 7.24- 7.34 (m, 3H), 7.67 (d, J = 8.5 Hz, 1H).

23		2.02 (m, 2H), 3.27-3.34 (m, 5H), 3.45 (s, 2H), 4.07 (s, 2H), 4.21 (t, J = 6.8 Hz, 2H), 5.78 (brs, 1H), 6.98-7.10 (m, 5H), 7.21 (brs, 1H), 7.30- 7.35 (m, 2H), 7.67 (m, 1H).

TABLE 4

Example	structural formula	¹H-NMR (CDCl₃) δ

24		1.42 (d, J = 6.8 Hz, 3H), 2.00-2.26 (m, 2H), 3.28 (s, 3H), 3.28-3.36 (m, 3H), 4.01 (d, J = 14.5 Hz, 1H), 4.07 (d, J = 14.5 Hz, 1H), 4.28 (t, J = 6.8 Hz, 2H), 5.47 (brs, 1H), 6.97-7.10 (m, 5H), 7.23 (brs, 1H), 7.29- 7.34 (m, 2H), 7.67 (m, 1H).

25		1.74-2.38 (m, 8H), 3.44 (s, 2H), 4.09 (s, 2H), 4.78 (m, 1H), 5.93 (brs, 1H), 6.93- 7.68 (m, 9H).

26		1.40-1.42 (m, 3H), 1.74- 2.21 (m, 8H), 3.30 (q, J = 6.8 Hz, 1H), 4.00-4.11 (m, 2H), 4.72-4.77 (m, 1H), 5.76 (brs, 1H), 6.94-7.68 (m, 9H).

27		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.34 (q, J = 7.0 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.1 Hz, 2H), 4.04 (d, J = 14.8 Hz, 1H), 4.12 (d, J = 14.8 Hz, 1H), 4.19-4.26 (m, 2H), 5.40 (brs, 1H), 6.90-7.00 (m, 4H), 7.23 (brs, 1H), 7.24- 7.30 (m, 2H), 7.69 (m, 1H).

28		1.09 (t, J = 7.0 Hz, 3H), 3.39 (q, J = 7.0 Hz, 1H), 3.42 (s, 2H), 3.69 (t, J = 5.0 Hz, 2H), 4.10 (s, 2H), 4.27 (t, J = 5.0 Hz, 2H), 6.90-7.00 (m, 4H), 7.18 (brs, 1H), 7.24-7.30 (m, 3H), 7.68 (m, 1H).

29		1.08 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.8 Hz, 3H), 3.30-3.42 (m, 3H), 3.68-3.70 (m, 2H), 4.04 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.21-4.32 (m, 2H), 5.73 (brs, 1H), 6.86-7.05 (m, 5H), 7.20-7.27 (m, 2H), 7.71 (m, 1H).

TABLE 5

Example	structural formula	¹H-NMR (CDCl₃)

30		1.09 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 3.39 (q, J = 7.0 Hz, 2H), 3.70 (t, J = 5.0 Hz, 2H), 4.04 (s, 2H), 4.27 (t, J = 5.0 Hz, 2H), 5.49 (brs, 1H), 6.85-7.06 (m, 5H), 7.23 (t, J = 8.1 Hz, 1H), 7.48 (brs, 1H), 7.71 (d, J = 8.4 Hz, 1H).

31		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.0 Hz, 2H), 4.03 (d, J = 14.8 Hz, 1H), 4.12 (d, J = 14.8 Hz, 1H), 4.22 (dt, J = 15.1, 5.0 Hz, 1H), 4.28 (dt, J = 15.1, 5.0 Hz, 1H), 5.63 (brs, 1H), 6.89-7.19 (m, 5H), 7.26 (brs, 1H), 7.47 (dd, J = 7.9, 1.6 Hz, 1H), 7.68 (dd, J = 8.4, 0.7 Hz, 1H).

32		1.09 (t, J = 7.0 Hz, 3H), 1.46 (s, 6H), 3.38 (q, J = 7.0 Hz, 2H), 3.69 (t, J = 5.1 Hz, 2H), 4.03 (s, 2H), 4.25 (t, J = 5.1 Hz, 2H), 5.55 (brs, 1H), 6.89-7.18 (m, 5H), 7.45-7.48 (m, 2H), 7.68 (d, J = 8.4 Hz, 1H).

33		1.47 (s, 6H), 1.86-2.04 (m, 2H), 2.45-2.57 (m, 2H), 2.77- 2.92 (m, 2H), 3.96 (s, 2H), 4.85 (m, 1H), 5.46 (brs, 1H), 6.94-7.11 (m, 4H), 7.29-7.37 (m, 4H), 7.67 (d, J = 8.8 Hz, 1H).

34		1.42 (d, J = 7.0 Hz, 3H), 1.82- 2.04 (m, 2H), 2.44-2.58 (m, 2H), 2.76-2.91 (m, 2H), 3.30 (q, J = 7.0 Hz, 1H), 3.99 (d, J = 14.1 Hz, 1H), 4.06 (d, J = 14.1 Hz, 1H), 4.87 (m, 1H), 5.52 (brs, 1H), 6.94-7.11 (m, 4H), 7.13 (brs, 1H), 7.30-7.37 (m, 3H), 7.66 (d, J = 8.8 Hz, 1H).

35		1.46 (s, 6H), 1.57 (m, 1H), 1.82-2.10 (m, 3H), 3.67-3.84 (m, 2H), 3.96-4.25 (m, 5H), 5.36 (brs, 1H), 6.96-7.11 (m, 5H), 7.28-7.35 (m, 2H), 7.48 (brs, 1H), 7.68 (d, J = 8.6 Hz, 1H).

TABLE 6

Example	structural formula	¹H-NMR (CDCl₃) δ

36		1.08 (t, J = 7.0 Hz, 3H), 1.40 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.0 Hz, 2H), 4.03 (d, J = 14.7 Hz, 1H), 4.12 (d, J = 14.7 Hz, 1H), 4.17- 4.32 (m, 2H), 5.95 (brs, 1H), 6.98-7.10 (m, 5H), 7.29-7.35 (m, 3H), 7.68 (m, 1H).

37		1.01 (t, J = 7.3 Hz, 3H), 1.08 (t, J = 7.0 Hz, 3H), 1.70-1.84 (m, 2H), 3.15 (t, J = 6.3 Hz, 1H), 3.37 (q, J = 7.3 Hz, 2H), 3.68 (t, J = 5.2 Hz, 2H), 4.01 (d, J = 14.6 Hz, 1H), 4.13 (d, J = 14.6 Hz, 1H), 4.21 (dt, J = 15.2, 5.2 Hz, 1H), 4.30 (dt, J = 15.2, 5.2 Hz, 1H), 5.56 (brs, 1H), 6.98-7.11 (m, 5H), 7.18 (brs, 1H), 7.27-7.35 (m, 2H), 7.68 (m, 1H).

38		0.99 (d, J 6.9 Hz, 3H), 1.02 (d, J = 6.9 Hz, 3H), 1.08 (t, J = 7.0 Hz, 3H), 2.08 (m, 1H), 2.97 (d, J = 5.3 Hz, 1H), 3.37 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.2 Hz, 2H), 3.99 (d, J = 14.4 Hz, 1H), 4.14 (d, J = 14.4 Hz, 1H), 4.22 (dt, J = 15.2, 5.2 Hz, 1H), 4.35 (dt, J = 15.2, 5.2 Hz, 1H), 5.80 (brs, 1H), 6.97-7.11 (m, 6H), 7.27-7.35 (m, 2H), 7.68 (m, 1H).

39		1.09 (t, J = 7.0 Hz, 3H), 1.46 (s, 6H), 3.39 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.0 Hz, 2H), 4.03 (s, 2H), 4.24 (t, J = 5.0 Hz, 2H), 5.76 (brs, 1H), 6.97-7.10 (m, 5H), 7.27-7.35 (m, 2H), 7.51 (brs, 1H), 7.69 (m, 1H).

40		1.08 (t, J = 7.0 Hz, 3H), 2.43 (s, 3H), 3.20 (s, 2H), 3.38 (q, J = 7.0 Hz, 2H), 3.71 (t, J = 5.2 Hz, 2H), 3.96 (s, 2H), 4.37 (t, J = 5.2 Hz, 2H), 5.84 (brs, 1H), 6.98-7.11 (m, 5H), 7.27-7.35 (m, 2H), 7.38 (brs, 1H), 7.69 (m, 1H).

41		1.01 (t, J = 7.4 Hz, 3H), 1.08 (t, J = 7.0 Hz, 3H), 1.69-1.86 (m, 2H), 3.15 (t, J = 6.3 Hz, 1H), 3.37 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.0 Hz, 2H), 4.00 (d, J = 14.6 Hz, 1H), 4.12 (d, J = 14.6 Hz, 1H), 4.19-4.33 (m, 2H), 5.79 (brs, 1H), 6.94-7.05 (m, 6H), 7.18 (brs, 1H), 7.67 (m, 1H).

TABLE 7

Example	structural formula	¹H-NMR (CDCl₃) δ

42		1.08 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.9 Hz, 3H), 2.33 (s, 3H), 3.33 (q, J = 6.9 Hz, 1H), 3.37 (q, J = 7.0 Hz, 2H), 3.67 (t, J = 5.1 Hz, 2H), 4.03 (d, J = 14.7 Hz, 1H), 4.11 (d, J = 14.7 Hz, 1H), 4.18- 4.32 (m, 2H), 5.62 (brs, 1H), 6.87-7.00 (m, 4H), 7.09-7.16 (m, 2H), 7.26 (brs, 1H), 7.65 (d, J = 9.4 Hz, 1H).

43		1.08 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.9 Hz, 3H), 3.34 (q, J = 6.9 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.69 (t, J = 5.0 Hz, 2H), 4.04 (d, J = 14.7Hz, 1H), 4.13 (d, J = 14.7 Hz, 1H), 4.19-4.36 (m, 2H), 5.75 (brs, 1H), 6.94- 7.04 (m, 4H), 7.13-7.20 (m, 2H), 7.25 (brs, 1H), 7.69 (d, J = 8.6 Hz, 1H).

44		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 2.27 (brs, 1H), 3.34 (q, J = 7.0 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.70 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.14 (d, J = 14.8 Hz, 1H), 4.23- 4.35 (m, 2H), 5.80 (brs, 1H), 6.51-6.64 (m, 2H), 6.92-7.08 (m, 2H), 7.21 (brs, 1H), 7.72 (d, J = 8.6 Hz, 1H).

45		1.08 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 6.9 Hz, 3H), 1.94 (brs, 1H), 3.34 (q, J = 6.9 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.70 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.14 (d, J = 14.8 Hz, 1H), 4.20- 4.37 (m, 2H), 5.63 (brs, 1H), 6.95-7.03 (m, 3H), 7.08 (d, J = 1.8 Hz, 1H), 7.19 (brs, 1H), 7.55-7.63 (m, 2H), 7.74 (d, J = 8.8 Hz, 1H).

46		1.08 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.32 (brs, 1H), 3.34 (q, J = 7.0 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.70 (t, J = 5.1 Hz, 2H), 4.05 (d, J = 14.7 Hz, 1H), 4.14 (d, J = 14.7 Hz, 1H), 4.20- 4.37 (m, 2H), 5.64 (brs, 1H), 6.97- 7.08 (m, 4H), 7.22 (brs, 1H), 7.56 (brd, J = 8.4 Hz, 2H), 7.72 (d, J = 8.6 Hz, 1H).

47		1.14 (t, J = 7.0 Hz, 3H), 1.39 (d, J = 7.0 Hz, 3H), 1.99 (m, 2H), 3.28- 3.41 (m, 5H), 3.99 (d, J = 14.6 Hz, 1H), 4.05 (d, J = 14.6 Hz, 1H), 4.18 (t, J = 7.0 Hz, 2H), 5.41 (brs, 1H), 6.71-7.02 (m, 6H), 7.16 (brs, 1H), 7.63 (d, J = 8.6 Hz, 1H).

TABLE 8

Example	structural formula	¹H-NMR (CDCl₃) δ

48		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.69 (t, J = 5.1 Hz, 2H), 4.04 (d, J = 14.8 Hz, 1H), 4.12 (d, J = 14.8 Hz, 1H), 4.20-4.33 (m, 2H), 5.43 (br, 1H), 6.71 (m, 1H), 6.80 (m, 1H), 6.95-7.00 (m, 2H), 7.10 (q, J = 9.0 Hz, 1H), 7.22 (br, 1H), 7.69 (d, J = 8.3 Hz, 1H).

49		1.08 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.0 Hz, 2H), 4.03 (d, J = 14.8 Hz, 1H), 4.11 (d, J = 14.8 Hz, 1H), 4.18-4.32 (m, 2H), 5.41 (br, 1H), 6.83 (m, 1H), 6.91-7.05 (m, 4H), 7.22 (br, 1H), 7.65 (m, 1H).

50		1.21 (s, 3H), 1.29 (s, 3H), 1.33 (d, J = 6.9 Hz, 3H), 3.35 (q, J = 6.9 Hz, 1H), 4.04 (d, J = 13.9 Hz, 1H), 4.10 (s, 2H), 4.11 (d, J = 13.9 Hz, 1H), 5.87 (brs, 1H), 6.91-7.05 (m, 6H), 7.09 (brs, 1H), 7.63 (d, J = 9.3 Hz, 1H).

51		1.40 (d, J = 7.0 Hz, 3H), 1.55 (m, 1H), 1.77-1.94 (m, 2H), 1.97-2.12 (m, 2H), 3.34 (q, J = 7.0 Hz, 1H), 3.65-3.83 (m, 2H), 3.96- 4.27 (m, 5H), 5.67 (brs, 1H), 6.91-7.06 (m, 6H), 7.24 (brs, 1H), 7.66 (dd, J = 8.4, 0.6 Hz, 1H).

52		1.07 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.1 Hz, 2H), 4.03 (d, J = 14.7 Hz, 1H), 4.12 (d, J = 14.7 Hz, 1H), 4.18- 4.32 (m, 2H), 5.43 (br, 1H), 6.95-7.23 (m, 6H), 7.25 (br, 1H), 7.66 (m, 1H).

53		1.09 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.34 (q, J = 7.0 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.69 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.19- 4.35 (m, 2H), 5.44 (br, 1H), 6.64-6.81 (m, 3H), 6.98-7.06 (m, 2H), 7.20-7.30 (m, 2H), 7.71 (d, J = 8.4 Hz, 1H).

TABLE 9

Example	structural formula	¹H-NMR (CDCl₃) δ

54		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.8 Hz, 3H), 3.33 (q, J = 6.8 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.68 (t, J = 5.2 Hz, 2H), 4.03 (d, J = 14.7 Hz, 1H), 4.12 (d, J = 14.7 Hz, 1H), 4.16- 4.32 (m, 2H), 5.41 (brs, 1H), 6.93-7.05 (m, 6H), 7.23 (brs, 1H), 7.67 (m, 1H).

55		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.69 (t, J = 5.0 Hz, 2H), 4.04 (d, J = 14.8 Hz, 1H), 4.12 (d, J = 14.8 Hz, 1H), 4.19-4.34 (m, 2H), 5.35 (br, 1H), 6.79-7.13 (m, 4H), 7.20 (br, 1H), 7.69 (d, J = 8.6 Hz, 1H).

56		1.41 (d, J = 6.8 Hz, 3H), 1.50- 2.10 (m, 4H), 3.32 (q, J = 6.8 Hz, 1H), 3.66-3.84 (m, 2H), 4.01-4.23 (m, 5H), 5.44 (br, 1H), 6.93-7.05 (m, 6H), 7.25 (m, 1H), 7.66 (d, J = 6.4 Hz, 1H).

57		1.08 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 3.34 (q, J = 6.8 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.70 (t, J = 5.1 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.20-4.35 (m, 2H), 5.47 (br, 1H), 6.39 (m, 1H), 6.65 (m, 1H), 7.01 (dd, J = 8.8, 2.4 Hz, 1H), 7.08 (d, J = 2.4 Hz, 1H), 7.20 (br, 1H), 7.72 (d, J = 8.8 Hz, 1H).

58		1.08 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.8 Hz, 3H), 3.33 (q, J = 6.8 Hz, 1H), 3.38 (q, J = 7.0 Hz, 2H), 3.69 (t, J = 5.0 Hz, 2H), 4.03 (d, J = 14.8 Hz, 1H), 4.12 (d, J = 14.8 Hz, 1H), 4.19- 4.34 (m, 2H), 5.52 (br, 1H), 6.72 (m, 1H), 6.87-7.04 (m, 4H), 7.23 (br, 1H), 7.68 (d, J = 8.6 Hz, 1H).

Reference Example 8

To a solution of the compound (0.22 g, 0.66 mmol) obtained in Reference Example 6 in tetrahydrofuran (3 mL) was added phosphorus tribromide (0.18 g, 0.66 mmol) under ice-cooling. After stirring for 1 hr, aqueous sodium hydrogen carbonate solution was added thereto, and the mixture was extracted with ethyl acetate, dried over magnesium sulfate, and concentrated under reduced pressure. The concentrate was directly used for the next reaction.
¹H-NMR (CDCl₃) δ 1.08 (t, J=7.0 Hz, 3H), 3.39 (q, J=7.0 Hz, 2H), 3.70 (t, J=5.1 Hz, 2H), 4.37 (t, J=5.1 Hz, 2H), 4.81 (s, 2H), 6.95-7.05 (m, 6H), 7.69 (m, 1H).

Example 59

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

To a solution of the compound (107 mg, 0.27 mmol) obtained in Reference Example 8 in acetonitrile (3 mL) were added diisopropylethylamine (0.10 ml, 0.55 mmol) and N-(2,4-dimethoxybenzyl)alaninamide (97.7 mg, 0.41 mmol). After stirring at 50° C. for 5 hr, aqueous sodium hydrogen carbonate solution was added thereto, and the mixture was extracted with chloroform. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. Trifluoroacetic acid (3 mL) was added thereto, and the mixture was further stirred at 50° C. for 2 hr, neutralized with aqueous sodium hydroxide solution, and extracted with ethyl acetate. The organic layer was dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was recrystallized from chloroform/2-propanol to give the object product (75 mg, 70%).
¹H-NMR (CDCl₃) δ1.08 (t, J=7.0 Hz, 3H), 1.41 (d, J=6.8 Hz, 3H), 3.33-3.41 (m, 3H), 3.68 (t, J=5.1 Hz, 2H), 4.03 (d, J=14.6 Hz, 1H), 4.12 (d, J=14.6 Hz, 1H), 4.23-4.27 (m, 2H), 5.58 (brs, 1H), 6.94-7.05 (m, 6H), 7.24 (brs, 1H), 7.67 (m, 1H).

Examples 60-65

The compounds of Examples 60-65 shown in Table 10 were prepared in the same manner as in Reference Examples 1-4, 8 and Example 59 from 2,4-difluoronitrobenzene and using commercially available or known compounds.

TABLE 10

Example	structural formula	¹H-NMR (CDCl₃) δ

60		1.41 (d, J = 7.0 Hz, 3H), 3.26 (s, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.65 (t, J = 4.9 Hz, 2H), 4.02 (d, J = 14.6 Hz, 1H), 4.10 (d, J = 14.6 Hz, 1H), 4.22- 4.28 (m, 2H), 5.34 (brs, 1H), 6.94-7.05 (m, 6H), 7.25 (brs, 1H), 7.67 (m, 1H).

61		1.02 (d, J = 6.2 Hz, 6H), 3.40- 3.48 (m, 3H), 3.68 (t, J = 5.1 Hz, 2H), 4.10 (s, 2H), 4.24 (t, J = 5.1 Hz, 2H), 5.45 (brs, 1H), 6.94-7.05 (m, 6H), 7.21 (brs, 1H), 7.67 (m, 1H).

62		1.01 (d, J = 6.0 Hz, 6H), 1.41 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 3.43 (m, 1H), 3.67 (t, J = 5.1 Hz, 2H), 4.04 (d, J = 14.8 Hz, 1H), 4.12 (d, J = 14.8 Hz, 1H), 4.22 (m, 2H), 5.33 (brs, 1H), 6.93-7.05 (m, 6H), 7.26 (brs, 1H), 7.67 (m, 1H).

63		3.25 (s, 3H), 3.40 (s, 2H), 3.64 (t, J = 5.0 Hz, 2H), 4.08 (s, 2H), 4.26 (t, J = 5.0 Hz, 2H), 6.34 (brs, 1H), 6.93-7.04 (m, 6H), 7.21 (brs, 1H), 7.65 (m, 1H).

64		1.42 (d, J = 7.0 Hz, 3H), 2.02 (quint, J = 6.7 Hz, 2H), 3.28 (s, 3H), 3.27-3.37 (m, 3H), 4.01 (d, J = 14.6 Hz, 1H), 4.07 (d, J = 14.6 Hz, 1H), 4.19 (t, J = 6.7 Hz, 2H), 5.36 (brs, 1H), 6.93-7.05 (m, 6H), 7.21 (brs, 1H), 7.66 (d, J = 8.8 Hz, 1H).

65		1.82-1.87 (m, 2H), 2.43-2.57 (m, 2H), 3.43 (s, 2H), 3.51-3.59 (m, 2H), 4.11 (s, 2H), 4.14-4.19 (m, 2H), 4.49 (m, 1H), 5.46 (brs, 1H), 6.80 (brs, 1H), 6.91- 7.05 (m, 5H), 7.25 (d, J = 2.0 Hz, 1H), 7.67 (d, J = 8.8 Hz, 1H).

Reference Example 9

The object product was obtained in the same manner as in Reference Examples 1, 3 and 4 from 2-fluoro-4-bromonitrobenzene.
¹H-NMR (CDCl₃) δ 1.12 (t, J=7.0 Hz, 3H), 3.43 (q, J=7.0 Hz, 2H), 3.75 (t, J=5.1 Hz, 2H), 4.37 (t, J=5.1 Hz, 2H), 4.88 (s, 2H), 7.36 (dd, J=8.6, 1.8 Hz, 1H), 7.49 (d, J=1.8 Hz, 1H), 7.59 (d, J=8.6 Hz, 1H).

Reference Example 10

The object product was obtained in the same manner as in Reference Example 5 from the compound obtained in Reference Example 9.
¹H-NMR (CDCl₃) δ 1.02 (t, J=7.0 Hz, 3H), 3.35 (q, J=7.0 Hz, 2H), 3.71 (t, J=5.1 Hz, 2H), 4.64 (t, J=5.1 Hz, 2H), 7.41 (m, 1H), 7.68-7.73 (m, 2H), 10.05 (s, 1H).

Reference Example 11

To a solution (4:1, 15 mL) of the compound (200 mg, 0.67 mmol) obtained in Reference Example 10 in a mixed solvent of dioxane-water were added potassium carbonate (280 mg, 2.02 mmol), phenylboronic acid (123 mg, 1.01 mmol) and tetrakis(triphenylphosphine)palladium (154 mg, 0.13 mmol), and the mixture was heated to 110° C. After refluxing for 2 hr, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column (hexane:ethyl acetate=90:10-75:25-50:50) to give the object product (115 mg, 58%).
¹H-NMR (CDCl₃) δ 1.07 (t, J=7.0 Hz, 3H), 3.42 (q, J=7.0 Hz, 2H), 3.81 (t, J=5.1 Hz, 2H), 4.81 (t, J=5.1 Hz, 2H), 7.39 (m, 1H), 7.48 (t, J=7.6 Hz, 2H), 7.63-7.67 (m, 3H), 7.76 (m, 1H), 7.96 (d, J=8.6 Hz, 1H), 10.11 (s, 1H).

Example 66

N²-{[1-(2-ethoxyethyl)-6-phenyl-1H-benzimidazol-2-yl]methyl}glycinamide

The object product (31 mg, 38%) was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 11 (68 mg, 0.23 mmol).
¹H-NMR (CDCl₃) δ1.08 (t, J=7.1 Hz, 3H), 3.38 (q, J=7.1 Hz, 2H), 3.41 (s, 2H), 3.75 (t, J=5.1 Hz, 2H), 4.11 (s, 2H), 4.35 (t, J=5.1 Hz, 2H), 5.68 (brs, 1H), 7.22 (brs, 1H), 7.33 (m, 1H), 7.42-7.51 (m, 4H), 7.61-7.63 (m, 2H), 7.76 (m, 1H).

Examples 67-73

The compounds of Examples 67-73 shown in Table 11 and Table 12 were prepared in the same manner as in Reference Examples 9-11 and Example 66.

TABLE 11

Example	structural formula	¹H-NMR (CDCl₃) δ

67		1.03 (t, J = 7.1 Hz, 3H), 3.29 (q, J = 7.1 Hz, 2H), 3.36 (s, 2H), 3.70 (t, J = 5.1 Hz, 2H), 4.06 (s, 2H), 4.30 (t, J = 5.1 Hz, 2H), 5.68 (brs, 1H), 7.06-7.09 (m, 2H), 7.16 (brs, 1H), 7.37- 7.39 (m, 2H), 7.49-7.53 (m, 2H), 7.70 (m, 1H).

68		1.08 (t, J = 7.1 Hz, 3H), 1.39 (d, J = 6.8 Hz, 3H), 3.32 (q, J = 6.8 Hz, 1H), 3.37 (q, J = 7.1 Hz, 2H), 3.73 (t, J = 5.0 Hz, 2H), 4.04 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.31 (dt, J = 15.9, 5.0 Hz, 1H), 4.36 (dt, J = 15.9, 5.0 Hz, 1H), 5.61 (brs, 1H), 7.10-7.14 (m, 2H), 7.25 (brs, 1H), 7.41-7.43 (m, 2H), 7.54- 7.57 (m, 2H), 7.74 (m, 1H).

69		1.08 (t, J = 7.0 Hz, 3H), 1.39 (d, J = 6.9 Hz, 3H), 3.30 (q, J = 6.9 Hz, 1H), 3.37 (q, J = 7.0 Hz, 2H), 3.73 (t, J = 4.8 Hz, 2H), 4.04 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.28-4.38 (m, 2H), 5.73 (brs, 1H), 7.28 (brs, 1H), 7.33 (m, 1H), 7.41-7.50 (m, 4H), 7.60- 7.63 (m, 2H), 7.75 (m, 1H).

70		1.10 (t, J = 7.0 Hz, 3H), 3.40 (q, J = 7.0 Hz, 2H), 3.44 (s, 2H), 3.75 (t, J = 5.0 Hz, 2H), 4.14 (s, 2H), 4.36 (t, J = 5.0 Hz, 2H), 5.60 (brs, 1H), 7.27-7.36 (m, 4H), 7.40-7.43 (m, 2H), 7.50 (m, 1H), 7.78 (m, 1H).

TABLE 12

Example	structural formula	¹H-NMR (CDCl₃) δ

71		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.35 (q, J = 7.0 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.74 (t, J = 5.0 Hz, 2H), 4.07 (d, J = 14.7 Hz, 1H), 4.16 (d, J = 14.7 Hz, 1H), 4.30 (dt, J = 15.0, 5.0 Hz, 1H), 4.37 (dt, J = 15.0, 5.0 Hz, 1H), 5.81 (brs, 1H), 7.26-7.36 (m, 4H), 7.39-7.42 (m, 2H), 7.50 (m, 1H), 7.78 (m, 1H).

72		1.10 (t, J = 7.0 Hz, 3H), 3.40 (q, J = 7.0 Hz, 2H), 3.43 (s, 2H), 3.77 (t, J = 5.1 Hz, 2H), 4.13 (s, 2H), 4.38 (t, J = 5.1 Hz, 2H), 5.65 (brs, 1H), 7.21 (brs, 1H), 7.41-7.49 (m, 4H), 7.54-7.58 (m, 2H), 7.78 (m, 1H).

73		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.35 (q, J = 7.0 Hz, 1H), 3.40 (q, J = 7.0 Hz, 2H), 3.76 (t, J = 5.0 Hz, 2H), 4.06 (d, J = 14.7 Hz, 1H), 4.16 (d, J = 14.7 Hz, 1H), 4.31- 4.44 (m, 2H), 5.81 (brs, 1H), 7.28 (brs, 1H), 7.40-7.47 (m, 4H), 7.53-7.57 (m, 2H), 7.78 (m, 1H).

Reference Example 12

Under a nitrogen atmosphere, to a solution of the compound (150 mg, 0.5 mmol) obtained in Reference Example 9 in N-methylpyrrolidinone (5 mL) were added cesium carbonate (489 mg, 1.5 mmol), 4-tert-butylphenol (225 mg, 1.5 mmol), 2,2,6,6-tetramethylheptane-3,5-dione (52 μl, 0.25 mmol) and copper(I) chloride (50 mg, 0.5 mmol), and the mixture was heated to 120° C. After stirring for 6 hr, the reaction mixture was added to 2 mol/L hydrochloric acid under ice-cooling, and the mixture was extracted with ethyl acetate. The organic layer was washed with 0.5 mol/L hydrochloric acid, 2 mol/L aqueous sodium hydroxide solution, water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column (hexane:ethyl acetate=100:0-0:100) to give the object product (56 mg, 30%).
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.32 (s, 9H), 3.41 (q, J=7.0 Hz, 2H), 3.72 (t, J=5.1 Hz, 2H), 4.35 (t, J=5.1 Hz, 2H), 4.89 (s, 2H), 6.89-7.02 (m, 4H), 7.31-7.36 (m, 2H), 7.64 (d, J=8.5 Hz, 1H).

Example 74

N²-{[6-(4-tert-butylphenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Reference Example 5 and Example 1 from the compound obtained in Reference Example 12.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.32 (s, 9H), 1.41 (d, J=6.9 Hz, 3H), 3.34 (q, J=6.9 Hz, 1H), 3.38 (q, J=7.0 Hz, 2H), 3.68 (t, J=5.1 Hz, 2H), 4.04 (d, J=14.9 Hz, 1H), 4.12 (d, J=14.9 Hz, 1H), 4.18-4.34 (m, 2H), 5.47 (brs, 1H), 6.89-6.95 (m, 2H), 6.97-7.02 (m, 2H), 7.29 (brs, 1H), 7.31-7.36 (m, 2H), 7.67 (d, J=8.5 Hz, 1H).

Reference Example 13

To a solution of the compound (1.20 g, 4 mmol) obtained in Reference Example 9 in N,N-dimethylformamide (15 mL) were added imidazole (1.36 g, 20 mmol) and tert-butyldimethylsilyl chloride (904 mg, 6 mmol). After stirring at room temperature for 2 hr, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column (hexane:ethyl acetate=100:0-85:15) to give the object product (1.65 g, 100%).
¹H-NMR (CDCl₃) δ0.11 (s, 6H), 0.91 (s, 9H), 1.12 (t, J=7.0 Hz, 3H), 3.41 (q, J=7.0 Hz, 2H), 3.74 (t, J=5.5 Hz, 2H), 4.44 (t, J=5.5 Hz, 2H), 4.99 (s, 2H), 7.34 (dd, J=1.9, 8.5 Hz, 1H), 7.56-7.62 (m, 2H).

Reference Example 14

Under a nitrogen atmosphere, to a solution of the compound (207 mg, 0.5 mmol) obtained in Reference Example 13 in N-methylpyrrolidinone (5 mL) were added cesium carbonate (489 mg, 1.5 mmol), 4-methoxyphenol (186 mg, 1.5 mmol), 2,2,6,6-tetramethylheptane-3,5-dione (52 μl, 0.25 mmol) and copper(I) chloride (50 mg, 0.5 mmol), and the mixture was heated to 120° C. After stirring for 4 hr, the reaction mixture was added to 2 mol/L hydrochloric acid under ice-cooling, and the mixture was extracted with ethyl acetate. The organic layer was washed with 0.5 mol/L hydrochloric acid, 2 mol/L aqueous sodium hydroxide solution, water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column (hexane:ethyl acetate=100:0-0:100) to give the object product (36 mg, 21%).
¹H-NMR (CDCl₃) δ 1.10 (t, J=7.0 Hz, 3H), 3.41 (q, J=7.0 Hz, 2H), 3.70 (t, J=5.0 Hz, 2H), 3.81 (s, 3H), 4.32 (t, J=5.0 Hz, 2H), 4.88 (s, 2H), 6.84-7.01 (m, 6H), 7.63 (d, J=8.8 Hz, 1H).

Example 75

N²-{[1-(2-ethoxyethyl)-6-(4-methoxyphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Reference Example 5 and Example 1 from the compound obtained in Reference Example 14.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.41 (d, J=6.8 Hz, 3H), 3.33 (q, J=6.8 Hz, 1H), 3.37 (q, J=7.0 Hz, 2H), 3.67 (t, J=5.1 Hz, 2H), 3.81 (s, 3H), 4.03 (d, J=14.7 Hz, 1H), 4.10 (d, J=14.7 Hz, 1H), 4.17-4.30 (m, 2H), 5.32 (brs, 1H), 6.85-7.00 (m, 6H), 7.27 (brs, 1H), 7.64 (d, J=8.8 Hz, 1H).

Reference Example 15

To a solution of 3-fluoro-4-nitrophenol (2.5 g, 16.0 mmol) in N,N-dimethylformamide (30 mL) were added potassium carbonate (3.3 g, 24.0 mmol) and benzyl bromide (2.1 ml, 17.6 mmol), and the mixture was heated at 70° C. After stirring for 1 hr, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure, and the obtained residue was directly used for the next reaction.
¹H-NMR (CDCl₃) δ5.14 (s, 2H), 6.79-6.86 (m, 2H), 7.38-7.43 (m, 5H), 8.10 (m, 1H).

Reference Example 16

The object product was obtained in the same manner as in Reference Examples 1 and 3-5 from the compound obtained in Reference Example 15.
¹H-NMR (CDCl₃) δ 1.08 (t, J=7.0 Hz, 3H), 3.40 (q, J=7.0 Hz, 2H), 3.77 (t, J=5.1 Hz, 2H), 4.71 (t, J=5.1 Hz, 2H), 5.15 (s, 2H), 7.04 (d, J=2.4 Hz, 1H), 7.11 (dd, J=9.0, 2.4 Hz, 1H), 7.35-7.49 (m, 5H), 7.79 (d, J=9.0 Hz, 1H), 10.01 (s, 1H).

Example 76

N²-{[6-(benzyloxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 16 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.39 (d, J=7.0 Hz, 3H), 3.32 (q, J=7.0 Hz, 1H), 3.37 (q, J=7.0 Hz, 2H), 3.68 (t, J=5.1 Hz, 2H), 4.00 (d, J=14.6 Hz, 1H), 4.09 (d, J=14.6 Hz, 1H), 4.16-4.32 (m, 2H), 5.11 (s, 2H), 5.75 (brs, 1H), 6.87 (d, J=2.2 Hz, 1H), 6.98 (dd, J=8.8, 2.2 Hz, 1H), 7.27-7.53 (m, 6H), 7.61 (d, J=8.8 Hz, 1H).

Example 77

N²-{[6-(benzyloxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-2-methylalaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 16 and 2-methylalaninamide.
¹H-NMR (CDCl₃) δ 1.10 (t, J=7.0 Hz, 3H), 1.45 (s, 6H), 3.37 (q, J=7.0 Hz, 2H), 3.69 (t, J=5.1 Hz, 2H), 4.00 (s, 2H), 4.24 (t, J=5.1 Hz, 2H), 5.12 (s, 2H), 5.47 (brs, 1H), 6.86 (d, J=2.4 Hz, 1H), 6.98 (dd, J=8.8, 2.4 Hz, 1H), 7.31-7.48 (m, 5H), 7.51 (brs, 1H), 7.62 (d, J=8.8 Hz, 1H).

Reference Example 17

The object product was obtained in the same manner as in Reference Examples 15, 1 and 3-5 from 3-fluoro-4-nitrophenol.
¹H-NMR (CDCl₃) δ 1.07 (t, J=7.0 Hz, 3H), 3.40 (q, J=7.0 Hz, 2H), 3.78 (t, J=5.3 Hz, 2H), 4.71 (t, J=5.3 Hz, 2H), 5.10 (s, 2H), 7.03 (d, J=2.2 Hz, 1H), 7.07-7.13 (m, 3H), 7.42-7.47 (m, 2H), 7.79 (d, J=9.0 Hz, 1H), 10.01 (s, 1H).

Example 78

N²-({1-(2-ethoxyethyl)-6-[(4-fluorobenzyl)oxy]-1H-benzimidazol-2-yl}methyl)-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 17 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.10 (t, J=7.0 Hz, 3H), 1.40 (d, J=7.0 Hz, 3H), 3.32 (q, J=7.0 Hz, 1H), 3.38 (q, J=7.0 Hz, 2H), 3.70 (t, J=5.1 Hz, 2H), 4.01 (d, J=14.6 Hz, 1H), 4.09 (d, J=14.6 Hz, 1H), 4.20-4.32 (m, 2H), 5.08 (s, 2H), 5.39 (brs, 1H), 6.86 (d, J=2.2 Hz, 1H), 6.96 (dd, J=8.8, 2.2 Hz, 1H), 7.06-7.10 (m, 2H), 7.25 (brs, 1H), 7.42-7.45 (m, 2H), 7.62 (d, J=8.8 Hz, 1H).

Reference Example 18

To a solution of 2,6-dichloro-3-nitropyridine (3.0 g, 15.5 mmol) in dioxane (50 mL) were added potassium carbonate (2.4 g, 17.0 mmol) and 2-ethoxyethylamine (1.4 g, 17.0 mmol), and the mixture was stirred at 50° C. After stirring for 3 hr, potassium carbonate (1.8 g, 13.0 mmol) and 2-ethoxyethylamine (0.9 g, 10.0 mmol) were added thereto, and the mixture was stirred at 50° C. for 3 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (ethyl acetate:hexane=1:5) to give the object product (3.4 g, 89%).
¹H-NMR (CDCl₃) δ 1.24 (t, J=7.0 Hz, 3H), 3.57 (q, J=7.0 Hz, 2H), 3.67 (t, J=5.2 Hz, 2H), 3.82 (q, J=5.2 Hz, 2H), 6.61 (d, J=8.5 Hz, 1H), 8.35 (d, J=8.5 Hz, 1H), 8.59 (br, 1H).

Reference Example 19

The object product was obtained in the same manner as in Reference Example 2 from the compound obtained in Reference Example 18.
¹H-NMR (CDCl₃) δ 1.18 (t, J=7.0 Hz, 3H), 3.39-3.50 (m, 6H), 6.20 (d, J=9.0 Hz, 1H), 7.12-7.17 (m, 2H), 7.25 (m, 1H), 7.37-7.44 (m, 2H), 8.42 (d, J=9.0 Hz, 1H), 8.66 (br, 1H).

Reference Example 20

The object product was obtained in the same manner as in Reference Examples 3-5 from the compound obtained in Reference Example 19.
¹H-NMR (CDCl₃) δ 1.01 (t, J=7.0 Hz, 3H), 3.38 (q, J=7.0 Hz, 2H), 3.72 (t, J=5.6 Hz, 2H), 4.70 (t, J=5.6 Hz, 2H), 6.98 (d, J=8.8 Hz, 1H), 7.17-7.28 (m, 3H), 7.37-7.46 (m, 2H), 8.16 (d, J=8.8 Hz, 1H), 10.00 (s, 1H).

Example 79

N²-{[3-(2-ethoxyethyl)-5-phenoxy-3H-imidazo[4,5-b]pyridin-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 1 from the compound obtained in Reference Example 20. ¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.41 (d, J=7.0 Hz, 3H), 3.35 (q, J=7.0 Hz, 1H), 3.38 (q, J=7.0 Hz, 2H), 3.71 (t, J=5.1 Hz, 2H), 4.06 (d, J=15.0 Hz, 1H), 4.14 (d, J=15.0 Hz, 1H), 4.32 (t, J=5.1 Hz, 2H), 5.56 (brs, 1H), 6.67 (d, J=8.6 Hz, 1H), 7.11-7.21 (m, 3H), 7.26 (brs, 1H), 7.35-7.42 (m, 2H), 7.95 (d, J=8.6 Hz, 1H).

Example 80

N²-{[3-(2-ethoxyethyl)-5-phenoxy-3H-imidazo[4,5-b]pyridin-2-yl]methyl}glycinamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 20. ¹H-NMR (CDCl₃) δ 1.08 (t, J=7.0 Hz, 3H), 3.38 (q, J=7.0 Hz, 2H), 3.42 (s, 2H), 3.72 (t, J=4.9 Hz, 2H), 4.12 (s, 2H), 4.33 (t, J=4.9 Hz, 2H), 5.73 (brs, 1H), 6.76 (d, J=8.4 Hz, 1H), 7.11-7.22 (m, 3H), 7.26 (brs, 1H), 7.35-7.42 (m, 2H), 7.95 (d, J=8.4 Hz, 1H).

Reference Example 21

The object product was obtained in the same manner as in Reference Example 1 from 2,4,5-trifluoronitrobenzene.
¹H-NMR (CDCl₃) δ 1.25 (t, J=7.1 Hz, 3H), 3.43 (q, J=5.1 Hz, 2H), 3.57 (q, J=7.1 Hz, 2H), 3.72 (t, J=5.1 Hz, 2H), 6.66 (dd, J=12.4, 6.6 Hz, 1H), 8.05 (dd, J=10.2, 8.6 Hz, 1H), 8.29 (br, 1H).

Reference Example 22

The object product was obtained in the same manner as in Reference Examples 2-5 from the compound obtained in Reference Example 21.
¹H-NMR (CDCl₃) δ 0.99 (t, J=7.0 Hz, 3H), 3.33 (q, J=7.0 Hz, 2H), 3.71 (t, J=5.1 Hz, 2H), 4.64 (t, J=5.1 Hz, 2H), 7.00-7.10 (m, 4H), 7.13 (d, J=7.1 Hz, 1H), 7.66 (d, J=10.3 Hz, 1H), 10.04 (s, 1H).

Example 81

N²-{[1-(2-ethoxyethyl)-5-fluoro-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 1 from the compound obtained in Reference Example 22.
¹H-NMR (CDCl₃) δ 1.07 (t, J=7.0 Hz, 3H), 1.41 (d, J=7.0 Hz, 3H), 3.32 (q, J=7.0 Hz, 1H), 3.37 (q, J=7.0 Hz, 2H), 3.66 (t, J=5.1 Hz, 2H), 4.02 (d, J=14.7 Hz, 1H), 4.11 (d, J=14.7 Hz, 1H), 4.17-4.32 (m, 2H), 5.38 (brs, 1H), 6.90-7.05 (m, 5H), 7.16 (brs, 1H), 7.52 (d, J=12.1 Hz, 1H).

Reference Example 23

The object product was obtained in the same manner as in Reference Examples 1-4 from 2,4-difluoronitrobenzene, 4-amino-(1-tert-butoxycarbonyl)piperidine and 4-fluorophenol.
¹H-NMR (CDCl₃) δ 1.48 (s, 9H), 1.91-1.95 (m, 2H), 2.22-2.37 (m, 2H), 2.76-2.93 (m, 2H), 4.30 (br, 2H), 4.60 (m, 1H), 4.86 (s, 2H), 6.86-7.05 (m, 5H), 7.14 (d, J=2.0 Hz, 1H), 7.58 (d, J=8.8 Hz, 1H).

Reference Example 24

The object product was obtained in the same manner as in Reference Example 5 from the compound obtained in Reference Example 23.
¹H-NMR (CDCl₃) δ 1.48 (s, 9H), 1.89-1.93 (m, 2H), 2.23-2.38 (m, 2H), 2.85-2.94 (m, 2H), 4.33 (br, 2H), 5.63 (m, 1H), 6.99-7.10 (m, 5H), 7.18 (d, J=2.0 Hz, 1H), 7.86 (d, J=8.8 Hz, 1H), 10.04 (s, 1H).

Example 82

tert-butyl 4-[2-({[(2S)-1-amino-1-oxopropan-2-yl]amino}methyl)-6-(4-fluorophenoxy)-1H-benzimidazol-1-yl]piperidine-1-carboxylate

The object product was obtained in the same manner as in Example 1 from the compound obtained in Reference Example 24.
¹H-NMR (CDCl₃) δ 1.38 (d, J=7.0 Hz, 3H), 1.48 (s, 9H), 1.86-1.89 (m, 2H), 2.30-2.34 (m, 2H), 2.81-2.89 (m, 2H), 3.28 (q, J=7.0 Hz, 1H), 4.02 (d, J=14.7 Hz, 1H), 4.10 (d, J=14.7 Hz, 1H), 4.31-4.42 (m, 3H), 6.02 (brs, 1H), 6.87-7.04 (m, 6H), 7.15 (d, J=2.0 Hz, 1H), 7.64 (d, J=8.8 Hz, 1H).

Example 83

N²-{[6-(4-fluorophenoxy)-1-(piperidin-4-yl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

To a solution of the compound (68 mg, 0.13 mmol) obtained in Example 82 in dichloromethane (1.3 mL) was added trifluoroacetic acid (260 μL), and the mixture was stirred at room temperature for 1 hr. Aqueous sodium hydroxide solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (ethyl acetate:methanol=99:1-80:20) to give the object product (38 mg, 71%).
¹H-NMR (CDCl₃) δ 1.41 (d, J=7.0 Hz, 3H), 1.86-1.89 (m, 2H), 2.26-2.40 (m, 2H), 2.72-2.81 (m, 2H), 3.26-3.33 (m, 3H), 4.02 (d, J=14.7 Hz, 1H), 4.10 (d, J=14.7 Hz, 1H), 4.30 (m, 1H), 5.89 (brs, 1H), 6.89-7.07 (m, 6H), 7.33 (d, J=2.0 Hz, 1H), 7.65 (d, J=8.8 Hz, 1H).

Reference Example 25

To a solution of the compound (300 mg, 0.68 mmol) obtained in Reference Example 24 in dichloromethane (6.8 mL) was added trifluoroacetic acid (1.4 mL), and the mixture was stirred at room temperature for 1 hr. Aqueous sodium hydroxide solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was dissolved in dichloromethane (6.8 mL), triethylamine (142 μL, 1.02 mmol) and isopropyl isocyanate (100 μL, 1.02 mmol) were added thereto, and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (chloroform:methanol=99:1-85:15) to give the object product (280 mg, 97%).
¹H-NMR (CDCl₃) δ 1.18 (d, J=6.6 Hz, 6H), 1.92-1.97 (m, 2H), 2.28-2.42 (m, 2H), 2.91-3.01 (m, 2H), 4.01 (m, 1H), 4.12-4.17 (m, 2H), 4.33 (m, 1H), 5.65 (m, 1H), 6.97-7.10 (m, 5H), 7.20 (d, J=2.0 Hz, 1H), 7.86 (d, J=8.8 Hz, 1H), 10.04 (s, 1H).

Example 84

4-[2-({[(2S)-1-amino-1-oxopropan-2-yl]amino}methyl)-6-(4-fluorophenoxy)-1H-benzimidazol-1-yl]-N-(propan-2-yl)piperidine-1-carboxamide

The object product was obtained in the same manner as in Example 1 from the compound obtained in Reference Example 25.
¹H-NMR (CDCl₃) δ 1.17 (d, J=6.6 Hz, 6H), 1.38 (d, J=7.0 Hz, 3H), 1.90-1.92 (m, 2H), 2.30-2.40 (m, 2H), 2.87-2.94 (m, 2H), 3.27 (q, J=7.0 Hz, 1H), 3.93-4.18 (m, 5H), 4.36-4.45 (m, 2H), 5.73 (brs, 1H), 6.89-7.03 (m, 6H), 7.16 (d, J=2.0 Hz, 1H), 7.65 (d, J=8.8 Hz, 1H).

Example 85

N²-{[1-(1-acetylpiperidin-4-yl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Reference Example 25 and Example 1 from the compound obtained in Reference Example 24 and acetyl chloride.
¹H-NMR (CDCl₃) δ 1.38 (d, J=7.0 Hz, 3H), 1.89-2.46 (m, 3H), 2.16 (s, 3H), 2.67 (m, 1H), 3.18-3.32 (m, 2H), 3.65 (m, 1H), 3.99-4.13 (m, 3H), 4.52 (m, 1H), 4.89 (m, 1H), 5.85 (brs, 1H), 6.88-7.05 (m, 6H), 7.11 (d, J=2.0 Hz, 1H), 7.65 (d, J=8.8 Hz, 1H).

Example 86

N²-({6-(4-fluorophenoxy)-1-[1-(methylsulfonyl)piperidin-4-yl]-1H-benzimidazol-2-yl}methyl)-L-alaninamide

The object product was obtained in the same manner as in Reference Example 25 and Example 1 from the compound obtained in Reference Example 24 and methanesulfonyl chloride.
¹H-NMR (CDCl₃) δ 1.37 (d, J=6.8 Hz, 3H), 2.00-2.16 (m, 3H), 2.48-2.61 (m, 2H), 2.88 (m, 1H), 2.86 (s, 3H), 3.25 (q, J=6.8 Hz, 1H), 3.99-4.16 (m, 4H), 4.46 (m, 1H), 5.87 (brs, 1H), 6.81 (brs, 1H), 6.89-7.05 (m, 5H), 7.21 (d, J=2.0 Hz, 1H), 7.65 (d, J=8.8 Hz, 1H).

Reference Example 26

To a solution of the compound (2.28 g, 6.9 mmol) obtained in Reference Example 7 in tetrahydrofuran (70 mL) were added (L)-alanine ethyl ester hydrochloride (2.15 g, 14 mmol), triethylamine (1.95 ml, 14 mmol) and sodium sulfate (10 g), and the mixture was stirred at room temperature. After stirring for 1 hr, sodium cyanoborohydride (503 mg, 8 mmol) was added thereto, and the mixture was stirred for 4 hr. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The organic layer was extracted, washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (chloroform:methanol=100:0-95:5) to give the object product (1.78 g, 60%).
¹H-NMR (CDCl₃) δ 1.08 (t, J=7.0 Hz, 3H), 1.28 (t, J=7.1 Hz, 3H), 1.35 (d, J=7.0 Hz, 3H), 3.38 (q, J=7.0 Hz, 2H), 3.48 (q, J=7.1 Hz, 1H), 3.70 (t, J=5.3 Hz, 2H), 4.02 (d, J=13.9 Hz, 1H), 4.10-4.23 (m, 3H), 4.31-4.42 (m, 2H), 6.90-7.05 (m, 6H), 7.66 (d, J=8.6 Hz, 1H).

Reference Example 27

To a solution of the compound (2.79 g, 6.5 mmol) obtained in Reference Example 26 in acetonitrile (65 mL) was added di-t-butyl dicarbonate (1.64 g, 7.5 mmol), and the mixture was stirred with heating at 60° C. for 3 hr and at 100° C. for 3 hr. After cooling to room temperature, the mixture was concentrated under reduced pressure, and the residue was purified by silica gel column (hexane:ethyl acetate=100:0-70:30) to give the object product (2.24 g, 65%).
¹H-NMR (CDCl₃) δ 1.00-1.18 (m, 6H), 1.40 (d, J=7.1 Hz, 3H), 1.44 (s, 9H), 3.38 (q, J=7.0 Hz, 2H), 3.68 (t, J=5.9 Hz, 2H), 3.86-4.12 (m, 2H), 4.19-4.55 (m, 3H), 4.75 (d, J=15.4 Hz, 1H), 4.98 (d, J=15.4 Hz, 1H), 6.90-7.08 (m, 6H), 7.64 (d, J=8.8 Hz, 1H).

Reference Example 28

To a solution of the compound (2.24 g, 4.2 mmol) obtained in Reference Example 27 in ethanol (40 mL) was added 2 mol/L aqueous sodium hydroxide solution (4.2 ml, 8.4 mmol) in an ice bath. After stirring for 30 min under the same conditions, water was added to the reaction mixture, and the aqueous layer was washed with ether. The aqueous layer was adjusted to pH=4 with 2 mol/L hydrochloric acid, and the mixture was extracted with chloroform. The organic layer was extracted, washed with saturated brine and dried over sodium sulfate to give the object product (2.02 g, 96%).
¹H-NMR (CDCl₃) δ 1.11 (t, J=7.0 Hz, 3H), 1.49 (s, 9H), 1.55 (d, J=7.2 Hz, 3H), 3.30-3.50 (m, 2H), 3.63-3.75 (m, 2H), 3.90 (brs, 1H), 4.13-4.29 (m, 2H), 4.54 (brs, 1H), 5.27 (brs, 1H), 6.91-7.08 (m, 6H), 7.63 (d, J=8.6 Hz, 1H).

Example 87

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-N-(2-hydroxy-2-methylpropyl)-L-alaninamide

To a solution of the compound (53 mg, 0.1 mmol) obtained in Reference Example 28 in dichloromethane (2 mL) were added 1-amino-2-methylpropan-2-ol (18 mg, 0.2 mmol) and PyBOP [registered trade mark, benzotriazol-1-yl-oxy-tris(pyrrolidino)phosphonium hexafluorophosphate (benzotriazol-1-yl-oxy-tris(pyrrolidino)phosphonium hexafluorophosphate)] (52 mg, 0.1 mmol), and the mixture was stirred at room temperature. After 16 hr, 10% aqueous citric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was extracted, washed with water and saturated brine, and dried over sodium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column (chloroform:methanol=100:0-98:2) to give the object product (51 mg, 89%). The product was dissolved in ethyl acetate (1 mL), 4 mol/L hydrogen chloride-ethyl acetate solution (1 ml, 4 mmol) was added thereto, and the mixture was stirred at room temperature. After 14 hr, the mixture was concentrated under reduced pressure. To the obtained residue was added 2 mol/L aqueous sodium hydroxide solution, and the mixture was extracted with chloroform. The organic layer was extracted, washed with saturated brine, and dried over sodium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column (chloroform:methanol=100:0-95:5) to give the object product (32 mg, 76%).
¹H-NMR (CDCl₃) δ 1.10 (t, J=7.0 Hz, 3H), 1.29 (s, 6H), 1.36 (d, J=6.8 Hz, 3H), 3.21 (dd, J=5.3, 3.6 Hz, 1H), 3.29-3.51 (m, 4H), 3.61-3.73 (m, 2H), 3.97 (d, J=14.3 Hz, 1H), 4.11 (d, J=14.3 Hz, 1H), 4.21 (dt, J=15.3, 4.2 Hz, 1H), 4.33 (m, 1H), 6.90-7.07 (m, 6H), 7.68 (dd, J=8.3, 0.9 Hz, 1H), 7.83 (brt, J=6.0 Hz, 1H).

Examples 88-90

The compounds of Examples 88-90 shown in Table 13 were prepared according to the methods described in the above-mentioned Reference Examples and Examples or methods analogous thereto.

TABLE 13

Example	structural formula	¹H-NMR (CDCl₃) δ

88		1.08 (t, J = 7.0 Hz, 3H), 1.37 (d, J = 7.0 Hz, 3H), 3.32 (q, J = 7.0 Hz, 1H), 3.35 (s, 3H), 3.38 (q, J = 7.0 Hz, 2H), 3.43-3.52 (m, 4H), 3.67 (t, J = 5.2 Hz, 2H), 3.99 (d, J = 14.7 Hz, 1H), 4.08 (d, J = 14.7 Hz, 1H), 4.26 (t, J = 5.2 Hz, 2H), 6.91-7.07 (m, 6H), 7.53 (brs, 1H), 7.64- 7.69 (m, 1H).

89		1.08 (t, J = 7.1 Hz, 3H), 1.37 (d, J = 6.8 Hz, 3H), 2.41-2.53 (m, 6H), 3.25- 3.45 (m, 5H), 3.62-3.72 (m, 6H), 4.00 (d, J = 14.9 Hz, 1H), 4.08 (d, J = 14.9 Hz, 1H), 4.17- 4.33 (m, 2H), 6.94-7.05 (m, 6H), 7.48 (brt, J = 5.2 Hz, 1H), 7.66 (m, 1H).

90		1.08 (t, J = 7.1 Hz, 3H), 1.19 (d, J = 7.0 Hz, 3H), 3.31-3.43 (m, 3H), 3.44- 3.80 (m, 10H), 3.96 (d, J = 14.1 Hz, 1H), 4.11 (d, J = 14.1 Hz, 1H), 4.32 (m, 1H), 4.46 (m, 1H), 6.90-7.06 (m, 6H), 7.63 (d, J = 8.6 Hz, 1H).

Reference Example 29

To a solution of alcohol (500 mg, 1.58 mmol) obtained in the same manner as in Reference Examples 1-4 in dichloromethane (16 mL) was added thionyl chloride (342 μL, 4.74 mmol), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was concentrated, and the obtained residue was dissolved in chloroform, aqueous sodium hydroxide solution was added thereto. The mixture was extracted with chloroform, and the organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give the object product (508 mg, 96%).
¹H-NMR (CDCl₃) δ 3.27 (s, 3H), 3.67 (t, J=5.1 Hz, 2H), 4.38 (t, J=5.1 Hz, 2H), 4.92 (s, 2H), 6.96-7.06 (m, 6H), 7.58 (d, J=8.4 Hz, 1H).

Example 91

N²-{[6-(4-fluorophenoxy)-1-(2-methoxyethyl)-1H-benzimidazol-2-yl]methyl}-2-methylalaninamide

To a solution of the compound (300 mg, 0.90 mmol) obtained in Reference Example 29 in acetonitrile (4.5 mL) were added 2,2-dimethylglycine (138 mg, 1.35 mmol), diisopropylethylamine (321 μL, 1.80 mmol) and sodium iodide (135 mg, 0.90 mmol), and the mixture was heated to 50° C. and stirred overnight. Water was added thereto, the mixture was extracted with chloroform, and the organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (ethyl acetate:methanol=99:1-80:20) to give the object product (169 mg, 47%).
¹H-NMR (CDCl₃) δ 1.45 (s, 6H), 3.26 (s, 3H), 3.66 (t, J=5.0 Hz, 2H), 4.00 (s, 2H), 4.25 (t, J=5.0 Hz, 2H), 5.57 (brs, 1H), 6.94-7.05 (m, 6H), 7.46 (brs, 1H), 7.67 (m, 1H).

Reference Example 30

To a solution of the compound (0.84 g, 2.8 mmol) obtained in Reference Example 10 in N,N-dimethylformamide (30 mL) was added N-chlorosuccinimide (0.95 g, 7.1 mmol), and the mixture was heated to 40° C. After stirring overnight, water was added thereto, the mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine, dried over magnesium sulfate, concentrated under reduced pressure and directly used for the next reaction.
¹H-NMR (CDCl₃) δ 1.07 (t, J=7.0 Hz, 3H), 3.39 (q, J=7.0 Hz, 2H), 3.76 (t, J=5.1 Hz, 2H), 4.72 (t, J=5.1 Hz, 2H), 8.01-8.02 (m, 2H), 10.09 (s, 1H).

Reference Example 31

The object product was obtained in the same manner as in Reference Example 11 from the compound obtained in Reference Example 30.
¹H-NMR (CDCl₃) δ 1.05 (t, J=7.0 Hz, 3H), 3.38 (q, J=7.0 Hz, 2H), 3.77 (t, J=5.1 Hz, 2H), 4.76 (t, J=5.1 Hz, 2H), 7.12-7.20 (m, 3H), 7.40-7.46 (m, 2H), 8.02 (s, 1H), 10.12 (s, 1H).

Example 92

N²-{[5-chloro-1-(2-ethoxyethyl)-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 1 from the compound obtained in Reference Example 31.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.41 (t, J=7.0 Hz, 3H), 3.32-3.42 (m, 3H), 3.71 (t, J=5.1 Hz, 2H), 4.05 (d, J=14.6 Hz, 1H), 4.14 (d, J=14.6 Hz, 1H), 4.23-4.38 (m, 2H), 5.39 (brs, 1H), 7.11-7.17 (m, 3H), 7.21 (brs, 1H), 7.41-7.45 (m, 2H), 7.83 (s, 1H).

Examples 93-108

The compounds of Examples 93-108 shown in Tables 14-16 were prepared according to the methods described in the above-mentioned Reference Examples and Examples or methods analogous thereto.

TABLE 14

Example	structural formula	¹H-NMR (CDCl₃) δ

93		1.11 (t, J = 7.0 Hz, 3H), 1.43 (d, J = 7.0 Hz, 3H), 3.32- 3.45 (m, 3H), 3.82 (t, J = 5.1 Hz, 2H), 4.07 (d, J = 14.9 Hz, 1H), 4.17 (d, J = 14.9 Hz, 1H), 4.65-4.68 (m, 2H), 5.35 (brs, 1H), 6.87- 7.04 (m, 6H), 7.58 (d, J = 8.8 Hz, 1H).

94		1.09 (t, J = 7.0 Hz, 3H), 1.24 (d, J = 7.0 Hz, 6H), 1.41 (d, J = 7.0 Hz, 3H), 2.90 (m, 1H), 3.31-3.40 (m, 3H), 3.68 (t, J = 5.1 Hz, 2H), 4.04 (d, J = 14.9 Hz, 1H), 4.11 (d, J = 14.9 Hz, 1H), 4.20-4.29 (m, 2H), 5.33 (brs, 1H), 6.90-6.99 (m, 4H), 7.16- 7.19 (m, 2H), 7.26 (brs, 1H), 7.66 (m, 1H).

95		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 2.06- 2.13 (m, 2H), 2.85-2.90 (m, 4H), 3.31-3.40 (m, 3H), 3.68 (t, J = 5.1 Hz, 2H), 4.03 (d, J = 14.6 Hz, 1H), 4.11 (d, J = 14.6 Hz, 1H), 4.18-4.30 (m, 2H), 5.33 (brs, 1H), 6.79 (d, J = 8.1 Hz, 1H), 6.86 (m, 1H), 6.97-6.99 (m, 3H), 7.15 (d, J = 8.3 Hz, 1H), 7.65 (d, J = 9.3 Hz, 1H).

96		1.38 (t, J = 7.1 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.32 (q, J = 7.0 Hz, 1H), 3.99 (d, J = 14.8 Hz, 1H), 4.06 (d, J = 14.8 Hz, 1H), 4.06-4.16 (m, 2H), 5.50 (br, 1H), 6.88-7.00 (m, 4H), 7.09-7.16 (m, 3H), 7.65 (m, 1H).

97		1.40 (t, J = 7.3 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.32 (q, J = 7.0 Hz, 1H), 4.00 (d, J = 15.0 Hz, 1H), 4.08 (d, J = 15.0 Hz, 1H), 4.09-4.20 (m, 2H), 5.52 (br, 1H), 6.71 (m, 1H), 6.80 (m, 1H), 6.87-7.15 (m, 4H), 7.69 (d, J = 8.6 Hz, 1H).

TABLE 15

Example	structural formula	¹H-NMR (CDCl₃) δ

98		1.39 (t, J = 7.1 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 3.31 (q, J = 6.8 Hz, 1H), 3.99 (d, J = 14.8 Hz, 1H), 4.06 (d, J = 14.8 Hz, 1H), 4.07-4.17 (m, 2H), 5.48 (br, 1H), 6.80-7.12 (m, 6H), 7.65 (m, 1H).

99		0.95-1.05 (m, 2H), 1.13-1.23 (m, 2H), 1.43 (d, J = 7.0 Hz, 3H), 3.18 (m, 1H), 3.30 (q, J = 7.0 Hz, 1H), 4.08 (d, J = 14.4 Hz, 1H) , 4.17 (d, J = 14.4 Hz, 1H), 5.52 (br, 1H), 6.80-7.06 (m, 4H), 7.13 (d, J = 2.4 Hz, 1H), 7.23 (br, 1H), 7.61 (d, J = 8.6 Hz, 1H).

100		0.98-1.08 (m, 2H), 1.15-1.25 (m, 2H), 1.44 (d, J = 6.8 Hz, 3H), 3.19 (m, 1H), 3.36 (q, J = 6.8 Hz, 1H), 4.10 (d, J = 15.4 Hz, 1H), 4.18 (d, J = 15.4 Hz, 1H), 5.44 (br, 1H), 6.93-7.00 (m, 3H), 7.14-7.26 (m, 4H), 7.66 (d, J = 8.6 Hz, 1H).

101		1.20 (s, 3H), 1.29 (s, 3H), 1.32 (d, J = 6.9 Hz, 3H), 2.33 (s, 3H), 3.34 (q, J = 6.9 Hz, 1H), 4.03 (d, J = 13.9 Hz, 1H), 4.07-4.14 (m, 3H), 5.91 (brs, 1H), 6.84-6.91 (m, 2H), 6.94-6.99 (m, 2H), 7.08- 7.15 (m, 3H), 7.61 (m, 1H).

102		1.06 (t, J = 7.0 Hz, 3H), 1.22 (t, J = 7.6 Hz, 3H), 1.38 (d, J = 6.8 Hz, 3H), 2.61 (q, J = 7.6 Hz, 2H), 3.30- 3.38 (m, 3H), 3.65 (t, J = 5.1 Hz, 2H), 4.03 (d, J = 14.6 Hz, 1H), 4.09 (d, J = 14.6 Hz, 1H), 4.16-4.28 (m, 2H), 5.41 (brs, 1H), 6.89-6.96 (m, 4H), 7.11-7.13 (m, 2H), 7.21 (brs, 1H), 7.62 (m, 1H).

TABLE 16

Example	structural formula	¹H-NMR (CDCl₃) δ

103		(CD₃OD) 1.24 (s, 3H), 1.25 (s, 3H), 1.61 (d, J = 7.1 Hz, 3H), 4.14 (q, J = 7.1 Hz, 1H), 4.27 (d, J = 15.3 Hz, 1H), 4.32 (d, J = 15.3 Hz, 1H), 4.62 (d, J = 15.1 Hz, 1H), 4.67 (d, J = 15.1 Hz, 1H), 7.00-7.10 (m, 3H), 7.22- 7.28 (m, 2H), 7.37 (d, J = 2.0 Hz, 1H), 7.73 (d, J = 8.8 Hz, 1H).

104		1.39 (t, J = 7.0 Hz, 3H), 1.43 (d, J = 7.0 Hz, 3H), 3.33 (q, J = 7.0 Hz, 1H), 4.00 (d, J = 14.9 Hz, 1H), 4.03 (d, J = 14.9 Hz, 1H), 4.14 (q, J = 7.0 Hz, 2H), 5.63 (brs, 1H), 6.94-7.03 (m, 4H), 7.09 (brs, 1H), 7.12-7.21 (m, 2H), 7.69 (d, J = 8.6 Hz, 1H).

105		(CD₃OD) 1.20 (s, 3H), 1.22 (s, 3H), 1.30 (d, J = 6.8 Hz, 3H), 3.25-3.36 (m, 1H), 4.03 (d, J = 14.3 Hz, 1H), 4.11 (d, J = 14.3 Hz, 1H), 4.18 (d, J = 15.0 Hz, 1H), 4.25 (d, J = 15.0 Hz, 1H), 6.87-6.96 (m, 2H), 7.03-7.18 (m, 3H), 7.57 (d, J = 8.8 Hz, 1H).

106		1.08 (t, J = 7.1 Hz, 3H), 1.21 (d, J = 7.0 Hz, 3H), 3.17-3.84 (m, 9H), 3.91- 4.35 (m, 5H), 4.45 (m, 1H), 6.73-7.07 (m, 7H), 7.61 (t, J = 8.6 Hz, 1H).

107		1.08 (t, J = 7.0 Hz, 3H), 1.23- 1.32 (m, 3H), 2.82-4.54 (m, 16H), 6.88-7.08 (m, 6H), 7.63 (m, 1H).

108		1.08 (t, J = 7.0 Hz, 3H), 1.13- 1.23 (m, 3H), 2.28 (m, 1H), 2.57-3.46 (m, 6H), 3.58-4.61 (m, 9H), 6.90-7.06 (m, 6H), 7.61 (m, 1H).

Reference Example 32

The object product was obtained in the same manner as in Reference Example 1 from 4-bromo-2,5-difluoronitrobenzene. ¹H-NMR (CDCl₃) δ 1.23 (t, J=7.0 Hz, 3H), 3.43 (q, J=5.2 Hz, 2H), 3.56 (q, J=7.0 Hz, 2H), 3.70 (t, J=5.2 Hz, 2H), 7.11 (d, J=5.9 Hz, 1H), 7.93 (d, J=8.6 Hz, 1H).

Reference Example 33

The object product was obtained in the same manner as in Reference Example 3-2 from the compound obtained in Reference Example 32.
¹H-NMR (CDCl₃) δ 1.21 (t, J=7.3 Hz, 3H), 3.51-3.58 (m, 4H), 3.65 (t, J=5.1 Hz, 2H), 6.49 (d, J=9.5 Hz, 1H), 6.72 (d, J=6.6 Hz, 1H).

Reference Example 34

The object product was obtained in the same manner as in Reference Example 4 from the compound obtained in Reference Example 33.
¹H-NMR (CDCl₃) δ 1.12 (t, J=7.0 Hz, 3H), 3.43 (q, J=7.0 Hz, 2H), 3.75 (t, J=5.0 Hz, 2H), 4.38 (t, J=5.0 Hz, 2H), 4.88 (s, 2H), 7.45 (d, J=8.8 Hz, 1H), 7.53 (d, J=5.9 Hz, 1H).

Reference Example 35

The object product was obtained in the same manner as in Reference Example 5 from the compound obtained in Reference Example 34.
¹H-NMR (CDCl₃) δ 1.07 (t, J=7.0 Hz, 3H), 3.40 (q, J=7.0 Hz, 2H), 3.76 (t, J=5.0 Hz, 2H), 4.73 (t, J=5.0 Hz, 2H), 7.63 (d, J=8.5 Hz, 1H), 7.87 (d, J=6.1 Hz, 1H), 10.09 (s, 1H).

Reference Example 36

The object product was obtained in the same manner as in Reference Example 11 from the compound obtained in Reference Example 35.
¹H-NMR (CDCl₃) δ 1.06 (t, J=7.0 Hz, 3H), 3.40 (q, J=7.0 Hz, 2H), 3.78 (t, J=5.1 Hz, 2H), 4.78 (t, J=5.1 Hz, 2H), 7.15-7.27 (m, 2H), 7.54-7.66 (m, 4H), 10.11 (s, 1H).

Example 109

N²-{[1-(2-ethoxyethyl)-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 36 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.40 (d, J=7.0 Hz, 3H), 3.31-3.41 (m, 3H), 3.72 (t, J=5.0 Hz, 2H), 4.04 (d, J=14.8 Hz, 1H), 4.12 (d, J=14.8 Hz, 1H), 4.26-4.38 (m, 2H), 5.82 (brs, 1H), 7.11-7.15 (m, 2H), 7.22 (brs, 1H), 7.27 (d, J=6.6 Hz, 1H), 7.47 (d, J=10.7 Hz, 1H), 7.49-7.53 (m, 2H).

Reference Example 37

The object product was obtained in the same manner as in Reference Examples 9-11 from 4-bromo-2-fluoronitrobenzene, ethylamine and 4-fluorophenylboranic acid.
¹H-NMR (CDCl₃) δ 1.49 (t, J=7.2 Hz, 3H), 4.71 (q, J=7.2 Hz, 2H), 7.18 (t, J=8.5 Hz, 2H), 7.58-7.64 (m, 4H), 7.98 (d, J=9.3 Hz, 1H), 10.12 (s, 1H).

Example 110

N²-{[1-ethyl-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 37 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.42-1.48 (m, 6H), 3.32 (q, J=7.0 Hz, 1H), 4.03 (d, J=14.8 Hz, 1H), 4.11 (d, J=14.8 Hz, 1H), 4.24 (q, J=7.0 Hz, 2H), 5.60 (brs, 1H), 7.12-7.18 (m, 3H), 7.43-7.46 (m, 2H), 7.57-7.62 (m, 2H), 7.77 (m, 1H).

Reference Example 38

The object product was obtained in the same manner as in Reference Example 37 from 4-bromo-2,5-difluoronitrobenzene.
¹H-NMR (CDCl₃) δ 1.48 (t, J=7.2 Hz, 3H), 4.68 (q, J=7.2 Hz, 2H), 7.14-7.20 (m, 2H), 7.46 (d, J=6.6 Hz, 1H), 7.53-7.59 (m, 2H), 7.67 (d, J=10.5 Hz, 1H), 10.11 (s, 1H).

Example 111

N²-{[1-ethyl-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 38 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.42-1.46 (m, 6H), 3.31 (q, J=7.0 Hz, 1H), 4.01 (d, J=14.6 Hz, 1H), 4.08 (d, J=14.6 Hz, 1H), 4.20 (q, J=7.0 Hz, 2H), 5.41 (brs, 1H), 7.04 (brs, 1H), 7.13-7.18 (m, 2H), 7.28 (d, J=6.6 Hz, 1H), 7.49 (d, J=11.0 Hz, 1H), 7.52-7.55 (m, 2H).

Reference Example 39

To a solution of 2-chloro-6-fluoroaniline (2.5 g, 17.2 mmol) in chloroform (40 mL) was added bromine (2.75 g, 17.2 mmol), and the mixture was stirred at room temperature for 2 hr. The reaction mixture was poured into aqueous sodium thiosulfate solution, and the mixture was extracted with chloroform. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (hexane:ethyl acetate=9:1-3:1) to give the object product (3.21 g, 83%).
¹H-NMR (CDCl₃) δ 7.07 (dd, J=10.0, 2.0 Hz, 1H), 7.19 (t, J=2.0 Hz, 1H).

Reference Example 40

A solution of sodium peroxoborate tetrahydrate (11.0 g, 71.5 mmol) in acetic acid (50 mL) was heated to 55° C., and a solution of the compound (3.21 g, 14.3 mmol) obtained in Reference Example 39 in acetic acid (30 mL) was added dropwise over 1 hr. After stirring for 3 hr, the mixture was allowed to cool to room temperature and insoluble material was filtered off. The filtrate was poured into water, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column (hexane:ethyl acetate=90:10-5:1) to give the object product (1.30 g, 36%).
¹H-NMR (CDCl₃) δ 7.39 (dd, J=8.3, 2.0 Hz, 1H), 7.50 (t, J=2.0 Hz, 1H).

Reference Example 41

The object product was obtained in the same manner as in Reference Examples 9-11 from the compound obtained in Reference Example 40 and 4-fluorophenylboronic acid.
¹H-NMR (CDCl₃) δ 1.04 (t, J=7.0 Hz, 3H), 3.38 (q, J=7.0 Hz, 2H), 3.79 (t, J=5.1 Hz, 2H), 4.79 (t, J=5.1 Hz, 2H), 7.12-7.18 (m, 2H), 7.51-7.62 (m, 4H), 10.12 (s, 1H).

Example 112

N²-{[4-chloro-1-(2-ethoxyethyl)-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 41 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.40 (d, J=7.0 Hz, 3H), 3.30-3.41 (m, 3H), 3.74 (t, J=5.0 Hz, 2H), 4.07 (d, J=14.8 Hz, 1H), 4.15 (d, J=14.8 Hz, 1H), 4.30-4.44 (m, 2H), 5.65 (brs, 1H), 7.11-7.16 (m, 2H), 7.27 (brs, 1H), 7.35 (d, J=1.4 Hz, 1H), 7.46 (d, J=1.4 Hz, 1H), 7.53-7.57 (m, 2H).

Reference Example 42

The object product was obtained in the same manner as in Reference Example 40 from 4-bromo-2-fluoro-5-methylaniline.
¹H-NMR (CDCl₃) δ 2.43 (s, 3H), 7.48 (d, J=10.0 Hz, 1H), 7.93 (d, J=7.8 Hz, 1H).

Reference Example 43

The object product was obtained in the same manner as in Reference Example 41 from the compound obtained in Reference Example 42.
¹H-NMR (CDCl₃) δ 1.05 (t, J=7.0 Hz, 3H), 2.34 (s, 3H), 3.40 (q, J=7.0 Hz, 2H), 3.77 (t, J=5.4 Hz, 2H), 4.75 (t, J=5.4 Hz, 2H), 7.11-7.16 (m, 2H), 7.29-7.33 (m, 2H), 7.40 (s, 1H), 7.70 (s, 1H), 10.10 (s, 1H).

Example 113

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenyl)-5-methyl-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 43 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.41 (d, J=6.8 Hz, 3H), 2.33 (s, 3H), 3.30-3.42 (m, 3H), 3.71 (t, J=5.0 Hz, 2H), 4.05 (d, J=14.8 Hz, 1H), 4.13 (d, J=14.8 Hz, 1H), 4.22-4.38 (m, 2H), 5.43 (brs, 1H), 7.09-7.14 (m, 3H), 7.29-7.34 (m, 3H), 7.61 (s, 1H).

Reference Example 44

The object product was obtained in the same manner as in Reference Example 40 from 4-bromo-2,6-difluoroaniline.
¹H-NMR (CDCl₃) δ 7.28-7.32 (m, 2H).

Reference Example 45

The object product was obtained in the same manner as in Reference Example 41 from the compound obtained in Reference Example 44.
¹H-NMR (CDCl₃) δ 1.06 (t, J=7.0 Hz, 3H), 3.41 (q, J=7.0 Hz, 2H), 3.81 (t, J=5.3 Hz, 2H), 4.81 (t, J=5.3 Hz, 2H), 7.15-7.19 (m, 2H), 7.27 (dd, J=11.0, 1.6 Hz, 1H), 7.51 (d, J=1.6 Hz, 1H), 7.57-7.61 (m, 2H), 10.16 (s, 1H).

Example 114

N²-{[1-(2-ethoxyethyl)-4-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 45 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.11 (t, J=7.0 Hz, 3H), 1.42 (d, J=6.8 Hz, 3H), 3.32-3.45 (m, 3H), 3.77 (t, J=5.0 Hz, 2H), 4.08 (d, J=14.6 Hz, 1H), 4.18 (d, J=14.6 Hz, 1H), 4.31-4.46 (m, 2H), 6.00 (brs, 1H), 7.12-7.29 (m, 5H), 7.52-7.59 (m, 2H).

Reference Example 46

The object product was obtained in the same manner as in Reference Example 40 from 4-bromo-6-fluoro-3-trifluoromethylaniline.

Reference Example 47

The object product was obtained in the same manner as in Reference Example 41 from the compound obtained in Reference Example 46.
¹H-NMR (CDCl₃) δ 1.03 (t, J=7.0 Hz, 3H), 3.38 (q, J=7.0 Hz, 2H), 3.77 (t, J=5.1 Hz, 2H), 4.78 (t, J=5.1 Hz, 2H), 7.09-7.13 (m, 2H), 7.31-7.35 (m, 2H), 7.53 (s, 1H), 8.32 (s, 1H), 10.16 (s, 1H).

Example 115

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenyl)-5-(trifluoromethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 47 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.09 (t, J=7.0 Hz, 3H), 1.43 (d, J=7.0 Hz, 3H), 3.31-3.42 (m, 3H), 3.71 (t, J=5.0 Hz, 2H), 4.09 (d, J=15.0 Hz, 1H), 4.18 (d, J=15.0 Hz, 1H), 4.27-4.38 (m, 2H), 5.34 (brs, 1H), 7.10 (t, J=8.7 Hz, 2H), 7.13 (brs, 1H), 7.25 (s, 1H), 7.31-7.36 (m, 2H), 8.13 (s, 1H).

Reference Example 48

The object product was obtained in the same manner as in Reference Examples 1, 3, 4 and 11 from 2,5-difluoro-4-bromonitrobenzene, 4-aminotetrahydropyran hydrochloride and 4-fluorophenylboronic acid.
¹H-NMR (CDCl₃) δ 1.94 (m, 2H), 2.58 (m, 2H), 3.62 (m, 2H), 4.20 (m, 2H), 4.69 (m, 1H), 4.92 (s, 2H), 7.12-7.21 (m, 2H), 7.45 (d, 1H, J=10.6 Hz), 7.48-7.57 (m, 3H).

Reference Example 49

To a solution of the compound (0.82 g, 2.38 mmol) obtained in Reference Example 48 in dichloromethane (20 mL) were added diisopropylethylamine (2.12 ml, 11.9 mmol) and thionyl chloride (1 mol/L dichloromethane solution, 11.9 ml, 11.9 mmol). After heating under reflux for 1 hr, the mixture was cooled to 0° C. and water was added thereto. The mixture was neutralized with 2 mol/L aqueous sodium hydroxide solution, and extracted with chloroform. The organic layer was washed with water and saturated brine, dried over sodium sulfate, concentrated under reduced pressure, and the obtained residue was directly used for the next reaction.
¹H-NMR (CDCl₃) δ 1.96-2.05 (m, 2H), 2.55-2.70 (m, 2H), 3.58-3.66 (m, 2H), 4.19-4.24 (m, 2H), 4.61 (m, 1H), 4.88 (s, 2H), 7.15-7.22 (m, 2H), 7.50-7.57 (m, 4H).

Example 116

N²-{[5-fluoro-6-(4-fluorophenyl)-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

To a solution of the compound (0.16 g, 0.44 mmol) obtained in Reference Example 49 in tetrahydrofuran (5 mL) were added N-(2,4-dimethoxybenzyl)alaninamide (0.12 g, 0.49 mmol), diisopropylethylamine (0.12 ml, 0.66 mmol) and sodium iodide (0.07 g, 0.44 mmol). After heating under reflux for 2 hr, the mixture was allowed to cool to room temperature and water was added thereto. The mixture was extracted with chloroform, and the organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. To the residue was added trifluoroacetic acid (2 mL) and the mixture was heated to 50° C. After stirring for 1 hr, the mixture was cooled to 0° C., chloroform was added thereto, and the mixture was neutralized with 2 mol/L aqueous sodium hydroxide solution, and extracted with chloroform. The organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column (chloroform:methanol=99:1-85:15) and recrystallized from ethyl acetate-hexane to give the object product (0.09 mg, 50%). ¹H-NMR (CDCl₃) δ 1.40 (d, J=7.0 Hz, 3H), 1.86-1.89 (m, 2H), 2.49-2.64 (m, 2H), 3.32 (m, 1H), 3.53-3.61 (m, 2H), 4.11-4.20 (m, 4H), 4.53 (m, 1H), 5.43 (brs, 1H), 7.08 (brs, 1H), 7.12-7.18 (m, 2H), 7.43-7.52 (m, 4H).

Reference Example 50

The object product was obtained in the same manner as in Reference Examples 1-3 from 2,4-difluoronitrobenzene, 2-aminoethanol and 4-fluorophenol.
¹H-NMR (CDCl₃) δ 3.23 (t, J=4.8 Hz, 2H), 3.84 (t, J=4.8 Hz, 2H), 6.28 (d, J=7.8 Hz, 1H), 6.37 (d, J=2.4 Hz, 1H), 6.66 (d, J=7.8 Hz, 1H), 6.27-6.98 (m, 4H).

Reference Example 51

To a solution of the compound (2.7 g, 10.5 mmol) obtained in Reference Example 50 in N,N-dimethylformamide (50 mL) were added t-butyl-diphenylsilyl chloride (3.6 ml, 12.6 mmol) and imidazole (1.1 g, 15.8 mmol), and the mixture was stirred at room temperature. After stirring for 1 hr, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure, and the obtained residue was directly used for the next reaction.
¹H-NMR (CDCl₃) δ 1.05 (s, 9H), 3.16 (t, J=5.1 Hz, 2H), 3.87 (t, J=5.1 Hz, 2H), 6.24-6.28 (m, 2H), 6.65 (d, J=8.1 Hz, 1H), 6.82-6.94 (m, 4H), 7.31-7.43 (m, 6H), 7.62-7.72 (m, 4H).

Reference Example 52

The object product was obtained in the same manner as in Reference Examples 4 and 5 and Example 2 from the compound obtained in Reference Example 51 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.02 (s, 9H), 1.45 (d, J=6.8 Hz, 3H), 3.34 (q, J=6.8 Hz, 1H), 3.95 (t, J=5.4 Hz, 2H), 4.09 (d, J=14.9 Hz, 1H), 4.14 (d, J=14.9 Hz, 1H), 4.23-4.36 (m, 2H), 6.08 (brs, 1H), 6.87-6.93 (m, 3H), 7.00-7.05 (m, 3H), 7.18 (brs, 1H), 7.30-7.36 (m, 4H), 7.41-7.47 (m, 6H), 7.79 (d, J=8.8 Hz, 1H).

Example 117

N²-{[6-(4-fluorophenoxy)-1-(2-hydroxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

To a solution (4 mL) of the compound (1.2 g, 2.0 mmol) obtained in Reference Example 52 in THF was added tetrabutylammonium fluoride (1 mol/L tetrahydrofuran solution, 3.0 ml, 3.0 mmol), and the mixture was stirred at room temperature. After stirring for 1 hr, water was added thereto, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column (chloroform:methanol=99:1-85:15) and recrystallized from chloroform-hexane to give the object product (300 mg, 40%).
¹H-NMR (CDCl₃) δ 1.32 (d, J=7.0 Hz, 3H), 3.33 (q, J=7.0 Hz, 1H), 3.92-3.98 (m, 2H), 4.03 (d, J=13.6 Hz, 1H), 4.08 (d, J=13.6 Hz, 1H), 4.30 (t, J=4.6 Hz, 2H), 5.50 (brs, 1H), 6.78 (brs, 1H), 6.92-7.03 (m, 6H), 7.64 (d, J=8.8 Hz, 1H).

Reference Example 53

To a solution of the compound (1.0 g, 4.4 mmol) obtained in Reference Example 1 in N,N-dimethylformamide (44 mL) was added N-chlorosuccinimide (0.64 g, 4.8 mmol), and the mixture was heated to 40° C. After stirring overnight, the mixture was allowed to cool to room temperature. Water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by silica gel column (hexane:ethyl acetate=95:5-90:10-75:25-50:50) to give the object product (0.82 g, 72%).
¹H-NMR (CDCl₃) δ 1.22 (t, J=7.0 Hz, 3H), 3.41 (q, J=5.2 Hz, 2H), 3.55 (q, J=7.0 Hz, 2H), 3.69 (t, J=5.2 Hz, 2H), 6.62 (d, J=11.5 Hz, 1H), 8.27 (d, J=7.8 Hz, 1H), 8.31 (brs, 1H).

Reference Example 54

The object product was obtained in the same manner as in Reference Examples 2-5 from the compound obtained in Reference Example 53.
¹H-NMR (CDCl₃) δ 0.95 (t, J=7.0 Hz, 3H), 3.29 (q, J=7.0 Hz, 2H), 3.67 (t, J=5.0 Hz, 2H), 4.59 (t, J=5.0 Hz, 2H), 6.96-7.10 (m, 5H), 7.98 (s, 1H), 10.02 (s, 1H).

Example 118

N²-{[5-chloro-1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide

The object product was obtained in the same manner as in Example 2 from the compound obtained in Reference Example 54 and (L)-alaninamide hydrochloride.
¹H-NMR (CDCl₃) δ 1.05 (t, J=7.0 Hz, 3H), 1.40 (d, J=6.8 Hz, 3H), 3.29-3.38 (m, 3H), 3.63 (t, J=5.0 Hz, 2H), 4.01 (d, J=14.8 Hz, 1H), 4.10 (d, J=14.8 Hz, 1H), 4.15-4.28 (m, 2H), 5.68 (brs, 1H), 6.87-6.91 (m, 2H), 6.97-7.02 (m, 3H), 7.16 (brs, 1H), 7.80 (s, 1H).

Examples 119-190

The compounds of Examples 119-190 shown in Tables 17-31 were prepared according to the methods described in the above-mentioned Reference Examples and Examples or methods analogous thereto.

TABLE 17

Example	structural formula	¹H-NMR (CDCl₃) δ

119		1.40 (d, J = 7.0 Hz, 3H), 1.55 (m, 1H), 1.80-1.95 (m, 2H), 2.03 (m, 1H), 2.33 (s, 3H), 3.32 (q, J = 7.0 Hz, 1H), 3.70 (m, 1H), 3.80 (m, 1H), 4.01- 4.21 (m, 5H), 5.57 (brs, 1H), 6.87-7.01 (m, 4H), 7.12 (d, J = 8.3 Hz, 2H), 7.27 (brs, 1H), 7.65 (d, J = 8.3 Hz, 1H).

120		1.41 (d, J = 7.0 Hz, 3H), 1.57 (m, 1H), 1.84-1.95 (m, 2H), 2.05 (m, 1H), 3.32 (q, J = 7.0 Hz, 1H), 3.71 (m, 1H), 3.80 (m, 1H), 4.03-4.25 (m, 5H), 5.61 (brs, 1H), 6.94-7.00 (m, 3H), 7.03 (d, J = 2.4 Hz, 1H), 7.16 (d, J = 8.4 Hz, 2H), 7.23 (brs, 1H), 7.69 (d, J = 8.4 Hz, 1H).

121		1.41 (d, J = 7.0 Hz, 3H), 1.57 (m, 1H), 1.80-2.10 (m, 3H), 3.31 (q, J = 7.0 Hz, 1H), 3.66- 3.84 (m, 2H), 4.00-4.24 (m, 5H), 5.40 (br, 1H), 6.78-7.05 (m, 5H), 7.24 (br, 1H), 7.65 (d, J = 8.6 Hz, 1H).

122		1.43 (d, J = 7.0 Hz, 3H), 2.03 (m, 2H), 3.28-3.38 (m, 6H), 4.02 (d, J = 14.7 Hz, 1H), 4.08 (d, J = 14.7 Hz, 1H), 4.21 (t, J = 6.8 Hz, 2H), 5.47 (br, 1H), 6.66-6.84 (m, 2H), 6.96 (dd, J = 8.6, 2.2 Hz, 1H), 7.04 (d, J = 2.2 Hz, 1H), 7.10 (m, 1H), 7.20 (br, 1H), 7.69 (d, J = 8.8 Hz, 1H).

123		1.42 (d, J = 7.0 Hz, 3H), 2.02 (m, 2H), 3.25-3.36 (m, 6H), 4.00 (d, J = 14.7 Hz, 1H), 4.06 (d, J = 14.7 Hz, 1H), 4.19 (t, J = 6.8 Hz, 2H), 5.55 (br, 1H), 6.79-7.06 (m, 5H), 7.21 (br, 1H), 7,.64 (d, J = 8.6 Hz, 1H).

TABLE 18

Example	structural formula	¹H-NMR (CDCl₃) δ

124		1.41 (d, J = 6.8 Hz, 3H), 1.55 (m, 1H), 1.75-2.10 (m, 3H), 3.35 (q, J = 6.8 Hz, 1H), 3.66-3.84 (m, 2H), 4.00-4.30 (m, 5H), 5.45 (br, 1H), 6.70 (m, 1H), 6.80 (m, 1H), 6.95 (dd, J = 8.6, 2.2 Hz, 1H), 7.01 (d, J = 2.2 Hz, 1H), 7.09 (m, 1H), 7.21 (br, 1H), 7.68 (d, J = 8.6 Hz, 1H).

125		1.40 (d, J = 7.0 Hz, 3H), 1.55 (m, 1H), 1.80-2.10 (m, 3H), 3.34 (q, J = 7.0 Hz, 1H), 3.66-3.83 (m, 2H), 3.98-4.28 (m, 5H), 5.44 (br, 1H), 6.79- 7.05 (m, 5H), 7.22 (br, 1H), 7.64 (d, J = 8.6 Hz, 1H).

126		1.42 (d, J = 7.0 Hz, 3H), 2.01 (m, 2H), 2.33 (s, 3H), 3.28 (s, 3H), 3.28 (m, 2H), 3.33 (q, J = 7.0 Hz, 1H), 4.00 (d, J = 14.7 Hz, 1H), 4.07 (d, J = 14.7 Hz, 1H), 4.18 (t, J = 6.8 Hz, 2H), 5.50 (br, 1H), 6.87-7.02 (m, 4H), 7.12 (m, 2H), 7.23 (br, 1H), 7.64 (d, J = 8.6 Hz, 1H).

127		1.42 (d, J = 6.8 Hz, 3H), 2.03 (m, 2H), 3.28 (s, 3H), 3.28- 3.38 (m, 3H), 4.02 (d, J = 14.8 Hz, 1H), 4.08 (d, J = 14.8 Hz, 1H), 4.21 (t, J = 6.9 Hz, 2H), 5.56 (br, 1H), 6.95-7.00 (m, 3H), 7.05 (d, J = 2.2 Hz, 1H), 7.14-7.25 (m, 3H), 7.69 (d, J = 8.8 Hz, 1H).

128		1.40 (d, J = 7.0 Hz, 3H), 1.80- 1.95 (m, 2H), 2.50 (m, 2H), 3.28 (q, J = 7.0 Hz, 1H), 3.56 (m, 2H), 4.00-4.22 (m, 4H), 4.50 (m, 1H), 5.59 (br, 1H), 6.65-6.83 (m, 2H), 6.90 (br, 1H), 6.95 (dd, J = 8.8, 2.2 Hz, 1H), 7.10 (m, 1H), 7.28 (d, J = 2.2 Hz, 1H), 7.69 (d, J = 8.8 Hz, 1H).

TABLE 19

Example	structural formula	¹H-NMR (CDCl₃) δ

129		1.40 (d, J = 6.9 Hz, 3H), 1.78-1.86 (m, 2H), 2.33 (s, 3H), 2.43-2.58 (m, 2H), 3.28 (q, J = 6.9 Hz, 1H), 3.50- 3.59 (m, 2H), 4.00-4.19 (m, 4H), 4.47 (m, 1H), 5.72 (brs, 1H), 6.87-7.00 (m, 4H), 7.10- 7.14 (m, 2H), 7.27 (d, J = 2.2 Hz, 1H), 7.65 (d, J = 8.8 Hz, 1H).

130		1.40 (d, J = 6.9 Hz, 3H), 1.80-1.91 (m, 2H), 2.44-2.59 (m, 2H), 3.29 (q, J = 6.6 Hz, 1H), 3.50-3.60 (m, 2H), 4.01- 4.21 (m, 4H), 4.50 (m, 1H), 5.86 (brs, 1H), 6.92-7.00 (m, 4H), 7.14-7.20 (m, 2H), 7.31 (d, J = 2.0 Hz, 1H), 7.69 (d, J = 8.8 Hz, 1H).

131		1.40 (d, J = 6.9 Hz, 3H), 1.55 (m, 1H), 1.78-1.89 (m, 2H), 2.01 (m, 1H), 2.33 (s, 3H), 3.34 (q, J = 6.9 Hz, 1H), 3.71 (m, 1H), 3.79 (m, 1H), 3.98-4.27 (m, 5H), 5.57 (brs, 1H), 6.86-6.91 (m, 2H), 6.93-7.01 (m, 2H), 7.12 (d, J = 8.3 Hz, 2H), 7.27 (brs, 1H), 7.65 (d, J = 8.3 Hz, 1H).

132		1.41 (d, J = 6.9 Hz, 3H), 1.56 (m, 1H), 1.79-1.95 (m, 2H), 2.05 (m, 1H), 3.35 (q, J = 6.9 Hz, 1H), 3.70 (m, 1H), 3.80 (m, 1H), 3.99-4.21 (m, 4H), 4.25 (dd, J = 14.8, 2.8 Hz, 1H), 5.68 (brs, 1H), 6.94-7.00 (m, 3H), 7.03 (d, J = 2.2 Hz, 1H), 7.13-7.19 (m, 2H), 7.22 (brs, 1H), 7.69 (d, J = 8.5 Hz, 1H).

133		1.38 (d, J = 6.8 Hz, 3H), 2.03- 2.09 (m, 2H), 3.36-3.55 (m, 3H), 4.06 (d, J = 14.3 Hz, 1H), 4.13 (d, J = 14.3 Hz, 1H), 4.22- 4.41 (m, 2H), 5.72 (brs, 1H), 6.95-7.18 (m, 7H), 7.68 (d, J = 8.6 Hz, 1H).

TABLE 20

Example	structural formula	¹H-NMR (CDCl₃) δ

134		1.32 (d, J = 7.0 Hz, 3H), 3.35 (q, J = 7.0 Hz, 1H), 3.96 (t, J = 4.8 Hz, 2H), 4.04 (d, J = 14.0 Hz, 1H), 4.10 (d, J = 14.0 Hz, 1H), 4.32 (t, J = 4.8 Hz, 2H), 5.65 (brs, 1H), 6.85 (brs, 1H), 6.95-7.00 (m, 4H), 7.15- 7.18 (m, 2H), 7.65 (d, J = 9.4 Hz, 1H).

135		1.38 (t, J = 7.2 Hz, 3H), 1.47 (s, 6H), 2.34 (s, 3H), 3.97 (s, 2H), 4.10 (q, J = 7.2 Hz, 2H), 5.45 (br, 1H), 6.85-7.00 (m, 4H), 7.13 (m, 2H), 7.32 (br, 1H), 7.65 (d, J = 8.8 Hz, 1H).

136		1.00-1.28 (m, 4H), 1.48 (s, 6H), 3.18 (m, 1H), 4.08 (s, 2H), 5.58 (br, 1H), 6.90-7.05 (m, 5H), 7.15 (d, J = 2.4 Hz, 1H), 7.42 (br, 1H), 7.64 (d, J = 8.8 Hz, 1H).

137		1.46 (s, 6H), 1.57 (m, 1H), 1.80-2.10 (m, 3H), 3.67-3.84 (m, 2H), 3.96-4.25 (m, 5H), 5.33 (br, 1H), 6.82 (m, 1H), 6.89-7.04 (m, 4H), 7.45 (br, 1H), 7.65 (d, J = 8.6 Hz, 1H).

138		1.31 (t, J = 7.3 Hz, 3H), 1.47 (s, 6H), 3.97 (s, 2H), 4.11 (q, J = 7.3 Hz, 2H), 5.59 (br, 1H), 6.92-7.06 (m, 6H), 7.30 (br, 1H), 7.67 (m, 1H).

TABLE 21

Example	structural formula	¹H-NMR (CDCl₃) δ

139		1.39 (t, J = 7.1 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 3.32 (q, J = 6.8 Hz, 1H), 3.39 (d, J = 14.8 Hz, 1H), 4.06 (d, J = 14.8 Hz, 1H), 4.12 (m, 2H), 5.50 (br, 1H), 6.92-7.14 (m, 7H), 7.67 (m, 1H).

140		1.47 (s, 6H), 1.78-1.86 (m, 2H), 2.33 (s, 3H), 2.44-2.58 (m, 2H), 3.48-3.58 (m, 2H), 4.00 (s, 2H), 4.12-4.20 (m, 2H), 4.41 (m, 1H), 5.65 (brs, 1H), 6.86-6.91 (m, 2H), 6.94 (dd, J = 8.8, 2.2 Hz, 1H), 7.10-7.14 (m, 2H), 7.17 (brs, 1H), 7.26 (d, J = 2.2 Hz, 1H), 7.65 (d, J = 8.8 Hz, 1H).

141		1.09 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 3.39 (q, J = 7.0 Hz, 2H), 3.70 (t, J = 5.0 Hz, 2H), 4.03 (s, 2H), 4.26 (t, J = 5.0 Hz, 2H), 5.41 (br, 1H), 6.70 (m, 1H), 6.80 (m, 1H), 6.94-7.15 (m, 3H), 7.46 (br, 1H), 7.70 (d, J = 8.4 Hz, 1H).

142		1.47 (s, 6H), 2.02 (m, 2H), 2.33 (s, 3H), 3.28 (s, 3H), 3.28 (m, 2H), 3.98 (s, 2H), 4.18 (t, J = 6.9 Hz, 2H), 5.48 (br, 1H), 6.87-7.02 (m, 4H), 7.10 (d, J = 8.2 Hz, 2H), 7.44 (br, 1H), 7.65 (d, J = 8.6 Hz, 1H).

143		1.45 (s, 6H), 3.96 (t, J = 4.8 Hz, 2H), 4.01 (s, 2H), 4.30 (t, J = 4.8 Hz, 2H), 5.39 (brs, 1H), 6.92-7.05 (m, 7H), 7.65 (d, J = 8.6 Hz, 1H).

TABLE 22

Example	structural formula	¹H-NMR (CDCl₃) δ

144		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.8 Hz, 3H), 2.38 (s, 3H), 3.33-3.43 (m, 3H), 3.74 (t, J = 5.1 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.15 (d, J = 14.8 Hz, 1H), 4.31- 4.43 (m, 2H), 5.89 (brs, 1H), 7.26-7.32 (m, 4H), 7.48-7.55 (m, 3H), 7.76 (d, J = 8.3 Hz, 1H).

145		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.32- 3.42 (m, 3H), 3.76 (t, J = 5.1 Hz, 2H), 4.07 (d, J = 14.8 Hz, 1H), 4.15 (d, J = 14.8 Hz, 1H), 4.30-4.41 (m, 2H), 5.75 (brs, 1H), 7.25-7.32 (m, 3H), 7.45-7.47 (m, 2H), 7.63- 7.65 (m, 2H), 7.78 (d, J = 9.0 Hz, 1H).

146		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.8 Hz, 3H), 3.32- 3.42 (m, 3H), 3.76 (t, J = 5.0 Hz, 2H), 4.07 (d, J = 14.6 Hz, 1H), 4.16 (d, J = 14.6 Hz, 1H), 4.31-4.43 (m, 2H), 5.70 (brs, 1H), 7.25 (brs, 1H), 7.49-7.52 (m, 2H), 7.68-7.74 (m, 4H), 7.80 (d, J = 8.3 Hz, 1H).

147		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.31- 3.43 (m, 3H), 3.75 (t, J = 5.0 Hz, 2H), 4.08 (d, J = 14.7 Hz, 1H), 4.17 (d, J = 14.7 Hz, 1H), 4.30-4.43 (m, 2H), 5.73 (brs, 1H), 6.90-7.00 (m, 2H), 7.28-7.50 (m, 4H), 7.79 (d, J = 8.4 Hz, 1H).

148		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.34-3.43 (m, 3H), 3.76 (t, J = 5.0 Hz, 2H), 4.08 (d, J = 14.8 Hz, 1H), 4.15 (d, J = 14.8 Hz, 1H), 4.29- 4.43 (m, 2H), 5.98 (brs, 1H), 7.18-7.44 (m, 6H), 7.77 (d, J = 8.4 Hz, 1H).

TABLE 23

Example	structural formula	¹H-NMR (CDCl₃) δ

149		1.11 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 3.40 (q, J = 7.0 Hz, 2H), 3.77 (t, J = 5.0 Hz, 2H), 4.06 (s, 2H), 4.36 (t, J = 5.0 Hz, 2H), 5.47 (brs, 1H), 7.12-7.17 (m, 2H), 7.44-7.46 (m, 2H), 7.51 (brs, 1H), 7.57-7.60 (m, 2H), 7.78 (m, 1H).

150		1.01 (t, J = 7.4 Hz, 3H), 1.10 (t, J = 7.0 Hz, 3H), 1.69-1.87 (m, 2H), 3.16 (t, J = 6.3 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.76 (t, J = 5.0 Hz, 2H), 4.04 (d, J = 14.6 Hz, 1H), 4.16 (d, J = 14.6 Hz, 1H), 4.30-4.45 (m, 2H), 5.96 (brs, 1H), 7.11-7.16 (m, 2H), 7.21 (brs, 1H), 7.43-7.46 (m, 2H), 7.56- 7.60 (m, 2H), 7.77 (m, 1H).

151		1.00 (d, J = 7.0 Hz, 3H), 1.02 (d, J = 7.0 Hz, 3H), 1.10 (t, J = 7.0 Hz, 3H), 2.08 (m, 1H), 2.98 (d, J = 5.6 Hz, 1H), 3.40 (q, J = 7.0 Hz, 2H), 3.76 (q, J = 5.2 Hz, 2H), 4.02 (d, J = 14.4 Hz, 1H), 4.18 (d, J = 14.4 Hz, 1H), 4.31- 4.49 (m, 2H), 5.66 (brs, 1H), 7.09 (brs, 1H), 7.12-7.17 (m, 2H), 7.44-7.46 (m, 2H), 7.57-7.60 (m, 2H), 7.76 (m, 1H).

152		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.8 Hz, 3H), 2.45 (s, 3H), 3.32-3.42 (m, 3H), 3.76 (t, J = 5.1 Hz, 2H), 4.06 (d, J = 14.8 Hz, 1H), 4.15 (d, J = 14.8 Hz, 1H), 4.30-4.42 (m, 2H), 5.68 (brs, 1H), 7.16-7.52 (m, 7H), 7.77 (m, 1H).

153		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.29 (s, 3H), 3.33- 3.42 (m, 3H), 3.73 (t, J = 5.1 Hz, 2H), 4.08 (d, J = 14.8 Hz, 1H), 4.16 (d, J = 14.8 Hz, 1H), 4.26- 4.38 (m, 2H), 5.66 (brs, 1H), 7.22- 7.30 (m, 7H), 7.75 (m, 1H).

TABLE 24

Example	structural formula	¹H-NMR (CDCl₃) δ

154		1.45 (t, J = 7.0 Hz, 3H), 1.48 (s, 6H), 4.01 (s, 2H), 4.22 (q, J = 7.0 Hz, 2H), 5.82 (brs, 1H), 7.11- 7.17 (m, 2H), 7.34 (brs, 1H), 7.42-7.45 (m, 2H), 7.56-7.61 (m, 2H), 7.77 (m, 1H).

155		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 3.32-3.42 (m, 3H), 3.74 (t, J = 5.1 Hz, 2H), 4.08 (d, J = 14.6 Hz, 1H), 4.16 (d, J = 14.6 Hz, 1H), 4.29-4.41 (m, 2H), 5.41 (brs, 1H), 7.06 (m, 1H), 7.24-7.30 (m, 3H), 7.35-7.39 (m, 2H), 7.77 (d, J = 8.3 Hz, 1H).

156		1.10 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 3.40 (q, J = 7.0 Hz, 2H), 3.75 (t, J = 5.1 Hz, 2H), 4.07 (s, 2H), 4.34 (t, J = 5.1 Hz, 2H), 5.37 (brs, 1H), 7.06 (m, 1H), 7.24-7.39 (m, 5H), 7.77 (d, J = 8.3 Hz, 1H).

157		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.27 (s, 3H), 3.33-3.42 (m, 3H), 3.73 (t, J = 5.4 Hz, 2H), 4.08 (d, J = 15.4 Hz, 1H), 4.15 (d, J = 15.4 Hz, 1H), 4.27-4.40 (m, 2H), 5.35 (brs, 1H), 6.92-7.01 (m, 2H), 7.17-7.25 (m, 3H), 7.29 (brs, 1H), 7.34 (d, J = 8.3 Hz, 1H).

158		1.11 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 2.26 (s, 3H), 3.40 (q, J = 7.0 Hz, 2H), 3.74 (t, J = 5.0 Hz, 2H), 4.07 (s, 2H), 4.33 (t, J = 5.0 Hz, 2H), 5.47 (brs, 1H), 6.92- 7.01 (m, 2H), 7.17-7.27 (m, 3H), 7.54 (brs, 1H), 7.75 (d, J = 8.3 Hz, 1H).

TABLE 25

Example	structural formula	¹H-NMR (CDCl₃) δ

159		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 2.26 (s, 3H), 2.38 (s, 3H), 3.32-3.42 (m, 3H), 3.72 (t, J = 5.1 Hz, 2H), 4.07 (d, J = 14.6 Hz, 1H), 4.15 (d, J = 14.6 Hz, 1H), 4.26-4.38 (m, 2H), 5.81 (brs, 1H), 7.07-7.27 (m, 5H), 7.33 (brs, 1H), 7.73 (d, J = 8.3 Hz, 1H).

160		1.10 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 2.26 (s, 3H), 2.38 (s, 3H), 3.39 (q, J = 7.0 Hz, 2H), 3.73 (t, J = 5.1 Hz, 2H), 4.06 (s, 2H), 4.32 (t, J = 5.1 Hz, 2H), 5.49 (brs, 1H), 7.06-7.26 (m, 5H), 7.55 (brs, 1H), 7.75 (d, J = 8.3 Hz, 1H).

161		1.11 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 2.32 (s, 3H), 2.36 (s, 3H), 3.31-3.43 (m, 3H), 3.76 (t, J = 5.0 Hz, 2H), 4.07 (d, J = 14.9 Hz, 1H), 4.16 (d, J = 14.9 Hz, 1H), 4.29-4.44 (m, 2H), 5.36 (brs, 1H), 7.23 (m, 1H), 7.36 (brs, 1H), 7.30-7.51 (m, 4H), 7.76 (d, J = 9.0 Hz, 1H).

162		1.10 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 2.32 (s, 3H), 2.36 (s, 3H), 3.39 (q, J = 7.0 Hz, 2H), 3.77 (t, J = 5.0 Hz, 2H), 4.06 (s, 2H), 4.36 (t, J = 5.0 Hz, 2H), 5.28 (brs, 1H), 7.22 (m, 1H), 7.37-7.51 (m, 4H), 7.55 (brs, 1H), 7.77 (d, J = 8.6 Hz, 1H).

163		1.01 (t, J = 7.5 Hz, 3H), 1.10 (t, J = 7.0 Hz, 3H), 1.65-1.85 (m, 2H), 2.32 (s, 3H), 2.36 (s, 3H), 3.16 (t, J = 6.3 Hz, 1H), 3.39 (q, J = 7.0 Hz, 2H), 3.76 (t, J = 5.2 Hz, 2H), 4.05 (d, J = 14.7 Hz, 1H), 4.16 (d, J = 14.7 Hz, 1H), 4.29-4.46 (m, 2H), 5.42 (brs, 1H), 7.22 (m, 2H), 7.36-7.52 (m, 4H), 7.76 (d, J = 9.0 Hz, 1H).

TABLE 26

Example	structural formula	¹H-NMR (CDCl₃) δ

164		1.09 (t, J = 7.0 Hz, 3H), 1.43 (d, J = 7.1 Hz, 3H), 2.01 (s, 6H), 2.35 (s, 3H), 3.33-3.41 (m, 3H), 3.76 (t, J = 5.0 Hz, 2H), 4.07 (d, J = 14.8 Hz, 1H), 4.14 (d, J = 14.8 Hz, 1H), 4.24-4.36 (m, 2H), 5.37 (brs, 1H), 6.97 (s, 2H), 7.04 (dd, J = 8.0, 1.6 Hz, 1H), 7.10 (d, J = 1.6 Hz, 1H), 7.32 (brs, 1H), 7.76 (d, J = 8.0 Hz, 1H).

165		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.41 (s, 3H), 3.31-3.43 (m, 3H), 3.75 (t, J = 5.1 Hz, 2H), 4.07 (d, J = 14.7 Hz, 1H), 4.16 (d, J = 14.7 Hz, 1H), 4.28-4.42 (m, 2H), 5.33 (brs, 1H), 6.98-7.06 (m, 2H), 7.27 (brs, 1H), 7.35-7.49 (m, 3H), 7.78 (d, J = 8.4 Hz, 1H).

166		1.10 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 2.41 (s, 3H), 3.39 (q, J = 7.0 Hz, 2H), 3.76 (t, J = 5.1 Hz, 2H), 4.07 (s, 2H), 4.35 (t, J = 5.1 Hz, 2H), 5.31 (brs, 1H), 6.96-7.05 (m, 2H), 7.35-7.49 (m, 3H), 7.52 (brs, 1H), 7.78 (d, J = 8.4 Hz, 1H).

167		1.11 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.36 (s, 3H), 3.31-3.44 (m, 3H), 3.76 (t, J = 5.2 Hz, 2H), 4.07 (d, J = 14.8 Hz, 1H), 4.16 (d, J = 14.8 Hz, 1H), 4.28-4.44 (m, 2H), 5.37 (brs, 1H), 7.08 (t, J = 8.9 Hz, 1H), 7.37-7.46 (m, 5H), 7.77 (d, J = 9.0 Hz, 1H).

168		1.11 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 2.36 (s, 3H), 3.40 (q, J = 7.0 Hz, 2H), 3.77 (t, J = 5.0 Hz, 2H), 4.06 (s, 2H), 4.36 (t, J = 5.0 Hz, 2H), 5.30 (brs, 1H), 7.08 (t, J = 8.8 Hz, 1H), 7.36- 7.46 (m, 4H), 7.51 (brs, 1H), 7.77 (d, J = 8.1 Hz, 1H).

TABLE 27

Example	structural formula	¹H-NMR (CDCl₃) δ

169		1.11 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.33 (s, 3H), 3.31-3.44 (m, 3H), 3.76 (t, J = 5.0 Hz, 2H), 4.07 (d, J = 14.8 Hz, 1H), 4.16 (d, J = 14.8 Hz, 1H), 4.29- 4.44 (m, 2H), 5.42 (brs, 1H), 7.23-7.33 (m, 4H), 7.42-7.49 (m, 2H), 7.77 (d, J = 8.8 Hz, 1H).

170		1.11 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 2.33 (s, 3H), 3.40 (q, J = 7.0 Hz, 2H), 3.77 (t, J = 5.0 Hz, 2H), 4.07 (s, 2H), 4.36 (t, J = 5.0 Hz, 2H), 5.35 (brs, 1H), 7.22-7.33 (m, 4H), 7.46-7.49 (m, 2H), 7.78 (d, J = 9.0 Hz, 1H).

171		1.09 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 3.34- 3.42 (m, 3H), 3.75 (t, J = 5.1 Hz, 2H), 4.09 (d, J = 14.8 Hz, 1H), 4.16 (d, J = 14.8 Hz, 1H), 4.29-4.41 (m, 2H), 5.67 (brs, 1H), 7.14-7.16 (m, 2H), 7.23-7.30 (m, 2H), 7.41- 7.52 (m, 2H), 7.80 (d, J = 8.5 Hz, 1H).

172		1.10 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.31- 3.42 (m, 3H), 3.74 (t, J = 5.1 Hz, 2H), 3.81 (s, 3H), 4.07 (d, J = 14.8 Hz, 1H), 4.15 (d, J = 14.8 Hz, 1H), 4.28- 4.40 (m, 2H), 5.37 (brs, 1H), 6.73-6.78 (m, 2H), 7.28-7.41 (m, 4H), 7.75 (d, J = 8.3 Hz, 1H).

173		1.11 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.32-3.43 (m, 3H), 3.76 (t, J = 5.0 Hz, 2H), 3.98 (s, 3H), 4.08 (d, J = 14.8 Hz, 1H), 4.16 (d, J = 14.8 Hz, 1H), 4.31-4.43 (m, 2H), 5.40 (brs, 1H), 7.13-7.20 (m, 4H), 7.44-7.46 (m, 2H), 7.78 (d, J = 9.0 Hz, 1H).

TABLE 28

Example	structural formula	¹H-NMR (CDCl₃) δ

174		1.11 (t, J = 7.0 Hz, 3H), 1.47 (s, 6H), 3.39 (q, J = 7.0 Hz, 2H), 3.75 (t, J = 5.1 Hz, 2H), 3.81 (s, 3H), 4.06 (s, 2H), 4.33 (t, J = 5.1 Hz, 2H), 5.36 (brs, 1H), 6.72-6.78 (m, 2H), 7.28-7.40 (m, 3H), 7.53 (brs, 1H), 7.75 (d, J = 8.3 Hz, 1H).

175		1.11 (t, J = 7.0 Hz, 3H), 1.48 (s, 6H), 3.39 (q, J = 7.0 Hz, 2H), 3.77 (t, J = 5.1 Hz, 2H), 3.98 (s, 3H), 4.07 (s, 2H), 4.37 (t, J = 5.1 Hz, 2H), 5.29 (brs, 1H), 7.14-7.20 (m, 4H), 7.44-7.51 (m, 2H), 7.78 (d, J = 8.0 Hz, 1H).

176		1.09 (t, J = 7.0 Hz, 3H), 1.41 (t, J = 7.0 Hz, 3H), 3.32- 3.42 (m, 3H), 3.71 (t, J = 5.1 Hz, 2H), 4.05 (d, J = 14.6 Hz, 1H), 4.14 (d, J = 14.6 Hz, 1H), 4.23-4.38 (m, 2H), 5.39 (brs, 1H), 7.11-7.17 (m, 3H), 7.21 (brs, 1H), 7.41- 7.45 (m, 2H), 7.83 (s, 1H).

177		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.31- 3.43 (m, 3H), 3.71 (t, J = 5.0 Hz, 2H), 4.07 (d, J = 14.8 Hz, 1H), 4.17 (d, J = 14.8 Hz, 1H), 4.24-4.39 (m, 2H), 5.60 (brs, 1H), 7.24-7.47 (m, 7H), 7.84 (s, 1H).

178		1.10 (t, J = 7.0 Hz, 3H), 1.43 (d, J = 7.0 Hz, 3H), 2.44 (s, 3H), 3.32-3.42 (m, 3H), 3.71 (t, J = 5.0 Hz, 2H), 4.07 (d, J = 14.8 Hz, 1H), 4.15 (d, J = 14.8 Hz, 1H), 4.25- 4.38 (m, 2H), 5.61 (brs, 1H), 7.26-7.39 (m, 6H), 7.83 (s, 1H).

TABLE 29

Example	structural formula	¹H-NMR (CDCl₃) δ

179		1.08 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.30-3.41 (m, 3H), 3.70 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 15.1 Hz, 1H), 4.13 (d, J = 15.1 Hz, 1H), 4.24- 4.36 (m, 2H), 5.67 (brs, 1H), 6.90-6.98 (m, 2H), 7.21 (brs, 1H), 7.28-7.34 (m, 2H), 7.84 (s, 1H).

180		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.30-3.41 (m, 3H), 3.71 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.25- 4.37 (m, 2H), 5.68 (brs, 1H), 7.15-7.30 (m, 5H), 7.81 (s, 1H).

181		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 7.0 Hz, 3H), 3.30-3.42 (m, 3H), 3.70 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 15.0 Hz, 1H), 4.14 (d, J = 15.0 Hz, 1H), 4.23- 4.38 (m, 2H), 5.63 (brs, 1H), 7.20 (brs, 1H), 7.26-7.30 (m, 3H), 7.47-7.50 (m, 2H), 7.83 (s, 1H).

182		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.37-3.44 (m, 3H), 3.72 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.14 (d, J = 14.8 Hz, 1H), 4.25- 4.35 (m, 2H), 7.31 (m, 1H), 7.56- 7.59 (m, 2H), 7.70-7.73 (m, 2H), 7.84 (s, 1H).

183		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.31-3.43 (m, 3H), 3.74 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.14 (d, J = 14.8 Hz, 1H), 4.28- 4.40 (m, 2H), 5.54 (brs, 1H), 7.18 (brs, 1H), 7.21-7.29 (m, 3H), 7.39 (m, 1H), 7.49 (s, 1H).

TABLE 30

Example	structural formula	¹H-NMR (CDCl₃) δ

184		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.42 (s, 3H), 3.31-3.42 (m, 3H), 3.73 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.26- 4.38 (m, 2H), 5.56 (brs, 1H), 7.24 (brs, 1H), 7.26-7.30 (m, 3H), 7.46-7.50 (m, 3H).

185		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 3.31- 3.42 (m, 3H), 3.73 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.27-4.39 (m, 2H), 5.58 (brs, 1H), 7.23 (brs, 1H), 7.32 (d, J = 6.3 Hz, 1H), 7.39 (m, 1H), 7.45-7.51 (m, 3H), 7.57-7.59 (m, 2H).

186		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 3.31- 3.42 (m, 3H), 3.73 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.27-4.39 (m, 2H), 5.36 (brs, 1H), 7.20 (brs, 1H), 7.29 (d, J = 6.6 Hz, 1H), 7.42- 7.44 (m, 3H), 7.48-7.52 (m, 2H).

187		1.45 (t, J = 7.0 Hz, 3H), 1.48 (s, 6H), 3.99 (s, 2H), 4.20 (q, J = 7.0 Hz, 2H), 5.50 (brs, 1H), 7.13-7.18 (m, 2H), 7.28 (d, J = 6.6 Hz, 1H), 7.49 (d, J = 11.0 Hz, 1H), 7.52- 7.56 (m, 2H).

188		1.11 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 7.0 Hz, 3H), 2.35 (s, 3H), 3.30-3.43 (m, 3H), 3.73 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.14 (d, J = 14.8 Hz, 1H), 4.27-4.39 (m, 2H), 5.35 (brs, 1H), 7.09 (t, J = 8.8 Hz, 1H), 7.23 (brs, 1H), 7.34-7.39 (m, 3H), 7.48 (d, J = 10.8 Hz, 1H).

TABLE 31

Example	structural formula	¹H-NMR (CDCl₃) δ

189		1.10 (t, J = 7.0 Hz, 3H), 1.42 (d, J = 6.8 Hz, 3H), 2.34 (s, 3H), 3.31-3.42 (m, 3H), 3.73 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.28-4.40 (m, 2H), 5.42 (brs, 1H), 7.22-7.31 (m, 5H), 7.49 (d, J = 10.7 Hz, 1H).

190		1.09 (t, J = 7.0 Hz, 3H), 1.41 (d, J = 6.8 Hz, 3H), 2.33 (s, 3H), 3.31-3.41 (m, 3H), 3.71 (t, J = 5.0 Hz, 2H), 4.05 (d, J = 14.8 Hz, 1H), 4.13 (d, J = 14.8 Hz, 1H), 4.24-4.36 (m, 2H), 5.41 (brs, 1H), 7.07-7.26 (m, 5H), 7.60 (s, 1H).

Reference Example 55

To a solution of the compound (1.4 g, 5.0 mmol) obtained in the same manner as in Reference Examples 9 and 10 from 2-fluoro-5-bromo-nitrobenzene in tetrahydrofuran (30 mL) were added anhydrous sodium sulfate (3.8 g, 26.8 mmol), triethylamine (2.1 ml, 15.4 mmol) and (L)-alaninamide hydrochloride (1.9 g, 15.2 mmol), and the mixture was stirred at room temperature for 30 min. Sodium cyanoborohydride (0.33 g, 5.2 mmol) was added to the reaction mixture, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated. The residue was purified by silica gel column (dichloromethane:methanol=99:1-95:5) to give the object product (0.89 g, 51%).

Reference Example 56

To a solution of the compound (0.48 g, 1.3 mmol) obtained in Reference Example 55 in dichloroethane (10 mL) were added di-tert-butyl bicarbonate (1.4 g, 6.5 mmol) and diisopropylethylamine (0.33 ml, 1.95 mmol), and the mixture was stirred at 80° C. for 14 hr. Dichloromethane was added to the reaction mixture, and the mixture was washed with water and saturated brine. The organic layer was dried over sodium sulfate, and concentrated. The residue was purified by silica gel column (dichloromethane:methanol=99:1-97:3) to give the object product (500 mg, 82%).

Reference Example 57

To a solution (3:1, 4 mL) of the compound (50 mg, 0.11 mmol) obtained in Reference Example 56 in aqueous acetonitrile were added 4-chlorophenylboranic acid (34 mg, 0.22 mmol), 3 mol/L aqueous sodium hydrogen carbonate solution (90 μl) and tetrakis(triphenylphosphine)palladium (13 mg, 0.00112 mmol), and the mixture was stirred at 85° C. for 5 hr under an argon atmosphere. The reaction mixture was filtered through celite, and the filtrate was concentrated. Ethyl acetate and saturated aqueous sodium hydrogen carbonate solution were added to partition the residue. The organic layer was washed with water, dried and concentrated. The residue was purified by silica gel column (ethyl acetate alone) to give the object product (48 mg, 90%).

Example 191

N²-{[5-(4-chlorophenyl)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide hydrochloride

A solution (3 mL) of the compound (48 mg, 0.10 mmol) obtained in Reference Example 57 in hydrochloric acid-dioxane was stirred at room temperature for 1 hr. The reaction mixture was concentrated, and the resulting powder was washed with diethyl ether to give the object product (25 mg, 76%).

Example 192

N²-{[1-(2-ethoxyethyl)-5-(4-methoxyphenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide trifluoroacetate

To a solution (3 mL) of the compound (62 mg, 0.13 mmol) obtained in the above-mentioned Reference Example in dichloromethane was added trifluoroacetic acid (0.3 mL) under ice-cooling. The mixture was allowed to warm to room temperature and stirred for 1 hr. The reaction mixture was concentrated and crystallized from diethyl ether to give the object product (48 mg, 76%).

Example 193-208

The compounds shown in Table 32 were prepared according to the methods described in the above-mentioned Reference Examples and Examples or methods analogous thereto.
The compounds were identified by LC/MS spectrum and retention time according to any of the following methods.

Analysis Conditions 1

detection instrument: LCMS/MS API2000 (manufactured by Applied Biosystems)
column: Phenomenex Gemini C18 4.6×50 mm, 5 μm
detection wavelength: 220 nm, 260 nm
flow rate: 1.2 mL/min
elution solvent composition: SOLUTION A: 0.05% aqueous TFA solution, 0.05% aqueous HCOOH solution or 10 mM aqueous ammonium acetate solution, SOLUTION B: acetonitrile
gradient: 0-0.01 min B 10%, 0.01-1.50 min B 10% to 30%, 1.50-3.00 min B 30% to 90%, 3.00-4.00 min B 90%, 4.00-5.00 min B 90% to 10%

Analysis Conditions 2

detection instrument: LCMS/MS API2000 (manufactured by Applied Biosystems)
column: Phenomenex Gemini C18 4.6×50 mm, 5 μm
detection wavelength: 220 nm, 260 nm
flow rate: 1 mL/min
elution solvent composition: SOLUTION A: 0.05% aqueous TFA solution, 0.05% aqueous HCOOH solution or 10 mM aqueous ammonium acetate solution, SOLUTION B: acetonitrile
gradient: 0-0.01 min B 5%, 0.01-1.00 min B 5%, 1.00-7.00 min B 5% to 50%, 7.00-10.00 min B 50% to 90%, 10.00-11.00 min B 90%, 11.00-12.00 min B 90% to 5%

TABLE 32

			molecular		retention	analysis
Example	R	salt	weight	m/e	time	conditions

191		HCl	400.1666	401.4	2.74	analysis conditions 1 MeCN—TFA

192		CF₃CO₂H	396.2161	397.4	2.61	analysis conditions 1 MeCN—TFA

193		HCl	366.2056	367.4	3.86	analysis conditions 1 MeCN—TFA

194		CF₃CO₂H	380.2212	381.4	6.29	analysis conditions 2 MeCN—TFA

195		HCl	394.2369	395.4	2.77	analysis conditions 1 MeCN—TFA

196		HCl	408.2525	409.4	2.84	analysis conditions 1 MeCN—TFA

197		HCl	384.1962	385.2	5.94	analysis conditions 2 MeCN—TFA

198		HCl	384.1962	385.2	5.94	analysis conditions 2 MeCN—TFA

199		HCl	402.1867	403.2	6.1	analysis conditions 2 MeCN—TFA

200		CF₃CO₂H	402.1867	403.4	2.75	analysis conditions 1 MeCN—TFA

201		HCl	420.1773	421.4	2.76	analysis conditions 1 MeCN—TFA

202		HCl	420.1773	421.2	6.25	analysis conditions 2 MeCN—TFA

203		HCl	410.2318	411.4	2.7	analysis conditions 1 MeCN—TFA

204		CF₃CO₂H	450.1879	451.2	2.78	analysis conditions 1 MeCN—TFA

205		CF₃CO₂H	434.193	435.4	2.79	analysis conditions 1 MeCN—TFA

206		HCl	420.1773	421.2	2.71	analysis conditions 1 MeCN—TFA

207		HCl	367.2008	368.6	5.99	analysis conditions 2 MeCN—TFA

208		HCl	391.2008	392.2	5.63	analysis conditions 2 MeCN—TFA

Reference Example 58

To a solution (25 mL) of iron (3.7 g, 66 mmol) and ammonium chloride (1.04 g, 19 mmol) in a mixed solvent (3:2:1) of tetrahydrofuran-methanol-water was added dropwise a solution (25 mL) of the compound (1.7 g, 6.9 mmol) obtained in Reference Example 18 in a mixed solvent (3:2:1) of tetrahydrofuran-methanol-water at 70° C. After 1.5 hr, the mixture was allowed to cool to room temperature, and the reaction mixture was filtered through celite. The filtrate was concentrated, water was added thereto, and the mixture was extracted with ethyl acetate. The organic layer was washed with water, dried and concentrated to give the object product (1.32 g, 89%). The product was used for the next reaction without purification.

Reference Example 59

The object product was obtained in the same manner as in Reference Examples 4, 5, 55 and 56.

Reference Example 60

To a solution of the compound (60 mg, 0.14 mmol) obtained in Reference Example 59 and 4-methylphenylboronic acid (38 mg, 0.28 mmol) in n-butanol (2 mL) were added potassium phosphate (60 mg, 0.28 mmol), palladium acetate (3.2 mg, 0.014 mmol) and S-phos (11.6 mg, 0.0038 mmol), and the mixture was stirred at 100° C. for 14 hr under an argon atmosphere. After cooling, the reaction mixture was filtered through celite, and washed with methanol. The filtrate was concentrated, ethyl acetate was added thereto, and the mixture was washed with saturated aqueous sodium hydrogen carbonate solution and saturated brine, dried and concentrated. The residue was purified by silica gel column (ethyl acetate:hexane=65:35) to give the object product (43 mg, 52%).

Example 209

N²-{[3-(2-ethoxyethyl)-5-(4-methylphenyl)-3H-imidazo[4,5-b]pyridin-2-yl]methyl}-L-alaninamide hydrochloride

To a solution of the compound (34 mg) obtained in Reference Example 60 in dioxane (1 mL) was added 4 mol/L hydrochloric acid-dioxane (2 mL) under ice-cooling. The mixture was allowed to warm to room temperature, and stirred for 10 hr. The reaction mixture was concentrated, and the resulting powder was washed with diethyl ether to give the object product (28 mg, 95%).

Examples 210-226

The compounds shown in Table 33 were prepared according to the methods described in the above-mentioned Reference Examples and Examples or methods analogous thereto.
The compounds were identified by LC/MS spectrum and retention time under the conditions similar to those described above.

TABLE 33

			molecular		retention	analysis
Example	R	salt	weight	m/e	time	conditions

209		HCl	381.2165	382.3	6.15	analysis conditions 2 MeCN—TFA

210		HCl	367.2008	368.5	3.04	analysis conditions 1 MeCN—NH₄OAc

211		HCl	395.2321	396.4	2.79	analysis conditions 1 MeCN—TFA

212		HCl	409.2478	410.2	2.86	analysis conditions 1 MeCN—TFA

213		HCl	385.1914	386.4	3.12	analysis conditions 1 MeCN—NH₄OAc

214		HCl	385.1914	386.2	2.63	analysis conditions 1 MeCN—TFA

215		HCl	385.1914	386.2	2.63	analysis conditions 1 MeCN—TFA

216		HCl	403.182	404.2	2.6	analysis conditions 1 MeCN—TFA

217		HCl	403.182	404.4	2.71	analysis conditions 1 MeCN—TFA

218		HCl	421.1726	422.2	2.71	analysis conditions 1 MeCN—TFA

219		HCl	421.1726	422.1	6.25	analysis conditions 2 MeCN—TFA

220		HCl	397.2114	398.2	2.67	analysis conditions 1 MeCN—TFA

221		HCl	411.227	412.4	6.22	analysis conditions 2 MeCN—TFA

222		HCl	435.1882	436.6	2.79	analysis conditions 1 MeCN—TFA

223		HCl	451.1831	452.2	6.85	analysis conditions 2 MeCN—TFA

224		HCl	392.1961	393.4	2.61	analysis conditions 1 MeCN—TFA

225		HCl	421.1726	422	2.65	analysis conditions 1 MeCN—TFA

226		HCl	368.1961	369.6	5.34	analysis conditions 2 MeCN—TFA

Example 227-237

The compounds of Examples 227-237 shown in Table 34 and Table 35 were prepared in the same manner as in Reference Examples 18-20 and Example 79.
The compounds were identified by LC/MS spectrum and retention time under the conditions similar to those described above.

TABLE 34

		molecular		retention	analysis
Example	R	weight	m/e	time	conditions

227		401.1863	402	2.64	analysis conditions 1 MeCN—TFA

228		417.1568	418	2.72	analysis conditions 1 MeCN—TFA

229		397.2114	398.2	2.67	analysis conditions 1 MeCN—TFA

230		419.1769	420.2	2.68	analysis conditions 1 MeCN—TFA

231		419.1769	420.2	2.67	analysis conditions 1 MeCN—TFA

232		437.1675	438	2.68	analysis conditions 1 MeCN—TFA

TABLE 35

		molecular		retention	analysis
Example	R	weight	m/e	time	conditions

233		383.1758	384.2	2.71	analysis conditions 1 MeCN—TFA

234		379.2008	380.4	2.78	analysis conditions 1 MeCN—TFA

235		401.1663	402.2	2.71	analysis conditions 1 MeCN—TFA

236		401.1663	402.2	2.72	analysis conditions 1 MeCN—TFA

237		419.1569	419.9	2.75	analysis conditions 1 MeCN—TFA

The compounds shown in Tables 36-38 can be prepared according to the methods described in the above-mentioned Reference Examples and Examples or methods analogous thereto.

TABLE 36

	No.	R²

	1

	2

	3

TABLE 37

	No.	R²

	4

	5

	6

TABLE 38

	No.	R²

	7

	8

	9

	10

	11

	12

	13

	14

	15

	16

	17

	18

	19

	20

	21

Experimental Example 1

Inhibition Experiment of TTX Resistant Na Channel on Human SNS Gene-Expressing Cell

Human SNS gene-expressing cell is obtained by incorporating human SNS gene into Chinese hamster ovary cell (CHO-K1) and allowing stable expression. Since CHO-K1 cell does not inherently have a TTX resistant Na channel component, TTX resistant Na channel component of human SNS gene-expressing cell is SNS and the compound of the present invention is considered an SNS inhibitor.

1) Construction of Human SNS-Expressing Cell and Confirmation Of Expression of SNS Function

Full-length human SNS α subunit gene was incorporated into an expression plasmid (pcDNA3.1Zeo(+)) having a Zeocin resistance gene, and full-length Annexin II light chain gene was introduced into an expression plasmid (pcDNA3.1 (+)) containing a Neomycin resistance gene. These two genes were simultaneously introduced into CHO-K1 cell by using lipofectamine 2000, cultured in F-12 medium containing Neomycin and Zeocin, and a cell resistant to the both drugs, namely, a cell harboring the both genes, was selected. The two drug-resistance strain was subjected to limiting dilution twice, and the SNS gene-incorporating cell was cloned. Transgenic SNS was confirmed by RT-PCR, a TTX resistant component responsive to Na channel stimulation was detected by using a membrane potential sensitive fluorescent indicator, and functional expression of SNS was confirmed.

2) Pharmacological Effect on TTX Resistant Na Channel of Human SNS Gene-Expressing Cell

Using the human SNS-expressing cell obtained in the aforementioned 1, the SNS inhibitory action of the compound of the present invention was evaluated. To be specific, a test compound was added in advance to a human SNS-expressing cell, veratridine (50 μM), an Na channel stimulant, was added about 30 min later in the presence of TTX (1 μM), the membrane potencial was increased via the TTX resistant Na channel, and the suppressive action on the membrane potencial increase of the test compound was evaluated.

3) Pharmacological Evaluation Method

SNS inhibitory rate of the test compound was determined by the following calculation formula.
SNS inhibitory rate (%)=100×[(peak value by veratridine stimulation alone without test compound)−(peak value by veratridine stimulation with test compound)]/[(peak value by veratridine stimulation alone without test compound)−(standard value without stimulation)]

4) Test Results

The compounds obtained in the Examples were evaluated for an inhibitory action (SNS inhibitory rate) on TTX resistant Na channel of human SNS-expressing cell. As a result, the compound of the present invention was observed to show an SNS inhibitory action. The SNS inhibitory rate (%) when the compound concentration was 12.5 μM is shown in Tables 39-47.

	TABLE 39

	compound	SNS inhibitory rate (%)

	Example 1	45.8
	Example 2	8.4
	Example 3	12.9
	Example 4	66.8
	Example 5	59.3
	Example 6	77.8
	Example 7	83.1
	Example 8	90.4
	Example 9	28.9
	Example 10	16.3
	Example 11	63.0
	Example 12	17.0
	Example 13	29.8
	Example 14	16.4
	Example 15	95.7
	Example 16	96.2
	Example 17	89.3
	Example 18	14.2
	Example 19	100
	Example 20	7.2
	Example 21	100
	Example 22	16.4
	Example 23	0.8
	Example 24	5.8
	Example 25	0.0
	Example 26	26.6
	Example 27	78.2
	Example 28	27.4
	Example 29	27.0
	Example 30	31.5

	TABLE 40

	compound	SNS inhibitory rate (%)

	Example 31	92.1
	Example 32	91.2
	Example 33	32.9
	Example 34	6.7
	Example 35	10.8
	Example 36	0.4
	Example 37	42.3
	Example 38	48.8
	Example 39	48.8
	Example 40	95.8
	Example 41	99.7
	Example 42	76.7
	Example 43	61.0
	Example 44	84.9
	Example 45	40.6
	Example 46	95.5
	Example 47	86.6
	Example 48	96.7
	Example 49	94.8
	Example 50	86.8
	Example 51	90.5
	Example 52	89.7
	Example 53	94.0
	Example 54	95.7
	Example 55	89.4
	Example 56	82.2
	Example 57	87.6
	Example 58	71.2
	Example 59	54.8
	Example 60	75.7

	TABLE 41

	compound	SNS inhibitory rate (%)

	Example 61	26.1
	Example 62	93.8
	Example 63	9.2
	Example 64	82.7
	Example 65	47.8
	Example 66	16.8
	Example 67	30.8
	Example 68	16.0
	Example 69	22.3
	Example 70	11.2
	Example 71	73.7
	Example 72	7.3
	Example 73	8.0
	Example 74	58.2
	Example 75	0.0
	Example 76	18.8
	Example 77	16.0
	Example 78	22.2
	Example 79	3.5
	Example 80	2.5
	Example 81	69.1
	Example 82	30.7
	Example 83	0.0
	Example 84	76.8
	Example 85	24.9
	Example 86	8.3
	Example 87	90.1
	Example 88	83.5
	Example 89	83.0
	Example 90	96.1

	TABLE 42

	compound	SNS inhibitory rate (%)

	Example 91	76.4
	Example 92	66.7
	Example 93	82.1
	Example 94	63.9
	Example 95	26.8
	Example 96	84.8
	Example 97	82.4
	Example 98	69.8
	Example 99	65.4
	Example 100	72.1
	Example 101	85.2
	Example 102	96.3
	Example 103	87.9
	Example 104	83.6
	Example 105	75.1
	Example 106	86.4
	Example 107	83.7
	Example 108	85.3

	TABLE 43

	compound	SNS inhibitory rate (%)

	Example 109	89.3
	Example 110	9.8
	Example 111	88.4
	Example 112	0
	Example 113	64.7
	Example 114	6.5
	Example 115	3.5
	Example 116	33.2
	Example 117	78.8
	Example 118	64.5
	Example 119	87.2
	Example 120	92.4
	Example 121	94.3
	Example 122	100
	Example 123	96.8
	Example 124	87.8
	Example 125	95.9
	Example 126	56.9
	Example 127	93.9
	Example 128	85
	Example 129	90.3
	Example 130	42.1
	Example 131	55.9
	Example 132	86.4
	Example 133	91.7
	Example 134	95.7
	Example 135	57.8
	Example 136	28.7
	Example 137	90.7
	Example 138	93.1

	TABLE 44

	compound	SNS inhibitory rate (%)

	Example 139	96
	Example 140	97.5
	Example 141	90.3
	Example 142	47.9
	Example 143	27.7
	Example 144	6.1
	Example 145	1.3
	Example 146	19.7
	Example 147	23.5
	Example 148	17
	Example 149	30.6
	Example 150	45.6
	Example 151	26.6
	Example 152	8.9
	Example 153	28.5
	Example 154	11.2
	Example 155	86.1
	Example 156	71.2
	Example 157	89.9
	Example 158	86.1
	Example 159	96.1
	Example 160	97
	Example 161	76.2
	Example 162	67.3
	Example 163	36.5
	Example 164	3.7
	Example 165	100
	Example 166	62.7
	Example 167	82.8
	Example 168	20.2

	TABLE 45

	compound	SNS inhibitory rate (%)

	Example 169	68.1
	Example 170	14.2
	Example 171	38.3
	Example 172	50.9
	Example 173	27.1
	Example 174	33.4
	Example 175	5.9
	Example 176	68.8
	Example 177	22.5
	Example 178	16
	Example 179	67.4
	Example 180	4.5
	Example 181	0
	Example 182	0
	Example 183	72.3
	Example 184	87.9
	Example 185	64.6
	Example 186	55.6
	Example 187	53.3
	Example 188	87
	Example 189	97.7
	Example 190	34.3
	Example 191	23.3
	Example 192	11.9
	Example 193	22.3
	Example 194	19.7
	Example 195	20.1
	Example 196	23
	Example 197	9.3
	Example 198	10.2

	TABLE 46

	compound	SNS inhibitory rate (%)

	Example 199	14.7
	Example 200	22.4
	Example 201	11.1
	Example 202	26
	Example 203	18.4
	Example 204	0
	Example 205	24.2
	Example 206	14.5
	Example 207	7
	Example 208	0
	Example 209	6.5
	Example 210	2.1
	Example 211	9.5
	Example 212	20.6
	Example 213	8.1
	Example 214	0.2
	Example 215	12.4
	Example 216	0.7
	Example 217	3.2
	Example 218	12.5
	Example 219	9.7
	Example 220	12.2
	Example 221	22
	Example 222	10.1
	Example 223	0
	Example 224	0
	Example 225	25.1
	Example 226	14
	Example 227	20.4
	Example 228	31

	TABLE 47

	compound	SNS inhibitory rate (%)

	Example 229	10.1
	Example 230	33.2
	Example 231	17.9
	Example 232	16.1
	Example 233	49.9
	Example 234	94.3
	Example 235	100
	Example 236	71
	Example 237	100

INDUSTRIAL APPLICABILITY

The novel bicyclic heterocyclic compound of the present invention can be used as a superior drug for the treatment or prophylaxis of pathology in which SNS is involved, specifically, diseases such as neuropathic pain, nociceptive pain, dysuria, multiple sclerosis and the like.

Claims

1. A method of inhibiting SNS in a patient, which comprises administering an effective amount of a compound represented by formula (1):

wherein

R¹is a hydrogen atom, a halogen atom, an alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms or a haloalkoxy group having 1 to 6 carbon atoms (R¹can substitute the benzene ring or pyridine ring at any substitutable position thereon),

L is a single bond, —O— or —CH₂O— (L can substitute the benzene ring or pyridine ring at any substitutable position thereon),

R²is a substituted or unsubstituted 6- to 10-membered aryl group, or a substituted or unsubstituted 5- to 10-membered aromatic heterocyclic group,

X is a carbon atom or a nitrogen atom,

R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 6 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered cycloalkenyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group,

R⁴is a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a substituted or unsubstituted 3- to 8-membered cycloalkyl group,

R^5aand R^5bare each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or R⁴and R^5aare optionally bonded to form, together with the nitrogen atom that R⁴is bonded to, a 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle (in this case, R^5bis a hydrogen atom),

R⁶and R⁷are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted alkenyl group having 2 to 6 carbon atoms, a substituted or unsubstituted alkynyl group having 2 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered cycloalkenyl group, a substituted or unsubstituted O-5 to 8-membered saturated aliphatic heterocyclic group, a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, a substituted or unsubstituted 6- to 10-membered aryl group, or a substituted or unsubstituted 5- to 10-membered aromatic heterocyclic group,

or R⁶and R⁷are optionally bonded to form, together with the nitrogen atom that they are bond to, a substituted or unsubstituted 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle, or a substituted or unsubstituted 5- to 10-membered unsaturated nitrogen-containing aliphatic heterocycle (the saturated or unsaturated nitrogen-containing aliphatic heterocycle contains 0 to 2 oxygen atoms, 0 to 2 sulfur atoms and 1 to 3 nitrogen atoms),

or a pharmaceutically acceptable salt thereof, to the patient, whereupon SNS is inhibited in the patient.

2. The method of claim 1, wherein the compound is represented by formula (2):

wherein R¹, R², R³, R⁴, R^5a, R^6b, R⁶, R⁷, L and X are as defined in claim 1, or a pharmaceutically acceptable salt thereof.

3. The method of claim 1, wherein the compound is represented by formula (3):

wherein R¹, R², R³, R⁴, R^5a, R^5b, R⁶, R⁷, L and X are as defined in claim 1, or a pharmaceutically acceptable salt thereof.

4. The method of claim 1, wherein R²is a substituted or unsubstituted phenyl group, or a pharmaceutically acceptable salt thereof.

5. The method of claim 1, wherein R³is a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, or a pharmaceutically acceptable salt thereof.

6. The method of claim 1, wherein R⁶and R⁷are each independently a hydrogen atom, a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, a haloalkyl group having 1 to 6 carbon atoms, a substituted or unsubstituted 3- to 8-membered cycloalkyl group, a substituted or unsubstituted 4- to 8-membered saturated aliphatic heterocyclic group, or a substituted or unsubstituted 5- to 10-membered unsaturated aliphatic heterocyclic group, or R⁶and R⁷are optionally bonded to form, together with the nitrogen atom that they are bond to, a substituted or unsubstituted 4- to 8-membered saturated nitrogen-containing aliphatic heterocycle, or a substituted or unsubstituted 5- to 10-membered unsaturated nitrogen-containing aliphatic heterocycle (the saturated or unsaturated nitrogen-containing aliphatic heterocycle contains 0 to 2 oxygen atoms, 0 to 2 sulfur atoms and 1 to 3 nitrogen atoms), or a pharmaceutically acceptable salt thereof.

7. The method of claim 1, wherein R⁴is a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a pharmaceutically acceptable salt thereof.

8. The method of claim 1, wherein R^5aand R^5bare each independently a hydrogen atom, or a substituted or unsubstituted alkyl group having 1 to 6 carbon atoms, or a pharmaceutically acceptable salt thereof.

9. The method of claim 1, wherein X is a carbon atom, or a pharmaceutically acceptable salt thereof.

10. The method of claim 1, wherein R¹is a hydrogen atom or a halogen atom, or a pharmaceutically acceptable salt thereof.

11. The method of claim 1, wherein L is a single bond, or a pharmaceutically acceptable salt thereof.

12. The method of claim 1, wherein L is —O—, or a pharmaceutically acceptable salt thereof.

13. The method of claim 1, wherein L is —CH₂O—, or a pharmaceutically acceptable salt thereof.

14. The method of claim 1, wherein the compound is selected from

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}glycinamide,

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-2-methylalaninamide,

N²-{[1-cyclopropyl-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[1-cyclobutyl-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[6-(4-chlorophenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[6-(4-fluorophenoxy)-1-(2-hydroxy-2-methylpropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[6-(4-fluorophenoxy)-1-(3-methoxypropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[6-(2-chloro-4-fluorophenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[1-ethyl-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[6-(2,4-difluorophenoxy)-1-(2-hydroxy-2-methylpropyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[1-(2-ethoxyethyl)-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[1-ethyl-5-fluoro-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[1-(3-methoxypropyl)-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[6-(4-methylphenoxy)-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

N²-{[5-chloro-1-(2-ethoxyethyl)-6-(4-fluorophenyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, and

N²-{[5-chloro-6-(3,4-difluorophenyl)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide,

and a pharmaceutically acceptable salt thereof.

15. The method of claim 1, wherein the compound is N²-{[1-(2-ethoxyethyl)-6-(4-fluorophenoxy)-1H-benzimidazol-2-yl]methyl}-2-methylalaninamide, or a pharmaceutically acceptable salt thereof.

16. The method of claim 1, wherein the compound is N²-{[6-(2-chloro-4-fluorophenoxy)-1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, or a pharmaceutically acceptable salt thereof.

17. The method of claim 1, wherein the compound is N²-{[1-ethyl-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, or a pharmaceutically acceptable salt thereof.

18. The method of claim 1, wherein the compound is N²-{[1-(3-methoxypropyl)-6-(4-methylphenoxy)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, or a pharmaceutically acceptable salt thereof.

19. The method of claim 1, wherein the compound is N²-{[6-(4-methylphenoxy)-1-(tetrahydro-2H-pyran-4-yl)-1H-benzimidazol-2-yl]methyl}-L-alaninamide, or a pharmaceutically acceptable salt thereof.