KR860001792A - 피롤 유도체의 제조방법 - Google Patents
피롤 유도체의 제조방법 Download PDFInfo
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- KR860001792A KR860001792A KR1019850005873A KR850005873A KR860001792A KR 860001792 A KR860001792 A KR 860001792A KR 1019850005873 A KR1019850005873 A KR 1019850005873A KR 850005873 A KR850005873 A KR 850005873A KR 860001792 A KR860001792 A KR 860001792A
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- 238000000034 method Methods 0.000 title claims 9
- 150000003233 pyrroles Chemical class 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 21
- 150000001875 compounds Chemical class 0.000 claims 16
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 125000005843 halogen group Chemical group 0.000 claims 10
- 239000002253 acid Substances 0.000 claims 9
- 239000007858 starting material Substances 0.000 claims 9
- 239000004480 active ingredient Substances 0.000 claims 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 8
- 244000045947 parasite Species 0.000 claims 7
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 150000002148 esters Chemical class 0.000 claims 6
- 125000001424 substituent group Chemical group 0.000 claims 6
- KGANAERDZBAECK-UHFFFAOYSA-N (3-phenoxyphenyl)methanol Chemical compound OCC1=CC=CC(OC=2C=CC=CC=2)=C1 KGANAERDZBAECK-UHFFFAOYSA-N 0.000 claims 5
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 238000004519 manufacturing process Methods 0.000 claims 5
- 241001465754 Metazoa Species 0.000 claims 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims 4
- 125000003118 aryl group Chemical group 0.000 claims 3
- 150000001721 carbon Chemical class 0.000 claims 3
- YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 claims 3
- 125000000524 functional group Chemical group 0.000 claims 3
- GXUQMKBQDGPMKZ-UHFFFAOYSA-N 2-hydroxy-2-(3-phenoxyphenyl)acetonitrile Chemical compound N#CC(O)C1=CC=CC(OC=2C=CC=CC=2)=C1 GXUQMKBQDGPMKZ-UHFFFAOYSA-N 0.000 claims 2
- 241000238876 Acari Species 0.000 claims 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims 2
- 230000000895 acaricidal effect Effects 0.000 claims 2
- 239000000642 acaricide Substances 0.000 claims 2
- 125000003710 aryl alkyl group Chemical group 0.000 claims 2
- 125000006165 cyclic alkyl group Chemical group 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 229910052736 halogen Inorganic materials 0.000 claims 2
- 150000002367 halogens Chemical class 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052760 oxygen Inorganic materials 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 2
- 229920006395 saturated elastomer Polymers 0.000 claims 2
- 229910052717 sulfur Inorganic materials 0.000 claims 2
- 125000004434 sulfur atom Chemical group 0.000 claims 2
- VPGDRFHIEUUXJB-UHFFFAOYSA-N (1-prop-2-ynylpyrrol-3-yl)methanol Chemical compound OCC=1C=CN(CC#C)C=1 VPGDRFHIEUUXJB-UHFFFAOYSA-N 0.000 claims 1
- AFEOKIGLYCQHAZ-UHFFFAOYSA-N (5-benzylfuran-3-yl)methanol Chemical compound OCC1=COC(CC=2C=CC=CC=2)=C1 AFEOKIGLYCQHAZ-UHFFFAOYSA-N 0.000 claims 1
- VTJMSIIXXKNIDJ-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-methylbutyric acid Chemical compound CC(C)C(C(O)=O)C1=CC=C(Cl)C=C1 VTJMSIIXXKNIDJ-UHFFFAOYSA-N 0.000 claims 1
- QQHOVRKETYPQHY-UHFFFAOYSA-N 2-(hydroxymethyl)-4,5,6,7-tetrahydroisoindole-1,3-dione Chemical compound O=C1N(CO)C(=O)C2=C1CCCC2 QQHOVRKETYPQHY-UHFFFAOYSA-N 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- MDIQXIJPQWLFSD-UHFFFAOYSA-N 3-(2,2-dibromoethenyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CC1(C)C(C=C(Br)Br)C1C(O)=O MDIQXIJPQWLFSD-UHFFFAOYSA-N 0.000 claims 1
- GNACAIQZXUOEEU-UHFFFAOYSA-N 3-(3-ethoxy-2-fluoro-3-oxoprop-1-enyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CCOC(=O)C(F)=CC1C(C(O)=O)C1(C)C GNACAIQZXUOEEU-UHFFFAOYSA-N 0.000 claims 1
- PZPGQLXLKXVMCT-UHFFFAOYSA-N 3-(3-ethoxy-3-oxoprop-1-enyl)-2,2-dimethylcyclopropane-1-carboxylic acid Chemical compound CCOC(=O)C=CC1C(C(O)=O)C1(C)C PZPGQLXLKXVMCT-UHFFFAOYSA-N 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 241000244206 Nematoda Species 0.000 claims 1
- AFVLVVWMAFSXCK-VMPITWQZSA-N alpha-cyano-4-hydroxycinnamic acid Chemical group OC(=O)C(\C#N)=C\C1=CC=C(O)C=C1 AFVLVVWMAFSXCK-VMPITWQZSA-N 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 150000001555 benzenes Chemical class 0.000 claims 1
- 125000001246 bromo group Chemical group Br* 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 229910052801 chlorine Inorganic materials 0.000 claims 1
- 239000000460 chlorine Substances 0.000 claims 1
- -1 cyano-3-phenoxybenzyl alcohols Chemical class 0.000 claims 1
- 125000004122 cyclic group Chemical group 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- 230000000694 effects Effects 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 125000000623 heterocyclic group Chemical group 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000005645 nematicide Substances 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000000575 pesticide Substances 0.000 claims 1
- 238000002360 preparation method Methods 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
- 125000004417 unsaturated alkyl group Chemical group 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/333—Radicals substituted by oxygen or sulfur atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23K—FODDER
- A23K20/00—Accessory food factors for animal feeding-stuffs
- A23K20/10—Organic substances
- A23K20/116—Heterocyclic compounds
- A23K20/132—Heterocyclic compounds containing only one nitrogen as hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/33—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/337—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/42—Nitro radicals
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Polymers & Plastics (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Dentistry (AREA)
- Food Science & Technology (AREA)
- Animal Husbandry (AREA)
- Pyrrole Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fodder In General (AREA)
- Medicinal Preparation (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Peptides Or Proteins (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Cephalosporin Compounds (AREA)
Abstract
Description
Claims (24)
- 다음 일반식(Ⅱ)의 알콜을 다음 일반식(Ⅲ)의 산 또는 이산의 작용 유도체로 반응시킴을 특징으로 하여 다음 일반식(Ⅰ)의 화합물을 제조하는 방법:상기식에서 -R2또는 R2기의 하나는기를 나타내며, 여기서 A는 ACO2H피레트리노이드 산의 잔기를 나타내며; Z는 수소원자, C,N,C CH,CF3그룹 또는 1내지 3탄소원자를 함유하는 알킬기를 나타내며, -R2또는 R2기의 어느 것이든지기를 나타내지 않을 뿐만 아니라 같거나 서로 다른 R4및 R5기는 수소원자, 할로겐원자, 18탄소원자까지 함유하는 알킬기, 14탄소원자까지 함유하는 아릴기, 18탄소원자까지 함유하는 아르알킬기, 시아노기, CF3기, 8탄소원자까지 함유하는 CO2알킬기, NO2기, 8탄소원자까지 함유하는 알콕시기,기를 나타내며;여기서 n은 0,1 또는 2이고, R′,R′1및 R′2기는 1내지 8탄소원자를 함유하는 알킬기이고, R4및 R5기는 8탄소원자까지 함유하는 포화 또는 불포화 탄소동종 사이클을 형성할 수 있고, -R1은이거나,기 이거나,기 이거나,기 일 수 있는데여기서 X 및 Y는 같거나 다르며 수소원자, 할로겐원자 1내지 8탄소원자 함유알킬기 또는 14탄소원자까지 함유하는 아릴기 이며, X′,Y′및 Y″는 같거나 다르며, 상기한 X 및 Y 에 나타낸 것과 같은 정의들의 하나를 나타내며, 파선은 탄소(1)과 (2)사이에 가능한 이중결합을 나타내며, r′는 할로겐, 시아노,)여기서 n은 1 또는 2이다)및를 제외하고 상기한 R4및 R5에 대하여 상기한 바와같고, R″및 R″′은 같거나 다르며, 수소원자, 1내지 18탄소원자함유 알킬기, 14탄소원자까지 함유하는 마릴기, 18탄소원자함유 아르알킬기, CF3기 8탄소원자까지 함유하는 CO2-알킬기 또는 8탄소원자까지 함유하는 알콕시기를 나타내며, 상기(Ⅱ)식에서 R″2및 R″3기의 하나는그룹을 나타내고, R″2및 R″3기의 다른 하나는 상기 R4및 R5에 대하여 상기한 바와 같다.
- 상기 1항에 있어, R1이 -CH2-C≡CH기를 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1또는 2항에 있어, R″2및 R″3기의 하나는그룹을 나타내고, 여기서 Z는 수소원자를 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1또는 2항에 있어, R″2및 R″3기의 하나는그룹을 나타내고, 여기서 Z는 시아노기를 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1또는 2항에 있어, R″3치환기는그룹을 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1내지 5항에 있서, R″2,R4및 R5치환기의 하나는 니트로기를 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1내지 5항의 어느 하나에 있어, R″2,R4및 R5치환기의 하나는 니트로기를 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1내지 5항의 어느 하나에 있어, R″2,R4및 R5치환기의 하나는 시아노기를 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1내지 5항의 어느 하나에 있어, R″2,R4및 R5치환기의 하나는 트리플루오로메틸기를 나타내는 일반식(Ⅱ)의 알콜을 출발물질로 사용함을 특징으로 하는 상기의 방법.
- 상기 1내지 9항의 어느 하나에 있어 -A가인 기를 나타내거나, -Z2가기를 나타내거나, -Z2가기를 나타내거나, -Z2가기를 나타내거나, A가기를 나타내며, 여기서 Z1과 Z2는 각각 메틸기를 나타내고, 또는 Z1은 수소원자를 나타내고, Z2는 상기한 것이거나, Z3는 수소원자 또는 할로겐원자를 나타내고, T1과 T2는 같거나 다르며, 수소원자, 할로겐원자, 1내지 8탄소원자 함유 알콕실 또는 알킬기, CF3또는 CN기 또는 할로겐에 의하여 치환이 가능한 페닐 핵 또는 T1과 T2가 다같이 3내지 6탄소원자를 함유하는 시클로 알킬기를 형성하거나기를 나타내며, 여기서 B는 산소 또는 황원자를 나타내며a,b,c및d는 같거나 다르며 각각 할로겐원자를 나타내며, D는 수소 또는 할로겐원자, 1내지 8탄소원자함유 알콕시기를 나타내고, G는 산소 또는 황원자를 나타내고, J는 우선하나 또는 그 이상의 같거나 다른 작용기로 치환이 가능한, 1내지 8탄소원자함유 직쇄, 측쇄 또는 환형의 포화 또는 불포화 알킬기이거나, 하는 또는 그 이상의 같거나 다른 작용기로 치한이 가능한 6내지 14탄소원자 함유 아릴 그룹이거나 하나 또는 그 이상의 같거나 다른 작용기로 치환이 가능한 헤테로고리기를 나타내며,U는 벤젠핵상의 어떤 위치에서, 할로겐 원자, 1내지 8탄소원자함유 알킬기 또는 1내지 8탄소원자함유 알콕시기를 나타내고, m은 0,1또는 2의 숫자를 나타내는 일반식(Ⅲ)의 화합물의 화합물과 상기 산을 반응시킴을 특징으로 하는 상기의 제조방법.
- 상기 10항에 있어, Hal은 할로겐원자를 나타내며, A는기를 나타내는 일반식(Ⅲ)의 화합물과 상기 산을 반응시킴을 특징으로 하는 상기의 제조방법.
- 상기 10항에 있어 J는 1내지 8탄소원자함유 직쇄, 측쇄 또는 고리화된 알킬기를 나타내며, 이중 결합은(Z)은 기하구조를 가지며, A는기를 나타내는 일반식(Ⅲ)의 화합물과 상기산을 반응시킴을 특징으로 하는 상기의 제조방법.
- 상기 10항에 있어, Hal은 할로겐 원자를 나타내고, J는 1내지 8탄소원자 함유 직쇄, 측쇄 또는 고리화된 알킬기를 나타내며, 이중결합은(E)기하구조를 가지며, A는기를 나타내는 일반식(Ⅲ)의 화합물과 상기 산을 반응시킴을 특징으로 하는 상기의 제조방법.
- 상기 13항에 있어, Hal은 불소원자를 나타내며, J는 1내지 8탄소원자함유 알킬기를 나타내며, 이중결합은(E) 기하구조를 가지며, A는기를 나타내는 일반식(Ⅲ)의 화합물과 상기산을 반응시킴을 특징으로 하는 상기의 제조방법.
- 상기 10항에 있어, 1R, 시스(ΔE) 2,2-디메틸 3-(3-에톡시 3-옥소 2-플루오로 1-프로페닐) 시클로프로판 카복실산 1R, 시스(ΔZ) 2,2-디메틸 3-(3-에톡시 3-옥소 1-프로페닐) 시클로프로판 카복실산 또는 1R, 시스(ΔE) 2,2-디메틸 3-(3-tert. -부톡시 3-옥소 2-플루오로 1-프로페닐)시클로프로판 카복실산 및 1-(2-프로피닐) 1H-피롤 3-메탄올 또는 1-(2-프로피닐) 2-트리플루오로메틸 1H-피롤 3-메탄올을 출발물질로 하는 상기의 제조방법.
- 상기 1내지 14항의 어느 하나에서 정의한 생성물을 활성성분으로 함유함을 특징으로 하여 온혈동물의 기생충·토지의 기생충 및 재배지의 기생충을 처치하기 위한 조성물.
- 상기 15항의 어느 하나에서 정의한 생성물을 활성성분으로 함유함을 특징하는 온혈동물의 기생충·토지의 기생충 및 재배지의 기생충을 처치하기 위한 조성물.
- 상기 1내지 15항의 어느 하나에 있어 정의한 생성물의 적어도 하나를 활성성분으로 함유하는 살충제.
- 상기 1내지 15항의 어느 하나에 있어 정의한 생성물의 적어도 하나를 활성성분으로 함유하는 살비제.
- 상기 1내지 15항의 어느 하나에 있어 정의한 생성물의 적어도 하나를 활성성분으로 함유하는 살선충제.
- 상기 1내지 15항의 어느 하나에 있어 정의한 생성물의 적어도 하나를 활성성분으로 함유하는 것으로 특히 진드기 및 진드기류인, 온혈동물의 기생충을 처치할 목적으로 된 살비조성물.
- 상기 1내지 15항의 어느 하나에 있어 정의한 생성물의 적어도 하나를 활성성분으로 함유하는 동물 사료용으로 제조된 조성물.
- 활성성분으로 한편은 일반식(Ⅰ)의 화합물의 적어도 하나를 함유하고, 또다른 한편은 3,4,5,6-테트라하이드로프탈이미도 메틸 알콜의 5-벤질-3-프릴메틸알콜의, 3-펜옥시벤질알콜의 그리고 크리산테민 산과 함께 α-시아노-3-펜옥시벤질알콜의 알레트롤론의 에스테르, 2,2-디메틸-3-(2-옥소-3-테트라하이드로티오페닐리덴메틸)시클로프로판-1-카복실린산과 함께 5-벤질-3-푸릴메틸 알콜의 에스테르 3-펜옥시벤질알콜 및 2,2-디메틸3-(2,2-디클로로베닐)시클로프로판-1-카복실린산과 함께 α-시아노-3-펜옥시벤질 알콜의 에스테르, 2,2-디메틸-3-(2,2-디브로모비닐)시클로프로판-1-카복실린 산과 함께 α-시아노-3-펜옥시벤질알콜의 에스테르, 2-파라클로로페닐-2-이소프로필아세트산과 함께 3-펜옥시벤질알콜의 에스테르, 3,4,5,6-테트라하이드 로프탈이미도메틸 알콜의, 5-벤질-3-프릴메틸알콜의 3-펜옥시벤질알콜의 그리고 2,2-디메틸-3-(1,2,2,2,2-테트라할로에틸)시클로프로판-1-카복실산과 함께 α-시아노-3-펜옥시벤질알콜의 알레트롤론의 에스테르로 구성돤 그룹으로부터 선택한 적어도 하나의 피레트리노이드 에스테르를 함유함을 특징으로 하는데, 여기서 "할로"는 불소, 염소 또는 브롬원자를 나타내고, 일반식(Ⅰ)의 화합물은 상기 피레트리노이드 에스테르의 산과 알콜코플라와 같이 그들의 모든 가능한 입체 이성체형으로 존재할 수 있는 살충제, 살비제 또는 살 선충활성을 갖는 조성물.
- 상기 16내지 23항의 어느 하나에 있어 그것들은 피레트리 노이드의 상승작용제를 함유함을 특징으로 하는 상기한 조성물.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR84-12791 | 1984-08-14 | ||
FR8412791A FR2569189B1 (fr) | 1984-08-14 | 1984-08-14 | Nouveaux derives du pyrrole, leur procede de preparation et leur application comme pesticides |
FR8506134A FR2580637B2 (fr) | 1984-08-14 | 1985-04-23 | Nouveaux derives du pyrrole, leur procede de preparation et leur application comme pesticides |
FR85-06134 | 1985-04-23 | ||
FR85-6134 | 1985-04-23 |
Publications (2)
Publication Number | Publication Date |
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KR860001792A true KR860001792A (ko) | 1986-03-22 |
KR920007553B1 KR920007553B1 (ko) | 1992-09-07 |
Family
ID=26224109
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019850005873A KR920007553B1 (ko) | 1984-08-14 | 1985-08-14 | 피롤 유도체의 제조방법 |
Country Status (27)
Country | Link |
---|---|
US (2) | US4737513A (ko) |
EP (1) | EP0176387B1 (ko) |
JP (1) | JPH0649680B2 (ko) |
KR (1) | KR920007553B1 (ko) |
AT (1) | ATE58525T1 (ko) |
AU (1) | AU577884B2 (ko) |
BG (1) | BG51232A3 (ko) |
BR (1) | BR8503835A (ko) |
CA (1) | CA1256882A (ko) |
DE (1) | DE3580638D1 (ko) |
EG (1) | EG18254A (ko) |
ES (1) | ES8706627A1 (ko) |
FR (2) | FR2569189B1 (ko) |
GR (1) | GR851967B (ko) |
HU (1) | HU194823B (ko) |
IL (1) | IL75959A (ko) |
MA (1) | MA20505A1 (ko) |
MX (1) | MX8274A (ko) |
NZ (1) | NZ213080A (ko) |
OA (1) | OA08082A (ko) |
PH (1) | PH23870A (ko) |
PT (1) | PT80942B (ko) |
RO (1) | RO92243B (ko) |
SU (1) | SU1493103A3 (ko) |
TR (1) | TR22482A (ko) |
YU (1) | YU45923B (ko) |
ZA (1) | ZA856077B (ko) |
Families Citing this family (21)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2569189B1 (fr) * | 1984-08-14 | 1986-12-19 | Roussel Uclaf | Nouveaux derives du pyrrole, leur procede de preparation et leur application comme pesticides |
FR2604173B1 (fr) * | 1986-09-18 | 1988-12-30 | Roussel Uclaf | Nouveaux derives de l'indole, leur procede de preparation et leur application comme pesticide |
FR2612184B1 (fr) * | 1987-03-09 | 1990-12-28 | Roussel Uclaf | Nouveaux derives du pyrrole substitues par un radical trifluoromethyle, leur procede de preparation et leur application comme pesticides |
FR2618432B1 (fr) * | 1987-07-20 | 1989-12-01 | Roussel Uclaf | Nouveaux derives pyrethrinoides comportant un heterocycle azote, leur procede de preparation et leurs applications comme pesticides |
US5455263A (en) * | 1987-07-29 | 1995-10-03 | American Cyanamid Company | Methods for the control and the protection of warm-blooded animals against infestation and infection by helminths, acarids and arthropod endo- and ectoparasites |
US5010098A (en) * | 1987-07-29 | 1991-04-23 | American Cyanamid Company | Arylpyrrole insecticidal acaricidal and nematicidal agents and methods for the preparation thereof |
JPS6483063A (en) * | 1987-09-24 | 1989-03-28 | Central Glass Co Ltd | Fluorine-containing monosubstituted pyrrole and production thereof |
FR2629452B1 (fr) * | 1988-03-31 | 1990-11-09 | Roussel Uclaf | Nouveau procede de preparation de derives trifluoromethylvinyliques a partir de derives halogenovinyliques correspondants |
DE3902216A1 (de) * | 1989-01-26 | 1990-08-02 | Basf Ag | Pyrrolderivate |
DE69019098T2 (de) * | 1989-02-27 | 1995-08-31 | Nippon Oils & Fats Co Ltd | Verfahren zur Herstellung von Fluoralkylderivaten. |
FR2658820B1 (fr) * | 1990-02-27 | 1994-06-03 | Roussel Uclaf | Nouveaux derives du pyrrole, leur procede de preparation et leur application comme pesticides. |
US5233052A (en) * | 1990-11-30 | 1993-08-03 | American Cyanamid Company | Insecticidal and acaricidal diarylpyrrolecarbonitrile and diarylnitropyrrole compounds |
US5180734A (en) * | 1990-11-30 | 1993-01-19 | American Cyanamid Company | Insecticidal and acaricidal diarylpyrrolecarbonitrile and diarylnitropyrrole compounds |
US5130328A (en) * | 1991-09-06 | 1992-07-14 | American Cyanamid Company | N-alkanoylaminomethyl and N-aroylaminomethyl pyrrole insecticidal and acaricidal agents |
US5286742A (en) * | 1992-11-03 | 1994-02-15 | American Cyanamid Company | Pyrrole thiocarboxamide insecticidal and acaricidal agents |
AU710683B2 (en) * | 1995-06-07 | 1999-09-30 | Nippon Shinyaku Co. Ltd. | Pyrrole derivatives and medicinal composition |
JP4126621B2 (ja) * | 1996-11-25 | 2008-07-30 | 日本農薬株式会社 | 殺虫・殺ダニ剤 |
GB0130517D0 (en) * | 2001-12-20 | 2002-02-06 | Syngenta Ltd | Chemical process |
US20080242648A1 (en) * | 2006-11-10 | 2008-10-02 | Syndax Pharmaceuticals, Inc., A California Corporation | COMBINATION OF ERa+ LIGANDS AND HISTONE DEACETYLASE INHIBITORS FOR THE TREATMENT OF CANCER |
WO2009015180A2 (en) * | 2007-07-23 | 2009-01-29 | Syndax Pharmaceuticals, Inc. | Novel compounds and methods of using them |
WO2009067453A1 (en) * | 2007-11-19 | 2009-05-28 | Syndax Pharmaceuticals, Inc. | Combinations of hdac inhibitors and proteasome inhibitors |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3850977A (en) * | 1968-06-06 | 1974-11-26 | Sumitomo Chemical Co | 3-substituted-benzyl cyclopropane-carboxylates |
GB1561502A (en) * | 1975-07-22 | 1980-02-20 | Kuraray Co | Y-lactone derivatives |
JPS6033106B2 (ja) * | 1977-10-07 | 1985-08-01 | 住友化学工業株式会社 | カルボン酸エステル、その製造法およびそれを有効成分とする殺虫、殺ダニ剤 |
US4229352A (en) * | 1979-08-13 | 1980-10-21 | Zoecon Corporation | Benzylpyrrolylmethyl esters of cyclopropane carboxylic acids |
FR2491060A1 (fr) * | 1980-10-01 | 1982-04-02 | Roussel Uclaf | Esters d'acides cyclopropanes carboxyliques apparentes a l'acide pyrethrique, leur procede de preparation et leur application a la lutte contre les parasites |
JPS57126470A (en) * | 1981-01-27 | 1982-08-06 | Mitsubishi Chem Ind Ltd | Carboxylic ester |
US4380656A (en) * | 1981-07-27 | 1983-04-19 | Emery Industries, Inc. | 2-Vinyl- and 2-ethylcyclopropane carboxylates |
US4418202A (en) * | 1981-12-21 | 1983-11-29 | Emery Industries, Inc. | 2-Vinyl- and 2-ethylcyclopropane monocarboxylates |
FR2569189B1 (fr) * | 1984-08-14 | 1986-12-19 | Roussel Uclaf | Nouveaux derives du pyrrole, leur procede de preparation et leur application comme pesticides |
-
1984
- 1984-08-14 FR FR8412791A patent/FR2569189B1/fr not_active Expired
-
1985
- 1985-04-23 FR FR8506134A patent/FR2580637B2/fr not_active Expired
- 1985-07-30 IL IL75959A patent/IL75959A/xx not_active IP Right Cessation
- 1985-08-09 AT AT85401627T patent/ATE58525T1/de not_active IP Right Cessation
- 1985-08-09 EP EP85401627A patent/EP0176387B1/fr not_active Expired - Lifetime
- 1985-08-09 DE DE8585401627T patent/DE3580638D1/de not_active Expired - Fee Related
- 1985-08-09 OA OA58662A patent/OA08082A/xx unknown
- 1985-08-12 GR GR851967A patent/GR851967B/el unknown
- 1985-08-12 RO RO119839A patent/RO92243B/ro unknown
- 1985-08-12 TR TR35183A patent/TR22482A/xx unknown
- 1985-08-12 ZA ZA856077A patent/ZA856077B/xx unknown
- 1985-08-13 ES ES546117A patent/ES8706627A1/es not_active Expired
- 1985-08-13 YU YU128985A patent/YU45923B/sh unknown
- 1985-08-13 PT PT80942A patent/PT80942B/pt not_active IP Right Cessation
- 1985-08-13 BG BG071439A patent/BG51232A3/xx unknown
- 1985-08-13 MA MA20731A patent/MA20505A1/fr unknown
- 1985-08-13 EG EG481/85A patent/EG18254A/xx active
- 1985-08-13 SU SU853947352A patent/SU1493103A3/ru active
- 1985-08-13 HU HU853101A patent/HU194823B/hu not_active IP Right Cessation
- 1985-08-13 NZ NZ213080A patent/NZ213080A/xx unknown
- 1985-08-13 CA CA000488586A patent/CA1256882A/fr not_active Expired
- 1985-08-13 BR BR8503835A patent/BR8503835A/pt not_active IP Right Cessation
- 1985-08-13 US US06/765,317 patent/US4737513A/en not_active Expired - Fee Related
- 1985-08-14 PH PH32641A patent/PH23870A/en unknown
- 1985-08-14 KR KR1019850005873A patent/KR920007553B1/ko not_active IP Right Cessation
- 1985-08-14 AU AU46194/85A patent/AU577884B2/en not_active Ceased
- 1985-08-14 JP JP60177796A patent/JPH0649680B2/ja not_active Expired - Lifetime
-
1987
- 1987-12-02 US US07/127,922 patent/US4798901A/en not_active Expired - Fee Related
-
1992
- 1992-06-10 MX MX9208274A patent/MX8274A/es unknown
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