JP2003012649A - N-(3-quinolyl)amide derivative - Google Patents

N-(3-quinolyl)amide derivative

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Publication number
JP2003012649A
JP2003012649A JP2002118645A JP2002118645A JP2003012649A JP 2003012649 A JP2003012649 A JP 2003012649A JP 2002118645 A JP2002118645 A JP 2002118645A JP 2002118645 A JP2002118645 A JP 2002118645A JP 2003012649 A JP2003012649 A JP 2003012649A
Authority
JP
Japan
Prior art keywords
group
meo
allyl
ipr
compound
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
JP2002118645A
Other languages
Japanese (ja)
Inventor
Hiroyuki Ito
寛之 伊藤
Hisako Tanaka
久子 田中
Hiroshi Ota
昊 太田
Toru Onishi
徹 大西
Tsuneaki Imai
秩明 今井
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sankyo Co Ltd
Original Assignee
Sankyo Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sankyo Co Ltd filed Critical Sankyo Co Ltd
Priority to JP2002118645A priority Critical patent/JP2003012649A/en
Publication of JP2003012649A publication Critical patent/JP2003012649A/en
Ceased legal-status Critical Current

Links

Abstract

PROBLEM TO BE SOLVED: To obtain both an N-(3-quinolyl)amide derivative or its salt and an agrochemical comprising the same as an active ingredient. SOLUTION: This N-(3-quinolyl)amide derivative is represented by general formula [...... is a single bond or a double bond; R is a 1-8C alkyl group, a 3-6C cycloalkyl group, a 2-6C alkyenyl group, or a 3-6C alkynyl group which may be substituted; X is a halogen atom, a 1-6C alkyl group which may be substituted, or a 1-6C alkoxy group which may be substituted; (m) is an integer of 0-6; (Z) is a 1-6C alkyl group; (n) is an integer of 0-6; when (n) is >=2, two Zs may be bonded to form a 1-4C alkylene group] or its salt.

Description

【発明の詳細な説明】Detailed Description of the Invention

【０００１】[0001]

【発明の属する技術分野】本発明は、Ｎ−（３−キノリ
ル）アミド誘導体又はその塩、それを有効成分として含
有する農薬に関する。TECHNICAL FIELD The present invention relates to an N- (3-quinolyl) amide derivative or a salt thereof, and an agricultural chemical containing the same as an active ingredient.

【０００２】[0002]

【従来の技術】Synlett 1999, No. 12, 1957-1959に
は、３−シクロヘキサンカルボニルアミドキノリンが記
載されているが、α位に置換基を有するシクロアルキル
カルボン酸と３−キノリルアミンが結合したＮ−アシル
体は記載されておらず、また、農園芸用殺菌剤に関する
記載もない。このように、Ｎ−（３−キノリル）アミド
誘導体が農園芸用殺菌剤として使用できることは従来知
られていない。2. Description of the Prior Art Synlett 1999, No. 12, 1957-1959 describes 3-cyclohexanecarbonylamidoquinoline, which is an N-bond in which a cycloalkylcarboxylic acid having a substituent at the α-position and 3-quinolylamine are bonded. -Acylate is not mentioned, nor is there any mention of fungicides for agriculture and horticulture. As described above, it has not hitherto been known that N- (3-quinolyl) amide derivatives can be used as agricultural and horticultural fungicides.

【０００３】[0003]

【発明が解決しようとする課題】本発明者らは、Ｎ−
（３−キノリル）アミド誘導体について鋭意研究を重ね
た結果、３−アミノキノリル基に、α位に置換基を有す
る、シクロヘキサンカルボン酸又はシクロヘキセンカル
ボン酸が結合したＮ−（３−キノリル）アミド誘導体
が、種々の植物病害に対し優れた殺菌活性を有し農薬の
有効成分として有用であり、特に、植物のかび病のなか
でも農園芸用作物に対してしばしば重篤な被害を与える
イネいもち病（Pyricularia oryzae）並びにトマト、キ
ュウリ及びインゲンの灰色かび病（Botrytis cinerea）
に対して低薬量で防除が可能であることを見出し、本発
明を完成した。DISCLOSURE OF THE INVENTION The present inventors have found that N-
As a result of earnest studies on the (3-quinolyl) amide derivative, an N- (3-quinolyl) amide derivative having a 3-aminoquinolyl group having a substituent at the α-position, to which cyclohexanecarboxylic acid or cyclohexenecarboxylic acid is bonded, It has excellent bactericidal activity against various plant diseases and is useful as an active ingredient of agricultural chemicals. In particular, among rice mold diseases of rice, rice blast disease (Pyricularia) often causes serious damage to agricultural and horticultural crops. oryzae) and gray mold (Botrytis cinerea) on tomato, cucumber and green beans
However, the inventors have found that it is possible to control with a low dose, and completed the present invention.

【０００４】[0004]

【課題を解決するための手段】本発明は、一般式The present invention has the general formula

【０００５】[0005]

【化２】 [Chemical 2]

【０００６】［式中、……は、単結合又は二重結合を表
し、Ｒは、置換されてよいＣ1〜Ｃ8アルキル基（当該置
換基は、同一又は異なった１〜４個のハロゲン原子、１
個のＣ3〜Ｃ6シクロアルキル基又は１個のＣ1〜Ｃ6アル
コキシ基である。）、Ｃ3〜Ｃ6シクロアルキル基、Ｃ2
〜Ｃ6アルケニル基又はＣ3〜Ｃ6アルキニル基を表し、
Ｘは、ハロゲン原子、置換されてよいＣ1〜Ｃ6アルキル
基（当該置換基は、同一又は異なった１〜３個のハロゲ
ン原子である。）又は置換されてよいＣ1〜Ｃ6アルコキ
シ基（当該アルコキシ基は、同一又は異なった１〜３個
のハロゲン原子である。）を表し、ｍは、０〜６の整数
を表し、ｍが２以上であるとき、複数のＸは同一であっ
ても異なっていてもよく、Ｚは、Ｃ1〜Ｃ6アルキル基で
あり、ｎは、０〜６の整数を表し、ｎが２以上であると
き、複数のＺは同一であっても異なっていてもよく、任
意の２個のＺが、一緒になって、Ｃ1〜Ｃ4アルキレン基
を形成してよい。］で表される化合物又はその塩であ
る。[Wherein, ... represents a single bond or a double bond, and R represents an optionally substituted C 1 -C 8 alkyl group (the said substituents are the same or different 1-4 halogens). Atom, 1
C 3 -C 6 cycloalkyl group or one C 1 -C 6 alkoxy group. ), C 3 -C 6 cycloalkyl groups, C 2
To C 6 alkenyl group or C 3 to C 6 alkynyl group,
X is a halogen atom, a C 1 -C 6 alkyl group which may be substituted (the said substituents are the same or different 1 to 3 halogen atoms) or a C 1 -C 6 alkoxy group which may be substituted. (The alkoxy groups are the same or different 1 to 3 halogen atoms.), M represents an integer of 0 to 6, and when m is 2 or more, a plurality of Xs are the same. Or Z may be different, Z is a C 1 to C 6 alkyl group, n represents an integer of 0 to 6, and when n is 2 or more, a plurality of Zs may be the same or different. even if well, any two Z together may form a C 1 -C 4 alkylene group. ] It is a compound or its salt represented by these.

【０００７】本発明において、「Ｃ1〜Ｃ8アルキル基」
は、例えば、メチル基、エチル基、プロピル基、イソプ
ロピル基、ブチル基、イソブチル基、ｓ−ブチル基、ｔ
−ブチル基、ペンチル基、イソペンチル基、２−メチル
ブチル基、ネオペンチル基、１−エチルプロピル基、へ
キシル基、４−メチルペンチル基、３−メチルペンチル
基、２−メチルペンチル基、１−メチルペンチル基、
３，３−ジメチルブチル基、２，２−ジメチルブチル
基、１，１−ジメチルブチル基、１，２−ジメチルブチ
ル基、１，３−ジメチルブチル基、２，３−ジメチルブ
チル基、２−エチルブチル基、ヘプチル基、オクチル基
のような炭素数１乃至８個の直鎖又は分枝鎖アルキル基
であり、好適には、炭素数１乃至６個の直鎖又は分枝鎖
アルキル基（Ｃ1〜Ｃ6アルキル基）であり、より好適に
は、炭素数１乃至５個の直鎖又は分枝鎖アルキル基（Ｃ
1〜Ｃ5アルキル基）であり、更により好適には、炭素数
１乃至４個の直鎖又は分枝鎖アルキル基（Ｃ1〜Ｃ4アル
キル基）であり、また更により好適には、炭素数１乃至
３個の直鎖又は分枝鎖アルキル基（Ｃ1〜Ｃ3アルキル
基）であり、特に好適には、メチル基、エチル基又はプ
ロピル基であり、最も好適には、メチル基又はエチル基
である。In the present invention, "C 1 -C 8 alkyl group"
Is, for example, methyl group, ethyl group, propyl group, isopropyl group, butyl group, isobutyl group, s-butyl group, t
-Butyl group, pentyl group, isopentyl group, 2-methylbutyl group, neopentyl group, 1-ethylpropyl group, hexyl group, 4-methylpentyl group, 3-methylpentyl group, 2-methylpentyl group, 1-methylpentyl group Base,
3,3-dimethylbutyl group, 2,2-dimethylbutyl group, 1,1-dimethylbutyl group, 1,2-dimethylbutyl group, 1,3-dimethylbutyl group, 2,3-dimethylbutyl group, 2- It is a linear or branched alkyl group having 1 to 8 carbon atoms such as an ethylbutyl group, a heptyl group, an octyl group, and preferably a linear or branched alkyl group having 1 to 6 carbon atoms (C 1 to C 6 alkyl group), and more preferably a linear or branched alkyl group having 1 to 5 carbon atoms (C
1 to C 5 alkyl group), and even more preferably a linear or branched alkyl group having 1 to 4 carbon atoms (C 1 to C 4 alkyl group), and even more preferably, It is a linear or branched alkyl group having 1 to 3 carbon atoms (C 1 -C 3 alkyl group), particularly preferably a methyl group, an ethyl group or a propyl group, and most preferably a methyl group. Or an ethyl group.

【０００８】本発明において、「ハロゲン原子」は、フ
ッ素原子、塩素原子、臭素原子又はヨウ素原子であり、
好適には、フッ素原子、塩素原子又は臭素原子であり、
より好適には、フッ素原子又は塩素原子であり、最も好
適には、フッ素原子である。In the present invention, the "halogen atom" is a fluorine atom, a chlorine atom, a bromine atom or an iodine atom,
Preferably, it is a fluorine atom, a chlorine atom or a bromine atom,
It is more preferably a fluorine atom or a chlorine atom, and most preferably a fluorine atom.

【０００９】本発明において、「Ｃ3〜Ｃ6シクロアルキ
ル基」は、シクロプロピル基、シクロブチル基、シクロ
ペンチル基又はシクロヘキシル基であり、好適には、シ
クロプロピル基又はシクロブチル基であり、より好適に
は、シクロプロピル基である。In the present invention, the "C 3 -C 6 cycloalkyl group" is a cyclopropyl group, a cyclobutyl group, a cyclopentyl group or a cyclohexyl group, preferably a cyclopropyl group or a cyclobutyl group, more preferably Is a cyclopropyl group.

【００１０】本発明において、「Ｃ1〜Ｃ6アルコキシ
基」は、例えば、メトキシ基、エトキシ基、プロポキシ
基、イソプロポキシ基、ブトキシ基、イソブトキシ基、
ｓ−ブトキシ基、ｔ−ブトキシ基、ペンチルオキシ基、
イソペンチルオキシ基、２−メチルブトキシ基、ネオペ
ンチルオキシ基、１−エチルプロポキシ基、へキシルオ
キシ基、（４−メチルペンチル）オキシ基、（３−メチ
ルペンチル）オキシ基、（２−メチルペンチル）オキシ
基、（１−メチルペンチル）オキシ基、３，３−ジメチ
ルブトキシ基、２，２−ジメチルブトキシ基、１，１−
ジメチルブトキシ基、１，２−ジメチルブトキシ基、
１，３−ジメチルブトキシ基、２，３−ジメチルブトキ
シ基、２−エチルブトキシ基のような炭素数１乃至６個
の直鎖又は分枝鎖アルコキシ基であり、好適には、炭素
数１乃至４個の直鎖又は分枝鎖アルコキシ基（Ｃ1〜Ｃ4
アルコキシ基）であり、より好適には、メトキシ基、エ
トキシ基又はイソプロポキシ基であり、更により好適に
は、メトキシ基又はエトキシ基であり、最も好適には、
メトキシ基である。In the present invention, "C 1 -C 6 alkoxy group" means, for example, methoxy group, ethoxy group, propoxy group, isopropoxy group, butoxy group, isobutoxy group,
s-butoxy group, t-butoxy group, pentyloxy group,
Isopentyloxy group, 2-methylbutoxy group, neopentyloxy group, 1-ethylpropoxy group, hexyloxy group, (4-methylpentyl) oxy group, (3-methylpentyl) oxy group, (2-methylpentyl) Oxy group, (1-methylpentyl) oxy group, 3,3-dimethylbutoxy group, 2,2-dimethylbutoxy group, 1,1-
Dimethylbutoxy group, 1,2-dimethylbutoxy group,
A straight-chain or branched-chain alkoxy group having 1 to 6 carbon atoms such as a 1,3-dimethylbutoxy group, a 2,3-dimethylbutoxy group, and a 2-ethylbutoxy group, and preferably having 1 to 6 carbon atoms. 4 straight or branched chain alkoxy groups (C 1 -C 4
An alkoxy group), more preferably a methoxy group, an ethoxy group or an isopropoxy group, even more preferably a methoxy group or an ethoxy group, and most preferably
It is a methoxy group.

【００１１】本発明において、「Ｃ1〜Ｃ8アルキル基
（当該置換基は、同一又は異なった１〜４個のハロゲン
原子、１個のＣ3〜Ｃ6シクロアルキル基又は１個のＣ1
〜Ｃ6アルコキシ基である。）」は、前記「Ｃ1〜Ｃ8ア
ルキル基」の他に、例えば、トリフルオロメチル基、ト
リクロロメチル基、ジフルオロメチル基、ジクロロメチ
ル基、ジブロモメチル基、フルオロメチル基、クロロメ
チル基、ブロモメチル基、ヨ−ドメチル基、２，２，２
−トリクロロエチル基、２，２，２−トリフルオロエチ
ル基、２−ブロモエチル基、２−クロロエチル基、２−
フルオロエチル基、３−クロロプロピル基、３，３，３
−トリフルオロプロピル基、４−フルオロブチル基、３
−フルオロ−２−メチルプロピル基、３，３，３−トリ
フルオロ−２−メチルプロピル基、６，６，６−トリク
ロロヘキシル基、３，３，４，４−テトラフルオロブチ
ル基のような同一又は異なった１〜４個の前記「ハロゲ
ン原子」により置換された前記「Ｃ1〜Ｃ8アルキル
基」、シクロプロピルメチル基、シクロブチルメチル
基、シクロペンチルメチル基、シクロヘキシルメチル基
のような１個の前記「Ｃ3〜Ｃ6シクロアルキル基」が結
合した前記「Ｃ1〜Ｃ8アルキル基」、又は、メトキシメ
チル基、エトキシメチル基、プロポキシメチル基、メト
キシエチル基、メトキシプロピル基、メトキシブトキシ
基、ペンチルオキシメチル基のような１個の前記「Ｃ1
〜Ｃ6アルコキシ基」が結合した前記「Ｃ1〜Ｃ8アルキ
ル基」であり、好適には、同一又は異なった１〜３個の
前記「ハロゲン原子」、１個の前記「Ｃ3〜Ｃ6シクロア
ルキル基」又は１個の前記「Ｃ1〜Ｃ6アルコキシ基」に
より置換されてよい前記「Ｃ1〜Ｃ6アルキル基」であ
り、より好適には、同一又は異なった１〜３個の前記
「ハロゲン原子」、１個の前記「Ｃ4〜Ｃ6シクロアルキ
ル基」又は１個の前記「Ｃ1〜Ｃ4アルコキシ基」により
置換されてよい前記「Ｃ1〜Ｃ4アルキル基」であり、更
により好適には、同一又は異なった１〜３個の「フッ素
原子又は塩素原子」、１個の「Ｃ4〜Ｃ6シクロアルキル
基」又は１個の「Ｃ1〜Ｃ3アルコキシ基」により置換さ
れてよい前記「Ｃ1〜Ｃ3アルキル基」であり、特に好適
には、メチル基、エチル基、プロピル基、クロロメチル
基、トリフルオロメチル基、シクロヘキシルメチル基、
シクロブチルメチル基、メトキシメチル基又はメトキシ
エチル基であり、最も好適には、メチル基、エチル基、
トリフルオロメチル基、シクロブチルメチル基又はメト
キシメチル基である。In the present invention, a "C 1 -C 8 alkyl group (the substituent is the same or different 1 to 4 halogen atoms, 1 C 3 -C 6 cycloalkyl group or 1 C 1
~C is 6 alkoxy group. ) ”Is, in addition to the above-mentioned“ C 1 -C 8 alkyl group ”, for example, a trifluoromethyl group, a trichloromethyl group, a difluoromethyl group, a dichloromethyl group, a dibromomethyl group, a fluoromethyl group, a chloromethyl group, a bromomethyl group. Group, iodomethyl group, 2,2,2
-Trichloroethyl group, 2,2,2-trifluoroethyl group, 2-bromoethyl group, 2-chloroethyl group, 2-
Fluoroethyl group, 3-chloropropyl group, 3,3,3
-Trifluoropropyl group, 4-fluorobutyl group, 3
Same as -fluoro-2-methylpropyl group, 3,3,3-trifluoro-2-methylpropyl group, 6,6,6-trichlorohexyl group, 3,3,4,4-tetrafluorobutyl group Or one such as the above "C 1 -C 8 alkyl group" substituted with 1 to 4 different "halogen atoms", cyclopropylmethyl group, cyclobutylmethyl group, cyclopentylmethyl group, cyclohexylmethyl group wherein said "C 3 -C 6 cycloalkyl group" is bound to "C 1 -C 8 alkyl group", or a methoxymethyl group, ethoxymethyl group, propoxymethyl group, methoxyethyl group, methoxypropyl group, methoxy butoxy Group, one of the above-mentioned "C 1
-C 6 wherein the alkoxy group "is bonded is" C 1 -C 8 alkyl group ", preferably, identical or different one to three of the" halogen atom ", one of the" C 3 -C 6 wherein that may be substituted by a cycloalkyl group "or one of the" C 1 -C 6 alkoxy group "is a" C 1 -C 6 alkyl group ", more preferably the same or different 1 to 3 was the "halogen atom", one of the "C 4 -C 6 cycloalkyl group" or one of the said that may be substituted by "C 1 -C 4 alkoxy group", "C 1 -C 4 alkyl group" And even more preferably, the same or different 1 to 3 "fluorine atom or chlorine atom", 1 "C 4 -C 6 cycloalkyl group" or 1 "C 1 -C 3 alkoxy" The above-mentioned "C 1 -C 3 alkyl group" which may be substituted by "group" is particularly preferable. Chill group, ethyl group, propyl group, chloromethyl group, trifluoromethyl group, cyclohexylmethyl group,
A cyclobutylmethyl group, a methoxymethyl group or a methoxyethyl group, most preferably a methyl group, an ethyl group,
It is a trifluoromethyl group, a cyclobutylmethyl group or a methoxymethyl group.

【００１２】本発明において、「Ｃ2〜Ｃ6アルケニル
基」は、例えば、ビニル基、アリル基、１−プロペニル
基、２−メチル−１−プロペニル基、２−メチル−２−
プロペニル基、３−ブテニル基、２−メチル−２−ブテ
ニル基、２−ペンテニル基、４−ペンテニル基、３−メ
チル−２−ブテニル基のような炭素数２乃至６個の直鎖
又は分枝鎖アルケニル基であり、好適には、炭素数２乃
至５個の直鎖又は分枝鎖アルケニル基であり、より好適
には、ビニル基、アリル基、４−ペンテニル基又は３−
メチル−２−ブテニル基であり、更により好適には、ア
リル基である。In the present invention, the "C 2 -C 6 alkenyl group" is, for example, vinyl group, allyl group, 1-propenyl group, 2-methyl-1-propenyl group, 2-methyl-2-.
A straight or branched chain having 2 to 6 carbon atoms such as propenyl group, 3-butenyl group, 2-methyl-2-butenyl group, 2-pentenyl group, 4-pentenyl group, 3-methyl-2-butenyl group A chain alkenyl group, preferably a linear or branched alkenyl group having 2 to 5 carbon atoms, and more preferably a vinyl group, an allyl group, a 4-pentenyl group or 3-
It is a methyl-2-butenyl group, and more preferably an allyl group.

【００１３】本発明において、「Ｃ3〜Ｃ6アルキニル
基」は、例えば、プロパルギル基、２−ペンチニル基、
３−ペンチニル基、２−ブチニル基のような炭素数３乃
至６個の直鎖又は分枝鎖アルキニル基であり、好適に
は、炭素数３又は４個のアルキニル基であり、更により
好適には、プロパルギル基又は２−ペンチニル基であ
り、特に好適には、２−ペンチニル基である。In the present invention, "C 3 -C 6 alkynyl group" means, for example, propargyl group, 2-pentynyl group,
A linear or branched alkynyl group having 3 to 6 carbon atoms such as a 3-pentynyl group or a 2-butynyl group, preferably an alkynyl group having 3 or 4 carbon atoms, and further preferably Is a propargyl group or a 2-pentynyl group, particularly preferably a 2-pentynyl group.

【００１４】本発明において、「Ｃ1〜Ｃ6アルキル基
（当該置換基は、同一又は異なった１〜３個のハロゲン
原子である。）」は、前記「Ｃ1〜Ｃ6アルキル基」の他
に、例えば、トリフルオロメチル基、トリクロロメチル
基、ジフルオロメチル基、ジクロロメチル基、ジブロモ
メチル基、フルオロメチル基、クロロメチル基、ブロモ
メチル基、ヨ−ドメチル基、２，２，２−トリクロロエ
チル基、２，２，２−トリフルオロエチル基、２−ブロ
モエチル基、２−クロロエチル基、２−フルオロエチル
基、３−クロロプロピル基、３，３，３−トリフルオロ
プロピル基、４−フルオロブチル基、３−フルオロ−２
−メチルプロピル基、３，３，３−トリフルオロ−２−
メチルプロピル基、６，６，６−トリクロロヘキシル基
のような同一又は異なった１〜３個の前記「ハロゲン原
子」により置換された前記「Ｃ1〜Ｃ6アルキル基」であ
り、好適には、同一又は異なった１〜３個の前記「ハロ
ゲン原子」により置換されてよい前記「Ｃ1〜Ｃ4アルキ
ル基」であり、より好適には、同一又は異なった１〜３
個の「フッ素原子又は塩素原子」により置換されてよい
前記「Ｃ1〜Ｃ3アルキル基」であり、更により好適に
は、メチル基、エチル基、プロピル基、クロロメチル基
又はトリフルオロメチル基であり、特に好適には、メチ
ル基、エチル基又はトリフルオロメチル基である。In the present invention, the "C 1 -C 6 alkyl group (the substituents are the same or different 1 to 3 halogen atoms)" means the above "C 1 -C 6 alkyl group". Besides, for example, trifluoromethyl group, trichloromethyl group, difluoromethyl group, dichloromethyl group, dibromomethyl group, fluoromethyl group, chloromethyl group, bromomethyl group, iodomethyl group, 2,2,2-trichloroethyl group Group, 2,2,2-trifluoroethyl group, 2-bromoethyl group, 2-chloroethyl group, 2-fluoroethyl group, 3-chloropropyl group, 3,3,3-trifluoropropyl group, 4-fluorobutyl group Group, 3-fluoro-2
-Methylpropyl group, 3,3,3-trifluoro-2-
The above-mentioned "C 1 -C 6 alkyl group" substituted with 1 to 3 of the same or different "halogen atoms" such as methylpropyl group and 6,6,6-trichlorohexyl group, and preferably , The same or different 1 to 3 “halogen atoms” which may be substituted with the above “C 1 to C 4 alkyl group”, more preferably the same or different 1 to 3
The above “C 1 -C 3 alkyl group” which may be substituted with “fluorine atom or chlorine atom”, and more preferably, methyl group, ethyl group, propyl group, chloromethyl group or trifluoromethyl group. And particularly preferably a methyl group, an ethyl group or a trifluoromethyl group.

【００１５】本発明において、「Ｃ1〜Ｃ6アルコキシ基
（当該置換基は、同一又は異なった１〜３個のハロゲン
原子である。）」は、前記「Ｃ1〜Ｃ6アルコキシ基」の
他に、例えば、トリフルオロメトキシ基、トリクロロメ
トキシ基、ジフルオロメトキシ基、ジクロロメトキシ
基、ジブロモメトキシ基、フルオロメトキシ基、クロロ
メトキシ基、ブロモメトキシ基、ヨ−ドメトキシ基、
２，２，２−トリクロロエトキシ基、２，２，２−トリ
フルオロエトキシ基、２−ブロモエトキシ基、２−クロ
ロエトキシ基、２−フルオロエトキシ基、３−クロロプ
ロポキシ基、３，３，３−トリフルオロプロポキシ基、
４−フルオロブトキシ基、３−フルオロ−２−メチルプ
ロポキシ基、３，３，３−トリフルオロ−２−メチルプ
ロポキシ基、６，６，６−トリクロロヘキシルオキシ基
のような同一又は異なった１〜３個の前記「ハロゲン原
子」により置換された前記「Ｃ1〜Ｃ6アルコキシ基」で
あり、好適には、同一又は異なった１〜３個の前記「ハ
ロゲン原子」により置換されてよい前記「Ｃ1〜Ｃ4アル
コキシ基」であり、より好適には、同一又は異なった１
〜３個の「フッ素原子又は塩素原子」により置換されて
よい前記「Ｃ1〜Ｃ3アルコキシ基」であり、更により好
適には、メトキシ基、エトキシ基、プロポキシ基又はト
リフルオロメトキシ基であり、最も好適には、メトキシ
基である。In the present invention, the "C 1 -C 6 alkoxy group (the substituents are the same or different 1 to 3 halogen atoms)" means the above "C 1 -C 6 alkoxy group". In addition, for example, trifluoromethoxy group, trichloromethoxy group, difluoromethoxy group, dichloromethoxy group, dibromomethoxy group, fluoromethoxy group, chloromethoxy group, bromomethoxy group, iodomethoxy group,
2,2,2-trichloroethoxy group, 2,2,2-trifluoroethoxy group, 2-bromoethoxy group, 2-chloroethoxy group, 2-fluoroethoxy group, 3-chloropropoxy group, 3,3,3 -Trifluoropropoxy group,
The same or different 1 to 4 groups such as 4-fluorobutoxy group, 3-fluoro-2-methylpropoxy group, 3,3,3-trifluoro-2-methylpropoxy group and 6,6,6-trichlorohexyloxy group. The above “C 1 -C 6 alkoxy group” substituted by 3 “halogen atoms”, and preferably the above “C 1 -C 6 alkoxy group”, which may be substituted by 1 to 3 the same or different “halogen atoms”. C 1 -C 4 alkoxy group ”, more preferably the same or different 1
To the above “C 1 to C 3 alkoxy group” which may be substituted with 3 “fluorine atoms or chlorine atoms”, and more preferably a methoxy group, an ethoxy group, a propoxy group or a trifluoromethoxy group. , Most preferably a methoxy group.

【００１６】本発明において「Ｃ1〜Ｃ4アルキレン基」
は、例えば、メチレン基、エチレン基、トリメチレン
基、プロピレン基、テトラメチレン基のような炭素数１
〜４個の直鎖又は分枝鎖アルキレン基であり、好適に
は、メチレン基又はエチレン基であり、より好適には、
メチレン基である。In the present invention, "C 1 -C 4 alkylene group"
Is a carbon number 1 such as methylene group, ethylene group, trimethylene group, propylene group, tetramethylene group.
To 4 linear or branched alkylene groups, preferably methylene groups or ethylene groups, and more preferably
It is a methylene group.

【００１７】本発明の化合物（Ｉ）において、（１）Ｒ
は、好適には、置換されてよいＣ1〜Ｃ6アルキル基（当
該置換基は、同一又は異なった１〜４個のフッ素原子若
しくは塩素原子、１個のＣ4〜Ｃ6シクロアルキル基又は
１個のＣ1〜Ｃ4アルコキシ基である。）、Ｃ3〜Ｃ4シク
ロアルキル基、Ｃ3〜Ｃ5アルケニル基又はＣ3〜Ｃ5アル
キニル基であり、より好適には、置換されてよいＣ1〜
Ｃ5アルキル基（当該置換基は、１〜３個のフッ素原
子、１個のシクロヘキシル基又は１個のメトキシ基であ
る。）、Ｃ3〜Ｃ5アルケニル基又はＣ3〜Ｃ5アルキニル
基であり、更により好適には、置換されてよいＣ1〜Ｃ4
アルキル基（当該置換基は、１〜３個のフッ素原子であ
る。）、Ｃ3〜Ｃ4アルケニル基又はＣ4〜Ｃ5アルキニル
基であり、特に好適には、メチル基、エチル基、プロピ
ル基、ブチル基、イソブチル基、ペンチル基、トリフル
オロメチル基、ビニル基、アリル基、４−ペンテニル
基、３−メチル−２−ブテニル基、プロパルギル基又は
２−ペンチニル基であり、最も好適には、メチル基、エ
チル基、トリフルオロメチル基、アリル基又は２−ペン
チニル基であり、（２）Ｘmは、好適には、Ｘが、フッ
素原子、塩素原子、臭素原子、ヨウ素原子、置換されて
よいＣ1〜Ｃ4アルキル基（当該置換基は、同一又は異な
った１〜３個のフッ素原子若しくは塩素原子である。）
又は置換されてよいＣ1〜Ｃ4アルコキシ基（当該置換基
は、同一又は異なった１〜３個のフッ素原子若しくは塩
素原子である。）であり、ｍが、０、１又は２であり、
より好適には、Ｘが、フッ素原子、塩素原子、Ｃ1〜Ｃ3
アルキル基又はＣ1〜Ｃ3アルコキシ基であり、ｍが、０
又は１であり、更により好適には、Ｘが、フッ素原子又
はメチル基であり、ｍが、０又は１であり、特に好適に
は、ｍが、０であり、（３）Ｚnは、好適には、Ｚが、
Ｃ1〜Ｃ4アルキル基であり、ｎが、０、１又は２であ
り、ｎが２であるとき、２個のＺが、一緒になって、Ｃ
1〜Ｃ2アルキレン基を形成してよく、より好適には、Ｚ
が、Ｃ1〜Ｃ3アルキル基であり、ｎが、０又は１であ
り、更により好適には、Ｚが、メチル基であり、ｎが、
０又は１であり、特に好適には、ｎが、０であり、
（４）……は、好適には、単結合〔本発明化合物（Ｉ）
のアシル基が、１位がＲにより置換されたシクロヘキサ
ンカルボニル基である。〕である。In the compound (I) of the present invention, (1) R
Is preferably an optionally substituted C 1 -C 6 alkyl group (the substituents are the same or different 1 to 4 fluorine atoms or chlorine atoms, 1 C 4 to C 6 cycloalkyl group or A C 1 -C 4 alkoxy group), a C 3 -C 4 cycloalkyl group, a C 3 -C 5 alkenyl group or a C 3 -C 5 alkynyl group, more preferably substituted. Good C 1 ~
A C 5 alkyl group (the substituent is 1 to 3 fluorine atoms, 1 cyclohexyl group or 1 methoxy group), a C 3 to C 5 alkenyl group or a C 3 to C 5 alkynyl group And even more preferably C 1 -C 4 which may be substituted
An alkyl group (the substituent is 1 to 3 fluorine atoms), a C 3 to C 4 alkenyl group or a C 4 to C 5 alkynyl group, particularly preferably a methyl group, an ethyl group, a propyl group. Group, butyl group, isobutyl group, pentyl group, trifluoromethyl group, vinyl group, allyl group, 4-pentenyl group, 3-methyl-2-butenyl group, propargyl group or 2-pentynyl group, most preferably , A methyl group, an ethyl group, a trifluoromethyl group, an allyl group or a 2-pentynyl group, and (2) X m is preferably such that X is a fluorine atom, a chlorine atom, a bromine atom, an iodine atom or a substituted one. Optionally a C 1 -C 4 alkyl group (the substituents are the same or different 1 to 3 fluorine atoms or chlorine atoms).
Or a C 1 -C 4 alkoxy group which may be substituted (the substituents are the same or different 1 to 3 fluorine atoms or chlorine atoms), and m is 0, 1 or 2,
More preferably, X is a fluorine atom, a chlorine atom, C 1 to C 3
An alkyl group or a C 1 -C 3 alkoxy group, m is 0
Or 1, even more preferably X is a fluorine atom or a methyl group, m is 0 or 1, and particularly preferably m is 0 and (3) Z n is Suitably Z is
When it is a C 1 -C 4 alkyl group, n is 0, 1 or 2, and n is 2, two Zs are taken together to form C
1- C 2 alkylene groups may be formed, more preferably Z
Is a C 1 -C 3 alkyl group, n is 0 or 1, and even more preferably Z is a methyl group and n is
0 or 1, particularly preferably n is 0,
(4) ...... is preferably a single bond [present compound (I)
The acyl group of is a cyclohexanecarbonyl group substituted at the 1-position with R. ].

【００１８】本発明の化合物（Ｉ）において、好適に
は、（ａ１）Ｒが、置換されてよいＣ1〜Ｃ6アルキル基
（当該置換基は、同一又は異なった１〜４個のフッ素原
子若しくは塩素原子、１個のＣ4〜Ｃ6シクロアルキル基
又は１個のＣ1〜Ｃ4アルコキシ基である。）、Ｃ3〜Ｃ4
シクロアルキル基、Ｃ 3〜Ｃ5アルケニル基又はＣ3〜Ｃ5
アルキニル基であり、（ａ２）Ｘが、フッ素原子、塩素
原子、臭素原子、ヨウ素原子、置換されてよいＣ1〜Ｃ4
アルキル基（当該置換基は、同一又は異なった１〜３個
のフッ素原子若しくは塩素原子である。）又は置換され
てよいＣ1〜Ｃ4アルコキシ基（当該置換基は、同一又は
異なった１〜３個のフッ素原子若しくは塩素原子であ
る。）であり、ｍが、０、１又は２であり、（ａ３）Ｚ
が、Ｃ1〜Ｃ4アルキル基であり、ｎが、０、１又は２で
あり、ｎが２であるとき、２個のＺが、一緒になって、
Ｃ1〜Ｃ2アルキレン基を形成してよく、（ａ４）……
が、単結合又は二重結合であり、より好適には、（ｂ
１）Ｒが、置換されてよいＣ1〜Ｃ5アルキル基（当該置
換基は、１〜３個のフッ素原子、１個のシクロヘキシル
基又は１個のメトキシ基である。）、Ｃ3〜Ｃ5アルケニ
ル基又はＣ3〜Ｃ5アルキニル基であり、（ｂ２）Ｘが、
フッ素原子、塩素原子、Ｃ1〜Ｃ3アルキル基又はＣ1〜
Ｃ3アルコキシ基であり、ｍが、０又は１であり、（ｂ
３）Ｚが、Ｃ1〜Ｃ3アルキル基であり、ｎが、０又は１
であり、（ｂ４）……が、単結合又は二重結合であり、
更により好適には、（ｃ１）Ｒが、置換されてよいＣ1
〜Ｃ4アルキル基（当該置換基は、１〜３個のフッ素原
子である。）、Ｃ3〜Ｃ4アルケニル基又はＣ4〜Ｃ5アル
キニル基であり、（ｃ２）Ｘが、フッ素原子又はメチル
基であり、ｍが、０又は１であり、（ｃ３）Ｚが、メチ
ル基であり、ｎが、０又は１であり、（ｃ４）……が、
単結合又は二重結合であり、特に好適には、（ｄ１）Ｒ
が、メチル基、エチル基、プロピル基、ブチル基、イソ
ブチル基、ペンチル基、トリフルオロメチル基、ビニル
基、アリル基、４−ペンテニル基、３−メチル−２−ブ
テニル基、プロパルギル基又は２−ペンチニル基であ
り、（ｄ２）ｍが、０であり、（ｄ３）ｎが、０であ
り、（ｄ４）……が、単結合又は二重結合であり、最も
好適には、（ｅ）化合物（Ｉ）が、１−メチル−N−
（３−キノリル）−１−シクロヘキサンカルボキサミ
ド、1-メチル-N-（8-フルオロ-3-キノリル）−１−シク
ロヘキサンカルボキサミド、1-メチル-N-（2-メチル-3-
キノリル）−１−シクロヘキサンカルボキサミド、1-メ
チル-N-（8-メチル-3-キノリル）−１−シクロヘキサン
カルボキサミド、1-エチル-N-（2-メチル-3-キノリル）
−１−シクロヘキサンカルボキサミド、1-エチル-N-（4
-メチル-3-キノリル）−１−シクロヘキサンカルボキサ
ミド、1-プロピル-N-（4-メチル-3-キノリル）−１−シ
クロヘキサンカルボキサミド、1-イソブチル-N-（4-メ
チル-3-キノリル）−１−シクロヘキサンカルボキサミ
ド、１−トリフルオロメチル−N−（３−キノリル）−
１−シクロヘキサンカルボキサミド、１−アリル−N−
（３−キノリル）−１−シクロヘキサンカルボキサミ
ド、1-アリル-N-（2-メチル-3-キノリル）−１−シクロ
ヘキサンカルボキサミド、1-アリル-N-（4-メチル-3-キ
ノリル）−１−シクロヘキサンカルボキサミド、1-（2-
メチルアリル）-N-（2-メチル-3-キノリル）−１−シク
ロヘキサンカルボキサミド、1-（2-メチルアリル）-N-
（4-メチル-3-キノリル）−１−シクロヘキサンカルボ
キサミド、1-プロパルギル-N-（3-キノリル）−１−シ
クロヘキサンカルボキサミド、1-（2-ペンチニル）-N-
（4-メチル-3-キノリル）−１−シクロヘキサンカルボ
キサミド、1-エチル-N-（2-メチル-3-キノリル）-3-シ
クロヘキセン−１−カルボキサミド、1-アリル-N-（4-
メチル-3-キノリル）-3-シクロヘキセン−１−カルボキ
サミド又は1,2-ジメチル-N-（3-キノリル）−１−シク
ロヘキサンカルボキサミドである。In the compound (I) of the present invention, preferably
Is C in which (a1) R may be substituted1~ C6Alkyl group
(The substituents are the same or different 1 to 4 fluorine atoms.
Child or chlorine atom, 1 CFour~ C6Cycloalkyl group
Or 1 C1~ CFourIt is an alkoxy group. ), C3~ CFour
Cycloalkyl group, C 3~ CFiveAlkenyl group or C3~ CFive
An alkynyl group, wherein (a2) X is a fluorine atom or chlorine
Atom, bromine atom, iodine atom, optionally substituted C1~ CFour
Alkyl group (the said substituents are the same or different 1 to 3)
Is a fluorine atom or chlorine atom. ) Or replaced
May be C1~ CFourAlkoxy group (the substituents are the same or
1 to 3 different fluorine or chlorine atoms
It ), M is 0, 1 or 2, and (a3) Z
But C1~ CFourAn alkyl group, n is 0, 1 or 2
And when n is 2, two Z's together
C1~ C2An alkylene group may be formed, (a4)......
Is a single bond or a double bond, and more preferably (b
1) R may be substituted C1~ CFiveAlkyl group
The substituent is 1 to 3 fluorine atoms, 1 cyclohexyl
A group or one methoxy group. ), C3~ CFiveArcheni
Ru radical or C3~ CFiveIs an alkynyl group, and (b2) X is
Fluorine atom, chlorine atom, C1~ C3Alkyl group or C1~
C3An alkoxy group, m is 0 or 1, and (b
3) Z is C1~ C3It is an alkyl group, and n is 0 or 1.
And (b4)......Is a single bond or a double bond,
Even more preferably, (c1) R is optionally substituted C1
~ CFourAlkyl group (the substituent is 1 to 3 fluorine atoms)
Is a child. ), C3~ CFourAlkenyl group or CFour~ CFiveAl
A quinyl group, (c2) X is a fluorine atom or methyl
A group, m is 0 or 1, and (c3) Z is methyl.
Is a group, n is 0 or 1, and (c4)......But,
A single bond or a double bond, and particularly preferably (d1) R
Is a methyl group, ethyl group, propyl group, butyl group, iso
Butyl group, pentyl group, trifluoromethyl group, vinyl
Group, allyl group, 4-pentenyl group, 3-methyl-2-bu
A tenyl group, a propargyl group or a 2-pentynyl group
And (d2) m is 0, and (d3) n is 0.
(D4)......Is a single bond or a double bond,
Preferably, (e) compound (I) is 1-methyl-N-
(3-quinolyl) -1-cyclohexanecarboxami
De, 1-methyl-N- (8-fluoro-3-quinolyl) -1-siku
Rohexanecarboxamide, 1-methyl-N- (2-methyl-3-
Quinolyl) -1-cyclohexanecarboxamide, 1-me
Cyl-N- (8-methyl-3-quinolyl) -1-cyclohexane
Carboxamide, 1-ethyl-N- (2-methyl-3-quinolyl)
-1-cyclohexanecarboxamide, 1-ethyl-N- (4
-Methyl-3-quinolyl) -1-cyclohexanecarboxa
Mido, 1-propyl-N- (4-methyl-3-quinolyl) -1-si
Chlorohexanecarboxamide, 1-isobutyl-N- (4-me
Cyl-3-quinolyl) -1-cyclohexanecarboxami
, 1-trifluoromethyl-N- (3-quinolyl)-
1-cyclohexanecarboxamide, 1-allyl-N-
(3-quinolyl) -1-cyclohexanecarboxami
1-allyl-N- (2-methyl-3-quinolyl) -1-cyclo
Hexanecarboxamide, 1-allyl-N- (4-methyl-3-ki
Noryl) -1-cyclohexanecarboxamide, 1- (2-
Methylallyl) -N- (2-methyl-3-quinolyl) -1-siku
Rohexanecarboxamide, 1- (2-methylallyl) -N-
(4-methyl-3-quinolyl) -1-cyclohexanecarbo
Xamide, 1-propargyl-N- (3-quinolyl) -1-si
Clohexane carboxamide, 1- (2-pentynyl) -N-
(4-methyl-3-quinolyl) -1-cyclohexanecarbo
Xamide, 1-ethyl-N- (2-methyl-3-quinolyl) -3-si
Chlohexene-1-carboxamide, 1-allyl-N- (4-
Methyl-3-quinolyl) -3-cyclohexene-1-carboxy
Samide or 1,2-dimethyl-N- (3-quinolyl) -1-siku
Rohexane carboxamide.

【００１９】本発明の化合物（Ｉ）は、例えば、硫酸
塩、塩酸塩、硝酸塩、リン酸塩、のような塩にすること
ができる。それらの塩は、農園芸用の殺菌剤として使用
できる限り、本発明に包含される。The compound (I) of the present invention can be converted into salts such as sulfates, hydrochlorides, nitrates and phosphates. Those salts are included in the present invention as long as they can be used as fungicides for agriculture and horticulture.

【００２０】本発明化合物（Ｉ）は溶媒和物にすること
ができ、それら溶媒和物も、本発明に包含される。その
ような溶媒和物は、好適には、水和物である。The compound (I) of the present invention can be a solvate, and these solvates are also included in the present invention. Such solvates are preferably hydrates.

【００２１】本発明化合物（Ｉ）中には、不斉炭素を有
する化合物もあり、その場合には、本願発明は、一種の
光学活性体及び数種の光学活性体の任意の割合の混合物
をも包含する。The compound (I) of the present invention also includes a compound having an asymmetric carbon. In such a case, the present invention comprises a mixture of one optically active substance and several optically active substances at any ratio. Also includes.

【００２２】本発明の代表化合物を下記表に例示する
が、本発明はこれらの化合物に限定されるものではな
い。Representative compounds of the present invention are exemplified in the following table, but the present invention is not limited to these compounds.

【００２３】以下、「……」において「単」は単結合
を、「……」において「二」は二重結合を、「Me」はメ
チル基を、「Et」はエチル基を、「Pr」はプロピル基
を、「iPr」はイソプロピル基を、「cPr」はシクロプロ
ピル基を、「Bu」はブチル基を、「iBu」はイソブチル
基を、「tBu」はtert-ブチル基を、「cBu」はシクロブ
チル基を、「Pent」はペンチル基を、「Hex」はヘキシ
ル基を、「cHex」はシクロヘキシル基を、「2-Et-Bu」
は２−エチルブチル基を、「Hept」はヘプチル基を、
「Oct」はオクチル基を、「Allyl」はアリル基を、「Vi
nyl」はビニル基を、「2,4-F2」はキノリン環の２位に
結合したフッ素原子及び４位に結合したフッ素原子を、
「Xm」において「H」はm=0を、「Yn」において「H」はn
=0を、「3,3,4,4-F4-Bu」は３，３，４，４−テトラフ
ルオロブチル基を、「Yn」において「2-5-CH2」はシク
ロヘキサン若しくはシクロヘキセン環の２位及び５位が
メチレン基で結ばれていることを、それぞれ示す。In the following, " ... " indicates a single bond, " ... " indicates a double bond, "Me" indicates a methyl group, "Et" indicates an ethyl group, and "Pr". Is a propyl group, "iPr" is an isopropyl group, "cPr" is a cyclopropyl group, "Bu" is a butyl group, "iBu" is an isobutyl group, "tBu" is a tert-butyl group, " cBu ”is a cyclobutyl group,“ Pent ”is a pentyl group,“ Hex ”is a hexyl group,“ cHex ”is a cyclohexyl group, and“ 2-Et-Bu ”.
Is a 2-ethylbutyl group, "Hept" is a heptyl group,
“Oct” is an octyl group, “Allyl” is an allyl group, and “Vi
“Nyl” is a vinyl group, and “2,4-F 2 ” is a fluorine atom bonded to the 2-position or 4-position of the quinoline ring,
In “X m ”, “H” is m = 0, and in “Y n ”, “H” is n.
= 0, "3,3,4,4-F 4 -Bu" is a 3,3,4,4-tetrafluorobutyl group, and in "Y n " 2-5-CH 2 "is cyclohexane or cyclohexene. It shows that the 2-position and 5-position of the ring are connected by a methylene group, respectively.

【００２４】[0024]

【表１】[Table 1]

【００２５】[0025]

【化３】 [Chemical 3]

【００２６】 ────────────────────────────────── 化合物 …… Ｒ Ｘm 化合物 …… Ｒ Ｘm 番号 番号 ────────────────────────────────── 1-1 単 Me H 1-2 単 Me 2-F 1-3 単 Me 4-F 1-4 単 Me 5-F 1-5 単 Me 6-F 1-6 単 Me 7-F 1-7 単 Me 8-F 1-8 単 Me 2-Cl 1-9 単 Me 4-Cl 1-10 単 Me 5-Cl 1-11 単 Me 6-Cl 1-12 単 Me 7-Cl 1-13 単 Me 8-Cl 1-14 単 Me 2-Br 1-15 単 Me 4-Br 1-16 単 Me 5-Br 1-17 単 Me 6-Br 1-18 単 Me 7-Br 1-19 単 Me 8-Br 1-20 単 Me 2-I 1-21 単 Me 4-I 1-22 単 Me 5-I 1-23 単 Me 6-I 1-24 単 Me 7-I 1-25 単 Me 8-I 1-26 単 Me 2-Me 1-27 単 Me 4-Me 1-28 単 Me 5-Me 1-29 単 Me 6-Me 1-30 単 Me 7-Me 1-31 単 Me 8-Me 1-32 単 Me 2-Et 1-33 単 Me 4-Et 1-34 単 Me 5-Et 1-35 単 Me 6-Et 1-36 単 Me 7-Et 1-37 単 Me 8-Et 1-38 単 Me 2-Pr 1-39 単 Me 4-Pr 1-40 単 Me 5-Pr 1-41 単 Me 6-Pr 1-42 単 Me 7-Pr 1-43 単 Me 8-Pr 1-44 単 Me 2-iPr 1-45 単 Me 4-iPr 1-46 単 Me 5-iPr 1-47 単 Me 6-iPr 1-48 単 Me 7-iPr 1-49 単 Me 8-iPr 1-50 単 Me 2-Bu 1-51 単 Me 4-Bu 1-52 単 Me 5-Bu 1-53 単 Me 6-Bu 1-54 単 Me 7-Bu 1-55 単 Me 8-Bu 1-56 単 Me 2-CF3 1-57 単 Me 4-CF3 1-58 単 Me 5-CF3 1-59 単 Me 6-CF3 1-60 単 Me 7-CF3 1-61 単 Me 8-CF3 1-62 単 Me 2-CF3CH2 1-63 単 Me 4-CF3CH2 1-64 単 Me 5-CF3CH2 1-65 単 Me 6-CF3CH2 1-66 単 Me 7-CF3CH2 1-67 単 Me 8-CF3CH2 1-68 単 Me 2-CF2H 1-69 単 Me 4-CF2H 1-70 単 Me 5-CF2H 1-71 単 Me 6-CF2H 1-72 単 Me 7-CF2H 1-73 単 Me 8-CF2H 1-74 単 Me 2-CF2H 1-75 単 Me 4-CF2H 1-76 単 Me 5-CF2H 1-77 単 Me 6-CF2H 1-78 単 Me 7-CF2H 1-79 単 Me 8-CF2H 1-80 単 Me 2-CClH2 1-81 単 Me 4-CClH2 1-82 単 Me 5-CClH2 1-83 単 Me 6-CClH2 1-84 単 Me 7-CClH2 1-85 単 Me 8-CClH2 1-86 単 Me 2-MeO 1-87 単 Me 4-MeO 1-88 単 Me 5-MeO 1-89 単 Me 6-MeO 1-90 単 Me 7-MeO 1-91 単 Me 8-MeO 1-92 単 Me 2-EtO 1-93 単 Me 4-EtO 1-94 単 Me 5-EtO 1-95 単 Me 6-EtO 1-96 単 Me 7-EtO 1-97 単 Me 8-EtO 1-98 単 Me 2-PrO 1-99 単 Me 4-PrO 1-100 単 Me 5-PrO 1-101 単 Me 6-PrO 1-102 単 Me 7-PrO 1-103 単 Me 8-PrO 1-104 単 Me 2-iPrO 1-105 単 Me 4-iPrO 1-106 単 Me 5-iPrO 1-107 単 Me 6-iPrO 1-108 単 Me 7-iPrO 1-109 単 Me 8-iPrO 1-110 単 Me 2-BuO 1-111 単 Me 4-BuO 1-112 単 Me 5-BuO 1-113 単 Me 6-BuO 1-114 単 Me 7-BuO 1-115 単 Me 8-BuO 1-116 単 Me 2-CF3O 1-117 単 Me 4-CF3O 1-118 単 Me 5-CF3O 1-119 単 Me 6-CF3O 1-120 単 Me 7-CF3O 1-121 単 Me 8-CF3O 1-122 単 Me 2-CF3CH2O 1-123 単 Me 4-CF3CH2O 1-124 単 Me 5-CF3CH2O 1-125 単 Me 6-CF3CH2O 1-126 単 Me 7-CF3CH2O 1-127 単 Me 8-CF3CH2O 1-128 単 Me 2-CF2HO 1-129 単 Me 4-CF2HO 1-130 単 Me 5-CF2HO 1-131 単 Me 6-CF2HO 1-132 単 Me 7-CF2HO 1-133 単 Me 8-CF2HO 1-134 単 Me 2-CF2HO 1-135 単 Me 4-CF2HO 1-136 単 Me 5-CF2HO 1-137 単 Me 6-CF2HO 1-138 単 Me 7-CF2HO 1-139 単 Me 8-CF2HO 1-140 単 Me 2-CClH2O 1-141 単 Me 4-CClH2O 1-142 単 Me 5-CClH2O 1-143 単 Me 6-CClH2O 1-144 単 Me 7-CClH2O 1-145 単 Me 8-CClH2O 1-146 単 Me 2,4-F2 1-147 単 Me 2,5-F2 1-148 単 Me 2,6-F2 1-149 単 Me 2,7-F2 1-150 単 Me 2,8-F2 1-151 単 Me 4,5-F2 1-152 単 Me 4,6-F2 1-153 単 Me 4,7-F2 1-154 単 Me 4,8-F2 1-155 単 Me 5,6-F2 1-156 単 Me 5,7-F2 1-157 単 Me 5,8-F2 1-158 単 Me 6,7-F2 1-159 単 Me 6,8-F2 1-160 単 Me 7,8-F2 1-161 単 Me 4,5-Cl2 1-162 単 Me 4,6-Cl2 1-163 単 Me 4,7-Cl2 1-164 単 Me 4,8-Cl2 1-165 単 Me 5,6-Cl2 1-166 単 Me 5,7-Cl2 1-167 単 Me 5,8-Cl2 1-168 単 Me 6,7-Cl2 1-169 単 Me 6,8-Cl2 1-170 単 Me 7,8-Cl2 1-171 単 Me 2,5-Me2 1-172 単 Me 2,6-Me2 1-173 単 Me 2,7-Me2 1-174 単 Me 2,8-Me2 1-175 単 Me 4,5-Me2 1-176 単 Me 4,6-Me2 1-177 単 Me 4,7-Me2 1-178 単 Me 4,8-Me2 1-179 単 Me 5,6-Me2 1-180 単 Me 5,7-Me2 1-181 単 Me 5,8-Me2 1-182 単 Me 6,7-Me2 1-183 単 Me 6,8-Me2 1-184 単 Me 7,8-Me2 1-185 単 Me 2,5-(MeO)2 1-186 単 Me 2,6-(MeO)2 1-187 単 Me 2,7-(MeO)2 1-188 単 Me 2,8-(MeO)2 1-189 単 Me 4,5-(MeO)2 1-190 単 Me 4,6-(MeO)2 1-191 単 Me 4,7-(MeO)2 1-192 単 Me 4,8-(MeO)2 1-193 単 Me 5,6-(MeO)2 1-194 単 Me 5,7-(MeO)2 1-195 単 Me 5,8-(MeO)2 1-196 単 Me 6,7-(MeO)2 1-197 単 Me 6,8-(MeO)2 1-198 単 Me 7,8-(MeO)2 1-199 単 Me 2-Me-5-F 1-200 単 Me 2-Me-6-F 1-201 単 Me 2-Me-7-F 1-202 単 Me 2-Me-8-F 1-203 単 Me 2-Me-5-Cl 1-204 単 Me 2-Me-6-Cl 1-205 単 Me 2-Me-7-Cl 1-206 単 Me 2-Me-8-Cl 1-207 単 Me 2-Me-5-MeO 1-208 単 Me 2-Me-6-MeO 1-209 単 Me 2-Me-7-MeO 1-210 単 Me 2-Me-8-MeO 1-211 単 Me 4-Cl-5-F 1-212 単 Me 4-Cl-6-F 1-213 単 Me 4-Cl-7-F 1-214 単 Me 4-Cl-8-F 1-215 単 Me 4-Cl-5-Me 1-216 単 Me 4-Cl-6-Me 1-217 単 Me 4-Cl-7-Me 1-218 単 Me 4-Cl-8-Me 1-219 単 Me 4-Cl-5-MeO 1-220 単 Me 4-Cl-6-MeO 1-221 単 Me 4-Cl-7-MeO 1-222 単 Me 4-Cl-8-MeO 1-223 単 Et H 1-224 単 Et 2-F 1-225 単 Et 4-F 1-226 単 Et 5-F 1-227 単 Et 6-F 1-228 単 Et 7-F 1-229 単 Et 8-F 1-230 単 Et 2-Cl 1-231 単 Et 4-Cl 1-232 単 Et 5-Cl 1-233 単 Et 6-Cl 1-234 単 Et 7-Cl 1-235 単 Et 8-Cl 1-236 単 Et 2-Br 1-237 単 Et 4-Br 1-238 単 Et 5-Br 1-239 単 Et 6-Br 1-240 単 Et 7-Br 1-241 単 Et 8-Br 1-242 単 Et 2-I 1-243 単 Et 4-I 1-244 単 Et 5-I 1-245 単 Et 6-I 1-246 単 Et 7-I 1-247 単 Et 8-I 1-248 単 Et 2-Me 1-249 単 Et 4-Me 1-250 単 Et 5-Me 1-251 単 Et 6-Me 1-252 単 Et 7-Me 1-253 単 Et 8-Me 1-254 単 Et 2-Et 1-255 単 Et 4-Et 1-256 単 Et 5-Et 1-257 単 Et 6-Et 1-258 単 Et 7-Et 1-259 単 Et 8-Et 1-260 単 Et 2-Pr 1-261 単 Et 4-Pr 1-262 単 Et 5-Pr 1-263 単 Et 6-Pr 1-264 単 Et 7-Pr 1-265 単 Et 8-Pr 1-266 単 Et 2-iPr 1-267 単 Et 4-iPr 1-268 単 Et 5-iPr 1-269 単 Et 6-iPr 1-270 単 Et 7-iPr 1-271 単 Et 8-iPr 1-272 単 Et 2-Bu 1-273 単 Et 4-Bu 1-274 単 Et 5-Bu 1-275 単 Et 6-Bu 1-276 単 Et 7-Bu 1-277 単 Et 8-Bu 1-278 単 Et 2-CF3 1-279 単 Et 4-CF3 1-280 単 Et 5-CF3 1-281 単 Et 6-CF3 1-282 単 Et 7-CF3 1-283 単 Et 8-CF3 1-284 単 Et 2-CF3CH2 1-285 単 Et 4-CF3CH2 1-286 単 Et 5-CF3CH2 1-287 単 Et 6-CF3CH2 1-288 単 Et 7-CF3CH2 1-289 単 Et 8-CF3CH2 1-290 単 Et 2-CF2H 1-291 単 Et 4-CF2H 1-292 単 Et 5-CF2H 1-293 単 Et 6-CF2H 1-294 単 Et 7-CF2H 1-295 単 Et 8-CF2H 1-296 単 Et 2-CF2H 1-297 単 Et 4-CF2H 1-298 単 Et 5-CF2H 1-299 単 Et 6-CF2H 1-300 単 Et 7-CF2H 1-301 単 Et 8-CF2H 1-302 単 Et 2-CClH2 1-303 単 Et 4-CClH2 1-304 単 Et 5-CClH2 1-305 単 Et 6-CClH2 1-306 単 Et 7-CClH2 1-307 単 Et 8-CClH2 1-308 単 Et 2-MeO 1-309 単 Et 4-MeO 1-310 単 Et 5-MeO 1-311 単 Et 6-MeO 1-312 単 Et 7-MeO 1-313 単 Et 8-MeO 1-314 単 Et 2-EtO 1-315 単 Et 4-EtO 1-316 単 Et 5-EtO 1-317 単 Et 6-EtO 1-318 単 Et 7-EtO 1-319 単 Et 8-EtO 1-320 単 Et 2-PrO 1-321 単 Et 4-PrO 1-322 単 Et 5-PrO 1-323 単 Et 6-PrO 1-324 単 Et 7-PrO 1-325 単 Et 8-PrO 1-326 単 Et 2-iPrO 1-327 単 Et 4-iPrO 1-328 単 Et 5-iPrO 1-329 単 Et 6-iPrO 1-330 単 Et 7-iPrO 1-331 単 Et 8-iPrO 1-332 単 Et 2-BuO 1-333 単 Et 4-BuO 1-334 単 Et 5-BuO 1-335 単 Et 6-BuO 1-336 単 Et 7-BuO 1-337 単 Et 8-BuO 1-338 単 Et 2-CF3O 1-339 単 Et 4-CF3O 1-340 単 Et 5-CF3O 1-341 単 Et 6-CF3O 1-342 単 Et 7-CF3O 1-343 単 Et 8-CF3O 1-344 単 Et 2-CF3CH2O 1-345 単 Et 4-CF3CH2O 1-346 単 Et 5-CF3CH2O 1-347 単 Et 6-CF3CH2O 1-348 単 Et 7-CF3CH2O 1-349 単 Et 8-CF3CH2O 1-350 単 Et 2-CF2HO 1-351 単 Et 4-CF2HO 1-352 単 Et 5-CF2HO 1-353 単 Et 6-CF2HO 1-354 単 Et 7-CF2HO 1-355 単 Et 8-CF2HO 1-356 単 Et 2-CF2HO 1-357 単 Et 4-CF2HO 1-358 単 Et 5-CF2HO 1-359 単 Et 6-CF2HO 1-360 単 Et 7-CF2HO 1-361 単 Et 8-CF2HO 1-362 単 Et 2-CClH2O 1-363 単 Et 4-CClH2O 1-364 単 Et 5-CClH2O 1-365 単 Et 6-CClH2O 1-366 単 Et 7-CClH2O 1-367 単 Et 8-CClH2O 1-368 単 Et 2,4-F2 1-369 単 Et 2,5-F2 1-370 単 Et 2,6-F2 1-371 単 Et 2,7-F2 1-372 単 Et 2,8-F2 1-373 単 Et 4,5-F2 1-374 単 Et 4,6-F2 1-375 単 Et 4,7-F2 1-376 単 Et 4,8-F2 1-377 単 Et 5,6-F2 1-378 単 Et 5,7-F2 1-379 単 Et 5,8-F2 1-380 単 Et 6,7-F2 1-381 単 Et 6,8-F2 1-382 単 Et 7,8-F2 1-383 単 Et 4,5-Cl2 1-384 単 Et 4,6-Cl2 1-385 単 Et 4,7-Cl2 1-386 単 Et 4,8-Cl2 1-387 単 Et 5,6-Cl2 1-388 単 Et 5,7-Cl2 1-389 単 Et 5,8-Cl2 1-390 単 Et 6,7-Cl2 1-391 単 Et 6,8-Cl2 1-392 単 Et 7,8-Cl2 1-393 単 Et 2,5-Me2 1-394 単 Et 2,6-Me2 1-395 単 Et 2,7-Me2 1-396 単 Et 2,8-Me2 1-397 単 Et 4,5-Me2 1-398 単 Et 4,6-Me2 1-399 単 Et 4,7-Me2 1-400 単 Et 4,8-Me2 1-401 単 Et 5,6-Me2 1-402 単 Et 5,7-Me2 1-403 単 Et 5,8-Me2 1-404 単 Et 6,7-Me2 1-405 単 Et 6,8-Me2 1-406 単 Et 7,8-Me2 1-407 単 Et 2,5-(MeO)2 1-408 単 Et 2,6-(MeO)2 1-409 単 Et 2,7-(MeO)2 1-410 単 Et 2,8-(MeO)2 1-411 単 Et 4,5-(MeO)2 1-412 単 Et 4,6-(MeO)2 1-413 単 Et 4,7-(MeO)2 1-414 単 Et 4,8-(MeO)2 1-415 単 Et 5,6-(MeO)2 1-416 単 Et 5,7-(MeO)2 1-417 単 Et 5,8-(MeO)2 1-418 単 Et 6,7-(MeO)2 1-419 単 Et 6,8-(MeO)2 1-420 単 Et 7,8-(MeO)2 1-421 単 Et 2-Me-5-F 1-422 単 Et 2-Me-6-F 1-423 単 Et 2-Me-7-F 1-424 単 Et 2-Me-8-F 1-425 単 Et 2-Me-5-Cl 1-426 単 Et 2-Me-6-Cl 1-427 単 Et 2-Me-7-Cl 1-428 単 Et 2-Me-8-Cl 1-429 単 Et 2-Me-5-MeO 1-430 単 Et 2-Me-6-MeO 1-431 単 Et 2-Me-7-MeO 1-432 単 Et 2-Me-8-MeO 1-433 単 Et 4-Cl-5-F 1-434 単 Et 4-Cl-6-F 1-435 単 Et 4-Cl-7-F 1-436 単 Et 4-Cl-8-F 1-437 単 Et 4-Cl-5-Me 1-438 単 Et 4-Cl-6-Me 1-439 単 Et 4-Cl-7-Me 1-440 単 Et 4-Cl-8-Me 1-441 単 Et 4-Cl-5-MeO 1-442 単 Et 4-Cl-6-MeO 1-443 単 Et 4-Cl-7-MeO 1-444 単 Et 4-Cl-8-MeO 1-445 単 Pr H 1-446 単 Pr 2-F 1-447 単 Pr 4-F 1-448 単 Pr 5-F 1-449 単 Pr 6-F 1-450 単 Pr 7-F 1-451 単 Pr 8-F 1-452 単 Pr 2-Cl 1-453 単 Pr 4-Cl 1-454 単 Pr 5-Cl 1-455 単 Pr 6-Cl 1-456 単 Pr 7-Cl 1-457 単 Pr 8-Cl 1-458 単 Pr 2-Br 1-459 単 Pr 4-Br 1-460 単 Pr 5-Br 1-461 単 Pr 6-Br 1-462 単 Pr 7-Br 1-463 単 Pr 8-Br 1-464 単 Pr 2-I 1-465 単 Pr 4-I 1-466 単 Pr 5-I 1-467 単 Pr 6-I 1-468 単 Pr 7-I 1-469 単 Pr 8-I 1-470 単 Pr 2-Me 1-471 単 Pr 4-Me 1-472 単 Pr 5-Me 1-473 単 Pr 6-Me 1-474 単 Pr 7-Me 1-475 単 Pr 8-Me 1-476 単 Pr 2-Et 1-477 単 Pr 4-Et 1-478 単 Pr 5-Et 1-479 単 Pr 6-Et 1-480 単 Pr 7-Et 1-481 単 Pr 8-Et 1-482 単 Pr 2-Pr 1-483 単 Pr 4-Pr 1-484 単 Pr 5-Pr 1-485 単 Pr 6-Pr 1-486 単 Pr 7-Pr 1-487 単 Pr 8-Pr 1-488 単 Pr 2-iPr 1-489 単 Pr 4-iPr 1-490 単 Pr 5-iPr 1-491 単 Pr 6-iPr 1-492 単 Pr 7-iPr 1-493 単 Pr 8-iPr 1-494 単 Pr 2-Bu 1-495 単 Pr 4-Bu 1-496 単 Pr 5-Bu 1-497 単 Pr 6-Bu 1-498 単 Pr 7-Bu 1-499 単 Pr 8-Bu 1-500 単 Pr 2-CF3 1-501 単 Pr 4-CF3 1-502 単 Pr 5-CF3 1-503 単 Pr 6-CF3 1-504 単 Pr 7-CF3 1-505 単 Pr 8-CF3 1-506 単 Pr 2-CF3CH2 1-507 単 Pr 4-CF3CH2 1-508 単 Pr 5-CF3CH2 1-509 単 Pr 6-CF3CH2 1-510 単 Pr 7-CF3CH2 1-511 単 Pr 8-CF3CH2 1-512 単 Pr 2-CF2H 1-513 単 Pr 4-CF2H 1-514 単 Pr 5-CF2H 1-515 単 Pr 6-CF2H 1-516 単 Pr 7-CF2H 1-517 単 Pr 8-CF2H 1-518 単 Pr 2-CF2H 1-519 単 Pr 4-CF2H 1-520 単 Pr 5-CF2H 1-521 単 Pr 6-CF2H 1-522 単 Pr 7-CF2H 1-523 単 Pr 8-CF2H 1-524 単 Pr 2-CClH2 1-525 単 Pr 4-CClH2 1-526 単 Pr 5-CClH2 1-527 単 Pr 6-CClH2 1-528 単 Pr 7-CClH2 1-529 単 Pr 8-CClH2 1-530 単 Pr 2-MeO 1-531 単 Pr 4-MeO 1-532 単 Pr 5-MeO 1-533 単 Pr 6-MeO 1-534 単 Pr 7-MeO 1-535 単 Pr 8-MeO 1-536 単 Pr 2-EtO 1-537 単 Pr 4-EtO 1-538 単 Pr 5-EtO 1-539 単 Pr 6-EtO 1-540 単 Pr 7-EtO 1-541 単 Pr 8-EtO 1-542 単 Pr 2-PrO 1-543 単 Pr 4-PrO 1-544 単 Pr 5-PrO 1-545 単 Pr 6-PrO 1-546 単 Pr 7-PrO 1-547 単 Pr 8-PrO 1-548 単 Pr 2-iPrO 1-549 単 Pr 4-iPrO 1-550 単 Pr 5-iPrO 1-551 単 Pr 6-iPrO 1-552 単 Pr 7-iPrO 1-553 単 Pr 8-iPrO 1-554 単 Pr 2-BuO 1-555 単 Pr 4-BuO 1-556 単 Pr 5-BuO 1-557 単 Pr 6-BuO 1-558 単 Pr 7-BuO 1-559 単 Pr 8-BuO 1-560 単 Pr 2-CF3O 1-561 単 Pr 4-CF3O 1-562 単 Pr 5-CF3O 1-563 単 Pr 6-CF3O 1-564 単 Pr 7-CF3O 1-565 単 Pr 8-CF3O 1-566 単 Pr 2-CF3CH2O 1-567 単 Pr 4-CF3CH2O 1-568 単 Pr 5-CF3CH2O 1-569 単 Pr 6-CF3CH2O 1-570 単 Pr 7-CF3CH2O 1-571 単 Pr 8-CF3CH2O 1-572 単 Pr 2-CF2HO 1-573 単 Pr 4-CF2HO 1-574 単 Pr 5-CF2HO 1-575 単 Pr 6-CF2HO 1-576 単 Pr 7-CF2HO 1-577 単 Pr 8-CF2HO 1-578 単 Pr 2-CF2HO 1-579 単 Pr 4-CF2HO 1-580 単 Pr 5-CF2HO 1-581 単 Pr 6-CF2HO 1-582 単 Pr 7-CF2HO 1-583 単 Pr 8-CF2HO 1-584 単 Pr 2-CClH2O 1-585 単 Pr 4-CClH2O 1-586 単 Pr 5-CClH2O 1-587 単 Pr 6-CClH2O 1-588 単 Pr 7-CClH2O 1-589 単 Pr 8-CClH2O 1-590 単 Pr 2,4-F2 1-591 単 Pr 2,5-F2 1-592 単 Pr 2,6-F2 1-593 単 Pr 2,7-F2 1-594 単 Pr 2,8-F2 1-595 単 Pr 4,5-F2 1-596 単 Pr 4,6-F2 1-597 単 Pr 4,7-F2 1-598 単 Pr 4,8-F2 1-599 単 Pr 5,6-F2 1-600 単 Pr 5,7-F2 1-601 単 Pr 5,8-F2 1-602 単 Pr 6,7-F2 1-603 単 Pr 6,8-F2 1-604 単 Pr 7,8-F2 1-605 単 Pr 4,5-Cl2 1-606 単 Pr 4,6-Cl2 1-607 単 Pr 4,7-Cl2 1-608 単 Pr 4,8-Cl2 1-609 単 Pr 5,6-Cl2 1-610 単 Pr 5,7-Cl2 1-611 単 Pr 5,8-Cl2 1-612 単 Pr 6,7-Cl2 1-613 単 Pr 6,8-Cl2 1-614 単 Pr 7,8-Cl2 1-615 単 Pr 2,5-Me2 1-616 単 Pr 2,6-Me2 1-617 単 Pr 2,7-Me2 1-618 単 Pr 2,8-Me2 1-619 単 Pr 4,5-Me2 1-620 単 Pr 4,6-Me2 1-621 単 Pr 4,7-Me2 1-622 単 Pr 4,8-Me2 1-623 単 Pr 5,6-Me2 1-624 単 Pr 5,7-Me2 1-625 単 Pr 5,8-Me2 1-626 単 Pr 6,7-Me2 1-627 単 Pr 6,8-Me2 1-628 単 Pr 7,8-Me2 1-629 単 Pr 2,5-(MeO)2 1-630 単 Pr 2,6-(MeO)2 1-631 単 Pr 2,7-(MeO)2 1-632 単 Pr 2,8-(MeO)2 1-633 単 Pr 4,5-(MeO)2 1-634 単 Pr 4,6-(MeO)2 1-635 単 Pr 4,7-(MeO)2 1-636 単 Pr 4,8-(MeO)2 1-637 単 Pr 5,6-(MeO)2 1-638 単 Pr 5,7-(MeO)2 1-639 単 Pr 5,8-(MeO)2 1-640 単 Pr 6,7-(MeO)2 1-641 単 Pr 6,8-(MeO)2 1-642 単 Pr 7,8-(MeO)2 1-643 単 Pr 2-Me-5-F 1-644 単 Pr 2-Me-6-F 1-645 単 Pr 2-Me-7-F 1-646 単 Pr 2-Me-8-F 1-647 単 Pr 2-Me-5-Cl 1-648 単 Pr 2-Me-6-Cl 1-649 単 Pr 2-Me-7-Cl 1-650 単 Pr 2-Me-8-Cl 1-651 単 Pr 2-Me-5-MeO 1-652 単 Pr 2-Me-6-MeO 1-653 単 Pr 2-Me-7-MeO 1-654 単 Pr 2-Me-8-MeO 1-655 単 Pr 4-Cl-5-F 1-656 単 Pr 4-Cl-6-F 1-657 単 Pr 4-Cl-7-F 1-658 単 Pr 4-Cl-8-F 1-659 単 Pr 4-Cl-5-Me 1-660 単 Pr 4-Cl-6-Me 1-661 単 Pr 4-Cl-7-Me 1-662 単 Pr 4-Cl-8-Me 1-663 単 Pr 4-Cl-5-MeO 1-664 単 Pr 4-Cl-6-MeO 1-665 単 Pr 4-Cl-7-MeO 1-666 単 Pr 4-Cl-8-MeO 1-667 単 iPr H 1-668 単 iPr 2-F 1-669 単 iPr 4-F 1-670 単 iPr 5-F 1-671 単 iPr 6-F 1-672 単 iPr 7-F 1-673 単 iPr 8-F 1-674 単 iPr 2-Cl 1-675 単 iPr 4-Cl 1-676 単 iPr 5-Cl 1-677 単 iPr 6-Cl 1-678 単 iPr 7-Cl 1-679 単 iPr 8-Cl 1-680 単 iPr 2-Br 1-681 単 iPr 4-Br 1-682 単 iPr 5-Br 1-683 単 iPr 6-Br 1-684 単 iPr 7-Br 1-685 単 iPr 8-Br 1-686 単 iPr 2-I 1-687 単 iPr 4-I 1-688 単 iPr 5-I 1-689 単 iPr 6-I 1-690 単 iPr 7-I 1-691 単 iPr 8-I 1-692 単 iPr 2-Me 1-693 単 iPr 4-Me 1-694 単 iPr 5-Me 1-695 単 iPr 6-Me 1-696 単 iPr 7-Me 1-697 単 iPr 8-Me 1-698 単 iPr 2-Et 1-699 単 iPr 4-Et 1-700 単 iPr 5-Et 1-701 単 iPr 6-Et 1-702 単 iPr 7-Et 1-703 単 iPr 8-Et 1-704 単 iPr 2-Pr 1-705 単 iPr 4-Pr 1-706 単 iPr 5-Pr 1-707 単 iPr 6-Pr 1-708 単 iPr 7-Pr 1-709 単 iPr 8-Pr 1-710 単 iPr 2-iPr 1-711 単 iPr 4-iPr 1-712 単 iPr 5-iPr 1-713 単 iPr 6-iPr 1-714 単 iPr 7-iPr 1-715 単 iPr 8-iPr 1-716 単 iPr 2-Bu 1-717 単 iPr 4-Bu 1-718 単 iPr 5-Bu 1-719 単 iPr 6-Bu 1-720 単 iPr 7-Bu 1-721 単 iPr 8-Bu 1-722 単 iPr 2-CF3 1-723 単 iPr 4-CF3 1-724 単 iPr 5-CF3 1-725 単 iPr 6-CF3 1-726 単 iPr 7-CF3 1-727 単 iPr 8-CF3 1-728 単 iPr 2-CF3CH2 1-729 単 iPr 4-CF3CH2 1-730 単 iPr 5-CF3CH2 1-731 単 iPr 6-CF3CH2 1-732 単 iPr 7-CF3CH2 1-733 単 iPr 8-CF3CH2 1-734 単 iPr 2-CF2H 1-735 単 iPr 4-CF2H 1-736 単 iPr 5-CF2H 1-737 単 iPr 6-CF2H 1-738 単 iPr 7-CF2H 1-739 単 iPr 8-CF2H 1-740 単 iPr 2-CF2H 1-741 単 iPr 4-CF2H 1-742 単 iPr 5-CF2H 1-743 単 iPr 6-CF2H 1-744 単 iPr 7-CF2H 1-745 単 iPr 8-CF2H 1-746 単 iPr 2-CClH2 1-747 単 iPr 4-CClH2 1-748 単 iPr 5-CClH2 1-749 単 iPr 6-CClH2 1-750 単 iPr 7-CClH2 1-751 単 iPr 8-CClH2 1-752 単 iPr 2-MeO 1-753 単 iPr 4-MeO 1-754 単 iPr 5-MeO 1-755 単 iPr 6-MeO 1-756 単 iPr 7-MeO 1-757 単 iPr 8-MeO 1-758 単 iPr 2-EtO 1-759 単 iPr 4-EtO 1-760 単 iPr 5-EtO 1-761 単 iPr 6-EtO 1-762 単 iPr 7-EtO 1-763 単 iPr 8-EtO 1-764 単 iPr 2-PrO 1-765 単 iPr 4-PrO 1-766 単 iPr 5-PrO 1-767 単 iPr 6-PrO 1-768 単 iPr 7-PrO 1-769 単 iPr 8-PrO 1-770 単 iPr 2-iPrO 1-771 単 iPr 4-iPrO 1-772 単 iPr 5-iPrO 1-773 単 iPr 6-iPrO 1-774 単 iPr 7-iPrO 1-775 単 iPr 8-iPrO 1-776 単 iPr 2-BuO 1-777 単 iPr 4-BuO 1-778 単 iPr 5-BuO 1-779 単 iPr 6-BuO 1-780 単 iPr 7-BuO 1-781 単 iPr 8-BuO 1-782 単 iPr 2-CF3O 1-783 単 iPr 4-CF3O 1-784 単 iPr 5-CF3O 1-785 単 iPr 6-CF3O 1-786 単 iPr 7-CF3O 1-787 単 iPr 8-CF3O 1-788 単 iPr 2-CF3CH2O 1-789 単 iPr 4-CF3CH2O 1-790 単 iPr 5-CF3CH2O 1-791 単 iPr 6-CF3CH2O 1-792 単 iPr 7-CF3CH2O 1-793 単 iPr 8-CF3CH2O 1-794 単 iPr 2-CF2HO 1-795 単 iPr 4-CF2HO 1-796 単 iPr 5-CF2HO 1-797 単 iPr 6-CF2HO 1-798 単 iPr 7-CF2HO 1-799 単 iPr 8-CF2HO 1-800 単 iPr 2-CF2HO 1-801 単 iPr 4-CF2HO 1-802 単 iPr 5-CF2HO 1-803 単 iPr 6-CF2HO 1-804 単 iPr 7-CF2HO 1-805 単 iPr 8-CF2HO 1-806 単 iPr 2-CClH2O 1-807 単 iPr 4-CClH2O 1-808 単 iPr 5-CClH2O 1-809 単 iPr 6-CClH2O 1-810 単 iPr 7-CClH2O 1-811 単 iPr 8-CClH2O 1-812 単 iPr 2,4-F2 1-813 単 iPr 2,5-F2 1-814 単 iPr 2,6-F2 1-815 単 iPr 2,7-F2 1-816 単 iPr 2,8-F2 1-817 単 iPr 4,5-F2 1-818 単 iPr 4,6-F2 1-819 単 iPr 4,7-F2 1-820 単 iPr 4,8-F2 1-821 単 iPr 5,6-F2 1-822 単 iPr 5,7-F2 1-823 単 iPr 5,8-F2 1-824 単 iPr 6,7-F2 1-825 単 iPr 6,8-F2 1-826 単 iPr 7,8-F2 1-827 単 iPr 4,5-Cl2 1-828 単 iPr 4,6-Cl2 1-829 単 iPr 4,7-Cl2 1-830 単 iPr 4,8-Cl2 1-831 単 iPr 5,6-Cl2 1-832 単 iPr 5,7-Cl2 1-833 単 iPr 5,8-Cl2 1-834 単 iPr 6,7-Cl2 1-835 単 iPr 6,8-Cl2 1-836 単 iPr 7,8-Cl2 1-837 単 iPr 2,5-Me2 1-838 単 iPr 2,6-Me2 1-839 単 iPr 2,7-Me2 1-840 単 iPr 2,8-Me2 1-841 単 iPr 4,5-Me2 1-842 単 iPr 4,6-Me2 1-843 単 iPr 4,7-Me2 1-844 単 iPr 4,8-Me2 1-845 単 iPr 5,6-Me2 1-846 単 iPr 5,7-Me2 1-847 単 iPr 5,8-Me2 1-848 単 iPr 6,7-Me2 1-849 単 iPr 6,8-Me2 1-850 単 iPr 7,8-Me2 1-851 単 iPr 2,5-(MeO)2 1-852 単 iPr 2,6-(MeO)2 1-853 単 iPr 2,7-(MeO)2 1-854 単 iPr 2,8-(MeO)2 1-855 単 iPr 4,5-(MeO)2 1-856 単 iPr 4,6-(MeO)2 1-857 単 iPr 4,7-(MeO)2 1-858 単 iPr 4,8-(MeO)2 1-859 単 iPr 5,6-(MeO)2 1-860 単 iPr 5,7-(MeO)2 1-861 単 iPr 5,8-(MeO)2 1-862 単 iPr 6,7-(MeO)2 1-863 単 iPr 6,8-(MeO)2 1-864 単 iPr 7,8-(MeO)2 1-865 単 iPr 2-Me-5-F 1-866 単 iPr 2-Me-6-F 1-867 単 iPr 2-Me-7-F 1-868 単 iPr 2-Me-8-F 1-869 単 iPr 2-Me-5-Cl 1-870 単 iPr 2-Me-6-Cl 1-871 単 iPr 2-Me-7-Cl 1-872 単 iPr 2-Me-8-Cl 1-873 単 iPr 2-Me-5-MeO 1-874 単 iPr 2-Me-6-MeO 1-875 単 iPr 2-Me-7-MeO 1-876 単 iPr 2-Me-8-MeO 1-877 単 iPr 4-Cl-5-F 1-878 単 iPr 4-Cl-6-F 1-879 単 iPr 4-Cl-7-F 1-880 単 iPr 4-Cl-8-F 1-881 単 iPr 4-Cl-5-Me 1-882 単 iPr 4-Cl-6-Me 1-883 単 iPr 4-Cl-7-Me 1-884 単 iPr 4-Cl-8-Me 1-885 単 iPr 4-Cl-5-MeO 1-886 単 iPr 4-Cl-6-MeO 1-887 単 iPr 4-Cl-7-MeO 1-888 単 iPr 4-Cl-8-MeO 1-889 単 Bu H 1-890 単 Bu 2-F 1-891 単 Bu 4-F 1-892 単 Bu 5-F 1-893 単 Bu 6-F 1-894 単 Bu 7-F 1-895 単 Bu 8-F 1-896 単 Bu 2-Cl 1-897 単 Bu 4-Cl 1-898 単 Bu 5-Cl 1-899 単 Bu 6-Cl 1-900 単 Bu 7-Cl 1-901 単 Bu 8-Cl 1-902 単 Bu 2-Br 1-903 単 Bu 4-Br 1-904 単 Bu 5-Br 1-905 単 Bu 6-Br 1-906 単 Bu 7-Br 1-907 単 Bu 8-Br 1-908 単 Bu 2-I 1-909 単 Bu 4-I 1-910 単 Bu 5-I 1-911 単 Bu 6-I 1-912 単 Bu 7-I 1-913 単 Bu 8-I 1-914 単 Bu 2-Me 1-915 単 Bu 4-Me 1-916 単 Bu 5-Me 1-917 単 Bu 6-Me 1-918 単 Bu 7-Me 1-919 単 Bu 8-Me 1-920 単 Bu 2-Et 1-921 単 Bu 4-Et 1-922 単 Bu 5-Et 1-923 単 Bu 6-Et 1-924 単 Bu 7-Et 1-925 単 Bu 8-Et 1-926 単 Bu 2-Pr 1-927 単 Bu 4-Pr 1-928 単 Bu 5-Pr 1-929 単 Bu 6-Pr 1-930 単 Bu 7-Pr 1-931 単 Bu 8-Pr 1-932 単 Bu 2-iPr 1-933 単 Bu 4-iPr 1-934 単 Bu 5-iPr 1-935 単 Bu 6-iPr 1-936 単 Bu 7-iPr 1-937 単 Bu 8-iPr 1-938 単 Bu 2-Bu 1-939 単 Bu 4-Bu 1-940 単 Bu 5-Bu 1-941 単 Bu 6-Bu 1-942 単 Bu 7-Bu 1-943 単 Bu 8-Bu 1-944 単 Bu 2-CF3 1-945 単 Bu 4-CF3 1-946 単 Bu 5-CF3 1-947 単 Bu 6-CF3 1-948 単 Bu 7-CF3 1-949 単 Bu 8-CF3 1-950 単 Bu 2-CF3CH2 1-951 単 Bu 4-CF3CH2 1-952 単 Bu 5-CF3CH2 1-953 単 Bu 6-CF3CH2 1-954 単 Bu 7-CF3CH2 1-955 単 Bu 8-CF3CH2 1-956 単 Bu 2-CF2H 1-957 単 Bu 4-CF2H 1-958 単 Bu 5-CF2H 1-959 単 Bu 6-CF2H 1-960 単 Bu 7-CF2H 1-961 単 Bu 8-CF2H 1-962 単 Bu 2-CF2H 1-963 単 Bu 4-CF2H 1-964 単 Bu 5-CF2H 1-965 単 Bu 6-CF2H 1-966 単 Bu 7-CF2H 1-967 単 Bu 8-CF2H 1-968 単 Bu 2-CClH2 1-969 単 Bu 4-CClH2 1-970 単 Bu 5-CClH2 1-971 単 Bu 6-CClH2 1-972 単 Bu 7-CClH2 1-973 単 Bu 8-CClH2 1-974 単 Bu 2-MeO 1-975 単 Bu 4-MeO 1-976 単 Bu 5-MeO 1-977 単 Bu 6-MeO 1-978 単 Bu 7-MeO 1-979 単 Bu 8-MeO 1-980 単 Bu 2-EtO 1-981 単 Bu 4-EtO 1-982 単 Bu 5-EtO 1-983 単 Bu 6-EtO 1-984 単 Bu 7-EtO 1-985 単 Bu 8-EtO 1-986 単 Bu 2-PrO 1-987 単 Bu 4-PrO 1-988 単 Bu 5-PrO 1-989 単 Bu 6-PrO 1-990 単 Bu ７−ＰｒＯ 1-993 単 Bu 4-iPrO 1-994 単 Bu 5-iPrO 1-995 単 Bu 6-iPrO 1-996 単 Bu 7-iPrO 1-997 単 Bu 8-iPrO 1-998 単 Bu 2-BuO 1-999 単 Bu 4-BuO 1-1000 単 Bu 5-BuO 1-1001 単 Bu 6-BuO 1-1002 単 Bu 7-BuO 1-1003 単 Bu 8-BuO 1-1004 単 Bu 2-CF3O 1-1005 単 Bu 4-CF3O 1-1006 単 Bu 5-CF3O 1-1007 単 Bu 6-CF3O 1-1008 単 Bu 7-CF3O 1-1009 単 Bu 8-CF3O 1-1010 単 Bu 2-CF3CH2O 1-1011 単 Bu 4-CF3CH2O 1-1012 単 Bu 5-CF3CH2O 1-1013 単 Bu 6-CF3CH2O 1-1014 単 Bu 7-CF3CH2O 1-1015 単 Bu 8-CF3CH2O 1-1016 単 Bu 2-CF2HO 1-1017 単 Bu 4-CF2HO 1-1018 単 Bu 5-CF2HO 1-1019 単 Bu 6-CF2HO 1-1020 単 Bu 7-CF2HO 1-1021 単 Bu 8-CF2HO 1-1022 単 Bu 2-CF2HO 1-1023 単 Bu 4-CF2HO 1-1024 単 Bu 5-CF2HO 1-1025 単 Bu 6-CF2HO 1-1026 単 Bu 7-CF2HO 1-1027 単 Bu 8-CF2HO 1-1028 単 Bu 2-CClH2O 1-1029 単 Bu 4-CClH2O 1-1030 単 Bu 5-CClH2O 1-1031 単 Bu 6-CClH2O 1-1032 単 Bu 7-CClH2O 1-1033 単 Bu 8-CClH2O 1-1034 単 Bu 2,4-F2 1-1035 単 Bu 2,5-F2 1-1036 単 Bu 2,6-F2 1-1037 単 Bu 2,7-F2 1-1038 単 Bu 2,8-F2 1-1039 単 Bu 4,5-F2 1-1040 単 Bu 4,6-F2 1-1041 単 Bu 4,7-F2 1-1042 単 Bu 4,8-F2 1-1043 単 Bu 5,6-F2 1-1044 単 Bu 5,7-F2 1-1045 単 Bu 5,8-F2 1-1046 単 Bu 6,7-F2 1-1047 単 Bu 6,8-F2 1-1048 単 Bu 7,8-F2 1-1049 単 Bu 4,5-Cl2 1-1050 単 Bu 4,6-Cl2 1-1051 単 Bu 4,7-Cl2 1-1052 単 Bu 4,8-Cl2 1-1053 単 Bu 5,6-Cl2 1-1054 単 Bu 5,7-Cl2 1-1055 単 Bu 5,8-Cl2 1-1056 単 Bu 6,7-Cl2 1-1057 単 Bu 6,8-Cl2 1-1058 単 Bu 7,8-Cl2 1-1059 単 Bu 2,5-Me2 1-1060 単 Bu 2,6-Me2 1-1061 単 Bu 2,7-Me2 1-1062 単 Bu 2,8-Me2 1-1063 単 Bu 4,5-Me2 1-1064 単 Bu 4,6-Me2 1-1065 単 Bu 4,7-Me2 1-1066 単 Bu 4,8-Me2 1-1067 単 Bu 5,6-Me2 1-1068 単 Bu 5,7-Me2 1-1069 単 Bu 5,8-Me2 1-1070 単 Bu 6,7-Me2 1-1071 単 Bu 6,8-Me2 1-1072 単 Bu 7,8-Me2 1-1073 単 Bu 2,5-(MeO)2 1-1074 単 Bu 2,6-(MeO)2 1-1075 単 Bu 2,7-(MeO)2 1-1076 単 Bu 2,8-(MeO)2 1-1077 単 Bu 4,5-(MeO)2 1-1078 単 Bu 4,6-(MeO)2 1-1079 単 Bu 4,7-(MeO)2 1-1080 単 Bu 4,8-(MeO)2 1-1081 単 Bu 5,6-(MeO)2 1-1082 単 Bu 5,7-(MeO)2 1-1083 単 Bu 5,8-(MeO)2 1-1084 単 Bu 6,7-(MeO)2 1-1085 単 Bu 6,8-(MeO)2 1-1086 単 Bu 7,8-(MeO)2 1-1087 単 Bu 2-Me-5-F 1-1088 単 Bu 2-Me-6-F 1-1089 単 Bu 2-Me-7-F 1-1090 単 Bu 2-Me-8-F 1-1091 単 Bu 2-Me-5-Cl 1-1092 単 Bu 2-Me-6-Cl 1-1093 単 Bu 2-Me-7-Cl 1-1094 単 Bu 2-Me-8-Cl 1-1095 単 Bu 2-Me-5-MeO 1-1096 単 Bu 2-Me-6-MeO 1-1097 単 Bu 2-Me-7-MeO 1-1098 単 Bu 2-Me-8-MeO 1-1099 単 Bu 4-Cl-5-F 1-1100 単 Bu 4-Cl-6-F 1-1101 単 Bu 4-Cl-7-F 1-1102 単 Bu 4-Cl-8-F 1-1103 単 Bu 4-Cl-5-Me 1-1104 単 Bu 4-Cl-6-Me 1-1105 単 Bu 4-Cl-7-Me 1-1106 単 Bu 4-Cl-8-Me 1-1107 単 Bu 4-Cl-5-MeO 1-1108 単 Bu 4-Cl-6-MeO 1-1109 単 Bu 4-Cl-7-MeO 1-1110 単 Bu 4-Cl-8-MeO 1-1111 単 iBu H 1-1112 単 iBu 2-F 1-1113 単 iBu 4-F 1-1114 単 iBu 5-F 1-1115 単 iBu 6-F 1-1116 単 iBu 7-F 1-1117 単 iBu 8-F 1-1118 単 iBu 2-Cl 1-1119 単 iBu 4-Cl 1-1120 単 iBu 5-Cl 1-1121 単 iBu 6-Cl 1-1122 単 iBu 7-Cl 1-1123 単 iBu 8-Cl 1-1124 単 iBu 2-Br 1-1125 単 iBu 4-Br 1-1126 単 iBu 5-Br 1-1127 単 iBu 6-Br 1-1128 単 iBu 7-Br 1-1129 単 iBu 8-Br 1-1130 単 iBu 2-I 1-1131 単 iBu 4-I 1-1132 単 iBu 5-I 1-1133 単 iBu 6-I 1-1134 単 iBu 7-I 1-1135 単 iBu 8-I 1-1136 単 iBu 2-Me 1-1137 単 iBu 4-Me 1-1138 単 iBu 5-Me 1-1139 単 iBu 6-Me 1-1140 単 iBu 7-Me 1-1141 単 iBu 8-Me 1-1142 単 iBu 2-Et 1-1143 単 iBu 4-Et 1-1144 単 iBu 5-Et 1-1145 単 iBu 6-Et 1-1146 単 iBu 7-Et 1-1147 単 iBu 8-Et 1-1148 単 iBu 2-Pr 1-1149 単 iBu 4-Pr 1-1150 単 iBu 5-Pr 1-1151 単 iBu 6-Pr 1-1152 単 iBu 7-Pr 1-1153 単 iBu 8-Pr 1-1154 単 iBu 2-iPr 1-1155 単 iBu 4-iPr 1-1156 単 iBu 5-iPr 1-1157 単 iBu 6-iPr 1-1158 単 iBu 7-iPr 1-1159 単 iBu 8-iPr 1-1160 単 iBu 2-Bu 1-1161 単 iBu 4-Bu 1-1162 単 iBu 5-Bu 1-1163 単 iBu 6-Bu 1-1164 単 iBu 7-Bu 1-1165 単 iBu 8-Bu 1-1166 単 iBu 2-CF3 1-1167 単 iBu 4-CF3 1-1168 単 iBu 5-CF3 1-1169 単 iBu 6-CF3 1-1170 単 iBu 7-CF3 1-1171 単 iBu 8-CF3 1-1172 単 iBu 2-CF3CH2 1-1173 単 iBu 4-CF3CH2 1-1174 単 iBu 5-CF3CH2 1-1175 単 iBu 6-CF3CH2 1-1176 単 iBu 7-CF3CH2 1-1177 単 iBu 8-CF3CH2 1-1178 単 iBu 2-CF2H 1-1179 単 iBu 4-CF2H 1-1180 単 iBu 5-CF2H 1-1181 単 iBu 6-CF2H 1-1182 単 iBu 7-CF2H 1-1183 単 iBu 8-CF2H 1-1184 単 iBu 2-CF2H 1-1185 単 iBu 4-CF2H 1-1186 単 iBu 5-CF2H 1-1187 単 iBu 6-CF2H 1-1188 単 iBu 7-CF2H 1-1189 単 iBu 8-CF2H 1-1190 単 iBu 2-CClH2 1-1191 単 iBu 4-CClH2 1-1192 単 iBu 5-CClH2 1-1193 単 iBu 6-CClH2 1-1194 単 iBu 7-CClH2 1-1195 単 iBu 8-CClH2 1-1196 単 iBu 2-MeO 1-1197 単 iBu 4-MeO 1-1198 単 iBu 5-MeO 1-1199 単 iBu 6-MeO 1-1200 単 iBu 7-MeO 1-1201 単 iBu 8-MeO 1-1202 単 iBu 2-EtO 1-1203 単 iBu 4-EtO 1-1204 単 iBu 5-EtO 1-1205 単 iBu 6-EtO 1-1206 単 iBu 7-EtO 1-1207 単 iBu 8-EtO 1-1208 単 iBu 2-PrO 1-1209 単 iBu 4-PrO 1-1210 単 iBu 5-PrO 1-1211 単 iBu 6-PrO 1-1212 単 iBu 7-PrO 1-1213 単 iBu 8-PrO 1-1214 単 iBu 2-iPrO 1-1215 単 iBu 4-iPrO 1-1216 単 iBu 5-iPrO 1-1217 単 iBu 6-iPrO 1-1218 単 iBu 7-iPrO 1-1219 単 iBu 8-iPrO 1-1220 単 iBu 2-BuO 1-1221 単 iBu 4-BuO 1-1222 単 iBu 5-BuO 1-1223 単 iBu 6-BuO 1-1224 単 iBu 7-BuO 1-1225 単 iBu 8-BuO 1-1226 単 iBu 2-CF3O 1-1227 単 iBu 4-CF3O 1-1228 単 iBu 5-CF3O 1-1229 単 iBu 6-CF3O 1-1230 単 iBu 7-CF3O 1-1231 単 iBu 8-CF3O 1-1232 単 iBu 2-CF3CH2O 1-1233 単 iBu 4-CF3CH2O 1-1234 単 iBu 5-CF3CH2O 1-1235 単 iBu 6-CF3CH2O 1-1236 単 iBu 7-CF3CH2O 1-1237 単 iBu 8-CF3CH2O 1-1238 単 iBu 2-CF2HO 1-1239 単 iBu 4-CF2HO 1-1240 単 iBu 5-CF2HO 1-1241 単 iBu 6-CF2HO 1-1242 単 iBu 7-CF2HO 1-1243 単 iBu 8-CF2HO 1-1244 単 iBu 2-CF2HO 1-1245 単 iBu 4-CF2HO 1-1246 単 iBu 5-CF2HO 1-1247 単 iBu 6-CF2HO 1-1248 単 iBu 7-CF2HO 1-1249 単 iBu 8-CF2HO 1-1250 単 iBu 2-CClH2O 1-1251 単 iBu 4-CClH2O 1-1252 単 iBu 5-CClH2O 1-1253 単 iBu 6-CClH2O 1-1254 単 iBu 7-CClH2O 1-1255 単 iBu 8-CClH2O 1-1256 単 iBu 2,4-F2 1-1257 単 iBu 2,5-F2 1-1258 単 iBu 2,6-F2 1-1259 単 iBu 2,7-F2 1-1260 単 iBu 2,8-F2 1-1261 単 iBu 4,5-F2 1-1262 単 iBu 4,6-F2 1-1263 単 iBu 4,7-F2 1-1264 単 iBu 4,8-F2 1-1265 単 iBu 5,6-F2 1-1266 単 iBu 5,7-F2 1-1267 単 iBu 5,8-F2 1-1268 単 iBu 6,7-F2 1-1269 単 iBu 6,8-F2 1-1270 単 iBu 7,8-F2 1-1271 単 iBu 4,5-Cl2 1-1272 単 iBu 4,6-Cl2 1-1273 単 iBu 4,7-Cl2 1-1274 単 iBu 4,8-Cl2 1-1275 単 iBu 5,6-Cl2 1-1276 単 iBu 5,7-Cl2 1-1277 単 iBu 5,8-Cl2 1-1278 単 iBu 6,7-Cl2 1-1279 単 iBu 6,8-Cl2 1-1280 単 iBu 7,8-Cl2 1-1281 単 iBu 2,5-Me2 1-1282 単 iBu 2,6-Me2 1-1283 単 iBu 2,7-Me2 1-1284 単 iBu 2,8-Me2 1-1285 単 iBu 4,5-Me2 1-1286 単 iBu 4,6-Me2 1-1287 単 iBu 4,7-Me2 1-1288 単 iBu 4,8-Me2 1-1289 単 iBu 5,6-Me2 1-1290 単 iBu 5,7-Me2 1-1291 単 iBu 5,8-Me2 1-1292 単 iBu 6,7-Me2 1-1293 単 iBu 6,8-Me2 1-1294 単 iBu 7,8-Me2 1-1295 単 iBu 2,5-(MeO)2 1-1296 単 iBu 2,6-(MeO)2 1-1297 単 iBu 2,7-(MeO)2 1-1298 単 iBu 2,8-(MeO)2 1-1299 単 iBu 4,5-(MeO)2 1-1300 単 iBu 4,6-(MeO)2 1-1301 単 iBu 4,7-(MeO)2 1-1302 単 iBu 4,8-(MeO)2 1-1303 単 iBu 5,6-(MeO)2 1-1304 単 iBu 5,7-(MeO)2 1-1305 単 iBu 5,8-(MeO)2 1-1306 単 iBu 6,7-(MeO)2 1-1307 単 iBu 6,8-(MeO)2 1-1308 単 iBu 7,8-(MeO)2 1-1309 単 iBu 2-Me-5-F 1-1310 単 iBu 2-Me-6-F 1-1311 単 iBu 2-Me-7-F 1-1312 単 iBu 2-Me-8-F 1-1313 単 iBu 2-Me-5-Cl 1-1314 単 iBu 2-Me-6-Cl 1-1315 単 iBu 2-Me-7-Cl 1-1316 単 iBu 2-Me-8-Cl 1-1317 単 iBu 2-Me-5-MeO 1-1318 単 iBu 2-Me-6-MeO 1-1319 単 iBu 2-Me-7-MeO 1-1320 単 iBu 2-Me-8-MeO 1-1321 単 iBu 4-Cl-5-F 1-1322 単 iBu 4-Cl-6-F 1-1323 単 iBu 4-Cl-7-F 1-1324 単 iBu 4-Cl-8-F 1-1325 単 iBu 4-Cl-5-Me 1-1326 単 iBu 4-Cl-6-Me 1-1327 単 iBu 4-Cl-7-Me 1-1328 単 iBu 4-Cl-8-Me 1-1329 単 iBu 4-Cl-5-MeO 1-1330 単 iBu 4-Cl-6-MeO 1-1331 単 iBu 4-Cl-7-MeO 1-1332 単 iBu 4-Cl-8-MeO 1-1333 単 CF3 H 1-1334 単 CF3 2-F 1-1335 単 CF3 4-F 1-1336 単 CF3 5-F 1-1337 単 CF3 6-F 1-1338 単 CF3 7-F 1-1339 単 CF3 8-F 1-1340 単 CF3 2-Cl 1-1341 単 CF3 4-Cl 1-1342 単 CF3 5-Cl 1-1343 単 CF3 6-Cl 1-1344 単 CF3 7-Cl 1-1345 単 CF3 8-Cl 1-1346 単 CF3 2-Br 1-1347 単 CF3 4-Br 1-1348 単 CF3 5-Br 1-1349 単 CF3 6-Br 1-1350 単 CF3 7-Br 1-1351 単 CF3 8-Br 1-1352 単 CF3 2-I 1-1353 単 CF3 4-I 1-1354 単 CF3 5-I 1-1355 単 CF3 6-I 1-1356 単 CF3 7-I 1-1357 単 CF3 8-I 1-1358 単 CF3 2-Me 1-1359 単 CF3 4-Me 1-1360 単 CF3 5-Me 1-1361 単 CF3 6-Me 1-1362 単 CF3 7-Me 1-1363 単 CF3 8-Me 1-1364 単 CF3 2-Et 1-1365 単 CF3 4-Et 1-1366 単 CF3 5-Et 1-1367 単 CF3 6-Et 1-1368 単 CF3 7-Et 1-1369 単 CF3 8-Et 1-1370 単 CF3 2-Pr 1-1371 単 CF3 4-Pr 1-1372 単 CF3 5-Pr 1-1373 単 CF3 6-Pr 1-1374 単 CF3 7-Pr 1-1375 単 CF3 8-Pr 1-1376 単 CF3 2-iPr 1-1377 単 CF3 4-iPr 1-1378 単 CF3 5-iPr 1-1379 単 CF3 6-iPr 1-1380 単 CF3 7-iPr 1-1381 単 CF3 8-iPr 1-1382 単 CF3 2-Bu 1-1383 単 CF3 4-Bu 1-1384 単 CF3 5-Bu 1-1385 単 CF3 6-Bu 1-1386 単 CF3 7-Bu 1-1387 単 CF3 8-Bu 1-1388 単 CF3 2-CF3 1-1389 単 CF3 4-CF3 1-1390 単 CF3 5-CF3 1-1391 単 CF3 6-CF3 1-1392 単 CF3 7-CF3 1-1393 単 CF3 8-CF3 1-1394 単 CF3 2-CF3CH2 1-1395 単 CF3 4-CF3CH2 1-1396 単 CF3 5-CF3CH2 1-1397 単 CF3 6-CF3CH2 1-1398 単 CF3 7-CF3CH2 1-1399 単 CF3 8-CF3CH2 1-1400 単 CF3 2-CF2H 1-1401 単 CF3 4-CF2H 1-1402 単 CF3 5-CF2H 1-1403 単 CF3 6-CF2H 1-1404 単 CF3 7-CF2H 1-1405 単 CF3 8-CF2H 1-1406 単 CF3 2-CF2H 1-1407 単 CF3 4-CF2H 1-1408 単 CF3 5-CF2H 1-1409 単 CF3 6-CF2H 1-1410 単 CF3 7-CF2H 1-1411 単 CF3 8-CF2H 1-1412 単 CF3 2-CClH2 1-1413 単 CF3 4-CClH2 1-1414 単 CF3 5-CClH2 1-1415 単 CF3 6-CClH2 1-1416 単 CF3 7-CClH2 1-1417 単 CF3 8-CClH2 1-1418 単 CF3 2-MeO 1-1419 単 CF3 4-MeO 1-1420 単 CF3 5-MeO 1-1421 単 CF3 6-MeO 1-1422 単 CF3 7-MeO 1-1423 単 CF3 8-MeO 1-1424 単 CF3 2-EtO 1-1425 単 CF3 4-EtO 1-1426 単 CF3 5-EtO 1-1427 単 CF3 6-EtO 1-1428 単 CF3 7-EtO 1-1429 単 CF3 8-EtO 1-1430 単 CF3 2-PrO 1-1431 単 CF3 4-PrO 1-1432 単 CF3 5-PrO 1-1433 単 CF3 6-PrO 1-1434 単 CF3 7-PrO 1-1435 単 CF3 8-PrO 1-1436 単 CF3 2-iPrO 1-1437 単 CF3 4-iPrO 1-1438 単 CF3 5-iPrO 1-1439 単 CF3 6-iPrO 1-1440 単 CF3 7-iPrO 1-1441 単 CF3 8-iPrO 1-1442 単 CF3 2-BuO 1-1443 単 CF3 4-BuO 1-1444 単 CF3 5-BuO 1-1445 単 CF3 6-BuO 1-1446 単 CF3 7-BuO 1-1447 単 CF3 8-BuO 1-1448 単 CF3 2-CF3O 1-1449 単 CF3 4-CF3O 1-1450 単 CF3 5-CF3O 1-1451 単 CF3 6-CF3O 1-1452 単 CF3 7-CF3O 1-1453 単 CF3 8-CF3O 1-1454 単 CF3 2-CF3CH2O 1-1455 単 CF3 4-CF3CH2O 1-1456 単 CF3 5-CF3CH2O 1-1457 単 CF3 6-CF3CH2O 1-1458 単 CF3 7-CF3CH2O 1-1459 単 CF3 8-CF3CH2O 1-1460 単 CF3 2-CF2HO 1-1461 単 CF3 4-CF2HO 1-1462 単 CF3 5-CF2HO 1-1463 単 CF3 6-CF2HO 1-1464 単 CF3 7-CF2HO 1-1465 単 CF3 8-CF2HO 1-1466 単 CF3 2-CF2HO 1-1467 単 CF3 4-CF2HO 1-1468 単 CF3 5-CF2HO 1-1469 単 CF3 6-CF2HO 1-1470 単 CF3 7-CF2HO 1-1471 単 CF3 8-CF2HO 1-1472 単 CF3 2-CClH2O 1-1473 単 CF3 4-CClH2O 1-1474 単 CF3 5-CClH2O 1-1475 単 CF3 6-CClH2O 1-1476 単 CF3 7-CClH2O 1-1477 単 CF3 8-CClH2O 1-1478 単 CF3 2,4-F2 1-1479 単 CF3 2,5-F2 1-1480 単 CF3 2,6-F2 1-1481 単 CF3 2,7-F2 1-1482 単 CF3 2,8-F2 1-1483 単 CF3 4,5-F2 1-1484 単 CF3 4,6-F2 1-1485 単 CF3 4,7-F2 1-1486 単 CF3 4,8-F2 1-1487 単 CF3 5,6-F2 1-1488 単 CF3 5,7-F2 1-1489 単 CF3 5,8-F2 1-1490 単 CF3 6,7-F2 1-1491 単 CF3 6,8-F2 1-1492 単 CF3 7,8-F2 1-1493 単 CF3 4,5-Cl2 1-1494 単 CF3 4,6-Cl2 1-1495 単 CF3 4,7-Cl2 1-1496 単 CF3 4,8-Cl2 1-1497 単 CF3 5,6-Cl2 1-1498 単 CF3 5,7-Cl2 1-1499 単 CF3 5,8-Cl2 1-1500 単 CF3 6,7-Cl2 1-1501 単 CF3 6,8-Cl2 1-1502 単 CF3 7,8-Cl2 1-1503 単 CF3 2,5-Me2 1-1504 単 CF3 2,6-Me2 1-1505 単 CF3 2,7-Me2 1-1506 単 CF3 2,8-Me2 1-1507 単 CF3 4,5-Me2 1-1508 単 CF3 4,6-Me2 1-1509 単 CF3 4,7-Me2 1-1510 単 CF3 4,8-Me2 1-1511 単 CF3 5,6-Me2 1-1512 単 CF3 5,7-Me2 1-1513 単 CF3 5,8-Me2 1-1514 単 CF3 6,7-Me2 1-1515 単 CF3 6,8-Me2 1-1516 単 CF3 7,8-Me2 1-1517 単 CF3 2,5-(MeO)2 1-1518 単 CF3 2,6-(MeO)2 1-1519 単 CF3 2,7-(MeO)2 1-1520 単 CF3 2,8-(MeO)2 1-1521 単 CF3 4,5-(MeO)2 1-1522 単 CF3 4,6-(MeO)2 1-1523 単 CF3 4,7-(MeO)2 1-1524 単 CF3 4,8-(MeO)2 1-1525 単 CF3 5,6-(MeO)2 1-1526 単 CF3 5,7-(MeO)2 1-1527 単 CF3 5,8-(MeO)2 1-1528 単 CF3 6,7-(MeO)2 1-1529 単 CF3 6,8-(MeO)2 1-1530 単 CF3 7,8-(MeO)2 1-1531 単 CF3 2-Me-5-F 1-1532 単 CF3 2-Me-6-F 1-1533 単 CF3 2-Me-7-F 1-1534 単 CF3 2-Me-8-F 1-1535 単 CF3 2-Me-5-Cl 1-1536 単 CF3 2-Me-6-Cl 1-1537 単 CF3 2-Me-7-Cl 1-1538 単 CF3 2-Me-8-Cl 1-1539 単 CF3 2-Me-5-MeO 1-1540 単 CF3 2-Me-6-MeO 1-1541 単 CF3 2-Me-7-MeO 1-1542 単 CF3 2-Me-8-MeO 1-1543 単 CF3 4-Cl-5-F 1-1544 単 CF3 4-Cl-6-F 1-1545 単 CF3 4-Cl-7-F 1-1546 単 CF3 4-Cl-8-F 1-1547 単 CF3 4-Cl-5-Me 1-1548 単 CF3 4-Cl-6-Me 1-1549 単 CF3 4-Cl-7-Me 1-1550 単 CF3 4-Cl-8-Me 1-1551 単 CF3 4-Cl-5-MeO 1-1552 単 CF3 4-Cl-6-MeO 1-1553 単 CF3 4-Cl-7-MeO 1-1554 単 CF3 4-Cl-8-MeO 1-1555 二 CH2Cl H 1-1556 二 CH2Cl 2-F 1-1557 二 CH2Cl 4-F 1-1558 二 CH2Cl 5-F 1-1559 二 CH2Cl 6-F 1-1560 二 CH2Cl 7-F 1-1561 二 CH2Cl 8-F 1-1562 二 CH2Cl 2-Cl 1-1563 二 CH2Cl 4-Cl 1-1564 二 CH2Cl 5-Cl 1-1565 二 CH2Cl 6-Cl 1-1566 二 CH2Cl 7-Cl 1-1567 二 CH2Cl 8-Cl 1-1568 二 CH2Cl 2-Br 1-1569 二 CH2Cl 4-Br 1-1570 二 CH2Cl 5-Br 1-1571 二 CH2Cl 6-Br 1-1572 二 CH2Cl 7-Br 1-1573 二 CH2Cl 8-Br 1-1574 二 CH2Cl 2-I 1-1575 二 CH2Cl 4-I 1-1576 二 CH2Cl 5-I 1-1577 二 CH2Cl 6-I 1-1578 二 CH2Cl 7-I 1-1579 二 CH2Cl 8-I 1-1580 二 CH2Cl 2-Me 1-1581 二 CH2Cl 4-Me 1-1582 二 CH2Cl 5-Me 1-1583 二 CH2Cl 6-Me 1-1584 二 CH2Cl 7-Me 1-1585 二 CH2Cl 8-Me 1-1586 二 CH2Cl 2-Et 1-1587 二 CH2Cl 4-Et 1-1588 二 CH2Cl 5-Et 1-1589 二 CH2Cl 6-Et 1-1590 二 CH2Cl 7-Et 1-1591 二 CH2Cl 8-Et 1-1592 二 CH2Cl 2-Pr 1-1593 二 CH2Cl 4-Pr 1-1594 二 CH2Cl 5-Pr 1-1595 二 CH2Cl 6-Pr 1-1596 二 CH2Cl 7-Pr 1-1597 二 CH2Cl 8-Pr 1-1598 二 CH2Cl 2-iPr 1-1599 二 CH2Cl 4-iPr 1-1600 二 CH2Cl 5-iPr 1-1601 二 CH2Cl 6-iPr 1-1602 二 CH2Cl 7-iPr 1-1603 二 CH2Cl 8-iPr 1-1604 二 CH2Cl 2-Bu 1-1605 二 CH2Cl 4-Bu 1-1606 二 CH2Cl 5-Bu 1-1607 二 CH2Cl 6-Bu 1-1608 二 CH2Cl 7-Bu 1-1609 二 CH2Cl 8-Bu 1-1610 二 CH2Cl 2-CF3 1-1611 二 CH2Cl 4-CF3 1-1612 二 CH2Cl 5-CF3 1-1613 二 CH2Cl 6-CF3 1-1614 二 CH2Cl 7-CF3 1-1615 二 CH2Cl 8-CF3 1-1616 二 CH2Cl 2-CF3CH2 1-1617 二 CH2Cl 4-CF3CH2 1-1618 二 CH2Cl 5-CF3CH2 1-1619 二 CH2Cl 6-CF3CH2 1-1620 二 CH2Cl 7-CF3CH2 1-1621 二 CH2Cl 8-CF3CH2 1-1622 二 CH2Cl 2-CF2H 1-1623 二 CH2Cl 4-CF2H 1-1624 二 CH2Cl 5-CF2H 1-1625 二 CH2Cl 6-CF2H 1-1626 二 CH2Cl 7-CF2H 1-1627 二 CH2Cl 8-CF2H 1-1628 二 CH2Cl 2-CF2H 1-1629 二 CH2Cl 4-CF2H 1-1630 二 CH2Cl 5-CF2H 1-1631 二 CH2Cl 6-CF2H 1-1632 二 CH2Cl 7-CF2H 1-1633 二 CH2Cl 8-CF2H 1-1634 二 CH2Cl 2-CClH2 1-1635 二 CH2Cl 4-CClH2 1-1636 二 CH2Cl 5-CClH2 1-1637 二 CH2Cl 6-CClH2 1-1638 二 CH2Cl 7-CClH2 1-1639 二 CH2Cl 8-CClH2 1-1640 二 CH2Cl 2-MeO 1-1641 二 CH2Cl 4-MeO 1-1642 二 CH2Cl 5-MeO 1-1643 二 CH2Cl 6-MeO 1-1644 二 CH2Cl 7-MeO 1-1645 二 CH2Cl 8-MeO 1-1646 二 CH2Cl 2-EtO 1-1647 二 CH2Cl 4-EtO 1-1648 二 CH2Cl 5-EtO 1-1649 二 CH2Cl 6-EtO 1-1650 二 CH2Cl 7-EtO 1-1651 二 CH2Cl 8-EtO 1-1652 二 CH2Cl 2-PrO 1-1653 二 CH2Cl 4-PrO 1-1654 二 CH2Cl 5-PrO 1-1655 二 CH2Cl 6-PrO 1-1656 二 CH2Cl 7-PrO 1-1657 二 CH2Cl 8-PrO 1-1658 二 CH2Cl 2-iPrO 1-1659 二 CH2Cl 4-iPrO 1-1660 二 CH2Cl 5-iPrO 1-1661 二 CH2Cl 6-iPrO 1-1662 二 CH2Cl 7-iPrO 1-1663 二 CH2Cl 8-iPrO 1-1664 二 CH2Cl 2-BuO 1-1665 二 CH2Cl 4-BuO 1-1666 二 CH2Cl 5-BuO 1-1667 二 CH2Cl 6-BuO 1-1668 二 CH2Cl 7-BuO 1-1669 二 CH2Cl 8-BuO 1-1670 二 CH2Cl 2-CF3O 1-1671 二 CH2Cl 4-CF3O 1-1672 二 CH2Cl 5-CF3O 1-1673 二 CH2Cl 6-CF3O 1-1674 二 CH2Cl 7-CF3O 1-1675 二 CH2Cl 8-CF3O 1-1676 二 CH2Cl 2-CF3CH2O 1-1677 二 CH2Cl 4-CF3CH2O 1-1678 二 CH2Cl 5-CF3CH2O 1-1679 二 CH2Cl 6-CF3CH2O 1-1680 二 CH2Cl 7-CF3CH2O 1-1681 二 CH2Cl 8-CF3CH2O 1-1682 二 CH2Cl 2-CF2HO 1-1683 二 CH2Cl 4-CF2HO 1-1684 二 CH2Cl 5-CF2HO 1-1685 二 CH2Cl 6-CF2HO 1-1686 二 CH2Cl 7-CF2HO 1-1687 二 CH2Cl 8-CF2HO 1-1688 二 CH2Cl 2-CF2HO 1-1689 二 CH2Cl 4-CF2HO 1-1690 二 CH2Cl 5-CF2HO 1-1691 二 CH2Cl 6-CF2HO 1-1692 二 CH2Cl 7-CF2HO 1-1693 二 CH2Cl 8-CF2HO 1-1694 二 CH2Cl 2-CClH2O 1-1695 二 CH2Cl 4-CClH2O 1-1696 二 CH2Cl 5-CClH2O 1-1697 二 CH2Cl 6-CClH2O 1-1698 二 CH2Cl 7-CClH2O 1-1699 二 CH2Cl 8-CClH2O 1-1700 二 CH2Cl 2,4-F2 1-1701 二 CH2Cl 2,5-F2 1-1702 二 CH2Cl 2,6-F2 1-1703 二 CH2Cl 2,7-F2 1-1704 二 CH2Cl 2,8-F2 1-1705 二 CH2Cl 4,5-F2 1-1706 二 CH2Cl 4,6-F2 1-1707 二 CH2Cl 4,7-F2 1-1708 二 CH2Cl 4,8-F2 1-1709 二 CH2Cl 5,6-F2 1-1710 二 CH2Cl 5,7-F2 1-1711 二 CH2Cl 5,8-F2 1-1712 二 CH2Cl 6,7-F2 1-1713 二 CH2Cl 6,8-F2 1-1714 二 CH2Cl 7,8-F2 1-1715 二 CH2Cl 4,5-Cl2 1-1716 二 CH2Cl 4,6-Cl2 1-1717 二 CH2Cl 4,7-Cl2 1-1718 二 CH2Cl 4,8-Cl2 1-1719 二 CH2Cl 5,6-Cl2 1-1720 二 CH2Cl 5,7-Cl2 1-1721 二 CH2Cl 5,8-Cl2 1-1722 二 CH2Cl 6,7-Cl2 1-1723 二 CH2Cl 6,8-Cl2 1-1724 二 CH2Cl 7,8-Cl2 1-1725 二 CH2Cl 2,5-Me2 1-1726 二 CH2Cl 2,6-Me2 1-1727 二 CH2Cl 2,7-Me2 1-1728 二 CH2Cl 2,8-Me2 1-1729 二 CH2Cl 4,5-Me2 1-1730 二 CH2Cl 4,6-Me2 1-1731 二 CH2Cl 4,7-Me2 1-1732 二 CH2Cl 4,8-Me2 1-1733 二 CH2Cl 5,6-Me2 1-1734 二 CH2Cl 5,7-Me2 1-1735 二 CH2Cl 5,8-Me2 1-1736 二 CH2Cl 6,7-Me2 1-1737 二 CH2Cl 6,8-Me2 1-1738 二 CH2Cl 7,8-Me2 1-1739 二 CH2Cl 2,5-(MeO)2 1-1740 二 CH2Cl 2,6-(MeO)2 1-1741 二 CH2Cl 2,7-(MeO)2 1-1742 二 CH2Cl 2,8-(MeO)2 1-1743 二 CH2Cl 4,5-(MeO)2 1-1744 二 CH2Cl 4,6-(MeO)2 1-1745 二 CH2Cl 4,7-(MeO)2 1-1746 二 CH2Cl 4,8-(MeO)2 1-1747 二 CH2Cl 5,6-(MeO)2 1-1748 二 CH2Cl 5,7-(MeO)2 1-1749 二 CH2Cl 5,8-(MeO)2 1-1750 二 CH2Cl 6,7-(MeO)2 1-1751 二 CH2Cl 6,8-(MeO)2 1-1752 二 CH2Cl 7,8-(MeO)2 1-1753 二 CH2Cl 2-Me-5-F 1-1754 二 CH2Cl 2-Me-6-F 1-1755 二 CH2Cl 2-Me-7-F 1-1756 二 CH2Cl 2-Me-8-F 1-1757 二 CH2Cl 2-Me-5-Cl 1-1758 二 CH2Cl 2-Me-6-Cl 1-1759 二 CH2Cl 2-Me-7-Cl 1-1760 二 CH2Cl 2-Me-8-Cl 1-1761 二 CH2Cl 2-Me-5-MeO 1-1762 二 CH2Cl 2-Me-6-MeO 1-1763 二 CH2Cl 2-Me-7-MeO 1-1764 二 CH2Cl 2-Me-8-MeO 1-1765 二 CH2Cl 4-Cl-5-F 1-1766 二 CH2Cl 4-Cl-6-F 1-1767 二 CH2Cl 4-Cl-7-F 1-1768 二 CH2Cl 4-Cl-8-F 1-1769 二 CH2Cl 4-Cl-5-Me 1-1770 二 CH2Cl 4-Cl-6-Me 1-1771 二 CH2Cl 4-Cl-7-Me 1-1772 二 CH2Cl 4-Cl-8-Me 1-1773 二 CH2Cl 4-Cl-5-MeO 1-1774 二 CH2Cl 4-Cl-6-MeO 1-1775 二 CH2Cl 4-Cl-7-MeO 1-1776 二 CH2Cl 4-Cl-8-MeO 1-1777 二 Me H 1-1778 二 Me 2-F 1-1779 二 Me 4-F 1-1780 二 Me 5-F 1-1781 二 Me 6-F 1-1782 二 Me 7-F 1-1783 二 Me 8-F 1-1784 二 Me 2-Cl 1-1785 二 Me 4-Cl 1-1786 二 Me 5-Cl 1-1787 二 Me 6-Cl 1-1788 二 Me 7-Cl 1-1789 二 Me 8-Cl 1-1790 二 Me 2-Br 1-1791 二 Me 4-Br 1-1792 二 Me 5-Br 1-1793 二 Me 6-Br 1-1794 二 Me 7-Br 1-1795 二 Me 8-Br 1-1796 二 Me 2-I 1-1797 二 Me 4-I 1-1798 二 Me 5-I 1-1799 二 Me 6-I 1-1800 二 Me 7-I 1-1801 二 Me 8-I 1-1802 二 Me 2-Me 1-1803 二 Me 4-Me 1-1804 二 Me 5-Me 1-1805 二 Me 6-Me 1-1806 二 Me 7-Me 1-1807 二 Me 8-Me 1-1808 二 Me 2-Et 1-1809 二 Me 4-Et 1-1810 二 Me 5-Et 1-1811 二 Me 6-Et 1-1812 二 Me 7-Et 1-1813 二 Me 8-Et 1-1814 二 Me 2-Pr 1-1815 二 Me 4-Pr 1-1816 二 Me 5-Pr 1-1817 二 Me 6-Pr 1-1818 二 Me 7-Pr 1-1819 二 Me 8-Pr 1-1820 二 Me 2-iPr 1-1821 二 Me 4-iPr 1-1822 二 Me 5-iPr 1-1823 二 Me 6-iPr 1-1824 二 Me 7-iPr 1-1825 二 Me 8-iPr 1-1826 二 Me 2-Bu 1-1827 二 Me 4-Bu 1-1828 二 Me 5-Bu 1-1829 二 Me 6-Bu 1-1830 二 Me 7-Bu 1-1831 二 Me 8-Bu 1-1832 二 Me 2-CF3 1-1833 二 Me 4-CF3 1-1834 二 Me 5-CF3 1-1835 二 Me 6-CF3 1-1836 二 Me 7-CF3 1-1837 二 Me 8-CF3 1-1838 二 Me 2-CF3CH2 1-1839 二 Me 4-CF3CH2 1-1840 二 Me 5-CF3CH2 1-1841 二 Me 6-CF3CH2 1-1842 二 Me 7-CF3CH2 1-1843 二 Me 8-CF3CH2 1-1844 二 Me 2-CF2H 1-1845 二 Me 4-CF2H 1-1846 二 Me 5-CF2H 1-1847 二 Me 6-CF2H 1-1848 二 Me 7-CF2H 1-1849 二 Me 8-CF2H 1-1850 二 Me 2-CF2H 1-1851 二 Me 4-CF2H 1-1852 二 Me 5-CF2H 1-1853 二 Me 6-CF2H 1-1854 二 Me 7-CF2H 1-1855 二 Me 8-CF2H 1-1856 二 Me 2-CClH2 1-1857 二 Me 4-CClH2 1-1858 二 Me 5-CClH2 1-1859 二 Me 6-CClH2 1-1860 二 Me 7-CClH2 1-1861 二 Me 8-CClH2 1-1862 二 Me 2-MeO 1-1863 二 Me 4-MeO 1-1864 二 Me 5-MeO 1-1865 二 Me 6-MeO 1-1866 二 Me 7-MeO 1-1867 二 Me 8-MeO 1-1868 二 Me 2-EtO 1-1869 二 Me 4-EtO 1-1870 二 Me 5-EtO 1-1871 二 Me 6-EtO 1-1872 二 Me 7-EtO 1-1873 二 Me 8-EtO 1-1874 二 Me 2-PrO 1-1875 二 Me 4-PrO 1-1876 二 Me 5-PrO 1-1877 二 Me 6-PrO 1-1878 二 Me 7-PrO 1-1879 二 Me 8-PrO 1-1880 二 Me 2-iPrO 1-1881 二 Me 4-iPrO 1-1882 二 Me 5-iPrO 1-1883 二 Me 6-iPrO 1-1884 二 Me 7-iPrO 1-1885 二 Me 8-iPrO 1-1886 二 Me 2-BuO 1-1887 二 Me 4-BuO 1-1888 二 Me 5-BuO 1-1889 二 Me 6-BuO 1-1890 二 Me 7-BuO 1-1891 二 Me 8-BuO 1-1892 二 Me 2-CF3O 1-1893 二 Me 4-CF3O 1-1894 二 Me 5-CF3O 1-1895 二 Me 6-CF3O 1-1896 二 Me 7-CF3O 1-1897 二 Me 8-CF3O 1-1898 二 Me 2-CF3CH2O 1-1899 二 Me 4-CF3CH2O 1-1900 二 Me 5-CF3CH2O 1-1901 二 Me 6-CF3CH2O 1-1902 二 Me 7-CF3CH2O 1-1903 二 Me 8-CF3CH2O 1-1904 二 Me 2-CF2HO 1-1905 二 Me 4-CF2HO 1-1906 二 Me 5-CF2HO 1-1907 二 Me 6-CF2HO 1-1908 二 Me 7-CF2HO 1-1909 二 Me 8-CF2HO 1-1910 二 Me 2-CF2HO 1-1911 二 Me 4-CF2HO 1-1912 二 Me 5-CF2HO 1-1913 二 Me 6-CF2HO 1-1914 二 Me 7-CF2HO 1-1915 二 Me 8-CF2HO 1-1916 二 Me 2-CClH2O 1-1917 二 Me 4-CClH2O 1-1918 二 Me 5-CClH2O 1-1919 二 Me 6-CClH2O 1-1920 二 Me 7-CClH2O 1-1921 二 Me 8-CClH2O 1-1922 二 Me 2,4-F2 1-1923 二 Me 2,5-F2 1-1924 二 Me 2,6-F2 1-1925 二 Me 2,7-F2 1-1926 二 Me 2,8-F2 1-1927 二 Me 4,5-F2 1-1928 二 Me 4,6-F2 1-1929 二 Me 4,7-F2 1-1930 二 Me 4,8-F2 1-1931 二 Me 5,6-F2 1-1932 二 Me 5,7-F2 1-1933 二 Me 5,8-F2 1-1934 二 Me 6,7-F2 1-1935 二 Me 6,8-F2 1-1936 二 Me 7,8-F2 1-1937 二 Me 4,5-Cl2 1-1938 二 Me 4,6-Cl2 1-1939 二 Me 4,7-Cl2 1-1940 二 Me 4,8-Cl2 1-1941 二 Me 5,6-Cl2 1-1942 二 Me 5,7-Cl2 1-1943 二 Me 5,8-Cl2 1-1944 二 Me 6,7-Cl2 1-1945 二 Me 6,8-Cl2 1-1946 二 Me 7,8-Cl2 1-1947 二 Me 2,5-Me2 1-1948 二 Me 2,6-Me2 1-1949 二 Me 2,7-Me2 1-1950 二 Me 2,8-Me2 1-1951 二 Me 4,5-Me2 1-1952 二 Me 4,6-Me2 1-1953 二 Me 4,7-Me2 1-1954 二 Me 4,8-Me2 1-1955 二 Me 5,6-Me2 1-1956 二 Me 5,7-Me2 1-1957 二 Me 5,8-Me2 1-1958 二 Me 6,7-Me2 1-1959 二 Me 6,8-Me2 1-1960 二 Me 7,8-Me2 1-1961 二 Me 2,5-(MeO)2 1-1962 二 Me 2,6-(MeO)2 1-1963 二 Me 2,7-(MeO)2 1-1964 二 Me 2,8-(MeO)2 1-1965 二 Me 4,5-(MeO)2 1-1966 二 Me 4,6-(MeO)2 1-1967 二 Me 4,7-(MeO)2 1-1968 二 Me 4,8-(MeO)2 1-1969 二 Me 5,6-(MeO)2 1-1970 二 Me 5,7-(MeO)2 1-1971 二 Me 5,8-(MeO)2 1-1972 二 Me 6,7-(MeO)2 1-1973 二 Me 6,8-(MeO)2 1-1974 二 Me 7,8-(MeO)2 1-1975 二 Me 2-Me-5-F 1-1976 二 Me 2-Me-6-F 1-1977 二 Me 2-Me-7-F 1-1978 二 Me 2-Me-8-F 1-1979 二 Me 2-Me-5-Cl 1-1980 二 Me 2-Me-6-Cl 1-1981 二 Me 2-Me-7-Cl 1-1982 二 Me 2-Me-8-Cl 1-1983 二 Me 2-Me-5-MeO 1-1984 二 Me 2-Me-6-MeO 1-1985 二 Me 2-Me-7-MeO 1-1986 二 Me 2-Me-8-MeO 1-1987 二 Me 4-Cl-5-F 1-1988 二 Me 4-Cl-6-F 1-1989 二 Me 4-Cl-7-F 1-1990 二 Me 4-Cl-8-F 1-1991 二 Me 4-Cl-5-Me 1-1992 二 Me 4-Cl-6-Me 1-1993 二 Me 4-Cl-7-Me 1-1994 二 Me 4-Cl-8-Me 1-1995 二 Me 4-Cl-5-MeO 1-1996 二 Me 4-Cl-6-MeO 1-1997 二 Me 4-Cl-7-MeO 1-1998 二 Me 4-Cl-8-MeO 1-1999 二 CF3 H 1-2000 二 CF3 2-F 1-2001 二 CF3 4-F 1-2002 二 CF3 5-F 1-2003 二 CF3 6-F 1-2004 二 CF3 7-F 1-2005 二 CF3 8-F 1-2006 二 CF3 2-Cl 1-2007 二 CF3 4-Cl 1-2008 二 CF3 5-Cl 1-2009 二 CF3 6-Cl 1-2010 二 CF3 7-Cl 1-2011 二 CF3 8-Cl 1-2012 二 CF3 2-Br 1-2013 二 CF3 4-Br 1-2014 二 CF3 5-Br 1-2015 二 CF3 6-Br 1-2016 二 CF3 7-Br 1-2017 二 CF3 8-Br 1-2018 二 CF3 2-I 1-2019 二 CF3 4-I 1-2020 二 CF3 5-I 1-2021 二 CF3 6-I 1-2022 二 CF3 7-I 1-2023 二 CF3 8-I 1-2024 二 CF3 2-Me 1-2025 二 CF3 4-Me 1-2026 二 CF3 5-Me 1-2027 二 CF3 6-Me 1-2028 二 CF3 7-Me 1-2029 二 CF3 8-Me 1-2030 二 CF3 2-Et 1-2031 二 CF3 4-Et 1-2032 二 CF3 5-Et 1-2033 二 CF3 6-Et 1-2034 二 CF3 7-Et 1-2035 二 CF3 8-Et 1-2036 二 CF3 2-Pr 1-2037 二 CF3 4-Pr 1-2038 二 CF3 5-Pr 1-2039 二 CF3 6-Pr 1-2040 二 CF3 7-Pr 1-2041 二 CF3 8-Pr 1-2042 二 CF3 2-iPr 1-2043 二 CF3 4-iPr 1-2044 二 CF3 5-iPr 1-2045 二 CF3 6-iPr 1-2046 二 CF3 7-iPr 1-2047 二 CF3 8-iPr 1-2048 二 CF3 2-Bu 1-2049 二 CF3 4-Bu 1-2050 二 CF3 5-Bu 1-2051 二 CF3 6-Bu 1-2052 二 CF3 7-Bu 1-2053 二 CF3 8-Bu 1-2054 二 CF3 2-CF3 1-2055 二 CF3 4-CF3 1-2056 二 CF3 5-CF3 1-2057 二 CF3 6-CF3 1-2058 二 CF3 7-CF3 1-2059 二 CF3 8-CF3 1-2060 二 CF3 2-CF3CH2 1-2061 二 CF3 4-CF3CH2 1-2062 二 CF3 5-CF3CH2 1-2063 二 CF3 6-CF3CH2 1-2064 二 CF3 7-CF3CH2 1-2065 二 CF3 8-CF3CH2 1-2066 二 CF3 2-CF2H 1-2067 二 CF3 4-CF2H 1-2068 二 CF3 5-CF2H 1-2069 二 CF3 6-CF2H 1-2070 二 CF3 7-CF2H 1-2071 二 CF3 8-CF2H 1-2072 二 CF3 2-CF2H 1-2073 二 CF3 4-CF2H 1-2074 二 CF3 5-CF2H 1-2075 二 CF3 6-CF2H 1-2076 二 CF3 7-CF2H 1-2077 二 CF3 8-CF2H 1-2078 二 CF3 2-CClH2 1-2079 二 CF3 4-CClH2 1-2080 二 CF3 5-CClH2 1-2081 二 CF3 6-CClH2 1-2082 二 CF3 7-CClH2 1-2083 二 CF3 8-CClH2 1-2084 二 CF3 2-MeO 1-2085 二 CF3 4-MeO 1-2086 二 CF3 5-MeO 1-2087 二 CF3 6-MeO 1-2088 二 CF3 7-MeO 1-2089 二 CF3 8-MeO 1-2090 二 CF3 2-EtO 1-2091 二 CF3 4-EtO 1-2092 二 CF3 5-EtO 1-2093 二 CF3 6-EtO 1-2094 二 CF3 7-EtO 1-2095 二 CF3 8-EtO 1-2096 二 CF3 2-PrO 1-2097 二 CF3 4-PrO 1-2098 二 CF3 5-PrO 1-2099 二 CF3 6-PrO 1-2100 二 CF3 7-PrO 1-2101 二 CF3 8-PrO 1-2102 二 CF3 2-iPrO 1-2103 二 CF3 4-iPrO 1-2104 二 CF3 5-iPrO 1-2105 二 CF3 6-iPrO 1-2106 二 CF3 7-iPrO 1-2107 二 CF3 8-iPrO 1-2108 二 CF3 2-BuO 1-2109 二 CF3 4-BuO 1-2110 二 CF3 5-BuO 1-2111 二 CF3 6-BuO 1-2112 二 CF3 7-BuO 1-2113 二 CF3 8-BuO 1-2114 二 CF3 2-CF3O 1-2115 二 CF3 4-CF3O 1-2116 二 CF3 5-CF3O 1-2117 二 CF3 6-CF3O 1-2118 二 CF3 7-CF3O 1-2119 二 CF3 8-CF3O 1-2120 二 CF3 2-CF3CH2O 1-2121 二 CF3 4-CF3CH2O 1-2122 二 CF3 5-CF3CH2O 1-2123 二 CF3 6-CF3CH2O 1-2124 二 CF3 7-CF3CH2O 1-2125 二 CF3 8-CF3CH2O 1-2126 二 CF3 2-CF2HO 1-2127 二 CF3 4-CF2HO 1-2128 二 CF3 5-CF2HO 1-2129 二 CF3 6-CF2HO 1-2130 二 CF3 7-CF2HO 1-2131 二 CF3 8-CF2HO 1-2132 二 CF3 2-CF2HO 1-2133 二 CF3 4-CF2HO 1-2134 二 CF3 5-CF2HO 1-2135 二 CF3 6-CF2HO 1-2136 二 CF3 7-CF2HO 1-2137 二 CF3 8-CF2HO 1-2138 二 CF3 2-CClH2O 1-2139 二 CF3 4-CClH2O 1-2140 二 CF3 5-CClH2O 1-2141 二 CF3 6-CClH2O 1-2142 二 CF3 7-CClH2O 1-2143 二 CF3 8-CClH2O 1-2144 二 CF3 2,4-F2 1-2145 二 CF3 2,5-F2 1-2146 二 CF3 2,6-F2 1-2147 二 CF3 2,7-F2 1-2148 二 CF3 2,8-F2 1-2149 二 CF3 4,5-F2 1-2150 二 CF3 4,6-F2 1-2151 二 CF3 4,7-F2 1-2152 二 CF3 4,8-F2 1-2153 二 CF3 5,6-F2 1-2154 二 CF3 5,7-F2 1-2155 二 CF3 5,8-F2 1-2156 二 CF3 6,7-F2 1-2157 二 CF3 6,8-F2 1-2158 二 CF3 7,8-F2 1-2159 二 CF3 4,5-Cl2 1-2160 二 CF3 4,6-Cl2 1-2161 二 CF3 4,7-Cl2 1-2162 二 CF3 4,8-Cl2 1-2163 二 CF3 5,6-Cl2 1-2164 二 CF3 5,7-Cl2 1-2165 二 CF3 5,8-Cl2 1-2166 二 CF3 6,7-Cl2 1-2167 二 CF3 6,8-Cl2 1-2168 二 CF3 7,8-Cl2 1-2169 二 CF3 2,5-Me2 1-2170 二 CF3 2,6-Me2 1-2171 二 CF3 2,7-Me2 1-2172 二 CF3 2,8-Me2 1-2173 二 CF3 4,5-Me2 1-2174 二 CF3 4,6-Me2 1-2175 二 CF3 4,7-Me2 1-2176 二 CF3 4,8-Me2 1-2177 二 CF3 5,6-Me2 1-2178 二 CF3 5,7-Me2 1-2179 二 CF3 5,8-Me2 1-2180 二 CF3 6,7-Me2 1-2181 二 CF3 6,8-Me2 1-2182 二 CF3 7,8-Me2 1-2183 二 CF3 2,5-(MeO)2 1-2184 二 CF3 2,6-(MeO)2 1-2185 二 CF3 2,7-(MeO)2 1-2186 二 CF3 2,8-(MeO)2 1-2187 二 CF3 4,5-(MeO)2 1-2188 二 CF3 4,6-(MeO)2 1-2189 二 CF3 4,7-(MeO)2 1-2190 二 CF3 4,8-(MeO)2 1-2191 二 CF3 5,6-(MeO)2 1-2192 二 CF3 5,7-(MeO)2 1-2193 二 CF3 5,8-(MeO)2 1-2194 二 CF3 6,7-(MeO)2 1-2195 二 CF3 6,8-(MeO)2 1-2196 二 CF3 7,8-(MeO)2 1-2197 二 CF3 2-Me-5-F 1-2198 二 CF3 2-Me-6-F 1-2199 二 CF3 2-Me-7-F 1-2200 二 CF3 2-Me-8-F 1-2201 二 CF3 2-Me-5-Cl 1-2202 二 CF3 2-Me-6-Cl 1-2203 二 CF3 2-Me-7-Cl 1-2204 二 CF3 2-Me-8-Cl 1-2205 二 CF3 2-Me-5-MeO 1-2206 二 CF3 2-Me-6-MeO 1-2207 二 CF3 2-Me-7-MeO 1-2208 二 CF3 2-Me-8-MeO 1-2209 二 CF3 4-Cl-5-F 1-2210 二 CF3 4-Cl-6-F 1-2211 二 CF3 4-Cl-7-F 1-2212 二 CF3 4-Cl-8-F 1-2213 二 CF3 4-Cl-5-Me 1-2214 二 CF3 4-Cl-6-Me 1-2215 二 CF3 4-Cl-7-Me 1-2216 二 CF3 4-Cl-8-Me 1-2217 二 CF3 4-Cl-5-MeO 1-2218 二 CF3 4-Cl-6-MeO 1-2219 二 CF3 4-Cl-7-MeO 1-2220 二 CF3 4-Cl-8-MeO 1-2221 単 cPr H 1-2222 単 cPr 2-F 1-2223 単 cPr 4-F 1-2224 単 cPr 5-F 1-2225 単 cPr 6-F 1-2226 単 cPr 7-F 1-2227 単 cPr 8-F 1-2228 単 cPr 2-Cl 1-2229 単 cPr 4-Cl 1-2230 単 cPr 5-Cl 1-2231 単 cPr 6-Cl 1-2232 単 cPr 7-Cl 1-2233 単 cPr 8-Cl 1-2234 単 cPr 2-Br 1-2235 単 cPr 4-Br 1-2236 単 cPr 5-Br 1-2237 単 cPr 6-Br 1-2238 単 cPr 7-Br 1-2239 単 cPr 8-Br 1-2240 単 cPr 2-I 1-2241 単 cPr 4-I 1-2242 単 cPr 5-I 1-2243 単 cPr 6-I 1-2244 単 cPr 7-I 1-2245 単 cPr 8-I 1-2246 単 cPr 2-Me 1-2247 単 cPr 4-Me 1-2248 単 cPr 5-Me 1-2249 単 cPr 6-Me 1-2250 単 cPr 7-Me 1-2251 単 cPr 8-Me 1-2252 単 cPr 2-Et 1-2253 単 cPr 4-Et 1-2254 単 cPr 5-Et 1-2255 単 cPr 6-Et 1-2256 単 cPr 7-Et 1-2257 単 cPr 8-Et 1-2258 単 cPr 2-Pr 1-2259 単 cPr 4-Pr 1-2260 単 cPr 5-Pr 1-2261 単 cPr 6-Pr 1-2262 単 cPr 7-Pr 1-2263 単 cPr 8-Pr 1-2264 単 cPr 2-iPr 1-2265 単 cPr 4-iPr 1-2266 単 cPr 5-iPr 1-2267 単 cPr 6-iPr 1-2268 単 cPr 7-iPr 1-2269 単 cPr 8-iPr 1-2270 単 cPr 2-Bu 1-2271 単 cPr 4-Bu 1-2272 単 cPr 5-Bu 1-2273 単 cPr 6-Bu 1-2274 単 cPr 7-Bu 1-2275 単 cPr 8-Bu 1-2276 単 cPr 2-CF3 1-2277 単 cPr 4-CF3 1-2278 単 cPr 5-CF3 1-2279 単 cPr 6-CF3 1-2280 単 cPr 7-CF3 1-2281 単 cPr 8-CF3 1-2282 単 cPr 2-CF3CH2 1-2283 単 cPr 4-CF3CH2 1-2284 単 cPr 5-CF3CH2 1-2285 単 cPr 6-CF3CH2 1-2286 単 cPr 7-CF3CH2 1-2287 単 cPr 8-CF3CH2 1-2288 単 cPr 2-CF2H 1-2289 単 cPr 4-CF2H 1-2290 単 cPr 5-CF2H 1-2291 単 cPr 6-CF2H 1-2292 単 cPr 7-CF2H 1-2293 単 cPr 8-CF2H 1-2294 単 cPr 2-CF2H 1-2295 単 cPr 4-CF2H 1-2296 単 cPr 5-CF2H 1-2297 単 cPr 6-CF2H 1-2298 単 cPr 7-CF2H 1-2299 単 cPr 8-CF2H 1-2300 単 cPr 2-CClH2 1-2301 単 cPr 4-CClH2 1-2302 単 cPr 5-CClH2 1-2303 単 cPr 6-CClH2 1-2304 単 cPr 7-CClH2 1-2305 単 cPr 8-CClH2 1-2306 単 cPr 2-MeO 1-2307 単 cPr 4-MeO 1-2308 単 cPr 5-MeO 1-2309 単 cPr 6-MeO 1-2310 単 cPr 7-MeO 1-2311 単 cPr 8-MeO 1-2312 単 cPr 2-EtO 1-2313 単 cPr 4-EtO 1-2314 単 cPr 5-EtO 1-2315 単 cPr 6-EtO 1-2316 単 cPr 7-EtO 1-2317 単 cPr 8-EtO 1-2318 単 cPr 2-PrO 1-2319 単 cPr 4-PrO 1-2320 単 cPr 5-PrO 1-2321 単 cPr 6-PrO 1-2322 単 cPr 7-PrO 1-2323 単 cPr 8-PrO 1-2324 単 cPr 2-iPrO 1-2325 単 cPr 4-iPrO 1-2326 単 cPr 5-iPrO 1-2327 単 cPr 6-iPrO 1-2328 単 cPr 7-iPrO 1-2329 単 cPr 8-iPrO 1-2330 単 cPr 2-BuO 1-2331 単 cPr 4-BuO 1-2332 単 cPr 5-BuO 1-2333 単 cPr 6-BuO 1-2334 単 cPr 7-BuO 1-2335 単 cPr 8-BuO 1-2336 単 cPr 2-CF3O 1-2337 単 cPr 4-CF3O 1-2338 単 cPr 5-CF3O 1-2339 単 cPr 6-CF3O 1-2340 単 cPr 7-CF3O 1-2341 単 cPr 8-CF3O 1-2342 単 cPr 2-CF3CH2O 1-2343 単 cPr 4-CF3CH2O 1-2344 単 cPr 5-CF3CH2O 1-2345 単 cPr 6-CF3CH2O 1-2346 単 cPr 7-CF3CH2O 1-2347 単 cPr 8-CF3CH2O 1-2348 単 cPr 2-CF2HO 1-2349 単 cPr 4-CF2HO 1-2350 単 cPr 5-CF2HO 1-2351 単 cPr 6-CF2HO 1-2352 単 cPr 7-CF2HO 1-2353 単 cPr 8-CF2HO 1-2354 単 cPr 2-CF2HO 1-2355 単 cPr 4-CF2HO 1-2356 単 cPr 5-CF2HO 1-2357 単 cPr 6-CF2HO 1-2358 単 cPr 7-CF2HO 1-2359 単 cPr 8-CF2HO 1-2360 単 cPr 2-CClH2O 1-2361 単 cPr 4-CClH2O 1-2362 単 cPr 5-CClH2O 1-2363 単 cPr 6-CClH2O 1-2364 単 cPr 7-CClH2O 1-2365 単 cPr 8-CClH2O 1-2366 単 cPr 2,4-F2 1-2367 単 cPr 2,5-F2 1-2368 単 cPr 2,6-F2 1-2369 単 cPr 2,7-F2 1-2370 単 cPr 2,8-F2 1-2371 単 cPr 4,5-F2 1-2372 単 cPr 4,6-F2 1-2373 単 cPr 4,7-F2 1-2374 単 cPr 4,8-F2 1-2375 単 cPr 5,6-F2 1-2376 単 cPr 5,7-F2 1-2377 単 cPr 5,8-F2 1-2378 単 cPr 6,7-F2 1-2379 単 cPr 6,8-F2 1-2380 単 cPr 7,8-F2 1-2381 単 cPr 4,5-Cl2 1-2382 単 cPr 4,6-Cl2 1-2383 単 cPr 4,7-Cl2 1-2384 単 cPr 4,8-Cl2 1-2385 単 cPr 5,6-Cl2 1-2386 単 cPr 5,7-Cl2 1-2387 単 cPr 5,8-Cl2 1-2388 単 cPr 6,7-Cl2 1-2389 単 cPr 6,8-Cl2 1-2390 単 cPr 7,8-Cl2 1-2391 単 cPr 2,5-Me2 1-2392 単 cPr 2,6-Me2 1-2393 単 cPr 2,7-Me2 1-2394 単 cPr 2,8-Me2 1-2395 単 cPr 4,5-Me2 1-2396 単 cPr 4,6-Me2 1-2397 単 cPr 4,7-Me2 1-2398 単 cPr 4,8-Me2 1-2399 単 cPr 5,6-Me2 1-2400 単 cPr 5,7-Me2 1-2401 単 cPr 5,8-Me2 1-2402 単 cPr 6,7-Me2 1-2403 単 cPr 6,8-Me2 1-2404 単 cPr 7,8-Me2 1-2405 単 cPr 2,5-(MeO)2 1-2406 単 cPr 2,6-(MeO)2 1-2407 単 cPr 2,7-(MeO)2 1-2408 単 cPr 2,8-(MeO)2 1-2409 単 cPr 4,5-(MeO)2 1-2410 単 cPr 4,6-(MeO)2 1-2411 単 cPr 4,7-(MeO)2 1-2412 単 cPr 4,8-(MeO)2 1-2413 単 cPr 5,6-(MeO)2 1-2414 単 cPr 5,7-(MeO)2 1-2415 単 cPr 5,8-(MeO)2 1-2416 単 cPr 6,7-(MeO)2 1-2417 単 cPr 6,8-(MeO)2 1-2418 単 cPr 7,8-(MeO)2 1-2419 単 cPr 2-Me-5-F 1-2420 単 cPr 2-Me-6-F 1-2421 単 cPr 2-Me-7-F 1-2422 単 cPr 2-Me-8-F 1-2423 単 cPr 2-Me-5-Cl 1-2424 単 cPr 2-Me-6-Cl 1-2425 単 cPr 2-Me-7-Cl 1-2426 単 cPr 2-Me-8-Cl 1-2427 単 cPr 2-Me-5-MeO 1-2428 単 cPr 2-Me-6-MeO 1-2429 単 cPr 2-Me-7-MeO 1-2430 単 cPr 2-Me-8-MeO 1-2431 単 cPr 4-Cl-5-F 1-2432 単 cPr 4-Cl-6-F 1-2433 単 cPr 4-Cl-7-F 1-2434 単 cPr 4-Cl-8-F 1-2435 単 cPr 4-Cl-5-Me 1-2436 単 cPr 4-Cl-6-Me 1-2437 単 cPr 4-Cl-7-Me 1-2438 単 cPr 4-Cl-8-Me 1-2439 単 cPr 4-Cl-5-MeO 1-2440 単 cPr 4-Cl-6-MeO 1-2441 単 cPr 4-Cl-7-MeO 1-2442 単 cPr 4-Cl-8-MeO 1-2443 単 Allyl H 1-2444 単 Allyl 2-F 1-2445 単 Allyl 4-F 1-2446 単 Allyl 5-F 1-2447 単 Allyl 6-F 1-2448 単 Allyl 7-F 1-2449 単 Allyl 8-F 1-2450 単 Allyl 2-Cl 1-2451 単 Allyl 4-Cl 1-2452 単 Allyl 5-Cl 1-2453 単 Allyl 6-Cl 1-2454 単 Allyl 7-Cl 1-2455 単 Allyl 8-Cl 1-2456 単 Allyl 2-Br 1-2457 単 Allyl 4-Br 1-2458 単 Allyl 5-Br 1-2459 単 Allyl 6-Br 1-2460 単 Allyl 7-Br 1-2461 単 Allyl 8-Br 1-2462 単 Allyl 2-I 1-2463 単 Allyl 4-I 1-2464 単 Allyl 5-I 1-2465 単 Allyl 6-I 1-2466 単 Allyl 7-I 1-2467 単 Allyl 8-I 1-2468 単 Allyl 2-Me 1-2469 単 Allyl 4-Me 1-2470 単 Allyl 5-Me 1-2471 単 Allyl 6-Me 1-2472 単 Allyl 7-Me 1-2473 単 Allyl 8-Me 1-2474 単 Allyl 2-Et 1-2475 単 Allyl 4-Et 1-2476 単 Allyl 5-Et 1-2477 単 Allyl 6-Et 1-2478 単 Allyl 7-Et 1-2479 単 Allyl 8-Et 1-2480 単 Allyl 2-Pr 1-2481 単 Allyl 4-Pr 1-2482 単 Allyl 5-Pr 1-2483 単 Allyl 6-Pr 1-2484 単 Allyl 7-Pr 1-2485 単 Allyl 8-Pr 1-2486 単 Allyl 2-iPr 1-2487 単 Allyl 4-iPr 1-2488 単 Allyl 5-iPr 1-2489 単 Allyl 6-iPr 1-2490 単 Allyl 7-iPr 1-2491 単 Allyl 8-iPr 1-2492 単 Allyl 2-Bu 1-2493 単 Allyl 4-Bu 1-2494 単 Allyl 5-Bu 1-2495 単 Allyl 6-Bu 1-2496 単 Allyl 7-Bu 1-2497 単 Allyl 8-Bu 1-2498 単 Allyl 2-CF3 1-2499 単 Allyl 4-CF3 1-2500 単 Allyl 5-CF3 1-2501 単 Allyl 6-CF3 1-2502 単 Allyl 7-CF3 1-2503 単 Allyl 8-CF3 1-2504 単 Allyl 2-CF3CH2 1-2505 単 Allyl 4-CF3CH2 1-2506 単 Allyl 5-CF3CH2 1-2507 単 Allyl 6-CF3CH2 1-2508 単 Allyl 7-CF3CH2 1-2509 単 Allyl 8-CF3CH2 1-2510 単 Allyl 2-CF2H 1-2511 単 Allyl 4-CF2H 1-2512 単 Allyl 5-CF2H 1-2513 単 Allyl 6-CF2H 1-2514 単 Allyl 7-CF2H 1-2515 単 Allyl 8-CF2H 1-2516 単 Allyl 2-CF2H 1-2517 単 Allyl 4-CF2H 1-2518 単 Allyl 5-CF2H 1-2519 単 Allyl 6-CF2H 1-2520 単 Allyl 7-CF2H 1-2521 単 Allyl 8-CF2H 1-2522 単 Allyl 2-CClH2 1-2523 単 Allyl 4-CClH2 1-2524 単 Allyl 5-CClH2 1-2525 単 Allyl 6-CClH2 1-2526 単 Allyl 7-CClH2 1-2527 単 Allyl 8-CClH2 1-2528 単 Allyl 2-MeO 1-2529 単 Allyl 4-MeO 1-2530 単 Allyl 5-MeO 1-2531 単 Allyl 6-MeO 1-2532 単 Allyl 7-MeO 1-2533 単 Allyl 8-MeO 1-2534 単 Allyl 2-EtO 1-2535 単 Allyl 4-EtO 1-2536 単 Allyl 5-EtO 1-2537 単 Allyl 6-EtO 1-2538 単 Allyl 7-EtO 1-2539 単 Allyl 8-EtO 1-2540 単 Allyl 2-PrO 1-2541 単 Allyl 4-PrO 1-2542 単 Allyl 5-PrO 1-2543 単 Allyl 6-PrO 1-2544 単 Allyl 7-PrO 1-2545 単 Allyl 8-PrO 1-2546 単 Allyl 2-iPrO 1-2547 単 Allyl 4-iPrO 1-2548 単 Allyl 5-iPrO 1-2549 単 Allyl 6-iPrO 1-2550 単 Allyl 7-iPrO 1-2551 単 Allyl 8-iPrO 1-2552 単 Allyl 2-BuO 1-2553 単 Allyl 4-BuO 1-2554 単 Allyl 5-BuO 1-2555 単 Allyl 6-BuO 1-2556 単 Allyl 7-BuO 1-2557 単 Allyl 8-BuO 1-2558 単 Allyl 2-CF3O 1-2559 単 Allyl 4-CF3O 1-2560 単 Allyl 5-CF3O 1-2561 単 Allyl 6-CF3O 1-2562 単 Allyl 7-CF3O 1-2563 単 Allyl 8-CF3O 1-2564 単 Allyl 2-CF3CH2O 1-2565 単 Allyl 4-CF3CH2O 1-2566 単 Allyl 5-CF3CH2O 1-2567 単 Allyl 6-CF3CH2O 1-2568 単 Allyl 7-CF3CH2O 1-2569 単 Allyl 8-CF3CH2O 1-2570 単 Allyl 2-CF2HO 1-2571 単 Allyl 4-CF2HO 1-2572 単 Allyl 5-CF2HO 1-2573 単 Allyl 6-CF2HO 1-2574 単 Allyl 7-CF2HO 1-2575 単 Allyl 8-CF2HO 1-2576 単 Allyl 2-CF2HO 1-2577 単 Allyl 4-CF2HO 1-2578 単 Allyl 5-CF2HO 1-2579 単 Allyl 6-CF2HO 1-2580 単 Allyl 7-CF2HO 1-2581 単 Allyl 8-CF2HO 1-2582 単 Allyl 2-CClH2O 1-2583 単 Allyl 4-CClH2O 1-2584 単 Allyl 5-CClH2O 1-2585 単 Allyl 6-CClH2O 1-2586 単 Allyl 7-CClH2O 1-2587 単 Allyl 8-CClH2O 1-2588 単 Allyl 2,4-F2 1-2589 単 Allyl 2,5-F2 1-2590 単 Allyl 2,6-F2 1-2591 単 Allyl 2,7-F2 1-2592 単 Allyl 2,8-F2 1-2593 単 Allyl 4,5-F2 1-2594 単 Allyl 4,6-F2 1-2595 単 Allyl 4,7-F2 1-2596 単 Allyl 4,8-F2 1-2597 単 Allyl 5,6-F2 1-2598 単 Allyl 5,7-F2 1-2599 単 Allyl 5,8-F2 1-2600 単 Allyl 6,7-F2 1-2601 単 Allyl 6,8-F2 1-2602 単 Allyl 7,8-F2 1-2603 単 Allyl 4,5-Cl2 1-2604 単 Allyl 4,6-Cl2 1-2605 単 Allyl 4,7-Cl2 1-2606 単 Allyl 4,8-Cl2 1-2607 単 Allyl 5,6-Cl2 1-2608 単 Allyl 5,7-Cl2 1-2609 単 Allyl 5,8-Cl2 1-2610 単 Allyl 6,7-Cl2 1-2611 単 Allyl 6,8-Cl2 1-2612 単 Allyl 7,8-Cl2 1-2613 単 Allyl 2,5-Me2 1-2614 単 Allyl 2,6-Me2 1-2615 単 Allyl 2,7-Me2 1-2616 単 Allyl 2,8-Me2 1-2617 単 Allyl 4,5-Me2 1-2618 単 Allyl 4,6-Me2 1-2619 単 Allyl 4,7-Me2 1-2620 単 Allyl 4,8-Me2 1-2621 単 Allyl 5,6-Me2 1-2622 単 Allyl 5,7-Me2 1-2623 単 Allyl 5,8-Me2 1-2624 単 Allyl 6,7-Me2 1-2625 単 Allyl 6,8-Me2 1-2626 単 Allyl 7,8-Me2 1-2627 単 Allyl 2,5-(MeO)2 1-2628 単 Allyl 2,6-(MeO)2 1-2629 単 Allyl 2,7-(MeO)2 1-2630 単 Allyl 2,8-(MeO)2 1-2631 単 Allyl 4,5-(MeO)2 1-2632 単 Allyl 4,6-(MeO)2 1-2633 単 Allyl 4,7-(MeO)2 1-2634 単 Allyl 4,8-(MeO)2 1-2635 単 Allyl 5,6-(MeO)2 1-2636 単 Allyl 5,7-(MeO)2 1-2637 単 Allyl 5,8-(MeO)2 1-2638 単 Allyl 6,7-(MeO)2 1-2639 単 Allyl 6,8-(MeO)2 1-2640 単 Allyl 7,8-(MeO)2 1-2641 単 Allyl 2-Me-5-F 1-2642 単 Allyl 2-Me-6-F 1-2643 単 Allyl 2-Me-7-F 1-2644 単 Allyl 2-Me-8-F 1-2645 単 Allyl 2-Me-5-Cl 1-2646 単 Allyl 2-Me-6-Cl 1-2647 単 Allyl 2-Me-7-Cl 1-2648 単 Allyl 2-Me-8-Cl 1-2649 単 Allyl 2-Me-5-MeO 1-2650 単 Allyl 2-Me-6-MeO 1-2651 単 Allyl 2-Me-7-MeO 1-2652 単 Allyl 2-Me-8-MeO 1-2653 単 Allyl 4-Cl-5-F 1-2654 単 Allyl 4-Cl-6-F 1-2655 単 Allyl 4-Cl-7-F 1-2656 単 Allyl 4-Cl-8-F 1-2657 単 Allyl 4-Cl-5-Me 1-2658 単 Allyl 4-Cl-6-Me 1-2659 単 Allyl 4-Cl-7-Me 1-2660 単 Allyl 4-Cl-8-Me 1-2661 単 Allyl 4-Cl-5-MeO 1-2662 単 Allyl 4-Cl-6-MeO 1-2663 単 Allyl 4-Cl-7-MeO 1-2664 単 Allyl 4-Cl-8-MeO 1-2665 単 tBu H 1-2666 単 tBu 2-F 1-2667 単 tBu 4-F 1-2668 単 tBu 5-F 1-2669 単 tBu 6-F 1-2670 単 tBu 7-F 1-2671 単 tBu 8-F 1-2672 単 tBu 2-Cl 1-2673 単 tBu 4-Cl 1-2674 単 tBu 5-Cl 1-2675 単 tBu 6-Cl 1-2676 単 tBu 7-Cl 1-2677 単 tBu 8-Cl 1-2678 単 tBu 2-Me 1-2679 単 tBu 4-Me 1-2680 単 tBu 5-Me 1-2681 単 tBu 6-Me 1-2682 単 tBu 7-Me 1-2683 単 tBu 8-Me 1-2684 単 tBu 2-Et 1-2685 単 tBu 4-Et 1-2686 単 tBu 5-Et 1-2687 単 tBu 6-Et 1-2688 単 tBu 7-Et 1-2689 単 tBu 8-Et 1-2690 単 tBu 2,4-F2 1-2691 単 tBu 2,5-F2 1-2692 単 tBu 2,6-F2 1-2693 単 tBu 2,7-F2 1-2694 単 tBu 2,8-F2 1-2695 単 tBu 4,5-F2 1-2696 単 tBu 4,6-F2 1-2697 単 tBu 4,7-F2 1-2698 単 tBu 4,8-F2 1-2699 単 tBu 5,6-F2 1-2700 単 tBu 5,7-F2 1-2701 単 tBu 5,8-F2 1-2702 単 tBu 6,7-F2 1-2703 単 tBu 6,8-F2 1-2704 単 tBu 7,8-F2 1-2705 単 tBu 2,4-Me2 1-2706 単 tBu 2,5-Me2 1-2707 単 tBu 2,6-Me2 1-2708 単 tBu 2,7-Me2 1-2709 単 tBu 2,8-Me2 1-2710 単 tBu 4,5-Me2 1-2711 単 tBu 4,6-Me2 1-2712 単 tBu 4,7-Me2 1-2713 単 tBu 4,8-Me2 1-2714 単 tBu 5,6-Me2 1-2715 単 tBu 5,7-Me2 1-2716 単 tBu 5,8-Me2 1-2717 単 tBu 6,7-Me2 1-2718 単 tBu 6,8-Me2 1-2719 単 tBu 7,8-Me2 1-2720 単 tBu 2-Me-5-F 1-2721 単 tBu 2-Me-6-F 1-2722 単 tBu 2-Me-7-F 1-2723 単 tBu 2-Me-8-F 1-2724 単 tBu 2-Me-5-Cl 1-2725 単 tBu 2-Me-6-Cl 1-2726 単 tBu 2-Me-7-Cl 1-2727 単 tBu 2-Me-8-Cl 1-2728 単 tBu 2-Me-5-MeO 1-2729 単 tBu 2-Me-6-MeO 1-2730 単 tBu 2-Me-7-MeO 1-2731 単 tBu 2-Me-8-MeO 1-2732 単 Pent H 1-2733 単 Pent 2-F 1-2734 単 Pent 4-F 1-2735 単 Pent 5-F 1-2736 単 Pent 6-F 1-2737 単 Pent 7-F 1-2738 単 Pent 8-F 1-2739 単 Pent 2-Cl 1-2740 単 Pent 4-Cl 1-2741 単 Pent 5-Cl 1-2742 単 Pent 6-Cl 1-2743 単 Pent 7-Cl 1-2744 単 Pent 8-Cl 1-2745 単 Pent 2-Me 1-2746 単 Pent 4-Me 1-2747 単 Pent 5-Me 1-2748 単 Pent 6-Me 1-2749 単 Pent 7-Me 1-2750 単 Pent 8-Me 1-2751 単 Pent 2-Et 1-2752 単 Pent 4-Et 1-2753 単 Pent 5-Et 1-2754 単 Pent 6-Et 1-2755 単 Pent 7-Et 1-2756 単 Pent 8-Et 1-2757 単 Pent 2,4-F2 1-2758 単 Pent 2,5-F2 1-2759 単 Pent 2,6-F2 1-2760 単 Pent 2,7-F2 1-2761 単 Pent 2,8-F2 1-2762 単 Pent 4,5-F2 1-2763 単 Pent 4,6-F2 1-2764 単 Pent 4,7-F2 1-2765 単 Pent 4,8-F2 1-2766 単 Pent 5,6-F2 1-2767 単 Pent 5,7-F2 1-2768 単 Pent 5,8-F2 1-2769 単 Pent 6,7-F2 1-2770 単 Pent 6,8-F2 1-2771 単 Pent 7,8-F2 1-2772 単 Pent 2,4-Me2 1-2773 単 Pent 2,5-Me2 1-2774 単 Pent 2,6-Me2 1-2775 単 Pent 2,7-Me2 1-2776 単 Pent 2,8-Me2 1-2777 単 Pent 4,5-Me2 1-2778 単 Pent 4,6-Me2 1-2779 単 Pent 4,7-Me2 1-2780 単 Pent 4,8-Me2 1-2781 単 Pent 5,6-Me2 1-2782 単 Pent 5,7-Me2 1-2783 単 Pent 5,8-Me2 1-2784 単 Pent 6,7-Me2 1-2785 単 Pent 6,8-Me2 1-2786 単 Pent 7,8-Me2 1-2787 単 Pent 2-Me-5-F 1-2788 単 Pent 2-Me-6-F 1-2789 単 Pent 2-Me-7-F 1-2790 単 Pent 2-Me-8-F 1-2791 単 Pent 2-Me-5-Cl 1-2792 単 Pent 2-Me-6-Cl 1-2793 単 Pent 2-Me-7-Cl 1-2794 単 Pent 2-Me-8-Cl 1-2795 単 Pent 2-Me-5-MeO 1-2796 単 Pent 2-Me-6-MeO 1-2797 単 Pent 2-Me-7-MeO 1-2798 単 Pent 2-Me-8-MeO 1-2799 単 Hex H 1-2800 単 Hex 2-F 1-2801 単 Hex 4-F 1-2802 単 Hex 5-F 1-2803 単 Hex 6-F 1-2804 単 Hex 7-F 1-2805 単 Hex 8-F 1-2806 単 Hex 2-Cl 1-2807 単 Hex 4-Cl 1-2808 単 Hex 5-Cl 1-2809 単 Hex 6-Cl 1-2810 単 Hex 7-Cl 1-2811 単 Hex 8-Cl 1-2812 単 Hex 2-Me 1-2813 単 Hex 4-Me 1-2814 単 Hex 5-Me 1-2815 単 Hex 6-Me 1-2816 単 Hex 7-Me 1-2817 単 Hex 8-Me 1-2818 単 Hex 2-Et 1-2819 単 Hex 4-Et 1-2820 単 Hex 5-Et 1-2821 単 Hex 6-Et 1-2822 単 Hex 7-Et 1-2823 単 Hex 8-Et 1-2824 単 Hex 2,4-F2 1-2825 単 Hex 2,5-F2 1-2826 単 Hex 2,6-F2 1-2827 単 Hex 2,7-F2 1-2828 単 Hex 2,8-F2 1-2829 単 Hex 4,5-F2 1-2830 単 Hex 4,6-F2 1-2831 単 Hex 4,7-F2 1-2832 単 Hex 4,8-F2 1-2833 単 Hex 5,6-F2 1-2834 単 Hex 5,7-F2 1-2835 単 Hex 5,8-F2 1-2836 単 Hex 6,7-F2 1-2837 単 Hex 6,8-F2 1-2838 単 Hex 7,8-F2 1-2839 単 Hex 2,4-Me2 1-2840 単 Hex 2,5-Me2 1-2841 単 Hex 2,6-Me2 1-2842 単 Hex 2,7-Me2 1-2843 単 Hex 2,8-Me2 1-2844 単 Hex 4,5-Me2 1-2845 単 Hex 4,6-Me2 1-2846 単 Hex 4,7-Me2 1-2847 単 Hex 4,8-Me2 1-2848 単 Hex 5,6-Me2 1-2849 単 Hex 5,7-Me2 1-2850 単 Hex 5,8-Me2 1-2851 単 Hex 6,7-Me2 1-2852 単 Hex 6,8-Me2 1-2853 単 Hex 7,8-Me2 1-2854 単 Hex 2-Me-5-F 1-2855 単 Hex 2-Me-6-F 1-2856 単 Hex 2-Me-7-F 1-2857 単 Hex 2-Me-8-F 1-2858 単 Hex 2-Me-5-Cl 1-2859 単 Hex 2-Me-6-Cl 1-2860 単 Hex 2-Me-7-Cl 1-2861 単 Hex 2-Me-8-Cl 1-2862 単 Hex 2-Me-5-MeO 1-2863 単 Hex 2-Me-6-MeO 1-2864 単 Hex 2-Me-7-MeO 1-2865 単 Hex 2-Me-8-MeO 1-2866 単 2-Et-Bu H 1-2867 単 2-Et-Bu 2-F 1-2868 単 2-Et-Bu 4-F 1-2869 単 2-Et-Bu 5-F 1-2870 単 2-Et-Bu 6-F 1-2871 単 2-Et-Bu 7-F 1-2872 単 2-Et-Bu 8-F 1-2873 単 2-Et-Bu 2-Cl 1-2874 単 2-Et-Bu 4-Cl 1-2875 単 2-Et-Bu 5-Cl 1-2876 単 2-Et-Bu 6-Cl 1-2877 単 2-Et-Bu 7-Cl 1-2878 単 2-Et-Bu 8-Cl 1-2879 単 2-Et-Bu 2-Me 1-2880 単 2-Et-Bu 4-Me 1-2881 単 2-Et-Bu 5-Me 1-2882 単 2-Et-Bu 6-Me 1-2883 単 2-Et-Bu 7-Me 1-2884 単 2-Et-Bu 8-Me 1-2885 単 2-Et-Bu 2-Et 1-2886 単 2-Et-Bu 4-Et 1-2887 単 2-Et-Bu 5-Et 1-2888 単 2-Et-Bu 6-Et 1-2889 単 2-Et-Bu 7-Et 1-2890 単 2-Et-Bu 8-Et 1-2891 単 2-Et-Bu 2,4-F2 1-2892 単 2-Et-Bu 2,5-F2 1-2893 単 2-Et-Bu 2,6-F2 1-2894 単 2-Et-Bu 2,7-F2 1-2895 単 2-Et-Bu 2,8-F2 1-2896 単 2-Et-Bu 4,5-F2 1-2897 単 2-Et-Bu 4,6-F2 1-2898 単 2-Et-Bu 4,7-F2 1-2899 単 2-Et-Bu 4,8-F2 1-2900 単 2-Et-Bu 5,6-F2 1-2901 単 2-Et-Bu 5,7-F2 1-2902 単 2-Et-Bu 5,8-F2 1-2903 単 2-Et-Bu 6,7-F2 1-2904 単 2-Et-Bu 6,8-F2 1-2905 単 2-Et-Bu 7,8-F2 1-2906 単 2-Et-Bu 2,4-Me2 1-2907 単 2-Et-Bu 2,5-Me2 1-2908 単 2-Et-Bu 2,6-Me2 1-2909 単 2-Et-Bu 2,7-Me2 1-2910 単 2-Et-Bu 2,8-Me2 1-2911 単 2-Et-Bu 4,5-Me2 1-2912 単 2-Et-Bu 4,6-Me2 1-2913 単 2-Et-Bu 4,7-Me2 1-2914 単 2-Et-Bu 4,8-Me2 1-2915 単 2-Et-Bu 5,6-Me2 1-2916 単 2-Et-Bu 5,7-Me2 1-2917 単 2-Et-Bu 5,8-Me2 1-2918 単 2-Et-Bu 6,7-Me2 1-2919 単 2-Et-Bu 6,8-Me2 1-2920 単 2-Et-Bu 7,8-Me2 1-2921 単 2-Et-Bu 2-Me-5-F 1-2922 単 2-Et-Bu 2-Me-6-F 1-2923 単 2-Et-Bu 2-Me-7-F 1-2924 単 2-Et-Bu 2-Me-8-F 1-2925 単 2-Et-Bu 2-Me-5-Cl 1-2926 単 2-Et-Bu 2-Me-6-Cl 1-2927 単 2-Et-Bu 2-Me-7-Cl 1-2928 単 2-Et-Bu 2-Me-8-Cl 1-2929 単 2-Et-Bu 2-Me-5-MeO 1-2930 単 2-Et-Bu 2-Me-6-MeO 1-2931 単 2-Et-Bu 2-Me-7-MeO 1-2932 単 2-Et-Bu 2-Me-8-MeO 1-2933 単 Hept H 1-2934 単 Hept 2-F 1-2935 単 Hept 4-F 1-2936 単 Hept 5-F 1-2937 単 Hept 6-F 1-2938 単 Hept 7-F 1-2939 単 Hept 8-F 1-2940 単 Hept 2-Cl 1-2941 単 Hept 4-Cl 1-2942 単 Hept 5-Cl 1-2943 単 Hept 6-Cl 1-2944 単 Hept 7-Cl 1-2945 単 Hept 8-Cl 1-2946 単 Hept 2-Me 1-2947 単 Hept 4-Me 1-2948 単 Hept 5-Me 1-2949 単 Hept 6-Me 1-2950 単 Hept 7-Me 1-2951 単 Hept 8-Me 1-2952 単 Hept 2-Et 1-2953 単 Hept 4-Et 1-2954 単 Hept 5-Et 1-2955 単 Hept 6-Et 1-2956 単 Hept 7-Et 1-2957 単 Hept 8-Et 1-2958 単 Hept 2,4-F2 1-2959 単 Hept 2,5-F2 1-2960 単 Hept 2,6-F2 1-2961 単 Hept 2,7-F2 1-2962 単 Hept 2,8-F2 1-2963 単 Hept 4,5-F2 1-2964 単 Hept 4,6-F2 1-2965 単 Hept 4,7-F2 1-2966 単 Hept 4,8-F2 1-2967 単 Hept 5,6-F2 1-2968 単 Hept 5,7-F2 1-2969 単 Hept 5,8-F2 1-2970 単 Hept 6,7-F2 1-2971 単 Hept 6,8-F2 1-2972 単 Hept 7,8-F2 1-2973 単 Hept 2,4-Me2 1-2974 単 Hept 2,5-Me2 1-2975 単 Hept 2,6-Me2 1-2976 単 Hept 2,7-Me2 1-2977 単 Hept 2,8-Me2 1-2978 単 Hept 4,5-Me2 1-2979 単 Hept 4,6-Me2 1-2980 単 Hept 4,7-Me2 1-2981 単 Hept 4,8-Me2 1-2982 単 Hept 5,6-Me2 1-2983 単 Hept 5,7-Me2 1-2984 単 Hept 5,8-Me2 1-2985 単 Hept 6,7-Me2 1-2986 単 Hept 6,8-Me2 1-2987 単 Hept 7,8-Me2 1-2988 単 Hept 2-Me-5-F 1-2989 単 Hept 2-Me-6-F 1-2990 単 Hept 2-Me-7-F 1-2991 単 Hept 2-Me-8-F 1-2992 単 Hept 2-Me-5-Cl 1-2993 単 Hept 2-Me-6-Cl 1-2994 単 Hept 2-Me-7-Cl 1-2995 単 Hept 2-Me-8-Cl 1-2996 単 Hept 2-Me-5-MeO 1-2997 単 Hept 2-Me-6-MeO 1-2998 単 Hept 2-Me-7-MeO 1-2999 単 Hept 2-Me-8-MeO 1-3000 単 Oct H 1-3001 単 Oct 2-F 1-3002 単 Oct 4-F 1-3003 単 Oct 5-F 1-3004 単 Oct 6-F 1-3005 単 Oct 7-F 1-3006 単 Oct 8-F 1-3007 単 Oct 2-Cl 1-3008 単 Oct 4-Cl 1-3009 単 Oct 5-Cl 1-3010 単 Oct 6-Cl 1-3011 単 Oct 7-Cl 1-3012 単 Oct 8-Cl 1-3013 単 Oct 2-Me 1-3014 単 Oct 4-Me 1-3015 単 Oct 5-Me 1-3016 単 Oct 6-Me 1-3017 単 Oct 7-Me 1-3018 単 Oct 8-Me 1-3019 単 Oct 2-Et 1-3020 単 Oct ４−Ｅｔ 1-3023 単 Oct 7-Et 1-3024 単 Oct 8-Et 1-3025 単 Oct 2,4-F2 1-3026 単 Oct 2,5-F2 1-3027 単 Oct 2,6-F2 1-3028 単 Oct 2,7-F2 1-3029 単 Oct 2,8-F2 1-3030 単 Oct 4,5-F2 1-3031 単 Oct 4,6-F2 1-3032 単 Oct 4,7-F2 1-3033 単 Oct 4,8-F2 1-3034 単 Oct 5,6-F2 1-3035 単 Oct 5,7-F2 1-3036 単 Oct 5,8-F2 1-3037 単 Oct 6,7-F2 1-3038 単 Oct 6,8-F2 1-3039 単 Oct 7,8-F2 1-3040 単 Oct 2,4-Me2 1-3041 単 Oct 2,5-Me2 1-3042 単 Oct 2,6-Me2 1-3043 単 Oct 2,7-Me2 1-3044 単 Oct 2,8-Me2 1-3045 単 Oct 4,5-Me2 1-3046 単 Oct 4,6-Me2 1-3047 単 Oct 4,7-Me2 1-3048 単 Oct 4,8-Me2 1-3049 単 Oct 5,6-Me2 1-3050 単 Oct 5,7-Me2 1-3051 単 Oct 5,8-Me2 1-3052 単 Oct 6,7-Me2 1-3053 単 Oct 6,8-Me2 1-3054 単 Oct 7,8-Me2 1-3055 単 Oct 2-Me-5-F 1-3056 単 Oct 2-Me-6-F 1-3057 単 Oct 2-Me-7-F 1-3058 単 Oct 2-Me-8-F 1-3059 単 Oct 2-Me-5-Cl 1-3060 単 Oct 2-Me-6-Cl 1-3061 単 Oct 2-Me-7-Cl 1-3062 単 Oct 2-Me-8-Cl 1-3063 単 Oct 2-Me-5-MeO 1-3064 単 Oct 2-Me-6-MeO 1-3065 単 Oct 2-Me-7-MeO 1-3066 単 Oct 2-Me-8-MeO 1-3067 単 FCH2 H 1-3068 単 FCH2 2-F 1-3069 単 FCH2 4-F 1-3070 単 FCH2 5-F 1-3071 単 FCH2 6-F 1-3072 単 FCH2 7-F 1-3073 単 FCH2 8-F 1-3074 単 FCH2 2-Cl 1-3075 単 FCH2 4-Cl 1-3076 単 FCH2 5-Cl 1-3077 単 FCH2 6-Cl 1-3078 単 FCH2 7-Cl 1-3079 単 FCH2 8-Cl 1-3080 単 FCH2 2-Me 1-3081 単 FCH2 4-Me 1-3082 単 FCH2 5-Me 1-3083 単 FCH2 6-Me 1-3084 単 FCH2 7-Me 1-3085 単 FCH2 8-Me 1-3086 単 FCH2 2-Et 1-3087 単 FCH2 4-Et 1-3088 単 FCH2 5-Et 1-3089 単 FCH2 6-Et 1-3090 単 FCH2 7-Et 1-3091 単 FCH2 8-Et 1-3092 単 FCH2 2,4-F2 1-3093 単 FCH2 2,5-F2 1-3094 単 FCH2 2,6-F2 1-3095 単 FCH2 2,7-F2 1-3096 単 FCH2 2,8-F2 1-3097 単 FCH2 4,5-F2 1-3098 単 FCH2 4,6-F2 1-3099 単 FCH2 4,7-F2 1-3100 単 FCH2 4,8-F2 1-3101 単 FCH2 5,6-F2 1-3102 単 FCH2 5,7-F2 1-3103 単 FCH2 5,8-F2 1-3104 単 FCH2 6,7-F2 1-3105 単 FCH2 6,8-F2 1-3106 単 FCH2 7,8-F2 1-3107 単 FCH2 2,4-Me2 1-3108 単 FCH2 2,5-Me2 1-3109 単 FCH2 2,6-Me2 1-3110 単 FCH2 2,7-Me2 1-3111 単 FCH2 2,8-Me2 1-3112 単 FCH2 4,5-Me2 1-3113 単 FCH2 4,6-Me2 1-3114 単 FCH2 4,7-Me2 1-3115 単 FCH2 4,8-Me2 1-3116 単 FCH2 5,6-Me2 1-3117 単 FCH2 5,7-Me2 1-3118 単 FCH2 5,8-Me2 1-3119 単 FCH2 6,7-Me2 1-3120 単 FCH2 6,8-Me2 1-3121 単 FCH2 7,8-Me2 1-3122 単 FCH2 2-Me-5-F 1-3123 単 FCH2 2-Me-6-F 1-3124 単 FCH2 2-Me-7-F 1-3125 単 FCH2 2-Me-8-F 1-3126 単 FCH2 2-Me-5-Cl 1-3127 単 FCH2 2-Me-6-Cl 1-3128 単 FCH2 2-Me-7-Cl 1-3129 単 FCH2 2-Me-8-Cl 1-3130 単 FCH2 2-Me-5-MeO 1-3131 単 FCH2 2-Me-6-MeO 1-3132 単 FCH2 2-Me-7-MeO 1-3133 単 FCH2 2-Me-8-MeO 1-3134 単 ClCH2 H 1-3135 単 ClCH2 2-F 1-3136 単 ClCH2 4-F 1-3137 単 ClCH2 5-F 1-3138 単 ClCH2 6-F 1-3139 単 ClCH2 7-F 1-3140 単 ClCH2 8-F 1-3141 単 ClCH2 2-Cl 1-3142 単 ClCH2 4-Cl 1-3143 単 ClCH2 5-Cl 1-3144 単 ClCH2 6-Cl 1-3145 単 ClCH2 7-Cl 1-3146 単 ClCH2 8-Cl 1-3147 単 ClCH2 2-Me 1-3148 単 ClCH2 4-Me 1-3149 単 ClCH2 5-Me 1-3150 単 ClCH2 6-Me 1-3151 単 ClCH2 7-Me 1-3152 単 ClCH2 8-Me 1-3153 単 ClCH2 2-Et 1-3154 単 ClCH2 4-Et 1-3155 単 ClCH2 5-Et 1-3156 単 ClCH2 6-Et 1-3157 単 ClCH2 7-Et 1-3158 単 ClCH2 8-Et 1-3159 単 ClCH2 2,4-F2 1-3160 単 ClCH2 2,5-F2 1-3161 単 ClCH2 2,6-F2 1-3162 単 ClCH2 2,7-F2 1-3163 単 ClCH2 2,8-F2 1-3164 単 ClCH2 4,5-F2 1-3165 単 ClCH2 4,6-F2 1-3166 単 ClCH2 4,7-F2 1-3167 単 ClCH2 4,8-F2 1-3168 単 ClCH2 5,6-F2 1-3169 単 ClCH2 5,7-F2 1-3170 単 ClCH2 5,8-F2 1-3171 単 ClCH2 6,7-F2 1-3172 単 ClCH2 6,8-F2 1-3173 単 ClCH2 7,8-F2 1-3174 単 ClCH2 2,4-Me2 1-3175 単 ClCH2 2,5-Me2 1-3176 単 ClCH2 2,6-Me2 1-3177 単 ClCH2 2,7-Me2 1-3178 単 ClCH2 2,8-Me2 1-3179 単 ClCH2 4,5-Me2 1-3180 単 ClCH2 4,6-Me2 1-3181 単 ClCH2 4,7-Me2 1-3182 単 ClCH2 4,8-Me2 1-3183 単 ClCH2 5,6-Me2 1-3184 単 ClCH2 5,7-Me2 1-3185 単 ClCH2 5,8-Me2 1-3186 単 ClCH2 6,7-Me2 1-3187 単 ClCH2 6,8-Me2 1-3188 単 ClCH2 7,8-Me2 1-3189 単 ClCH2 2-Me-5-F 1-3190 単 ClCH2 2-Me-6-F 1-3191 単 ClCH2 2-Me-7-F 1-3192 単 ClCH2 2-Me-8-F 1-3193 単 ClCH2 2-Me-5-Cl 1-3194 単 ClCH2 2-Me-6-Cl 1-3195 単 ClCH2 2-Me-7-Cl 1-3196 単 ClCH2 2-Me-8-Cl 1-3197 単 ClCH2 2-Me-5-MeO 1-3198 単 ClCH2 2-Me-6-MeO 1-3199 単 ClCH2 2-Me-7-MeO 1-3200 単 ClCH2 2-Me-8-MeO 1-3201 単 3,3,4,4-F4-Bu H 1-3202 単 3,3,4,4-F4-Bu 2-F 1-3203 単 3,3,4,4-F4-Bu 4-F 1-3204 単 3,3,4,4-F4-Bu 5-F 1-3205 単 3,3,4,4-F4-Bu 6-F 1-3206 単 3,3,4,4-F4-Bu 7-F 1-3207 単 3,3,4,4-F4-Bu 8-F 1-3208 単 3,3,4,4-F4-Bu 2-Cl 1-3209 単 3,3,4,4-F4-Bu 4-Cl 1-3210 単 3,3,4,4-F4-Bu 5-Cl 1-3211 単 3,3,4,4-F4-Bu 6-Cl 1-3212 単 3,3,4,4-F4-Bu 7-Cl 1-3213 単 3,3,4,4-F4-Bu 8-Cl 1-3214 単 3,3,4,4-F4-Bu 2-Me 1-3215 単 3,3,4,4-F4-Bu 4-Me 1-3216 単 3,3,4,4-F4-Bu 5-Me 1-3217 単 3,3,4,4-F4-Bu 6-Me 1-3218 単 3,3,4,4-F4-Bu 7-Me 1-3219 単 3,3,4,4-F4-Bu 8-Me 1-3220 単 3,3,4,4-F4-Bu 2-Et 1-3221 単 3,3,4,4-F4-Bu 4-Et 1-3222 単 3,3,4,4-F4-Bu 5-Et 1-3223 単 3,3,4,4-F4-Bu 6-Et 1-3224 単 3,3,4,4-F4-Bu 7-Et 1-3225 単 3,3,4,4-F4-Bu 8-Et 1-3226 単 3,3,4,4-F4-Bu 2,4-F2 1-3227 単 3,3,4,4-F4-Bu 2,5-F2 1-3228 単 3,3,4,4-F4-Bu 2,6-F2 1-3229 単 3,3,4,4-F4-Bu 2,7-F2 1-3230 単 3,3,4,4-F4-Bu 2,8-F2 1-3231 単 3,3,4,4-F4-Bu 4,5-F2 1-3232 単 3,3,4,4-F4-Bu 4,6-F2 1-3233 単 3,3,4,4-F4-Bu 4,7-F2 1-3234 単 3,3,4,4-F4-Bu 4,8-F2 1-3235 単 3,3,4,4-F4-Bu 5,6-F2 1-3236 単 3,3,4,4-F4-Bu 5,7-F2 1-3237 単 3,3,4,4-F4-Bu 5,8-F2 1-3238 単 3,3,4,4-F4-Bu 6,7-F2 1-3239 単 3,3,4,4-F4-Bu 6,8-F2 1-3240 単 3,3,4,4-F4-Bu 7,8-F2 1-3241 単 3,3,4,4-F4-Bu 2,4-Me2 1-3242 単 3,3,4,4-F4-Bu 2,5-Me2 1-3243 単 3,3,4,4-F4-Bu 2,6-Me2 1-3244 単 3,3,4,4-F4-Bu 2,7-Me2 1-3245 単 3,3,4,4-F4-Bu 2,8-Me2 1-3246 単 3,3,4,4-F4-Bu 4,5-Me2 1-3247 単 3,3,4,4-F4-Bu 4,6-Me2 1-3248 単 3,3,4,4-F4-Bu 4,7-Me2 1-3249 単 3,3,4,4-F4-Bu 4,8-Me2 1-3250 単 3,3,4,4-F4-Bu 5,6-Me2 1-3251 単 3,3,4,4-F4-Bu 5,7-Me2 1-3252 単 3,3,4,4-F4-Bu 5,8-Me2 1-3253 単 3,3,4,4-F4-Bu 6,7-Me2 1-3254 単 3,3,4,4-F4-Bu 6,8-Me2 1-3255 単 3,3,4,4-F4-Bu 7,8-Me2 1-3256 単 3,3,4,4-F4-Bu 2-Me-5-F 1-3257 単 3,3,4,4-F4-Bu 2-Me-6-F 1-3258 単 3,3,4,4-F4-Bu 2-Me-7-F 1-3259 単 3,3,4,4-F4-Bu 2-Me-8-F 1-3260 単 3,3,4,4-F4-Bu 2-Me-5-Cl 1-3261 単 3,3,4,4-F4-Bu 2-Me-6-Cl 1-3262 単 3,3,4,4-F4-Bu 2-Me-7-Cl 1-3263 単 3,3,4,4-F4-Bu 2-Me-8-Cl 1-3264 単 3,3,4,4-F4-Bu 2-Me-5-MeO 1-3265 単 3,3,4,4-F4-Bu 2-Me-6-MeO 1-3266 単 3,3,4,4-F4-Bu 2-Me-7-MeO 1-3267 単 cBuCH2 H 1-3268 単 cBuCH2 2-F 1-3269 単 cBuCH2 4-F 1-3270 単 cBuCH2 5-F 1-3271 単 cBuCH2 6-F 1-3272 単 cBuCH2 7-F 1-3273 単 cBuCH2 8-F 1-3274 単 cBuCH2 2-Cl 1-3275 単 cBuCH2 4-Cl 1-3276 単 cBuCH2 5-Cl 1-3277 単 cBuCH2 6-Cl 1-3278 単 cBuCH2 7-Cl 1-3279 単 cBuCH2 8-Cl 1-3280 単 cBuCH2 2-Me 1-3281 単 cBuCH2 4-Me 1-3282 単 cBuCH2 5-Me 1-3283 単 cBuCH2 6-Me 1-3284 単 cBuCH2 7-Me 1-3285 単 cBuCH2 8-Me 1-3286 単 cBuCH2 2-Et 1-3287 単 cBuCH2 4-Et 1-3288 単 cBuCH2 5-Et 1-3289 単 cBuCH2 6-Et 1-3290 単 cBuCH2 7-Et 1-3291 単 cBuCH2 8-Et 1-3292 単 cBuCH2 2,4-F2 1-3293 単 cBuCH2 2,5-F2 1-3294 単 cBuCH2 2,6-F2 1-3295 単 cBuCH2 2,7-F2 1-3296 単 cBuCH2 2,8-F2 1-3297 単 cBuCH2 4,5-F2 1-3298 単 cBuCH2 4,6-F2 1-3299 単 cBuCH2 4,7-F2 1-3300 単 cBuCH2 4,8-F2 1-3301 単 cBuCH2 5,6-F2 1-3302 単 cBuCH2 5,7-F2 1-3303 単 cBuCH2 5,8-F2 1-3304 単 cBuCH2 6,7-F2 1-3305 単 cBuCH2 6,8-F2 1-3306 単 cBuCH2 7,8-F2 1-3307 単 cBuCH2 2,4-Me2 1-3308 単 cBuCH2 2,5-Me2 1-3309 単 cBuCH2 2,6-Me2 1-3310 単 cBuCH2 2,7-Me2 1-3311 単 cBuCH2 2,8-Me2 1-3312 単 cBuCH2 4,5-Me2 1-3313 単 cBuCH2 4,6-Me2 1-3314 単 cBuCH2 4,7-Me2 1-3315 単 cBuCH2 4,8-Me2 1-3316 単 cBuCH2 5,6-Me2 1-3317 単 cBuCH2 5,7-Me2 1-3318 単 cBuCH2 5,8-Me2 1-3319 単 cBuCH2 6,7-Me2 1-3320 単 cBuCH2 6,8-Me2 1-3321 単 cBuCH2 7,8-Me2 1-3322 単 cBuCH2 2-Me-5-F 1-3323 単 cBuCH2 2-Me-6-F 1-3324 単 cBuCH2 2-Me-7-F 1-3325 単 cBuCH2 2-Me-8-F 1-3326 単 cBuCH2 2-Me-5-Cl 1-3327 単 cBuCH2 2-Me-6-Cl 1-3328 単 cBuCH2 2-Me-7-Cl 1-3329 単 cBuCH2 2-Me-8-Cl 1-3330 単 cBuCH2 2-Me-5-MeO 1-3331 単 cBuCH2 2-Me-6-MeO 1-3332 単 cBuCH2 2-Me-7-MeO 1-3333 単 cBuCH2 2-Me-8-MeO 1-3334 単 cHexCH2 H 1-3335 単 cHexCH2 2-F 1-3336 単 cHexCH2 4-F 1-3337 単 cHexCH2 5-F 1-3338 単 cHexCH2 6-F 1-3339 単 cHexCH2 7-F 1-3340 単 cHexCH2 8-F 1-3341 単 cHexCH2 2-Cl 1-3342 単 cHexCH2 4-Cl 1-3343 単 cHexCH2 5-Cl 1-3344 単 cHexCH2 6-Cl 1-3345 単 cHexCH2 7-Cl 1-3346 単 cHexCH2 8-Cl 1-3347 単 cHexCH2 2-Me 1-3348 単 cHexCH2 4-Me 1-3349 単 cHexCH2 5-Me 1-3350 単 cHexCH2 6-Me 1-3351 単 cHexCH2 7-Me 1-3352 単 cHexCH2 8-Me 1-3353 単 cHexCH2 2-Et 1-3354 単 cHexCH2 4-Et 1-3355 単 cHexCH2 5-Et 1-3356 単 cHexCH2 6-Et 1-3357 単 cHexCH2 7-Et 1-3358 単 cHexCH2 8-Et 1-3359 単 cHexCH2 2,4-F2 1-3360 単 cHexCH2 2,5-F2 1-3361 単 cHexCH2 2,6-F2 1-3362 単 cHexCH2 2,7-F2 1-3363 単 cHexCH2 2,8-F2 1-3364 単 cHexCH2 4,5-F2 1-3365 単 cHexCH2 4,6-F2 1-3366 単 cHexCH2 4,7-F2 1-3367 単 cHexCH2 4,8-F2 1-3368 単 cHexCH2 5,6-F2 1-3369 単 cHexCH2 5,7-F2 1-3370 単 cHexCH2 5,8-F2 1-3371 単 cHexCH2 6,7-F2 1-3372 単 cHexCH2 6,8-F2 1-3373 単 cHexCH2 7,8-F2 1-3374 単 cHexCH2 2,4-Me2 1-3375 単 cHexCH2 2,5-Me2 1-3376 単 cHexCH2 2,6-Me2 1-3377 単 cHexCH2 2,7-Me2 1-3378 単 cHexCH2 2,8-Me2 1-3379 単 cHexCH2 4,5-Me2 1-3380 単 cHexCH2 4,6-Me2 1-3381 単 cHexCH2 4,7-Me2 1-3382 単 cHexCH2 4,8-Me2 1-3383 単 cHexCH2 5,6-Me2 1-3384 単 cHexCH2 5,7-Me2 1-3385 単 cHexCH2 5,8-Me2 1-3386 単 cHexCH2 6,7-Me2 1-3387 単 cHexCH2 6,8-Me2 1-3388 単 cHexCH2 7,8-Me2 1-3389 単 cHexCH2 2-Me-5-F 1-3390 単 cHexCH2 2-Me-6-F 1-3391 単 cHexCH2 2-Me-7-F 1-3392 単 cHexCH2 2-Me-8-F 1-3393 単 cHexCH2 2-Me-5-Cl 1-3394 単 cHexCH2 2-Me-6-Cl 1-3395 単 cHexCH2 2-Me-7-Cl 1-3396 単 cHexCH2 2-Me-8-Cl 1-3397 単 cHexCH2 2-Me-5-MeO 1-3398 単 cHexCH2 2-Me-6-MeO 1-3399 単 cHexCH2 2-Me-7-MeO 1-3400 単 cHexCH2 2-Me-8-MeO 1-3401 単 Vinyl H 1-3402 単 Vinyl 2-F 1-3403 単 Vinyl 4-F 1-3404 単 Vinyl 5-F 1-3405 単 Vinyl 6-F 1-3406 単 Vinyl 7-F 1-3407 単 Vinyl 8-F 1-3408 単 Vinyl 2-Cl 1-3409 単 Vinyl 4-Cl 1-3410 単 Vinyl 5-Cl 1-3411 単 Vinyl 6-Cl 1-3412 単 Vinyl 7-Cl 1-3413 単 Vinyl 8-Cl 1-3414 単 Vinyl 2-Me 1-3415 単 Vinyl 4-Me 1-3416 単 Vinyl 5-Me 1-3417 単 Vinyl 6-Me 1-3418 単 Vinyl 7-Me 1-3419 単 Vinyl 8-Me 1-3420 単 Vinyl 2-Et 1-3421 単 Vinyl 4-Et 1-3422 単 Vinyl 5-Et 1-3423 単 Vinyl 6-Et 1-3424 単 Vinyl 7-Et 1-3425 単 Vinyl 8-Et 1-3426 単 Vinyl 2,4-F2 1-3427 単 Vinyl 2,5-F2 1-3428 単 Vinyl 2,6-F2 1-3429 単 Vinyl 2,7-F2 1-3430 単 Vinyl 2,8-F2 1-3431 単 Vinyl 4,5-F2 1-3432 単 Vinyl 4,6-F2 1-3433 単 Vinyl 4,7-F2 1-3434 単 Vinyl 4,8-F2 1-3435 単 Vinyl 5,6-F2 1-3436 単 Vinyl 5,7-F2 1-3437 単 Vinyl 5,8-F2 1-3438 単 Vinyl 6,7-F2 1-3439 単 Vinyl 6,8-F2 1-3440 単 Vinyl 7,8-F2 1-3441 単 Vinyl 2,4-Me2 1-3442 単 Vinyl 2,5-Me2 1-3443 単 Vinyl 2,6-Me2 1-3444 単 Vinyl 2,7-Me2 1-3445 単 Vinyl 2,8-Me2 1-3446 単 Vinyl 4,5-Me2 1-3447 単 Vinyl 4,6-Me2 1-3448 単 Vinyl 4,7-Me2 1-3449 単 Vinyl 4,8-Me2 1-3450 単 Vinyl 5,6-Me2 1-3451 単 Vinyl 5,7-Me2 1-3452 単 Vinyl 5,8-Me2 1-3453 単 Vinyl 6,7-Me2 1-3454 単 Vinyl 6,8-Me2 1-3455 単 Vinyl 7,8-Me2 1-3456 単 Vinyl 2-Me-5-F 1-3457 単 Vinyl 2-Me-6-F 1-3458 単 Vinyl 2-Me-7-F 1-3459 単 Vinyl 2-Me-8-F 1-3460 単 Vinyl 2-Me-5-Cl 1-3461 単 Vinyl 2-Me-6-Cl 1-3462 単 Vinyl 2-Me-7-Cl 1-3463 単 Vinyl 2-Me-8-Cl 1-3464 単 Vinyl 2-Me-5-MeO 1-3465 単 Vinyl 2-Me-6-MeO 1-3466 単 Vinyl 2-Me-7-MeO 1-3467 単 Vinyl 2-Me-8-MeO 1-3468 単 Methallyl H 1-3469 単 Methallyl 2-F 1-3470 単 Methallyl 4-F 1-3471 単 Methallyl 5-F 1-3472 単 Methallyl 6-F 1-3473 単 Methallyl 7-F 1-3474 単 Methallyl 8-F 1-3475 単 Methallyl 2-Cl 1-3476 単 Methallyl 4-Cl 1-3477 単 Methallyl 5-Cl 1-3478 単 Methallyl 6-Cl 1-3479 単 Methallyl 7-Cl 1-3480 単 Methallyl 8-Cl 1-3481 単 Methallyl 2-Me 1-3482 単 Methallyl 4-Me 1-3483 単 Methallyl 5-Me 1-3484 単 Methallyl 6-Me 1-3485 単 Methallyl 7-Me 1-3486 単 Methallyl 8-Me 1-3487 単 Methallyl 2-Et 1-3488 単 Methallyl 4-Et 1-3489 単 Methallyl 5-Et 1-3490 単 Methallyl 6-Et 1-3491 単 Methallyl 7-Et 1-3492 単 Methallyl 8-Et 1-3493 単 Methallyl 2,4-F2 1-3494 単 Methallyl 2,5-F2 1-3495 単 Methallyl 2,6-F2 1-3496 単 Methallyl 2,7-F2 1-3497 単 Methallyl 2,8-F2 1-3498 単 Methallyl 4,5-F2 1-3499 単 Methallyl 4,6-F2 1-3500 単 Methallyl 4,7-F2 1-3501 単 Methallyl 4,8-F2 1-3502 単 Methallyl 5,6-F2 1-3503 単 Methallyl 5,7-F2 1-3504 単 Methallyl 5,8-F2 1-3505 単 Methallyl 6,7-F2 1-3506 単 Methallyl 6,8-F2 1-3507 単 Methallyl 7,8-F2 1-3508 単 Methallyl 2,4-Me2 1-3509 単 Methallyl 2,5-Me2 1-3510 単 Methallyl 2,6-Me2 1-3511 単 Methallyl 2,7-Me2 1-3512 単 Methallyl 2,8-Me2 1-3513 単 Methallyl 4,5-Me2 1-3514 単 Methallyl 4,6-Me2 1-3515 単 Methallyl 4,7-Me2 1-3516 単 Methallyl 4,8-Me2 1-3517 単 Methallyl 5,6-Me2 1-3518 単 Methallyl 5,7-Me2 1-3519 単 Methallyl 5,8-Me2 1-3520 単 Methallyl 6,7-Me2 1-3521 単 Methallyl 6,8-Me2 1-3522 単 Methallyl 7,8-Me2 1-3523 単 Methallyl 2-Me-5-F 1-3524 単 Methallyl 2-Me-6-F 1-3525 単 Methallyl 2-Me-7-F 1-3526 単 Methallyl 2-Me-8-F 1-3527 単 Methallyl 2-Me-5-Cl 1-3528 単 Methallyl 2-Me-6-Cl 1-3529 単 Methallyl 2-Me-7-Cl 1-3530 単 Methallyl 2-Me-8-Cl 1-3531 単 Methallyl 2-Me-5-MeO 1-3532 単 Methallyl 2-Me-6-MeO 1-3533 単 Methallyl 2-Me-7-MeO 1-3534 単 Methallyl 2-Me-8-MeO 1-3535 単 3-Me-2-butenyl H 1-3536 単 3-Me-2-butenyl 2-F 1-3537 単 3-Me-2-butenyl 4-F 1-3538 単 3-Me-2-butenyl 5-F 1-3539 単 3-Me-2-butenyl 6-F 1-3540 単 3-Me-2-butenyl 7-F 1-3541 単 3-Me-2-butenyl 8-F 1-3542 単 3-Me-2-butenyl 2-Cl 1-3543 単 3-Me-2-butenyl 4-Cl 1-3544 単 3-Me-2-butenyl 5-Cl 1-3545 単 3-Me-2-butenyl 6-Cl 1-3546 単 3-Me-2-butenyl 7-Cl 1-3547 単 3-Me-2-butenyl 8-Cl 1-3548 単 3-Me-2-butenyl 2-Me 1-3549 単 3-Me-2-butenyl 4-Me 1-3550 単 3-Me-2-butenyl 5-Me 1-3551 単 3-Me-2-butenyl 6-Me 1-3552 単 3-Me-2-butenyl 7-Me 1-3553 単 3-Me-2-butenyl 8-Me 1-3554 単 3-Me-2-butenyl 2-Et 1-3555 単 3-Me-2-butenyl 4-Et 1-3556 単 3-Me-2-butenyl 5-Et 1-3557 単 3-Me-2-butenyl 6-Et 1-3558 単 3-Me-2-butenyl 7-Et 1-3559 単 3-Me-2-butenyl 8-Et 1-3560 単 3-Me-2-butenyl 2,4-F2 1-3561 単 3-Me-2-butenyl 2,5-F2 1-3562 単 3-Me-2-butenyl 2,6-F2 1-3563 単 3-Me-2-butenyl 2,7-F2 1-3564 単 3-Me-2-butenyl 2,8-F2 1-3565 単 3-Me-2-butenyl 4,5-F2 1-3566 単 3-Me-2-butenyl 4,6-F2 1-3567 単 3-Me-2-butenyl 4,7-F2 1-3568 単 3-Me-2-butenyl 4,8-F2 1-3569 単 3-Me-2-butenyl 5,6-F2 1-3570 単 3-Me-2-butenyl 5,7-F2 1-3571 単 3-Me-2-butenyl 5,8-F2 1-3572 単 3-Me-2-butenyl 6,7-F2 1-3573 単 3-Me-2-butenyl 6,8-F2 1-3574 単 3-Me-2-butenyl 7,8-F2 1-3575 単 3-Me-2-butenyl 2,4-Me2 1-3576 単 3-Me-2-butenyl 2,5-Me2 1-3577 単 3-Me-2-butenyl 2,6-Me2 1-3578 単 3-Me-2-butenyl 2,7-Me2 1-3579 単 3-Me-2-butenyl 2,8-Me2 1-3580 単 3-Me-2-butenyl 4,5-Me2 1-3581 単 3-Me-2-butenyl 4,6-Me2 1-3582 単 3-Me-2-butenyl 4,7-Me2 1-3583 単 3-Me-2-butenyl 4,8-Me2 1-3584 単 3-Me-2-butenyl 5,6-Me2 1-3585 単 3-Me-2-butenyl 5,7-Me2 1-3586 単 3-Me-2-butenyl 5,8-Me2 1-3587 単 3-Me-2-butenyl 6,7-Me2 1-3588 単 3-Me-2-butenyl 6,8-Me2 1-3589 単 3-Me-2-butenyl 7,8-Me2 1-3590 単 3-Me-2-butenyl 2-Me-5-F 1-3591 単 3-Me-2-butenyl 2-Me-6-F 1-3592 単 3-Me-2-butenyl 2-Me-7-F 1-3593 単 3-Me-2-butenyl 2-Me-8-F 1-3594 単 3-Me-2-butenyl 2-Me-5-Cl 1-3595 単 3-Me-2-butenyl 2-Me-6-Cl 1-3596 単 3-Me-2-butenyl 2-Me-7-Cl 1-3597 単 3-Me-2-butenyl 2-Me-8-Cl 1-3598 単 3-Me-2-butenyl 2-Me-5-MeO 1-3599 単 3-Me-2-butenyl 2-Me-6-MeO 1-3600 単 3-Me-2-butenyl 2-Me-7-MeO 1-3601 単 3-Me-2-butenyl 2-Me-8-MeO 1-3602 単 3-Butenyl H 1-3603 単 3-Butenyl 2-F 1-3604 単 3-Butenyl 4-F 1-3605 単 3-Butenyl 5-F 1-3606 単 3-Butenyl 6-F 1-3607 単 3-Butenyl 7-F 1-3608 単 3-Butenyl 8-F 1-3609 単 3-Butenyl 2-Cl 1-3610 単 3-Butenyl 4-Cl 1-3611 単 3-Butenyl 5-Cl 1-3612 単 3-Butenyl 6-Cl 1-3613 単 3-Butenyl 7-Cl 1-3614 単 3-Butenyl 8-Cl 1-3615 単 3-Butenyl 2-Me 1-3616 単 3-Butenyl 4-Me 1-3617 単 3-Butenyl 5-Me 1-3618 単 3-Butenyl 6-Me 1-3619 単 3-Butenyl 7-Me 1-3620 単 3-Butenyl 8-Me 1-3621 単 3-Butenyl 2-Et 1-3622 単 3-Butenyl 4-Et 1-3623 単 3-Butenyl 5-Et 1-3624 単 3-Butenyl 6-Et 1-3625 単 3-Butenyl 7-Et 1-3626 単 3-Butenyl 8-Et 1-3627 単 3-Butenyl 2,4-F2 1-3628 単 3-Butenyl 2,5-F2 1-3629 単 3-Butenyl 2,6-F2 1-3630 単 3-Butenyl 2,7-F2 1-3631 単 3-Butenyl 2,8-F2 1-3632 単 3-Butenyl 4,5-F2 1-3633 単 3-Butenyl 4,6-F2 1-3634 単 3-Butenyl 4,7-F2 1-3635 単 3-Butenyl 4,8-F2 1-3636 単 3-Butenyl 5,6-F2 1-3637 単 3-Butenyl 5,7-F2 1-3638 単 3-Butenyl 5,8-F2 1-3639 単 3-Butenyl 6,7-F2 1-3640 単 3-Butenyl 6,8-F2 1-3641 単 3-Butenyl 7,8-F2 1-3642 単 3-Butenyl 2,4-Me2 1-3643 単 3-Butenyl 2,5-Me2 1-3644 単 3-Butenyl 2,6-Me2 1-3645 単 3-Butenyl 2,7-Me2 1-3646 単 3-Butenyl 2,8-Me2 1-3647 単 3-Butenyl 4,5-Me2 1-3648 単 3-Butenyl 4,6-Me2 1-3649 単 3-Butenyl 4,7-Me2 1-3650 単 3-Butenyl 4,8-Me2 1-3651 単 3-Butenyl 5,6-Me2 1-3652 単 3-Butenyl 5,7-Me2 1-3653 単 3-Butenyl 5,8-Me2 1-3654 単 3-Butenyl 6,7-Me2 1-3655 単 3-Butenyl 6,8-Me2 1-3656 単 3-Butenyl 7,8-Me2 1-3657 単 3-Butenyl 2-Me-5-F 1-3658 単 3-Butenyl 2-Me-6-F 1-3659 単 3-Butenyl 2-Me-7-F 1-3660 単 3-Butenyl 2-Me-8-F 1-3661 単 3-Butenyl 2-Me-5-Cl 1-3662 単 3-Butenyl 2-Me-6-Cl 1-3663 単 3-Butenyl 2-Me-7-Cl 1-3664 単 3-Butenyl 2-Me-8-Cl 1-3665 単 3-Butenyl 2-Me-5-MeO 1-3666 単 3-Butenyl 2-Me-6-MeO 1-3667 単 3-Butenyl 2-Me-7-MeO 1-3668 単 3-Butenyl 2-Me-8-MeO 1-3669 単 4-Pentenyl H 1-3670 単 4-Pentenyl 2-F 1-3671 単 4-Pentenyl 4-F 1-3672 単 4-Pentenyl 5-F 1-3673 単 4-Pentenyl 6-F 1-3674 単 4-Pentenyl 7-F 1-3675 単 4-Pentenyl 8-F 1-3676 単 4-Pentenyl 2-Cl 1-3677 単 4-Pentenyl 4-Cl 1-3678 単 4-Pentenyl 5-Cl 1-3679 単 4-Pentenyl 6-Cl 1-3680 単 4-Pentenyl 7-Cl 1-3681 単 4-Pentenyl 8-Cl 1-3682 単 4-Pentenyl 2-Me 1-3683 単 4-Pentenyl 4-Me 1-3684 単 4-Pentenyl 5-Me 1-3685 単 4-Pentenyl 6-Me 1-3686 単 4-Pentenyl 7-Me 1-3687 単 4-Pentenyl 8-Me 1-3688 単 4-Pentenyl 2-Et 1-3689 単 4-Pentenyl 4-Et 1-3690 単 4-Pentenyl 5-Et 1-3691 単 4-Pentenyl 6-Et 1-3692 単 4-Pentenyl 7-Et 1-3693 単 4-Pentenyl 8-Et 1-3694 単 4-Pentenyl 2,4-F2 1-3695 単 4-Pentenyl 2,5-F2 1-3696 単 4-Pentenyl 2,6-F2 1-3697 単 4-Pentenyl 2,7-F2 1-3698 単 4-Pentenyl 2,8-F2 1-3699 単 4-Pentenyl 4,5-F2 1-3700 単 4-Pentenyl 4,6-F2 1-3701 単 4-Pentenyl 4,7-F2 1-3702 単 4-Pentenyl 4,8-F2 1-3703 単 4-Pentenyl 5,6-F2 1-3704 単 4-Pentenyl 5,7-F2 1-3705 単 4-Pentenyl 5,8-F2 1-3706 単 4-Pentenyl 6,7-F2 1-3707 単 4-Pentenyl 6,8-F2 1-3708 単 4-Pentenyl 7,8-F2 1-3709 単 4-Pentenyl 2,4-Me2 1-3710 単 4-Pentenyl 2,5-Me2 1-3711 単 4-Pentenyl 2,6-Me2 1-3712 単 4-Pentenyl 2,7-Me2 1-3713 単 4-Pentenyl 2,8-Me2 1-3714 単 4-Pentenyl 4,5-Me2 1-3715 単 4-Pentenyl 4,6-Me2 1-3716 単 4-Pentenyl 4,7-Me2 1-3717 単 4-Pentenyl 4,8-Me2 1-3718 単 4-Pentenyl 5,6-Me2 1-3719 単 4-Pentenyl 5,7-Me2 1-3720 単 4-Pentenyl 5,8-Me2 1-3721 単 4-Pentenyl 6,7-Me2 1-3722 単 4-Pentenyl 6,8-Me2 1-3723 単 4-Pentenyl 7,8-Me2 1-3724 単 4-Pentenyl 2-Me-5-F 1-3725 単 4-Pentenyl 2-Me-6-F 1-3726 単 4-Pentenyl 2-Me-7-F 1-3727 単 4-Pentenyl 2-Me-8-F 1-3728 単 4-Pentenyl 2-Me-5-Cl 1-3729 単 4-Pentenyl 2-Me-6-Cl 1-3730 単 4-Pentenyl 2-Me-7-Cl 1-3731 単 4-Pentenyl 2-Me-8-Cl 1-3732 単 4-Pentenyl 2-Me-5-MeO 1-3733 単 4-Pentenyl 2-Me-6-MeO 1-3734 単 4-Pentenyl 2-Me-7-MeO 1-3735 単 4-Pentenyl 2-Me-8-MeO 1-3736 単 Propargyl H 1-3737 単 Propargyl 2-F 1-3738 単 Propargyl 4-F 1-3739 単 Propargyl 5-F 1-3740 単 Propargyl 6-F 1-3741 単 Propargyl 7-F 1-3742 単 Propargyl 8-F 1-3743 単 Propargyl 2-Cl 1-3744 単 Propargyl 4-Cl 1-3745 単 Propargyl 5-Cl 1-3746 単 Propargyl 6-Cl 1-3747 単 Propargyl 7-Cl 1-3748 単 Propargyl 8-Cl 1-3749 単 Propargyl 2-Me 1-3750 単 Propargyl 4-Me 1-3751 単 Propargyl 5-Me 1-3752 単 Propargyl 6-Me 1-3753 単 Propargyl 7-Me 1-3754 単 Propargyl 8-Me 1-3755 単 Propargyl 2-Et 1-3756 単 Propargyl 4-Et 1-3757 単 Propargyl 5-Et 1-3758 単 Propargyl 6-Et 1-3759 単 Propargyl 7-Et 1-3760 単 Propargyl 8-Et 1-3761 単 Propargyl 2,4-F2 1-3762 単 Propargyl 2,5-F2 1-3763 単 Propargyl 2,6-F2 1-3764 単 Propargyl 2,7-F2 1-3765 単 Propargyl 2,8-F2 1-3766 単 Propargyl 4,5-F2 1-3767 単 Propargyl 4,6-F2 1-3768 単 Propargyl 4,7-F2 1-3769 単 Propargyl 4,8-F2 1-3770 単 Propargyl 5,6-F2 1-3771 単 Propargyl 5,7-F2 1-3772 単 Propargyl 5,8-F2 1-3773 単 Propargyl 6,7-F2 1-3774 単 Propargyl 6,8-F2 1-3775 単 Propargyl 7,8-F2 1-3776 単 Propargyl 2,4-Me2 1-3777 単 Propargyl 2,5-Me2 1-3778 単 Propargyl 2,6-Me2 1-3779 単 Propargyl 2,7-Me2 1-3780 単 Propargyl 2,8-Me2 1-3781 単 Propargyl 4,5-Me2 1-3782 単 Propargyl 4,6-Me2 1-3783 単 Propargyl 4,7-Me2 1-3784 単 Propargyl 4,8-Me2 1-3785 単 Propargyl 5,6-Me2 1-3786 単 Propargyl 5,7-Me2 1-3787 単 Propargyl 5,8-Me2 1-3788 単 Propargyl 6,7-Me2 1-3789 単 Propargyl 6,8-Me2 1-3790 単 Propargyl 7,8-Me2 1-3791 単 Propargyl 2-Me-5-F 1-3792 単 Propargyl 2-Me-6-F 1-3793 単 Propargyl 2-Me-7-F 1-3794 単 Propargyl 2-Me-8-F 1-3795 単 Propargyl 2-Me-5-Cl 1-3796 単 Propargyl 2-Me-6-Cl 1-3797 単 Propargyl 2-Me-7-Cl 1-3798 単 Propargyl 2-Me-8-Cl 1-3799 単 Propargyl 2-Me-5-MeO 1-3800 単 Propargyl 2-Me-6-MeO 1-3801 単 Propargyl 2-Me-7-MeO 1-3802 単 Propargyl 2-Me-8-MeO 1-3803 単 2-Pentynyl H 1-3804 単 2-Pentynyl 2-F 1-3805 単 2-Pentynyl 4-F 1-3806 単 2-Pentynyl 5-F 1-3807 単 2-Pentynyl 6-F 1-3808 単 2-Pentynyl 7-F 1-3809 単 2-Pentynyl 8-F 1-3810 単 2-Pentynyl 2-Cl 1-3811 単 2-Pentynyl 4-Cl 1-3812 単 2-Pentynyl 5-Cl 1-3813 単 2-Pentynyl 6-Cl 1-3814 単 2-Pentynyl 7-Cl 1-3815 単 2-Pentynyl 8-Cl 1-3816 単 2-Pentynyl 2-Me 1-3817 単 2-Pentynyl 4-Me 1-3818 単 2-Pentynyl 5-Me 1-3819 単 2-Pentynyl 6-Me 1-3820 単 2-Pentynyl 7-Me 1-3821 単 2-Pentynyl 8-Me 1-3822 単 2-Pentynyl 2-Et 1-3823 単 2-Pentynyl 4-Et 1-3824 単 2-Pentynyl 5-Et 1-3825 単 2-Pentynyl 6-Et 1-3826 単 2-Pentynyl 7-Et 1-3827 単 2-Pentynyl 8-Et 1-3828 単 2-Pentynyl 2,4-F2 1-3829 単 2-Pentynyl 2,5-F2 1-3830 単 2-Pentynyl 2,6-F2 1-3831 単 2-Pentynyl 2,7-F2 1-3832 単 2-Pentynyl 2,8-F2 1-3833 単 2-Pentynyl 4,5-F2 1-3834 単 2-Pentynyl 4,6-F2 1-3835 単 2-Pentynyl 4,7-F2 1-3836 単 2-Pentynyl 4,8-F2 1-3837 単 2-Pentynyl 5,6-F2 1-3838 単 2-Pentynyl 5,7-F2 1-3839 単 2-Pentynyl 5,8-F2 1-3840 単 2-Pentynyl 6,7-F2 1-3841 単 2-Pentynyl 6,8-F2 1-3842 単 2-Pentynyl 7,8-F2 1-3843 単 2-Pentynyl 2,4-Me2 1-3844 単 2-Pentynyl 2,5-Me2 1-3845 単 2-Pentynyl 2,6-Me2 1-3846 単 2-Pentynyl 2,7-Me2 1-3847 単 2-Pentynyl 2,8-Me2 1-3848 単 2-Pentynyl 4,5-Me2 1-3849 単 2-Pentynyl 4,6-Me2 1-3850 単 2-Pentynyl 4,7-Me2 1-3851 単 2-Pentynyl 4,8-Me2 1-3852 単 2-Pentynyl 5,6-Me2 1-3853 単 2-Pentynyl 5,7-Me2 1-3854 単 2-Pentynyl 5,8-Me2 1-3855 単 2-Pentynyl 6,7-Me2 1-3856 単 2-Pentynyl 6,8-Me2 1-3857 単 2-Pentynyl 7,8-Me2 1-3858 単 2-Pentynyl 2-Me-5-F 1-3859 単 2-Pentynyl 2-Me-6-F 1-3860 単 2-Pentynyl 2-Me-7-F 1-3861 単 2-Pentynyl 2-Me-8-F 1-3862 単 2-Pentynyl 2-Me-5-Cl 1-3863 単 2-Pentynyl 2-Me-6-Cl 1-3864 単 2-Pentynyl 2-Me-7-Cl 1-3865 単 2-Pentynyl 2-Me-8-Cl 1-3866 単 2-Pentynyl 2-Me-5-MeO 1-3867 単 2-Pentynyl 2-Me-6-MeO 1-3868 単 2-Pentynyl 2-Me-7-MeO 1-3869 単 2-Pentynyl 2-Me-8-MeO 1-3870 単 MeOCH2 H 1-3871 単 MeOCH2 2-F 1-3872 単 MeOCH2 4-F 1-3873 単 MeOCH2 5-F 1-3874 単 MeOCH2 6-F 1-3875 単 MeOCH2 7-F 1-3876 単 MeOCH2 8-F 1-3877 単 MeOCH2 2-Cl 1-3878 単 MeOCH2 4-Cl 1-3879 単 MeOCH2 5-Cl 1-3880 単 MeOCH2 6-Cl 1-3881 単 MeOCH2 7-Cl 1-3882 単 MeOCH2 8-Cl 1-3883 単 MeOCH2 2-Me 1-3884 単 MeOCH2 4-Me 1-3885 単 MeOCH2 5-Me 1-3886 単 MeOCH2 6-Me 1-3887 単 MeOCH2 7-Me 1-3888 単 MeOCH2 8-Me 1-3889 単 MeOCH2 2-Et 1-3890 単 MeOCH2 4-Et 1-3891 単 MeOCH2 5-Et 1-3892 単 MeOCH2 6-Et 1-3893 単 MeOCH2 7-Et 1-3894 単 MeOCH2 8-Et 1-3895 単 MeOCH2 2,4-F2 1-3896 単 MeOCH2 2,5-F2 1-3897 単 MeOCH2 2,6-F2 1-3898 単 MeOCH2 2,7-F2 1-3899 単 MeOCH2 2,8-F2 1-3900 単 MeOCH2 4,5-F2 1-3901 単 MeOCH2 4,6-F2 1-3902 単 MeOCH2 4,7-F2 1-3903 単 MeOCH2 4,8-F2 1-3904 単 MeOCH2 5,6-F2 1-3905 単 MeOCH2 5,7-F2 1-3906 単 MeOCH2 5,8-F2 1-3907 単 MeOCH2 6,7-F2 1-3908 単 MeOCH2 6,8-F2 1-3909 単 MeOCH2 7,8-F2 1-3910 単 MeOCH2 2,4-Me2 1-3911 単 MeOCH2 2,5-Me2 1-3912 単 MeOCH2 2,6-Me2 1-3913 単 MeOCH2 2,7-Me2 1-3914 単 MeOCH2 2,8-Me2 1-3915 単 MeOCH2 4,5-Me2 1-3916 単 MeOCH2 4,6-Me2 1-3917 単 MeOCH2 4,7-Me2 1-3918 単 MeOCH2 4,8-Me2 1-3919 単 MeOCH2 5,6-Me2 1-3920 単 MeOCH2 5,7-Me2 1-3921 単 MeOCH2 5,8-Me2 1-3922 単 MeOCH2 6,7-Me2 1-3923 単 MeOCH2 6,8-Me2 1-3924 単 MeOCH2 7,8-Me2 1-3925 単 MeOCH2 2-Me-5-F 1-3926 単 MeOCH2 2-Me-6-F 1-3927 単 MeOCH2 2-Me-7-F 1-3928 単 MeOCH2 2-Me-8-F 1-3929 単 MeOCH2 2-Me-5-Cl 1-3930 単 MeOCH2 2-Me-6-Cl 1-3931 単 MeOCH2 2-Me-7-Cl 1-3932 単 MeOCH2 2-Me-8-Cl 1-3933 単 MeOCH2 2-Me-5-MeO 1-3934 単 MeOCH2 2-Me-6-MeO 1-3935 単 MeOCH2 2-Me-7-MeO 1-3936 単 MeOCH2 2-Me-8-MeO 1-3937 単 MeOCH2CH2 H 1-3938 単 MeOCH2CH2 2-F 1-3939 単 MeOCH2CH2 4-F 1-3940 単 MeOCH2CH2 5-F 1-3941 単 MeOCH2CH2 6-F 1-3942 単 MeOCH2CH2 7-F 1-3943 単 MeOCH2CH2 8-F 1-3944 単 MeOCH2CH2 2-Cl 1-3945 単 MeOCH2CH2 4-Cl 1-3946 単 MeOCH2CH2 5-Cl 1-3947 単 MeOCH2CH2 6-Cl 1-3948 単 MeOCH2CH2 7-Cl 1-3949 単 MeOCH2CH2 8-Cl 1-3950 単 MeOCH2CH2 2-Me 1-3951 単 MeOCH2CH2 4-Me 1-3952 単 MeOCH2CH2 5-Me 1-3953 単 MeOCH2CH2 6-Me 1-3954 単 MeOCH2CH2 7-Me 1-3955 単 MeOCH2CH2 8-Me 1-3956 単 MeOCH2CH2 2-Et 1-3957 単 MeOCH2CH2 4-Et 1-3958 単 MeOCH2CH2 5-Et 1-3959 単 MeOCH2CH2 6-Et 1-3960 単 MeOCH2CH2 7-Et 1-3961 単 MeOCH2CH2 8-Et 1-3962 単 MeOCH2CH2 2,4-F2 1-3963 単 MeOCH2CH2 2,5-F2 1-3964 単 MeOCH2CH2 2,6-F2 1-3965 単 MeOCH2CH2 2,7-F2 1-3966 単 MeOCH2CH2 2,8-F2 1-3967 単 MeOCH2CH2 4,5-F2 1-3968 単 MeOCH2CH2 4,6-F2 1-3969 単 MeOCH2CH2 4,7-F2 1-3970 単 MeOCH2CH2 4,8-F2 1-3971 単 MeOCH2CH2 5,6-F2 1-3972 単 MeOCH2CH2 5,7-F2 1-3973 単 MeOCH2CH2 5,8-F2 1-3974 単 MeOCH2CH2 6,7-F2 1-3975 単 MeOCH2CH2 6,8-F2 1-3976 単 MeOCH2CH2 7,8-F2 1-3977 単 MeOCH2CH2 2,4-Me2 1-3978 単 MeOCH2CH2 2,5-Me2 1-3979 単 MeOCH2CH2 2,6-Me2 1-3980 単 MeOCH2CH2 2,7-Me2 1-3981 単 MeOCH2CH2 2,8-Me2 1-3982 単 MeOCH2CH2 4,5-Me2 1-3983 単 MeOCH2CH2 4,6-Me2 1-3984 単 MeOCH2CH2 4,7-Me2 1-3985 単 MeOCH2CH2 4,8-Me2 1-3986 単 MeOCH2CH2 5,6-Me2 1-3987 単 MeOCH2CH2 5,7-Me2 1-3988 単 MeOCH2CH2 5,8-Me2 1-3989 単 MeOCH2CH2 6,7-Me2 1-3990 単 MeOCH2CH2 6,8-Me2 1-3991 単 MeOCH2CH2 7,8-Me2 1-3992 単 MeOCH2CH2 2-Me-5-F 1-3993 単 MeOCH2CH2 2-Me-6-F 1-3994 単 MeOCH2CH2 2-Me-7-F 1-3995 単 MeOCH2CH2 2-Me-8-F 1-3996 単 MeOCH2CH2 2-Me-5-Cl 1-3997 単 MeOCH2CH2 2-Me-6-Cl 1-3998 単 MeOCH2CH2 2-Me-7-Cl 1-3999 単 MeOCH2CH2 2-Me-8-Cl 1-4000 単 MeOCH2CH2 2-Me-5-MeO 1-4001 単 MeOCH2CH2 2-Me-6-MeO 1-4002 単 MeOCH2CH2 2-Me-7-MeO 1-4003 単 MeOCH2CH2 2-Me-8-MeO 1-4004 二 Et H 1-4005 二 Et 2-F 1-4006 二 Et 4-F 1-4007 二 Et 5-F 1-4008 二 Et 6-F 1-4009 二 Et 7-F 1-4010 二 Et 8-F 1-4011 二 Et 2-Cl 1-4012 二 Et 4-Cl 1-4013 二 Et 5-Cl 1-4014 二 Et 6-Cl 1-4015 二 Et 7-Cl 1-4016 二 Et 8-Cl 1-4017 二 Et 2-Me 1-4018 二 Et 4-Me 1-4019 二 Et 5-Me 1-4020 二 Et 6-Me 1-4021 二 Et 7-Me 1-4022 二 Et 8-Me 1-4023 二 Et 2-Et 1-4024 二 Et 4-Et 1-4025 二 Et 5-Et 1-4026 二 Et 6-Et 1-4027 二 Et 7-Et 1-4028 二 Et 8-Et 1-4029 二 Et 2,4-F2 1-4030 二 Et 2,5-F2 1-4031 二 Et 2,6-F2 1-4032 二 Et 2,7-F2 1-4033 二 Et 2,8-F2 1-4034 二 Et 4,5-F2 1-4035 二 Et 4,6-F2 1-4036 二 Et 4,7-F2 1-4037 二 Et 4,8-F2 1-4038 二 Et 5,6-F2 1-4039 二 Et 5,7-F2 1-4040 二 Et 5,8-F2 1-4041 二 Et 6,7-F2 1-4042 二 Et 6,8-F2 1-4043 二 Et 7,8-F2 1-4044 二 Et 2,4-Me2 1-4045 二 Et 2,5-Me2 1-4046 二 Et 2,6-Me2 1-4047 二 Et 2,7-Me2 1-4048 二 Et 2,8-Me2 1-4049 二 Et 4,5-Me2 1-4050 二 Et 4,6-Me2 1-4051 二 Et 4,7-Me2 1-4052 二 Et 4,8-Me2 1-4053 二 Et 5,6-Me2 1-4054 二 Et 5,7-Me2 1-4055 二 Et 5,8-Me2 1-4056 二 Et 6,7-Me2 1-4057 二 Et 6,8-Me2 1-4058 二 Et 7,8-Me2 1-4059 二 Et 2-Me-5-F 1-4060 二 Et 2-Me-6-F 1-4061 二 Et 2-Me-7-F 1-4062 二 Et 2-Me-8-F 1-4063 二 Et 2-Me-5-Cl 1-4064 二 Et 2-Me-6-Cl 1-4065 二 Et 2-Me-7-Cl 1-4066 二 Et 2-Me-8-Cl 1-4067 二 Et 2-Me-5-MeO 1-4068 二 Et 2-Me-6-MeO 1-4069 二 Et 2-Me-7-MeO 1-4070 二 Et 2-Me-8-MeO 1-4071 二 Pr H 1-4072 二 Pr 2-F 1-4073 二 Pr 4-F 1-4074 二 Pr 5-F 1-4075 二 Pr 6-F 1-4076 二 Pr 7-F 1-4077 二 Pr 8-F 1-4078 二 Pr 2-Cl 1-4079 二 Pr 4-Cl 1-4080 二 Pr 5-Cl 1-4081 二 Pr 6-Cl 1-4082 二 Pr 7-Cl 1-4083 二 Pr 8-Cl 1-4084 二 Pr 2-Me 1-4085 二 Pr 4-Me 1-4086 二 Pr 5-Me 1-4087 二 Pr 6-Me 1-4088 二 Pr 7-Me 1-4089 二 Pr 8-Me 1-4090 二 Pr 2-Et 1-4091 二 Pr 4-Et 1-4092 二 Pr 5-Et 1-4093 二 Pr 6-Et 1-4094 二 Pr 7-Et 1-4095 二 Pr 8-Et 1-4096 二 Pr 2,4-F2 1-4097 二 Pr 2,5-F2 1-4098 二 Pr 2,6-F2 1-4099 二 Pr 2,7-F2 1-4100 二 Pr 2,8-F2 1-4101 二 Pr 4,5-F2 1-4102 二 Pr 4,6-F2 1-4103 二 Pr 4,7-F2 1-4104 二 Pr 4,8-F2 1-4105 二 Pr 5,6-F2 1-4106 二 Pr 5,7-F2 1-4107 二 Pr 5,8-F2 1-4108 二 Pr 6,7-F2 1-4109 二 Pr 6,8-F2 1-4110 二 Pr 7,8-F2 1-4111 二 Pr 2,4-Me2 1-4112 二 Pr 2,5-Me2 1-4113 二 Pr 2,6-Me2 1-4114 二 Pr 2,7-Me2 1-4115 二 Pr 2,8-Me2 1-4116 二 Pr 4,5-Me2 1-4117 二 Pr 4,6-Me2 1-4118 二 Pr 4,7-Me2 1-4119 二 Pr 4,8-Me2 1-4120 二 Pr 5,6-Me2 1-4121 二 Pr 5,7-Me2 1-4122 二 Pr 5,8-Me2 1-4123 二 Pr 6,7-Me2 1-4124 二 Pr 6,8-Me2 1-4125 二 Pr 7,8-Me2 1-4126 二 Pr 2-Me-5-F 1-4127 二 Pr 2-Me-6-F 1-4128 二 Pr 2-Me-7-F 1-4129 二 Pr 2-Me-8-F 1-4130 二 Pr 2-Me-5-Cl 1-4131 二 Pr 2-Me-6-Cl 1-4132 二 Pr 2-Me-7-Cl 1-4133 二 Pr 2-Me-8-Cl 1-4134 二 Pr 2-Me-5-MeO 1-4135 二 Pr 2-Me-6-MeO 1-4136 二 Pr 2-Me-7-MeO 1-4137 二 Pr 2-Me-8-MeO 1-4138 二 Allyl H 1-4139 二 Allyl 2-F 1-4140 二 Allyl 4-F 1-4141 二 Allyl 5-F 1-4142 二 Allyl 6-F 1-4143 二 Allyl 7-F 1-4144 二 Allyl 8-F 1-4145 二 Allyl 2-Cl 1-4146 二 Allyl 4-Cl 1-4147 二 Allyl 5-Cl 1-4148 二 Allyl 6-Cl 1-4149 二 Allyl 7-Cl 1-4150 二 Allyl 8-Cl 1-4151 二 Allyl 2-Me 1-4152 二 Allyl 4-Me 1-4153 二 Allyl 5-Me 1-4154 二 Allyl 6-Me 1-4155 二 Allyl 7-Me 1-4156 二 Allyl 8-Me 1-4157 二 Allyl 2-Et 1-4158 二 Allyl 4-Et 1-4159 二 Allyl 5-Et 1-4160 二 Allyl 6-Et 1-4161 二 Allyl 7-Et 1-4162 二 Allyl 8-Et 1-4163 二 Allyl 2,4-F2 1-4164 二 Allyl 2,5-F2 1-4165 二 Allyl 2,6-F2 1-4166 二 Allyl 2,7-F2 1-4167 二 Allyl 2,8-F2 1-4168 二 Allyl 4,5-F2 1-4169 二 Allyl 4,6-F2 1-4170 二 Allyl 4,7-F2 1-4171 二 Allyl 4,8-F2 1-4172 二 Allyl 5,6-F2 1-4173 二 Allyl 5,7-F2 1-4174 二 Allyl 5,8-F2 1-4175 二 Allyl 6,7-F2 1-4176 二 Allyl 6,8-F2 1-4177 二 Allyl 7,8-F2 1-4178 二 Allyl 2,4-Me2 1-4179 二 Allyl 2,5-Me2 1-4180 二 Allyl 2,6-Me2 1-4181 二 Allyl 2,7-Me2 1-4182 二 Allyl 2,8-Me2 1-4183 二 Allyl 4,5-Me2 1-4184 二 Allyl 4,6-Me2 1-4185 二 Allyl 4,7-Me2 1-4186 二 Allyl 4,8-Me2 1-4187 二 Allyl 5,6-Me2 1-4188 二 Allyl 5,7-Me2 1-4189 二 Allyl 5,8-Me2 1-4190 二 Allyl 6,7-Me2 1-4191 二 Allyl 6,8-Me2 1-4192 二 Allyl 7,8-Me2 1-4193 二 Allyl 2-Me-5-F 1-4194 二 Allyl 2-Me-6-F 1-4195 二 Allyl 2-Me-7-F 1-4196 二 Allyl 2-Me-8-F 1-4197 二 Allyl 2-Me-5-Cl 1-4198 二 Allyl 2-Me-6-Cl 1-4199 二 Allyl 2-Me-7-Cl 1-4200 二 Allyl 2-Me-8-Cl 1-4201 二 Allyl 2-Me-5-MeO 1-4202 二 Allyl 2-Me-6-MeO 1-4203 二 Allyl 2-Me-7-MeO 1-4204 二 Allyl 2-Me-8-MeO 1-4205 単 Me 2,4-Me2 1-4206 単 Et 2,4-Me2 1-4207 単 CF3 2,4-Me2 1-4208 単 Allyl 2,4-Me2 1-4209 単 MeOCH2 2,4-Me2 ──────────────────────────────────────────────────────────────────── Compound ...... R Xm compound ...... RXm number Number ────────────────────────────────── 1-1 Single Me H 1-2 Single Me 2 -F 1-3 Single Me 4-F 1-4 Single Me 5-F 1-5 Single Me 6-F 1-6 Single Me 7-F 1-7 Single Me 8-F 1-8 Single Me 2-Cl 1-9 Single Me 4-Cl 1-10 Single Me 5-Cl 1-11 Single Me 6-Cl 1-12 Single Me 7-Cl 1-13 Single Me 8-Cl 1-14 Single Me 2-Br 1- 15 Single Me 4-Br 1-16 Single Me 5-Br 1-17 Single Me 6-Br 1-18 Single Me 7-Br 1-19 Single Me 8-Br 1-20 Single Me 2-I 1-21 Single Me 4-I 1-22 single Me 5-I 1-23 single Me 6-I 1-24 single Me 7-I 1-25 single Me 8-I 1-26 single Me 2-Me 1-27 single Me 4 -Me 1-28 single Me 5-Me 1-29 single Me 6-Me 1-30 single Me 7-Me 1-31 single Me 8-Me 1-32 single Me 2-Et 1-33 single Me 4-Et 1-34 Single Me 5-Et 1-35 Single Me 6-Et 1-36 Single Me 7-Et 1-37 Single Me 8-Et 1-38 Single Me 2-Pr 1-39 Single Me 4-Pr 1- 40 Single Me 5-Pr 1-41 Single Me 6-Pr 1-42 Single Me 7-Pr 1-43 Single Me 8-Pr 1-44 Single Me 2-iPr 1-45 Single Me 4-iPr 1-46 Single Me 5-iPr 1-47 single Me 6-iPr 1-48 single Me 7-iPr 1-49 single Me 8-iPr 1-50 single Me 2-Bu 1-51 single Me 4-Bu 1-52 single Me 5 -Bu 1-53 single Me 6-Bu 1-54 Single Me 7-Bu 1-55 Single Me 8-Bu 1-56 Single Me 2-CF 3 1-57 Single Me 4-CF 3 1-58 Single Me 5-CF 3 1-59 Single Me 6-CF 3 1-60 Single Me 7-CF 3 1-61 Single Me 8-CF 3 1-62 Single Me 2-CF 3 CH 2 1-63 Single Me 4-CF 3 CH 2 1-64 Single Me 5-CF 3 CH 2 1-65 Single Me 6-CF 3 CH 2 1-66 Single Me 7-CF 3 CH 2 1-67 Single Me 8-CF 3 CH 2 1-68 Single Me 2-CF 2 H 1-69 Single Me 4-CF 2 H 1-70 Single Me 5-CF 2 H 1-71 Single Me 6-CF 2 H 1-72 Single Me 7-CF 2 H 1-73 Single Me 8-CF 2 H 1-74 Single Me 2-CF 2 H 1-75 Single Me 4-CF 2 H 1-76 Single Me 5-CF 2 H 1-77 Single Me 6-CF 2 H 1-78 Single Me 7-CF 2 H 1-79 Single Me 8-CF 2 H 1-80 Single Me 2-CClH 2 1-81 Single Me 4-CClH 2 1-82 Single Me 5-CClH 2 1-83 Single Me 6-CClH 2 1-84 Single Me 7-CClH 2 1-85 Single Me 8-CClH 2 1-86 Single Me 2-MeO 1-87 Single Me 4-MeO 1-88 Single Me 5-MeO 1-89 Single Me 6-MeO 1-90 Single Me 7-MeO 1-91 Single Me 8-MeO 1- 92 Single Me 2-EtO 1-93 Single Me 4-EtO 1-94 Single Me 5-EtO 1-95 Single Me 6-EtO 1-96 Single Me 7-EtO 1-97 Single Me 8-EtO 1-98 Single Me 2-PrO 1-99 Single Me 4-PrO 1-100 Single Me 5-PrO 1-101 Single Me 6-PrO 1-102 Single Me 7-PrO 1-103 Single Me 8-PrO 1-104 Single Me 2 -iPrO 1-105 Single Me 4-iPrO 1-106 Single Me 5-iPrO 1-107 Single Me 6-iPrO 1-108 Single Me 7-iPrO 1-109 Single Me 8-iPrO 1-110 Single Me 2-BuO 1-111 Single Me 4-BuO 1-112 Single Me 5-BuO 1-113 Single Me 6-BuO 1-114 Single Me 7-BuO 1-115 Single Me 8-BuO 1-116 Single Me 2-CF 3 O 1-117 Single Me 4-CF 3 O 1-118 Single Me 5-CF 3 O 1-119 Single Me 6-CF 3 O 1-120 Single Me 7-CF 3 O 1-121 Single Me 8-CF 3 O 1-122 Single Me 2-CF 3 CH 2 O 1-123 Single Me 4-CF 3 CH 2 O 1-124 Single Me 5-CF 3 CH 2 O 1-125 Single Me 6-CF 3 CH 2 O 1-126 Single Me 7-CF 3 CH 2 O 1-127 Single Me 8-CF 3 CH 2 O 1-128 Single Me 2-CF 2 HO 1-129 Single Me 4-CF 2 HO 1-130 Single Me 5-CF 2 HO 1-131 Single Me 6-CF 2 HO 1-132 Single Me 7-CF 2 HO 1-133 Single Me 8-CF 2 HO 1-134 Single Me 2-CF 2 HO 1-135 Single Me 4-CF 2 HO 1-136 Single Me 5-CF 2 HO 1-137 Single Me 6-CF 2 HO 1-138 Single Me 7-CF 2 HO 1-139 Single Me 8-CF 2 HO 1-140 Single Me 2-CClH 2 O 1-141 Single Me 4-CClH 2 O 1-142 Single Me 5-CClH 2 O 1-143 Single Me 6-CClH 2 O 1-144 Single Me 7-CClH 2 O 1-145 Single Me 8-CClH 2 O 1-146 Single Me 2,4-F 2 1-147 Single Me 2,5-F 2 1-148 Single Me 2,6-F 2 1-149 Single Me 2,7-F 2 1-150 Single Me 2,8-F 2 1-151 Single Me 4,5-F 2 1-152 Single Me 4,6-F 2 1-153 Single Me 4,7-F 2 1-154 Single Me 4,8-F 2 1-155 Single Me 5,6-F 2 1-156 Single Me 5,7-F 2 1-157 Single Me 5,8-F 2 1-158 Single Me 6,7-F 2 1-159 Single Me 6,8-F 2 1-160 Single Me 7,8-F 2 1-161 Single Me 4,5-Cl 2 1-162 Single Me 4,6-Cl 2 1-163 Single Me 4,7-Cl 2 1-164 Single Me 4,8-Cl 2 1-165 Single Me 5,6-Cl 2 1-166 Single Me 5,7-Cl 2 1-167 Single Me 5,8-Cl 2 1-168 Single Me 6,7-Cl 2 1-169 Single Me 6,8-Cl 2 1-170 Single Me 7,8-Cl 2 1-171 Single Me 2,5-Me 2 1-172 Single Me 2,6-Me 2 1-173 Single Me 2,7-Me 2 1-174 Single Me 2,8-Me 2 1-175 Single Me 4,5-Me 2 1-176 Single Me 4,6-Me 2 1-177 Single Me 4,7-Me 2 1-178 Single Me 4,8-Me 2 1-179 Single Me 5,6-Me 2 1-180 Single Me 5,7-Me 2 1-181 Single Me 5,8-Me 2 1-182 Single Me 6,7-Me 2 1-183 Single Me 6,8-Me 2 1-184 Single Me 7,8-Me 2 1-185 Single Me 2,5- (MeO) 2 1-186 Single Me 2,6- (MeO) 2 1-187 Single Me 2,7- (MeO) 2 1-188 Single Me 2,8- (MeO) 2 1-189 Single Me 4,5- (MeO) 2 1-190 Single Me 4,6- (MeO) 2 1-191 Single Me 4,7- (MeO) 2 1-192 Single Me 4,8- (MeO) 2 1-193 Single Me 5,6- (MeO) 2 1-194 Single Me 5,7- (MeO) 2 1-195 Single Me 5,8- (MeO) 2 1-196 Single Me 6,7- (MeO) 2 1-197 Single Me 6,8- (MeO) 2 1-198 Single Me 7,8- (MeO) 2 1-199 Single Me 2-Me-5-F 1-200 Single Me 2-Me-6-F 1-201 Single Me 2-Me-7-F 1-202 Single Me 2-Me-8-F 1- 203 Single Me 2-Me-5-Cl 1-204 Single Me 2-Me-6-Cl 1-205 Single Me 2-Me-7-Cl 1-206 Single Me 2-Me-8-Cl 1-207 Single Me 2-Me-5-MeO 1-208 single Me 2-Me-6-MeO 1-209 single Me 2-Me-7-MeO 1-210 single Me 2-Me-8-MeO 1-211 single Me 4 -Cl-5-F 1-212 Single Me 4-Cl-6-F 1-213 Single Me 4-Cl-7-F 1-214 Single Me 4-Cl-8-F 1-215 Single Me 4-Cl -5-Me 1-216 Single Me 4-Cl-6-Me 1-217 Single Me 4-Cl-7-Me 1-218 Single Me 4-Cl-8-Me 1-219 Single Me 4-Cl-5 -MeO 1-220 single Me 4-Cl-6-MeO 1-221 single Me 4-Cl-7-MeO 1-222 single Me 4-Cl-8-MeO 1-223 single Et H 1-224 single Et 2 -F 1-225 Single Et 4-F 1-226 Single Et 5-F 1-227 Single Et 6-F 1-228 Single Et 7-F 1-229 Single Et 8-F 1-230 Single Et 2-Cl 1-231 Single Et 4-Cl 1-22 Single Et 5-Cl 1-233 Single Et 6-Cl 1-234 Single Et 7-Cl 1-235 Single Et 8-Cl 1-236 Single Et 2-Br 1- 237 Single Et 4-Br 1-238 Single Et 5-Br 1-239 Single Et 6-Br 1-240 Single Et 7-Br 1-241 Single Et 8-Br 1-242 Single Et 2-I 1-243 Single Et 4-I 1-244 single Et 5-I 1-245 single Et 6-I 1-246 single Et 7-I 1-247 single Et 8-I 1-248 single Et 2-Me 1-249 single Et 4-Me 1-250 single Et 5-Me 1-251 single Et 6-Me 1-252 single Et 7-Me 1-253 single Et 8-Me 1-254 single Et 2- Et 1-255 Single Et 4-Et 1-256 Single Et 5-Et 1-257 Single Et 6-Et 1-258 Single Et 7-Et 1-259 Single Et 8-Et 1-260 Single Et 2-Pr 1 -261 Single Et 4-Pr 1-262 Single Et 5-Pr 1-263 Single Et 6-Pr 1-264 Single Et 7-Pr 1-265 Single Et 8-Pr 1-266 Single Et 2-iPr 1-267 Single Et 4-iPr 1-268 Single Et 5-iPr 1-269 Single Et 6-iPr 1-270 Single Et 7-iPr 1-271 Single Et 8-iPr 1-272 Single Et 2-Bu 1-273 Single Et 4-Bu 1-274 single Et 5-Bu 1-275 single Et 6-Bu 1-276 single Et 7-Bu 1-277 single Et 8-Bu 1-278 single Et 2-CF 3 1-279 Single Et 4-CF 3 1-280 Single Et 5-CF 3 1-281 Single Et 6-CF 3 1-282 Single Et 7-CF 3 1-283 Single Et 8-CF 3 1-284 Single Et 2-CF 3 CH 2 1-285 Single Et 4-CF 3 CH 2 1-286 Single Et 5-CF 3 CH 2 1-287 Single Et 6-CF 3 CH 2 1-288 Single Et 7-CF 3 CH 2 1-289 Single Et 8-CF 3 CH 2 1-290 Single Et 2-CF 2 H 1-291 Single Et 4-CF 2 H 1-292 Single Et 5-CF 2 H 1-293 Single Et 6-CF 2 H 1-294 Single Et 7-CF 2 H 1-295 Single Et 8-CF 2 H 1-296 Single Et 2-CF 2 H 1-297 Single Et 4-CF 2 H 1-298 Single Et 5-CF 2 H 1-299 Single Et 6-CF 2 H 1-300 Single Et 7-CF 2 H 1-301 Single Et 8-CF 2 H 1-302 Single Et 2-CClH 2 1-303 Single Et 4-CClH 2 1-304 Single Et 5-CClH 2 1-305 Single Et 6-CClH 2 1-306 Single Et 7-CClH 2 1-307 Single Et 8-CClH 2 1-308 Single Et 2-MeO 1-309 Single Et 4-MeO 1-310 Single Et 5-MeO 1-311 Single Et 6-MeO 1-312 Single Et 7-MeO 1-313 Single Et 8-MeO 1- 314 Single Et 2-EtO 1-315 Single Et 4-EtO 1-316 Single Et 5-EtO 1-317 Single Et 6-EtO 1-318 Single Et 7-EtO 1-319 Single Et 8-EtO 1-320 Single Et 2-PrO 1-321 single Et 4-PrO 1-322 single Et 5-PrO 1-323 single Et 6-PrO 1-324 single Et 7-PrO 1-325 single Et 8-PrO 1-326 single Et 2 -iPrO 1-327 single Et 4-iPrO 1-328 single Et 5-iPrO 1-329 single Et 6-iPrO 1-330 single Et 7-iPrO 1-331 single Et 8-iPrO 1-332 single Et 2-BuO 1-333 Single Et 4-BuO 1-334 Single Et 5-BuO 1-335 Single Et 6-BuO 1-336 Single Et 7-BuO 1-337 Single Et 8-BuO 1-338 Single Et 2-CF 3 O 1-339 Single Et 4-CF 3 O 1-340 Single Et 5-CF 3 O 1-341 Single Et 6-CF 3 O 1-342 Single Et 7-CF 3 O 1-343 Single Et 8-CF 3 O 1-344 Single Et 2-CF 3 CH 2 O 1-345 Single Et 4-CF 3 CH 2 O 1-346 Single Et 5-CF 3 CH 2 O 1-347 Single Et 6-CF 3 CH 2 O 1-348 Single Et 7-CF 3 CH 2 O 1-349 Single Et 8-CF 3 CH 2 O 1-350 Single Et 2-CF 2 HO 1-351 Single Et 4-CF 2 HO 1-352 Single Et 5-CF 2 HO 1-353 Single Et 6-CF 2 HO 1-354 Single Et 7-CF 2 HO 1-355 Single Et 8-CF 2 HO 1-356 Single Et 2-CF 2 HO 1-357 Single Et 4-CF 2 HO 1-358 Single Et 5-CF 2 HO 1-359 Single Et 6-CF 2 HO 1-360 Single Et 7-CF 2 HO 1-361 Single Et 8-CF 2 HO 1-362 Single Et 2-CClH 2 O 1-363 Single Et 4-CClH 2 O 1-364 Single Et 5-CClH 2 O 1-365 Single Et 6-CClH 2 O 1-366 Single Et 7-CClH 2 O 1-367 Single Et 8-CClH 2 O 1-368 Single Et 2,4-F 2 1-369 Single Et 2,5-F 2 1-370 Single Et 2,6-F 2 1-371 Single Et 2,7-F 2 1-372 Single Et 2,8-F 2 1-373 Single Et 4,5-F 2 1-374 Single Et 4,6-F 2 1-375 Single Et 4,7-F 2 1-376 Single Et 4,8-F 2 1-377 Single Et 5,6-F 2 1-378 Single Et 5,7-F 2 1-379 Single Et 5,8-F 2 1-380 Single Et 6,7-F 2 1-381 Single Et 6,8-F 2 1-382 Single Et 7,8-F 2 1-383 Single Et 4,5-Cl 2 1-384 Single Et 4,6-Cl 2 1-385 Single Et 4,7-Cl 2 1-386 Single Et 4,8-Cl 2 1-387 Single Et 5,6-Cl 2 1-388 Single Et 5,7-Cl 2 1-389 Single Et 5,8-Cl 2 1-390 Single Et 6,7-Cl 2 1-391 Single Et 6,8-Cl 2 1-392 Single Et 7,8-Cl 2 1-393 Single Et 2,5-Me 2 1-394 Single Et 2,6-Me 2 1-395 Single Et 2,7-Me 2 1-396 Single Et 2,8-Me 2 1-397 Single Et 4,5-Me 2 1-398 Single Et 4,6-Me 2 1-399 Single Et 4,7-Me 2 1-400 Single Et 4,8-Me 2 1-401 Single Et 5,6-Me 2 1-402 Single Et 5,7-Me 2 1-403 Single Et 5,8-Me 2 1-404 Single Et 6,7-Me 2 1-405 Single Et 6,8-Me 2 1-406 Single Et 7,8-Me 2 1-407 Single Et 2,5- (MeO) 2 1-408 Single Et 2,6- (MeO) 2 1-409 Single Et 2,7- (MeO) 2 1-410 Single Et 2,8- (MeO) 2 1-411 Single Et 4,5- (MeO) 2 1-412 Single Et 4,6- (MeO) 2 1-413 Single Et 4,7- (MeO) 2 1-414 Single Et 4,8- (MeO) 2 1-415 Single Et 5,6- (MeO) 2 1-416 Single Et 5,7- (MeO) 2 1-417 Single Et 5,8- (MeO) 2 1-418 Single Et 6,7- (MeO) 2 1-419 Single Et 6,8- (MeO) 2 1-420 Single Et 7,8- (MeO) 2 1-421 Single Et 2-Me-5-F 1-422 Single Et 2-Me-6-F 1-423 Single Et 2-Me-7-F 1-424 Single Et 2-Me-8-F 1- 425 Single Et 2-Me-5-Cl 1-426 Single Et 2-Me-6-Cl 1-427 Single Et 2-Me-7-Cl 1-428 Single Et 2-Me-8-Cl 1-429 Single Et 2-Me-5-MeO 1-430 single Et 2-Me-6-MeO 1-431 single Et 2-Me-7-MeO 1-432 single Et 2-Me-8-MeO 1-433 single Et 4 -Cl-5-F 1-434 Single Et 4-Cl-6-F 1-435 Single Et 4-Cl-7-F 1-436 Single Et 4-Cl-8-F 1-437 Single Et 4-Cl -5-Me 1-438 Single Et 4-Cl-6-Me 1-439 Single Et 4-Cl-7-Me 1-440 Single Et 4-Cl-8-Me 1-441 Single Et 4-Cl-5 -MeO 1-442 single Et 4-Cl-6-MeO 1-443 single Et 4-Cl-7-MeO 1-444 single Et 4-Cl-8-MeO 1-445 single Pr H 1-446 single Pr 2 -F 1-447 Single Pr 4-F 1-448 Single Pr 5-F 1-449 Single Pr 6-F 1-450 Single Pr 7-F 1-451 Single Pr 8-F 1-452 Single Pr 2-Cl 1-453 Single Pr 4-Cl 1-454 Single Pr 5-Cl 1-455 Single Pr 6-Cl 1-456 Single Pr 7-Cl 1-457 Single Pr 8-Cl 1-458 Single Pr 2-Br 1- 459 Single Pr 4-Br 1-460 Single Pr 5-Br 1-461 Single Pr 6-Br 1-462 Single Pr 7-Br 1-463 Single Pr 8-Br 1-464 Single Pr 2-I 1-465 Single Pr 4-I 1-466 single Pr 5-I 1-467 single Pr 6-I 1-468 single Pr 7-I 1-469 single Pr 8-I 1-470 single Pr 2-Me 1-471 Single Pr 4-Me 1-472 Single Pr 5-Me 1-473 Single Pr 6-Me 1-474 Single Pr 7-Me 1-475 Single Pr 8-Me 1-476 Single Pr 2- Et 1-477 Single Pr 4-Et 1-478 Single Pr 5-Et 1-479 Single Pr 6-Et 1-480 Single Pr 7-Et 1-481 Single Pr 8-Et 1-482 Single Pr 2-Pr 1 -483 Single Pr 4-Pr 1-484 Single Pr 5-Pr 1-485 Single Pr 6-Pr 1-486 Single Pr 7-Pr 1-487 Single Pr 8-Pr 1-488 Single Pr 2-iPr 1-489 Single Pr 4-iPr 1-490 Single Pr 5-iPr 1-491 Single Pr 6-iPr 1-492 Single Pr 7-iPr 1-493 Single Pr 8-iPr 1-494 Single Pr 2-Bu 1-495 Single Pr 4-Bu 1-496 Single Pr 5-Bu 1-497 Single Pr 6-Bu 1-498 Single Pr 7-Bu 1-499 Single Pr 8-Bu 1-500 Single Pr 2-CF 3 1-501 Single Pr 4-CF 3 1-502 Single Pr 5-CF 3 1-503 Single Pr 6-CF 3 1-504 Single Pr 7-CF 3 1-505 Single Pr 8-CF 3 1-506 Single Pr 2-CF 3 CH 2 1-507 Single Pr 4-CF 3 CH 2 1-508 Single Pr 5-CF 3 CH 2 1-509 Single Pr 6-CF 3 CH 2 1-510 Single Pr 7-CF 3 CH 2 1-511 Single Pr 8-CF 3 CH 2 1-512 Single Pr 2-CF 2 H 1-513 Single Pr 4-CF 2 H 1-514 Single Pr 5-CF 2 H 1-515 Single Pr 6-CF 2 H 1-516 Single Pr 7-CF 2 H 1-517 Single Pr 8-CF 2 H 1-518 Single Pr 2-CF 2 H 1-519 Single Pr 4-CF 2 H 1-520 Single Pr 5-CF 2 H 1-521 Single Pr 6-CF 2 H 1-522 Single Pr 7-CF 2 H 1-523 Single Pr 8-CF 2 H 1-524 Single Pr 2-CClH 2 1-525 Single Pr 4-CClH 2 1-526 Single Pr 5-CClH 2 1-527 Single Pr 6-CClH 2 1-528 Single Pr 7-CClH 2 1-529 Single Pr 8-CClH 2 1-530 Single Pr 2-MeO 1-531 Single Pr 4-MeO 1-532 Single Pr 5-MeO 1-533 Single Pr 6-MeO 1-534 Single Pr 7-MeO 1-535 Single Pr 8-MeO 1- 536 Single Pr 2-EtO 1-537 Single Pr 4-EtO 1-538 Single Pr 5-EtO 1-539 Single Pr 6-EtO 1-540 Single Pr 7-EtO 1-541 Single Pr 8-EtO 1-542 Single Pr 2-PrO 1-543 Single Pr 4-PrO 1-544 Single Pr 5-PrO 1-545 Single Pr 6-PrO 1-546 Single Pr 7-PrO 1-547 Single Pr 8-PrO 1-548 Single Pr 2 -iPrO 1-549 Single Pr 4-iPrO 1-550 Single Pr 5-iPrO 1-551 Single Pr 6-iPrO 1-552 Single Pr 7-iPrO 1-553 Single Pr 8-iPrO 1-554 Single Pr 2-BuO 1-555 Single Pr 4-BuO 1-556 Single Pr 5-BuO 1-557 Single Pr 6-BuO 1-558 Single Pr 7-BuO 1-559 Single Pr 8-BuO 1-560 Single Pr 2-CF 3 O 1-561 Single Pr 4-CF 3 O 1-562 Single Pr 5-CF 3 O 1-563 Single Pr 6-CF 3 O 1-564 Single Pr 7-CF 3 O 1-565 Single Pr 8-CF 3 O 1-566 Single Pr 2-CF 3 CH 2 O 1-567 Single Pr 4-CF 3 CH 2 O 1-568 Single Pr 5-CF 3 CH 2 O 1-569 Single Pr 6-CF 3 CH 2 O 1-570 Single Pr 7-CF 3 CH 2 O 1-571 Single Pr 8-CF 3 CH 2 O 1-572 Single Pr 2-CF 2 HO 1-573 Single Pr 4-CF 2 HO 1-574 Single Pr 5-CF 2 HO 1-575 Single Pr 6-CF 2 HO 1-576 Single Pr 7-CF 2 HO 1-577 Single Pr 8-CF 2 HO 1-578 Single Pr 2-CF 2 HO 1-579 Single Pr 4-CF 2 HO 1-580 Single Pr 5-CF 2 HO 1-581 Single Pr 6-CF 2 HO 1-582 Single Pr 7-CF 2 HO 1-583 Single Pr 8-CF 2 HO 1-584 Single Pr 2-CClH 2 O 1-585 Single Pr 4-CClH 2 O 1-586 Single Pr 5-CClH 2 O 1-587 Single Pr 6-CClH 2 O 1-588 Single Pr 7-CClH 2 O 1-589 Single Pr 8-CClH 2 O 1-590 Single Pr 2,4-F 2 1-591 Single Pr 2,5-F 2 1-592 Single Pr 2,6-F 2 1-593 Single Pr 2,7-F 2 1-594 Single Pr 2,8-F 2 1-595 Single Pr 4,5-F 2 1-596 Single Pr 4,6-F 2 1-597 Single Pr 4,7-F 2 1-598 Single Pr 4,8-F 2 1-599 Single Pr 5,6-F 2 1-600 Single Pr 5,7-F 2 1-601 Single Pr 5,8-F 2 1-602 Single Pr 6,7-F 2 1-603 Single Pr 6,8-F 2 1-604 Single Pr 7,8-F 2 1-605 Single Pr 4,5-Cl 2 1-606 Single Pr 4,6-Cl 2 1-607 Single Pr 4,7-Cl 2 1-608 Single Pr 4,8-Cl 2 1-609 Single Pr 5,6-Cl 2 1-610 Single Pr 5,7-Cl 2 1-611 Single Pr 5,8-Cl 2 1-612 Single Pr 6,7-Cl 2 1-613 Single Pr 6,8-Cl 2 1-614 Single Pr 7,8-Cl 2 1-615 Single Pr 2,5-Me 2 1-616 Single Pr 2,6-Me 2 1-617 Single Pr 2,7-Me 2 1-618 Single Pr 2,8-Me 2 1-619 Single Pr 4,5-Me 2 1-620 Single Pr 4,6-Me 2 1-621 Single Pr 4,7-Me 2 1-622 Single Pr 4,8-Me 2 1-623 Single Pr 5,6-Me 2 1-624 Single Pr 5,7-Me 2 1-625 Single Pr 5,8-Me 2 1-626 Single Pr 6,7-Me 2 1-627 Single Pr 6,8-Me 2 1-628 Single Pr 7,8-Me 2 1-629 Single Pr 2,5- (MeO) 2 1-630 Single Pr 2,6- (MeO) 2 1-631 Single Pr 2,7- (MeO) 2 1-632 Single Pr 2,8- (MeO) 2 1-633 Single Pr 4,5- (MeO) 2 1-634 Single Pr 4,6- (MeO) 2 1-635 Single Pr 4,7- (MeO) 2 1-636 Single Pr 4,8- (MeO) 2 1-637 Single Pr 5,6- (MeO) 2 1-638 Single Pr 5,7- (MeO) 2 1-639 Single Pr 5,8- (MeO) 2 1-640 Single Pr 6,7- (MeO) 2 1-641 Single Pr 6,8- (MeO) 2 1-642 Single Pr 7,8- (MeO) 2 1-643 Single Pr 2-Me-5-F 1-644 Single Pr 2-Me-6-F 1-645 Single Pr 2-Me-7-F 1-646 Single Pr 2-Me-8-F 1- 647 Single Pr 2-Me-5-Cl 1-648 Single Pr 2-Me-6-Cl 1-649 Single Pr 2-Me-7-Cl 1-650 Single Pr 2-Me-8-Cl 1-651 Single Pr 2-Me-5-MeO 1-652 Single Pr 2-Me-6-MeO 1-653 Single Pr 2-Me-7-MeO 1-654 Single Pr 2-Me-8-MeO 1-655 Single Pr 4 -Cl-5-F 1-656 Single Pr 4-Cl-6-F 1-657 Single Pr 4-Cl-7-F 1-658 Single Pr 4-Cl-8-F 1-659 Single Pr 4-Cl -5-Me 1-660 Single Pr 4-Cl-6-Me 1-661 Single Pr 4-Cl-7-Me 1-662 Single Pr 4-Cl-8-Me 1-663 Single Pr 4-Cl-5 -MeO 1-664 Single Pr 4-Cl-6-MeO 1-665 Single Pr 4-Cl-7-MeO 1-666 Single Pr 4-Cl-8-MeO 1-667 Single iPr H 1-668 Single iPr 2 -F 1-669 Single iPr 4-F 1-670 Single iPr 5-F 1-671 Single iPr 6-F 1-672 Single iPr 7-F 1-673 Single iPr 8-F 1-674 Single iPr 2-Cl 1-675 Single iPr 4-Cl 1-676 Single iPr 5-Cl 1-677 Single iPr 6-Cl 1-678 Single iPr 7-Cl 1-679 Single iPr 8-Cl 1-680 Single iPr 2-Br 1- 681 Single iPr 4-Br 1-682 Single iPr 5-Br 1-683 Single iPr 6-Br 1-684 Single iPr 7-Br 1-685 Single iPr 8-Br 1-686 Single iPr 2-I 1-687 Single iPr 4-I 1-688 Single iPr 5-I 1-689 Single iPr 6-I 1-690 Single iPr 7-I 1-691 Single iPr 8-I 1-692 Single iPr 2-Me 1-693 Single iPr 4-Me 1-694 Single iPr 5-Me 1-695 Single iPr 6-Me 1-696 Single iPr 7-Me 1-697 Single iPr 8-Me 1-698 Single iPr 2-Et 1-699 Single iPr 4-Et 1-700 Single iPr 5-Et 1-701 Single iPr 6-Et 1-702 Single iPr 7-Et 1-703 Single iPr 8- Et 1-704 Single iPr 2-Pr 1-705 Single iPr 4-Pr 1-706 Single iPr 5-Pr 1-707 Single iPr 6-Pr 1-708 Single iPr 7-Pr 1-709 Single iPr 8-Pr 1 -710 Single iPr 2-iPr 1-711 Single iPr 4-iPr 1-712 Single iPr 5-iPr 1-713 Single iPr 6-iPr 1-714 Single iPr 7-iPr 1-715 Single iPr 8-iPr 1-716 Single iPr 2-Bu 1-717 Single iPr 4-Bu 1-718 Single iPr 5-Bu 1-719 Single iPr 6-Bu 1-720 Single iPr 7-Bu 1-721 Single iPr 8-Bu 1-722 Single iPr 2-CF 3 1-723 Single iPr 4-CF 3 1-724 Single iPr 5-CF 3 1-725 Single iPr 6-CF 3 1-726 Single iPr 7-CF 3 1-727 Single iPr 8-CF 3 1-728 Single iPr 2-CF 3 CH 2 1-729 Single iPr 4-CF 3 CH 2 1-730 Single iPr 5-CF 3 CH 2 1-731 Single iPr 6-CF 3 CH 2 1-732 Single iPr 7-CF 3 CH 2 1-733 Single iPr 8-CF 3 CH 2 1-734 Single iPr 2-CF 2 H 1-735 Single iPr 4-CF 2 H 1-736 Single iPr 5-CF 2 H 1-737 Single iPr 6-CF 2 H 1-738 Single iPr 7-CF 2 H 1-739 Single iPr 8-CF 2 H 1-740 Single iPr 2-CF 2 H 1-741 Single iPr 4-CF 2 H 1-742 Single iPr 5-CF 2 H 1-743 Single iPr 6-CF 2 H 1-744 Single iPr 7-CF 2 H 1-745 Single iPr 8-CF 2 H 1-746 Single iPr 2-CClH 2 1-747 Single iPr 4-CClH 2 1-748 Single iPr 5-CClH 2 1-749 Single iPr 6-CClH 2 1-750 Single iPr 7-CClH 2 1-751 Single iPr 8-CClH 2 1-752 Single iPr 2-MeO 1-753 Single iPr 4-MeO 1-754 Single iPr 5-MeO 1-755 Single iPr 6-MeO 1-756 Single iPr 7-MeO 1-757 Single iPr 8-MeO 1- 758 Single iPr 2-EtO 1-759 Single iPr 4-EtO 1-760 Single iPr 5-EtO 1-761 Single iPr 6-EtO 1-762 Single iPr 7-EtO 1-763 Single iPr 8-EtO 1-764 Single iPr 2-PrO 1-765 Single iPr 4-PrO 1-766 Single iPr 5-PrO 1-767 Single iPr 6-PrO 1-768 Single iPr 7-PrO 1-769 Single iPr 8-PrO 1-770 Single iPr 2 -iPrO 1-771 single iPr 4-iPrO 1-772 single iPr 5-iPrO 1-773 single iPr 6-iPrO 1-774 single iPr 7-iPrO 1-775 single iPr 8-iPrO 1-776 single iPr 2-BuO 1-777 Single iPr 4-BuO 1-778 Single iPr 5-BuO 1-779 Single iPr 6-BuO 1-780 Single iPr 7-BuO 1-781 Single iPr 8-BuO 1-782 Single iPr 2-CF 3 O 1-783 Single iPr 4-CF 3 O 1-784 Single iPr 5-CF 3 O 1-785 Single iPr 6-CF 3 O 1-786 Single iPr 7-CF 3 O 1-787 Single iPr 8-CF 3 O 1-788 Single iPr 2-CF 3 CH 2 O 1-789 Single iPr 4-CF 3 CH 2 O 1-790 Single iPr 5-CF 3 CH 2 O 1-791 Single iPr 6-CF 3 CH 2 O 1-792 Single iPr 7-CF 3 CH 2 O 1-793 Single iPr 8-CF 3 CH 2 O 1-794 Single iPr 2-CF 2 HO 1-795 Single iPr 4-CF 2 HO 1-796 Single iPr 5-CF 2 HO 1-797 Single iPr 6-CF 2 HO 1-798 Single iPr 7-CF 2 HO 1-799 Single iPr 8-CF 2 HO 1-800 Single iPr 2-CF 2 HO 1-801 Single iPr 4-CF 2 HO 1-802 Single iPr 5-CF 2 HO 1-803 Single iPr 6-CF 2 HO 1-804 Single iPr 7-CF 2 HO 1-805 Single iPr 8-CF 2 HO 1-806 Single iPr 2-CClH 2 O 1-807 Single iPr 4-CClH 2 O 1-808 Single iPr 5-CClH 2 O 1-809 Single iPr 6-CClH 2 O 1-810 Single iPr 7-CClH 2 O 1-811 Single iPr 8-CClH 2 O 1-812 Single iPr 2,4-F 2 1-813 Single iPr 2,5-F 2 1-814 Single iPr 2,6-F 2 1-815 Single iPr 2,7-F 2 1-816 Single iPr 2,8-F 2 1-817 Single iPr 4,5-F 2 1-818 Single iPr 4,6-F 2 1-819 Single iPr 4,7-F 2 1-820 Single iPr 4,8-F 2 1-821 Single iPr 5,6-F 2 1-822 Single iPr 5,7-F 2 1-823 Single iPr 5,8-F 2 1-824 Single iPr 6,7-F 2 1-825 Single iPr 6,8-F 2 1-826 Single iPr 7,8-F 2 1-827 Single iPr 4,5-Cl 2 1-828 Single iPr 4,6-Cl 2 1-829 Single iPr 4,7-Cl 2 1-830 Single iPr 4,8-Cl 2 1-831 Single iPr 5,6-Cl 2 1-832 Single iPr 5,7-Cl 2 1-833 Single iPr 5,8-Cl 2 1-834 Single iPr 6,7-Cl 2 1-835 Single iPr 6,8-Cl 2 1-836 Single iPr 7,8-Cl 2 1-837 Single iPr 2,5-Me 2 1-838 Single iPr 2,6-Me 2 1-839 Single iPr 2,7-Me 2 1-840 Single iPr 2,8-Me 2 1-841 Single iPr 4,5-Me 2 1-842 Single iPr 4,6-Me 2 1-843 Single iPr 4,7-Me 2 1-844 Single iPr 4,8-Me 2 1-845 Single iPr 5,6-Me 2 1-846 Single iPr 5,7-Me 2 1-847 Single iPr 5,8-Me 2 1-848 Single iPr 6,7-Me 2 1-849 Single iPr 6,8-Me 2 1-850 Single iPr 7,8-Me 2 1-851 Single iPr 2,5- (MeO) 2 1-852 Single iPr 2,6- (MeO) 2 1-853 Single iPr 2,7- (MeO) 2 1-854 Single iPr 2,8- (MeO) 2 1-855 Single iPr 4,5- (MeO) 2 1-856 Single iPr 4,6- (MeO) 2 1-857 Single iPr 4,7- (MeO) 2 1-858 Single iPr 4,8- (MeO) 2 1-859 Single iPr 5,6- (MeO) 2 1-860 Single iPr 5,7- (MeO) 2 1-861 Single iPr 5,8- (MeO) 2 1-862 Single iPr 6,7- (MeO) 2 1-863 Single iPr 6,8- (MeO) 2 1-864 Single iPr 7,8- (MeO) 2 1-865 Single iPr 2-Me-5-F 1-866 Single iPr 2-Me-6-F 1-867 Single iPr 2-Me-7-F 1-868 Single iPr 2-Me-8-F 1- 869 Single iPr 2-Me-5-Cl 1-870 Single iPr 2-Me-6-Cl 1-871 Single iPr 2-Me-7-Cl 1-872 Single iPr 2-Me-8-Cl 1-873 Single iPr 2-Me-5-MeO 1-874 Single iPr 2-Me-6-MeO 1-875 Single iPr 2-Me-7-MeO 1-876 Single iPr 2-Me-8-MeO 1-877 Single iPr 4 -Cl-5-F 1-878 Single iPr 4-Cl-6-F 1-879 Single iPr 4-Cl-7-F 1-880 Single iPr 4-Cl-8-F 1-881 Single iPr 4-Cl -5-Me 1-882 Single iPr 4-Cl-6-Me 1-883 Single iPr 4-Cl-7-Me 1-884 Single iPr 4-Cl-8-Me 1-885 Single iPr 4-Cl-5 -MeO 1-886 Single iPr 4-Cl-6-MeO 1-887 Single iPr 4-Cl-7-MeO 1-888 Single iPr 4-Cl-8-MeO 1-889 Single Bu H 1-890 Single Bu 2 -F 1-891 Single Bu 4-F 1-892 Single Bu 5-F 1-893 Single Bu 6-F 1-894 Single Bu 7-F 1-895 Single Bu 8-F 1-896 Single Bu 2-Cl 1-897 Single Bu 4-Cl 1-898 Single Bu 5-Cl 1-899 Single Bu 6-Cl 1-900 Single Bu 7-Cl 1-901 Single Bu 8-Cl 1-902 Single Bu 2-Br 1- 903 Single Bu 4-Br 1-904 Single Bu 5-Br 1-905 Single Bu 6-Br 1-906 Single Bu 7-Br 1-907 Single Bu 8-Br 1-908 Single Bu 2-I 1-909 Single Bu 4-I 1-910 single Bu 5-I 1-911 single Bu 6-I 1-912 single Bu 7-I 1-913 Single Bu 8-I 1-914 Single Bu 2-Me 1-915 Single Bu 4-Me 1-916 Single Bu 5-Me 1-917 Single Bu 6-Me 1-918 Single Bu 7-Me 1-919 Single Bu 8-Me 1-920 Single Bu 2-Et 1-921 Single Bu 4-Et 1-922 Single Bu 5-Et 1-923 Single Bu 6-Et 1-924 Single Bu 7-Et 1-925 Single Bu 8- Et 1-926 Single Bu 2-Pr 1-927 Single Bu 4-Pr 1-928 Single Bu 5-Pr 1-929 Single Bu 6-Pr 1-930 Single Bu 7-Pr 1-931 Single Bu 8-Pr 1 -932 Single Bu 2-iPr 1-933 Single Bu 4-iPr 1-934 Single Bu 5-iPr 1-935 Single Bu 6-iPr 1-936 Single Bu 7-iPr 1-937 Single Bu 8-iPr 1-938 Single Bu 2-Bu 1-939 Single Bu 4-Bu 1-940 Single Bu 5-Bu 1-941 Single Bu 6-Bu 1-942 Single Bu 7-Bu 1-943 Single Bu 8-Bu 1-944 Single Bu 2-CF 3 1-945 Single Bu 4-CF 3 1-946 Single Bu 5-CF 3 1-947 Single Bu 6-CF 3 1-948 Single Bu 7-CF 3 1-949 Single Bu 8-CF 3 1-950 Single Bu 2-CF 3 CH 2 1-951 Single Bu 4-CF 3 CH 2 1-952 Single Bu 5-CF 3 CH 2 1-953 Single Bu 6-CF 3 CH 2 1-954 Single Bu 7-CF 3 CH 2 1-955 Single Bu 8-CF 3 CH 2 1-956 Single Bu 2-CF 2 H 1-957 Single Bu 4-CF 2 H 1-958 Single Bu 5-CF 2 H 1-959 Single Bu 6-CF 2 H 1-960 Single Bu 7-CF 2 H 1-961 Single Bu 8-CF 2 H 1-962 Single Bu 2-CF 2 H 1-963 Single Bu 4-CF 2 H 1-964 Single Bu 5-CF 2 H 1-965 Single Bu 6-CF 2 H 1-966 Single Bu 7-CF 2 H 1-967 Single Bu 8-CF 2 H 1-968 Single Bu 2-CClH 2 1-969 Single Bu 4-CClH 2 1-970 Single Bu 5-CClH 2 1-971 Single Bu 6-CClH 2 1-972 Single Bu 7-CClH 2 1-973 Single Bu 8-CClH 2 1-974 Single Bu 2-MeO 1-975 Single Bu 4-MeO 1-976 Single Bu 5-MeO 1-977 Single Bu 6-MeO 1-978 Single Bu 7-MeO 1-979 Single Bu 8-MeO 1- 980 Single Bu 2-EtO 1-981 Single Bu 4-EtO 1-982 Single Bu 5-EtO 1-983 Single Bu 6-EtO 1-984 Single Bu 7-EtO 1-985 Single Bu 8-EtO 1-986 Single Bu 2-PrO 1-987 single Bu 4-PrO 1-988 single Bu 5-PrO 1-989 single Bu 6-PrO 1-990 single Bu 7-PrO 1-993 single Bu 4-iPrO 1-994 single Bu 5 -iPrO 1-995 single Bu 6-iPrO 1-996 single Bu 7-iPrO 1-997 single Bu 8-iPrO 1-998 single Bu 2-BuO 1-999 single Bu 4-BuO 1-1000 single Bu 5-BuO 1-1001 Single Bu 6-BuO 1-1002 Single Bu 7-BuO 1-1003 Single Bu 8-BuO 1-1004 Single Bu 2-CF 3 O 1-1005 Single Bu 4-CF 3 O 1-1006 Single Bu 5-CF 3 O 1-1007 Single Bu 6-CF 3 O 1-1008 Single Bu 7-CF 3 O 1-1009 Single Bu 8-CF 3 O 1-1010 Single Bu 2-CF 3 CH 2 O 1-1011 Single Bu 4-CF 3 CH 2 O 1-1012 Single Bu 5-CF 3 CH 2 O 1-1013 Single Bu 6-CF 3 CH 2 O 1-1014 Single Bu 7-CF 3 CH 2 O 1-1015 Single Bu 8-CF 3 CH 2 O 1-1016 Single Bu 2-CF 2 HO 1-1017 Single Bu 4-CF 2 HO 1-1018 Single Bu 5-CF 2 HO 1-1019 Single Bu 6-CF 2 HO 1-1020 Single Bu 7-CF 2 HO 1-1021 Single Bu 8-CF 2 HO 1-1022 Single Bu 2-CF 2 HO 1-1023 Single Bu 4-CF 2 HO 1-1024 Single Bu 5-CF 2 HO 1-1025 Single Bu 6-CF 2 HO 1-1026 Single Bu 7-CF 2 HO 1-1027 Single Bu 8-CF 2 HO 1-1028 Single Bu 2-CClH 2 O 1-1029 Single Bu 4-CClH 2 O 1-1030 Single Bu 5-CClH 2 O 1-1031 Single Bu 6-CClH 2 O 1-1032 Single Bu 7-CClH 2 O 1-1033 Single Bu 8-CClH 2 O 1-1034 Single Bu 2,4-F 2 1-1035 Single Bu 2,5-F 2 1-1036 Single Bu 2,6-F 2 1-1037 Single Bu 2,7-F 2 1-1038 Single Bu 2,8-F 2 1-1039 Single Bu 4,5-F 2 1-1040 Single Bu 4,6-F 2 1-1041 Single Bu 4,7-F 2 1-1042 Single Bu 4,8-F 2 1-1043 Single Bu 5,6-F 2 1-1044 Single Bu 5,7-F 2 1-1045 Single Bu 5,8-F 2 1-1046 Single Bu 6,7-F 2 1-1047 Single Bu 6,8-F 2 1-1048 Single Bu 7,8-F 2 1-1049 Single Bu 4,5-Cl 2 1-1050 Single Bu 4,6-Cl 2 1-1051 Single Bu 4,7-Cl 2 1-1052 Single Bu 4,8-Cl 2 1-1053 Single Bu 5,6-Cl 2 1-1054 Single Bu 5,7-Cl 2 1-1055 Single Bu 5,8-Cl 2 1-1056 Single Bu 6,7-Cl 2 1-1057 Single Bu 6,8-Cl 2 1-1058 Single Bu 7,8-Cl 2 1-1059 Single Bu 2,5-Me 2 1-1060 Single Bu 2,6-Me 2 1-1061 Single Bu 2,7-Me 2 1-1062 Single Bu 2,8-Me 2 1-1063 Single Bu 4,5-Me 2 1-1064 Single Bu 4,6-Me 2 1-1065 Single Bu 4,7-Me 2 1-1066 Single Bu 4,8-Me 2 1-1067 Single Bu 5,6-Me 2 1-1068 Single Bu 5,7-Me 2 1-1069 Single Bu 5,8-Me 2 1-1070 Single Bu 6,7-Me 2 1-1071 Single Bu 6,8-Me 2 1-1072 Single Bu 7,8-Me 2 1-1073 Single Bu 2,5- (MeO) 2 1-1074 Single Bu 2,6- (MeO) 2 1-1075 Single Bu 2,7- (MeO) 2 1-1076 Single Bu 2,8- (MeO) 2 1-1077 Single Bu 4,5- (MeO) 2 1-1078 Single Bu 4,6- (MeO) 2 1-1079 Single Bu 4,7- (MeO) 2 1-1080 Single Bu 4,8- (MeO) 2 1-1081 Single Bu 5,6- (MeO) 2 1-1082 Single Bu 5,7- (MeO) 2 1-1083 Single Bu 5,8- (MeO) 2 1-1084 Single Bu 6,7- (MeO) 2 1-1085 Single Bu 6,8- (MeO) 2 1-1086 Single Bu 7,8- (MeO) 2 1-1087 Single Bu 2-Me-5-F 1-1088 Single Bu 2-Me-6-F 1-1089 Single Bu 2-Me-7-F 1-1090 Single Bu 2-Me-8-F 1- 1091 Single Bu 2-Me-5-Cl 1-1092 Single Bu 2-Me-6-Cl 1-1093 Single Bu 2-Me-7-Cl 1-1094 Single Bu 2-Me-8-Cl 1-1095 Single Bu 2-Me-5-MeO 1-1096 single Bu 2-Me-6-MeO 1-1097 single Bu 2-Me-7-MeO 1-1098 single Bu 2-Me-8-MeO 1-1099 single Bu 4 -Cl-5-F 1-1100 Single Bu 4-Cl-6-F 1-1101 Single Bu 4-Cl-7-F 1-1102 Single Bu 4-Cl-8-F 1-1103 Single Bu 4-Cl -5-Me 1-1104 Single Bu 4-Cl-6-Me 1-1105 Single Bu 4-Cl-7-Me 1-1106 Single Bu 4-Cl-8-Me 1-1107 Single Bu 4-Cl-5 -MeO 1-1108 Single Bu 4-Cl-6-MeO 1-1109 Single Bu 4-Cl-7-MeO 1-1110 Single Bu 4-Cl-8-MeO 1-1111 Single iBu H 1-1112 Single iBu 2 -F 1-1113 Single iBu 4-F 1-1114 Single iBu 5-F 1-1115 Single iBu 6-F 1-1116 Single iBu 7-F 1-1117 Single iBu 8-F 1-1118 Single iBu 2-Cl 1-1119 Single iBu 4-Cl 1-1120 Single iBu 5-Cl 1-1121 Single iBu 6-Cl 1-1122 Single iBu 7-Cl 1-1123 Single iBu 8-Cl 1-1124 Single iBu 2-Br 1- 1125 Single iBu 4-Br 1-1126 Single iBu 5-Br 1-1127 Single iBu 6-Br 1-1128 Single iBu 7-Br 1-1129 Single iBu 8-Br 1-1130 Single iBu 2-I 1-1131 Single iBu 4-I 1-1132 Single iBu 5-I 1-1133 Single iBu 6-I 1-1134 Single iBu 7-I 1-1135 Single iBu 8-I 1-1136 Single iBu 2-Me 1-1137 Single iBu 4-Me 1-1138 Single iBu 5- Me 1-1139 Single iBu 6-Me 1-1140 Single iBu 7-Me 1-1141 Single iBu 8-Me 1-1142 Single iBu 2-Et 1-1143 Single iBu 4-Et 1-1144 Single iBu 5-Et 1 -1145 Single iBu 6-Et 1-1146 Single iBu 7-Et 1-1147 Single iBu 8-Et 1-1148 Single iBu 2-Pr 1-1149 Single iBu 4-Pr 1-1150 Single iBu 5-Pr 1-1151 Single iBu 6-Pr 1-1152 Single iBu 7-Pr 1-1153 Single iBu 8-Pr 1-1154 Single iBu 2-iPr 1-1155 Single iBu 4-iPr 1-1156 Single iBu 5-iPr 1-1157 Single iBu 6-iPr 1-1158 Single iBu 7-iPr 1-1159 Single iBu 8-iPr 1-1160 Single iBu 2-Bu 1-1161 Single iBu 4-Bu 1-1162 Single iBu 5-Bu 1-1163 Single iBu 6- Bu 1-1164 Single iBu 7-Bu 1-1165 Single iBu 8-Bu 1-1166 Single iBu 2-CF 3 1-1167 Single iBu 4-CF 3 1-1168 Single iBu 5-CF 3 1-1169 Single iBu 6-CF 3 1-1170 Single iBu 7-CF 3 1-1171 Single iBu 8-CF 3 1-1172 Single iBu 2-CF 3 CH 2 1-1173 Single iBu 4-CF 3 CH 2 1-1174 Single iBu 5-CF 3 CH 2 1-1175 Single iBu 6-CF 3 CH 2 1-1176 Single iBu 7-CF 3 CH 2 1-1177 Single iBu 8-CF 3 CH 2 1-1178 Single iBu 2-CF 2 H 1-1179 Single iBu 4-CF 2 H 1-1180 Single iBu 5-CF 2 H 1-1181 Single iBu 6-CF 2 H 1-1182 Single iBu 7-CF 2 H 1-1183 Single iBu 8-CF 2 H 1-1184 Single iBu 2-CF 2 H 1-1185 Single iBu 4-CF 2 H 1-1186 Single iBu 5-CF 2 H 1-1187 Single iBu 6-CF 2 H 1-1188 Single iBu 7-CF 2 H 1-1189 Single iBu 8-CF 2 H 1-1190 Single iBu 2-CClH 2 1-1191 Single iBu 4-CClH 2 1-1192 Single iBu 5-CClH 2 1-1193 Single iBu 6-CClH 2 1-1194 Single iBu 7-CClH 2 1-1195 Single iBu 8-CClH 2 1-1196 Single iBu 2-MeO 1-1197 Single iBu 4-MeO 1-1198 Single iBu 5-MeO 1-1199 Single iBu 6-MeO 1-1200 Single iBu 7-MeO 1-1201 Single iBu 8-MeO 1- 1202 Single iBu 2-EtO 1-1203 Single iBu 4-EtO 1-1204 Single iBu 5-EtO 1-1205 Single iBu 6-EtO 1-1206 Single iBu 7-EtO 1-1207 Single iBu 8-EtO 1-1208 Single iBu 2-PrO 1-1209 single iBu 4-PrO 1-1210 single iBu 5-PrO 1-1211 single iBu 6-PrO 1-1212 single iBu 7-PrO 1-1213 single iBu 8-PrO 1-1214 single iBu 2 -iPrO 1-1215 Single iBu 4-iPrO 1-1216 Single iBu 5-iPrO 1-1217 Single iBu 6-iPrO 1-1218 Single iBu 7-iPrO 1-1219 Single iBu 8-iPrO 1-1220 Single iBu 2-BuO 1-1221 Single iBu 4-BuO 1-1222 Single iBu 5-BuO 1-1223 Single iBu 6-BuO 1-1224 Single iBu 7-BuO 1-1225 Single iBu 8-BuO 1-1226 Single iBu 2-CF 3 O 1-1227 Single iBu 4-CF 3 O 1-1228 Single iBu 5-CF 3 O 1-1229 Single iBu 6-CF 3 O 1-1230 Single iBu 7-CF 3 O 1-1231 Single iBu 8-CF 3 O 1-1232 Single iBu 2-CF 3 CH 2 O 1-1233 Single iBu 4-CF 3 CH 2 O 1-1234 Single iBu 5-CF 3 CH 2 O 1-1235 Single iBu 6-CF 3 CH 2 O 1-1236 Single iBu 7-CF 3 CH 2 O 1-1237 Single iBu 8-CF 3 CH 2 O 1-1238 Single iBu 2-CF 2 HO 1-1239 Single iBu 4-CF 2 HO 1-1240 Single iBu 5-CF 2 HO 1-1241 Single iBu 6-CF 2 HO 1-1242 Single iBu 7-CF 2 HO 1-1243 Single iBu 8-CF 2 HO 1-1244 Single iBu 2-CF 2 HO 1-1245 Single iBu 4-CF 2 HO 1-1246 Single iBu 5-CF 2 HO 1-1247 Single iBu 6-CF 2 HO 1-1248 Single iBu 7-CF 2 HO 1-1249 Single iBu 8-CF 2 HO 1-1250 Single iBu 2-CClH 2 O 1-1251 Single iBu 4-CClH 2 O 1-1252 Single iBu 5-CClH 2 O 1-1253 Single iBu 6-CClH 2 O 1-1254 Single iBu 7-CClH 2 O 1-1255 Single iBu 8-CClH 2 O 1-1256 Single iBu 2,4-F 2 1-1257 Single iBu 2,5-F 2 1-1258 Single iBu 2,6-F 2 1-1259 Single iBu 2,7-F 2 1-1260 Single iBu 2,8-F 2 1-1261 Single iBu 4,5-F 2 1-1262 Single iBu 4,6-F 2 1-1263 Single iBu 4,7-F 2 1-1264 Single iBu 4,8-F 2 1-1265 Single iBu 5,6-F 2 1-1266 Single iBu 5,7-F 2 1-1267 Single iBu 5,8-F 2 1-1268 Single iBu 6,7-F 2 1-1269 Single iBu 6,8-F 2 1-1270 Single iBu 7,8-F 2 1-1271 Single iBu 4,5-Cl 2 1-1272 Single iBu 4,6-Cl 2 1-1273 Single iBu 4,7-Cl 2 1-1274 Single iBu 4,8-Cl 2 1-1275 Single iBu 5,6-Cl 2 1-1276 Single iBu 5,7-Cl 2 1-1277 Single iBu 5,8-Cl 2 1-1278 Single iBu 6,7-Cl 2 1-1279 Single iBu 6,8-Cl 2 1-1280 Single iBu 7,8-Cl 2 1-1281 Single iBu 2,5-Me 2 1-1282 Single iBu 2,6-Me 2 1-1283 Single iBu 2,7-Me 2 1-1284 Single iBu 2,8-Me 2 1-1285 Single iBu 4,5-Me 2 1-1286 Single iBu 4,6-Me 2 1-1287 Single iBu 4,7-Me 2 1-1288 Single iBu 4,8-Me 2 1-1289 Single iBu 5,6-Me 2 1-1290 Single iBu 5,7-Me 2 1-1291 Single iBu 5,8-Me 2 1-1292 Single iBu 6,7-Me 2 1-1293 Single iBu 6,8-Me 2 1-1294 Single iBu 7,8-Me 2 1-1295 Single iBu 2,5- (MeO) 2 1-1296 Single iBu 2,6- (MeO) 2 1-1297 Single iBu 2,7- (MeO) 2 1-1298 Single iBu 2,8- (MeO) 2 1-1299 Single iBu 4,5- (MeO) 2 1-1300 Single iBu 4,6- (MeO) 2 1-1301 Single iBu 4,7- (MeO) 2 1-1302 Single iBu 4,8- (MeO) 2 1-1303 Single iBu 5,6- (MeO) 2 1-1304 Single iBu 5,7- (MeO) 2 1-1305 Single iBu 5,8- (MeO) 2 1-1306 Single iBu 6,7- (MeO) 2 1-1307 Single iBu 6,8- (MeO) 2 1-1308 Single iBu 7,8- (MeO) 2 1-1309 Single iBu 2-Me-5-F 1-1310 Single iBu 2-Me-6-F 1-1311 Single iBu 2-Me-7-F 1-1312 Single iBu 2-Me-8-F 1- 1313 Single iBu 2-Me-5-Cl 1-1314 Single iBu 2-Me-6-Cl 1-1315 Single iBu 2-Me-7-Cl 1-1316 Single iBu 2-Me-8-Cl 1-1317 Single iBu 2-Me-5-MeO 1-1318 single iBu 2-Me-6-MeO 1-1319 single iBu 2-Me-7-MeO 1-1320 single iBu 2-Me-8-MeO 1-1321 single iBu 4 -Cl-5-F 1-1322 Single iBu 4-Cl-6-F 1-1323 Single iBu 4-Cl-7-F 1-1324 Single iBu 4-Cl-8-F 1-1325 Single iBu 4-Cl -5-Me 1-1326 Single iBu 4-Cl-6-Me 1-1327 Single iBu 4-Cl-7-Me 1-1328 Single iBu 4-Cl-8-Me 1-1329 Single iBu 4-Cl-5 -MeO 1-1330 Single iBu 4-Cl-6-MeO 1-1331 Single iBu 4-Cl-7-MeO 1-1332 Single iBu 4-Cl-8-MeO 1-1333 Single CF 3 H 1-1334 Single CF 3 2-F 1-1335 Single CF 3 4-F 1-1336 Single CF 3 5-F 1-1337 Single CF 3 6-F 1-1338 Single CF 3 7-F 1-1339 Single CF 3 8-F 1-1340 Single CF 3 2-Cl 1-1341 Single CF 3 4-Cl 1-1342 Single CF 3 5-Cl 1-1343 Single CF 3 6-Cl 1-1344 Single CF 3 7-Cl 1-1345 Single CF 3 8-Cl 1-1346 Single CF 3 2-Br 1-1347 Single CF 3 4-Br 1-1348 Single CF 3 5-Br 1-1349 Single CF 3 6-Br 1-1350 Single CF 3 7-Br 1-1351 Single CF 3 8-Br 1-1352 Single CF 3 2-I 1-1353 Single CF 3 4-I 1-1354 Single CF 3 5-I 1-1355 Single CF 3 6-I 1-1356 Single CF 3 7-I 1-1357 Single CF 3 8-I 1-1358 Single CF 3 2-Me 1-1359 Single CF 3 4-Me 1-1360 Single CF 3 5-Me 1-1361 Single CF 3 6-Me 1-1362 Single CF 3 7-Me 1-1363 Single CF 3 8-Me 1-1364 Single CF 3 2-Et 1-1365 Single CF 3 4-Et 1-1366 Single CF 3 5-Et 1-1367 Single CF 3 6-Et 1-1368 Single CF 3 7-Et 1-1369 Single CF 3 8-Et 1-1370 Single CF 3 2-Pr 1-1371 Single CF 3 4-Pr 1-1372 Single CF 3 5-Pr 1-1373 Single CF 3 6-Pr 1-1374 Single CF 3 7-Pr 1-1375 Single CF 3 8-Pr 1-1376 Single CF 3 2-iPr 1-1377 Single CF 3 4-iPr 1-1378 Single CF 3 5-iPr 1-1379 Single CF 3 6-iPr 1-1380 Single CF 3 7-iPr 1-1381 Single CF 3 8-iPr 1-1382 Single CF 3 2-Bu 1-1383 Single CF 3 4-Bu 1-1384 Single CF 3 5-Bu 1-1385 Single CF 3 6-Bu 1-1386 Single CF 3 7-Bu 1-1387 Single CF 3 8-Bu 1-1388 Single CF 3 2-CF 3 1-1389 Single CF 3 4-CF 3 1-1390 Single CF 3 5-CF 3 1-1391 Single CF 3 6-CF 3 1-1392 Single CF 3 7-CF 3 1-1393 Single CF 3 8-CF 3 1-1394 Single CF 3 2-CF 3 CH 2 1-1395 Single CF 3 4-CF 3 CH 2 1-1396 Single CF 3 5-CF 3 CH 2 1-1397 Single CF 3 6-CF 3 CH 2 1-1398 Single CF 3 7-CF 3 CH 2 1-1399 Single CF 3 8-CF 3 CH 2 1-1400 Single CF 3 2-CF 2 H 1-1401 Single CF 3 4-CF 2 H 1-1402 Single CF 3 5-CF 2 H 1-1403 Single CF 3 6-CF 2 H 1-1404 Single CF 3 7-CF 2 H 1-1405 Single CF 3 8-CF 2 H 1-1406 Single CF 3 2-CF 2 H 1-1407 Single CF 3 4-CF 2 H 1-1408 Single CF 3 5-CF 2 H 1-1409 Single CF 3 6-CF 2 H 1-1410 Single CF 3 7-CF 2 H 1-1411 Single CF 3 8-CF 2 H 1-1412 Single CF 3 2-CClH 2 1-1413 Single CF 3 4-CClH 2 1-1414 Single CF 3 5-CClH 2 1-1415 Single CF 3 6-CClH 2 1-1416 Single CF 3 7-CClH 2 1-1417 Single CF 3 8-CClH 2 1-1418 Single CF 3 2-MeO 1-1419 Single CF 3 4-MeO 1-1420 Single CF 3 5-MeO 1-1421 Single CF 3 6-MeO 1-1422 Single CF 3 7-MeO 1-1423 Single CF 3 8-MeO 1-1424 Single CF 3 2-EtO 1-1425 Single CF 3 4-EtO 1-1426 Single CF 3 5-EtO 1-1427 Single CF 3 6-EtO 1-1428 Single CF 3 7-EtO 1-1429 Single CF 3 8-EtO 1-1430 Single CF 3 2-PrO 1-1431 Single CF 3 4-PrO 1-1432 Single CF 3 5-PrO 1-1433 Single CF 3 6-PrO 1-1434 Single CF 3 7-PrO 1-1435 Single CF 3 8-PrO 1-1436 Single CF 3 2-iPrO 1-1437 Single CF 3 4-iPrO 1-1438 Single CF 3 5-iPrO 1-1439 Single CF 3 6-iPrO 1-1440 Single CF 3 7-iPrO 1-1441 Single CF 3 8-iPrO 1-1442 Single CF 3 2-BuO 1-1443 Single CF 3 4-BuO 1-1444 Single CF 3 5-BuO 1-1445 Single CF 3 6-BuO 1-1446 Single CF 3 7-BuO 1-1447 Single CF 3 8-BuO 1-1448 Single CF 3 2-CF 3 O 1-1449 Single CF 3 4-CF 3 O 1-1450 Single CF 3 5-CF 3 O 1-1451 Single CF 3 6-CF 3 O 1-1452 Single CF 3 7-CF 3 O 1-1453 Single CF 3 8-CF 3 O 1-1454 Single CF 3 2-CF 3 CH 2 O 1-1455 Single CF 3 4-CF 3 CH 2 O 1-1456 Single CF 3 5-CF 3 CH 2 O 1-1457 Single CF 3 6-CF 3 CH 2 O 1-1458 Single CF 3 7-CF 3 CH 2 O 1-1459 Single CF 3 8-CF 3 CH 2 O 1-1460 Single CF 3 2-CF 2 HO 1-1461 Single CF 3 4-CF 2 HO 1-1462 Single CF 3 5-CF 2 HO 1-1463 Single CF 3 6-CF 2 HO 1-1464 Single CF 3 7-CF 2 HO 1-1465 Single CF 3 8-CF 2 HO 1-1466 Single CF 3 2-CF 2 HO 1-1467 Single CF 3 4-CF 2 HO 1-1468 Single CF 3 5-CF 2 HO 1-1469 Single CF 3 6-CF 2 HO 1-1470 Single CF 3 7-CF 2 HO 1-1471 Single CF 3 8-CF 2 HO 1-1472 Single CF 3 2-CClH 2 O 1-1473 Single CF 3 4-CClH 2 O 1-1474 Single CF 3 5-CClH 2 O 1-1475 Single CF 3 6-CClH 2 O 1-1476 Single CF 3 7-CClH 2 O 1-1477 Single CF 3 8-CClH 2 O 1-1478 Single CF 3 2,4-F 2 1-1479 Single CF 3 2,5-F 2 1-1480 Single CF 3 2,6-F 2 1-1481 Single CF 3 2,7-F 2 1-1482 Single CF 3 2,8-F 2 1-1483 Single CF 3 4,5-F 2 1-1484 Single CF 3 4,6-F 2 1-1485 Single CF 3 4,7-F 2 1-1486 Single CF 3 4,8-F 2 1-1487 Single CF 3 5,6-F 2 1-1488 Single CF 3 5,7-F 2 1-1489 Single CF 3 5,8-F 2 1-1490 Single CF 3 6,7-F 2 1-1491 Single CF 3 6,8-F 2 1-1492 Single CF 3 7,8-F 2 1-1493 Single CF 3 4,5-Cl 2 1-1494 Single CF 3 4,6-Cl 2 1-1495 Single CF 3 4,7-Cl 2 1-1496 Single CF 3 4,8-Cl 2 1-1497 Single CF 3 5,6-Cl 2 1-1498 Single CF 3 5,7-Cl 2 1-1499 Single CF 3 5,8-Cl 2 1-1500 Single CF 3 6,7-Cl 2 1-1501 Single CF 3 6,8-Cl 2 1-1502 Single CF 3 7,8-Cl 2 1-1503 Single CF 3 2,5-Me 2 1-1504 Single CF 3 2,6-Me 2 1-1505 Single CF 3 2,7-Me 2 1-1506 Single CF 3 2,8-Me 2 1-1507 Single CF 3 4,5-Me 2 1-1508 Single CF 3 4,6-Me 2 1-1509 Single CF 3 4,7-Me 2 1-1510 Single CF 3 4,8-Me 2 1-1511 Single CF 3 5,6-Me 2 1-1512 Single CF 3 5,7-Me 2 1-1513 Single CF 3 5,8-Me 2 1-1514 Single CF 3 6,7-Me 2 1-1515 Single CF 3 6,8-Me 2 1-1516 Single CF 3 7,8-Me 2 1-1517 Single CF 3 2,5- (MeO) 2 1-1518 Single CF 3 2,6- (MeO) 2 1-1519 Single CF 3 2,7- (MeO) 2 1-1520 Single CF 3 2,8- (MeO) 2 1-1521 Single CF 3 4,5- (MeO) 2 1-1522 Single CF 3 4,6- (MeO) 2 1-1523 Single CF 3 4,7- (MeO) 2 1-1524 Single CF 3 4,8- (MeO) 2 1-1525 Single CF 3 5,6- (MeO) 2 1-1526 Single CF 3 5,7- (MeO) 2 1-1527 Single CF 3 5,8- (MeO) 2 1-1528 Single CF 3 6,7- (MeO) 2 1-1529 Single CF 3 6,8- (MeO) 2 1-1530 Single CF 3 7,8- (MeO) 2 1-1531 Single CF 3 2-Me-5-F 1-1532 Single CF 3 2-Me-6-F 1-1533 Single CF 3 2-Me-7-F 1-1534 Single CF 3 2-Me-8-F 1-1535 Single CF 3 2-Me-5-Cl 1-1536 Single CF 3 2-Me-6-Cl 1-1537 Single CF 3 2-Me-7-Cl 1-1538 Single CF 3 2-Me-8-Cl 1-1539 Single CF 3 2-Me-5-MeO 1-1540 Single CF 3 2-Me-6-MeO 1-1541 Single CF 3 2-Me-7-MeO 1-1542 Single CF 3 2-Me-8-MeO 1-1543 Single CF 3 4-Cl-5-F 1-1544 Single CF 3 4-Cl-6-F 1-1545 Single CF 3 4-Cl-7-F 1-1546 Single CF 3 4-Cl-8-F 1-1547 Single CF 3 4-Cl-5-Me 1-1548 Single CF 3 4-Cl-6-Me 1-1549 Single CF 3 4-Cl-7-Me 1-1550 Single CF 3 4-Cl-8-Me 1-1551 Single CF 3 4-Cl-5-MeO 1-1552 Single CF 3 4-Cl-6-MeO 1-1553 Single CF 3 4-Cl-7-MeO 1-1554 Single CF 3 4-Cl-8-MeO 1-1555 Two CH 2 Cl H 1-1556 Two CH 2 Cl 2-F 1-1557 Two CH 2 Cl 4-F 1-1558 Two CH 2 Cl 5-F 1-1559 Two CH 2 Cl 6-F 1-1560 Two CH 2 Cl 7-F 1-1561 Two CH 2 Cl 8-F 1-1562 Two CH 2 Cl 2-Cl 1-1563 Two CH 2 Cl 4-Cl 1-1564 Two CH 2 Cl 5-Cl 1-1565 Two CH 2 Cl 6-Cl 1-1566 Two CH 2 Cl 7-Cl 1-1567 Two CH 2 Cl 8-Cl 1-1568 Two CH 2 Cl 2-Br 1-1569 Two CH 2 Cl 4-Br 1-1570 Two CH 2 Cl 5-Br 1-1571 Two CH 2 Cl 6-Br 1-1572 Two CH 2 Cl 7-Br 1-1573 Two CH 2 Cl 8-Br 1-1574 Two CH 2 Cl 2-I 1-1575 Two CH 2 Cl 4-I 1-1576 Two CH 2 Cl 5-I 1-1577 Two CH 2 Cl 6-I 1-1578 Two CH 2 Cl 7-I 1-1579 Two CH 2 Cl 8-I 1-1580 Two CH 2 Cl 2-Me 1-1581 Two CH 2 Cl 4-Me 1-1582 Two CH 2 Cl 5-Me 1-1583 Two CH 2 Cl 6-Me 1-1584 Two CH 2 Cl 7-Me 1-1585 Two CH 2 Cl 8-Me 1-1586 Two CH 2 Cl 2-Et 1-1587 Two CH 2 Cl 4-Et 1-1588 Two CH 2 Cl 5-Et 1-1589 Two CH 2 Cl 6-Et 1-1590 Two CH 2 Cl 7-Et 1-1591 Two CH 2 Cl 8-Et 1-1592 Two CH 2 Cl 2-Pr 1-1593 Two CH 2 Cl 4-Pr 1-1594 Two CH 2 Cl 5-Pr 1-1595 Two CH 2 Cl 6-Pr 1-1596 Two CH 2 Cl 7-Pr 1-1597 Two CH 2 Cl 8-Pr 1-1598 Two CH 2 Cl 2-iPr 1-1599 Two CH 2 Cl 4-iPr 1-1600 Two CH 2 Cl 5-iPr 1-1601 Two CH 2 Cl 6-iPr 1-1602 Two CH 2 Cl 7-iPr 1-1603 Two CH 2 Cl 8-iPr 1-1604 Two CH 2 Cl 2-Bu 1-1605 Two CH 2 Cl 4-Bu 1-1606 Two CH 2 Cl 5-Bu 1-1607 Two CH 2 Cl 6-Bu 1-1608 Two CH 2 Cl 7-Bu 1-1609 Two CH 2 Cl 8-Bu 1-1610 Two CH 2 Cl 2-CF 3 1-1611 Two CH 2 Cl 4-CF 3 1-1612 Two CH 2 Cl 5-CF 3 1-1613 Two CH 2 Cl 6-CF 3 1-1614 Two CH 2 Cl 7-CF 3 1-1615 Two CH 2 Cl 8-CF 3 1-1616 Two CH 2 Cl 2-CF 3 CH 2 1-1617 Two CH 2 Cl 4-CF 3 CH 2 1-1618 Two CH 2 Cl 5-CF 3 CH 2 1-1619 Two CH 2 Cl 6-CF 3 CH 2 1-1620 Two CH 2 Cl 7-CF 3 CH 2 1-1621 Two CH 2 Cl 8-CF 3 CH 2 1-1622 Two CH 2 Cl 2-CF 2 H 1-1623 Two CH 2 Cl 4-CF 2 H 1-1624 Two CH 2 Cl 5-CF 2 H 1-1625 Two CH 2 Cl 6-CF 2 H 1-1626 Two CH 2 Cl 7-CF 2 H 1-1627 Two CH 2 Cl 8-CF 2 H 1-1628 Two CH 2 Cl 2-CF 2 H 1-1629 Two CH 2 Cl 4-CF 2 H 1-1630 Two CH 2 Cl 5-CF 2 H 1-1631 Two CH 2 Cl 6-CF 2 H 1-1632 Two CH 2 Cl 7-CF 2 H 1-1633 Two CH 2 Cl 8-CF 2 H 1-1634 Two CH 2 Cl 2-CClH 2 1-1635 Two CH 2 Cl 4-CClH 2 1-1636 Two CH 2 Cl 5-CClH 2 1-1637 Two CH 2 Cl 6-CClH 2 1-1638 Two CH 2 Cl 7-CClH 2 1-1639 Two CH 2 Cl 8-CClH 2 1-1640 Two CH 2 Cl 2-MeO 1-1641 Two CH 2 Cl 4-MeO 1-1642 Two CH 2 Cl 5-MeO 1-1643 Two CH 2 Cl 6-MeO 1-1644 Two CH 2 Cl 7-MeO 1-1645 Two CH 2 Cl 8-MeO 1-1646 Two CH 2 Cl 2-EtO 1-1647 Two CH 2 Cl 4-EtO 1-1648 Two CH 2 Cl 5-EtO 1-1649 Two CH 2 Cl 6-EtO 1-1650 Two CH 2 Cl 7-EtO 1-1651 Two CH 2 Cl 8-EtO 1-1652 Two CH 2 Cl 2-PrO 1-1653 Two CH 2 Cl 4-PrO 1-1654 Two CH 2 Cl 5-PrO 1-1655 Two CH 2 Cl 6-PrO 1-1656 Two CH 2 Cl 7-PrO 1-1657 Two CH 2 Cl 8-PrO 1-1658 Two CH 2 Cl 2-iPrO 1-1659 Two CH 2 Cl 4-iPrO 1-1660 Two CH 2 Cl 5-iPrO 1-1661 Two CH 2 Cl 6-iPrO 1-1662 Two CH 2 Cl 7-iPrO 1-1663 Two CH 2 Cl 8-iPrO 1-1664 Two CH 2 Cl 2-BuO 1-1665 Two CH 2 Cl 4-BuO 1-1666 Two CH 2 Cl 5-BuO 1-1667 Two CH 2 Cl 6-BuO 1-1668 Two CH 2 Cl 7-BuO 1-1669 Two CH 2 Cl 8-BuO 1-1670 Two CH 2 Cl 2-CF 3 O 1-1671 Two CH 2 Cl 4-CF 3 O 1-1672 Two CH 2 Cl 5-CF 3 O 1-1673 Two CH 2 Cl 6-CF 3 O 1-1674 Two CH 2 Cl 7-CF 3 O 1-1675 Two CH 2 Cl 8-CF 3 O 1-1676 Two CH 2 Cl 2-CF 3 CH 2 O 1-1677 Two CH 2 Cl 4-CF 3 CH 2 O 1-1678 Two CH 2 Cl 5-CF 3 CH 2 O 1-1679 Two CH 2 Cl 6-CF 3 CH 2 O 1-1680 Two CH 2 Cl 7-CF 3 CH 2 O 1-1681 Two CH 2 Cl 8-CF 3 CH 2 O 1-1682 Two CH 2 Cl 2-CF 2 HO 1-1683 Two CH 2 Cl 4-CF 2 HO 1-1684 Two CH 2 Cl 5-CF 2 HO 1-1685 Two CH 2 Cl 6-CF 2 HO 1-1686 Two CH 2 Cl 7-CF 2 HO 1-1687 Two CH 2 Cl 8-CF 2 HO 1-1688 Two CH 2 Cl 2-CF 2 HO 1-1689 Two CH 2 Cl 4-CF 2 HO 1-1690 Two CH 2 Cl 5-CF 2 HO 1-1691 Two CH 2 Cl 6-CF 2 HO 1-1692 Two CH 2 Cl 7-CF 2 HO 1-1693 Two CH 2 Cl 8-CF 2 HO 1-1694 Two CH 2 Cl 2-CClH 2 O 1-1695 Two CH 2 Cl 4-CClH 2 O 1-1696 Two CH 2 Cl 5-CClH 2 O 1-1697 Two CH 2 Cl 6-CClH 2 O 1-1698 Two CH 2 Cl 7-CClH 2 O 1-1699 Two CH 2 Cl 8-CClH 2 O 1-1700 Two CH 2 Cl 2,4-F 2 1-1701 Two CH 2 Cl 2,5-F 2 1-1702 Two CH 2 Cl 2,6-F 2 1-1703 Two CH 2 Cl 2,7-F 2 1-1704 Two CH 2 Cl 2,8-F 2 1-1705 Two CH 2 Cl 4,5-F 2 1-1706 Two CH 2 Cl 4,6-F 2 1-1707 Two CH 2 Cl 4,7-F 2 1-1708 Two CH 2 Cl 4,8-F 2 1-1709 Two CH 2 Cl 5,6-F 2 1-1710 Two CH 2 Cl 5,7-F 2 1-1711 Two CH 2 Cl 5,8-F 2 1-1712 Two CH 2 Cl 6,7-F 2 1-1713 Two CH 2 Cl 6,8-F 2 1-1714 Two CH 2 Cl 7,8-F 2 1-1715 Two CH 2 Cl 4,5-Cl 2 1-1716 Two CH 2 Cl 4,6-Cl 2 1-1717 Two CH 2 Cl 4,7-Cl 2 1-1718 Two CH 2 Cl 4,8-Cl 2 1-1719 Two CH 2 Cl 5,6-Cl 2 1-1720 Two CH 2 Cl 5,7-Cl 2 1-1721 Two CH 2 Cl 5,8-Cl 2 1-1722 Two CH 2 Cl 6,7-Cl 2 1-1723 Two CH 2 Cl 6,8-Cl 2 1-1724 Two CH 2 Cl 7,8-Cl 2 1-1725 Two CH 2 Cl 2,5-Me 2 1-1726 Two CH 2 Cl 2,6-Me 2 1-1727 Two CH 2 Cl 2,7-Me 2 1-1728 Two CH 2 Cl 2,8-Me 2 1-1729 Two CH 2 Cl 4,5-Me 2 1-1730 Two CH 2 Cl 4,6-Me 2 1-1731 Two CH 2 Cl 4,7-Me 2 1-1732 Two CH 2 Cl 4,8-Me 2 1-1733 Two CH 2 Cl 5,6-Me 2 1-1734 Two CH 2 Cl 5,7-Me 2 1-1735 Two CH 2 Cl 5,8-Me 2 1-1736 Two CH 2 Cl 6,7-Me 2 1-1737 Two CH 2 Cl 6,8-Me 2 1-1738 Two CH 2 Cl 7,8-Me 2 1-1739 Two CH 2 Cl 2,5- (MeO) 2 1-1740 Two CH 2 Cl 2,6- (MeO) 2 1-1741 Two CH 2 Cl 2,7- (MeO) 2 1-1742 Two CH 2 Cl 2,8- (MeO) 2 1-1743 Two CH 2 Cl 4,5- (MeO) 2 1-1744 Two CH 2 Cl 4,6- (MeO) 2 1-1745 Two CH 2 Cl 4,7- (MeO) 2 1-1746 Two CH 2 Cl 4,8- (MeO) 2 1-1747 Two CH 2 Cl 5,6- (MeO) 2 1-1748 Two CH 2 Cl 5,7- (MeO) 2 1-1749 Two CH 2 Cl 5,8- (MeO) 2 1-1750 Two CH 2 Cl 6,7- (MeO) 2 1-1751 Two CH 2 Cl 6,8- (MeO) 2 1-1752 Two CH 2 Cl 7,8- (MeO) 2 1-1753 Two CH 2 Cl 2-Me-5-F 1-1754 Two CH 2 Cl 2-Me-6-F 1-1755 Two CH 2 Cl 2-Me-7-F 1-1756 Two CH 2 Cl 2-Me-8-F 1-1757 Two CH 2 Cl 2-Me-5-Cl 1-1758 Two CH 2 Cl 2-Me-6-Cl 1-1759 Two CH 2 Cl 2-Me-7-Cl 1-1760 Two CH 2 Cl 2-Me-8-Cl 1-1761 Two CH 2 Cl 2-Me-5-MeO 1-1762 Two CH 2 Cl 2-Me-6-MeO 1-1763 Two CH 2 Cl 2-Me-7-MeO 1-1764 Two CH 2 Cl 2-Me-8-MeO 1-1765 Two CH 2 Cl 4-Cl-5-F 1-1766 Two CH 2 Cl 4-Cl-6-F 1-1767 Two CH 2 Cl 4-Cl-7-F 1-1768 Two CH 2 Cl 4-Cl-8-F 1-1769 Two CH 2 Cl 4-Cl-5-Me 1-1770 Two CH 2 Cl 4-Cl-6-Me 1-1771 Two CH 2 Cl 4-Cl-7-Me 1-1772 Two CH 2 Cl 4-Cl-8-Me 1-1773 Two CH 2 Cl 4-Cl-5-MeO 1-1774 Two CH 2 Cl 4-Cl-6-MeO 1-1775 Two CH 2 Cl 4-Cl-7-MeO 1-1776 Two CH 2 Cl 4-Cl-8-MeO 1-1777 II Me H 1-1778 II Me 2-F 1-1779 II Me 4-F 1-1780 II Me 5-F 1-1781 II Me 6-F 1-1782 II Me 7-F 1-1783 Second Me 8-F 1-1784 Second Me 2-Cl 1-1785 Second Me 4-Cl 1-1786 Second Me 5-Cl 1-1787 Second Me 6-Cl 1-1788 Second Me 7 -Cl 1-1789 Two Me 8-Cl 1-1790 Two Me 2-Br 1-1791 Two Me 4-Br 1-1792 Two Me 5-Br 1-1793 Two Me 6-Br 1-1794 Two Me 7-Br 1-1795 Two Me 8-Br 1-1796 Two Me 2-I 1-1797 Two Me 4-I 1-1798 Two Me 5-I 1-1799 Two Me 6-I 1-1800 Two Me 7-I 1- 1801 Two Me 8-I 1-1802 Two Me 2-Me 1-1803 Two Me 4-Me 1-1804 Two Me 5-Me 1-1805 Two Me 6-Me 1-1806 Two Me 7-Me 1-1807 Two Me 8-Me 1-1808 Two Me 2-Et 1-1809 Two Me 4-Et 1-1810 Two Me 5-Et 1-1811 Two Me 6-Et 1-1812 Two Me 7-Et 1-1813 Two Me 8 -Et 1-1814 Two Me 2-Pr 1-1815 Two Me 4-Pr 1-1816 Two Me 5-Pr 1-1817 Two Me 6-Pr 1-1818 Two Me 7-Pr 1-1819 Two Me 8-Pr 1-1820 Two Me 2-iPr 1-1821 Two Me 4-iPr 1-1822 Two Me 5-iPr 1-1823 Two Me 6-iPr 1-1824 Two Me 7-iPr 1-1825 Two Me 8-iPr 1- 1826 Two Me 2-Bu 1-1827 Two Me 4-Bu 1-1828 Two Me 5-Bu 1-1829 Second Me 6-Bu 1-1830 Second Me 7-Bu 1-1831 Second Me 8-Bu 1-1832 Second Me 2-CF 3 1-1833 Two Me 4-CF 3 1-1834 Two Me 5-CF 3 1-1835 Two Me 6-CF 3 1-1836 Two Me 7-CF 3 1-1837 Two Me 8-CF 3 1-1838 Two Me 2-CF 3 CH 2 1-1839 Two Me 4-CF 3 CH 2 1-1840 Two Me 5-CF 3 CH 2 1-1841 Two Me 6-CF 3 CH 2 1-1842 Two Me 7-CF 3 CH 2 1-1843 Two Me 8-CF 3 CH 2 1-1844 Two Me 2-CF 2 H 1-1845 Two Me 4-CF 2 H 1-1846 Two Me 5-CF 2 H 1-1847 Two Me 6-CF 2 H 1-1848 Two Me 7-CF 2 H 1-1849 Two Me 8-CF 2 H 1-1850 Two Me 2-CF 2 H 1-1851 Two Me 4-CF 2 H 1-1852 Two Me 5-CF 2 H 1-1853 Two Me 6-CF 2 H 1-1854 Two Me 7-CF 2 H 1-1855 Two Me 8-CF 2 H 1-1856 Two Me 2-CClH 2 1-1857 Two Me 4-CClH 2 1-1858 Two Me 5-CClH 2 1-1859 Two Me 6-CClH 2 1-1860 Two Me 7-CClH 2 1-1861 Two Me 8-CClH 2 1-1862 Two Me 2-MeO 1-1863 Two Me 4-MeO 1-1864 Two Me 5-MeO 1-1865 Two Me 6-MeO 1-1866 Two Me 7-MeO 1-1867 Two Me 8-MeO 1- 1868 Two Me 2-EtO 1-1869 Two Me 4-EtO 1-1870 Two Me 5-EtO 1-1871 Two Me 6-EtO 1-1872 Two Me 7-EtO 1-1873 Two Me 8-EtO 1-1874 Two Me 2-PrO 1-1875 II Me 4-PrO 1-1876 II Me 5-PrO 1-1877 II Me 6-PrO 1-1878 II Me 7-PrO 1-1879 II Me 8-PrO 1-1880 II Me 2 -iPrO 1-1881 two Me 4-iPrO 1-1882 two Me 5-iPrO 1-1883 two Me 6-iPrO 1-1884 two Me 7-iPrO 1-1885 two Me 8-iPrO 1-1886 two Me 2-BuO 1-1887 Two Me 4-BuO 1-1888 Two Me 5-BuO 1-1889 Two Me 6-BuO 1-1890 Two Me 7-BuO 1-1891 Two Me 8-BuO 1-1892 Two Me 2-CF 3 O 1-1893 Two Me 4-CF 3 O 1-1894 Two Me 5-CF 3 O 1-1895 Two Me 6-CF 3 O 1-1896 Two Me 7-CF 3 O 1-1897 Two Me 8-CF 3 O 1-1898 Two Me 2-CF 3 CH 2 O 1-1899 Two Me 4-CF 3 CH 2 O 1-1900 Two Me 5-CF 3 CH 2 O 1-1901 Two Me 6-CF 3 CH 2 O 1-1902 Two Me 7-CF 3 CH 2 O 1-1903 Two Me 8-CF 3 CH 2 O 1-1904 Two Me 2-CF 2 HO 1-1905 Two Me 4-CF 2 HO 1-1906 Two Me 5-CF 2 HO 1-1907 Two Me 6-CF 2 HO 1-1908 Two Me 7-CF 2 HO 1-1909 Two Me 8-CF 2 HO 1-1910 Two Me 2-CF 2 HO 1-1911 Two Me 4-CF 2 HO 1-1912 Two Me 5-CF 2 HO 1-1913 Two Me 6-CF 2 HO 1-1914 Two Me 7-CF 2 HO 1-1915 Two Me 8-CF 2 HO 1-1916 Two Me 2-CClH 2 O 1-1917 Two Me 4-CClH 2 O 1-1918 Two Me 5-CClH 2 O 1-1919 Two Me 6-CClH 2 O 1-1920 Two Me 7-CClH 2 O 1-1921 Two Me 8-CClH 2 O 1-1922 Two Me 2,4-F 2 1-1923 Two Me 2,5-F 2 1-1924 Two Me 2,6-F 2 1-1925 Two Me 2,7-F 2 1-1926 Two Me 2,8-F 2 1-1927 Two Me 4,5-F 2 1-1928 Two Me 4,6-F 2 1-1929 Two Me 4,7-F 2 1-1930 Two Me 4,8-F 2 1-1931 Two Me 5,6-F 2 1-1932 Two Me 5,7-F 2 1-1933 Two Me 5,8-F 2 1-1934 Two Me 6,7-F 2 1-1935 Two Me 6,8-F 2 1-1936 Two Me 7,8-F 2 1-1937 Two Me 4,5-Cl 2 1-1938 Two Me 4,6-Cl 2 1-1939 Two Me 4,7-Cl 2 1-1940 Two Me 4,8-Cl 2 1-1941 Two Me 5,6-Cl 2 1-1942 Two Me 5,7-Cl 2 1-1943 Two Me 5,8-Cl 2 1-1944 Two Me 6,7-Cl 2 1-1945 Two Me 6,8-Cl 2 1-1946 Two Me 7,8-Cl 2 1-1947 Two Me 2,5-Me 2 1-1948 Two Me 2,6-Me 2 1-1949 Two Me 2,7-Me 2 1-1950 Two Me 2,8-Me 2 1-1951 Two Me 4,5-Me 2 1-1952 Two Me 4,6-Me 2 1-1953 Two Me 4,7-Me 2 1-1954 Two Me 4,8-Me 2 1-1955 Two Me 5,6-Me 2 1-1956 Two Me 5,7-Me 2 1-1957 Two Me 5,8-Me 2 1-1958 Two Me 6,7-Me 2 1-1959 Two Me 6,8-Me 2 1-1960 Two Me 7,8-Me 2 1-1961 Two Me 2,5- (MeO) 2 1-1962 Two Me 2,6- (MeO) 2 1-1963 Two Me 2,7- (MeO) 2 1-1964 Two Me 2,8- (MeO) 2 1-1965 Two Me 4,5- (MeO) 2 1-1966 Two Me 4,6- (MeO) 2 1-1967 Two Me 4,7- (MeO) 2 1-1968 Two Me 4,8- (MeO) 2 1-1969 Two Me 5,6- (MeO) 2 1-1970 Two Me 5,7- (MeO) 2 1-1971 Two Me 5,8- (MeO) 2 1-1972 Two Me 6,7- (MeO) 2 1-1973 Two Me 6,8- (MeO) 2 1-1974 Two Me 7,8- (MeO) 2 1-1975 Two Me 2-Me-5-F 1-1976 Two Me 2-Me-6-F 1-1977 Two Me 2-Me-7-F 1-1978 Two Me 2-Me-8-F 1- 1979 Two Me 2-Me-5-Cl 1-1980 Two Me 2-Me-6-Cl 1-1981 Two Me 2-Me-7-Cl 1-1982 Two Me 2-Me-8-Cl 1-1983 Two Me 2-Me-5-MeO 1-1984 Two Me 2-Me-6-MeO 1-1985 Two Me 2-Me-7-MeO 1-1986 Two Me 2-Me-8-MeO 1-1987 Two Me 4 -Cl-5-F 1-1988 Two Me 4-Cl-6-F 1-1989 Two Me 4-Cl-7-F 1-1990 Two Me 4-Cl-8-F 1-1991 Two Me 4-Cl -5-Me 1-1992 II Me 4-Cl-6-Me 1-1993 II Me 4-Cl-7-Me 1-1994 II Me 4-Cl-8-Me 1-1995 II Me 4-Cl-5 -MeO 1-1996 II Me 4-Cl-6-MeO 1-1997 II Me 4-Cl-7-MeO 1-1998 II Me 4-Cl-8-MeO 1-1999 II CF 3 H 1-2000 Two CF 3 2-F 1-2001 Two CF 3 4-F 1-2002 Two CF 3 5-F 1-2003 Two CF 3 6-F 1-2004 Two CF 3 7-F 1-2005 Two CF 3 8-F 1-2006 Two CF 3 2-Cl 1-2007 Two CF 3 4-Cl 1-2008 Two CF 3 5-Cl 1-2009 Two CF 3 6-Cl 1-2010 Two CF 3 7-Cl 1-2011 Two CF 3 8-Cl 1-2012 Two CF 3 2-Br 1-2013 Two CF 3 4-Br 1-2014 Two CF 3 5-Br 1-2015 Two CF 3 6-Br 1-2016 Two CF 3 7-Br 1-2017 Two CF 3 8-Br 1-2018 Two CF 3 2-I 1-2019 Two CF 3 4-I 1-2020 Two CF 3 5-I 1-2021 Two CF 3 6-I 1-2022 Two CF 3 7-I 1-2023 Two CF 3 8-I 1-2024 Two CF 3 2-Me 1-2025 Two CF 3 4-Me 1-2026 Two CF 3 5-Me 1-2027 Two CF 3 6-Me 1-2028 Two CF 3 7-Me 1-2029 Two CF 3 8-Me 1-2030 Two CF 3 2-Et 1-2031 Two CF 3 4-Et 1-2032 Two CF 3 5-Et 1-2033 Two CF 3 6-Et 1-2034 Two CF 3 7-Et 1-2035 Two CF 3 8-Et 1-2036 Two CF 3 2-Pr 1-2037 Two CF 3 4-Pr 1-2038 Two CF 3 5-Pr 1-2039 Two CF 3 6-Pr 1-2040 Two CF 3 7-Pr 1-2041 Two CF 3 8-Pr 1-2042 Two CF 3 2-iPr 1-2043 Two CF 3 4-iPr 1-2044 Two CF 3 5-iPr 1-2045 Two CF 3 6-iPr 1-2046 Two CF 3 7-iPr 1-2047 Two CF 3 8-iPr 1-2048 Two CF 3 2-Bu 1-2049 Two CF 3 4-Bu 1-2050 Two CF 3 5-Bu 1-2051 Two CF 3 6-Bu 1-2052 Two CF 3 7-Bu 1-2053 Two CF 3 8-Bu 1-2054 Two CF 3 2-CF 3 1-2055 Two CF 3 4-CF 3 1-2056 Two CF 3 5-CF 3 1-2057 Two CF 3 6-CF 3 1-2058 two CF 3 7-CF 3 1-2059 Two CF 3 8-CF 3 1-2060 two CF 3 2-CF 3 CH 2 1-2061 Two CF 3 4-CF 3 CH 2 1-2062 two CF 3 5-CF 3 CH 2 1-2063 Two CF 3 6-CF 3 CH 2 1-2064 Two CF 3 7-CF 3 CH 2 1-2065 Two CF 3 8-CF 3 CH 2 1-2066 Two CF 3 2-CF 2 H 1-2067 Two CF 3 4-CF 2 H 1-2068 Two CF 3 5-CF 2 H 1-2069 Two CF 3 6-CF 2 H 1-2070 Two CF 3 7-CF 2 H 1-2071 Two CF 3 8-CF 2 H 1-2072 Two CF 3 2-CF 2 H 1-2073 Two CF 3 4-CF 2 H 1-2074 Two CF 3 5-CF 2 H 1-2075 Two CF 3 6-CF 2 H 1-2076 Two CF 3 7-CF 2 H 1-2077 Two CF 3 8-CF 2 H 1-2078 Two CF 3 2-CClH 2 1-2079 Two CF 3 4-CClH 2 1-2080 Two CF 3 5-CClH 2 1-2081 Two CF 3 6-CClH 2 1-2082 Two CF 3 7-CClH 2 1-2083 Two CF 3 8-CClH 2 1-2084 Two CF 3 2-MeO 1-2085 Two CF 3 4-MeO 1-2086 Two CF 3 5-MeO 1-2087 Two CF 3 6-MeO 1-2088 Two CF 3 7-MeO 1-2089 Two CF 3 8-MeO 1-2090 Two CF 3 2-EtO 1-2091 Two CF 3 4-EtO 1-2092 Two CF 3 5-EtO 1-2093 Two CF 3 6-EtO 1-2094 Two CF 3 7-EtO 1-2095 Two CF 3 8-EtO 1-2096 Two CF 3 2-PrO 1-2097 Two CF 3 4-PrO 1-2098 Two CF 3 5-PrO 1-2099 Two CF 3 6-PrO 1-2100 Two CF 3 7-PrO 1-2101 Two CF 3 8-PrO 1-2102 two CF 3 2-iPrO 1-2103 Two CF 3 4-iPrO 1-2104 Two CF 3 5-iPrO 1-2105 two CF 3 6-iPrO 1-2106 Two CF 3 7-iPrO 1-2107 Two CF 3 8-iPrO 1-2108 two CF 3 2-BuO 1-2109 Two CF 3 4-BuO 1-2110 two CF 3 5-BuO 1-2111 Two CF 3 6-BuO 1-2112 Two CF 3 7-BuO 1-2113 Two CF 3 8-BuO 1-2114 two CF 3 2-CF 3 O 1-2115 Two CF 3 4-CF 3 O 1-2116 Two CF 3 5-CF 3 O 1-2117 two CF 3 6-CF 3 O 1-2118 Two CF 3 7-CF 3 O 1-2119 Two CF 3 8-CF 3 O 1-2120 two CF 3 2-CF 3 CH 2 O 1-2121 Two CF 3 4-CF 3 CH 2 O 1-2122 Two CF 3 5-CF 3 CH 2 O 1-2123 two CF 3 6-CF 3 CH 2 O 1-2124 Two CF 3 7-CF 3 CH 2 O 1-2125 two CF 3 8-CF 3 CH 2 O 1-2126 Two CF 3 2-CF 2 HO 1-2127 Two CF 3 4-CF 2 HO 1-2128 Two CF 3 5-CF 2 HO 1-2129 Two CF 3 6-CF 2 HO 1-2130 Two CF 3 7-CF 2 HO 1-2131 Two CF 3 8-CF 2 HO 1-2132 Two CF 3 2-CF 2 HO 1-2133 Two CF 3 4-CF 2 HO 1-2134 Two CF 3 5-CF 2 HO 1-2135 Two CF 3 6-CF 2 HO 1-2136 Two CF 3 7-CF 2 HO 1-2137 Two CF 3 8-CF 2 HO 1-2138 Two CF 3 2-CClH 2 O 1-2139 Two CF 3 4-CClH 2 O 1-2140 Two CF 3 5-CClH 2 O 1-2141 Two CF 3 6-CClH 2 O 1-2142 Two CF 3 7-CClH 2 O 1-2143 Two CF 3 8-CClH 2 O 1-2144 Two CF 3 2,4-F 2 1-2145 two CF 3 2,5-F 2 1-2146 two CF 3 2,6-F 2 1-2147 two CF 3 2,7-F 2 1-2148 Two CF 3 2,8-F 2 1-2149 Two CF 3 4,5-F 2 1-2150 two CF 3 4,6-F 2 1-2151 Two CF 3 4,7-F 2 1-2152 Two CF 3 4,8-F 2 1-2153 Two CF 3 5,6-F 2 1-2154 Two CF 3 5,7-F 2 1-2155 two CF 3 5,8-F 2 1-2156 Two CF 3 6,7-F 2 1-2157 Two CF 3 6,8-F 2 1-2158 Two CF 3 7,8-F 2 1-2159 Two CF 3 4,5-Cl 2 1-2160 two CF 3 4,6-Cl 2 1-2161 Two CF 3 4,7-Cl 2 1-2162 Two CF 3 4,8-Cl 2 1-2163 Two CF 3 5,6-Cl 2 1-2164 Two CF 3 5,7-Cl 2 1-2165 Two CF 3 5,8-Cl 2 1-2166 Two CF 3 6,7-Cl 2 1-2167 Two CF 3 6,8-Cl 2 1-2168 Two CF 3 7,8-Cl 2 1-2169 Two CF 3 2,5-Me 2 1-2170 Two CF 3 2,6-Me 2 1-2171 two CF 3 2,7-Me 2 1-2172 two CF 3 2,8-Me 2 1-2173 two CF 3 4,5-Me 2 1-2174 two CF 3 4,6-Me 2 1-2175 two CF 3 4,7-Me 2 1-2176 two CF 3 4,8-Me 2 1-2177 Two CF 3 5,6-Me 2 1-2178 Two CF 3 5,7-Me 2 1-2179 Two CF 3 5,8-Me 2 1-2180 Two CF 3 6,7-Me 2 1-2181 Two CF 3 6,8-Me 2 1-2182 Two CF 3 7,8-Me 2 1-2183 Two CF 3 2,5- (MeO) 2 1-2184 Two CF 3 2,6- (MeO) 2 1-2185 two CF 3 2,7- (MeO) 2 1-2186 Two CF 3 2,8- (MeO) 2 1-2187 two CF 3 4,5- (MeO) 2 1-2188 Two CF 3 4,6- (MeO) 2 1-2189 two CF 3 4,7- (MeO) 2 1-2190 two CF 3 4,8- (MeO) 2 1-2191 Two CF 3 5,6- (MeO) 2 1-2192 two CF 3 5,7- (MeO) 2 1-2193 Two CF 3 5,8- (MeO) 2 1-2194 Two CF 3 6,7- (MeO) 2 1-2195 Two CF 3 6,8- (MeO) 2 1-2196 Two CF 3 7,8- (MeO) 2 1-2197 Two CF 3 2-Me-5-F 1-2198 Two CF 3 2-Me-6-F 1-2199 Two CF 3 2-Me-7-F 1-2200 Two CF 3 2-Me-8-F 1-2201 Two CF 3 2-Me-5-Cl 1-2202 Two CF 3 2-Me-6-Cl 1-2203 Two CF 3 2-Me-7-Cl 1-2204 Two CF 3 2-Me-8-Cl 1-2205 Two CF 3 2-Me-5-MeO 1-2206 Two CF 3 2-Me-6-MeO 1-2207 Two CF 3 2-Me-7-MeO 1-2208 Two CF 3 2-Me-8-MeO 1-2209 Two CF 3 4-Cl-5-F 1-2210 Two CF 3 4-Cl-6-F 1-2211 Two CF 3 4-Cl-7-F 1-2212 Two CF 3 4-Cl-8-F 1-2213 Two CF 3 4-Cl-5-Me 1-2214 Two CF 3 4-Cl-6-Me 1-2215 Two CF 3 4-Cl-7-Me 1-2216 Two CF 3 4-Cl-8-Me 1-2217 Two CF 3 4-Cl-5-MeO 1-2218 Two CF 3 4-Cl-6-MeO 1-2219 Two CF 3 4-Cl-7-MeO 1-2220 Two CF 3 4-Cl-8-MeO 1-2221 Single cPr H 1-2222 Single cPr 2-F 1-2223 Single cPr 4-F 1-2224 Single cPr 5-F 1-2225 Single cPr 6-F 1-2226 Single cPr 7-F 1-2227 Single cPr 8-F 1-2228 Single cPr 2-Cl 1-2229 Single cPr 4-Cl 1-2230 Single cPr 5-Cl 1-2231 Single cPr 6-Cl 1-2232 Single cPr 7- Cl 1-2233 Single cPr 8-Cl 1-2234 Single cPr 2-Br 1-2235 Single cPr 4-Br 1-2236 Single cPr 5-Br 1-2237 Single cPr 6-Br 1-2238 Single cPr 7-Br 1 -2239 Single cPr 8-Br 1-2240 Single cPr 2-I 1-2241 Single cPr 4-I 1-2242 Single cPr 5-I 1-2243 Single cPr 6-I 1-2244 Single cPr 7-I 1-2245 Single cPr 8-I 1-2246 Single cPr 2-Me 1-2247 Single cPr 4-Me 1-2248 Single cPr 5-Me 1-2249 Single cPr 6-Me 1-2250 Single cPr 7-Me 1-2251 Single cPr 8-Me 1-2252 Single cPr 2-Et 1-2253 Single cPr 4-Et 1-2254 Single cPr 5-Et 1-2255 Single cPr 6-Et 1-2256 Single cPr 7-Et 1-2257 Single cPr 8- Et 1-2258 Single cPr 2-Pr 1-2259 Single cPr 4-Pr 1-2260 Single cPr 5-Pr 1-2261 Single cPr 6-Pr 1-2262 Single cPr 7-Pr 1-2263 Single cPr 8-Pr 1 -2264 Single cPr 2-iPr 1-2265 Single cPr 4-iPr 1-2266 Single cPr 5-iPr 1-2267 Single cPr 6-iPr 1-2268 Single cPr 7-iPr 1-2269 Single cPr 8-iPr 1-2270 Single cPr 2-B u 1-2271 Single cPr 4-Bu 1-2272 Single cPr 5-Bu 1-2273 Single cPr 6-Bu 1-2274 Single cPr 7-Bu 1-2275 Single cPr 8-Bu 1-2276 Single cPr 2-CF 3 1-2277 Single cPr 4-CF 3 1-2278 Single cPr 5-CF 3 1-2279 Single cPr 6-CF 3 1-2280 Single cPr 7-CF 3 1-2281 Single cPr 8-CF 3 1-2282 Single cPr 2-CF 3 CH 2 1-2283 Single cPr 4-CF 3 CH 2 1-2284 Single cPr 5-CF 3 CH 2 1-2285 Single cPr 6-CF 3 CH 2 1-2286 Single cPr 7-CF 3 CH 2 1-2287 Single cPr 8-CF 3 CH 2 1-2288 Single cPr 2-CF 2 H 1-2289 Single cPr 4-CF 2 H 1-2290 Single cPr 5-CF 2 H 1-2291 Single cPr 6-CF 2 H 1-2292 Single cPr 7-CF 2 H 1-2293 Single cPr 8-CF 2 H 1-2294 Single cPr 2-CF 2 H 1-2295 Single cPr 4-CF 2 H 1-2296 Single cPr 5-CF 2 H 1-2297 Single cPr 6-CF 2 H 1-2298 Single cPr 7-CF 2 H 1-2299 Single cPr 8-CF 2 H 1-2300 Single cPr 2-CClH 2 1-2301 Single cPr 4-CClH 2 1-2302 Single cPr 5-CClH 2 1-2303 Single cPr 6-CClH 2 1-2304 Single cPr 7-CClH 2 1-2305 Single cPr 8-CClH 2 1-2306 Single cPr 2-MeO 1-2307 Single cPr 4-MeO 1-2308 Single cPr 5-MeO 1-2309 Single cPr 6-MeO 1-2310 Single cPr 7-MeO 1-2311 Single cPr 8-MeO 1- 2312 Single cPr 2-EtO 1-2313 Single cPr 4-EtO 1-2314 Single cPr 5-EtO 1-2315 Single cPr 6-EtO 1-2316 Single cPr 7-EtO 1-2317 Single cPr 8-EtO 1-2318 Single cPr 2-PrO 1-2319 single cPr 4-PrO 1-2320 single cPr 5-PrO 1-2321 single cPr 6-PrO 1-2322 single cPr 7-PrO 1-2323 single cPr 8-PrO 1-2324 single cPr 2 -iPrO 1-2325 single cPr 4-iPrO 1-2326 single cPr 5-iPrO 1-2327 single cPr 6-iPrO 1-2328 single cPr 7-iPrO 1-2329 single cPr 8-iPrO 1-2330 single cPr 2-BuO 1-2331 Single cPr 4-BuO 1-2332 Single cPr 5-BuO 1-2333 Single cPr 6-BuO 1-2334 Single cPr 7-BuO 1-2335 Single cPr 8-BuO 1-2336 Single cPr 2-CF 3 O 1-2337 Single cPr 4-CF 3 O 1-2338 Single cPr 5-CF 3 O 1-2339 Single cPr 6-CF 3 O 1-2340 Single cPr 7-CF 3 O 1-2341 Single cPr 8-CF 3 O 1-2342 Single cPr 2-CF 3 CH 2 O 1-2343 Single cPr 4-CF 3 CH 2 O 1-2344 Single cPr 5-CF 3 CH 2 O 1-2345 Single cPr 6-CF 3 CH 2 O 1-2346 Single cPr 7-CF 3 CH 2 O 1-2347 Single cPr 8-CF 3 CH 2 O 1-2348 Single cPr 2-CF 2 HO 1-2349 Single cPr 4-CF 2 HO 1-2350 Single cPr 5-CF 2 HO 1-2351 Single cPr 6-CF 2 HO 1-2352 Single cPr 7-CF 2 HO 1-2353 Single cPr 8-CF 2 HO 1-2354 Single cPr 2-CF 2 HO 1-2355 Single cPr 4-CF 2 HO 1-2356 Single cPr 5-CF 2 HO 1-2357 Single cPr 6-CF 2 HO 1-2358 Single cPr 7-CF 2 HO 1-2359 Single cPr 8-CF 2 HO 1-2360 Single cPr 2-CClH 2 O 1-2361 Single cPr 4-CClH 2 O 1-2362 Single cPr 5-CClH 2 O 1-2363 Single cPr 6-CClH 2 O 1-2364 Single cPr 7-CClH 2 O 1-2365 Single cPr 8-CClH 2 O 1-2366 Single cPr 2,4-F 2 1-2367 Single cPr 2,5-F 2 1-2368 Single cPr 2,6-F 2 1-2369 Single cPr 2,7-F 2 1-2370 Single cPr 2,8-F 2 1-2371 Single cPr 4,5-F 2 1-2372 Single cPr 4,6-F 2 1-2373 Single cPr 4,7-F 2 1-2374 Single cPr 4,8-F 2 1-2375 Single cPr 5,6-F 2 1-2376 Single cPr 5,7-F 2 1-2377 Single cPr 5,8-F 2 1-2378 Single cPr 6,7-F 2 1-2379 Single cPr 6,8-F 2 1-2380 Single cPr 7,8-F 2 1-2381 Single cPr 4,5-Cl 2 1-2382 Single cPr 4,6-Cl 2 1-2383 Single cPr 4,7-Cl 2 1-2384 Single cPr 4,8-Cl 2 1-2385 Single cPr 5,6-Cl 2 1-2386 Single cPr 5,7-Cl 2 1-2387 Single cPr 5,8-Cl 2 1-2388 Single cPr 6,7-Cl 2 1-2389 Single cPr 6,8-Cl 2 1-2390 Single cPr 7,8-Cl 2 1-2391 Single cPr 2,5-Me 2 1-2392 Single cPr 2,6-Me 2 1-2393 Single cPr 2,7-Me 2 1-2394 Single cPr 2,8-Me 2 1-2395 Single cPr 4,5-Me 2 1-2396 Single cPr 4,6-Me 2 1-2397 Single cPr 4,7-Me 2 1-2398 Single cPr 4,8-Me 2 1-2399 Single cPr 5,6-Me 2 1-2400 Single cPr 5,7-Me 2 1-2401 Single cPr 5,8-Me 2 1-2402 Single cPr 6,7-Me 2 1-2403 Single cPr 6,8-Me 2 1-2404 Single cPr 7,8-Me 2 1-2405 Single cPr 2,5- (MeO) 2 1-2406 Single cPr 2,6- (MeO) 2 1-2407 Single cPr 2,7- (MeO) 2 1-2408 Single cPr 2,8- (MeO) 2 1-2409 Single cPr 4,5- (MeO) 2 1-2410 Single cPr 4,6- (MeO) 2 1-2411 Single cPr 4,7- (MeO) 2 1-2412 Single cPr 4,8- (MeO) 2 1-2413 Single cPr 5,6- (MeO) 2 1-2414 Single cPr 5,7- (MeO) 2 1-2415 Single cPr 5,8- (MeO) 2 1-2416 Single cPr 6,7- (MeO) 2 1-2417 Single cPr 6,8- (MeO) 2 1-2418 Single cPr 7,8- (MeO) 2 1-2419 Single cPr 2-Me-5-F 1-2420 Single cPr 2-Me-6-F 1-2421 Single cPr 2-Me-7-F 1-2422 Single cPr 2-Me-8-F 1- 2423 Single cPr 2-Me-5-Cl 1-2424 Single cPr 2-Me-6-Cl 1-2425 Single cPr 2-Me-7-Cl 1-2426 Single cPr 2-Me-8-Cl 1-2427 Single cPr 2-Me-5-MeO 1-2428 single cPr 2-Me-6-MeO 1-2429 single cPr 2-Me-7-MeO 1-2430 single cPr 2-Me-8-MeO 1-2431 single cPr 4 -Cl-5-F 1-2432 Single cPr 4-Cl-6-F 1-2433 Single cPr 4-Cl-7-F 1-2434 Single cPr 4-Cl-8-F 1-2435 Single cPr 4-Cl -5-Me 1-2436 Single cPr 4-Cl-6-Me 1-2437 Single cPr 4-Cl-7-Me 1-2438 Single cPr 4-Cl-8-Me 1-2439 Single cPr 4-Cl-5 -MeO 1-2440 single cPr 4-Cl-6-MeO 1-2441 single cPr 4-Cl-7-MeO 1-2442 single cPr 4-Cl-8-MeO 1-2443 single Allyl H 1-2444 single Allyl 2 -F 1-2445 Single Allyl 4-F 1-2446 Single Allyl 5-F 1-2447 Single Allyl 6-F 1-2448 Single Allyl 7-F 1-2449 Single Allyl 8-F 1-2450 Single Allyl 2-Cl 1-2451 Single Allyl 4-Cl 1-2452 Single Allyl 5-Cl 1-2453 Single Allyl 6-Cl 1-2454 Single Allyl 7-Cl 1-2455 Single Allyl 8-Cl 1-2456 Single Allyl 2-Br 1- 2457 Single Allyl 4-Br 1-2458 Single Allyl 5-Br 1-2459 Single Allyl 6-Br 1-2460 Single Allyl 7-Br 1-2461 Single Al lyl 8-Br 1-2462 Single Allyl 2-I 1-2463 Single Allyl 4-I 1-2464 Single Allyl 5-I 1-2465 Single Allyl 6-I 1-2466 Single Allyl 7-I 1-2467 Single Allyl 8 -I 1-2468 Single Allyl 2-Me 1-2469 Single Allyl 4-Me 1-2470 Single Allyl 5-Me 1-2471 Single Allyl 6-Me 1-2472 Single Allyl 7-Me 1-2473 Single Allyl 8-Me 1-2474 Single Allyl 2-Et 1-2475 Single Allyl 4-Et 1-2476 Single Allyl 5-Et 1-2477 Single Allyl 6-Et 1-2478 Single Allyl 7-Et 1-2479 Single Allyl 8-Et 1- 2480 Single Allyl 2-Pr 1-2481 Single Allyl 4-Pr 1-2482 Single Allyl 5-Pr 1-2483 Single Allyl 6-Pr 1-2484 Single Allyl 7-Pr 1-2485 Single Allyl 8-Pr 1-2486 Single Allyl 2-iPr 1-2487 single Allyl 4-iPr 1-2488 single Allyl 5-iPr 1-2489 single Allyl 6-iPr 1-2490 single Allyl 7-iPr 1-2491 single Allyl 8-iPr 1-2492 single Allyl 2 -Bu 1-2493 Single Allyl 4-Bu 1-2494 Single Allyl 5-Bu 1-2495 Single Allyl 6-Bu 1-2496 Single Allyl 7-Bu 1-2497 Single Allyl 8-Bu 1-2498 Single Allyl 2-CF 3 1-2499 Single Allyl 4-CF 3 1-2500 Single Allyl 5-CF 3 1-2501 Single Allyl 6-CF 3 1-2502 Single Allyl 7-CF 3 1-2503 Single Allyl 8-CF 3 1-2504 Single Allyl 2-CF 3 CH 2 1-2505 Single Allyl 4-CF 3 CH 2 1-2506 Single Allyl 5-CF 3 CH 2 1-2507 Single Allyl 6-CF 3 CH 2 1-2508 Single Allyl 7-CF 3 CH 2 1-2509 Single Allyl 8-CF 3 CH 2 1-2510 Single Allyl 2-CF 2 H 1-2511 Single Allyl 4-CF 2 H 1-2512 Single Allyl 5-CF 2 H 1-2513 Single Allyl 6-CF 2 H 1-2514 Single Allyl 7-CF 2 H 1-2515 Single Allyl 8-CF 2 H 1-2516 Single Allyl 2-CF 2 H 1-2517 Single Allyl 4-CF 2 H 1-2518 Single Allyl 5-CF 2 H 1-2519 Single Allyl 6-CF 2 H 1-2520 Single Allyl 7-CF 2 H 1-2521 Single Allyl 8-CF 2 H 1-2522 Single Allyl 2-CClH 2 1-2523 Single Allyl 4-CClH 2 1-2524 Single Allyl 5-CClH 2 1-2525 Single Allyl 6-CClH 2 1-2526 Single Allyl 7-CClH 2 1-2527 Single Allyl 8-CClH 2 1-2528 Single Allyl 2-MeO 1-2529 Single Allyl 4-MeO 1-2530 Single Allyl 5-MeO 1-2531 Single Allyl 6-MeO 1-2532 Single Allyl 7-MeO 1-2533 Single Allyl 8-MeO 1- 2534 Single Allyl 2-EtO 1-2535 Single Allyl 4-EtO 1-2536 Single Allyl 5-EtO 1-2537 Single Allyl 6-EtO 1-2538 Single Allyl 7-EtO 1-2539 Single Allyl 8-EtO 1-2540 Single Allyl 2-PrO 1-2541 Single Allyl 4-PrO 1-2542 Single Allyl 5-PrO 1-2543 Single Allyl 6-PrO 1-2544 Single Allyl 7-PrO 1-2545 Single Allyl 8-PrO 1-2546 Single Allyl 2 -iPrO 1-2547 Single Allyl 4-iPrO 1-2548 Single Allyl 5-iPrO 1-2549 Single Allyl 6-iPrO 1-2550 Single Allyl 7-iPrO 1-2551 Single Allyl 8-iPrO 1-2552 Single Allyl 2-BuO 1-2553 Single Allyl 4-BuO 1-2554 Single Allyl 5-BuO 1-2555 Single Allyl 6-BuO 1-2556 Single Allyl 7-BuO 1-2557 Single Allyl 8-BuO 1-2558 Single Allyl 2-CF 3 O 1-2559 Single Allyl 4-CF 3 O 1-2560 Single Allyl 5-CF 3 O 1-2561 Single Allyl 6-CF 3 O 1-2562 Single Allyl 7-CF 3 O 1-2563 Single Allyl 8-CF 3 O 1-2564 Single Allyl 2-CF 3 CH 2 O 1-2565 Single Allyl 4-CF 3 CH 2 O 1-2566 Single Allyl 5-CF 3 CH 2 O 1-2567 Single Allyl 6-CF 3 CH 2 O 1-2568 Single Allyl 7-CF 3 CH 2 O 1-2569 Single Allyl 8-CF 3 CH 2 O 1-2570 Single Allyl 2-CF 2 HO 1-2571 Single Allyl 4-CF 2 HO 1-2572 Single Allyl 5-CF 2 HO 1-2573 Single Allyl 6-CF 2 HO 1-2574 Single Allyl 7-CF 2 HO 1-2575 Single Allyl 8-CF 2 HO 1-2576 Single Allyl 2-CF 2 HO 1-2577 Single Allyl 4-CF 2 HO 1-2578 Single Allyl 5-CF 2 HO 1-2579 Single Allyl 6-CF 2 HO 1-2580 Single Allyl 7-CF 2 HO 1-2581 Single Allyl 8-CF 2 HO 1-2582 Single Allyl 2-CClH 2 O 1-2583 Single Allyl 4-CClH 2 O 1-2584 Single Allyl 5-CClH 2 O 1-2585 Single Allyl 6-CClH 2 O 1-2586 Single Allyl 7-CClH 2 O 1-2587 Single Allyl 8-CClH 2 O 1-2588 Single Allyl 2,4-F 2 1-2589 Single Allyl 2,5-F 2 1-2590 Single Allyl 2,6-F 2 1-2591 Single Allyl 2,7-F 2 1-2592 Single Allyl 2,8-F 2 1-2593 Single Allyl 4,5-F 2 1-2594 Single Allyl 4,6-F 2 1-2595 Single Allyl 4,7-F 2 1-2596 Single Allyl 4,8-F 2 1-2597 Single Allyl 5,6-F 2 1-2598 Single Allyl 5,7-F 2 1-2599 Single Allyl 5,8-F 2 1-2600 Single Allyl 6,7-F 2 1-2601 Single Allyl 6,8-F 2 1-2602 Single Allyl 7,8-F 2 1-2603 Single Allyl 4,5-Cl 2 1-2604 Single Allyl 4,6-Cl 2 1-2605 Single Allyl 4,7-Cl 2 1-2606 Single Allyl 4,8-Cl 2 1-2607 Single Allyl 5,6-Cl 2 1-2608 Single Allyl 5,7-Cl 2 1-2609 Single Allyl 5,8-Cl 2 1-2610 Single Allyl 6,7-Cl 2 1-2611 Single Allyl 6,8-Cl 2 1-2612 Single Allyl 7,8-Cl 2 1-2613 Single Allyl 2,5-Me 2 1-2614 Single Allyl 2,6-Me 2 1-2615 Single Allyl 2,7-Me 2 1-2616 Single Allyl 2,8-Me 2 1-2617 Single Allyl 4,5-Me 2 1-2618 Single Allyl 4,6-Me 2 1-2619 Single Allyl 4,7-Me 2 1-2620 Single Allyl 4,8-Me 2 1-2621 Single Allyl 5,6-Me 2 1-2622 Single Allyl 5,7-Me 2 1-2623 Single Allyl 5,8-Me 2 1-2624 Single Allyl 6,7-Me 2 1-2625 Single Allyl 6,8-Me 2 1-2626 Single Allyl 7,8-Me 2 1-2627 Single Allyl 2,5- (MeO) 2 1-2628 Single Allyl 2,6- (MeO) 2 1-2629 Single Allyl 2,7- (MeO) 2 1-2630 Single Allyl 2,8- (MeO) 2 1-2631 Single Allyl 4,5- (MeO) 2 1-2632 Single Allyl 4,6- (MeO) 2 1-2633 Single Allyl 4,7- (MeO) 2 1-2634 Single Allyl 4,8- (MeO) 2 1-2635 Single Allyl 5,6- (MeO) 2 1-2636 Single Allyl 5,7- (MeO) 2 1-2637 Single Allyl 5,8- (MeO) 2 1-2638 Single Allyl 6,7- (MeO) 2 1-2639 Single Allyl 6,8- (MeO) 2 1-2640 Single Allyl 7,8- (MeO) 2 1-2641 Single Allyl 2-Me-5-F 1-2642 Single Allyl 2-Me-6-F 1-2643 Single Allyl 2-Me-7-F 1-2644 Single Allyl 2-Me-8-F 1- 2645 Mono Allyl 2-Me-5-Cl 1-2646 Mono Allyl 2-Me-6-Cl 1-2647 Mono Allyl 2-Me-7-Cl 1-2648 Mono Allyl 2-Me-8-Cl 1-2649 Mono Allyl 2-Me-5-MeO 1-2650 Single Allyl 2-Me-6-MeO 1-2651 Single Allyl 2-Me-7-MeO 1-2652 Single Allyl 2-Me-8-MeO 1-2653 Single Allyl 4 -Cl-5-F 1-2654 Mono Allyl 4-Cl-6-F 1-2655 Mono Allyl 4-Cl-7-F 1-2656 Mono Allyl 4-Cl-8-F 1-2657 Mono Allyl 4-Cl -5-Me 1-2658 Single Allyl 4-Cl-6-Me 1-2659 Single Allyl 4-Cl-7-Me 1-2660 Single Allyl 4-Cl-8-Me 1-2661 Single Allyl 4-Cl-5 -MeO 1-2662 Single Allyl 4-Cl-6-MeO 1-2663 Single Allyl 4-Cl-7-MeO 1-2664 Single Allyl 4-Cl-8-MeO 1-2665 Single tBu H 1-2666 Single tBu 2 -F 1-2667 Single tBu 4-F 1-2668 Single tBu 5-F 1-2669 Single tBu 6-F 1-2670 Single tBu 7-F 1-2671 Single tBu 8-F 1-2672 Single tBu 2-Cl 1-2673 Single tBu 4-Cl 1-2674 Single tBu 5-Cl 1-2675 Single tBu 6-Cl 1-2676 Single tBu 7-Cl 1-2677 Single tBu 8-Cl 1-2678 Single tBu 2-Me 1- 2679 Single tBu 4-Me 1-2680 Single tBu 5-Me 1-2681 Single tBu 6-Me 1-2682 Single tBu 7-Me 1 -2683 Single tBu 8-Me 1-2684 Single tBu 2-Et 1-2685 Single tBu 4-Et 1-2686 Single tBu 5-Et 1-2687 Single tBu 6-Et 1-2688 Single tBu 7-Et 1-2689 Single tBu 8-Et 1-2690 Single tBu 2,4-F 2 1-2691 Single tBu 2,5-F 2 1-2692 Single tBu 2,6-F 2 1-2693 Single tBu 2,7-F 2 1-2694 Single tBu 2,8-F 2 1-2695 Single tBu 4,5-F 2 1-2696 Single tBu 4,6-F 2 1-2697 Single tBu 4,7-F 2 1-2698 Single tBu 4,8-F 2 1-2699 Single tBu 5,6-F 2 1-2700 Single tBu 5,7-F 2 1-2701 Single tBu 5,8-F 2 1-2702 Single tBu 6,7-F 2 1-2703 Single tBu 6,8-F 2 1-2704 Single tBu 7,8-F 2 1-2705 Single tBu 2,4-Me 2 1-2706 Single tBu 2,5-Me 2 1-2707 Single tBu 2,6-Me 2 1-2708 Single tBu 2,7-Me 2 1-2709 Single tBu 2,8-Me 2 1-2710 Single tBu 4,5-Me 2 1-2711 Single tBu 4,6-Me 2 1-2712 Single tBu 4,7-Me 2 1-2713 Single tBu 4,8-Me 2 1-2714 Single tBu 5,6-Me 2 1-2715 Single tBu 5,7-Me 2 1-2716 Single tBu 5,8-Me 2 1-2717 Single tBu 6,7-Me 2 1-2718 Single tBu 6,8-Me 2 1-2719 Single tBu 7,8-Me 2 1-2720 Single tBu 2-Me-5-F 1-2721 Single tBu 2-Me-6-F 1-2722 Single tBu 2-Me-7-F 1-2723 Single tBu 2-Me-8-F 1- 2724 Single tBu 2-Me-5-Cl 1-2725 Single tBu 2-Me-6-Cl 1-2726 Single tBu 2-Me-7-Cl 1-2727 Single tBu 2-Me-8-Cl 1-2728 Single tBu 2-Me-5-MeO 1-2729 single tBu 2-Me-6-MeO 1-2730 single tBu 2-Me-7-MeO 1-2731 single tBu 2-Me-8-MeO 1-2732 single Pent H 1-2733 Single Pent 2-F 1-2734 Single Pent 4-F 1-2735 Single Pent 5-F 1-2736 Single Pent 6-F 1-2737 Single Pent 7-F 1-2738 Single Pent 8-F 1- 2739 Single Pent 2-Cl 1-2740 Single Pent 4-Cl 1-2741 Single Pent 5-Cl 1-2742 Single Pent 6-Cl 1-2743 Single Pent 7-Cl 1-2744 Single Pent 8-Cl 1-2745 Single Pent 2-Me 1-2746 Single Pent 4-Me 1-2747 Single Pent 5-Me 1-2748 Single Pent 6-Me 1-2749 Single Pent 7-Me 1-2750 Single Pent 8-Me 1-2751 Single Pent 2 -Et 1-2752 Single Pent 4-Et 1-2753 Single Pent 5-Et 1-2754 Single Pent 6-Et 1-2755 Single Pent 7-Et 1-2756 Single Pent 8-Et 1-2757 Single Pent 2,4 -F 2 1-2758 Single Pent 2,5-F 2 1-2759 Single Pent 2,6-F 2 1-2760 Single Pent 2,7-F 2 1-2761 Single Pent 2,8-F 2 1-2762 Single Pent 4,5-F 2 1-2763 Single Pent 4,6-F 2 1-2764 Single Pent 4,7-F 2 1-2765 Single Pent 4,8-F 2 1-2766 Single Pent 5,6-F 2 1-2767 Single Pent 5,7-F 2 1-2768 Single Pent 5,8-F 2 1-2769 Single Pent 6,7-F 2 1-2770 Single Pent 6,8-F 2 1-2771 Single Pent 7,8-F 2 1-2772 Single Pent 2,4-Me 2 1-2773 Single Pent 2,5-Me 2 1-2774 Single Pent 2,6-Me 2 1-2775 Single Pent 2,7-Me 2 1-2776 Single Pent 2,8-Me 2 1-2777 Single Pent 4,5-Me 2 1-2778 Single Pent 4,6-Me 2 1-2779 Single Pent 4,7-Me 2 1-2780 Single Pent 4,8-Me 2 1-2781 Single Pent 5,6-Me 2 1-2782 Single Pent 5,7-Me 2 1-2783 Single Pent 5,8-Me 2 1-2784 Single Pent 6,7-Me 2 1-2785 Single Pent 6,8-Me 2 1-2786 Single Pent 7,8-Me 2 1-2787 Single Pent 2-Me-5-F 1-2788 Single Pent 2-Me-6-F 1-2789 Single Pent 2-Me-7-F 1-2790 Single Pent 2-Me-8-F 1- 2791 Single Pent 2-Me-5-Cl 1-2792 Single Pent 2-Me-6-Cl 1-2793 Single Pent 2-Me-7-Cl 1-2794 Single Pent 2-Me-8-Cl 1-2795 Single Pent 2-Me-5-MeO 1-2796 Single Pent 2-Me-6-MeO 1-2797 Single Pent 2-Me-7-MeO 1-2798 Single Pent 2-Me-8-MeO 1-2799 Single Hex H 1-2800 Single Hex 2-F 1-2801 Single Hex 4-F 1-2802 Single Hex 5-F 1-2803 Single Hex 6-F 1-2804 Single Hex 7-F 1-2805 Single Hex 8-F 1- 2806 Single Hex 2-Cl 1-2807 Single Hex 4-Cl 1-2808 Single Hex 5-Cl 1-2809 Single Hex 6-Cl 1-2810 Single Hex 7-Cl 1-2811 Single Hex 8-Cl 1-2812 Single Hex 2-Me 1-2813 Single Hex 4-Me 1-2814 Single Hex 5-Me 1-2815 Single Hex 6-Me 1-2816 Single Hex 7-Me 1-2817 Single Hex 8-Me 1-2818 Single Hex 2 -Et 1-2819 Single Hex 4-Et 1-2820 Single Hex 5-Et 1-2821 Single Hex 6-Et 1-2822 Single Hex 7-Et 1-2823 Single Hex 8-Et 1-2824 Single Hex 2,4 -F 2 1-2825 Single Hex 2,5-F 2 1-2826 Single Hex 2,6-F 2 1-2827 Single Hex 2,7-F 2 1-2828 Single Hex 2,8-F 2 1-2829 Single Hex 4,5-F 2 1-2830 Single Hex 4,6-F 2 1-2831 Single Hex 4,7-F 2 1-2832 Single Hex 4,8-F 2 1-2833 Single Hex 5,6-F 2 1-2834 Single Hex 5,7-F 2 1-2835 Single Hex 5,8-F 2 1-2836 Single Hex 6,7-F 2 1-2837 Single Hex 6,8-F 2 1-2838 Single Hex 7,8-F 2 1-2839 Single Hex 2,4-Me 2 1-2840 Single Hex 2,5-Me 2 1-2841 Single Hex 2,6-Me 2 1-2842 Single Hex 2,7-Me 2 1-2843 Single Hex 2,8-Me 2 1-2844 Single Hex 4,5-Me 2 1-2845 Single Hex 4,6-Me 2 1-2846 Single Hex 4,7-Me 2 1-2847 Single Hex 4,8-Me 2 1-2848 Single Hex 5,6-Me 2 1-2849 Single Hex 5,7-Me 2 1-2850 Single Hex 5,8-Me 2 1-2851 Single Hex 6,7-Me 2 1-2852 Single Hex 6,8-Me 2 1-2853 Single Hex 7,8-Me 2 1-2854 Single Hex 2-Me-5-F 1-2855 Single Hex 2-Me-6-F 1-2856 Single Hex 2-Me-7-F 1-2857 Single Hex 2-Me-8-F 1- 2858 Single Hex 2-Me-5-Cl 1-2859 Single Hex 2-Me-6-Cl 1-2860 Single Hex 2-Me-7-Cl 1-2861 Single Hex 2-Me-8-Cl 1-2862 Single Hex 2-Me-5-MeO 1-2863 single Hex 2-Me-6-MeO 1-2864 single Hex 2-Me-7-MeO 1-2865 single Hex 2-Me-8-MeO 1-2866 single 2- Et-Bu H 1-2867 Single 2-Et-Bu 2-F 1-2868 Single 2-Et-Bu 4-F 1-2869 Single 2-Et-Bu 5-F 1-2870 Single 2-Et-Bu 6 -F 1-2871 Single 2-Et-Bu 7-F 1-2872 Single 2-Et-Bu 8-F 1-2873 Single 2-Et-Bu 2-Cl 1-2874 Single 2-Et-Bu 4-Cl 1-2875 Single 2-Et-Bu 5-Cl 1-2876 Single 2-Et-Bu 6-Cl 1-2877 Single 2-Et-Bu 7-Cl 1-2878 Single 2-Et-Bu 8-Cl 1- 2879 Single 2-Et-Bu 2-Me 1-2880 Single 2-Et-Bu 4-Me 1-2881 Single 2-Et-Bu 5-Me 1-2882 Single 2-Et-Bu 6-Me 1-2883 Single 2-Et-Bu 7-Me 1-2884 Single 2-Et-Bu 8-Me 1-2885 Single 2-Et-Bu 2-Et 1-2886 Single 2-Et-Bu 4-Et 1-2887 Single 2- Et-Bu 5-Et 1-2888 Single 2-Et-Bu 6-Et 1-2889 Single 2-Et-Bu 7-Et 1-2890 Single 2-Et-Bu 8-Et 1-2891 Single 2-Et- Bu 2,4-F 2 1-2892 Single 2-Et-Bu 2,5-F 2 1-2893 Single 2-Et-Bu 2,6-F 2 1-2894 Single 2-Et-Bu 2,7-F 2 1-2895 Single 2-Et-Bu 2,8-F 2 1-2896 Single 2-Et-Bu 4,5-F 2 1-2897 Single 2-Et-Bu 4,6-F 2 1-2898 Single 2-Et-Bu 4,7-F 2 1-2899 Single 2-Et-Bu 4,8-F 2 1-2900 Single 2-Et-Bu 5,6-F 2 1-2901 Single 2-Et-Bu 5,7-F 2 1-2902 Single 2-Et-Bu 5,8-F 2 1-2903 Single 2-Et-Bu 6,7-F 2 1-2904 Single 2-Et-Bu 6,8-F 2 1-2905 Single 2-Et-Bu 7,8-F 2 1-2906 Single 2-Et-Bu 2,4-Me 2 1-2907 Single 2-Et-Bu 2,5-Me 2 1-2908 Single 2-Et-Bu 2,6-Me 2 1-2909 Single 2-Et-Bu 2,7-Me 2 1-2910 Single 2-Et-Bu 2,8-Me 2 1-2911 Single 2-Et-Bu 4,5-Me 2 1-2912 Single 2-Et-Bu 4,6-Me 2 1-2913 Single 2-Et-Bu 4,7-Me 2 1-2914 Single 2-Et-Bu 4,8-Me 2 1-2915 Single 2-Et-Bu 5,6-Me 2 1-2916 Single 2-Et-Bu 5,7-Me 2 1-2917 Single 2-Et-Bu 5,8-Me 2 1-2918 Single 2-Et-Bu 6,7-Me 2 1-2919 Single 2-Et-Bu 6,8-Me 2 1-2920 Single 2-Et-Bu 7,8-Me 2 1-2921 Single 2-Et-Bu 2-Me-5-F 1-2922 Single 2-Et-Bu 2-Me-6-F 1-2923 Single 2-Et-Bu 2-Me-7-F 1- 2924 Single 2-Et-Bu 2-Me-8-F 1-2925 Single 2-Et-Bu 2-Me-5-Cl 1-2926 Single 2-Et-Bu 2-Me-6-Cl 1-2927 Single 2-Et-Bu 2-Me-7-Cl 1-2928 Single 2-Et-Bu 2-Me-8-Cl 1-2929 Single 2-Et-Bu 2-Me-5-MeO 1-2930 Single 2- Et-Bu 2-Me-6-MeO 1-2931 Single 2-Et-Bu 2-Me-7-MeO 1-2932 Single 2-Et-Bu 2-Me-8-MeO 1-2933 Single Hept H 1- 2934 Single Hept 2-F 1-2935 Single Hept 4-F 1-2936 Single Hept 5-F 1-2937 Single Hept 6-F 1-2938 Single Hept 7-F 1-2939 Single Hept 8-F 1-2940 Single Hept 2-Cl 1-2941 Single Hept 4-Cl 1-2942 Single Hept 5-Cl 1-2943 Single Hept 6-Cl 1-2944 Single Hept 7-Cl 1-2945 Single Hept 8-Cl 1-2946 Single Hept 2 -Me 1-2947 Single Hept 4-Me 1-2948 Single Hept 5-Me 1-2949 Single Hept 6-Me 1-2950 Single Hept 7-Me 1-2951 Single Hept 8-Me 1-2952 Single Hept 2-Et 1-2953 Single Hept 4-Et 1-2954 Single Hept 5-Et 1-2955 Single Hept 6-Et 1-2956 Single Hept 7-Et 1-2957 Single Hept 8-Et 1-2958 Single Hept 2,4-F 2 1-2959 Single Hept 2,5-F 2 1-2960 Single Hept 2,6-F 2 1-2961 Single Hept 2,7-F 2 1-2962 Single Hept 2,8-F 2 1-2963 Single Hept 4,5-F 2 1-2964 Single Hept 4,6-F 2 1-2965 Single Hept 4,7-F 2 1-2966 Single Hept 4,8-F 2 1-2967 Single Hept 5,6-F 2 1-2968 Single Hept 5,7-F 2 1-2969 Single Hept 5,8-F 2 1-2970 Single Hept 6,7-F 2 1-2971 Single Hept 6,8-F 2 1-2972 Single Hept 7,8-F 2 1-2973 Single Hept 2,4-Me 2 1-2974 Single Hept 2,5-Me 2 1-2975 Single Hept 2,6-Me 2 1-2976 Single Hept 2,7-Me 2 1-2977 Single Hept 2,8-Me 2 1-2978 Single Hept 4,5-Me 2 1-2979 Single Hept 4,6-Me 2 1-2980 Single Hept 4,7-Me 2 1-2981 Single Hept 4,8-Me 2 1-2982 Single Hept 5,6-Me 2 1-2983 Single Hept 5,7-Me 2 1-2984 Single Hept 5,8-Me 2 1-2985 Single Hept 6,7-Me 2 1-2986 Single Hept 6,8-Me 2 1-2987 Single Hept 7,8-Me 2 1-2988 Single Hept 2-Me-5-F 1-2989 Single Hept 2-Me-6-F 1-2990 Single Hept 2-Me-7-F 1-2991 Single Hept 2-Me-8-F 1- 2992 Single Hept 2-Me-5-Cl 1-2993 Single Hept 2-Me-6-Cl 1-2994 Single Hept 2-Me-7-Cl 1-2995 Single Hept 2-Me-8-Cl 1-2996 Single Hept 2-Me-5-MeO 1-2997 Single Hept 2-Me-6-MeO 1-2998 Single Hept 2-Me-7-MeO 1-2999 Single Hept 2-Me-8-MeO 1-3000 Single Oct H 1-3001 Single Oct 2-F 1-3002 Single Oct 4-F 1-3003 Single Oct 5-F 1-3004 Single Oct 6-F 1-3005 Single Oct 7-F 1-3006 Single Oct 8-F 1- 3007 single Oct 2-Cl 1-3008 single Oct 4-Cl 1-3009 single Oct 5-Cl 1-3010 single Oct 6-Cl 1-3011 single Oct 7-Cl 1-3012 single Oct 8-Cl 1-3013 single Oct 2-Me 1-3014 single Oct 4-Me 1-3015 single Oct 5-Me 1-3016 single Oct 6-Me 1-3017 single Oct 7-Me 1-3018 single Oct 8-Me 1-3019 single Oct 2 -Et 1-3020 Single Oct 4-Et 1-3023 Single Oct 7-Et 1-3024 Single Oct 8-Et 1-3025 Single Oct 2,4-F 2 1-3026 Single Oct 2,5-F 2 1-3027 Single Oct 2,6-F 2 1-3028 Single Oct 2,7-F 2 1-3029 Single Oct 2,8-F 2 1-3030 Single Oct 4,5-F 2 1-3031 Single Oct 4,6-F 2 1-3032 Single Oct 4,7-F 2 1-3033 Single Oct 4,8-F 2 1-3034 Single Oct 5,6-F 2 1-3035 Single Oct 5,7-F 2 1-3036 Single Oct 5,8-F 2 1-3037 Single Oct 6,7-F 2 1-3038 Single Oct 6,8-F 2 1-3039 Single Oct 7,8-F 2 1-3040 Single Oct 2,4-Me 2 1-3041 Single Oct 2,5-Me 2 1-3042 Single Oct 2,6-Me 2 1-3043 Single Oct 2,7-Me 2 1-3044 Single Oct 2,8-Me 2 1-3045 Single Oct 4,5-Me 2 1-3046 Single Oct 4,6-Me 2 1-3047 Single Oct 4,7-Me 2 1-3048 Single Oct 4,8-Me 2 1-3049 Single Oct 5,6-Me 2 1-3050 Single Oct 5,7-Me 2 1-3051 Single Oct 5,8-Me 2 1-3052 Single Oct 6,7-Me 2 1-3053 Single Oct 6,8-Me 2 1-3054 Single Oct 7,8-Me 2 1-3055 Single Oct 2-Me-5-F 1-3056 Single Oct 2-Me-6-F 1-3057 Single Oct 2-Me-7-F 1-3058 Single Oct 2-Me-8-F 1- 3059 Single Oct 2-Me-5-Cl 1-3060 Single Oct 2-Me-6-Cl 1-3061 Single Oct 2-Me-7-Cl 1-3062 Single Oct 2-Me-8-Cl 1-3063 Single Oct 2-Me-5-MeO 1-3064 single Oct 2-Me-6-MeO 1-3065 single Oct 2-Me-7-MeO 1-3066 single Oct 2-Me-8-MeO 1-3067 single FCH 2 H 1-3068 Single FCH 2 2-F 1-3069 Single FCH 2 4-F 1-3070 Single FCH 2 5-F 1-3071 Single FCH 2 6-F 1-3072 Single FCH 2 7-F 1-3073 Single FCH 2 8-F 1-3074 Single FCH 2 2-Cl 1-3075 Single FCH 2 4-Cl 1-3076 Single FCH 2 5-Cl 1-3077 Single FCH 2 6-Cl 1-3078 Single FCH 2 7-Cl 1-3079 Single FCH 2 8-Cl 1-3080 Single FCH 2 2-Me 1-3081 Single FCH 2 4-Me 1-3082 Single FCH 2 5-Me 1-3083 Single FCH 2 6-Me 1-3084 Single FCH 2 7-Me 1-3085 Single FCH 2 8-Me 1-3086 Single FCH 2 2-Et 1-3087 Single FCH 2 4-Et 1-3088 Single FCH 2 5-Et 1-3089 Single FCH 2 6-Et 1-3090 Single FCH 2 7-Et 1-3091 Single FCH 2 8-Et 1-3092 Single FCH 2 2,4-F 2 1-3093 Single FCH 2 2,5-F 2 1-3094 Single FCH 2 2,6-F 2 1-3095 Single FCH 2 2,7-F 2 1-3096 Single FCH 2 2,8-F 2 1-3097 Single FCH 2 4,5-F 2 1-3098 Single FCH 2 4,6-F 2 1-3099 Single FCH 2 4,7-F 2 1-3100 Single FCH 2 4,8-F 2 1-3101 Single FCH 2 5,6-F 2 1-3102 Single FCH 2 5,7-F 2 1-3103 Single FCH 2 5,8-F 2 1-3104 Single FCH 2 6,7-F 2 1-3105 Single FCH 2 6,8-F 2 1-3106 Single FCH 2 7,8-F 2 1-3107 Single FCH 2 2,4-Me 2 1-3108 Single FCH 2 2,5-Me 2 1-3109 Single FCH 2 2,6-Me 2 1-3110 Single FCH 2 2,7-Me 2 1-3111 Single FCH 2 2,8-Me 2 1-3112 Single FCH 2 4,5-Me 2 1-3113 Single FCH 2 4,6-Me 2 1-3114 Single FCH 2 4,7-Me 2 1-3115 Single FCH 2 4,8-Me 2 1-3116 Single FCH 2 5,6-Me 2 1-3117 Single FCH 2 5,7-Me 2 1-3118 Single FCH 2 5,8-Me 2 1-3119 Single FCH 2 6,7-Me 2 1-3120 Single FCH 2 6,8-Me 2 1-3121 Single FCH 2 7,8-Me 2 1-3122 Single FCH 2 2-Me-5-F 1-3123 Single FCH 2 2-Me-6-F 1-3124 Single FCH 2 2-Me-7-F 1-3125 Single FCH 2 2-Me-8-F 1-3126 Single FCH 2 2-Me-5-Cl 1-3127 Single FCH 2 2-Me-6-Cl 1-3128 Single FCH 2 2-Me-7-Cl 1-3129 Single FCH 2 2-Me-8-Cl 1-3130 Single FCH 2 2-Me-5-MeO 1-3131 Single FCH 2 2-Me-6-MeO 1-3132 Single FCH 2 2-Me-7-MeO 1-3133 Single FCH 2 2-Me-8-MeO 1-3134 Single ClCH 2 H 1-3135 Single ClCH 2 2-F 1-3136 Single ClCH 2 4-F 1-3137 Single ClCH 2 5-F 1-3138 Single ClCH 2 6-F 1-3139 Single ClCH 2 7-F 1-3140 Single ClCH 2 8-F 1-3141 Single ClCH 2 2-Cl 1-3142 Single ClCH 2 4-Cl 1-3143 Single ClCH 2 5-Cl 1-3144 Single ClCH 2 6-Cl 1-3145 Single ClCH 2 7-Cl 1-3146 Single ClCH 2 8-Cl 1-3147 Single ClCH 2 2-Me 1-3148 Single ClCH 2 4-Me 1-3149 Single ClCH 2 5-Me 1-3150 Single ClCH 2 6-Me 1-3151 Single ClCH 2 7-Me 1-3152 Single ClCH 2 8-Me 1-3153 Single ClCH 2 2-Et 1-3154 Single ClCH 2 4-Et 1-3155 Single ClCH 2 5-Et 1-3156 Single ClCH 2 6-Et 1-3157 Single ClCH 2 7-Et 1-3158 Single ClCH 2 8-Et 1-3159 Single ClCH 2 2,4-F 2 1-3160 Single ClCH 2 2,5-F 2 1-3161 Single ClCH 2 2,6-F 2 1-3162 Single ClCH 2 2,7-F 2 1-3163 Single ClCH 2 2,8-F 2 1-3164 Single ClCH 2 4,5-F 2 1-3165 Single ClCH 2 4,6-F 2 1-3166 Single ClCH 2 4,7-F 2 1-3167 Single ClCH 2 4,8-F 2 1-3168 Single ClCH 2 5,6-F 2 1-3169 Single ClCH 2 5,7-F 2 1-3170 Single ClCH 2 5,8-F 2 1-3171 Single ClCH 2 6,7-F 2 1-3172 Single ClCH 2 6,8-F 2 1-3173 Single ClCH 2 7,8-F 2 1-3174 Single ClCH 2 2,4-Me 2 1-3175 Single ClCH 2 2,5-Me 2 1-3176 Single ClCH 2 2,6-Me 2 1-3177 Single ClCH 2 2,7-Me 2 1-3178 Single ClCH 2 2,8-Me 2 1-3179 Single ClCH 2 4,5-Me 2 1-3180 Single ClCH 2 4,6-Me 2 1-3181 Single ClCH 2 4,7-Me 2 1-3182 Single ClCH 2 4,8-Me 2 1-3183 Single ClCH 2 5,6-Me 2 1-3184 Single ClCH 2 5,7-Me 2 1-3185 Single ClCH 2 5,8-Me 2 1-3186 Single ClCH 2 6,7-Me 2 1-3187 Single ClCH 2 6,8-Me 2 1-3188 Single ClCH 2 7,8-Me 2 1-3189 Single ClCH 2 2-Me-5-F 1-3190 Single ClCH 2 2-Me-6-F 1-3191 Single ClCH 2 2-Me-7-F 1-3192 Single ClCH 2 2-Me-8-F 1-3193 Single ClCH 2 2-Me-5-Cl 1-3194 Single ClCH 2 2-Me-6-Cl 1-3195 Single ClCH 2 2-Me-7-Cl 1-3196 Single ClCH 2 2-Me-8-Cl 1-3197 Single ClCH 2 2-Me-5-MeO 1-3198 Single ClCH 2 2-Me-6-MeO 1-3199 Single ClCH 2 2-Me-7-MeO 1-3200 Single ClCH 2 2-Me-8-MeO 1-3201 Single 3,3,4,4-F Four -Bu H 1-3202 Single 3,3,4,4-F Four -Bu 2-F 1-3203 Single 3,3,4,4-F Four -Bu 4-F 1-3204 Single 3,3,4,4-F Four -Bu 5-F 1-3205 Single 3,3,4,4-F Four -Bu 6-F 1-3206 Single 3,3,4,4-F Four -Bu 7-F 1-3207 Single 3,3,4,4-F Four -Bu 8-F 1-3208 Single 3,3,4,4-F Four -Bu 2-Cl 1-3209 Single 3,3,4,4-F Four -Bu 4-Cl 1-3210 Single 3,3,4,4-F Four -Bu 5-Cl 1-3211 Single 3,3,4,4-F Four -Bu 6-Cl 1-3212 Single 3,3,4,4-F Four -Bu 7-Cl 1-3213 Single 3,3,4,4-F Four -Bu 8-Cl 1-3214 Single 3,3,4,4-F Four -Bu 2-Me 1-3215 Single 3,3,4,4-F Four -Bu 4-Me 1-3216 Single 3,3,4,4-F Four -Bu 5-Me 1-3217 Single 3,3,4,4-F Four -Bu 6-Me 1-3218 Single 3,3,4,4-F Four -Bu 7-Me 1-3219 Single 3,3,4,4-F Four -Bu 8-Me 1-3220 Single 3,3,4,4-F Four -Bu 2-Et 1-3221 Single 3,3,4,4-F Four -Bu 4-Et 1-3222 Single 3,3,4,4-F Four -Bu 5-Et 1-3223 Single 3,3,4,4-F Four -Bu 6-Et 1-3224 Single 3,3,4,4-F Four -Bu 7-Et 1-3225 Single 3,3,4,4-F Four -Bu 8-Et 1-3226 Single 3,3,4,4-F Four -Bu 2,4-F 2 1-3227 Single 3,3,4,4-F Four -Bu 2,5-F 2 1-3228 Single 3,3,4,4-F Four -Bu 2,6-F 2 1-3229 Single 3,3,4,4-F Four -Bu 2,7-F 2 1-3230 Single 3,3,4,4-F Four -Bu 2,8-F 2 1-3231 Single 3,3,4,4-F Four -Bu 4,5-F 2 1-3232 Single 3,3,4,4-F Four -Bu 4,6-F 2 1-3233 Single 3,3,4,4-F Four -Bu 4,7-F 2 1-3234 Single 3,3,4,4-F Four -Bu 4,8-F 2 1-3235 Single 3,3,4,4-F Four -Bu 5,6-F 2 1-3236 Single 3,3,4,4-F Four -Bu 5,7-F 2 1-3237 Single 3,3,4,4-F Four -Bu 5,8-F 2 1-3238 Single 3,3,4,4-F Four -Bu 6,7-F 2 1-3239 Single 3,3,4,4-F Four -Bu 6,8-F 2 1-3240 Single 3,3,4,4-F Four -Bu 7,8-F 2 1-3241 Single 3,3,4,4-F Four -Bu 2,4-Me 2 1-3242 Single 3,3,4,4-F Four -Bu 2,5-Me 2 1-3243 Single 3,3,4,4-F Four -Bu 2,6-Me 2 1-3244 Single 3,3,4,4-F Four -Bu 2,7-Me 2 1-3245 Single 3,3,4,4-F Four -Bu 2,8-Me 2 1-3246 Single 3,3,4,4-F Four -Bu 4,5-Me 2 1-3247 Single 3,3,4,4-F Four -Bu 4,6-Me 2 1-3248 Single 3,3,4,4-F Four -Bu 4,7-Me 2 1-3249 Single 3,3,4,4-F Four -Bu 4,8-Me 2 1-3250 Single 3,3,4,4-F Four -Bu 5,6-Me 2 1-3251 Single 3,3,4,4-F Four -Bu 5,7-Me 2 1-3252 Single 3,3,4,4-F Four -Bu 5,8-Me 2 1-3253 Single 3,3,4,4-F Four -Bu 6,7-Me 2 1-3254 Single 3,3,4,4-F Four -Bu 6,8-Me 2 1-3255 Single 3,3,4,4-F Four -Bu 7,8-Me 2 1-3256 Single 3,3,4,4-F Four -Bu 2-Me-5-F 1-3257 Single 3,3,4,4-F Four -Bu 2-Me-6-F 1-3258 Single 3,3,4,4-F Four -Bu 2-Me-7-F 1-3259 Single 3,3,4,4-F Four -Bu 2-Me-8-F 1-3260 Single 3,3,4,4-F Four -Bu 2-Me-5-Cl 1-3261 Single 3,3,4,4-F Four -Bu 2-Me-6-Cl 1-3262 Single 3,3,4,4-F Four -Bu 2-Me-7-Cl 1-3263 Single 3,3,4,4-F Four -Bu 2-Me-8-Cl 1-3264 Single 3,3,4,4-F Four -Bu 2-Me-5-MeO 1-3265 Single 3,3,4,4-F Four -Bu 2-Me-6-MeO 1-3266 Single 3,3,4,4-F Four -Bu 2-Me-7-MeO 1-3267 Single cBuCH 2 H 1-3268 Single cBuCH 2 2-F 1-3269 Single cBuCH 2 4-F 1-3270 Single cBuCH 2 5-F 1-3271 Single cBuCH 2 6-F 1-3272 Single cBuCH 2 7-F 1-3273 Single cBuCH 2 8-F 1-3274 Single cBuCH 2 2-Cl 1-3275 Single cBuCH 2 4-Cl 1-3276 Single cBuCH 2 5-Cl 1-3277 Single cBuCH 2 6-Cl 1-3278 Single cBuCH 2 7-Cl 1-3279 Single cBuCH 2 8-Cl 1-3280 Single cBuCH 2 2-Me 1-3281 Single cBuCH 2 4-Me 1-3282 Single cBuCH 2 5-Me 1-3283 Single cBuCH 2 6-Me 1-3284 Single cBuCH 2 7-Me 1-3285 Single cBuCH 2 8-Me 1-3286 Single cBuCH 2 2-Et 1-3287 Single cBuCH 2 4-Et 1-3288 Single cBuCH 2 5-Et 1-3289 Single cBuCH 2 6-Et 1-3290 Single cBuCH 2 7-Et 1-3291 Single cBuCH 2 8-Et 1-3292 Single cBuCH 2 2,4-F 2 1-3293 Single cBuCH 2 2,5-F 2 1-3294 Single cBuCH 2 2,6-F 2 1-3295 Single cBuCH 2 2,7-F 2 1-3296 Single cBuCH 2 2,8-F 2 1-3297 Single cBuCH 2 4,5-F 2 1-3298 Single cBuCH 2 4,6-F 2 1-3299 Single cBuCH 2 4,7-F 2 1-3300 Single cBuCH 2 4,8-F 2 1-3301 Single cBuCH 2 5,6-F 2 1-3302 Single cBuCH 2 5,7-F 2 1-3303 Single cBuCH 2 5,8-F 2 1-3304 Single cBuCH 2 6,7-F 2 1-3305 Single cBuCH 2 6,8-F 2 1-3306 Single cBuCH 2 7,8-F 2 1-3307 Single cBuCH 2 2,4-Me 2 1-3308 Single cBuCH 2 2,5-Me 2 1-3309 Single cBuCH 2 2,6-Me 2 1-3310 Single cBuCH 2 2,7-Me 2 1-3311 Single cBuCH 2 2,8-Me 2 1-3312 Single cBuCH 2 4,5-Me 2 1-3313 Single cBuCH 2 4,6-Me 2 1-3314 Single cBuCH 2 4,7-Me 2 1-3315 Single cBuCH 2 4,8-Me 2 1-3316 Single cBuCH 2 5,6-Me 2 1-3317 Single cBuCH 2 5,7-Me 2 1-3318 Single cBuCH 2 5,8-Me 2 1-3319 Single cBuCH 2 6,7-Me 2 1-3320 Single cBuCH 2 6,8-Me 2 1-3321 Single cBuCH 2 7,8-Me 2 1-3322 Single cBuCH 2 2-Me-5-F 1-3323 Single cBuCH 2 2-Me-6-F 1-3324 Single cBuCH 2 2-Me-7-F 1-3325 Single cBuCH 2 2-Me-8-F 1-3326 Single cBuCH 2 2-Me-5-Cl 1-3327 Single cBuCH 2 2-Me-6-Cl 1-3328 Single cBuCH 2 2-Me-7-Cl 1-3329 Single cBuCH 2 2-Me-8-Cl 1-3330 Single cBuCH 2 2-Me-5-MeO 1-3331 Single cBuCH 2 2-Me-6-MeO 1-3332 Single cBuCH 2 2-Me-7-MeO 1-3333 Single cBuCH 2 2-Me-8-MeO 1-3334 Single cHexCH 2 H 1-3335 Single cHexCH 2 2-F 1-3336 Single cHexCH 2 4-F 1-3337 Single cHexCH 2 5-F 1-3338 Single cHexCH 2 6-F 1-3339 Single cHexCH 2 7-F 1-3340 Single cHexCH 2 8-F 1-3341 Single cHexCH 2 2-Cl 1-3342 Single cHexCH 2 4-Cl 1-3343 Single cHexCH 2 5-Cl 1-3344 Single cHexCH 2 6-Cl 1-3345 Single cHexCH 2 7-Cl 1-3346 Single cHexCH 2 8-Cl 1-3347 Single cHexCH 2 2-Me 1-3348 Single cHexCH 2 4-Me 1-3349 Single cHexCH 2 5-Me 1-3350 Single cHexCH 2 6-Me 1-3351 Single cHexCH 2 7-Me 1-3352 Single cHexCH 2 8-Me 1-3353 Single cHexCH 2 2-Et 1-3354 Single cHexCH 2 4-Et 1-3355 Single cHexCH 2 5-Et 1-3356 Single cHexCH 2 6-Et 1-3357 Single cHexCH 2 7-Et 1-3358 Single cHexCH 2 8-Et 1-3359 Single cHexCH 2 2,4-F 2 1-3360 Single cHexCH 2 2,5-F 2 1-3361 Single cHexCH 2 2,6-F 2 1-3362 Single cHexCH 2 2,7-F 2 1-3363 Single cHexCH 2 2,8-F 2 1-3364 Single cHexCH 2 4,5-F 2 1-3365 Single cHexCH 2 4,6-F 2 1-3366 Single cHexCH 2 4,7-F 2 1-3367 Single cHexCH 2 4,8-F 2 1-3368 Single cHexCH 2 5,6-F 2 1-3369 Single cHexCH 2 5,7-F 2 1-3370 Single cHexCH 2 5,8-F 2 1-3371 Single cHexCH 2 6,7-F 2 1-3372 Single cHexCH 2 6,8-F 2 1-3373 Single cHexCH 2 7,8-F 2 1-3374 Single cHexCH 2 2,4-Me 2 1-3375 Single cHexCH 2 2,5-Me 2 1-3376 Single cHexCH 2 2,6-Me 2 1-3377 Single cHexCH 2 2,7-Me 2 1-3378 Single cHexCH 2 2,8-Me 2 1-3379 Single cHexCH 2 4,5-Me 2 1-3380 Single cHexCH 2 4,6-Me 2 1-3381 Single cHexCH 2 4,7-Me 2 1-3382 Single cHexCH 2 4,8-Me 2 1-3383 Single cHexCH 2 5,6-Me 2 1-3384 Single cHexCH 2 5,7-Me 2 1-3385 Single cHexCH 2 5,8-Me 2 1-3386 Single cHexCH 2 6,7-Me 2 1-3387 Single cHexCH 2 6,8-Me 2 1-3388 Single cHexCH 2 7,8-Me 2 1-3389 Single cHexCH 2 2-Me-5-F 1-3390 Single cHexCH 2 2-Me-6-F 1-3391 Single cHexCH 2 2-Me-7-F 1-3392 Single cHexCH 2 2-Me-8-F 1-3393 Single cHexCH 2 2-Me-5-Cl 1-3394 Single cHexCH 2 2-Me-6-Cl 1-3395 Single cHexCH 2 2-Me-7-Cl 1-3396 Single cHexCH 2 2-Me-8-Cl 1-3397 Single cHexCH 2 2-Me-5-MeO 1-3398 Single cHexCH 2 2-Me-6-MeO 1-3399 Single cHexCH 2 2-Me-7-MeO 1-3400 Single cHexCH 2 2-Me-8-MeO 1-3401 Single Vinyl H 1-3402 Single Vinyl 2-F 1-3403 Single Vinyl 4-F 1-3404 Single Vinyl 5-F 1-3405 Single Vinyl 6-F 1-3406 Single Vinyl 7-F 1-3407 Single Vinyl 8-F 1-3408 Single Vinyl 2-Cl 1-3409 Single Vinyl 4-Cl 1-3410 Single Vinyl 5-Cl 1-3411 Single Vinyl 6-Cl 1-3412 Single Vinyl 7- Cl 1-3413 Single Vinyl 8-Cl 1-3414 Single Vinyl 2-Me 1-3415 Single Vinyl 4-Me 1-3416 Single Vinyl 5-Me 1-3417 Single Vinyl 6-Me 1-3418 Single Vinyl 7-Me 1 -3419 Single Vinyl 8-Me 1-3420 Single Vinyl 2-Et 1-3421 Single Vinyl 4-Et 1-3422 Single Vinyl 5-Et 1-3423 Single Vinyl 6-Et 1-3424 Single Vinyl 7-Et 1-3425 Single Vinyl 8-Et 1-3426 Single Vinyl 2,4-F 2 1-3427 Single Vinyl 2,5-F 2 1-3428 Single Vinyl 2,6-F 2 1-3429 Single Vinyl 2,7-F 2 1-3430 Single Vinyl 2,8-F 2 1-3431 Single Vinyl 4,5-F 2 1-3432 Single Vinyl 4,6-F 2 1-3433 Single Vinyl 4,7-F 2 1-3434 Single Vinyl 4,8-F 2 1-3435 Single Vinyl 5,6-F 2 1-3436 Single Vinyl 5,7-F 2 1-3437 Single Vinyl 5,8-F 2 1-3438 Single Vinyl 6,7-F 2 1-3439 Single Vinyl 6,8-F 2 1-3440 Single Vinyl 7,8-F 2 1-3441 Single Vinyl 2,4-Me 2 1-3442 Single Vinyl 2,5-Me 2 1-3443 Single Vinyl 2,6-Me 2 1-3444 Single Vinyl 2,7-Me 2 1-3445 Single Vinyl 2,8-Me 2 1-3446 Single Vinyl 4,5-Me 2 1-3447 Single Vinyl 4,6-Me 2 1-3448 Single Vinyl 4,7-Me 2 1-3449 Single Vinyl 4,8-Me 2 1-3450 Single Vinyl 5,6-Me 2 1-3451 Single Vinyl 5,7-Me 2 1-3452 Single Vinyl 5,8-Me 2 1-3453 Single Vinyl 6,7-Me 2 1-3454 Single Vinyl 6,8-Me 2 1-3455 Single Vinyl 7,8-Me 2 1-3456 Single Vinyl 2-Me-5-F 1-3457 Single Vinyl 2-Me-6-F 1-3458 Single Vinyl 2-Me-7-F 1-3459 Single Vinyl 2-Me-8-F 1- 3460 Single Vinyl 2-Me-5-Cl 1-3461 Single Vinyl 2-Me-6-Cl 1-3462 Single Vinyl 2-Me-7-Cl 1-3463 Single Vinyl 2-Me-8-Cl 1-3464 Single Vinyl 2-Me-5-MeO 1-3465 Single Vinyl 2-Me-6-MeO 1-3466 Single Vinyl 2-Me-7-MeO 1-3467 Single Vinyl 2-Me-8-MeO 1-3468 Single Methallyl H 1-3469 Single Methallyl 2-F 1-3470 Single Methallyl 4-F 1-3471 Single Methallyl 5-F 1-3472 Single Methallyl 6-F 1-3473 Single Methallyl 7-F 1-3474 Single Methallyl 8-F 1- 3475 Single Methallyl 2-Cl 1-3476 Single Methallyl 4-Cl 1-3477 Single Methallyl 5-Cl 1-3478 Single Methallyl 6-Cl 1-3479 Single Methallyl 7-Cl 1-3480 Single Methallyl 8-Cl 1-3481 Single Methallyl 2-Me 1-3482 single Methallyl 4-Me 1-3483 single Methallyl 5-Me 1-3484 single Methallyl 6-Me 1-3485 single Methallyl 7-Me 1-3486 single Methallyl 8-Me 1-3487 single Methallyl 2 -Et 1-3488 Single Methallyl 4-Et 1-3489 Single Methallyl 5-Et 1-3490 Single Methallyl 6-Et 1-3491 Single Methallyl 7-Et 1-3492 Single Methallyl 8-Et 1-3493 Single Methallyl 2,4 -F 2 1-3494 Single Methallyl 2,5-F 2 1-3495 Single Methallyl 2,6-F 2 1-3496 Single Methallyl 2,7-F 2 1-3497 Single Methallyl 2,8-F 2 1-3498 Single Methallyl 4,5-F 2 1-3499 Single Methallyl 4,6-F 2 1-3500 Single Methallyl 4,7-F 2 1-3501 Single Methallyl 4,8-F 2 1-3502 Single Methallyl 5,6-F 2 1-3503 Single Methallyl 5,7-F 2 1-3504 Single Methallyl 5,8-F 2 1-3505 Single Methallyl 6,7-F 2 1-3506 Single Methallyl 6,8-F 2 1-3507 Single Methallyl 7,8-F 2 1-3508 Single Methallyl 2,4-Me 2 1-3509 Single Methallyl 2,5-Me 2 1-3510 Single Methallyl 2,6-Me 2 1-3511 Single Methallyl 2,7-Me 2 1-3512 Single Methallyl 2,8-Me 2 1-3513 Single Methallyl 4,5-Me 2 1-3514 Single Methallyl 4,6-Me 2 1-3515 Single Methallyl 4,7-Me 2 1-3516 Single Methallyl 4,8-Me 2 1-3517 Single Methallyl 5,6-Me 2 1-3518 Single Methallyl 5,7-Me 2 1-3519 Single Methallyl 5,8-Me 2 1-3520 Single Methallyl 6,7-Me 2 1-3521 Single Methallyl 6,8-Me 2 1-3522 Single Methallyl 7,8-Me 2 1-3523 Single Methallyl 2-Me-5-F 1-3524 Single Methallyl 2-Me-6-F 1-3525 Single Methallyl 2-Me-7-F 1-3526 Single Methallyl 2-Me-8-F 1- 3527 Single Methallyl 2-Me-5-Cl 1-3528 Single Methallyl 2-Me-6-Cl 1-3529 Single Methallyl 2-Me-7-Cl 1-3530 Single Methallyl 2-Me-8-Cl 1-3531 Single Methallyl 2-Me-5-MeO 1-3532 single Methallyl 2-Me-6-MeO 1-3533 single Methallyl 2-Me-7-MeO 1-3534 single Methallyl 2-Me-8-MeO 1-3535 single 3- Me-2-butenyl H 1-3536 single 3-Me-2-butenyl 2-F 1-3537 single 3-Me-2-butenyl 4-F 1-3538 single 3-Me-2-butenyl 5-F 1- 3539 Single 3-Me-2-butenyl 6-F 1-3540 Single 3-Me-2-butenyl 7-F 1-3541 Single 3-Me-2-butenyl 8-F 1-3542 Single 3-Me-2- butenyl 2-Cl 1-3543 single 3-Me-2-butenyl 4-Cl 1-3544 single 3-Me-2-butenyl 5-Cl 1-3545 single 3-Me-2-butenyl 6-Cl 1-3546 single 3-Me-2-butenyl 7-Cl 1-3547 single 3-Me-2-butenyl 8-Cl 1-3548 single 3-Me-2-butenyl 2-Me 1-3549 single 3-Me-2-butenyl 4 -Me 1-3550 single 3-Me-2-butenyl 5-Me 1-3551 single 3-Me-2-butenyl 6-Me 1-3552 single 3-Me-2-butenyl 7-Me 1-3553 single 3- Me-2-butenyl 8-Me 1-3554 Single 3-Me-2-butenyl 2-Et 1-3555 Single 3-Me-2 -butenyl 4-Et 1-3556 single 3-Me-2-butenyl 5-Et 1-3557 single 3-Me-2-butenyl 6-Et 1-3558 single 3-Me-2-butenyl 7-Et 1-3559 Single 3-Me-2-butenyl 8-Et 1-3560 Single 3-Me-2-butenyl 2,4-F 2 1-3561 Single 3-Me-2-butenyl 2,5-F 2 1-3562 Single 3-Me-2-butenyl 2,6-F 2 1-3563 Single 3-Me-2-butenyl 2,7-F 2 1-3564 Single 3-Me-2-butenyl 2,8-F 2 1-3565 Single 3-Me-2-butenyl 4,5-F 2 1-3566 Single 3-Me-2-butenyl 4,6-F 2 1-3567 Single 3-Me-2-butenyl 4,7-F 2 1-3568 Single 3-Me-2-butenyl 4,8-F 2 1-3569 Single 3-Me-2-butenyl 5,6-F 2 1-3570 Single 3-Me-2-butenyl 5,7-F 2 1-3571 Single 3-Me-2-butenyl 5,8-F 2 1-3572 Single 3-Me-2-butenyl 6,7-F 2 1-3573 Single 3-Me-2-butenyl 6,8-F 2 1-3574 Single 3-Me-2-butenyl 7,8-F 2 1-3575 Single 3-Me-2-butenyl 2,4-Me 2 1-3576 Single 3-Me-2-butenyl 2,5-Me 2 1-3577 Single 3-Me-2-butenyl 2,6-Me 2 1-3578 Single 3-Me-2-butenyl 2,7-Me 2 1-3579 Single 3-Me-2-butenyl 2,8-Me 2 1-3580 Single 3-Me-2-butenyl 4,5-Me 2 1-3581 Single 3-Me-2-butenyl 4,6-Me 2 1-3582 Single 3-Me-2-butenyl 4,7-Me 2 1-3583 Single 3-Me-2-butenyl 4,8-Me 2 1-3584 Single 3-Me-2-butenyl 5,6-Me 2 1-3585 Single 3-Me-2-butenyl 5,7-Me 2 1-3586 Single 3-Me-2-butenyl 5,8-Me 2 1-3587 Single 3-Me-2-butenyl 6,7-Me 2 1-3588 Single 3-Me-2-butenyl 6,8-Me 2 1-3589 Single 3-Me-2-butenyl 7,8-Me 2 1-3590 Single 3-Me-2-butenyl 2-Me-5-F 1-3591 Single 3-Me-2-butenyl 2-Me-6-F 1-3592 Single 3-Me-2-butenyl 2-Me -7-F 1-3593 Single 3-Me-2-butenyl 2-Me-8-F 1-3594 Single 3-Me-2-butenyl 2-Me-5-Cl 1-3595 Single 3-Me-2- butenyl 2-Me-6-Cl 1-3596 single 3-Me-2-butenyl 2-Me-7-Cl 1-3597 single 3-Me-2-butenyl 2-Me-8-Cl 1-3598 single 3- Me-2-butenyl 2-Me-5-MeO 1-3599 Single 3-Me-2-butenyl 2-Me-6-MeO 1-3600 Single 3-Me-2-butenyl 2-Me-7-MeO 1- 3601 Single 3-Me-2-butenyl 2-Me-8-MeO 1-3602 Single 3-Butenyl H 1-3603 Single 3-Butenyl 2-F 1-3604 Single 3-Butenyl 4-F 1-3605 Single 3- Butenyl 5-F 1-3606 Single 3-Butenyl 6-F 1-3607 Single 3-Butenyl 7-F 1-3608 Single 3-Butenyl 8-F 1-3609 Single 3-Butenyl 2-Cl 1-3610 Single 3- Butenyl 4-Cl 1-3611 Single 3-Butenyl 5-Cl 1-3612 Single 3-Butenyl 6-Cl 1-3613 Single 3-Butenyl 7-Cl 1-3614 Single 3-Butenyl 8-Cl 1-3615 Single 3- Butenyl 2-Me 1-3616 Single 3-Butenyl 4-Me 1-3617 Single 3-Butenyl 5-Me 1-3618 Single 3-Butenyl 6-Me 1-3619 Single 3-Butenyl 7-Me 1-3620 Single 3- Butenyl 8-Me 1-3621 Single 3-Butenyl 2-Et 1-3622 Single 3-Butenyl 4-Et 1-3623 Single 3-Butenyl 5-Et 1-362 4 Single 3-Butenyl 6-Et 1-3625 Single 3-Butenyl 7-Et 1-3626 Single 3-Butenyl 8-Et 1-3627 Single 3-Butenyl 2,4-F 2 1-3628 Single 3-Butenyl 2,5-F 2 1-3629 Single 3-Butenyl 2,6-F 2 1-3630 Single 3-Butenyl 2,7-F 2 1-3631 Single 3-Butenyl 2,8-F 2 1-3632 Single 3-Butenyl 4,5-F 2 1-3633 Single 3-Butenyl 4,6-F 2 1-3634 Single 3-Butenyl 4,7-F 2 1-3635 Single 3-Butenyl 4,8-F 2 1-3636 Single 3-Butenyl 5,6-F 2 1-3637 Single 3-Butenyl 5,7-F 2 1-3638 Single 3-Butenyl 5,8-F 2 1-3639 Single 3-Butenyl 6,7-F 2 1-3640 Single 3-Butenyl 6,8-F 2 1-3641 Single 3-Butenyl 7,8-F 2 1-3642 Single 3-Butenyl 2,4-Me 2 1-3643 Single 3-Butenyl 2,5-Me 2 1-3644 Single 3-Butenyl 2,6-Me 2 1-3645 Single 3-Butenyl 2,7-Me 2 1-3646 Single 3-Butenyl 2,8-Me 2 1-3647 Single 3-Butenyl 4,5-Me 2 1-3648 Single 3-Butenyl 4,6-Me 2 1-3649 Single 3-Butenyl 4,7-Me 2 1-3650 Single 3-Butenyl 4,8-Me 2 1-3651 Single 3-Butenyl 5,6-Me 2 1-3652 Single 3-Butenyl 5,7-Me 2 1-3653 Single 3-Butenyl 5,8-Me 2 1-3654 Single 3-Butenyl 6,7-Me 2 1-3655 Single 3-Butenyl 6,8-Me 2 1-3656 Single 3-Butenyl 7,8-Me 2 1-3657 Single 3-Butenyl 2-Me-5-F 1-3658 Single 3-Butenyl 2-Me-6-F 1-3659 Single 3-Butenyl 2-Me-7-F 1-3660 Single 3-Butenyl 2 -Me-8-F 1-3661 Single 3-Butenyl 2-Me-5-Cl 1-3662 Single 3-Butenyl 2-Me-6-Cl 1-3663 Single 3-Butenyl 2-Me-7-Cl 1- 3664 Single 3-Butenyl 2-Me-8-Cl 1-3665 Single 3-Butenyl 2-Me-5-MeO 1-3666 Single 3-Butenyl 2-Me-6-MeO 1-3667 Single 3-Butenyl 2-Me -7-MeO 1-3668 Single 3-Butenyl 2-Me-8-MeO 1-3669 Single 4-Pentenyl H 1-3670 Single 4-Pentenyl 2-F 1-3671 Single 4-Pentenyl 4-F 1-3672 Single 4-Pentenyl 5-F 1-3673 Single 4-Pentenyl 6-F 1-3674 Single 4-Pentenyl 7-F 1-3675 Single 4-Pentenyl 8-F 1-3676 Single 4-Pentenyl 2-Cl 1-3677 Single 4-Pentenyl 4-Cl 1-3678 Single 4-Pentenyl 5-Cl 1-3679 Single 4-Pentenyl 6-Cl 1-3680 Single 4-Pentenyl 7-Cl 1-3681 Single 4-Pentenyl 8-Cl 1-3682 Single 4-Pentenyl 2-Me 1-3683 Single 4-Pentenyl 4-Me 1-3684 Single 4-Pentenyl 5-Me 1-3685 Single 4-Pentenyl 6-Me 1-3686 Single 4-Pentenyl 7-Me 1-3687 Single 4-Pentenyl 8-Me 1-3688 Single 4-Pentenyl 2-Et 1-3689 Single 4-Pentenyl 4-Et 1-3690 Single 4-Pentenyl 5-Et 1-3691 Single 4-Pentenyl 6-Et 1-3692 Single 4-Pen tenyl 7-Et 1-3693 Single 4-Pentenyl 8-Et 1-3694 Single 4-Pentenyl 2,4-F 2 1-3695 Single 4-Pentenyl 2,5-F 2 1-3696 Single 4-Pentenyl 2,6-F 2 1-3697 Single 4-Pentenyl 2,7-F 2 1-3698 Single 4-Pentenyl 2,8-F 2 1-3699 Single 4-Pentenyl 4,5-F 2 1-3700 Single 4-Pentenyl 4,6-F 2 1-3701 Single 4-Pentenyl 4,7-F 2 1-3702 Single 4-Pentenyl 4,8-F 2 1-3703 Single 4-Pentenyl 5,6-F 2 1-3704 Single 4-Pentenyl 5,7-F 2 1-3705 Single 4-Pentenyl 5,8-F 2 1-3706 Single 4-Pentenyl 6,7-F 2 1-3707 Single 4-Pentenyl 6,8-F 2 1-3708 Single 4-Pentenyl 7,8-F 2 1-3709 Single 4-Pentenyl 2,4-Me 2 1-3710 Single 4-Pentenyl 2,5-Me 2 1-3711 Single 4-Pentenyl 2,6-Me 2 1-3712 Single 4-Pentenyl 2,7-Me 2 1-3713 Single 4-Pentenyl 2,8-Me 2 1-3714 Single 4-Pentenyl 4,5-Me 2 1-3715 Single 4-Pentenyl 4,6-Me 2 1-3716 Single 4-Pentenyl 4,7-Me 2 1-3717 Single 4-Pentenyl 4,8-Me 2 1-3718 Single 4-Pentenyl 5,6-Me 2 1-3719 Single 4-Pentenyl 5,7-Me 2 1-3720 Single 4-Pentenyl 5,8-Me 2 1-3721 Single 4-Pentenyl 6,7-Me 2 1-3722 Single 4-Pentenyl 6,8-Me 2 1-3723 Single 4-Pentenyl 7,8-Me 2 1-3724 Single 4-Pentenyl 2-Me-5-F 1-3725 Single 4-Pentenyl 2-Me-6-F 1-3726 Single 4-Pentenyl 2-Me-7-F 1-3727 Single 4-Pentenyl 2 -Me-8-F 1-3728 Single 4-Pentenyl 2-Me-5-Cl 1-3729 Single 4-Pentenyl 2-Me-6-Cl 1-3730 Single 4-Pentenyl 2-Me-7-Cl 1- 3731 Single 4-Pentenyl 2-Me-8-Cl 1-3732 Single 4-Pentenyl 2-Me-5-MeO 1-3733 Single 4-Pentenyl 2-Me-6-MeO 1-3734 Single 4-Pentenyl 2-Me -7-MeO 1-3735 Single 4-Pentenyl 2-Me-8-MeO 1-3736 Single Propargyl H 1-3737 Single Propargyl 2-F 1-3738 Single Propargyl 4-F 1-3739 Single Propargyl 5-F 1- 3740 Single Propargyl 6-F 1-3741 Single Propargyl 7-F 1-3742 Single Propargyl 8-F 1-3743 Single Propargyl 2-Cl 1-3744 Single Propargyl 4-Cl 1-3745 Single Propargyl 5-Cl 1-3746 Single Propargyl 6-Cl 1-3747 Single Propargyl 7-Cl 1-3748 Single Propargyl 8-Cl 1-3749 Single Propargyl 2-Me 1-3750 Single Propargyl 4-Me 1-3751 Single Propargyl 5-Me 1-3752 Single Propargyl 6 -Me 1-3753 Single Propargyl 7-Me 1-3754 Single Propargyl 8-Me 1-3755 Single Propargyl 2-Et 1-3756 Single Propargyl 4-Et 1-3757 Single Propargyl 5-Et 1-3758 Single Propargyl 6-Et 1-3759 Single Propargyl 7-Et 1 -3760 Single Propargyl 8-Et 1-3761 Single Propargyl 2,4-F 2 1-3762 Single Propargyl 2,5-F 2 1-3763 Single Propargyl 2,6-F 2 1-3764 Single Propargyl 2,7-F 2 1-3765 Single Propargyl 2,8-F 2 1-3766 Single Propargyl 4,5-F 2 1-3767 Single Propargyl 4,6-F 2 1-3768 Single Propargyl 4,7-F 2 1-3769 Single Propargyl 4,8-F 2 1-3770 Single Propargyl 5,6-F 2 1-3771 Single Propargyl 5,7-F 2 1-3772 Single Propargyl 5,8-F 2 1-3773 Single Propargyl 6,7-F 2 1-3774 Single Propargyl 6,8-F 2 1-3775 Single Propargyl 7,8-F 2 1-3776 Single Propargyl 2,4-Me 2 1-3777 Single Propargyl 2,5-Me 2 1-3778 Single Propargyl 2,6-Me 2 1-3779 Single Propargyl 2,7-Me 2 1-3780 Single Propargyl 2,8-Me 2 1-3781 Single Propargyl 4,5-Me 2 1-3782 Single Propargyl 4,6-Me 2 1-3783 Single Propargyl 4,7-Me 2 1-3784 Single Propargyl 4,8-Me 2 1-3785 Single Propargyl 5,6-Me 2 1-3786 Single Propargyl 5,7-Me 2 1-3787 Single Propargyl 5,8-Me 2 1-3788 Single Propargyl 6,7-Me 2 1-3789 Single Propargyl 6,8-Me 2 1-3790 Single Propargyl 7,8-Me 2 1-3791 Single Propargyl 2-Me-5-F 1-3792 Single Propargyl 2-Me-6-F 1-3793 Single Propargyl 2-Me-7-F 1-3794 Single Propargyl 2-Me-8-F 1- 3795 Single Propargyl 2-Me-5-Cl 1-3796 Single Propargyl 2-Me-6-Cl 1-3797 Single Propargyl 2-Me-7-Cl 1-3798 Single Propargyl 2-Me-8-Cl 1-3799 Single Propargyl 2-Me-5-MeO 1-3800 Single Propargyl 2-Me-6-MeO 1-3801 Single Propargyl 2-Me-7-MeO 1-3802 Single Propargyl 2-Me-8-MeO 1-3803 Single 2- Pentynyl H 1-3804 Single 2-Pentynyl 2-F 1-3805 Single 2-Pentynyl 4-F 1-3806 Single 2-Pentynyl 5-F 1-3807 Single 2-Pentynyl 6-F 1-3808 Single 2-Pentynyl 7 -F 1-3809 Single 2-Pentynyl 8-F 1-3810 Single 2-Pentynyl 2-Cl 1-3811 Single 2-Pentynyl 4-Cl 1-3812 Single 2-Pentynyl 5-Cl 1-3813 Single 2-Pentynyl 6 -Cl 1-3814 Single 2-Pentynyl 7-Cl 1-3815 Single 2-Pentynyl 8-Cl 1-3816 Single 2-Pentynyl 2-Me 1-3817 Single 2-Pentynyl 4-Me 1-3818 Single 2-Pentynyl 5 -Me 1-3819 Single 2-Pentynyl 6-Me 1-3820 Single 2-Pentynyl 7-Me 1-3821 Single 2-Pentynyl 8-Me 1-3822 Single 2-Pentynyl 2-Et 1-3823 Single 2-Pentynyl 4 -Et 1-3824 Single 2-Pentynyl 5-Et 1-3825 Single 2-Pentynyl 6-Et 1-3826 Single 2-Pen tynyl 7-Et 1-3827 Single 2-Pentynyl 8-Et 1-3828 Single 2-Pentynyl 2,4-F 2 1-3829 Single 2-Pentynyl 2,5-F 2 1-3830 Single 2-Pentynyl 2,6-F 2 1-3831 Single 2-Pentynyl 2,7-F 2 1-3832 Single 2-Pentynyl 2,8-F 2 1-3833 Single 2-Pentynyl 4,5-F 2 1-3834 Single 2-Pentynyl 4,6-F 2 1-3835 Single 2-Pentynyl 4,7-F 2 1-3836 Single 2-Pentynyl 4,8-F 2 1-3837 Single 2-Pentynyl 5,6-F 2 1-3838 Single 2-Pentynyl 5,7-F 2 1-3839 Single 2-Pentynyl 5,8-F 2 1-3840 Single 2-Pentynyl 6,7-F 2 1-3841 Single 2-Pentynyl 6,8-F 2 1-3842 Single 2-Pentynyl 7,8-F 2 1-3843 Single 2-Pentynyl 2,4-Me 2 1-3844 Single 2-Pentynyl 2,5-Me 2 1-3845 Single 2-Pentynyl 2,6-Me 2 1-3846 Single 2-Pentynyl 2,7-Me 2 1-3847 Single 2-Pentynyl 2,8-Me 2 1-3848 Single 2-Pentynyl 4,5-Me 2 1-3849 Single 2-Pentynyl 4,6-Me 2 1-3850 Single 2-Pentynyl 4,7-Me 2 1-3851 Single 2-Pentynyl 4,8-Me 2 1-3852 Single 2-Pentynyl 5,6-Me 2 1-3853 Single 2-Pentynyl 5,7-Me 2 1-3854 Single 2-Pentynyl 5,8-Me 2 1-3855 Single 2-Pentynyl 6,7-Me 2 1-3856 Single 2-Pentynyl 6,8-Me 2 1-3857 Single 2-Pentynyl 7,8-Me 2 1-3858 Single 2-Pentynyl 2-Me-5-F 1-3859 Single 2-Pentynyl 2-Me-6-F 1-3860 Single 2-Pentynyl 2-Me-7-F 1-3861 Single 2-Pentynyl 2 -Me-8-F 1-3862 Single 2-Pentynyl 2-Me-5-Cl 1-3863 Single 2-Pentynyl 2-Me-6-Cl 1-3864 Single 2-Pentynyl 2-Me-7-Cl 1- 3865 Mono 2-Pentynyl 2-Me-8-Cl 1-3866 Mono 2-Pentynyl 2-Me-5-MeO 1-3867 Mono 2-Pentynyl 2-Me-6-MeO 1-3868 Mono 2-Pentynyl 2-Me -7-MeO 1-3869 Single 2-Pentynyl 2-Me-8-MeO 1-3870 Single MeOCH 2 H 1-3871 Single MeOCH 2 2-F 1-3872 Single MeOCH 2 4-F 1-3873 Single MeOCH 2 5-F 1-3874 Single MeOCH 2 6-F 1-3875 Single MeOCH 2 7-F 1-3876 Single MeOCH 2 8-F 1-3877 Single MeOCH 2 2-Cl 1-3878 Single MeOCH 2 4-Cl 1-3879 Single MeOCH 2 5-Cl 1-3880 Single MeOCH 2 6-Cl 1-3881 Single MeOCH 2 7-Cl 1-3882 Single MeOCH 2 8-Cl 1-3883 Single MeOCH 2 2-Me 1-3884 Single MeOCH 2 4-Me 1-3885 Single MeOCH 2 5-Me 1-3886 Single MeOCH 2 6-Me 1-3887 Single MeOCH 2 7-Me 1-3888 Single MeOCH 2 8-Me 1-3889 Single MeOCH 2 2-Et 1-3890 Single MeOCH 2 4-Et 1-3891 Single MeOCH 2 5-Et 1-3892 Single MeOCH 2 6-Et 1-3893 Single MeOCH 2 7-Et 1-3894 Single MeOCH 2 8-Et 1-3895 Single MeOCH 2 2,4-F 2 1-3896 Single MeOCH 2 2,5-F 2 1-3897 Single MeOCH 2 2,6-F 2 1-3898 Single MeOCH 2 2,7-F 2 1-3899 Single MeOCH 2 2,8-F 2 1-3900 Single MeOCH 2 4,5-F 2 1-3901 Single MeOCH 2 4,6-F 2 1-3902 Single MeOCH 2 4,7-F 2 1-3903 Single MeOCH 2 4,8-F 2 1-3904 Single MeOCH 2 5,6-F 2 1-3905 Single MeOCH 2 5,7-F 2 1-3906 Single MeOCH 2 5,8-F 2 1-3907 Single MeOCH 2 6,7-F 2 1-3908 Single MeOCH 2 6,8-F 2 1-3909 Single MeOCH 2 7,8-F 2 1-3910 Single MeOCH 2 2,4-Me 2 1-3911 Single MeOCH 2 2,5-Me 2 1-3912 Single MeOCH 2 2,6-Me 2 1-3913 Single MeOCH 2 2,7-Me 2 1-3914 Single MeOCH 2 2,8-Me 2 1-3915 Single MeOCH 2 4,5-Me 2 1-3916 Single MeOCH 2 4,6-Me 2 1-3917 Single MeOCH 2 4,7-Me 2 1-3918 Single MeOCH 2 4,8-Me 2 1-3919 Single MeOCH 2 5,6-Me 2 1-3920 Single MeOCH 2 5,7-Me 2 1-3921 Single MeOCH 2 5,8-Me 2 1-3922 Single MeOCH 2 6,7-Me 2 1-3923 Single MeOCH 2 6,8-Me 2 1-3924 Single MeOCH 2 7,8-Me 2 1-3925 Single MeOCH 2 2-Me-5-F 1-3926 Single MeOCH 2 2-Me-6-F 1-3927 Single MeOCH 2 2-Me-7-F 1-3928 Single MeOCH 2 2-Me-8-F 1-3929 Single MeOCH 2 2-Me-5-Cl 1-3930 Single MeOCH 2 2-Me-6-Cl 1-3931 Single MeOCH 2 2-Me-7-Cl 1-3932 Single MeOCH 2 2-Me-8-Cl 1-3933 Single MeOCH 2 2-Me-5-MeO 1-3934 Single MeOCH 2 2-Me-6-MeO 1-3935 Single MeOCH 2 2-Me-7-MeO 1-3936 Single MeOCH 2 2-Me-8-MeO 1-3937 Single MeOCH 2 CH 2 H 1-3938 Single MeOCH 2 CH 2 2-F 1-3939 Single MeOCH 2 CH 2 4-F 1-3940 Single MeOCH 2 CH 2 5-F 1-3941 Single MeOCH 2 CH 2 6-F 1-3942 Single MeOCH 2 CH 2 7-F 1-3943 Single MeOCH 2 CH 2 8-F 1-3944 Single MeOCH 2 CH 2 2-Cl 1-3945 Single MeOCH 2 CH 2 4-Cl 1-3946 Single MeOCH 2 CH 2 5-Cl 1-3947 Single MeOCH 2 CH 2 6-Cl 1-3948 Single MeOCH 2 CH 2 7-Cl 1-3949 Single MeOCH 2 CH 2 8-Cl 1-3950 Single MeOCH 2 CH 2 2-Me 1-3951 Single MeOCH 2 CH 2 4-Me 1-3952 Single MeOCH 2 CH 2 5-Me 1-3953 Single MeOCH 2 CH 2 6-Me 1-3954 Single MeOCH 2 CH 2 7-Me 1-3955 Single MeOCH 2 CH 2 8-Me 1-3956 Single MeOCH 2 CH 2 2-Et 1-3957 Single MeOCH 2 CH 2 4-Et 1-3958 Single MeOCH 2 CH 2 5-Et 1-3959 Single MeOCH 2 CH 2 6-Et 1-3960 Single MeOCH 2 CH 2 7-Et 1-3961 Single MeOCH 2 CH 2 8-Et 1-3962 Single MeOCH 2 CH 2 2,4-F 2 1-3963 Single MeOCH 2 CH 2 2,5-F 2 1-3964 Single MeOCH 2 CH 2 2,6-F 2 1-3965 Single MeOCH 2 CH 2 2,7-F 2 1-3966 Single MeOCH 2 CH 2 2,8-F 2 1-3967 Single MeOCH 2 CH 2 4,5-F 2 1-3968 Single MeOCH 2 CH 2 4,6-F 2 1-3969 Single MeOCH 2 CH 2 4,7-F 2 1-3970 Single MeOCH 2 CH 2 4,8-F 2 1-3971 Single MeOCH 2 CH 2 5,6-F 2 1-3972 Single MeOCH 2 CH 2 5,7-F 2 1-3973 Single MeOCH 2 CH 2 5,8-F 2 1-3974 Single MeOCH 2 CH 2 6,7-F 2 1-3975 Single MeOCH 2 CH 2 6,8-F 2 1-3976 Single MeOCH 2 CH 2 7,8-F 2 1-3977 Single MeOCH 2 CH 2 2,4-Me 2 1-3978 Single MeOCH 2 CH 2 2,5-Me 2 1-3979 Single MeOCH 2 CH 2 2,6-Me 2 1-3980 Single MeOCH 2 CH 2 2,7-Me 2 1-3981 Single MeOCH 2 CH 2 2,8-Me 2 1-3982 Single MeOCH 2 CH 2 4,5-Me 2 1-3983 Single MeOCH 2 CH 2 4,6-Me 2 1-3984 Single MeOCH 2 CH 2 4,7-Me 2 1-3985 Single MeOCH 2 CH 2 4,8-Me 2 1-3986 Single MeOCH 2 CH 2 5,6-Me 2 1-3987 Single MeOCH 2 CH 2 5,7-Me 2 1-3988 Single MeOCH 2 CH 2 5,8-Me 2 1-3989 Single MeOCH 2 CH 2 6,7-Me 2 1-3990 Single MeOCH 2 CH 2 6,8-Me 2 1-3991 Single MeOCH 2 CH 2 7,8-Me 2 1-3992 Single MeOCH 2 CH 2 2-Me-5-F 1-3993 Single MeOCH 2 CH 2 2-Me-6-F 1-3994 Single MeOCH 2 CH 2 2-Me-7-F 1-3995 Single MeOCH 2 CH 2 2-Me-8-F 1-3996 Single MeOCH 2 CH 2 2-Me-5-Cl 1-3997 Single MeOCH 2 CH 2 2-Me-6-Cl 1-3998 Single MeOCH 2 CH 2 2-Me-7-Cl 1-3999 Single MeOCH 2 CH 2 2-Me-8-Cl 1-4000 Single MeOCH 2 CH 2 2-Me-5-MeO 1-4001 Single MeOCH 2 CH 2 2-Me-6-MeO 1-4002 Single MeOCH 2 CH 2 2-Me-7-MeO 1-4003 Single MeOCH 2 CH 2 2-Me-8-MeO 1-4004 two Et H 1-4005 two Et 2-F 1-4006 two Et 4-F 1-4007 two Et 5-F 1-4008 two Et 6-F 1-4009 two Et 7-F 1-4010 2 Et 8-F 1-4011 2 Et 2-Cl 1-4012 2 Et 4-Cl 1-4013 2 Et 5-Cl 1-4014 2 Et 6-Cl 1-4015 2 Et 7- Cl 1-4016 Two Et 8-Cl 1-4017 Two Et 2-Me 1-4018 Two Et 4-Me 1-4019 Two Et 5-Me 1-4020 Two Et 6-Me 1-4021 Two Et 7-Me 1 -4022 Two Et 8-Me 1-4023 Two Et 2-Et 1-4024 Two Et 4-Et 1-4025 Two Et 5-Et 1-4026 Two Et 6-Et 1-4027 Two Et 7-Et 1-4028 Ni Et 8-Et 1-4029 Ni Et 2,4-F 2 1-4030 Two Et 2,5-F 2 1-4031 Two Et 2,6-F 2 1-4032 Two Et 2,7-F 2 1-4033 Two Et 2,8-F 2 1-4034 Two Et 4,5-F 2 1-4035 Two Et 4,6-F 2 1-4036 Two Et 4,7-F 2 1-4037 Two Et 4,8-F 2 1-4038 Two Et 5,6-F 2 1-4039 Two Et 5,7-F 2 1-4040 Two Et 5,8-F 2 1-4041 Two Et 6,7-F 2 1-4042 Two Et 6,8-F 2 1-4043 Two Et 7,8-F 2 1-4044 Two Et 2,4-Me 2 1-4045 Two Et 2,5-Me 2 1-4046 Two Et 2,6-Me 2 1-4047 Two Et 2,7-Me 2 1-4048 Two Et 2,8-Me 2 1-4049 Two Et 4,5-Me 2 1-4050 Two Et 4,6-Me 2 1-4051 Two Et 4,7-Me 2 1-4052 Two Et 4,8-Me 2 1-4053 Two Et 5,6-Me 2 1-4054 Two Et 5,7-Me 2 1-4055 Two Et 5,8-Me 2 1-4056 Two Et 6,7-Me 2 1-4057 Two Et 6,8-Me 2 1-4058 Two Et 7,8-Me 2 1-4059 Ni Et 2-Me-5-F 1-4060 Ni Et 2-Me-6-F 1-4061 Ni Et 2-Me-7-F 1-4062 Ni Et 2-Me-8-F 1- 4063 Ni Et 2-Me-5-Cl 1-4064 Ni Et 2-Me-6-Cl 1-4065 Ni Et 2-Me-7-Cl 1-4066 Ni Et 2-Me-8-Cl 1-4067 Ni Et 2-Me-5-MeO 1-4068 2 Et 2-Me-6-MeO 1-4069 2 Et 2-Me-7-MeO 1-4070 2 Et 2-Me-8-MeO 1-4071 2 Pr H 1-4072 Two Pr 2-F 1-4073 Two Pr 4-F 1-4074 Two Pr 5-F 1-4075 Two Pr 6-F 1-4076 Two Pr 7-F 1-4077 Two Pr 8-F 1- 4078 Two Pr 2-Cl 1-4079 Two Pr 4-Cl 1-4080 Two Pr 5-Cl 1-4081 Two Pr 6-Cl 1-4082 Two Pr 7-Cl 1-4083 Two Pr 8-Cl 1-4084 Two Pr 2-Me 1-4085 two Pr 4-Me 1-4086 two Pr 5-Me 1-4087 two Pr 6-Me 1-4088 two Pr 7-Me 1-4089 two Pr 8-Me 1-4090 two Pr 2 -Et 1-4091 two Pr 4-Et 1-4092 two Pr 5-Et 1-4093 two Pr 6-Et 1-4094 two Pr 7-Et 1-4095 two Pr 8-Et 1-4096 two Pr 2,4 -F 2 1-4097 Two Pr 2,5-F 2 1-4098 Two Pr 2,6-F 2 1-4099 Two Pr 2,7-F 2 1-4100 Two Pr 2,8-F 2 1-4101 Two Pr 4,5-F 2 1-4102 Two Pr 4,6-F 2 1-4103 Two Pr 4,7-F 2 1-4104 Two Pr 4,8-F 2 1-4105 Two Pr 5,6-F 2 1-4106 Two Pr 5,7-F 2 1-4107 Two Pr 5,8-F 2 1-4108 Two Pr 6,7-F 2 1-4109 Two Pr 6,8-F 2 1-4110 Two Pr 7,8-F 2 1-4111 Two Pr 2,4-Me 2 1-4112 Two Pr 2,5-Me 2 1-4113 Two Pr 2,6-Me 2 1-4114 Two Pr 2,7-Me 2 1-4115 Two Pr 2,8-Me 2 1-4116 Two Pr 4,5-Me 2 1-4117 Two Pr 4,6-Me 2 1-4118 Two Pr 4,7-Me 2 1-4119 Two Pr 4,8-Me 2 1-4120 Two Pr 5,6-Me 2 1-4121 Two Pr 5,7-Me 2 1-4122 Two Pr 5,8-Me 2 1-4123 Two Pr 6,7-Me 2 1-4124 Two Pr 6,8-Me 2 1-4125 Two Pr 7,8-Me 2 1-4126 Two Pr 2-Me-5-F 1-4127 Two Pr 2-Me-6-F 1-4128 Two Pr 2-Me-7-F 1-4129 Two Pr 2-Me-8-F 1- 4130 Two Pr 2-Me-5-Cl 1-4131 Two Pr 2-Me-6-Cl 1-4132 Two Pr 2-Me-7-Cl 1-4133 Two Pr 2-Me-8-Cl 1-4134 Two Pr 2-Me-5-MeO 1-4135 two Pr 2-Me-6-MeO 1-4136 two Pr 2-Me-7-MeO 1-4137 two Pr 2-Me-8-MeO 1-4138 two Allyl H 1-4139 Two Allyl 2-F 1-4140 Two Allyl 4-F 1-4141 Two Allyl 5-F 1-4142 Two Allyl 6-F 1-4143 Two Allyl 7-F 1-4144 Two Allyl 8-F 1- 4145 II Allyl 2-Cl 1-4146 II Allyl 4-Cl 1-4147 II Allyl 5-Cl 1-4148 II Allyl 6-Cl 1-4149 II Allyl 7-Cl 1-4150 II Allyl 8-Cl 1-4151 II Allyl 2-Me 1-4152 two Allyl 4-Me 1-4153 two Allyl 5-Me 1-4154 two Allyl 6-Me 1-4155 two Allyl 7-Me 1-4156 two Allyl 8-Me 1-4157 two Allyl 2 -Et 1-4158 two Allyl 4-Et 1-4159 two Allyl 5-Et 1-4160 two Allyl 6-Et 1-4161 two Allyl 7-Et 1-4162 two Allyl 8-Et 1-4163 two Allyl 2,4 -F 2 1-4164 Two Allyl 2,5-F 2 1-4165 Two Allyl 2,6-F 2 1-4166 Two Allyl 2,7-F 2 1-4167 Two Allyl 2,8-F 2 1-4168 Two Allyl 4,5-F 2 1-4169 Two Allyl 4,6-F 2 1-4170 Two Allyl 4,7-F 2 1-4171 Two Allyl 4,8-F 2 1-4172 Two Allyl 5,6-F 2 1-4173 Two Allyl 5,7-F 2 1-4174 Two Allyl 5,8-F 2 1-4175 Two Allyl 6,7-F 2 1-4176 Two Allyl 6,8-F 2 1-4177 Two Allyl 7,8-F 2 1-4178 Two Allyl 2,4-Me 2 1-4179 Two Allyl 2,5-Me 2 1-4180 Two Allyl 2,6-Me 2 1-4181 Two Allyl 2,7-Me 2 1-4182 Two Allyl 2,8-Me 2 1-4183 Two Allyl 4,5-Me 2 1-4184 Two Allyl 4,6-Me 2 1-4185 Two Allyl 4,7-Me 2 1-4186 Two Allyl 4,8-Me 2 1-4187 Two Allyl 5,6-Me 2 1-4188 Two Allyl 5,7-Me 2 1-4189 Two Allyl 5,8-Me 2 1-4190 Two Allyl 6,7-Me 2 1-4191 Two Allyl 6,8-Me 2 1-4192 two Allyl 7,8-Me 2 1-4193 II Allyl 2-Me-5-F 1-4194 II Allyl 2-Me-6-F 1-4195 II Allyl 2-Me-7-F 1-4196 II Allyl 2-Me-8-F 1- 4197 Two Allyl 2-Me-5-Cl 1-4198 Two Allyl 2-Me-6-Cl 1-4199 Two Allyl 2-Me-7-Cl 1-4200 Two Allyl 2-Me-8-Cl 1-4201 Two Allyl 2-Me-5-MeO 1-4202 II Allyl 2-Me-6-MeO 1-4203 II Allyl 2-Me-7-MeO 1-4204 II Allyl 2-Me-8-MeO 1-4205 Single Me 2 , 4-Me 2 1-4206 Single Et 2,4-Me 2 1-4207 Single CF 3 2,4-Me 2 1-4208 Single Allyl 2,4-Me 2 1-4209 Single MeOCH 2 2,4-Me 2 ───────────────────────────────────

【００２７】[0027]

【表２】[Table 2]

【００２８】[0028]

【化４】 [Chemical 4]

【００２９】 ────────────────────────────────── 化合物番号 …… Ｒ Ｘm Ｚn ────────────────────────────────── 2-1 単 Me H 2-Me 2-2 単 Me H 3-Me 2-3 単 Me H 4-Me 2-4 単 Me H 2,2-Me2 2-5 単 Me H 2-5-CH2 2-6 単 Me 2-Me 2-Me 2-7 単 Me 2-Me 3-Me 2-8 単 Me 2-Me 4-Me 2-9 単 Me 2-Me 2,2-Me2 2-10 単 Me 2-Me 2-5-CH2 2-11 単 Me 4-Me 2-Me 2-12 単 Me 4-Me 3-Me 2-13 単 Me 4-Me 4-Me 2-14 単 Me 4-Me 2,2-Me2 2-15 単 Me 4-Me 2-5-CH2 2-16 単 Me 8-Me 2-Me 2-17 単 Me 8-Me 3-Me 2-18 単 Me 8-Me 4-Me 2-19 単 Me 8-Me 2,2-Me2 2-20 単 Me 8-Me 2-5-CH2 2-21 単 Et H 2-Me 2-22 単 Et H 3-Me 2-23 単 Et H 4-Me 2-24 単 Et H 2,2-Me2 2-25 単 Et H 2-5-CH2 2-26 単 CF3 H 2-Me 2-27 単 CF3 H 3-Me 2-28 単 CF3 H 4-Me 2-29 単 CF3 H 2,2-Me2 2-30 単 CF3 H 2-5-CH2 2-31 単 Allyl H 2-Me 2-32 単 Allyl H 3-Me 2-33 単 Allyl H 4-Me 2-34 単 Allyl H 2,2-Me2 2-35 単 Allyl H 2-5-CH2 2-36 単 2-Pentynyl H 2-Me 2-37 単 2-Pentynyl H 3-Me 2-38 単 2-Pentynyl H 4-Me 2-39 単 2-Pentynyl H 2,2-Me2 2-40 単 2-Pentynyl H 2-5-CH2 2-41 二 Me H 2-Me 2-42 二 Me H 3-Me 2-43 二 Me H 4-Me 2-44 二 Me H 2,2-Me2 2-45 二 Me H 2-5-CH2 ────────────────────────────────── 上記の例示化合物中、好適な化合物は、化合物番号１−
１、１−６、１−７、１−２６、１−２７、１−２８、
１−２９、１−３１、１−２１６、１−２２３、１−２
４８、１−２４９、１−４４５、１−４７０、１−４７
１、１−６６７、１−６９２、１−８８９、１−１１１
１、１−１１３７、１−１３３３、１−１８０３、１−
１９９９、１−２４４３、１−２４６８、１−２４６
９、１−２７３２、１−２７９９、１−３０００、１−
３３３４、１−３４０１、１−３４８１、１−３４８
２、１−３５３５、１−３６０２、１−３６６９、１−
３７３６、１−３７４９、１−３７５０、１−３８０
３、１−３８１６、１−３８１７、１−３８７０、１−
３８８４、１−４００４、１−４０１７、１−４０１
８、１−４１５２、２−１、２−４及び２−５番の化合
物であり、より好適には、化合物番号１−１、１−７、
１−２６、１−２７、１−３１、１−２２３、１−２４
８、１−２４９、１−４４５、１−４７１、１−６６
７、１−８８９、１−１１１１、１−１１３７、１−１
３３３、１−１８０３、１−１９９９、１−２４４３、
１−２４６８、１−２４６９、１−２７３２、１−３４
８１、１−３４８２、１−３６６９、１−３７３６、１
−３７４９、１−３７５０、１−３８１６、１−３８１
７、１−４０１７、１−４１５２、２−１及び２−４番
の化合物であり、更により好適には、化合物番号１−
１、１−７、１−２６、１−３１、１−２４８、１−２
４９、１−４７１、１−１１３７、１−１３３３、１−
２４４３、１−２４６８、１−２４６９、１−３４８
１、１−３４８２、１−３７３６、１−３８１７、１−
４０１７、１−４１５２及び２−１番の化合物である。────────────────────────────────── Compound number …… R Xm Zn ─────── ──────────────────────────── 2-1 Single Me H 2-Me 2-2 Single Me H 3-Me 2-3 Single Me H 4-Me 2-4 single Me H 2,2-Me 2 2-5 single Me H 2-5-CH 2 2-6 single Me 2-Me 2-Me 2-7 single Me 2-Me 3- Me 2-8 Single Me 2-Me 4-Me 2-9 Single Me 2-Me 2,2-Me 2 2-10 Single Me 2-Me 2-5-CH 2 2-11 Single Me 4-Me 2- Me 2-12 Single Me 4-Me 3-Me 2-13 Single Me 4-Me 4-Me 2-14 Single Me 4-Me 2,2-Me 2 2-15 Single Me 4-Me 2-5-CH 2 2-16 Single Me 8-Me 2-Me 2-17 Single Me 8-Me 3-Me 2-18 Single Me 8-Me 4-Me 2-19 Single Me 8-Me 2,2-Me 2 2- 20 Single Me 8-Me 2-5-CH 2 2-21 Single Et H 2-Me 2-22 Single Et H 3-Me 2-23 Single Et H 4-Me 2-24 Single Et H 2,2-Me 2 2-25 Single Et H 2-5-CH 2 2-26 Single CF3 H 2-Me 2-27 Single CF3 H 3-Me 2-28 Single CF3 H 4-Me 2-29 Single CF3 H 2,2- Me 2 2-30 Single CF3 H 2-5-CH 2 2-31 Single Allyl H 2-Me 2-32 Single Allyl H 3-Me 2-33 Single Allyl H 4-Me 2-34 Single Allyl H 2,2-Me 2 2-35 Single Allyl H 2-5-CH 2 2-36 Single 2-Pentynyl H 2-Me 2-37 Single 2-Pentynyl H 3-Me 2-38 Single 2-Pentynyl H 4 -Me 2-39 Single 2-Pentynyl H 2,2-Me 2 2-40 Single 2-Pentynyl H 2-5-CH 2 2-41 Secondary Me H 2-Me 2-42 Secondary Me H 3-Me 2- 43 Two Me H 4-Me 2-44 Two Me H 2,2-Me 2 2-45 Two Me H 2-5-CH 2 ─────────────────── ─────────────── Among the above-exemplified compounds, preferred compounds are compound numbers 1-
1, 1-6, 1-7, 1-26, 1-27, 1-28,
1-29, 1-31, 1-216, 1-223, 1-2
48, 1-249, 1-445, 1-470, 1-47
1, 1-667, 1-692, 1-889, 1-111
1, 1-1137, 1-1333, 1-1803, 1-
1999, 1-2443, 1-2468, 1-246
9, 1-2732, 1-2799, 1-3000, 1-
3334, 1-3401, 1-3481, 1-348
2, 1-3535, 1-3602, 1-3669, 1-
3736, 1-3749, 1-3750, 1-380
3, 1-3816, 1-3817, 1-3870, 1-
3884, 1-4004, 1-4017, 1-401
Nos. 8, 1-41522, 2-1, 2-4 and 2-5 compounds, more preferably compound numbers 1-1, 1-7,
1-26, 1-27, 1-31, 1-223, 1-24
8, 1-249, 1-445, 1-471, 1-66
7, 1-889, 1-1111, 1-1137, 1-1
333, 1-1803, 1-1999, 1-2443,
1-2468, 1-2469, 1-2732, 1-34
81, 1-3482, 1-3669, 1-3736, 1
-3749, 1-3750, 1-3816, 1-381
Nos. 7, 1-4017, 1-4152, 2-1, and 2-4, and even more preferably compound No. 1-
1, 1-7, 1-26, 1-31, 1-248, 1-2
49, 1-471, 1-1137, 1-1333, 1-
2443, 1-2468, 1-2469, 1-348
1, 1-3482, 1-3736, 1-3817, 1-
Nos. 4017, 1-4152, and 2-1.

【００３０】[0030]

【発明の実施の形態】本発明のＮ−（３−キノリル）ア
ミド誘導体は、以下に記載する工程Ａ又はＢの方法によ
って製造することができる。BEST MODE FOR CARRYING OUT THE INVENTION The N- (3-quinolyl) amide derivative of the present invention can be produced by the method of step A or B described below.

【００３１】（工程Ａ）(Step A)

【００３２】[0032]

【化５】 [Chemical 5]

【００３３】上式中、……、Ｒ、Ｘ、ｍ、Ｚ及びｎは、
前記と同意義を示す。In the above equation, ... , R, X, m, Z and n are
Same meaning as above.

【００３４】工程Ａは、一般式（II）で表されるアミン
類を、不活性溶媒中、塩基の存在下又は非存在下、縮合
剤の存在下又は非存在下、一般式（III）で表されるカ
ルボン酸誘導体と脱水縮合することにより、本発明の一
般式（I）で表されるN−（３−キノリル）アミド誘導体
を製造する工程である。In the step A, the amine represented by the general formula (II) is reacted with the general formula (III) in an inert solvent in the presence or absence of a base, in the presence or absence of a condensing agent. It is a step of producing an N- (3-quinolyl) amide derivative represented by the general formula (I) of the present invention by dehydration condensation with the represented carboxylic acid derivative.

【００３５】用いられる化合物（III）の量は、化合物
（II）１モルに対し、通常、1〜3モルであり、好適に
は、1.1〜1.5モルである。The amount of the compound (III) used is usually 1 to 3 mol, preferably 1.1 to 1.5 mol, per 1 mol of the compound (II).

【００３６】本発明で塩基を用いる場合、用いられる塩
基は、通常の反応において塩基として使用されるもので
あれば特に限定はないが、例えば、炭酸ナトリウム、炭
酸カリウムのようなアルカリ金属炭酸塩；炭酸水素ナト
リウム、炭酸水素カリウムのようなアルカリ金属炭酸水
素塩；水素化ナトリウム、水素化リチウム、水素化カリ
ウムのようなアルカリ金属水素化物；水酸化ナトリウ
ム、水酸化カリウム、水酸化バリウムのようなアルカリ
金属水酸化物若しくはアルカリ土類金属水酸化物；ナト
リウムメトキシド、ナトリウムエトキシド、カリウムｔ
−ブトキシドのようなアルカリ金属アルコキシド類；ト
リエチルアミン、トリブチルアミン、ジイソプロピルエ
チルアミン、Ｎ−メチルモルホリン、ピリジン、４−
（Ｎ，Ｎ−ジメチルアミノ）ピリジン、Ｎ，Ｎ−ジメチ
ルアニリン、Ｎ，Ｎ−ジエチルアニリン、１，５−ジア
ザビシクロ［４．３．０］ノナ−５−エン、１，４−ジ
アザビシクロ［２．２．２］オクタン（ＤＡＢＣＯ）、
１，８−ジアザビシクロ［５．４．０］−７−ウンデセ
ン（ＤＢＵ）のような有機塩基類又はブチルリチウム、
リチウムジイソプロピルアミドのような有機金属類であ
り得、好適には、有機塩基類であり、更に好適には、ト
リエチルアミンである。When a base is used in the present invention, the base used is not particularly limited as long as it is used as a base in a usual reaction, and examples thereof include alkali metal carbonates such as sodium carbonate and potassium carbonate; Alkali metal hydrogen carbonate such as sodium hydrogen carbonate, potassium hydrogen carbonate; Alkali metal hydride such as sodium hydride, lithium hydride, potassium hydride; Alkali such as sodium hydroxide, potassium hydroxide, barium hydroxide Metal hydroxide or alkaline earth metal hydroxide; sodium methoxide, sodium ethoxide, potassium t
-Alkali metal alkoxides such as butoxide; triethylamine, tributylamine, diisopropylethylamine, N-methylmorpholine, pyridine, 4-
(N, N-dimethylamino) pyridine, N, N-dimethylaniline, N, N-diethylaniline, 1,5-diazabicyclo [4.3.0] non-5-ene, 1,4-diazabicyclo [2. 2.2] Octane (DABCO),
Organic bases such as 1,8-diazabicyclo [5.4.0] -7-undecene (DBU) or butyllithium,
It may be an organometallic such as lithium diisopropylamide, preferably an organic base, more preferably triethylamine.

【００３７】用いられる塩基の量は、化合物（II）１モ
ルに対し、通常、1〜30モルであり、好適には、1.1〜15
モルである。The amount of the base used is usually 1 to 30 mol, preferably 1.1 to 15 mol, relative to 1 mol of the compound (II).
It is a mole.

【００３８】本発明で縮合剤を用いる場合、用いられる
縮合剤は、通常の脱水縮合反応において縮合剤として使
用されるものであれば特に限定はないが、例えば、ジシ
クロヘキシルカルボジイミド（DCC）、ジイソプロピル
カルボジイミド（DIPC）、N−エチル−N'−エチル−
（３−ジメチルアミノプロピル）カルボジイミド（ED
C）のようなカルボジイミド類；ジエチルリン酸シアニ
ド（DEPC）、ジフェニルリン酸アジド（DPPA）、ベンズ
イソオキサゾール−１−イル−トリス（ジメチルアミ
ノ）ホスホニウム ヘキサフルオロリン化物塩（BOP）
のようなリン酸類；沃化１−メチル−２−クロロピリジ
ニウム、１−エチル−２−フルオロピリジニウム＝テト
ラフルオロボレートのようなピリジニウム塩類；又は、
カルボニルジイミダゾール（CDI）であり得、好適に
は、ピリジニウム塩類であり、更に好適には、沃化１−
メチル−２−クロロピリジニウムである。When the condensing agent is used in the present invention, the condensing agent to be used is not particularly limited as long as it is used as a condensing agent in a usual dehydration condensation reaction, and examples thereof include dicyclohexylcarbodiimide (DCC) and diisopropylcarbodiimide. (DIPC), N-ethyl-N'-ethyl-
(3-Dimethylaminopropyl) carbodiimide (ED
C) carbodiimides such as diethylphosphate cyanide (DEPC), diphenylphosphate azide (DPPA), benzisoxazol-1-yl-tris (dimethylamino) phosphonium hexafluorophosphide salt (BOP)
Or a phosphoric acid; a pyridinium salt such as 1-methyl-2-chloropyridinium iodide, 1-ethyl-2-fluoropyridinium = tetrafluoroborate; or
It may be carbonyldiimidazole (CDI), preferably a pyridinium salt, more preferably 1-iodide
It is methyl-2-chloropyridinium.

【００３９】用いられる縮合剤の量は、化合物（II）１
モルに対し、通常、1〜30モルであり、好適には、1.1〜
15モルである。The amount of the condensing agent used is the compound (II) 1
It is usually 1 to 30 mol, and preferably 1.1 to 30 mol, based on mol.
It is 15 mol.

【００４０】本工程で用いられる溶媒は、反応を阻害し
ないものであれば特に限定はないが、例えば、ヘキサ
ン、シクロヘキサン、ベンゼン、トルエン等の炭化水素
類；ジクロロメタン、ジクロロエタン、クロロホルム、
テトラクロロエタン等のハロゲン化炭化水素類；ジオキ
サン、ジエチルエーテル、テトラヒドロフラン（ＴＨ
Ｆ）、エチレングリコールジメチルエーテル等のエーテ
ル類；ジメチルホルムアミド、ジメチルアセトアミド、
ヘキサメチルリン酸トリアミド（ＨＭＰＡ）等のアミド
類；アセトン、メチルエチルケトン、メチルイソブチル
ケトン、シクロヘキサノン等のケトン類；アセトニトリ
ル、イソブチロニトリル等のニトリル類；又は、酢酸メ
チル、酢酸エチル、酢酸プロピル等のエステル類であ
り、好適には、ハロゲン化炭化水素類又はエーテル類で
あり、更に好適には、ジクロロメタン、ジクロロエタン
又はＴＨＦである。The solvent used in this step is not particularly limited as long as it does not inhibit the reaction. For example, hydrocarbons such as hexane, cyclohexane, benzene, toluene; dichloromethane, dichloroethane, chloroform,
Halogenated hydrocarbons such as tetrachloroethane; dioxane, diethyl ether, tetrahydrofuran (TH
F), ethers such as ethylene glycol dimethyl ether; dimethylformamide, dimethylacetamide,
Hexamethylphosphoric triamide (HMPA) and other amides; acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and other ketones; acetonitrile, isobutyronitrile and other nitriles; or methyl acetate, ethyl acetate, propyl acetate, etc. Esters, preferably halogenated hydrocarbons or ethers, more preferably dichloromethane, dichloroethane or THF.

【００４１】反応温度は、原料化合物、反応試薬及び溶
媒などにより異なるが、通常、−２０℃〜１５０℃であ
り、好適には、０℃〜４０℃である。The reaction temperature will differ depending on the starting compounds, reaction reagents, solvent, etc., but will usually be -20 ° C to 150 ° C, and is preferably 0 ° C to 40 ° C.

【００４２】反応時間は、原料化合物、反応試薬、溶媒
及び反応温度などにより異なるが、通常１０分間〜１２
０時間であり、好適には３０分間〜７２時間である。The reaction time varies depending on the raw material compound, the reaction reagent, the solvent, the reaction temperature and the like, but is usually 10 minutes to 12 minutes.
It is 0 hour, preferably 30 minutes to 72 hours.

【００４３】本工程に使用される化合物（II）は公知化
合物であるか、又は公知の方法を組み合わせて（例え
ば、ジャーナル・オブ・メディシナル・ケミストリーJ.
Med.Chem.,３９巻２３号４６８２頁（１９９６年）に記
載された方法によって得られる４−ヒドロキシ−３−ニ
トロキノリン−２−オンから、ジャーナル・オブ・プラ
クティカル・ケミストリーJ.Prakt.Chem.,３３６巻４号
３１１頁（１９９４年）に記載された方法で２，４−ジ
クロロ−３−ニトロキノリンを得、これをケミシュ・ベ
リヒテChem.Ber.,51巻、１５０９頁（１９１８年）に記
載された方法で目的物を得る）製造することができる。The compound (II) used in this step is a known compound or a combination of known methods (for example, Journal of Medicinal Chemistry J.
Med. Chem., Vol. 39, No. 23, page 4682 (1996), from 4-hydroxy-3-nitroquinolin-2-one obtained from Journal of Practical Chemistry J. Prakt. Chem. ., 336, No. 4, page 311 (1994), to obtain 2,4-dichloro-3-nitroquinoline, which is Chemis Berichte Chem. Ber., 51, 1509 (1918). The desired product can be obtained by the method described in (1) above.

【００４４】本工程に使用される化合物（III）は公知
化合物であるか、又は公知の方法（例えば、オーガニッ
ク・シンセシスOrg.Synth.,４６巻７２頁（１９６６
年）又は、テトラヘドロンTetrahedron,５３巻２７号９
０２３頁（１９９７年）に記載された方法）に準じて製
造することができる。The compound (III) used in this step is a known compound, or a known method (for example, Organic Synthesis Org. Synth., Vol. 46, p. 72 (1966)).
Or Tetrahedron, 53, 27, 9
It can be manufactured according to the method described on page 023 (1997).

【００４５】（工程Ｂ）(Step B)

【００４６】[0046]

【化６】 [Chemical 6]

【００４７】上式中、……、Ｒ、Ｘ、ｍ、Ｚ及びｎは、
前記と同意義を示し、Ｑは、ハロゲンを示す。In the above equation, ... , R, X, m, Z and n are
It has the same meaning as above and Q represents halogen.

【００４８】工程Ｂは、一般式（II）で表されるアミン
類を、不活性溶媒中、塩基の存在下又は非存在下、一般
式（IV）で表されるアシル誘導体によりアシル化するこ
とにより、本発明の一般式（I）で表されるN−（３−キ
ノリル）アミド誘導体を製造する工程である。Step B is to acylate the amines represented by the general formula (II) with an acyl derivative represented by the general formula (IV) in an inert solvent in the presence or absence of a base. Is a step of producing the N- (3-quinolyl) amide derivative represented by the general formula (I) of the present invention.

【００４９】用いられる化合物（IV）の量は、化合物
（II）１モルに対し、通常、1〜3モルであり、好適に
は、1.1〜1.5モルである。The amount of the compound (IV) used is usually 1 to 3 mol, preferably 1.1 to 1.5 mol, per 1 mol of the compound (II).

【００５０】本発明で塩基を用いる場合、用いられる塩
基は、通常の反応において塩基として使用されるもので
あれば特に限定はないが、例えば、炭酸ナトリウム、炭
酸カリウムのようなアルカリ金属炭酸塩；炭酸水素ナト
リウム、炭酸水素カリウムのようなアルカリ金属炭酸水
素塩；水素化ナトリウム、水素化リチウム、水素化カリ
ウムのようなアルカリ金属水素化物；水酸化ナトリウ
ム、水酸化カリウム、水酸化バリウムのようなアルカリ
金属水酸化物又はアルカリ土類金属水酸化物；ナトリウ
ムメトキシド、ナトリウムエトキシド、カリウムｔ−ブ
トキシドのようなアルカリ金属アルコキシド類；トリエ
チルアミン、トリブチルアミン、ジイソプロピルエチル
アミン、Ｎ−メチルモルホリン、ピリジン、４−（Ｎ，
Ｎ−ジメチルアミノ）ピリジン、Ｎ，Ｎ−ジメチルアニ
リン、Ｎ，Ｎ−ジエチルアニリン、１，５−ジアザビシ
クロ［４．３．０］ノナ−５−エン、１，４−ジアザビ
シクロ［２．２．２］オクタン（ＤＡＢＣＯ）、１，８
−ジアザビシクロ［５．４．０］−７−ウンデセン（Ｄ
ＢＵ）のような有機塩基類；又は、ブチルリチウム、リ
チウムジイソプロピルアミドのような有機金属類であり
得、好適には、有機塩基類であり、更に好適には、ピリ
ジンである。When a base is used in the present invention, the base used is not particularly limited as long as it is used as a base in a usual reaction, and examples thereof include alkali metal carbonates such as sodium carbonate and potassium carbonate; Alkali metal hydrogen carbonate such as sodium hydrogen carbonate, potassium hydrogen carbonate; Alkali metal hydride such as sodium hydride, lithium hydride, potassium hydride; Alkali such as sodium hydroxide, potassium hydroxide, barium hydroxide Metal hydroxides or alkaline earth metal hydroxides; alkali metal alkoxides such as sodium methoxide, sodium ethoxide, potassium t-butoxide; triethylamine, tributylamine, diisopropylethylamine, N-methylmorpholine, pyridine, 4- (N,
N-dimethylamino) pyridine, N, N-dimethylaniline, N, N-diethylaniline, 1,5-diazabicyclo [4.3.0] non-5-ene, 1,4-diazabicyclo [2.2.2] ] Octane (DABCO), 1,8
-Diazabicyclo [5.4.0] -7-undecene (D
BU), or an organic metal such as butyllithium or lithium diisopropylamide, preferably an organic base, more preferably pyridine.

【００５１】用いられる塩基の量は、化合物（II）１モ
ルに対し、通常、1〜30モルであり、好適には、1.1〜15
モルである。The amount of the base used is usually 1 to 30 mol, preferably 1.1 to 15 mol, relative to 1 mol of the compound (II).
It is a mole.

【００５２】本工程で用いられる溶媒は、反応を阻害し
ないものであれば特に限定はないが、例えば、ヘキサ
ン、シクロヘキサン、ベンゼン、トルエン等の炭化水素
類；ジクロロメタン、ジクロロエタン、クロロホルム、
テトラクロロエタン等のハロゲン化炭化水素類；ジオキ
サン、ジエチルエーテル、テトラヒドロフラン（ＴＨ
Ｆ）、エチレングリコールジメチルエーテル等のエーテ
ル類；ジメチルホルムアミド、ジメチルアセトアミド、
ヘキサメチルリン酸トリアミド（ＨＭＰＡ）等のアミド
類；アセトン、メチルエチルケトン、メチルイソブチル
ケトン、シクロヘキサノン等のケトン類；アセトニトリ
ル、イソブチロニトリル等のニトリル類；又は、酢酸メ
チル、酢酸エチル、酢酸プロピル等のエステル類であり
得、好適には、ハロゲン化炭化水素類又はエーテル類で
あり、更に好適には、ジクロロメタン、ジクロロエタン
又はＴＨＦである。The solvent used in this step is not particularly limited as long as it does not inhibit the reaction, but for example, hydrocarbons such as hexane, cyclohexane, benzene, toluene; dichloromethane, dichloroethane, chloroform,
Halogenated hydrocarbons such as tetrachloroethane; dioxane, diethyl ether, tetrahydrofuran (TH
F), ethers such as ethylene glycol dimethyl ether; dimethylformamide, dimethylacetamide,
Hexamethylphosphoric triamide (HMPA) and other amides; acetone, methyl ethyl ketone, methyl isobutyl ketone, cyclohexanone and other ketones; acetonitrile, isobutyronitrile and other nitriles; or methyl acetate, ethyl acetate, propyl acetate, etc. It may be an ester, preferably a halogenated hydrocarbon or an ether, more preferably dichloromethane, dichloroethane or THF.

【００５３】反応温度は、原料化合物、反応試薬及び溶
媒などにより異なるが、通常、−２０℃〜１５０℃であ
り、好適には、０℃〜４０℃である。The reaction temperature will differ depending on the starting compounds, reaction reagents, solvent and the like, but will usually be -20 ° C to 150 ° C, and is preferably 0 ° C to 40 ° C.

【００５４】反応時間は、原料化合物、反応試薬、溶媒
及び反応温度などにより異なるが、通常、１０分間〜１
２０時間であり、好適には、３０分間〜７２時間であ
る。The reaction time varies depending on the raw material compound, the reaction reagent, the solvent, the reaction temperature and the like, but is usually 10 minutes to 1
20 hours, preferably 30 minutes to 72 hours.

【００５５】本工程に使用される化合物（IV）は公知化
合物であるか、又は公知の方法（例えば、新実験化学講
座（丸善株式会社、１９７７年）、１４巻、有機化合物
の合成と反応(II)、の１１０６頁（５・５酸ハロゲン化
物の章の５・５・２カルボン酸又はその誘導体からの合
成）に記載された方法）に準じて化合物（III）から製
造することができる。The compound (IV) used in this step is a known compound, or a known method (for example, New Experimental Chemistry Course (Maruzen Co., Ltd., 1977), Volume 14, Synthesis and Reaction of Organic Compound ( II), page 1106 (synthesis from 5.5.2 carboxylic acid or its derivative in the section of 5/5 acid halides)).

【００５６】上記各反応終了後、各反応の目的化合物
は、常法に従って反応混合物から採取することができ
る。例えば、反応混合物を適宜中和し、又、不溶物が存
在する場合には濾過により除去した後、水と酢酸エチル
のような混和しない有機溶媒を加え、水洗後、目的化合
物を含む有機層を分離し、無水硫酸マグネシウム等で乾
燥後、溶剤を留去することによって得られる。After completion of each of the above reactions, the target compound of each reaction can be collected from the reaction mixture according to a conventional method. For example, the reaction mixture is appropriately neutralized, and if insolubles are present, they are removed by filtration, water and an immiscible organic solvent such as ethyl acetate are added, and the mixture is washed with water to form an organic layer containing the target compound. It is obtained by separating, drying over anhydrous magnesium sulfate and the like, and distilling off the solvent.

【００５７】得られた目的化合物は必要ならば、常法、
例えば再結晶、再沈殿又はクロマトグラフィー等によっ
て更に精製できる。If necessary, the desired compound thus obtained is subjected to a conventional method,
It can be further purified by, for example, recrystallization, reprecipitation or chromatography.

【００５８】本発明の化合物（I）の塩を製造する工程
は、各工程で製造した本願化合物（I）を含む反応混合
物の抽出濃縮物、又は、化合物（I）を適当な溶媒に溶
解させた液に酸を加えることによって行われる。The steps for producing the salt of compound (I) of the present invention include the extraction concentrate of the reaction mixture containing compound (I) of the present invention produced in each step, or compound (I) is dissolved in a suitable solvent. It is carried out by adding an acid to the solution.

【００５９】反応に使用される酸は、フッ化水素酸、塩
酸、臭化水素酸、沃化水素酸のようなハロゲン化水素
酸、硝酸、過塩素酸、硫酸、燐酸等の無機酸；メタンス
ルホン酸、トリフルオロメタンスルホン酸、エタンスル
ホン酸のような低級アルキルスルホン酸、ベンゼンスル
ホン酸、ｐ−トルエンスルホン酸のようなアリールスル
ホン酸、コハク酸、蓚酸等の有機酸塩；及びサッカリン
のような有機酸アミド化合物を挙げることができる。The acid used in the reaction is hydrofluoric acid, hydrochloric acid, hydrobromic acid, hydrohalic acid such as hydroiodic acid, nitric acid, perchloric acid, sulfuric acid, phosphoric acid and other inorganic acids; methane. Lower alkyl sulfonic acids such as sulfonic acid, trifluoromethane sulfonic acid, ethane sulfonic acid, benzene sulfonic acid, aryl sulfonic acids such as p-toluene sulfonic acid, organic acid salts such as succinic acid, oxalic acid; and saccharin An organic acid amide compound can be mentioned.

【００６０】酸は、通常１当量乃至１０当量用いられ、
好適には１当量乃至５当量である。The acid is usually used in an amount of 1 to 10 equivalents,
It is preferably 1 equivalent to 5 equivalents.

【００６１】反応に使用される溶媒は、本反応を阻害し
ない限り特に限定は無いが、好適には、エーテル、ジイ
ソプロピルエーテル、テトラヒドロフラン（THF）、ジ
オキサン等のエーテル類、メタノール、エタノール等の
アルコール類を挙げることができる。The solvent used in the reaction is not particularly limited as long as it does not inhibit this reaction, but preferably ethers such as ether, diisopropyl ether, tetrahydrofuran (THF) and dioxane, alcohols such as methanol and ethanol. Can be mentioned.

【００６２】反応温度は、−２０℃〜５０℃であり、好
適には−１０℃〜３０℃である。The reaction temperature is -20 ° C to 50 ° C, preferably -10 ° C to 30 ° C.

【００６３】反応時間は、用いられる溶媒の種類及び温
度などにより異なるが、通常１０分間〜１時間である。The reaction time varies depending on the type of solvent used and the temperature, but it is usually 10 minutes to 1 hour.

【００６４】生成した塩は常法によって単離される。即
ち、結晶として析出する場合は濾取によって、水溶性の
場合には、有機溶媒と水との分液によって水溶液として
単離される。The salt formed is isolated by conventional methods. That is, when it precipitates as crystals, it is isolated by filtration, and when it is water-soluble, it is isolated as an aqueous solution by separating the organic solvent and water.

【００６５】本発明化合物は、有害生物防除剤の有効成
分として有用である。例えば農園芸用殺菌剤としては各
種の植物病原菌によって引き起こされる病害に対し優れ
た防除効果を示す。特にイネいもち病、穂枯病、アズ
キ、トマト、キュウリ及びインゲンの灰色かび病、菌核
病、タマネギ白斑葉枯病、コムギの雪腐病、うどんこ
病、リンゴのモニリア病、斑点落葉病、茶のたんそ病、
ナシの赤星病、黒斑病、ブドウの黒とう病、カンキツの
黒点病等の各種病害などに対して優れた防除効果を示
す。本発明化合物は優れた治療効果を有することから感
染後の処理による病害防除が可能である。The compound of the present invention is useful as an active ingredient of a pest control agent. For example, as an agricultural and horticultural fungicide, it exhibits an excellent control effect against diseases caused by various plant pathogens. Especially rice blast, panicle blight, adzuki bean, tomato, gray mold of cucumber and kidney bean, sclerotium disease, onion white leaf blight, snow rot of wheat, powdery mildew, monili disease of apple, leaf spot disease, Tea anthracnose,
It shows an excellent control effect against various diseases such as red scab of pear, black spot, grape black scab, and black spot of citrus. Since the compound of the present invention has an excellent therapeutic effect, disease control by treatment after infection is possible.

【００６６】本発明化合物の使用に際しては、従来の農
薬製剤の場合と同様に、補助剤と共に、乳剤、粉剤、水
和剤、液剤、粒剤、懸濁製剤などの種々の形態に製剤す
ることができる。これらの製剤の実際の使用に際して
は、そのまま使用するか、又は水などの希釈剤で所定濃
度に希釈して使用することができる。When the compound of the present invention is used, it may be formulated into various forms such as emulsions, powders, wettable powders, liquids, granules and suspensions together with auxiliary agents, as in the case of conventional pesticide formulations. You can In the actual use of these preparations, they can be used as they are or diluted with a diluent such as water to a predetermined concentration before use.

【００６７】用いられる補助剤としては、担体、乳化
剤、懸濁剤、分散剤、展着剤、浸透剤、湿潤剤、増粘
剤、安定剤などが挙げられ、必要に応じ適宜添加するこ
とができる。Examples of the auxiliary agent used include a carrier, an emulsifier, a suspending agent, a dispersing agent, a spreading agent, a penetrating agent, a wetting agent, a thickening agent, a stabilizer and the like, which may be appropriately added if necessary. it can.

【００６８】用いられる担体は、固体担体と液体担体に
分けられ、固体担体は、澱粉、砂糖、セルロース粉、シ
クロデキストリン、活性炭、大豆粉、小麦粉、もみがら
粉、木粉、魚粉、粉乳などの動植物性粉末；又は、タル
ク、カオリン、ベントナイト、有機ベントナイト、炭酸
カルシウム、硫酸カルシウム、重炭酸ナトリウム、ゼオ
ライト、珪藻土、ホワイトカーボン、クレー、アルミ
ナ、シリカ、硫黄粉末などの鉱物性粉末などであり得、
液体担体は、水；大豆油、棉実油、トウモロコシ油など
の動植物油；エチルアルコール、エチレングリコールな
どのアルコール類；アセトン、メチルエチルケトンなど
のケトン類；ジオキサン、テトラヒドロフランなどのエ
ーテル類；ケロシン、灯油、流動パラフィンなどの脂肪
族炭化水素類；キシレン、トリメチルベンゼン、テトラ
メチルベンゼン、シクロヘキサン、ソルベントナフサな
どの芳香族炭化水素類；クロロホルム、クロロベンゼン
などのハロゲン化炭化水素類；ジメチルホルムアミドな
どの酸アミド類；酢酸エチルエステル、脂肪酸のグリセ
リンエステルなどのエステル類；アセトニトリルなどの
ニトリル類；ジメチルスルホキシドなどの含硫化合物
類；又は、Ｎ−メチルピロリドンなどであり得る。The carriers used are divided into solid carriers and liquid carriers. The solid carriers include starch, sugar, cellulose powder, cyclodextrin, activated carbon, soybean flour, wheat flour, chaff flour, wood flour, fish meal, milk powder and the like. Animal and plant powders; or may be mineral powders such as talc, kaolin, bentonite, organic bentonite, calcium carbonate, calcium sulfate, sodium bicarbonate, zeolite, diatomaceous earth, white carbon, clay, alumina, silica, sulfur powder, etc.,
Liquid carriers include water; animal and vegetable oils such as soybean oil, cottonseed oil, and corn oil; alcohols such as ethyl alcohol and ethylene glycol; ketones such as acetone and methyl ethyl ketone; ethers such as dioxane and tetrahydrofuran; kerosene, kerosene, Aliphatic hydrocarbons such as liquid paraffin; aromatic hydrocarbons such as xylene, trimethylbenzene, tetramethylbenzene, cyclohexane, solvent naphtha; halogenated hydrocarbons such as chloroform and chlorobenzene; acid amides such as dimethylformamide; It may be ethyl acetate, esters such as glycerin ester of fatty acid; nitriles such as acetonitrile; sulfur-containing compounds such as dimethyl sulfoxide; or N-methylpyrrolidone.

【００６９】本発明化合物と補助剤との配合質量比は、
通常０．０５：９９．９５〜９０：１０であり、好適に
は０．２：９９．８〜８０：２０である。The compounding mass ratio of the compound of the present invention and the auxiliary agent is
Usually, it is 0.05: 99.95 to 90:10, and preferably 0.2: 99.8 to 80:20.

【００７０】本発明化合物の使用濃度又は使用量は、対
象作物、使用方法、製剤形態、施用量などの違いによっ
て異なるが、茎葉処理の場合、有効成分当たり普通０．
１〜１００００ｐｐｍであり、好適には１〜１０００ｐ
ｐｍであり、土壌処理の場合には、普通１０〜１０００
００ｇ／ｈａであり、好適には２００〜２００００ｇ／
ｈａである。The concentration or amount of the compound of the present invention to be used varies depending on the target crop, the method of use, the form of preparation, the amount applied, etc.
1 to 10000 ppm, preferably 1 to 1000 p
pm, usually 10 to 1000 in the case of soil treatment
00 g / ha, preferably 200 to 20000 g / ha
It is ha.

【００７１】本発明化合物は必要に応じて他の農薬、例
えば殺虫剤、殺ダニ剤、誘引剤、殺線虫剤、殺菌剤、抗
ウイルス剤、除草剤、植物生長調整剤などと混用又は併
用することができ、好適には、殺虫剤、殺ダニ剤、殺線
虫剤又は殺菌剤である。The compound of the present invention is optionally mixed with or used in combination with other agricultural chemicals such as insecticides, acaricides, attractants, nematicides, fungicides, antiviral agents, herbicides, plant growth regulators and the like. And preferably an insecticide, acaricide, nematicide or fungicide.

【００７２】用いられる殺虫剤、殺ダニ剤又は殺線虫剤
は、例えばＯ−（４−ブロモ−２−クロロフェニル）Ｏ
−エチルＳ−プロピルホスホロチオエート（一般名：プ
ロフェノホス）、Ｏ−（２，２−ジクロロビニル）
Ｏ，Ｏ−ジメチルホスフェート（一般名：ジクロルボ
ス）、Ｏ−エチル Ｏ−｛３−メチル−４−（メチルチ
オ）フェニル｝ Ｎ−イソプロピルホスホロアミデート
（一般名：フェナミホス）、Ｏ，Ｏ−ジメチル Ｏ−
（４−ニトロ−ｍ−トリル）ホスホロチオエート（一般
名：フェニトロチオン）、Ｏ−エチル Ｏ−（４−ニト
ロフェニル）フェニルホスホノチオエート（一般名：Ｅ
ＰＮ）、Ｏ，Ｏ−ジエチル Ｏ−（２−イソプロピル−
６−メチルピリミジン−４−イル）ホスホロチオエート
（一般名：ダイアジノン）、Ｏ，Ｏ−ジメチル Ｏ−
（３，５，６−トリクロロ−２−ピリジル）ホスホロチ
オエート（一般名：クロルピリホスメチル）、Ｏ，Ｓ−
ジメチルＮ−アセチルホスホロアミドチオエート（一般
名：アセフェート）、Ｏ−（２，４−ジクロロフェニ
ル） Ｏ−エチル Ｓ−プロピルホスホロジチオエート
（一般名：プロチオホス）のような有機リン酸エステル
系化合物；１−ナフチル Ｎ−メチルカーバメート（一
般名：カルバリル）、２−イソプロポキシフェニル Ｎ
−メチルカーバメート（一般名：プロポキスル）、２−
メチル−２−（メチルチオ）プロピオンアルデヒド Ｏ
−メチルカルバモイルオキシム（一般名：アルジカル
ブ）、２，３−ジヒドロ−２，２−ジメチルベンゾフラ
ン−７−イル Ｎ−メチルカーバメート（一般名：カル
ボフラン）、ジメチルＮ，Ｎ’−〔チオビス｛（メチル
イミノ）カルボニルオキシ｝〕ビスエタンイミドチオエ
ート（一般名：チオジカルブ）、Ｓ−メチル Ｎ−（メ
チルカルバモイルオキシ）チオアセトイミデート（一般
名：メソミル）、Ｎ，Ｎ−ジメチル−２−メチルカルバ
モイルオキシイミノ−２−（メチルチオ）アセトアミド
（一般名：オキサミル）、２−（エチルチオメチル）フ
ェニル Ｎ−メチルカーバメート（一般名：エチオフェ
ンカルブ）、２−ジメチルアミノ−５，６−ジメチルピ
リミジン−４−イル Ｎ，Ｎ−ジメチルカーバメート
（一般名：ピリミカーブ）、２−ｓｅｃ−ブチルフェニ
ル Ｎ−メチルカーバメート（一般名：フェノブカル
ブ）のようなカーバメート系化合物；Ｓ，Ｓ’−２−ジ
メチルアミノトリメチレンビス（チオカーバメート）
（一般名：カルタップ）、Ｎ，Ｎ−ジメチル−１，２，
３−トリチアン−５−イルアミン（一般名：チオシクラ
ム）のようなネライストキシン誘導体；２，２，２−ト
リクロロ−１，１−ビス（４−クロロフェニル）エタノ
ール（一般名：ジコホル）、４−クロロフェニル−２，
４，５−トリクロロフェニルスルホン（一般名：テトラ
ジホン）のような有機塩素系化合物；ビス｛トリス（２
−メチル−２−フェニルプロピル）チン｝オキシド（一
般名：酸化フェンブタスズ）のような有機金属系化合
物；（ＲＳ）−α−シアノ−３−フェノキシベンジル
（ＲＳ）−２−（４−クロロフェニル）−３−メチルブ
チレート（一般名：フェンバレレート）、３−フェノキ
シベンジル（１ＲＳ）−シス，トランス−３−（２，２
−ジクロロビニル）−２，２−ジメチルシクロプロパン
カルボキシレート（一般名：ペルメトリン）、（ＲＳ）
−α−シアノ−３−フェノキシベンジル（１ＲＳ）−シ
ス，トランス−３−（２，２−ジクロロビニル）−２，
２−ジメチルシクロプロパンカルボキシレート（一般
名：シペルメトリン）、（Ｓ）−α−シアノ−３−フェ
ノキシベンジル（１Ｒ）−シス−３−（２，２−ジブロ
モビニル）−２，２−ジメチルシクロプロパンカルボキ
シレート（一般名：デルタメトリン）、（ＲＳ）−α−
シアノ−３−フェノキシベンジル（１ＲＳ）−シス，ト
ランス−３−（２−クロロ−３，３，３−トリフルオロ
プロペニル）−２，２−ジメチルシクロプロパンカルボ
キシレート（一般名：シハロトリン）、４−メチル−
２，３，５，６−テトラフルオロベンジル−３−（２−
クロロ−３，３，３−トリフルオロ−１−プロペニル）
−２，２−ジメチルシクロプロパンカルボキシレート
（一般名：テフルトリン）、２−（４−エトキシフェニ
ル）−２−メチルプロピル ３−フェノキシベンジルエ
ーテル（一般名：エトフェンプロックス）のようなピレ
スロイド系化合物；１−（４−クロロフェニル）−３−
（２，６−ジフルオロベンゾイル）ウレア（一般名：ジ
フルベンズロン）、１−〔３，５−ジクロロ−４−（３
−クロロ−５−トリフルオロメチル−２−ピリジルオキ
シ）フェニル〕−３−（２，６−ジフルオロベンゾイ
ル）ウレア（一般名：クロルフルアズロン）、１−
（３，５−ジクロロ−２，４−ジフルオロフェニル）−
３−（２，６−ジフルオロベンゾイル）ウレア（一般
名：テフルベンズロン）のようなベンゾイルウレア系化
合物；イソプロピル （２Ｅ，４Ｅ）−１１−メトキシ
−３，７，１１−トリメチル−２，４−ドテカジエノエ
ート（一般名：メトプレン）のような幼若ホルモン様化
合物；２−ｔ−ブチル−５−（４−ｔ−ブチルベンジル
チオ）−４−クロロ−３（２Ｈ）−ピリダジノン（一般
名：ピリダベン）のようなピリダジノン系化合物；ｔ−
ブチル ４−｛（１，３−ジメチル−５−フェノキシピ
ラゾール−４−イル）メチレンアミノオキシメチル｝ベ
ンゾエート（一般名：フェンピロキシメート）のような
ピラゾール系化合物；１−（６−クロロ−３−ピリジル
メチル）−Ｎ−ニトロ−イミダゾリジン−２−イリデン
アミン（一般名：イミダクロプリド）などのニトロ系化
合物；ジニトロ系化合物、有機硫黄化合物、尿素系化合
物、トリアジン系化合物、ヒドラジン系化合物、また、
その他の化合物として、２−ｔｅｒｔ−ブチルイミノ−
３−イソプロピル−５−フェニル−３，４，５，６−テ
トラヒドロ−２Ｈ−１，３，５−チアジアジン−４−オ
ン（一般名：ブブロフェジン）、トランス−（４−クロ
ロフェニル）−Ｎ−シクロヘキシル−４−メチル−２−
オキソチアゾリジノン−３−カルボキサミド（一般名：
ヘキシチアゾクス）、Ｎ−メチルビス（２，４−キシリ
ルイミノメチル）アミン（一般名：アミトラズ）、Ｎ’
−（４−クロロ−ｏ−トリル）−Ｎ，Ｎ−ジメチルホル
ムアミジン（一般名：クロルジメホルム）、（４−エト
キシフェニル）−｛３−（４−フルオロ−３−フェノキ
シフェニル）プロピル｝（ジメチル）シラン（一般名：
シラフルオフェン）のような化合物であり得る。更に、
本発明化合物は、ＢＴ剤、昆虫病原ウイルス剤などのよ
うな微生物農薬、アベルメクチン、ミルベマイシンのよ
うな抗生物質などと、混用、併用することもできる。The insecticide, acaricide or nematicide used is, for example, O- (4-bromo-2-chlorophenyl) O.
-Ethyl S-propyl phosphorothioate (generic name: profenofos), O- (2,2-dichlorovinyl)
O, O-dimethyl phosphate (generic name: dichlorvos), O-ethyl O- {3-methyl-4- (methylthio) phenyl} N-isopropyl phosphoramidate (generic name: fenamiphos), O, O-dimethyl O −
(4-Nitro-m-tolyl) phosphorothioate (generic name: fenitrothion), O-ethyl O- (4-nitrophenyl) phenylphosphonothioate (generic name: E
PN), O, O-diethyl O- (2-isopropyl-
6-Methylpyrimidin-4-yl) phosphorothioate (generic name: diazinon), O, O-dimethyl O-
(3,5,6-Trichloro-2-pyridyl) phosphorothioate (generic name: chlorpyrifosmethyl), O, S-
Organic phosphate compounds such as dimethyl N-acetylphosphoramidothioate (generic name: acephate), O- (2,4-dichlorophenyl) O-ethyl S-propyl phosphorodithioate (generic name: prothiophos) 1-naphthyl N-methylcarbamate (generic name: carbaryl), 2-isopropoxyphenyl N
-Methyl carbamate (generic name: propoxur), 2-
Methyl-2- (methylthio) propionaldehyde O
-Methylcarbamoyl oxime (generic name: aldicarb), 2,3-dihydro-2,2-dimethylbenzofuran-7-yl N-methylcarbamate (generic name: carbofuran), dimethyl N, N '-[thiobis {(methylimino)] Carbonyloxy}] bisethaneimidothioate (generic name: thiodicarb), S-methyl N- (methylcarbamoyloxy) thioacetimidate (generic name: mesomil), N, N-dimethyl-2-methylcarbamoyloxyimino- 2- (Methylthio) acetamide (generic name: oxamyl), 2- (ethylthiomethyl) phenyl N-methylcarbamate (generic name: etiophencarb), 2-dimethylamino-5,6-dimethylpyrimidin-4-yl N, N -Dimethyl carbamate (generic name: pirimicarb), -sec- butyl phenyl N- methylcarbamate (common name: Fenobucarb) carbamate compounds such as; S, S'-2- dimethylaminotrimethylene-bis (thiocarbamate)
(General name: cartap), N, N-dimethyl-1,2,
Nereistoxin derivatives such as 3-trithian-5-ylamine (generic name: thiocyclam); 2,2,2-trichloro-1,1-bis (4-chlorophenyl) ethanol (generic name: dicofol), 4-chlorophenyl -2
Organochlorine compounds such as 4,5-trichlorophenyl sulfone (generic name: tetradiphone); bis {tris (2
-Methyl-2-phenylpropyl) tin} oxide (generic name: fenbutatin oxide); (RS) -α-cyano-3-phenoxybenzyl (RS) -2- (4-chlorophenyl)- 3-methylbutyrate (generic name: fenvalerate), 3-phenoxybenzyl (1RS) -cis, trans-3- (2,2)
-Dichlorovinyl) -2,2-dimethylcyclopropanecarboxylate (generic name: permethrin), (RS)
-Α-cyano-3-phenoxybenzyl (1RS) -cis, trans-3- (2,2-dichlorovinyl) -2,
2-Dimethylcyclopropanecarboxylate (generic name: cypermethrin), (S) -α-cyano-3-phenoxybenzyl (1R) -cis-3- (2,2-dibromovinyl) -2,2-dimethylcyclo Propane carboxylate (generic name: deltamethrin), (RS) -α-
Cyano-3-phenoxybenzyl (1RS) -cis, trans-3- (2-chloro-3,3,3-trifluoropropenyl) -2,2-dimethylcyclopropanecarboxylate (generic name: cyhalothrin), 4- Methyl-
2,3,5,6-tetrafluorobenzyl-3- (2-
Chloro-3,3,3-trifluoro-1-propenyl)
A pyrethroid-based compound such as -2,2-dimethylcyclopropanecarboxylate (generic name: tefluthrin), 2- (4-ethoxyphenyl) -2-methylpropyl 3-phenoxybenzyl ether (generic name: etofenprox); 1- (4-chlorophenyl) -3-
(2,6-Difluorobenzoyl) urea (generic name: diflubenzuron), 1- [3,5-dichloro-4- (3
-Chloro-5-trifluoromethyl-2-pyridyloxy) phenyl] -3- (2,6-difluorobenzoyl) urea (generic name: chlorfluazuron), 1-
(3,5-dichloro-2,4-difluorophenyl)-
Benzoyl urea-based compounds such as 3- (2,6-difluorobenzoyl) urea (generic name: teflubenzuron); isopropyl (2E, 4E) -11-methoxy-3,7,11-trimethyl-2,4-dotecad Juvenile hormone-like compounds such as enoate (generic name: methoprene); 2-t-butyl-5- (4-t-butylbenzylthio) -4-chloro-3 (2H) -pyridazinone (generic name: pyridaben) ) Like pyridazinone compounds; t-
Pyrazole compounds such as butyl 4-{(1,3-dimethyl-5-phenoxypyrazol-4-yl) methyleneaminooxymethyl} benzoate (generic name: fenpyroximate); 1- (6-chloro-3-pyridylmethyl ) -N-Nitro-imidazolidin-2-ylideneamine (general name: imidacloprid) and other nitro compounds; dinitro compounds, organic sulfur compounds, urea compounds, triazine compounds, hydrazine compounds, and
Other compounds include 2-tert-butylimino-
3-Isopropyl-5-phenyl-3,4,5,6-tetrahydro-2H-1,3,5-thiadiazin-4-one (generic name: bubrofedin), trans- (4-chlorophenyl) -N-cyclohexyl- 4-methyl-2-
Oxothiazolidinone-3-carboxamide (generic name:
Hexthiazox), N-methylbis (2,4-xylyliminomethyl) amine (generic name: amitraz), N ′
-(4-Chloro-o-tolyl) -N, N-dimethylformamidine (generic name: chlordimeform), (4-ethoxyphenyl)-{3- (4-fluoro-3-phenoxyphenyl) propyl} (dimethyl) Silane (generic name:
A compound such as silafluofen). Furthermore,
The compound of the present invention can be mixed and used in combination with a microbial agent such as a BT agent and an insect pathogenic virus agent, an antibiotic such as avermectin and milbemycin, and the like.

【００７３】用いられる殺菌剤は、例えば、２−アニリ
ノ−４−メチル−６−（１−プロピニル）ピリミジン
（一般名：メパニピリム）、４，６−ジメチル−Ｎ−フ
ェニル−２−ピリミジナミン（一般名：ピリメサニル）
のようなピリミジナミン系化合物；１−（４−クロロフ
ェノキシ）−３，３−ジメチル−１−（１Ｈ−１，２，
４−トリアゾール−１−イル）ブタノン（一般名：トリ
アジメホン）、１−（ビフェニル−４−イルオキシ）−
３，３−ジメチル−１−（１Ｈ，１，２，４−トリアゾ
ール−１−イル）ブタン−２−オール（一般名：ビテル
タノール）、１−｛Ｎ−（４−クロロ−２−トリフルオ
ロメチルフェニル）−２−プロポキシアセトイミドイ
ル｝イミダゾール（一般名：トリフルミゾール）、１−
｛２−（２，４−ジクロロフェニル）−４−エチル−
１，３−ジオキソラン−２−イルメチル｝−１Ｈ−１，
２，４−トリアゾール（一般名：エタコナゾール）、１
−｛２−（２，４−ジクロロフェニル）−４−プロピル
−１，３−ジオキソラン−２−イルメチル｝−１Ｈ−
１，２，４−トリアゾール（一般名：プロピコナゾー
ル）、１−｛２−（２，４−ジクロロフェニル）ペンチ
ル｝−１Ｈ−１，２，４−トリアゾール（一般名：ペン
コナゾール）、ビス（４−フルオロフェニル）（メチ
ル）（１Ｈ−１，２，４−トリアゾール−１−イルメチ
ル）シラン（一般名：フルシラゾール）、２−（４−ク
ロロフェニル）−２−（１Ｈ−１，２，４−トリアゾー
ル−１−イルメチル）ヘキサンニトリル（一般名：マイ
クロブタニル）、（２ＲＳ、３ＲＳ）−２−（４−クロ
ロフェニル）−３−シクロプロピル−１−（１Ｈ−１，
２，４−トリアゾール−１−イル）ブタン−２−オール
（一般名：シプロコナゾール）、（ＲＳ）−１−（４−
クロロフェニル）−４，４−ジメチル−３−（１Ｈ−
１，２，４−トリアゾール−１−イルメチル）ペンタン
−３−オール（一般名：ターブコナゾール）、（ＲＳ）
−２−（２，４−ジクロロフェニル）−１−（１Ｈ−
１，２，４−トリアゾール−１−イル）ヘキサン−２−
オール（一般名：ヘキサコナゾール）、（２ＲＳ，５Ｒ
Ｓ）−５−（２，４−ジクロロフェニル）テトラヒドロ
−５−（１Ｈ−１，２，４−トリアゾール−１−イルメ
チル）−２−フリル２，２，２−トリフルオロエチルエ
ーテル（一般名：ファーコナゾールシス）、Ｎ−プロピ
ル−Ｎ−｛２−（２，４，６−トリクロロフェノキシ）
エチル｝イミダゾール−１−カルボキサミド（一般名：
プロクロラズ）、２−（４−フルオロフェニル−１−
（１Ｈ−１，２，４トリアゾール−１−イル）−３−ト
リメチルシリルプロパン−２−オール（一般名：シメコ
ナゾール）のようなアゾール系化合物；６−メチル−
１，３−ジチオロ〔４，５−ｂ〕キノキサリン−２−オ
ン（一般名：キノメチオネート）のようなキノキサリン
系化合物；マンガニーズエチレンビス（ジチオカーバメ
ート）の重合物（一般名：マンネブ）、ジンクエチレン
ビス（ジチオカーバメート）の重合物（一般名：ジネ
ブ）、ジンク（亜鉛）とマンガニーズエチレンビス（ジ
チオカーバメート）（マンネブ）の錯化合物（一般名：
マンゼブ）、ジジンクビス（ジメチルジチオカーバメー
ト）エチレンビス（ジチオカーバメート）（一般名：ポ
リカーバメート）、ジンクプロピレンビス（ジチオカー
バメート）の重合物（一般名：プロビネブ）のようなジ
チオカーバメート系化合物；４，５，６，７−テトラク
ロロフタリド（一般名：フサライド）、テトラクロロイ
ソフタロニトリル（一般名：クロロタロニル）、ペンタ
クロロニトロベンゼン（一般名：キントゼン）のような
有機塩素系化合物；メチル １−（ブチルカルバモイ
ル）ベンズイミダゾール−２−イルカーバメート（一般
名：ベノミル）、ジメチル４，４’−（ｏ−フェニレ
ン）ビス（３−チオアロファネート）（一般名：チオフ
ァネートメチル）、メチルベンズイミダゾール−２−イ
ルカーバメート（一般名：カーベンダジム）のようなベ
ンズイミダゾール系化合物；３−クロロ−Ｎ−（３−ク
ロロ−２，６−ジニトロ−４−α，α，α−トリフルオ
ロトリル）−５−トリフルオロメチル−２−ピリジナミ
ン（一般名：フルアジナム）のようなピリジナミン系化
合物；１−（２−シアノ−２−メトキシイミノアセチ
ル）−３−エチル尿素（一般名：シモキサニル）のよう
なシアノアセトアミド系化合物；メチル Ｎ−（２−メ
トキシアセチル）−Ｎ−（２，６−キシリル）−ＤＬ−
アラニネート（一般名：メタラキシル）、２−メトキシ
−Ｎ−（２−オキソ−１，３−オキサゾリジン−３−イ
ル）アセト−２’，６’−キシリジド（一般名：オキサ
ジキシル）、（±）−α−２−クロロ−Ｎ−（２，６−
キシリルアセトアミド）−γ−ブチロラクトン（一般
名：オフレース）、メチル Ｎ−フェニルアセチル−Ｎ
−（２，６−キシリル）−ＤＬ−アラニネート（一般
名：ベナラキシル）、メチル Ｎ−（２−フロイル）−
Ｎ−（２，６−キシリル）−ＤＬ−アラニネート（一般
名：フララキシル）、（±）−α−〔Ｎ−（３−クロロ
フェニル）シクロプロパンカルボキサミド〕−γ−ブチ
ロラクトン（一般名：シプロフラン）のようなフェニル
アミド系化合物；Ｎ−ジクロロフルオロメチルチオ−
Ｎ’，Ｎ’−ジメチル−Ｎ−フェニルスルファミド（一
般名：ジクロフルアニド）のようなスルフェン酸系化合
物；水酸化第二銅（一般名：水酸化第二銅）、カッパー
８−キノリノレート（一般名：有機銅）のような銅系
化合物；５−メチルイソキサゾール−３−オール（一般
名：ヒドロキシイソキサゾール）のようなイソキサゾー
ル系化合物；アルミニウムトリス（エチルホスホネー
ト）（一般名：ホセチルアルミニウム）、Ｏ−２，６−
ジクロロ−ｐ−トリル−Ｏ，Ｏ−ジメチルホスホロチオ
エート（一般名：トルクロホス−メチル）、Ｓ−ベンジ
ル Ｏ，Ｏ−ジイソプロピルホスホロチオエート、Ｏ−
エチル Ｓ，Ｓ−ジフェニルホスホロジチオエート、ア
ルミニウムエチルハイドロゲンホスホネートのような有
機リン系化合物；Ｎ−（トリクロロメチルチオ）シクロ
ヘキシ−４−エン−１，２−ジカルボキシミド（一般
名：キャプタン）、Ｎ−（１，１，２，２−テトラクロ
ロエチルチオ）シクロヘキシ−４−エン−１，２−ジカ
ルボキシミド（一般名：キャプタホル）、Ｎ−（トリク
ロロメチルチオ）フタルイミド（一般名：フォルペッ
ト）のようなＮ−ハロゲノチオアルキル系化合物；Ｎ−
（３，５−ジクロロフェニル）−１，２−ジメチルシク
ロプロパン−１，２−ジカルボキシミド（一般名：プロ
シミドン）、３−（３，５−ジクロロフェニル）−Ｎ−
イソプロピル−２，４−ジオキソイミダゾリジン−１−
カルボキサミド（一般名：イプロジオン）、（ＲＳ）−
３−（３，５−ジクロロフェニル）−５−メチル−５−
ビニル−１，３−オキサゾリジン−２，４−ジオン（一
般名：ビンクロゾリン）のようなジカルボキシイミド系
化合物；α，α，α−トリフルオロ−３’−イソプロポ
キシ−ｏ−トルアニリド（一般名：フルトラニル）、
３’−イソプロポキシ−ｏ−トルアニリド（一般名：メ
プロニル）のようなベンズアニリド系化合物；Ｎ，Ｎ’
−〔ピペラジン−１，４−ジイルビス｛（トリクロロメ
チル）メチレン｝〕ジホルムアミド（一般名：トリホリ
ン）のようなピペラジン系化合物；２’，４’−ジクロ
ロ−２−（３−ピリジル）アセトフェノン Ｏ−メチル
オキシム（一般名：ピリフェノックス）のようなピリジ
ン系化合物；（±）−２，４’−ジクロロ−α−（ピリ
ミジン−５−イル）ベンズヒドリルアルコール（一般
名：フェナリモル）、（±）−２，４’−ジフルオロ−
α−（１Ｈ−１，２，４−トリアゾール−１−イルメチ
ル）ベンズヒドリルアルコール（一般名：フルトリアフ
ォル）のようなカルビノール系化合物；（ＲＳ）−１−
｛３−（４−ターシャリーブチルフェニル）−２−メチ
ルプロピル｝ピペリジン（一般名：フェンプロピディ
ン）のようなピペリジン系化合物；（±）−シス−４−
｛３−（４−ターシャリーブチルフェニル）−２−メチ
ルプロピル｝−２，６−ジメチルモルフォリン（一般
名：フェンプロピモルフ）のようなモルフォリン系化合
物；トリフェニルチンヒドロキシド（一般名：フェンチ
ンヒドロキシド）、トリフェニルチンアセテート（一般
名：フェンチンアセテート）のような有機スズ系化合
物；１−（４−クロロベンジル）−１−シクロペンチル
−３−フェニルウレア（一般名：ペンシキュロン）のよ
うな尿素系化合物；（Ｅ，Ｚ）４−｛３−（４−クロロ
フェニル）−３−（３，４−ジメトキシフェニル）アク
リロイル｝モリフォリン（一般名：ジメトモルフ）のよ
うなシンナミック酸系化合物；イソプロピル ３，４−
ジエトキシカルバニレート（一般名：ジエトフェンカル
ブ）のようなフェニルカーバメート系化合物；３−シア
ノ−４−（２，２−ジフルオロ−１，３−ベンゾジオキ
ソール−４−イル）ピロール（一般名：フルジオキソニ
ル）、３−（２’，３’−ジクロロフェニル）−４−シ
アノ−ピロール（一般名：フェンピクロニル）のような
シアノピロール系化合物であり得る。The fungicides used are, for example, 2-anilino-4-methyl-6- (1-propynyl) pyrimidine (generic name: mepanipyrim), 4,6-dimethyl-N-phenyl-2-pyrimidinamine (generic name). : Pyrimesanil)
A pyrimidinamine-based compound such as 1- (4-chlorophenoxy) -3,3-dimethyl-1- (1H-1,2,
4-triazol-1-yl) butanone (generic name: triadimefon), 1- (biphenyl-4-yloxy)-
3,3-Dimethyl-1- (1H, 1,2,4-triazol-1-yl) butan-2-ol (generic name: bitertanol), 1- {N- (4-chloro-2-trifluoromethyl) Phenyl) -2-propoxyacetimidoyl} imidazole (generic name: triflumizole), 1-
{2- (2,4-dichlorophenyl) -4-ethyl-
1,3-dioxolan-2-ylmethyl} -1H-1,
2,4-triazole (generic name: etaconazole), 1
-{2- (2,4-dichlorophenyl) -4-propyl-1,3-dioxolan-2-ylmethyl} -1H-
1,2,4-triazole (generic name: propiconazole), 1- {2- (2,4-dichlorophenyl) pentyl} -1H-1,2,4-triazole (generic name: penconazole), bis (4 -Fluorophenyl) (methyl) (1H-1,2,4-triazol-1-ylmethyl) silane (generic name: flusilazole), 2- (4-chlorophenyl) -2- (1H-1,2,4-triazole -1-ylmethyl) hexanenitrile (generic name: microbutanyl), (2RS, 3RS) -2- (4-chlorophenyl) -3-cyclopropyl-1- (1H-1,
2,4-triazol-1-yl) butan-2-ol (generic name: cyproconazole), (RS) -1- (4-
Chlorophenyl) -4,4-dimethyl-3- (1H-
1,2,4-triazol-1-ylmethyl) pentan-3-ol (generic name: turbuconazole), (RS)
-2- (2,4-dichlorophenyl) -1- (1H-
1,2,4-triazol-1-yl) hexane-2-
All (generic name: hexaconazole), (2RS, 5R
S) -5- (2,4-Dichlorophenyl) tetrahydro-5- (1H-1,2,4-triazol-1-ylmethyl) -2-furyl 2,2,2-trifluoroethyl ether (generic name: fur Conazol cis), N-propyl-N- {2- (2,4,6-trichlorophenoxy)
Ethyl} imidazole-1-carboxamide (generic name:
Prochloraz), 2- (4-fluorophenyl-1-)
Azole compounds such as (1H-1,2,4triazol-1-yl) -3-trimethylsilylpropan-2-ol (generic name: cimeconazole); 6-methyl-
A quinoxaline compound such as 1,3-dithiolo [4,5-b] quinoxalin-2-one (generic name: quinomethionate); a polymer of manganese ethylene bis (dithiocarbamate) (generic name: manneb), zinc ethylene Polymer of bis (dithiocarbamate) (generic name: Zineb), complex compound of zinc (zinc) and Manganese ethylene bis (dithiocarbamate) (Manneb) (generic name:
Dithiocarbamate compounds such as manzeb), dizinc bis (dimethyldithiocarbamate) ethylene bis (dithiocarbamate) (generic name: polycarbamate), zinc propylene bis (dithiocarbamate) (generic name: provineb); , 6,7-Tetrachlorophthalide (generic name: phthalide), tetrachloroisophthalonitrile (generic name: chlorothalonil), pentachloronitrobenzene (generic name: quintozene), an organochlorine compound; methyl 1- (butyl Lucarbamoyl) benzimidazol-2-ylcarbamate (generic name: benomyl), dimethyl 4,4 '-(o-phenylene) bis (3-thioallophanate) (generic name: thiophanate methyl), methylbenzimidazol-2-ylcarbamate ( common name Carbendazim) -like benzimidazole compounds; 3-chloro-N- (3-chloro-2,6-dinitro-4-α, α, α-trifluorotolyl) -5-trifluoromethyl-2-pyridinamine ( Pyridinamine-based compounds such as common name: fluazinam); Cyanoacetamide-based compounds such as 1- (2-cyano-2-methoxyiminoacetyl) -3-ethylurea (general name: Simoxanil); Methyl N- (2- Methoxyacetyl) -N- (2,6-xylyl) -DL-
Alaninate (generic name: metalaxyl), 2-methoxy-N- (2-oxo-1,3-oxazolidin-3-yl) aceto-2 ′, 6′-xylidide (generic name: oxadixyl), (±) -α -2-chloro-N- (2,6-
Xylylacetamide) -γ-butyrolactone (generic name: offlace), methyl N-phenylacetyl-N
-(2,6-xylyl) -DL-alaninate (generic name: benalaxyl), methyl N- (2-furoyl)-
Like N- (2,6-xylyl) -DL-alaninate (generic name: furaraxyl), (±) -α- [N- (3-chlorophenyl) cyclopropanecarboxamide] -γ-butyrolactone (generic name: cyprofuran) Phenylamide compounds; N-dichlorofluoromethylthio-
Sulfenic acid compounds such as N ', N'-dimethyl-N-phenylsulfamide (generic name: diclofluanide); cupric hydroxide (generic name: cupric hydroxide), kappa 8-quinolinolate A copper-based compound such as (common name: organic copper); An isoxazole-based compound such as 5-methylisoxazol-3-ol (common name: hydroxyisoxazole); Aluminum tris (ethylphosphonate) (common name: Fosetyl aluminum), O-2,6-
Dichloro-p-tolyl-O, O-dimethylphosphorothioate (generic name: tolclofos-methyl), S-benzyl O, O-diisopropylphosphorothioate, O-
Organophosphorus compounds such as ethyl S, S-diphenylphosphorodithioate, aluminum ethylhydrogenphosphonate; N- (trichloromethylthio) cyclohex-4-ene-1,2-dicarboximide (generic name: captan), N Such as-(1,1,2,2-tetrachloroethylthio) cyclohex-4-ene-1,2-dicarboximide (generic name: captafol), N- (trichloromethylthio) phthalimide (generic name: folpet) N-halogenothioalkyl compounds; N-
(3,5-Dichlorophenyl) -1,2-dimethylcyclopropane-1,2-dicarboximide (generic name: procymidone), 3- (3,5-dichlorophenyl) -N-
Isopropyl-2,4-dioxoimidazolidine-1-
Carboxamide (generic name: iprodione), (RS)-
3- (3,5-dichlorophenyl) -5-methyl-5-
Dicarboximide-based compounds such as vinyl-1,3-oxazolidine-2,4-dione (generic name: vinclozolin); α, α, α-trifluoro-3′-isopropoxy-o-toluanilide (generic name: Flutolanil),
Benzanilide compounds such as 3'-isopropoxy-o-toluanilide (generic name: mepronil); N, N '
-Piperazine-based compounds such as [piperazine-1,4-diylbis {(trichloromethyl) methylene}] diformamide (generic name: triphorine); 2 ', 4'-dichloro-2- (3-pyridyl) acetophenone O- Pyridine compounds such as methyl oxime (generic name: pyriphenox); (±) -2,4′-dichloro-α- (pyrimidin-5-yl) benzhydryl alcohol (generic name: phenalimol), (± ) -2,4'-Difluoro-
Carbinol compounds such as α- (1H-1,2,4-triazol-1-ylmethyl) benzhydryl alcohol (generic name: flutriafol); (RS) -1-
Piperidine-based compounds such as {3- (4-tert-butylphenyl) -2-methylpropyl} piperidine (generic name: phenpropidin); (±) -cis-4-
Morpholine-based compounds such as {3- (4-tert-butylphenyl) -2-methylpropyl} -2,6-dimethylmorpholine (generic name: phenpropimorph); triphenyltin hydroxide (generic name: Fentin hydroxide), triphenyltin acetate (generic name: fentine acetate) such as organotin compounds; 1- (4-chlorobenzyl) -1-cyclopentyl-3-phenylurea (generic name: peniculone) Urea-based compounds such as; (E, Z) 4- {3- (4-chlorophenyl) -3- (3,4-dimethoxyphenyl) acryloyl} morpholine (generic name: dimethomorph), cinnamic acid-based compounds; isopropyl 3,4-
Phenylcarbamate compounds such as diethoxycarbanilate (generic name: dietofencarb); 3-cyano-4- (2,2-difluoro-1,3-benzodioxol-4-yl) pyrrole (generic name: It may be a cyanopyrrole-based compound such as fludioxonil) or 3- (2 ′, 3′-dichlorophenyl) -4-cyano-pyrrole (generic name: fenpiclonyl).

【００７４】以下に、実施例、製剤例及び試験例を挙げ
て本発明化合物を具体的に説明するが、本発明はこれら
に限定されるものではない。The compounds of the present invention will be specifically described below with reference to Examples, Formulation Examples and Test Examples, but the present invention is not limited thereto.

【００７５】[0075]

【実施例】【Example】

【００７６】[0076]

【実施例１】１−メチル−N−（３−キノリル）−１−
シクロヘキサンカルボキサミド（化合物番号１−１） １−メチルシクロヘキサンカルボン酸（７１mg、０．５
ミリモル）を塩化メチレン（１mL）に溶かし、この溶液
に、沃化２−クロロー１−メチルピリジニウム（１９０
mg、０．７５ミリモル）、３−アミノキノリン（７２m
g、０．５ミリモル）及びトリエチルアミン（０．２m
L、１．５ミリモル）を順次加え、室温で３時間攪拌し
た。この反応溶液を氷水中に注ぎ、酢酸エチルで抽出
し、有機層を濃縮して得た残渣を薄層クロマトグラフィ
ー（溶出溶媒：ヘキサン／酢酸エチル＝１／１）により
精製することにより、目的物３０mg（収率２２％）を得
た。 融点：126-129℃。1 H-NMR (200MHz, CDCl3) δppm : 1.32 (3H, s), 1.42-
1.63 (8H, m), 2.05-2.12 (2H, m), 7.48-7.66 (2H,
m), 7.70 (1H, bs), 7.78 (1H, dd, J=1.8, 8.1Hz), 8.
03 (1H, d, J=8.4Hz), 8.73 (1H, d, J=2.6Hz), 8.82
(1H, d, J=2.6Hz). MS m/z : 268(M+), 144, 97, 83。Example 1 1-Methyl-N- (3-quinolyl) -1-
Cyclohexanecarboxamide (Compound No. 1-1) 1-Methylcyclohexanecarboxylic acid (71 mg, 0.5
Mmol) in methylene chloride (1 mL) and added to this solution 2-chloro-1-methylpyridinium iodide (190
mg, 0.75 mmol), 3-aminoquinoline (72 m
g, 0.5 mmol) and triethylamine (0.2 m
L, 1.5 mmol) were added successively and the mixture was stirred at room temperature for 3 hours. This reaction solution was poured into ice water, extracted with ethyl acetate, and the residue obtained by concentrating the organic layer was purified by thin layer chromatography (eluting solvent: hexane / ethyl acetate = 1/1) to give the desired product. 30 mg (yield 22%) was obtained. Melting point: 126-129 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.32 (3H, s), 1.42-
1.63 (8H, m), 2.05-2.12 (2H, m), 7.48-7.66 (2H,
m), 7.70 (1H, bs), 7.78 (1H, dd, J = 1.8, 8.1Hz), 8.
03 (1H, d, J = 8.4Hz), 8.73 (1H, d, J = 2.6Hz), 8.82
(1H, d, J = 2.6Hz). MS m / z: 268 (M + ), 144, 97, 83.

【００７７】[0077]

【実施例２】１−トリフルオロメチル−N−（３−キノ
リル）−３−シクロヘキセン−１−カルボキサミド（化
合物番号１−１９９９） １−トリフルオロメチル−３−シクロヘキセンカルボン
酸（２００mg、１．０ミリモル）をベンゼン（４mL）に
溶かし、この溶液に、塩化オキザリル（０．５mL、６．
０ミリモル）及びN,N-ジメチルホルムアミド（１滴）を
順次加え、室温で１２時間攪拌した。この反応溶液を濃
縮して得た残渣をアセトニトリル（１mL）に溶解させ、
３−アミノキノリン（１４０mg、１．０ミリモル）及び
ピリジン（０．１６mL、２．０ミリモル）を加え、室温
で６時間攪拌した。この反応液を氷水中に注ぎ、酢酸エ
チルで抽出し、有機層を濃縮して得た残渣を薄層クロマ
トグラフィー（溶出溶媒：ヘキサン／酢酸エチル＝１／
１）により精製することにより、目的物１４０mg（収率
４４％）を得た。 融点：157-160℃。1 H-NMR (200MHz, CDCl3) δppm : 1.89-2.04 (1H, m),
2.24-2.30 (2H, m), 2.40-2.50 (2H, m), 2.84-2.94 (1
H, m), 5.77 (2H, bs), 7.48-7.71 (3H, m), 7.95 (1H,
d, J=8.4Hz), 8.56-8.64 (3H, m). MS m/z : 320(M+), 251, 171, 144。Example 2 1-Trifluoromethyl-N- (3-quinolyl) -3-cyclohexene-1-carboxamide (Compound No. 1-1999) 1-Trifluoromethyl-3-cyclohexenecarboxylic acid (200 mg, 1.0 Mmol) in benzene (4 mL) and to this solution oxalyl chloride (0.5 mL, 6.
0 mmol) and N, N-dimethylformamide (1 drop) were sequentially added, and the mixture was stirred at room temperature for 12 hours. The residue obtained by concentrating the reaction solution was dissolved in acetonitrile (1 mL),
3-Aminoquinoline (140 mg, 1.0 mmol) and pyridine (0.16 mL, 2.0 mmol) were added, and the mixture was stirred at room temperature for 6 hours. The reaction mixture was poured into ice water, extracted with ethyl acetate, the organic layer was concentrated, and the resulting residue was subjected to thin layer chromatography (elution solvent: hexane / ethyl acetate = 1 /
Purification by 1) yielded 140 mg of the desired product (yield 44%). Melting point: 157-160 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.89-2.04 (1H, m),
2.24-2.30 (2H, m), 2.40-2.50 (2H, m), 2.84-2.94 (1
H, m), 5.77 (2H, bs), 7.48-7.71 (3H, m), 7.95 (1H,
d, J = 8.4Hz), 8.56-8.64 (3H, m). MS m / z: 320 (M + ), 251, 171, 144.

【００７８】実施例１、２と同様にして、以下の化合物
を合成した。The following compounds were synthesized in the same manner as in Examples 1 and 2.

【００７９】[0079]

【実施例３】１−エチル−N−（３−キノリル）−１−
シクロヘキサンカルボキサミド（化合物番号１−２２
３） 融点：113-116℃。1 H-NMR (200MHz, CDCl3) δppm : 0.90 (3H, t, J=7.5H
z), 1.26-1.71 (10H, m), 2.04-2.13 (2H, m), 7.47-7.
65 (2H, m), 7.76 (1H, d, J=8.4Hz), 7.78 (1H,bs),
8.02 (1H, d, J=8.1Hz), 8.74 (1H, d, J=2.6Hz), 8.80
(1H, d, J=2.6Hz). MS m/z : 282(M+), 144, 111。Example 3 1-Ethyl-N- (3-quinolyl) -1-
Cyclohexanecarboxamide (Compound No. 1-22
3) Melting point: 113-116 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.90 (3H, t, J = 7.5H
z), 1.26-1.71 (10H, m), 2.04-2.13 (2H, m), 7.47-7.
65 (2H, m), 7.76 (1H, d, J = 8.4Hz), 7.78 (1H, bs),
8.02 (1H, d, J = 8.1Hz), 8.74 (1H, d, J = 2.6Hz), 8.80
(1H, d, J = 2.6Hz) .MS m / z: 282 (M + ), 144, 111.

【００８０】[0080]

【実施例４】１−プロピル−N−（３−キノリル）−１
−シクロヘキサンカルボキサミド（化合物番号１−４４
５） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 0.88 (3H, t, J=7.1H
z), 1.22-1.62 (12H, m), 2.04-2.13 (2H, m), 7.46-7.
65 (2H, m), 7.74 (1H, dd, J=1.1, 7.7Hz), 7.86 (1H,
bs), 8.00 (1H, d, J=8.4Hz), 8.73 (1H, d, J=2.6H
z), 8.78 (1H, d, J=2.6Hz). MS m/z : 296(M+), 144, 125。Example 4 1-Propyl-N- (3-quinolyl) -1
-Cyclohexanecarboxamide (Compound No. 1-44
5) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.88 (3H, t, J = 7.1H
z), 1.22-1.62 (12H, m), 2.04-2.13 (2H, m), 7.46-7.
65 (2H, m), 7.74 (1H, dd, J = 1.1, 7.7Hz), 7.86 (1H,
bs), 8.00 (1H, d, J = 8.4Hz), 8.73 (1H, d, J = 2.6H
z), 8.78 (1H, d, J = 2.6Hz). MS m / z: 296 (M + ), 144, 125.

【００８１】[0081]

【実施例５】１−トリフルオロメチル−N−（３−キノ
リル）−１−シクロヘキサンカルボキサミド（化合物番
号１−１３３３） 融点：152℃。1 H-NMR (200MHz, CDCl3) δppm : 1.07-1.88 (8H, m),
2.37-2.44 (2H, m), 7.52-7.71 (2H, m), 7.80 (1H, b
s), 7.80-7.84 (1H, m), 8.07 (1H, d, J=8.8Hz),8.75
(1H, d, J=2.6Hz), 8.81 (1H, d, J=2.6Hz). MS m/z : 322(M+), 144, 131。Example 5 1-Trifluoromethyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-1333) Melting point: 152 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.07-1.88 (8H, m),
2.37-2.44 (2H, m), 7.52-7.71 (2H, m), 7.80 (1H, b
s), 7.80-7.84 (1H, m), 8.07 (1H, d, J = 8.8Hz), 8.75
(1H, d, J = 2.6Hz), 8.81 (1H, d, J = 2.6Hz). MS m / z: 322 (M + ), 144, 131.

【００８２】[0082]

【実施例６】１−メチル−N−（５−メチル−３−キノ
リル）−１−シクロヘキサンカルボキサミド（化合物番
号１−２８） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 1.34 (3H, s), 1.38-
1.72 (8H, m), 2.04-2.15 (2H, m), 2.70 (3H, s), 7.3
7 (1H, d, J=6.8Hz), 7.48-7.56 (1H, m), 7.59(1H, b
s), 7.90 (1H, d, J=8.4Hz), 8.72 (1H, d, J=2.6Hz),
8.98 (1H, d, J=2.6Hz). MS m/z : 282(M+), 184, 158, 130, 103, 97。Example 6 1-Methyl-N- (5-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-28) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.34 (3H, s), 1.38-
1.72 (8H, m), 2.04-2.15 (2H, m), 2.70 (3H, s), 7.3
7 (1H, d, J = 6.8Hz), 7.48-7.56 (1H, m), 7.59 (1H, b
s), 7.90 (1H, d, J = 8.4Hz), 8.72 (1H, d, J = 2.6Hz),
8.98 (1H, d, J = 2.6Hz) .MS m / z: 282 (M + ), 184, 158, 130, 103, 97.

【００８３】[0083]

【実施例７】１−メチル−N−（６−メチル−３−キノ
リル）−１−シクロヘキサンカルボキサミド（化合物番
号１−２９） 融点：140-143℃。1 H-NMR (200MHz, CDCl3) δppm : 1.32 (3H, s), 1.25-
2.08 (10H, m), 2.52 (3H, s), 7.45 (1H, d, J=8.4H
z), 7.52 (1H, s), 7.62 (1H, bs), 7.91 (1H, d,J=8.4
Hz), 8.64 (1H, d, J=2.4Hz), 8.70 (1H, d, J=2.4Hz). MS m/z : 282(M+), 158, 130, 97, 55。Example 7 1-Methyl-N- (6-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-29) Melting point: 140-143 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.32 (3H, s), 1.25-
2.08 (10H, m), 2.52 (3H, s), 7.45 (1H, d, J = 8.4H
z), 7.52 (1H, s), 7.62 (1H, bs), 7.91 (1H, d, J = 8.4
Hz), 8.64 (1H, d, J = 2.4Hz), 8.70 (1H, d, J = 2.4Hz). MS m / z: 282 (M + ), 158, 130, 97, 55.

【００８４】[0084]

【実施例８】１−メチル−N−（４−クロロ−６−メチ
ル−３−キノリル）−１−シクロヘキサンカルボキサミ
ド（化合物番号１−２１６） 融点：90-91℃。1 H-NMR (200MHz, CDCl3) δppm : 1.33 (3H, s), 1.40-
2.20 (10H, m), 2.52 (3H, s), 7.47 (1H, d, J=8.8H
z), 7.56 (1H, s), 7.83 (1H, d, J=8.8Hz), 8.23(1H,
bs), 9.14 (1H, s). MS m/z : 318(M++2), 316(M+), 281, 192, 164, 155。Example 8 1-Methyl-N- (4-chloro-6-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-216) Melting point: 90-91 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.33 (3H, s), 1.40-
2.20 (10H, m), 2.52 (3H, s), 7.47 (1H, d, J = 8.8H
z), 7.56 (1H, s), 7.83 (1H, d, J = 8.8Hz), 8.23 (1H,
bs), 9.14 (1H, s). MS m / z: 318 (M + +2), 316 (M + ), 281, 192, 164, 155.

【００８５】[0085]

【実施例９】１−アリル−N−（３−キノリル）−１−
シクロヘキサンカルボキサミド（化合物番号１−２４４
３番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.30-1.75 (8H, m),
2.08-2.19 (2H, m), 2.37 (2H, d, J=7.3Hz), 5.04-5.1
0 (2H, m), 5.71-5.92 (1H, m), 7.46-7.65 (2H,m), 7.
74 (1H, dd, J=1.5, 7.3Hz), 7.83 (1H, bs), 8.02 (1
H, d, J=7.7Hz),8.72 (1H, d, J=2.6Hz), 8.75 (1H, d,
J=2.6Hz). MS m/z : 294(M+), 144, 123。Example 9 1-allyl-N- (3-quinolyl) -1-
Cyclohexanecarboxamide (Compound No. 1-244
No. 3) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.30-1.75 (8H, m),
2.08-2.19 (2H, m), 2.37 (2H, d, J = 7.3Hz), 5.04-5.1
0 (2H, m), 5.71-5.92 (1H, m), 7.46-7.65 (2H, m), 7.
74 (1H, dd, J = 1.5, 7.3Hz), 7.83 (1H, bs), 8.02 (1
H, d, J = 7.7Hz), 8.72 (1H, d, J = 2.6Hz), 8.75 (1H, d,
J = 2.6Hz) .MS m / z: 294 (M + ), 144, 123.

【００８６】[0086]

【実施例１０】1-メチル-N-（5-フルオロ-3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
４番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.33 (3H, s), 1.50-
1.62 (8H, m), 2.05-2.14 (2H, m), 7.17-7.25 (1H,
m), 7.45-7.60 (1H, m), 7.63 (1H, s), 7.85 (1H,d, J
=7.9Hz), 8.84 (1H, d, J=2.6Hz), 8.92 (1H, d, J=2.6
Hz). MS m/z : 286(M+), 162, 134, 125, 107。Example 10 1-Methyl-N- (5-fluoro-3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 4) Physical property: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.33 (3H, s), 1.50-
1.62 (8H, m), 2.05-2.14 (2H, m), 7.17-7.25 (1H,
m), 7.45-7.60 (1H, m), 7.63 (1H, s), 7.85 (1H, d, J
= 7.9Hz), 8.84 (1H, d, J = 2.6Hz), 8.92 (1H, d, J = 2.6
Hz) .MS m / z: 286 (M + ), 162, 134, 125, 107.

【００８７】[0087]

【実施例１１】1-メチル-N-（6-フルオロ-3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
５番） 融点：128-130℃。1 H-NMR (200MHz, CDCl3) δppm : 1.32 (3H, s), 1.22-
2.11 (10H, m), 7.32-7.43 (2H, m) 7.63 (1H, bs), 7.
98-8.05 (1H, m), 8.65-8.80 (2H, m). MS m/z : 286(M+), 162, 125, 107, 97。Example 11 1-Methyl-N- (6-fluoro-3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 5) Melting point: 128-130 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.32 (3H, s), 1.22-
2.11 (10H, m), 7.32-7.43 (2H, m) 7.63 (1H, bs), 7.
98-8.05 (1H, m), 8.65-8.80 (2H, m). MS m / z: 286 (M + ), 162, 125, 107, 97.

【００８８】[0088]

【実施例１２】1-メチル-N-（7-フルオロ-3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
６番） 融点：126-127℃。1 H-NMR (200MHz, CDCl3) δppm : 1.33 (3H, s), 1.49-
1.67 (8H, m), 2.05-2.12 (2H, m), 7.33 (1H, dt, J=
2.4, 9.3Hz), 7.61 (1H, s), 7.67 (1H, dd, J=2.4, 9.
3Hz), 7.78 (1H, dd, J=6.1, 9.3Hz), 8.71 (1H, d, J=
2.6Hz), 8.84 (1H,d, J=2.6Hz). MS m/z : 286(M+), 162, 134, 125, 107。Example 12 1-Methyl-N- (7-fluoro-3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 6) Melting point: 126-127 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.33 (3H, s), 1.49-
1.67 (8H, m), 2.05-2.12 (2H, m), 7.33 (1H, dt, J =
2.4, 9.3Hz), 7.61 (1H, s), 7.67 (1H, dd, J = 2.4, 9.
3Hz), 7.78 (1H, dd, J = 6.1, 9.3Hz), 8.71 (1H, d, J =
2.6Hz), 8.84 (1H, d, J = 2.6Hz) .MS m / z: 286 (M + ), 162, 134, 125, 107.

【００８９】[0089]

【実施例１３】1-メチル-N-（8-フルオロ-3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
７番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.33 (3H, s), 1.50-
1.65 (8H, m), 2.08-2.13 (2H, m), 7.30-7.64 (4H,
m), 8.72 (1H, s), 8.94 (1H, s). MS m/z : 286(M+), 162, 134, 125, 97。Example 13 1-Methyl-N- (8-fluoro-3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 7) Physical property: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.33 (3H, s), 1.50-
1.65 (8H, m), 2.08-2.13 (2H, m), 7.30-7.64 (4H,
m), 8.72 (1H, s), 8.94 (1H, s). MS m / z: 286 (M + ), 162, 134, 125, 97.

【００９０】[0090]

【実施例１４】1-メチル-N-（2-クロロ-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−８
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.34 (3H, s), 1.50-
1.65 (8H, m), 2.06-2.09 (2H, m), 7.51-7.68 (2H,
m), 7.81 (1H, d, J=8.1Hz), 7.94 (1H, d, J=8.1Hz),
8.26 (1H, s), 9.24 (1H, s). MS m/z : 302(M+), 267, 178, 142, 115。Example 14 1-Methyl-N- (2-chloro-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-8
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.34 (3H, s), 1.50-
1.65 (8H, m), 2.06-2.09 (2H, m), 7.51-7.68 (2H,
m), 7.81 (1H, d, J = 8.1Hz), 7.94 (1H, d, J = 8.1Hz),
8.26 (1H, s), 9.24 (1H, s). MS m / z: 302 (M + ), 267, 178, 142, 115.

【００９１】[0091]

【実施例１５】1-メチル-N-（7-クロロ-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−１
２番） 融点：125-127℃。1 H-NMR (200MHz, CDCl3) δppm : 1.32 (3H, s), 1.45-
1.65 (8H, m), 2.04-2.11 (2H, m), 7.48 (1H, dd, J=
2.1, 8.7Hz), 7.61 (1H, s), 7.72 (1H, d, J=8.7Hz),
8.03 (1H, d, J=2.1Hz), 8.70 (1H, d, J=2.6Hz), 8.83
(1H, d, J=2.6Hz). MS m/z : 302(M+), 178, 150, 125, 97。Example 15 1-Methyl-N- (7-chloro-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-1
No. 2) Melting point: 125-127 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.32 (3H, s), 1.45-
1.65 (8H, m), 2.04-2.11 (2H, m), 7.48 (1H, dd, J =
2.1, 8.7Hz), 7.61 (1H, s), 7.72 (1H, d, J = 8.7Hz),
8.03 (1H, d, J = 2.1Hz), 8.70 (1H, d, J = 2.6Hz), 8.83
(1H, d, J = 2.6Hz) .MS m / z: 302 (M + ), 178, 150, 125, 97.

【００９２】[0092]

【実施例１６】1-メチル-N-（2-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−２
６番） 融点：122-125℃。1 H-NMR (200MHz, CDCl3) δppm : 1.34 (3H, s), 1.28-
2.09 (10H, m), 2.72 (3H, s) 7.43-7.65 (3H, m), 7.7
7 (1H, dd, J=1.5, 8.0 Hz), 7.95, (1H, d, J=8.4Hz),
8.84 (1H, s). MS m/z : 282(M+), 158, 130, 97, 89。Example 16 1-Methyl-N- (2-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-2
No. 6) Melting point: 122-125 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.34 (3H, s), 1.28-
2.09 (10H, m), 2.72 (3H, s) 7.43-7.65 (3H, m), 7.7
7 (1H, dd, J = 1.5, 8.0 Hz), 7.95, (1H, d, J = 8.4Hz),
8.84 (1H, s) .MS m / z: 282 (M + ), 158, 130, 97, 89.

【００９３】[0093]

【実施例１７】1-メチル-N-（4-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−２
７番） 融点：135-137℃。1 H-NMR (200MHz, CDCl3) δppm : 1.28 (3H, s), 1.35-
1.60 (8H, m), 2.00-2.10 (2H, m), 2.35 (3H, s), 7.4
0-7.70 (2H, m), 7.72 (1H, bs), 7.81 (1H, dd,J=1.3,
8.2Hz), 8.00 (1H, dd, J=1.1, 8.4Hz), 8.69 (1H,
s). MS m/z : 282(M+), 159, 130。Example 17 1-Methyl-N- (4-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-2
No. 7) Melting point: 135-137 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.28 (3H, s), 1.35-
1.60 (8H, m), 2.00-2.10 (2H, m), 2.35 (3H, s), 7.4
0-7.70 (2H, m), 7.72 (1H, bs), 7.81 (1H, dd, J = 1.3,
8.2Hz), 8.00 (1H, dd, J = 1.1, 8.4Hz), 8.69 (1H,
s) .MS m / z: 282 (M + ), 159, 130.

【００９４】[0094]

【実施例１８】1-メチル-N-（7-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−３
０番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.33 (3H, s), 1.43-
1.65 (8H, m), 2.05-2.12 (2H, m), 2.55 (3H, s), 7.3
7 (1H, d, J=8.4Hz), 7.54 (1H, s), 7.69 (1H,d, J=8.
4Hz), 7.81(1H, s), 8.67 (1H, d, J=2.6Hz), 8.78 (1
H, d, J=2.6Hz). MS m/z : 282(M+), 158, 130, 103, 97。Example 18 1-Methyl-N- (7-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-3
No. 0) Physical property: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.33 (3H, s), 1.43-
1.65 (8H, m), 2.05-2.12 (2H, m), 2.55 (3H, s), 7.3
7 (1H, d, J = 8.4Hz), 7.54 (1H, s), 7.69 (1H, d, J = 8.
4Hz), 7.81 (1H, s), 8.67 (1H, d, J = 2.6Hz), 8.78 (1
H, d, J = 2.6Hz). MS m / z: 282 (M + ), 158, 130, 103, 97.

【００９５】[0095]

【実施例１９】1-メチル-N-（8-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−３
１番） 融点：116-118℃。1 H-NMR (200MHz, CDCl3) δppm : 1.33 (3H, s), 1.43-
1.65 (8H, m), 2.05-2.12 (2H, m), 2.78 (3H, s), 7.3
7-7.48 (2H, m), 7.58-7.66 (2H, m), 8.71 (1H,d, J=
2.6Hz), 8.81 (1H, d, J=2.6Hz). MS m/z : 282(M+), 158, 130, 103, 97。Example 19 1-Methyl-N- (8-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-3
No. 1) Melting point: 116-118 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.33 (3H, s), 1.43-
1.65 (8H, m), 2.05-2.12 (2H, m), 2.78 (3H, s), 7.3
7-7.48 (2H, m), 7.58-7.66 (2H, m), 8.71 (1H, d, J =
2.6Hz), 8.81 (1H, d, J = 2.6Hz) .MS m / z: 282 (M + ), 158, 130, 103, 97.

【００９６】[0096]

【実施例２０】1-メチル-N-（2-プロピル-3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
３８番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 1.09 (3H, t, J=7.
3), 1.33 (1H, s), 1.45-1.70 (8H, m), 1.85 (2H, m),
2.00-2.10 (2H, m), 2.95 (1H, t, J=7.9Hz), 7.40-7.
70 (3H, m), 7.76 (1H, d, J=8.1Hz), 7.98 (1H, d, J=
8.4Hz), 8.87 (1H,s). MS m/z : 310(M+), 282, 213, 185, 158。Example 20 1-Methyl-N- (2-propyl-3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 38) Physical property: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.09 (3H, t, J = 7.
3), 1.33 (1H, s), 1.45-1.70 (8H, m), 1.85 (2H, m),
2.00-2.10 (2H, m), 2.95 (1H, t, J = 7.9Hz), 7.40-7.
70 (3H, m), 7.76 (1H, d, J = 8.1Hz), 7.98 (1H, d, J =
8.4Hz), 8.87 (1H, s) .MS m / z: 310 (M + ), 282, 213, 185, 158.

【００９７】[0097]

【実施例２１】1-メチル-N-（2-イソプロピル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−４４番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 1.34 (3H, s), 1.44
(6H, d, J=6.7Hz), 1.40-1.70 (8H, m), 1.95-2.15 (2
H, m), 3.23 (1H, m), 7.40-7.65 (3H, m), 7.76(1H,
d, J=8.8Hz), 7.99 (1H, d, J=8.4Hz), 8.84 (1H, s). MS m/z : 310(M+), 267, 213, 171, 158。Example 21 1-Methyl-N- (2-isopropyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-44) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.34 (3H, s), 1.44
(6H, d, J = 6.7Hz), 1.40-1.70 (8H, m), 1.95-2.15 (2
H, m), 3.23 (1H, m), 7.40-7.65 (3H, m), 7.76 (1H,
d, J = 8.8Hz), 7.99 (1H, d, J = 8.4Hz), 8.84 (1H, s). MS m / z: 310 (M + ), 267, 213, 171, 158.

【００９８】[0098]

【実施例２２】1-メチル-N-（5,7-ジメチル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−１８０番） 物性：ガム状。1 H-NMR (200MHz, CDCl3) δppm : 1.33 (3H, s), 1.44-
2.10 (10H, m), 2.49 (3H, s), 2.63 (3H, s), 7.20 (1
H, s), 7.65 (1H, s), 7.70 (1H, bs), 8.68 (1H, bs),
8.88 (1H, d, J=2.5Hz). MS m/z : 296(M+), 172, 157, 144, 97。Example 22 1-Methyl-N- (5,7-dimethyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-180) Physical properties: Gummy. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.33 (3H, s), 1.44-
2.10 (10H, m), 2.49 (3H, s), 2.63 (3H, s), 7.20 (1
H, s), 7.65 (1H, s), 7.70 (1H, bs), 8.68 (1H, bs),
8.88 (1H, d, J = 2.5Hz) .MS m / z: 296 (M + ), 172, 157, 144, 97.

【００９９】[0099]

【実施例２３】1-エチル-N-（2-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−２
４８番） 融点：115-118℃。1 H-NMR (200MHz, CDCl3) δppm : 0.94 (3H, t, J=7.5H
z), 1.26-2.15 (12H, m), 2.72 (3H, s), 7.43-7.65 (3
H, m), 7.78 (1H, dd, J=1.5, 7.7Hz), 7.96, (1H, d,
J=8.4Hz), 8.87 (1H, s). MS m/z : 296(M+), 158, 130, 111, 89, 69。Example 23 1-Ethyl-N- (2-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-2
No. 48) Melting point: 115-118 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.94 (3H, t, J = 7.5H
z), 1.26-2.15 (12H, m), 2.72 (3H, s), 7.43-7.65 (3
H, m), 7.78 (1H, dd, J = 1.5, 7.7Hz), 7.96, (1H, d,
J = 8.4Hz), 8.87 (1H, s) .MS m / z: 296 (M + ), 158, 130, 111, 89, 69.

【０１００】[0100]

【実施例２４】1-エチル-N-（4-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−２
４９番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.99 (3H, t, J=7.5H
z), 1.39-1.76 (8H, m),2.09-2.15 (2H, m), 2.56 (3H,
s), 7.38 (1H, bs), 7.52-7.72 (2H, m), 7.99(1H, d,
J=9.2Hz), 8.08 (1H, d, J=8.0Hz), 8.89 (1H, s). MS m/z : 296(M+), 158。Example 24 1-Ethyl-N- (4-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-2
No. 49) Physical property: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.99 (3H, t, J = 7.5H
z), 1.39-1.76 (8H, m), 2.09-2.15 (2H, m), 2.56 (3H,
s), 7.38 (1H, bs), 7.52-7.72 (2H, m), 7.99 (1H, d,
J = 9.2Hz), 8.08 (1H, d, J = 8.0Hz), 8.89 (1H, s). MS m / z: 296 (M + ), 158.

【０１０１】[0101]

【実施例２５】1-プロピル-N-（2-メチル-3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
４７０番） 融点：148-149℃。1 H-NMR (200MHz, CDCl3) δppm : 0.91 (3H, t, J=7.0H
z), 1.26-2.15 (14H, m), 2.72 (3H, s), 7.43-7.65 (3
H, m), 7.77 (1H, dd, J=1.1, 8.0Hz), 7.96, (1H, d,
J=8.4Hz), 8.87 (1H, s). MS m/z : 310(M+), 268, 158, 142, 125, 89。Example 25 1-Propyl-N- (2-methyl-3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 470) Melting point: 148-149 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.91 (3H, t, J = 7.0H
z), 1.26-2.15 (14H, m), 2.72 (3H, s), 7.43-7.65 (3
H, m), 7.77 (1H, dd, J = 1.1, 8.0Hz), 7.96, (1H, d,
J = 8.4Hz), 8.87 (1H, s) .MS m / z: 310 (M + ), 268, 158, 142, 125, 89.

【０１０２】[0102]

【実施例２６】1-プロピル-N-（4-メチル-3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
４７１番） 融点：130-132℃。1 H-NMR (200MHz, CDCl3) δppm : 0.95 (3H, t, J=7.0H
z), 1.22-1.67 (12H, m), 2.04-2.15 (2H, m), 2.56 (3
H, s), 7.37 (1H, bs), 7.53-7.71 (2H, m), 7.99 (1H,
d, J=8.0Hz), 8.08 (1H, d, J=8.0Hz), 8.90 (1H, s). MS m/z : 310(M+), 268, 158。Example 26 1-Propyl-N- (4-methyl-3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 471) Melting point: 130-132 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.95 (3H, t, J = 7.0H
z), 1.22-1.67 (12H, m), 2.04-2.15 (2H, m), 2.56 (3
H, s), 7.37 (1H, bs), 7.53-7.71 (2H, m), 7.99 (1H,
d, J = 8.0Hz), 8.08 (1H, d, J = 8.0Hz), 8.90 (1H, s). MS m / z: 310 (M + ), 268, 158.

【０１０３】[0103]

【実施例２７】1-イソプロピル-N-（3-キノリル）−１
−シクロヘキサンカルボキサミド（化合物番号１−６６
７番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.99 (6H, d, J=7.0H
z), 1.40-1.85 (9H, m),2.13-2.20 (2H, m), 7.45-7.65
(3H, m), 7.80 (1H, d, J=8.1Hz), 8.04 (1H,dd, J=1.
6, 8.1Hz), 8.70 (1H, d, J=2.6Hz), 8.84 (1H, d, J=
2.6Hz). MS m/z : 296(M+), 279, 265, 167, 149。Example 27 1-Isopropyl-N- (3-quinolyl) -1
-Cyclohexanecarboxamide (Compound No. 1-66
No. 7) Physical property: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.99 (6H, d, J = 7.0H
z), 1.40-1.85 (9H, m), 2.13-2.20 (2H, m), 7.45-7.65
(3H, m), 7.80 (1H, d, J = 8.1Hz), 8.04 (1H, dd, J = 1.
6, 8.1Hz), 8.70 (1H, d, J = 2.6Hz), 8.84 (1H, d, J =
2.6Hz) .MS m / z: 296 (M + ), 279, 265, 167, 149.

【０１０４】[0104]

【実施例２８】1-イソプロピル-N-（2-メチル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−６９２番） 物性：ガム状。1 H-NMR (200MHz, CDCl3) δppm : 1.01 (6H, d, J=6.6H
z), 1.26-2.16 (11H, m), 2.72 (3H, s), 7.43-7.65 (3
H, m), 7.77 (1H, d, J=7.7Hz), 7.96, (1H, d,J=8.4H
z), 8.91 (1H, s). MS m/z : 310(M+), 158, 142, 125, 89。Example 28 1-Isopropyl-N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-692) Physical properties: gummy. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.01 (6H, d, J = 6.6H
z), 1.26-2.16 (11H, m), 2.72 (3H, s), 7.43-7.65 (3
H, m), 7.77 (1H, d, J = 7.7Hz), 7.96, (1H, d, J = 8.4H
z), 8.91 (1H, s). MS m / z: 310 (M + ), 158, 142, 125, 89.

【０１０５】[0105]

【実施例２９】1-ブチル-N-（3-キノリル）−１−シク
ロヘキサンカルボキサミド（化合物番号１−８８９番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 0.87 (3H, t, J=6.6H
z), 1.10-1.70 (14H, m), 2.00-2.15 (2H, m), 7.50-7.
70 (3H, m), 7.80 (1H, d, J=8.1Hz), 8.04 (1H,d, J=
8.4Hz), 8.72 (1H, d, J=2.6Hz), 8.85 (1H, d, J=2.6H
z). MS m/z : 310(M+), 254, 144, 139。Example 29 1-Butyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-889) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.87 (3H, t, J = 6.6H
z), 1.10-1.70 (14H, m), 2.00-2.15 (2H, m), 7.50-7.
70 (3H, m), 7.80 (1H, d, J = 8.1Hz), 8.04 (1H, d, J =
8.4Hz), 8.72 (1H, d, J = 2.6Hz), 8.85 (1H, d, J = 2.6H
z). MS m / z: 310 (M + ), 254, 144, 139.

【０１０６】[0106]

【実施例３０】1-イソブチル-N-（3-キノリル）−１−
シクロヘキサンカルボキサミド（化合物番号１−１１１
１番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 0.88 (6H, d, J=6.6H
z), 1.40-1.90 (9H, m),1.58 (2H, d, J=5.9Hz), 2.05-
2.15 (2H, m), 7.45-7.65 (1H, m), 7.77 (1H,d, J=8.1
Hz), 7.85 (1H, bs), 8.02 (1H, d, J=8.4Hz), 8.76 (1
H, d, J=2.4Hz), 8.83 (1H, d, J=2.4Hz). MS m/z : 310(M+), 254, 145, 139。Example 30 1-Isobutyl-N- (3-quinolyl) -1-
Cyclohexanecarboxamide (Compound No. 1-111
No. 1) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.88 (6H, d, J = 6.6H
z), 1.40-1.90 (9H, m), 1.58 (2H, d, J = 5.9Hz), 2.05-
2.15 (2H, m), 7.45-7.65 (1H, m), 7.77 (1H, d, J = 8.1
Hz), 7.85 (1H, bs), 8.02 (1H, d, J = 8.4Hz), 8.76 (1
H, d, J = 2.4Hz), 8.83 (1H, d, J = 2.4Hz). MS m / z: 310 (M + ), 254, 145, 139.

【０１０７】[0107]

【実施例３１】1-イソブチル-N-（2-メチル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−１１３６番） 融点：120-123℃。1 H-NMR (200MHz, CDCl3) δppm : 0.91 (6H, d, J=6.6H
z), 1.26-2.15 (13H, m), 2.73 (3H, s), 7.43-7.65 (3
H, m), 7.78 (1H, dd, J=8.0,1.5Hz), 7.96, (1H, d, J
=8.4Hz), 8.89 (1H, s). MS m/z : 324(M+), 268, 158, 139, 130, 115, 97, 8
3。Example 31 1-isobutyl-N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-1136) Melting point: 120-123 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.91 (6H, d, J = 6.6H
z), 1.26-2.15 (13H, m), 2.73 (3H, s), 7.43-7.65 (3
H, m), 7.78 (1H, dd, J = 8.0,1.5Hz), 7.96, (1H, d, J
= 8.4Hz), 8.89 (1H, s) .MS m / z: 324 (M + ), 268, 158, 139, 130, 115, 97, 8
3.

【０１０８】[0108]

【実施例３２】1-イソブチル-N-（4-メチル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−１１３７番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 0.97 (6H, d, J=6.6H
z), 1.57-1.89 (11H, m), 2.05-2.15 (2H, m), 2.58 (3
H, s), 7.36 (1H, bs), 7.53-7.71 (2H, m), 8.00 (1H,
d, J=9.8Hz), 8.09 (1H, d, J=7.8Hz), 8.95 (1H, s). MS m/z : 324(M+), 279, 268, 167, 158。Example 32 1-Isobutyl-N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-1137) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.97 (6H, d, J = 6.6H
z), 1.57-1.89 (11H, m), 2.05-2.15 (2H, m), 2.58 (3
H, s), 7.36 (1H, bs), 7.53-7.71 (2H, m), 8.00 (1H,
d, J = 9.8Hz), 8.09 (1H, d, J = 7.8Hz), 8.95 (1H, s). MS m / z: 324 (M + ), 279, 268, 167, 158.

【０１０９】[0109]

【実施例３３】1-メチル-N-（3-キノリル）-3-シクロヘ
キセン−１−カルボキサミド（化合物番号１−１７７７
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.38 (3H, s), 1.74
(1H, dd, J=6.3, 14.5Hz), 2.00-2.20 (4H, m), 2.62
(1H, d, J=14.5Hz), 5.72-5.83 (2H, m), 7.45-7.65 (2
H, m), 7.76 (1H, d, J=8.1Hz), 7.95 (1H, bs), 8.02
(1H, d, J=8.1Hz),8.70 (1H, d, J=2.6Hz), 8.78 (1H,
d, J=2.6Hz). MS m/z : 266(M+), 144, 128, 116。Example 33 1-Methyl-N- (3-quinolyl) -3-cyclohexene-1-carboxamide (Compound No. 1-1777)
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.38 (3H, s), 1.74
(1H, dd, J = 6.3, 14.5Hz), 2.00-2.20 (4H, m), 2.62
(1H, d, J = 14.5Hz), 5.72-5.83 (2H, m), 7.45-7.65 (2
H, m), 7.76 (1H, d, J = 8.1Hz), 7.95 (1H, bs), 8.02
(1H, d, J = 8.1Hz), 8.70 (1H, d, J = 2.6Hz), 8.78 (1H,
d, J = 2.6Hz) .MS m / z: 266 (M + ), 144, 128, 116.

【０１１０】[0110]

【実施例３４】1-メチル-N-（2-メチル-3-キノリル）-3
-シクロヘキセン−１−カルボキサミド（化合物番号１
−１８０２番） 融点：91-93℃。1 H-NMR (200MHz, CDCl3) δppm : 1.40 (3H, s), 1.65-
2.57 (6H, m), 2.67 (3H, s), 5.82-5.95 (2H, m), 7.4
3-7.64 (2H, m), 7.76 (1H, dd, J=1.5, 8.0Hz),7.95,
(1H, d, J=8.4Hz), 8.89 (1H, s). MS m/z : 280(M+), 265, 184, 158, 130, 95。Example 34 1-Methyl-N- (2-methyl-3-quinolyl) -3
-Cyclohexene-1-carboxamide (Compound No. 1
-1802) Melting point: 91-93 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.40 (3H, s), 1.65-
2.57 (6H, m), 2.67 (3H, s), 5.82-5.95 (2H, m), 7.4
3-7.64 (2H, m), 7.76 (1H, dd, J = 1.5, 8.0Hz), 7.95,
(1H, d, J = 8.4Hz), 8.89 (1H, s). MS m / z: 280 (M + ), 265, 184, 158, 130, 95.

【０１１１】[0111]

【実施例３５】1-メチル-N-（4-メチル-3-キノリル）-3
-シクロヘキセン−１−カルボキサミド（化合物番号１
−１８０３番） 融点：96-98℃。1 H-NMR (200MHz, CDCl3) δppm : 1.42 (3H, s), 1.61-
1.81 (1H, m), 2.05-2.25 (4H, m), 2.54 (3H, s), 2.6
1-2.70 (1H, m), 5.87 (2H, bs), 7.51-7.71 (3H, m),
8.00 (1H, d, J=8.4Hz), 8.09 (1H, d, J=7.0Hz), 8.94
(1H, s). MS m/z : 280(M+), 265, 158。Example 35 1-Methyl-N- (4-methyl-3-quinolyl) -3
-Cyclohexene-1-carboxamide (Compound No. 1
-1803) Melting point: 96-98 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.42 (3H, s), 1.61-
1.81 (1H, m), 2.05-2.25 (4H, m), 2.54 (3H, s), 2.6
1-2.70 (1H, m), 5.87 (2H, bs), 7.51-7.71 (3H, m),
8.00 (1H, d, J = 8.4Hz), 8.09 (1H, d, J = 7.0Hz), 8.94
(1H, s). MS m / z: 280 (M + ), 265, 158.

【０１１２】[0112]

【実施例３６】1-アリル-N-（2-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−２
４６８番） 融点：117-119℃。1 H-NMR (200MHz, CDCl3) δppm : 1.42-2.15 (10H, m),
2.39 (2H, d, J=7.7Hz), 2.71 (3H, s), 5.06-5.16 (2
H, m), 5.72-5.93 (1H, m), 7.43-7.65 (3H, m),7.77
(1H, dd, J=1.5, 8.0Hz), 7.96, (1H, d, J=8.4Hz), 8.
85 (1H, s). MS m/z : 308(M+), 293, 266, 158, 142, 130, 123。Example 36 1-allyl-N- (2-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-2
No. 468) Melting point: 117-119 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.42-2.15 (10H, m),
2.39 (2H, d, J = 7.7Hz), 2.71 (3H, s), 5.06-5.16 (2
H, m), 5.72-5.93 (1H, m), 7.43-7.65 (3H, m), 7.77
(1H, dd, J = 1.5, 8.0Hz), 7.96, (1H, d, J = 8.4Hz), 8.
85 (1H, s) .MS m / z: 308 (M + ), 293, 266, 158, 142, 130, 123.

【０１１３】[0113]

【実施例３７】1-アリル-N-（4-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−２
４６９番） 融点：156-158℃。1 H-NMR (200MHz, CDCl3) δppm : 1.42-1.69 (8H, m),
2.05-2.16 (2H, m), 2.42 (2H, d, J=7.8Hz), 2.57 (3
H, s), 5.14 (1H, d, J=2.6Hz), 5.20 (1H, s), 5.80-
6.00 (1H, m), 7.32 (1H, bs), 7.53-7.72 (2H, m), 8.
00 (1H, d, J=8.0Hz), 8.09 (1H, d, J=7.8Hz), 8.89
(1H, s). MS m/z : 308(M+), 266, 158。Example 37 1-allyl-N- (4-methyl-3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-2
No. 469) Melting point: 156-158 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.42-1.69 (8H, m),
2.05-2.16 (2H, m), 2.42 (2H, d, J = 7.8Hz), 2.57 (3
H, s), 5.14 (1H, d, J = 2.6Hz), 5.20 (1H, s), 5.80-
6.00 (1H, m), 7.32 (1H, bs), 7.53-7.72 (2H, m), 8.
00 (1H, d, J = 8.0Hz), 8.09 (1H, d, J = 7.8Hz), 8.89
(1H, s). MS m / z: 308 (M + ), 266, 158.

【０１１４】[0114]

【実施例３８】1-ｔ-ブチル-N-（3-キノリル）−１−シ
クロヘキサンカルボキサミド（化合物番号１−２６６５
番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 1.03 (9H, s), 1.30-
1.85 (8H, m), 2.20-2.30 (2H, m), 7.50-7.70 (3H,
m), 7.80 (1H, d, J=8.4Hz), 8.04 (1H, d, J=8.4Hz),
8.71 (1H, d, J=2.6Hz), 8.85 (1H, d, J=2.6Hz). MS m/z : 310(M+), 254, 144, 139。Example 38 1-t-butyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-2665)
No.) Physical property: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.03 (9H, s), 1.30-
1.85 (8H, m), 2.20-2.30 (2H, m), 7.50-7.70 (3H,
m), 7.80 (1H, d, J = 8.4Hz), 8.04 (1H, d, J = 8.4Hz),
8.71 (1H, d, J = 2.6Hz), 8.85 (1H, d, J = 2.6Hz). MS m / z: 310 (M + ), 254, 144, 139.

【０１１５】[0115]

【実施例３９】1-ペンチル-N-（3-キノリル）−１−シ
クロヘキサンカルボキサミド（化合物番号１−２７３２
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.81-0.87 (3H, m),
1.26-1.65 (16H, m), 2.05-2.12 (2H, m), 7.49-7.67
(3H, m), 7.80 (1H, d, J=8.1Hz), 8.04 (1H, d,J=8.1H
z), 8.70 (1H, d, J=2.6Hz), 8.84 (1H, d, J=2.6Hz). MS m/z : 324(M+), 254, 153, 144, 128。Example 39 1-Pentyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-2732)
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.81-0.87 (3H, m),
1.26-1.65 (16H, m), 2.05-2.12 (2H, m), 7.49-7.67
(3H, m), 7.80 (1H, d, J = 8.1Hz), 8.04 (1H, d, J = 8.1H
z), 8.70 (1H, d, J = 2.6Hz), 8.84 (1H, d, J = 2.6Hz). MS m / z: 324 (M + ), 254, 153, 144, 128.

【０１１６】[0116]

【実施例４０】1-ヘキシル-N-（3-キノリル）−１−シ
クロヘキサンカルボキサミド（化合物番号１−２７９９
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.81-0.89 (3H, m),
1.25-1.64 (18H, m), 2.05-2.12 (2H, m), 7.49-7.66
(3H, m), 7.80 (1H, d, J=7.7Hz), 8.04 (1H, d,J=8.8H
z), 8.71 (1H, d, J=2.4Hz), 8.85 (1H, d, J=2.4Hz). MS m/z : 338(M+), 254, 167, 144, 128。Example 40 1-hexyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-2799)
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.81-0.89 (3H, m),
1.25-1.64 (18H, m), 2.05-2.12 (2H, m), 7.49-7.66
(3H, m), 7.80 (1H, d, J = 7.7Hz), 8.04 (1H, d, J = 8.8H
z), 8.71 (1H, d, J = 2.4Hz), 8.85 (1H, d, J = 2.4Hz). MS m / z: 338 (M + ), 254, 167, 144, 128.

【０１１７】[0117]

【実施例４１】1-（2-エチルブチル）-N-（3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−２８６６番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.75-0.90 (6H, m),
1.19-2.37 (17H, m), 7.49-7.67 (3H, m), 7.80 (1H,
d, J=8.1Hz), 8.04 (1H, d, J=8.1Hz), 8.73 (1H,s),
8.82(1H, s). MS m/z : 338(M+), 254, 167, 144, 128。Example 41 1- (2-Ethylbutyl) -N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-2866) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.75-0.90 (6H, m),
1.19-2.37 (17H, m), 7.49-7.67 (3H, m), 7.80 (1H,
d, J = 8.1Hz), 8.04 (1H, d, J = 8.1Hz), 8.73 (1H, s),
8.82 (1H, s). MS m / z: 338 (M + ), 254, 167, 144, 128.

【０１１８】[0118]

【実施例４２】1-ヘプチル-N-（3-キノリル）−１−シ
クロヘキサンカルボキサミド（化合物番号１−２９３３
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.81-0.84 (3H, m),
1.25-1.60 (20H, m), 2.07-2.10 (2H, m), 7.50-7.67
(3H, m), 7.80 (1H, d, J=7.7Hz), 8.04 (1H, d,J=8.8H
z), 8.71 (1H, s), 8.84 (1H, s). MS m/z : 352(M+), 254, 181, 144, 111。Example 42 1-heptyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-2933)
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.81-0.84 (3H, m),
1.25-1.60 (20H, m), 2.07-2.10 (2H, m), 7.50-7.67
(3H, m), 7.80 (1H, d, J = 7.7Hz), 8.04 (1H, d, J = 8.8H
z), 8.71 (1H, s), 8.84 (1H, s). MS m / z: 352 (M + ), 254, 181, 144, 111.

【０１１９】[0119]

【実施例４３】1-オクチル-N-（3-キノリル）−１−シ
クロヘキサンカルボキサミド（化合物番号１−３０００
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.81-0.84 (3H, m),
1.22-1.60 (22H, m), 2.07-2.12 (2H, m), 7.49-7.67
(3H, m), 7.80 (1H, d, J=7.7Hz), 8.04 (1H, d,J=8.4H
z), 8.71 (1H, s), 8.83 (1H, s). MS m/z : 366(M+), 254, 195, 144, 111。Example 43 1-octyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3000)
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.81-0.84 (3H, m),
1.22-1.60 (22H, m), 2.07-2.12 (2H, m), 7.49-7.67
(3H, m), 7.80 (1H, d, J = 7.7Hz), 8.04 (1H, d, J = 8.4H
z), 8.71 (1H, s), 8.83 (1H, s). MS m / z: 366 (M + ), 254, 195, 144, 111.

【０１２０】[0120]

【実施例４４】1-クロロメチル-N-（3-キノリル）−１
−シクロヘキサンカルボキサミド（化合物番号１−３１
３４番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.40-1.90 (8H, m),
2.10-2.30 (2H, m), 3.75 (2H, s), 7.50-7.70 (2H,
m), 7.78 (1H, bs), 7.81 (1H, dd, J=1.7, 8.1Hz), 8.
05 (1H, d, J=8.1Hz), 8.75 (1H, d, J=2.8Hz), 8.79
(1H, d, J=2.8Hz). MS m/z : 304(M++2), 302(M+), 267, 144, 131, 116。Example 44 1-Chloromethyl-N- (3-quinolyl) -1
-Cyclohexanecarboxamide (Compound No. 1-31
No. 34) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.40-1.90 (8H, m),
2.10-2.30 (2H, m), 3.75 (2H, s), 7.50-7.70 (2H,
m), 7.78 (1H, bs), 7.81 (1H, dd, J = 1.7, 8.1Hz), 8.
05 (1H, d, J = 8.1Hz), 8.75 (1H, d, J = 2.8Hz), 8.79
(1H, d, J = 2.8Hz) .MS m / z: 304 (M + +2), 302 (M + ), 267, 144, 131, 116.

【０１２１】[0121]

【実施例４５】1-（3,3,4,4-テトラフルオロブチル）-N
-（3-キノリル）−１−シクロヘキサンカルボキサミド
（化合物番号１−３２０１番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 1.35-2.15 (14H, m),
5.41-5.98 (1H, m), 7.50-7.69 (3H, m), 7.81 (1H,
d, J=8.4Hz), 8.05 (1H, d, J=8.4Hz), 8.73 (1H, d,
J=2.6Hz), 8.81 (1H, d, J=2.6Hz). MS m/z : 382(M+), 211, 169, 144, 128。Example 45 1- (3,3,4,4-tetrafluorobutyl) -N
-(3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3201) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.35-2.15 (14H, m),
5.41-5.98 (1H, m), 7.50-7.69 (3H, m), 7.81 (1H,
d, J = 8.4Hz), 8.05 (1H, d, J = 8.4Hz), 8.73 (1H, d,
J = 2.6Hz), 8.81 (1H, d, J = 2.6Hz). MS m / z: 382 (M + ), 211, 169, 144, 128.

【０１２２】[0122]

【実施例４６】1-シクロブチルメチル-N-（3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−３２６７番） 融点：174-177℃。1 H-NMR (200MHz, CDCl3) δppm : 1.43-2.48 (19H, m),
7.49-7.66 (3H, m), 7.80 (1H, d, J=7.7Hz), 8.04 (1
H, d, J=8.4Hz), 8.71 (1H, s), 8.84 (1H, s). MS m/z : 322(M+), 254, 226, 151, 144。Example 46 1-Cyclobutylmethyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3267) Melting point: 174-177 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.43-2.48 (19H, m),
7.49-7.66 (3H, m), 7.80 (1H, d, J = 7.7Hz), 8.04 (1
H, d, J = 8.4Hz), 8.71 (1H, s), 8.84 (1H, s). MS m / z: 322 (M + ), 254, 226, 151, 144.

【０１２３】[0123]

【実施例４７】1-シクロヘキシルメチル-N-（3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−３３３４番） 融点：167-169℃。1 H-NMR (200MHz, CDCl3) δppm : 0.85-2.11 (23H, m),
7.49-7.67 (3H, m), 7.81 (1H, d, J=8.4Hz), 8.04
(1H, d, J=8.4Hz), 8.71 (1H, d, J=2.6Hz), 8.80(1H,
d, J=2.6Hz). MS m/z : 350(M+), 254, 179, 144, 97。Example 47 1-Cyclohexylmethyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3334) Melting point: 167-169 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.85-2.11 (23H, m),
7.49-7.67 (3H, m), 7.81 (1H, d, J = 8.4Hz), 8.04
(1H, d, J = 8.4Hz), 8.71 (1H, d, J = 2.6Hz), 8.80 (1H,
d, J = 2.6Hz) .MS m / z: 350 (M + ), 254, 179, 144, 97.

【０１２４】[0124]

【実施例４８】1-ビニル-N-（3-キノリル）−１−シク
ロヘキサンカルボキサミド（化合物番号１−３４０１
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.40-1.80 (8H, m),
2.10-2.20 (2H, m), 5.34 (1H, d, J=17.6Hz), 5.40 (1
H, d, J=10.6Hz), 5.94 (1H, dd, J=10.6, 17.6Hz), 7.
45-7.60 (2H, m), 7.69 (1H, dd, J=1.7, 8.1Hz), 7.98
(1H, d, J=8.4Hz), 8.20 (1H, bs), 8.70 (1H, d, J=
2.6Hz), 8.73 (1H, d, J=2.6Hz). MS m/z : 280(M+), 171, 144, 109。Example 48 1-Vinyl-N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3401
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.40-1.80 (8H, m),
2.10-2.20 (2H, m), 5.34 (1H, d, J = 17.6Hz), 5.40 (1
H, d, J = 10.6Hz), 5.94 (1H, dd, J = 10.6, 17.6Hz), 7.
45-7.60 (2H, m), 7.69 (1H, dd, J = 1.7, 8.1Hz), 7.98
(1H, d, J = 8.4Hz), 8.20 (1H, bs), 8.70 (1H, d, J =
2.6Hz), 8.73 (1H, d, J = 2.6Hz) .MS m / z: 280 (M + ), 171, 144, 109.

【０１２５】[0125]

【実施例４９】1-（2-メチルアリル）-N-（3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−３４６８番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.30-1.80 (8H, m),
1.69 (3H, s), 2.10-2.20 (2H, m), 2.36 (2H, s), 4.7
4 (1H, bs), 4.90 (1H, bs), 7.45-7.65 (2H, m), 7.75
-7.85 (2H, m), 8.03 (1H, dd, J=0.7, 8.4Hz), 8.73
(1H, d, J=2.6Hz),8.80 (1H, d, J=2.6Hz). MS m/z : 308(M+), 252, 144, 137。Example 49 1- (2-methylallyl) -N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-33468) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.30-1.80 (8H, m),
1.69 (3H, s), 2.10-2.20 (2H, m), 2.36 (2H, s), 4.7
4 (1H, bs), 4.90 (1H, bs), 7.45-7.65 (2H, m), 7.75
-7.85 (2H, m), 8.03 (1H, dd, J = 0.7, 8.4Hz), 8.73
(1H, d, J = 2.6Hz), 8.80 (1H, d, J = 2.6Hz). MS m / z: 308 (M + ), 252, 144, 137.

【０１２６】[0126]

【実施例５０】1-（2-メチルアリル）-N-（2-メチル-3-
キノリル）−１−シクロヘキサンカルボキサミド（化合
物番号１−３４８１番） 融点：125-128℃。1 H-NMR (200MHz, CDCl3) δppm : 1.26-2.71 (10H, m),
1.71 (3H, s), 2.37 (2H, s), 2.71 (3H, s), 4.77-4.
94 (2H, m), 7.43-7.65 (3H, m), 7.78 (1H, d,d, J=8.
0,1.5Hz), 7.96, (1H, d, J=8.4Hz), 8.96 (1H, s). MS m/z : 322(M+), 307, 266, 158, 137, 130, 109, 9
5。Example 50 1- (2-methylallyl) -N- (2-methyl-3-
Quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3481) Melting point: 125-128 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.26-2.71 (10H, m),
1.71 (3H, s), 2.37 (2H, s), 2.71 (3H, s), 4.77-4.
94 (2H, m), 7.43-7.65 (3H, m), 7.78 (1H, d, d, J = 8.
0,1.5Hz), 7.96, (1H, d, J = 8.4Hz), 8.96 (1H, s) .MS m / z: 322 (M + ), 307, 266, 158, 137, 130, 109, 9
Five.

【０１２７】[0127]

【実施例５１】1-（2-メチルアリル）-N-（4-メチル-3-
キノリル）−１−シクロヘキサンカルボキサミド（化合
物番号１−３４８２番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.41-1.69 (8H, m),
1.79 (3H, s), 2.14-2.22 (2H, m), 2.40 (1H, s), 2.5
6 (3H, s), 4.81 (1H, s), 4.96 (1H, s), 7.41(1H, b
s), 7.52-7.71 (2H, m), 7.98 (1H, d, J=8.4Hz), 8.08
(1H, d, J=8.4Hz), 8.97 (1H, s). MS m/z : 322(M+), 307, 266, 158。Example 51 1- (2-methylallyl) -N- (4-methyl-3-
Quinolyl-1-cyclohexanecarboxamide (Compound No. 1-3482) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.41-1.69 (8H, m),
1.79 (3H, s), 2.14-2.22 (2H, m), 2.40 (1H, s), 2.5
6 (3H, s), 4.81 (1H, s), 4.96 (1H, s), 7.41 (1H, b
s), 7.52-7.71 (2H, m), 7.98 (1H, d, J = 8.4Hz), 8.08
(1H, d, J = 8.4Hz), 8.97 (1H, s). MS m / z: 322 (M + ), 307, 266, 158.

【０１２８】[0128]

【実施例５２】1-（3-メチル-2-ブテニル）-N-（3-キノ
リル）−１−シクロヘキサンカルボキサミド（化合物番
号１−３５３５番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.47-1.73 (14H, m),
2.08-2.12 (2H, m), 2.31 (1H, d, J=8.1Hz), 5.19-5.
27 (1H, m), 7.49-7.67 (3H, m), 7.80 (1H, d,J=7.7H
z), 8.03 (1H, d, J=8.4Hz), 8.64 (1H, d, J=2.6Hz),
8.81 (1H, d, J=2.6Hz). MS m/z : 322(M+), 254, 151, 144, 128。Example 52 1- (3-Methyl-2-butenyl) -N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3535) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.47-1.73 (14H, m),
2.08-2.12 (2H, m), 2.31 (1H, d, J = 8.1Hz), 5.19-5.
27 (1H, m), 7.49-7.67 (3H, m), 7.80 (1H, d, J = 7.7H
z), 8.03 (1H, d, J = 8.4Hz), 8.64 (1H, d, J = 2.6Hz),
8.81 (1H, d, J = 2.6Hz) .MS m / z: 322 (M + ), 254, 151, 144, 128.

【０１２９】[0129]

【実施例５３】1-(3-ブテニル)-N-（3-キノリル）−１
−シクロヘキサンカルボキサミド（化合物番号１−３６
０２番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 1.30-1.75 (10H, m),
2.00-2.20 (4H, m), 4.92 (1H, d, J=10.3Hz), 4.99
(1H, d, J=17.2Hz), 5.65-5.85 (1H, m), 7.45-7.65 (2
H, m), 7.75-7.80 (2H, m), 8.02 (1H, d, J=8.4Hz),
8.73 (1H, d, J=2.6Hz), 8.79 (1H, d, J=2.6Hz). MS m/z : 308(M+), 254, 144, 137。Example 53 1- (3-butenyl) -N- (3-quinolyl) -1
-Cyclohexanecarboxamide (Compound No. 1-36
No. 02) Physical property: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.30-1.75 (10H, m),
2.00-2.20 (4H, m), 4.92 (1H, d, J = 10.3Hz), 4.99
(1H, d, J = 17.2Hz), 5.65-5.85 (1H, m), 7.45-7.65 (2
H, m), 7.75-7.80 (2H, m), 8.02 (1H, d, J = 8.4Hz),
8.73 (1H, d, J = 2.6Hz), 8.79 (1H, d, J = 2.6Hz). MS m / z: 308 (M + ), 254, 144, 137.

【０１３０】[0130]

【実施例５４】1-（4-ペンテニル）-N-（3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
３６６９番） 融点：98-101℃。1 H-NMR (200MHz, CDCl3) δppm : 1.24-1.66 (12H, m),
2.02-2.12 (4H, m), 4.92-5.02 (2H, m), 5.64-5.85
(1H, m), 7.49-7.67 (3H, m), 7.80 (1H, d, J=8.1Hz),
8.04 (1H, d, J=8.4Hz), 8.70 (1H, d, J=2.6Hz), 8.8
5 (1H, d, J=2.6Hz). MS m/z : 322(M+), 254, 151, 144, 128。Example 54 1- (4-Pentenyl) -N- (3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 3669) Melting point: 98-101 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.24-1.66 (12H, m),
2.02-2.12 (4H, m), 4.92-5.02 (2H, m), 5.64-5.85
(1H, m), 7.49-7.67 (3H, m), 7.80 (1H, d, J = 8.1Hz),
8.04 (1H, d, J = 8.4Hz), 8.70 (1H, d, J = 2.6Hz), 8.8
5 (1H, d, J = 2.6Hz) .MS m / z: 322 (M + ), 254, 151, 144, 128.

【０１３１】[0131]

【実施例５５】1-プロパルギル-N-（3-キノリル）−１
−シクロヘキサンカルボキサミド（化合物番号１−３７
３６番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.45-1.65 (8H, m),
2.05-2.15 (2H, m), 2.20 (1H, t, J=2.7Hz), 2.53 (2
H, d, J=2.7Hz), 7.45-7.70 (1H, m), 7.78 (1H,d, J=
7.3Hz), 8.03 (1H, d, J=8.4Hz), 8.09 (1H, bs), 8.73
(1H, d, J=2.6Hz), 8.79 (1H, d, J=2.6Hz). MS m/z : 292(M+), 144, 121。Example 55 1-Propargyl-N- (3-quinolyl) -1
-Cyclohexanecarboxamide (Compound No. 1-37
No. 36) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.45-1.65 (8H, m),
2.05-2.15 (2H, m), 2.20 (1H, t, J = 2.7Hz), 2.53 (2
H, d, J = 2.7Hz), 7.45-7.70 (1H, m), 7.78 (1H, d, J =
7.3Hz), 8.03 (1H, d, J = 8.4Hz), 8.09 (1H, bs), 8.73
(1H, d, J = 2.6Hz), 8.79 (1H, d, J = 2.6Hz). MS m / z: 292 (M + ), 144, 121.

【０１３２】[0132]

【実施例５６】1-プロパルギル-N-（2-メチル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−３７４９番） 物性：ガム状。1 H-NMR (200MHz, CDCl3) δppm : 1.26-2.23 (11H, m),
2.56 (2H, d, J=2.6Hz), 2.75 (3H, s), 7.43-7.66 (2
H, m), 7.77 (1H, dd, J=8.0,1.5Hz), 7.83 (1H,bs),
7.96, (1H, d, J=8.4Hz), 8.87 (1H, s). MS m/z : 306(M+), 291, 251, 158, 142, 130, 121, 11
5。Example 56 1-Propargyl-N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3749) Physical properties: gum-like. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.26-2.23 (11H, m),
2.56 (2H, d, J = 2.6Hz), 2.75 (3H, s), 7.43-7.66 (2
H, m), 7.77 (1H, dd, J = 8.0,1.5Hz), 7.83 (1H, bs),
7.96, (1H, d, J = 8.4Hz), 8.87 (1H, s) .MS m / z: 306 (M + ), 291, 251, 158, 142, 130, 121, 11
Five.

【０１３３】[0133]

【実施例５７】1-プロパルギル-N-（4-メチル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−３７５０番） 融点：124-125℃。1 H-NMR (200MHz, CDCl3) δppm : 1.41-1.65 (8H, m),
2.21-2.26 (3H, m), 2.57 (2H, q, J=2.8Hz), 2.60 (3
H, s), 7.53-7.72 (3H, m), 8.01 (1H, d, J=8.4Hz),
8.09 (1H, d, J=8.2Hz), 8.91 (1H, s). MS m/z : 306(M+), 291, 251, 158。Example 57 1-Propargyl-N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3750) Melting point: 124-125 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.41-1.65 (8H, m),
2.21-2.26 (3H, m), 2.57 (2H, q, J = 2.8Hz), 2.60 (3
H, s), 7.53-7.72 (3H, m), 8.01 (1H, d, J = 8.4Hz),
8.09 (1H, d, J = 8.2Hz), 8.91 (1H, s) .MS m / z: 306 (M + ), 291, 251, 158.

【０１３４】[0134]

【実施例５８】1-（2-ペンチニル）-N-（3-キノリル）
−１−シクロヘキサンカルボキサミド（化合物番号１−
３８０３番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.11 (3H, t, J=7.3H
z), 1.30-1.65 (8H, m),2.10-2.30 (4H, m), 2.48 (2H,
t, J=2.4Hz), 7.40-7.65 (2H, m), 7.73 (1H,dd, J=1.
3, 8.3Hz), 8.00 (1H, d, J=8.8Hz), 8.43 (1H, bs),
8.72 (1H, d, J=2.6Hz), 8.78 (1H, d, J=2.6Hz). MS m/z : 320(M+), 149, 145, 128, 116, 107。Example 58 1- (2-Pentynyl) -N- (3-quinolyl)
-1-Cyclohexanecarboxamide (Compound No. 1-
No. 3803) Physical property: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.11 (3H, t, J = 7.3H
z), 1.30-1.65 (8H, m), 2.10-2.30 (4H, m), 2.48 (2H,
t, J = 2.4Hz), 7.40-7.65 (2H, m), 7.73 (1H, dd, J = 1.
3, 8.3Hz), 8.00 (1H, d, J = 8.8Hz), 8.43 (1H, bs),
8.72 (1H, d, J = 2.6Hz), 8.78 (1H, d, J = 2.6Hz). MS m / z: 320 (M + ), 149, 145, 128, 116, 107.

【０１３５】[0135]

【実施例５９】1-（2-ペンチニル）-N-（2-メチル-3-キ
ノリル）−１−シクロヘキサンカルボキサミド（化合物
番号１−３８１６番） 融点：142-143℃。1 H-NMR (200MHz, CDCl3) δppm : 1.09 (3H, t, J=7.5H
z), 1.57-2.26 (12H, m), 2.52 (2H, t, J=2.5Hz), 2.7
6 (3H, s), 7.44-7.65 (2H, m), 7.77 (1H, d, J=7.0H
z), 7.94 (1H, bs), 7.96, (1H, d, J=7.7Hz), 8.89(1
H, s). MS m/z : 334(M+), 319, 306, 291, 265, 167, 158。Example 59 1- (2-Pentynyl) -N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3816) Melting point: 142-143 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.09 (3H, t, J = 7.5H
z), 1.57-2.26 (12H, m), 2.52 (2H, t, J = 2.5Hz), 2.7
6 (3H, s), 7.44-7.65 (2H, m), 7.77 (1H, d, J = 7.0H
z), 7.94 (1H, bs), 7.96, (1H, d, J = 7.7Hz), 8.89 (1
H, s) .MS m / z: 334 (M + ), 319, 306, 291, 265, 167, 158.

【０１３６】[0136]

【実施例６０】1-（2-ペンチニル）-N-（4-メチル-3-キ
ノリル）−１−シクロヘキサンカルボキサミド（化合物
番号１−３８１７番） 融点：97-99℃。1 H-NMR (200MHz, CDCl3) δppm : 1.13 (3H, t, J=7.5H
z), 1.45-1.61 (8H, m),2.14-2.30 (4H, m), 2.53 (2H,
t, J=2.4Hz), 2.59 (3H, s), 7.52-7.72 (2H,m), 7.82
(1H, bs), 8.00 (1H, d, J=9.6Hz), 8.09 (1H, d, J=
8.6Hz), 8.89 (1H, s). MS m/z : 334(M+), 319, 305, 158。Example 60 1- (2-Pentynyl) -N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3817) Melting point: 97-99 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.13 (3H, t, J = 7.5H
z), 1.45-1.61 (8H, m), 2.14-2.30 (4H, m), 2.53 (2H,
t, J = 2.4Hz), 2.59 (3H, s), 7.52-7.72 (2H, m), 7.82
(1H, bs), 8.00 (1H, d, J = 9.6Hz), 8.09 (1H, d, J =
8.6Hz), 8.89 (1H, s) .MS m / z: 334 (M + ), 319, 305, 158.

【０１３７】[0137]

【実施例６１】1-メトキシメチル-N-（3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号１−３
８７０番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.45-1.65 (8H, m),
1.95-2.05 (2H, m), 3.50 (3H, s), 3.53 (2H, s), 7.4
5-7.65 (2H, m), 7.78 (1H, d, J=7.1Hz), 8.03(1H, d,
J=8.0Hz), 8.69 (1H, bs), 8.80 (1H, s), 8.95 (1H,
s). MS m/z : 298(M+), 144, 127。Example 61 1-Methoxymethyl-N- (3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 1-3
No. 870) Physical property: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.45-1.65 (8H, m),
1.95-2.05 (2H, m), 3.50 (3H, s), 3.53 (2H, s), 7.4
5-7.65 (2H, m), 7.78 (1H, d, J = 7.1Hz), 8.03 (1H, d,
J = 8.0Hz), 8.69 (1H, bs), 8.80 (1H, s), 8.95 (1H,
s). MS m / z: 298 (M + ), 144, 127.

【０１３８】[0138]

【実施例６２】1-メトキシメチル-N-（2-メチル-3-キノ
リル）−１−シクロヘキサンカルボキサミド（化合物番
号１−３８８３番） 融点：90-96℃。1 H-NMR (200MHz, CDCl3) δppm : 1.53-2.04 (10H, m),
2.70 (3H, s), 3.53 (3H, s), 3.57 (2H, s), 7.42-7.
62 (2H, m), 7.76 (1H, dd, J=8.0,1.1Hz), 7.94, (1H,
d, J=8.4Hz), 8.97 (1H, s), 9.02(1H, bs). MS m/z : 312(M+), 280, 158, 142, 127, 95, 89。Example 62 1-Methoxymethyl-N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3883) Melting point: 90-96 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.53-2.04 (10H, m),
2.70 (3H, s), 3.53 (3H, s), 3.57 (2H, s), 7.42-7.
62 (2H, m), 7.76 (1H, dd, J = 8.0,1.1Hz), 7.94, (1H,
d, J = 8.4Hz), 8.97 (1H, s), 9.02 (1H, bs). MS m / z: 312 (M + ), 280, 158, 142, 127, 95, 89.

【０１３９】[0139]

【実施例６３】1-メトキシメチル-N-（4-メチル-3-キノ
リル）−１−シクロヘキサンカルボキサミド（化合物番
号１−３８８４番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.55-1.62 (8H, m),
2.05-2.11 (2H, m), 2.55 (3H, s), 3.51 (3H, s), 3.5
6 (2H, s), 7.52-7.69 (2H, m), 7.99 (1H, d, J=8.4H
z), 8.09 (1H, d, J=8.4Hz), 8.52 (1H, bs), 9.08 (1
H, s). MS m/z : 312(M+), 280, 173, 158。Example 63 1-Methoxymethyl-N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3884) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.55-1.62 (8H, m),
2.05-2.11 (2H, m), 2.55 (3H, s), 3.51 (3H, s), 3.5
6 (2H, s), 7.52-7.69 (2H, m), 7.99 (1H, d, J = 8.4H
z), 8.09 (1H, d, J = 8.4Hz), 8.52 (1H, bs), 9.08 (1
H, s). MS m / z: 312 (M + ), 280, 173, 158.

【０１４０】[0140]

【実施例６４】1-（2-メトキシエチル）-N-（3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−３９３７番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.45-1.65 (8H, m),
1.93 (2H, t, J=6.4Hz),2.05-2.20 (2H, m), 3.33 (3H,
s), 3.52 (2H, t, J=6.4Hz), 7.45-7.65 (2H,m), 7.75
(1H, dd, J=1.8, 8.1Hz), 8.01 (1H, d, J=8.4Hz), 8.
73 (1H, bs), 8.73 (1H, d, J=2.6Hz), 8.79 (1H, d, J
=2.6Hz). MS m/z : 312(M+), 254, 169, 144, 109。Example 64 1- (2-methoxyethyl) -N- (3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-3937) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.45-1.65 (8H, m),
1.93 (2H, t, J = 6.4Hz), 2.05-2.20 (2H, m), 3.33 (3H,
s), 3.52 (2H, t, J = 6.4Hz), 7.45-7.65 (2H, m), 7.75
(1H, dd, J = 1.8, 8.1Hz), 8.01 (1H, d, J = 8.4Hz), 8.
73 (1H, bs), 8.73 (1H, d, J = 2.6Hz), 8.79 (1H, d, J
= 2.6Hz) .MS m / z: 312 (M + ), 254, 169, 144, 109.

【０１４１】[0141]

【実施例６５】1-エチル-N-（3-キノリル）-3-シクロヘ
キセン−１−カルボキサミド（化合物番号１−４００４
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.94 (3H, t, J=7.5H
z), 1.22-2.22 (7H, m),2.63 (1H, d, J=17.5Hz), 5.72
-5.88 (2H, m), 7.45-7.65 (2H, m), 7.75 (1H,d, J=7.
9Hz), 7.92 (1H, bs), 8.02 (1H, d, J=8.4Hz), 8.69
(1H, d, J=2.6Hz), 8.79 (1H, d, J=2.6Hz). MS m/z : 280(M+), 144, 109。Example 65 1-Ethyl-N- (3-quinolyl) -3-cyclohexene-1-carboxamide (Compound No. 1-4004)
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.94 (3H, t, J = 7.5H
z), 1.22-2.22 (7H, m), 2.63 (1H, d, J = 17.5Hz), 5.72
-5.88 (2H, m), 7.45-7.65 (2H, m), 7.75 (1H, d, J = 7.
9Hz), 7.92 (1H, bs), 8.02 (1H, d, J = 8.4Hz), 8.69
(1H, d, J = 2.6Hz), 8.79 (1H, d, J = 2.6Hz). MS m / z: 280 (M + ), 144, 109.

【０１４２】[0142]

【実施例６６】1-エチル-N-（2-メチル-3-キノリル）-3
-シクロヘキセン−１−カルボキサミド（化合物番号１
−４０１７番） 物性：ガム状。1 H-NMR (200MHz, CDCl3) δppm : 0.97 (3H, t, J=7.3H
z), 1.44-2.59 (8H, m),2.67 (3H, s), 5.83-5.96 (2H,
m), 7.43-7.64 (2H, m), 7.74 (1H, bs), 7.76(1H, d
d, J=8.0,1.5Hz), 7.95, (1H, d, J=8.8Hz), 8.89 (1H,
s). MS m/z : 294(M+), 265, 158, 142, 130, 109, 89。Example 66 1-Ethyl-N- (2-methyl-3-quinolyl) -3
-Cyclohexene-1-carboxamide (Compound No. 1
No.-4017) Physical properties: gum-like. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.97 (3H, t, J = 7.3H
z), 1.44-2.59 (8H, m), 2.67 (3H, s), 5.83-5.96 (2H,
m), 7.43-7.64 (2H, m), 7.74 (1H, bs), 7.76 (1H, d
d, J = 8.0,1.5Hz), 7.95, (1H, d, J = 8.8Hz), 8.89 (1H,
s) .MS m / z: 294 (M + ), 265, 158, 142, 130, 109, 89.

【０１４３】[0143]

【実施例６７】1-エチル-N-（4-メチル-3-キノリル）-3
-シクロヘキセン−１−カルボキサミド（化合物番号１
−４０１８番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.26 (3H, t, J=7.2H
z), 1.47-2.19 (7H, m),2.53 (3H, s), 2.62-2.70 (1H,
m), 5.81-5.95 (2H, m), 7.52-7.71 (3H, m),7.99 (1
H, d, J=8.0Hz), 8.08 (1H, d, J=8.4Hz), 8.91 (1H,
s). MS m/z : 294(M+), 265, 158。Example 67 1-Ethyl-N- (4-methyl-3-quinolyl) -3
-Cyclohexene-1-carboxamide (Compound No. 1
-4018) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.26 (3H, t, J = 7.2H
z), 1.47-2.19 (7H, m), 2.53 (3H, s), 2.62-2.70 (1H,
m), 5.81-5.95 (2H, m), 7.52-7.71 (3H, m), 7.99 (1
H, d, J = 8.0Hz), 8.08 (1H, d, J = 8.4Hz), 8.91 (1H,
s) .MS m / z: 294 (M + ), 265, 158.

【０１４４】[0144]

【実施例６８】1-プロピル-N-（3-キノリル）-3-シクロ
ヘキセン−１−カルボキサミド（化合物番号１−４０７
１番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.92 (3H, t, J=5.1H
z), 1.22-2.25 (9H, m),2.63 (1H, d, J=17.6Hz), 5.72
-5.88 (2H, m), 7.45-7.65 (2H, m), 7.78 (1H,d, J=8.
1Hz), 7.90 (1H, bs), 8.02 (1H, d, J=8.1Hz), 8.69
(1H, d, J=2.6Hz), 8.79 (1H, d, J=2.6Hz). MS m/z : 294(M+), 251, 144, 123。Example 68 1-Propyl-N- (3-quinolyl) -3-cyclohexene-1-carboxamide (Compound No. 1-407)
No. 1) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.92 (3H, t, J = 5.1H
z), 1.22-2.25 (9H, m), 2.63 (1H, d, J = 17.6Hz), 5.72
-5.88 (2H, m), 7.45-7.65 (2H, m), 7.78 (1H, d, J = 8.
1Hz), 7.90 (1H, bs), 8.02 (1H, d, J = 8.1Hz), 8.69
(1H, d, J = 2.6Hz), 8.79 (1H, d, J = 2.6Hz). MS m / z: 294 (M + ), 251, 144, 123.

【０１４５】[0145]

【実施例６９】1-アリル-N-（3-キノリル）-3-シクロヘ
キセン−１−カルボキサミド（化合物番号１−４１３８
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.70-2.75 (8H, m),
5.10-5.19 (2H, m), 5.72-5.91 (3H, m), 7.45-7.65 (2
H, m), 7.76 (1H, d, J=7.3Hz), 7.91 (1H, bs),8.02
(1H, d, J=8.4Hz), 8.67 (1H, d, J=2.4Hz), 8.77 (1H,
d, J=2.4Hz). MS m/z : 292(M+), 251, 144, 121。Example 69 1-allyl-N- (3-quinolyl) -3-cyclohexene-1-carboxamide (Compound No. 1-4138
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.70-2.75 (8H, m),
5.10-5.19 (2H, m), 5.72-5.91 (3H, m), 7.45-7.65 (2
H, m), 7.76 (1H, d, J = 7.3Hz), 7.91 (1H, bs), 8.02
(1H, d, J = 8.4Hz), 8.67 (1H, d, J = 2.4Hz), 8.77 (1H,
d, J = 2.4Hz). MS m / z: 292 (M + ), 251, 144, 121.

【０１４６】[0146]

【実施例７０】1-アリル-N-（2-メチル-3-キノリル）-3
-シクロヘキセン−１−カルボキサミド（化合物番号１
−４１５１番） 融点：86℃。1 H-NMR (200MHz, CDCl3) δppm : 1.69-2.79 (8H, m),
2.66 (3H, s), 5.11-5.20 (2H, m), 5.75-5.96 (3H,
m), 7.43-7.65 (2H, m), 7.74 (1H, bs), 7.76 (1H, d,
J=8.0Hz), 7.95, (1H, d, J=8.4Hz), 8.89 (1H, s). MS m/z : 306(M+), 265, 158, 121, 93, 79。Example 70 1-allyl-N- (2-methyl-3-quinolyl) -3
-Cyclohexene-1-carboxamide (Compound No. 1
-4151) Melting point: 86 ° C. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.69-2.79 (8H, m),
2.66 (3H, s), 5.11-5.20 (2H, m), 5.75-5.96 (3H,
m), 7.43-7.65 (2H, m), 7.74 (1H, bs), 7.76 (1H, d,
J = 8.0Hz), 7.95, (1H, d, J = 8.4Hz), 8.89 (1H, s) .MS m / z: 306 (M + ), 265, 158, 121, 93, 79.

【０１４７】[0147]

【実施例７１】1-アリル-N-（4-メチル-3-キノリル）-3
-シクロヘキセン−１−カルボキサミド（化合物番号１
−４１５２番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.70-1.84 (1H, m),
2.05-2.35 (5H, m), 2.52 (3H, s), 2.56-2.77 (2H,
m), 5.15 (1H, bs), 5.22 (1H, d, J=7.0Hz), 5.81-5.9
3 (3H, m), 7.52-7.72 (3H, m), 7.98 (1H, d, J=9.2H
z), 8.08 (1H, d, J=8.4Hz), 8.89 (1H, s). MS m/z : 306(M+), 265, 158。Example 71 1-allyl-N- (4-methyl-3-quinolyl) -3
-Cyclohexene-1-carboxamide (Compound No. 1
-4152) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.70-1.84 (1H, m),
2.05-2.35 (5H, m), 2.52 (3H, s), 2.56-2.77 (2H,
m), 5.15 (1H, bs), 5.22 (1H, d, J = 7.0Hz), 5.81-5.9
3 (3H, m), 7.52-7.72 (3H, m), 7.98 (1H, d, J = 9.2H
z), 8.08 (1H, d, J = 8.4Hz), 8.89 (1H, s). MS m / z: 306 (M + ), 265, 158.

【０１４８】[0148]

【実施例７２】1-メチル-N-（2,4-ジメチル-3-キノリ
ル）−１−シクロヘキサンカルボキサミド（化合物番号
１−４２０５番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 1.22 (3H, s), 1.25-
1.60 (8H, m), 1.90-2.10 (2H, m), 2.24 (3H, s), 2.4
8 (3H, s), 7.41 (1H, t, J=8.2Hz), 7.55-7.75(3H,
m), 7.93 (1H, dd, J=0.7, 8.4Hz). MS m/z : 296(M+), 172, 144。Example 72 1-Methyl-N- (2,4-dimethyl-3-quinolyl) -1-cyclohexanecarboxamide (Compound No. 1-4205) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.22 (3H, s), 1.25-
1.60 (8H, m), 1.90-2.10 (2H, m), 2.24 (3H, s), 2.4
8 (3H, s), 7.41 (1H, t, J = 8.2Hz), 7.55-7.75 (3H,
m), 7.93 (1H, dd, J = 0.7, 8.4Hz) .MS m / z: 296 (M + ), 172, 144.

【０１４９】[0149]

【実施例７３】1,2-ジメチル-N-（3-キノリル）−１−
シクロヘキサンカルボキサミド（化合物番号２−１番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.80-1.10 (3H, m),
1.20-2.10 (12H, m), 7.50-7.70 (3H, m), 7.78 (1H, d
d, J=1.7, 7.7Hz), 8.02 (1H, d, J=8.8Hz), 8.70-8.80
(2H, m). MS m/z : 282(M+), 144, 111。Example 73 1,2-Dimethyl-N- (3-quinolyl) -1-
Cyclohexanecarboxamide (Compound No. 2-1) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.80-1.10 (3H, m),
1.20-2.10 (12H, m), 7.50-7.70 (3H, m), 7.78 (1H, d
d, J = 1.7, 7.7Hz), 8.02 (1H, d, J = 8.8Hz), 8.70-8.80
(2H, m). MS m / z: 282 (M + ), 144, 111.

【０１５０】[0150]

【実施例７４】1,3-ジメチル-N-（3-キノリル）−１−
シクロヘキサンカルボキサミド（化合物番号２−２番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 0.80-1.00 (6H, m),
1.20-2.10 (9H, m), 7.45-7.65 (2H,m), 7.75(1H, d, J
=8.1Hz), 8.01 (1H, d, J=8.4Hz), 8.19 (1H, bs), 8.7
5-8.85 (2H, m). MS m/z : 282(M+), 268, 144。Example 74 1,3-Dimethyl-N- (3-quinolyl) -1-
Cyclohexanecarboxamide (Compound No. 2-2) Physical properties: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.80-1.00 (6H, m),
1.20-2.10 (9H, m), 7.45-7.65 (2H, m), 7.75 (1H, d, J
= 8.1Hz), 8.01 (1H, d, J = 8.4Hz), 8.19 (1H, bs), 8.7
5-8.85 (2H, m) .MS m / z: 282 (M + ), 268, 144.

【０１５１】[0151]

【実施例７５】1,4-ジメチル-N-（3-キノリル）−１−
シクロヘキサンカルボキサミド（化合物番号２−３番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 0.80-0.95 (3H, m),
1.20-2.10 (12H, m), 7.50-7.65 (2H, m), 7.70-7.80
(2H, m), 8.00-8.05 (1H, m), 8.70-8.90 (2H, m). MS m/z : 282(M+), 268, 144, 111。Example 75 1,4-Dimethyl-N- (3-quinolyl) -1-
Cyclohexanecarboxamide (Compound No. 2-3) Physical properties: oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.80-0.95 (3H, m),
1.20-2.10 (12H, m), 7.50-7.65 (2H, m), 7.70-7.80
(2H, m), 8.00-8.05 (1H, m), 8.70-8.90 (2H, m) .MS m / z: 282 (M + ), 268, 144, 111.

【０１５２】[0152]

【実施例７６】1,2,2-トリメチル-N-（3-キノリル）−
１−シクロヘキサンカルボキサミド（化合物番号２−４
番） 物性：アモルファス。1 H-NMR (200MHz, CDCl3) δppm : 0.80-0.95 (6H, m),
1.28 (3H, s), 1.20-1.90 (6H, m), 2.10-2.30 (2H,
m), 7.45-7.65 (2H, m), 7.75 (1H, d, J=8.1Hz),7.85
(1H, bs), 8.02 (1H, d, J=8.4Hz), 8.73-8.80 (2H,
m). MS m/z : 296(M+), 282, 144, 125, 111。Example 76 1,2,2-trimethyl-N- (3-quinolyl)-
1-Cyclohexanecarboxamide (Compound No. 2-4
No.) Physical property: amorphous. 1 H-NMR (200MHz, CDCl 3 ) δppm: 0.80-0.95 (6H, m),
1.28 (3H, s), 1.20-1.90 (6H, m), 2.10-2.30 (2H,
m), 7.45-7.65 (2H, m), 7.75 (1H, d, J = 8.1Hz), 7.85
(1H, bs), 8.02 (1H, d, J = 8.4Hz), 8.73-8.80 (2H,
m). MS m / z: 296 (M + ), 282, 144, 125, 111.

【０１５３】[0153]

【実施例７７】2-メチル-N-（3-キノリル）バイシクロ
[2,2,1]ヘプタン-2-カルボキサミド（化合物番号２−５
番） 物性：油状物。1 H-NMR (200MHz, CDCl3) δppm : 1.10-1.80 (6H, m),
1.95-2.10 (1H, m), 2.30-2.60 (3H, m), 7.45-7.65 (2
H, m), 7.75 (1H, dd, J=1.5, 7.7Hz), 8.01 (1H, d, J
=8.1Hz), 8.20 (1H, bs), 8.75 (1H, d, J=2.4Hz), 8.7
9 (1H, d, J=2.6Hz). MS m/z : 280(M+), 266, 144。Example 77 2-Methyl-N- (3-quinolyl) bicyclo
[2,2,1] Heptane-2-carboxamide (Compound No. 2-5
No.) Physical property: Oily substance. 1 H-NMR (200MHz, CDCl 3 ) δppm: 1.10-1.80 (6H, m),
1.95-2.10 (1H, m), 2.30-2.60 (3H, m), 7.45-7.65 (2
H, m), 7.75 (1H, dd, J = 1.5, 7.7Hz), 8.01 (1H, d, J
= 8.1Hz), 8.20 (1H, bs), 8.75 (1H, d, J = 2.4Hz), 8.7
9 (1H, d, J = 2.6Hz) .MS m / z: 280 (M + ), 266, 144.

【０１５４】[0154]

【製剤例１】粉剤 実施例１の化合物（１．０質量部）、ドリレスＡ（アル
キルエーテルリン酸エステル、日本化薬株式会社製、
０．４質量部）、カープレックス＃８０−Ｄ（ホワイト
カーボン、塩野義製薬株式会社製、１．５質量部）、炭
酸カルシウム（足立石灰株式会社製、０．５質量部）及
び啓和クレー風ヒ（啓和炉材株式会社製、３２．１質量
部）を混合後、エックサンプルＫＩＩ−１型（ハンマー
ミル）、不二パウダル株式会社製）で粉砕し、得られた
粉砕物の質量に対して１．５倍量のＤＬクレー啓和（啓
和炉材株式会社製）を加え混合し、粉剤ＤＬを得た。[Formulation Example 1] Dust formulation The compound of Example 1 (1.0 parts by mass), Doloreth A (alkyl ether phosphate, manufactured by Nippon Kayaku Co., Ltd.,
0.4 parts by mass), Carplex # 80-D (white carbon, Shionogi Pharmaceutical Co., Ltd., 1.5 parts by mass), calcium carbonate (Adachi Lime Co., Ltd., 0.5 parts by mass) and Keiwa Clay Kazehi (manufactured by Keiwa Furnace Co., Ltd., 32.1 parts by mass) was mixed, and then ground with Ecksample KII-1 type (hammer mill) manufactured by Fuji Paudal Co., Ltd., and the mass of the obtained ground product. 1.5 times the amount of DL clay Keiwa (manufactured by Keiwa Furnace Co., Ltd.) was added and mixed to obtain powder DL.

【０１５５】[0155]

【製剤例２】乳剤 実施例２の化合物（１０質量部）をキシレン（和光純薬
株式会社製、４０質量部）とＤＭＳＯ（和光純薬株式会
社製、３５質量部）の混合溶液に溶解し、この溶液にＰ
ａｒａｋｏｌＫＰＳ（アニオン界面活性剤とノニオン界
面活性剤の混合物、日本乳化剤株式会社製、２５質量
部）を添加混合し、乳剤を得た。[Formulation Example 2] Emulsion The compound of Example 2 (10 parts by mass) was dissolved in a mixed solution of xylene (Wako Pure Chemical Industries, Ltd., 40 parts by mass) and DMSO (Wako Pure Chemical Industries, Ltd., 35 parts by mass). , P to this solution
Arakol KPS (mixture of anionic surfactant and nonionic surfactant, manufactured by Nippon Emulsifier Co., Ltd., 25 parts by mass) was added and mixed to obtain an emulsion.

【０１５６】[0156]

【製剤例３】水和剤 実施例３の化合物（１質量部）、カープレックス＃８０
−Ｄ（１０質量部）、ゴーセノールＧＬ０５（ポリビニ
ルアルコール、日本合成化学株式会社製、２質量部）、
ニューコール２９１ＰＧ（ジオクチルスルホコハク酸ナ
トリウム塩、日本乳化剤株式会社製、０．５質量部）、
ネオゲンパウダー（直鎖アルキルベンゼンスルホン酸ナ
トリウム塩）、第一工業製薬株式会社製、５質量部）、
ラジオライト＃２００（焼成珪藻土）、昭和化学工業株
式会社製、１０質量部）及びＨ微分（カオリナイトクレ
ー）、啓和炉材株式会社製、７１．５質量部）を充分に
混合し、エックサンプルＫＩＩ−１型で粉砕し、水和剤
を得た。Formulation Example 3 Wettable powder Compound of Example 3 (1 part by mass), Carplex # 80
-D (10 parts by mass), Gohsenol GL05 (polyvinyl alcohol, manufactured by Nippon Synthetic Chemical Industry, 2 parts by mass),
Newcol 291PG (dioctyl sulfosuccinic acid sodium salt, manufactured by Nippon Emulsifier Co., Ltd., 0.5 parts by mass),
Neogen powder (straight chain alkylbenzene sulfonic acid sodium salt), Daiichi Kogyo Seiyaku Co., Ltd., 5 parts by mass),
Radiolite # 200 (calcined diatomaceous earth), Showa Kagaku Kogyo Co., Ltd., 10 parts by mass) and H derivative (kaolinite clay), Keiwa Furnace Co., Ltd., 71.5 parts by mass) are thoroughly mixed, and Eck The sample KII-1 was crushed to obtain a wettable powder.

【０１５７】[0157]

【製剤例４】粒剤 実施例４の化合物（２質量部）、トリポリリン酸ナトリ
ウム（三井化学株式会社製、２質量部）、アミコールＮ
Ｏ．１（デキストリン、日本澱粉化学株式会社製、１．
５質量部）、ベントナイト（豊順鉱業株式会社製、２５
質量部）及びカルヒン６００（炭酸カルシウム、足立石
灰株式会社製、６９．５質量部）を混合し、ドームグラ
ン（不二パウダル株式会社製、スクリーン０．９ｍｍ
φ）を用いて押し出し造粒した。得られた造粒物を棚型
乾燥機（タバイ株式会社製、PERFECT OVEN PS-222 型、
６０℃）にて乾燥した後、６００〜１１８０μｍに篩分
して、粒剤を得た。[Formulation Example 4] Granules The compound of Example 4 (2 parts by mass), sodium tripolyphosphate (manufactured by Mitsui Chemicals, Inc., 2 parts by mass), Amycol N
O. 1 (dextrin, manufactured by Nippon Starch Chemical Co., Ltd., 1.
5 parts by mass), bentonite (manufactured by Toyojun Mining Co., Ltd., 25
(Parts by mass) and Calhin 600 (calcium carbonate, Adachi Lime Co., Ltd., 69.5 parts by mass) are mixed and Dome Gran (Fuji Paudal Co., Ltd., screen 0.9 mm)
φ) was used for extrusion granulation. The resulting granulated product was used as a shelf type dryer (Tabay Co., Ltd., PERFECT OVEN PS-222 type,
After drying at 60 ° C.), it was sieved to 600 to 1180 μm to obtain granules.

【０１５８】[0158]

【試験例１】イネいもち病防除試験（治療効果） 第３〜４葉期のポット栽培供試植物（イネ：幸風）に病
原菌胞子懸濁液を噴霧接種し、室温が２０〜２３℃の接
種室に当該ポットを入れ発病を促した。本発明化合物を
ジメチルスルホキシド−メタノール混合溶液（容積比：
７／３）に溶解せしめ、本発明化合物を３００ppm含有
する散布液を調整し、当該ポットに均一に散布した。接
種７日後の発病程度を調査した。試験は２連で行った。[Test Example 1] Rice blast control test (therapeutic effect) A 3rd to 4th leaf stage pot cultivation test plant (rice: Kofu) was spray-inoculated with a pathogenic spore suspension and the room temperature was 20 to 23 ° C. The pot was put in the inoculation room to promote the disease. The compound of the present invention was mixed with dimethylsulfoxide-methanol mixed solution (volume ratio:
It was dissolved in 7/3) to prepare a spray solution containing the compound of the present invention in an amount of 300 ppm, and the solution was uniformly sprayed in the pot. The degree of illness was investigated 7 days after the inoculation. The test was performed in duplicate.

【０１５９】なお、発病程度は、試験植物の発病程度を
肉眼観察し、下記の基準で判定し、０〜３の４段階で表
した。 発病程度が０：発病が全く無い。The degree of disease onset was expressed in 4 stages from 0 to 3 by visually observing the degree of disease on the test plant and judging according to the following criteria. Degree of illness is 0: There is no illness.

【０１６０】１：発病程度が無処理区の４０％未満 ２：発病程度が４０％以上８０％未満 ３：発病程度が８０％以上 本試験の結果、実施例１（化合物番号１−１）、実施例
２（化合物番号１−１９９９）、実施例３（化合物番号
１−２２３）、実施例４（化合物番号１−４４５）、実
施例５（化合物番号１−１３３３）、実施例６（化合物
番号１−２４４３）、実施例１３（化合物番号１−
７）、実施例１６（化合物番号１−２６）、実施例２３
（化合物番号１−２４８）、実施例２４（化合物番号１
−２４９）、実施例２６（化合物番号１−４７１）、実
施例２８（化合物番号１−６９２）、実施例３２（化合
物番号１−１１３７）、実施例３７（化合物番号１−２
４６９）、実施例４３（化合物番号１−３０００）、実
施例４７（化合物番号１−３３３４）、実施例４８（化
合物番号１−３４０１）、実施例５０（化合物番号１−
３４８１）、実施例５１（化合物番号１−３４８２）、
実施例５５（化合物番号１−３７３６）、実施例５６
（化合物番号１−３７４９）、実施例５９（化合物番号
１−３８１６）、実施例６０（化合物番号１−３８１
７）、実施例６１（化合物番号１−３８７０）、実施例
６６（化合物番号１−４０１７）及び実施例７１（化合
物番号１−４１５２）の化合物は、発病程度が０であっ
た。1: The degree of disease is less than 40% of the untreated section 2: The degree of disease is 40% or more and less than 80% 3: The degree of disease is 80% or more As a result of this test, Example 1 (Compound No. 1-1), Example 2 (Compound No. 1-1999), Example 3 (Compound No. 1-223), Example 4 (Compound No. 1-445), Example 5 (Compound No. 1-1333), Example 6 (Compound No.) 1-2443), Example 13 (Compound No. 1-
7), Example 16 (Compound No. 1-26), Example 23
(Compound No. 1-248), Example 24 (Compound No. 1)
-249), Example 26 (Compound No. 1-471), Example 28 (Compound No. 1-692), Example 32 (Compound No. 1-1137), Example 37 (Compound No. 1-2).
469), Example 43 (Compound No. 1-3000), Example 47 (Compound No. 1-3334), Example 48 (Compound No. 1-3401), Example 50 (Compound No. 1-).
3481), Example 51 (Compound No. 1-3482),
Example 55 (Compound No. 1-3736), Example 56
(Compound No. 1-3749), Example 59 (Compound No. 1-3816), Example 60 (Compound No. 1-381)
7), Example 61 (Compound No. 1-3870), Example 66 (Compound No. 1-4017), and Example 71 (Compound No. 1-4152) had a disease severity of 0.

【０１６１】[0161]

【試験例２】トマト灰色かび病防除試験（予防効果） 第２〜３葉期のポット栽培供試植物（トマト：大型福
寿）に、原体をジメチルスルホキサイドとメタノール
（容積比７：３）に溶解せしめ、本発明化合物を３００
ppm含有する散布液を均一に散布した。１日栽培後、当
該ポットに病原菌胞子懸濁液を噴霧接種し、室温が２０
〜２３度の接種室に当該ポットを入れ発病を促した。接
種２日後の発病程度を調査した。試験は２連で行った。[Test Example 2] Tomato gray mold control test (preventive effect) A potted plant for the second to third leaf stage (tomato: large Fukuju) was used as a raw material for dimethyl sulfoxide and methanol (volume ratio 7: 3). ), The compound of the present invention is dissolved in 300
The spray solution containing ppm was uniformly sprayed. After cultivating for 1 day, the pot was inoculated with the pathogenic spore suspension by spraying, and the temperature was 20
The pot was put in an inoculation room at -23 ° C to promote illness. The degree of disease onset 2 days after the inoculation was investigated. The test was performed in duplicate.

【０１６２】なお、発病程度は、試験植物の発病程度を
肉眼観察し、下記の基準で判定し、０〜３の４段階で表
した。発病程度が０：発病が全く無い。The degree of disease onset was expressed in 4 stages from 0 to 3 by visually observing the degree of disease on the test plant and judging according to the following criteria. Degree of illness is 0: There is no illness.

【０１６３】１：発病程度が無処理区の４０％未満 ２：発病程度が４０％以上８０％未満 ３：発病程度が８０％以上 本試験の結果、実施例１（化合物番号１−１）、実施例
５（化合物番号１−１３３３）、実施例９（化合物番号
１−２４４３）、実施例１２（化合物番号１−６）、実
施例１３（化合物番号１−７）、実施例１６（化合物番
号１−２６）、実施例１９（化合物番号１−３１）、実
施例２３（化合物番号１−２４８）、実施例２４（化合
物番号１−２４９）、実施例２５（化合物番号１−４７
０）、実施例２６（化合物番号１−４７１）、実施例２
７（化合物番号１−６６７）、実施例２９（化合物番号
１−８８９）、実施例３０（化合物番号１−１１１
１）、実施例３２（化合物番号１−１１３７）、実施例
３５（化合物番号１−１８０３）、実施例３６（化合物
番号１−２４６８）、実施例３７（化合物番号１−２４
６９）、実施例３９（化合物番号１−２７３２）、実施
例４０（化合物番号１−２７９９）、実施例５０（化合
物番号１−３４８１）、実施例５１（化合物番号１−３
４８２）、実施例５３（化合物番号１−３６０２）、実
施例５４（化合物番号１−３６６９）、実施例５５（化
合物番号１−３７３６）、実施例５７（化合物番号１−
３７５０）、実施例５８（化合物番号１−３８０３）、
実施例６０（化合物番号１−３８１７）、実施例６５
（化合物番号１−４００４）、実施例６６（化合物番号
１−４０１７）、実施例７１（化合物番号１−４１５
２）及び実施例７３（化合物番号２−１）の化合物は、
発病程度が０であった。1: The degree of disease is less than 40% of the untreated section 2: The degree of disease is 40% or more and less than 80% 3: The degree of disease is 80% or more As a result of this test, Example 1 (Compound No. 1-1), Example 5 (Compound No. 1-1333), Example 9 (Compound No. 1-2443), Example 12 (Compound No. 1-6), Example 13 (Compound No. 1-7), Example 16 (Compound No.) 1-26), Example 19 (Compound No. 1-31), Example 23 (Compound No. 1-248), Example 24 (Compound No. 1-249), Example 25 (Compound No. 1-47).
0), Example 26 (Compound No. 1-471), Example 2
7 (Compound No. 1-667), Example 29 (Compound No. 1-889), Example 30 (Compound No. 1-111)
1), Example 32 (Compound No. 1-1137), Example 35 (Compound No. 1-1803), Example 36 (Compound No. 1-2468), Example 37 (Compound No. 1-24)
69), Example 39 (Compound No. 1-2732), Example 40 (Compound No. 1-2799), Example 50 (Compound No. 1-3481), Example 51 (Compound No. 1-3).
482), Example 53 (Compound No. 1-3602), Example 54 (Compound No. 1-3669), Example 55 (Compound No. 1-3736), Example 57 (Compound No. 1-).
3750), Example 58 (Compound No. 1-3803),
Example 60 (Compound No. 1-3817), Example 65
(Compound No. 1-4004), Example 66 (Compound No. 1-4017), Example 71 (Compound No. 1-415).
2) and the compound of Example 73 (Compound No. 2-1) are
The illness was 0.

【０１６４】[0164]

【発明の効果】本発明化合物は、農園芸用殺菌剤として
用いることができ、宿主植物に被害を与えることなく、
種々の植物病原菌、特にイネいもち病に対して卓効を示
すことから、農園芸用殺菌剤として優れたものである。INDUSTRIAL APPLICABILITY The compound of the present invention can be used as an agricultural and horticultural fungicide, without damaging the host plant.
It is excellent as a fungicide for agricultural and horticultural use because it shows excellent effects against various plant pathogens, especially rice blast.

【０１６５】本発明化合物が優れた効力を発揮する植物
病害としては、例えばイネいもち病(Pyricularia oryza
e)並びにキュウリ、トマト及びインゲンの灰色かび病(B
otrytis cinerea)が挙げられるが、本発明化合物の殺菌
スペクトラムは、これらに限定されない。Examples of plant diseases in which the compound of the present invention exerts excellent efficacy include, for example, rice blast (Pyricularia oryza).
e) and gray mold of cucumber, tomato and green beans (B
otrytis cinerea), but the bactericidal spectrum of the compound of the present invention is not limited thereto.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 太田 昊 滋賀県野洲郡野洲町野洲1041 三共株式会 社内 (72)発明者 大西 徹 滋賀県野洲郡野洲町野洲1041 三共株式会 社内 (72)発明者 今井 秩明 滋賀県野洲郡野洲町野洲1041 三共株式会 社内 Ｆターム(参考） 4C031 JA07 4H011 AA01 BA01 BB09 BC01 BC03 BC07 BC17 BC18 DA02 DA15 DA16 DC05 DC06 DD03    ─────────────────────────────────────────────────── ─── Continued front page    (72) Inventor Hajime Ota             1041 Yasu, Yasu-cho, Yasu-gun, Shiga Sankyo Stock Association             In-house (72) Inventor Tohru Onishi             1041 Yasu, Yasu-cho, Yasu-gun, Shiga Sankyo Stock Association             In-house (72) Inventor Noriaki Imai             1041 Yasu, Yasu-cho, Yasu-gun, Shiga Sankyo Stock Association             In-house F-term (reference) 4C031 JA07                 4H011 AA01 BA01 BB09 BC01 BC03                       BC07 BC17 BC18 DA02 DA15                       DA16 DC05 DC06 DD03

Claims (16)

【特許請求の範囲】[Claims] 【請求項１】一般式 【化１】 ［式中、……は、単結合又は二重結合を表し、Ｒは、置
換されてよいＣ1〜Ｃ8アルキル基（当該置換基は、同一
又は異なった１〜４個のハロゲン原子、１個のＣ3〜Ｃ6
シクロアルキル基又は１個のＣ1〜Ｃ6アルコキシ基であ
る。）、Ｃ3〜Ｃ6シクロアルキル基、Ｃ2〜Ｃ6アルケニ
ル基又はＣ3〜Ｃ6アルキニル基を表し、Ｘは、ハロゲン
原子、置換されてよいＣ1〜Ｃ6アルキル基（当該置換基
は、同一又は異なった１〜３個のハロゲン原子であ
る。）又は置換されてよいＣ1〜Ｃ6アルコキシ基（当該
アルコキシ基は、同一又は異なった１〜３個のハロゲン
原子である。）を表し、ｍは、０〜６の整数を表し、ｍ
が２以上であるとき、複数のＸは同一であっても異なっ
ていてもよく、Ｚは、Ｃ1〜Ｃ6アルキル基であり、ｎ
は、０〜６の整数を表し、ｎが２以上であるとき、複数
のＺは同一であっても異なっていてもよく、任意の２個
のＺが、一緒になって、Ｃ1〜Ｃ4アルキレン基であって
もよい。］で表される化合物又はその塩。1. A general formula: [Wherein ... represents a single bond or a double bond, R represents an optionally substituted C 1 to C 8 alkyl group (the substituents are the same or different 1 to 4 halogen atoms, 1 C 3 to C 6
It is a cycloalkyl group or one C 1 -C 6 alkoxy group. ), C 3 -C 6 cycloalkyl group, a C 2 -C 6 alkenyl or C 3 -C 6 alkynyl group, X is a halogen atom may be substituted C 1 -C 6 alkyl group (the substituent Are the same or different 1 to 3 halogen atoms) or an optionally substituted C 1 -C 6 alkoxy group (the alkoxy group is the same or different 1 to 3 halogen atoms). Represents, m represents an integer of 0 to 6, m
Is 2 or more, a plurality of X may be the same or different, Z is a C 1 -C 6 alkyl group, and n is
Represents an integer of 0 to 6, and when n is 2 or more, a plurality of Zs may be the same or different, and any two Zs are taken together to form C 1 to C. It may be a 4- alkylene group. ] The compound or its salt represented by these. 【請求項２】Ｒが、置換されてよいＣ1〜Ｃ6アルキル基
（当該置換基は、同一又は異なった１〜４個のフッ素原
子若しくは塩素原子、１個のＣ4〜Ｃ6シクロアルキル基
又は１個のＣ1〜Ｃ4アルコキシ基である。）、Ｃ3〜Ｃ4
シクロアルキル基、Ｃ3〜Ｃ5アルケニル基又はＣ3〜Ｃ5
アルキニル基である、請求項１に記載の化合物又はその
塩。2. R is an optionally substituted C 1 -C 6 alkyl group (the said substituents are the same or different 1 to 4 fluorine atoms or chlorine atoms, 1 C 4 -C 6 cycloalkyl group). A group or one C 1 -C 4 alkoxy group), C 3 -C 4
Cycloalkyl group, C 3 -C 5 alkenyl or C 3 -C 5
The compound or a salt thereof according to claim 1, which is an alkynyl group. 【請求項３】Ｒが、置換されてよいＣ1〜Ｃ5アルキル基
（当該置換基は、１〜３個のフッ素原子、１個のシクロ
ヘキシル基又は１個のメトキシ基である。）、Ｃ3〜Ｃ5
アルケニル基又はＣ3〜Ｃ5アルキニル基である、請求項
１に記載の化合物又はその塩。3. R is an optionally substituted C 1 -C 5 alkyl group (the said substituents are 1 to 3 fluorine atoms, 1 cyclohexyl group or 1 methoxy group), C 3 ~ C 5
The compound or salt thereof according to claim 1, which is an alkenyl group or a C 3 -C 5 alkynyl group. 【請求項４】Ｒが、置換されてよいＣ1〜Ｃ4アルキル基
（当該置換基は、１〜３個のフッ素原子である。）、Ｃ
3〜Ｃ4アルケニル基又はＣ4〜Ｃ5アルキニル基である、
請求項１に記載の化合物又はその塩。4. R is an optionally substituted C 1 -C 4 alkyl group (the said substituents are 1 to 3 fluorine atoms), C
3 is -C 4 alkenyl group or a C 4 -C 5 alkynyl group,
The compound according to claim 1, or a salt thereof. 【請求項５】Ｒが、メチル基、エチル基、プロピル基、
ブチル基、イソブチル基、ペンチル基、トリフルオロメ
チル基、ビニル基、アリル基、４−ペンテニル基、３−
メチル−２−ブテニル基、プロパルギル基又は２−ペン
チニル基である、請求項１に記載の化合物又はその塩。5. R is a methyl group, an ethyl group, a propyl group,
Butyl group, isobutyl group, pentyl group, trifluoromethyl group, vinyl group, allyl group, 4-pentenyl group, 3-
The compound or a salt thereof according to claim 1, which is a methyl-2-butenyl group, a propargyl group or a 2-pentynyl group. 【請求項６】Ｒが、メチル基、エチル基、トリフルオロ
メチル基、アリル基又は２−ペンチニル基である、請求
項１に記載の化合物又はその塩。6. The compound or a salt thereof according to claim 1, wherein R is a methyl group, an ethyl group, a trifluoromethyl group, an allyl group or a 2-pentynyl group. 【請求項７】Ｘが、フッ素原子、塩素原子、臭素原子、
ヨウ素原子、置換されてよいＣ1〜Ｃ4アルキル基（当該
置換基は、同一又は異なった１〜３個のフッ素原子若し
くは塩素原子である。）又は置換されてよいＣ1〜Ｃ4ア
ルコキシ基（当該置換基は、同一又は異なった１〜３個
のフッ素原子若しくは塩素原子である。）であり、ｍ
が、０、１又は２である、請求項１〜６のいずれか１つ
に記載の化合物又は塩。7. X is a fluorine atom, a chlorine atom, a bromine atom,
Iodine atom, C 1 -C 4 alkyl group which may be substituted (the said substituents are the same or different 1 to 3 fluorine atoms or chlorine atoms) or C 1 -C 4 alkoxy group which may be substituted (The said substituent is 1 or 3 same or different fluorine atoms or chlorine atoms.), And m
Is 0, 1 or 2, 7. The compound or salt according to any one of claims 1 to 6. 【請求項８】Ｘが、フッ素原子、塩素原子、Ｃ1〜Ｃ3ア
ルキル基又はＣ1〜Ｃ3アルコキシ基であり、ｍが、０又
は１である、請求項１〜６のいずれか１つに記載の化合
物又は塩。8. The method according to claim 1, wherein X is a fluorine atom, a chlorine atom, a C 1 -C 3 alkyl group or a C 1 -C 3 alkoxy group, and m is 0 or 1. Or a compound or salt thereof. 【請求項９】Ｘが、フッ素原子又はメチル基であり、ｍ
が、０又は１である、請求項１〜６のいずれか１つに記
載の化合物又は塩。9. X is a fluorine atom or a methyl group, and m
Is 0 or 1, The compound or salt as described in any one of Claims 1-6. 【請求項１０】ｍが、０である、請求項１〜６のいずれ
か１つに記載の化合物又は塩。10. The compound or salt according to any one of claims 1 to 6, wherein m is 0. 【請求項１１】Ｚが、Ｃ1〜Ｃ4アルキル基であり、ｎ
が、０、１又は２であり、ｎが２であるとき、２個のＺ
が、一緒になって、Ｃ1〜Ｃ2アルキレン基を形成してよ
い、請求項１〜１０のいずれか１つに記載の化合物又は
塩。11. Z is a C 1 -C 4 alkyl group, and n
Is 0, 1 or 2, and n is 2, two Z
But together, they may form a C 1 -C 2 alkylene group, the compound or salt according to any one of claims 1 to 10. 【請求項１２】Ｚが、Ｃ1〜Ｃ3アルキル基であり、ｎ
が、０又は１である、請求項１〜１０のいずれか１つに
記載の化合物又は塩。12. Z is a C 1 -C 3 alkyl group, and n
Is 0 or 1, The compound or salt as described in any one of Claims 1-10. 【請求項１３】Ｚが、メチル基であり、ｎが、０又は１
である、請求項１〜１０のいずれか１つに記載の化合物
又は塩。13. Z is a methyl group, and n is 0 or 1.
The compound or salt according to any one of claims 1 to 10, which is: 【請求項１４】ｎが、０である、請求項１〜１０のいず
れか１つに記載の化合物又は塩。14. The compound or salt according to any one of claims 1 to 10, wherein n is 0. 【請求項１５】……が、単結合である、請求項１〜１４
のいずれか１つに記載の化合物又は塩。15. The structure according to claim 1, wherein ... Is a single bond.
The compound or salt according to any one of 1. 【請求項１６】請求項１〜１４のいずれか１つに記載
の、１−メチル−N−（３−キノリル）−１−シクロヘ
キサンカルボキサミド、1-メチル-N-（8-フルオロ-3-キ
ノリル）−１−シクロヘキサンカルボキサミド、1-メチ
ル-N-（2-メチル-3-キノリル）−１−シクロヘキサンカ
ルボキサミド、1-メチル-N-（8-メチル-3-キノリル）−
１−シクロヘキサンカルボキサミド、1-エチル-N-（2-
メチル-3-キノリル）−１−シクロヘキサンカルボキサ
ミド、1-エチル-N-（4-メチル-3-キノリル）−１−シク
ロヘキサンカルボキサミド、1-プロピル-N-（4-メチル-
3-キノリル）−１−シクロヘキサンカルボキサミド、1-
イソブチル-N-（4-メチル-3-キノリル）−１−シクロヘ
キサンカルボキサミド、１−トリフルオロメチル−N−
（３−キノリル）−１−シクロヘキサンカルボキサミ
ド、１−アリル−N−（３−キノリル）−１−シクロヘ
キサンカルボキサミド、1-アリル-N-（2-メチル-3-キノ
リル）−１−シクロヘキサンカルボキサミド、1-アリル
-N-（4-メチル-3-キノリル）−１−シクロヘキサンカル
ボキサミド、1-（2-メチルアリル）-N-（2-メチル-3-キ
ノリル）−１−シクロヘキサンカルボキサミド、1-（2-
メチルアリル）-N-（4-メチル-3-キノリル）−１−シク
ロヘキサンカルボキサミド、1-プロパルギル-N-（3-キ
ノリル）−１−シクロヘキサンカルボキサミド、1-（2-
ペンチニル）-N-（4-メチル-3-キノリル）−１−シクロ
ヘキサンカルボキサミド、1-エチル-N-（2-メチル-3-キ
ノリル）-3-シクロヘキセン−１−カルボキサミド、1-
アリル-N-（4-メチル-3-キノリル）-3-シクロヘキセン
−１−カルボキサミド又は1,2-ジメチル-N-（3-キノリ
ル）−１−シクロヘキサンカルボキサミド。16. 1-Methyl-N- (3-quinolyl) -1-cyclohexanecarboxamide, 1-methyl-N- (8-fluoro-3-quinolyl) according to any one of claims 1 to 14. ) -1-Cyclohexanecarboxamide, 1-methyl-N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1-methyl-N- (8-methyl-3-quinolyl)-
1-cyclohexanecarboxamide, 1-ethyl-N- (2-
Methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1-ethyl-N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1-propyl-N- (4-methyl-
3-quinolyl) -1-cyclohexanecarboxamide, 1-
Isobutyl-N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1-trifluoromethyl-N-
(3-quinolyl) -1-cyclohexanecarboxamide, 1-allyl-N- (3-quinolyl) -1-cyclohexanecarboxamide, 1-allyl-N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1 -Allyl
-N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1- (2-methylallyl) -N- (2-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1- (2-
Methylallyl) -N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1-propargyl-N- (3-quinolyl) -1-cyclohexanecarboxamide, 1- (2-
Pentynyl) -N- (4-methyl-3-quinolyl) -1-cyclohexanecarboxamide, 1-ethyl-N- (2-methyl-3-quinolyl) -3-cyclohexene-1-carboxamide, 1-
Allyl-N- (4-methyl-3-quinolyl) -3-cyclohexene-1-carboxamide or 1,2-dimethyl-N- (3-quinolyl) -1-cyclohexanecarboxamide.
JP2002118645A 2001-04-24 2002-04-22 N-(3-quinolyl)amide derivative Ceased JP2003012649A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2002118645A JP2003012649A (en) 2001-04-24 2002-04-22 N-(3-quinolyl)amide derivative

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP2001125661 2001-04-24
JP2001-125661 2001-04-24
JP2002118645A JP2003012649A (en) 2001-04-24 2002-04-22 N-(3-quinolyl)amide derivative

Publications (1)

Publication Number Publication Date
JP2003012649A true JP2003012649A (en) 2003-01-15

Family

ID=26614074

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002118645A Ceased JP2003012649A (en) 2001-04-24 2002-04-22 N-(3-quinolyl)amide derivative

Country Status (1)

Country Link
JP (1) JP2003012649A (en)

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