KR960037663A - 디히드로피리다지논과 피리다지논 화합물, 이를 포함하는 조성물 및 이를 이용한 균 방제 방법 - Google Patents
디히드로피리다지논과 피리다지논 화합물, 이를 포함하는 조성물 및 이를 이용한 균 방제 방법 Download PDFInfo
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- KR960037663A KR960037663A KR1019960011980A KR19960011980A KR960037663A KR 960037663 A KR960037663 A KR 960037663A KR 1019960011980 A KR1019960011980 A KR 1019960011980A KR 19960011980 A KR19960011980 A KR 19960011980A KR 960037663 A KR960037663 A KR 960037663A
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- alkyl
- compound
- halo
- alkenyl
- hydrogen
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- 239000000203 mixture Substances 0.000 title claims abstract 5
- SSDAKJLEKSSAMH-UHFFFAOYSA-N 2,4-dihydro-1h-pyridazin-3-one Chemical compound O=C1CC=CNN1 SSDAKJLEKSSAMH-UHFFFAOYSA-N 0.000 title claims abstract 3
- AAILEWXSEQLMNI-UHFFFAOYSA-N 1h-pyridazin-6-one Chemical class OC1=CC=CN=N1 AAILEWXSEQLMNI-UHFFFAOYSA-N 0.000 title 1
- 244000052616 bacterial pathogen Species 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims abstract 19
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract 8
- 239000001257 hydrogen Substances 0.000 claims abstract 8
- -1 pyridazinone compound Chemical class 0.000 claims abstract 6
- 125000003118 aryl group Chemical group 0.000 claims abstract 5
- 229910052760 oxygen Inorganic materials 0.000 claims abstract 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract 2
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 8
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 6
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 4
- 125000004648 C2-C8 alkenyl group Chemical group 0.000 claims 4
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims 3
- 125000001475 halogen functional group Chemical group 0.000 claims 3
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims 2
- 125000006282 2-chlorobenzyl group Chemical group [H]C1=C([H])C(Cl)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000004847 2-fluorobenzyl group Chemical group [H]C1=C([H])C(F)=C(C([H])=C1[H])C([H])([H])* 0.000 claims 2
- 125000003852 3-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(Cl)=C1[H])C([H])([H])* 0.000 claims 2
- 125000006284 3-fluorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C(F)=C1[H])C([H])([H])* 0.000 claims 2
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 claims 2
- 125000001318 4-trifluoromethylbenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C([H])([H])*)C(F)(F)F 0.000 claims 2
- 241000894006 Bacteria Species 0.000 claims 2
- 241000196324 Embryophyta Species 0.000 claims 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000002946 cyanobenzyl group Chemical group 0.000 claims 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 2
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 2
- 125000006505 p-cyanobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1C#N)C([H])([H])* 0.000 claims 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 2
- 229920002554 vinyl polymer Polymers 0.000 claims 2
- 125000004642 (C1-C12) alkoxy group Chemical group 0.000 claims 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 239000004593 Epoxy Substances 0.000 claims 1
- 241000238631 Hexapoda Species 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000005466 alkylenyl group Chemical group 0.000 claims 1
- 125000005018 aryl alkenyl group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 230000002070 germicidal effect Effects 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 125000004953 trihalomethyl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 230000000844 anti-bacterial effect Effects 0.000 abstract 1
- 230000000749 insecticidal effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
- C07D237/14—Oxygen 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three 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
- C07D237/14—Oxygen atoms
- C07D237/16—Two oxygen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/06—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
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- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
Abstract
디히드로피리다지논 및 피리다지논 화합물의 구조식(1)은 다음과 같다.
여기서, W는 CH3-O-A=C-CO(V)CH3이고 ; n은 0 혹은 1이며 ; A는 N 혹은 CH이고 ; V는 0 혹은 NH이고 ; Y는 O, S, NR1혹은 R6이고, R4및 R5를 갖는 상기 고리 결합은 단일 혹은 이중 결합이고, R4및 R5는 하이드로겐 및 치환되었거나 치환되지 않은 알킬과 아릴 그룹으로부터 독립적으로 선택된다. 상기 화합물 및 이를 함유한 조성물은 살균성 및 살충성을 갖는다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (20)
- 하기 구조식을 갖는 디히드로피리다지논 및 피리다지논 화합물단 여기서, W는 CH3-O-A=C-CO(V)CH3이며 ; A는 N 혹은 CH이며 ; V는 0 혹은 NH이며 ; Y는 O, S, NR1혹은 R6이고, R4및 R5를 갖는 고리 결합은 단일 혹은 이중 결합이고 ; n은 0 혹은 1이며 ; X는 하이드로겐(수소), 할로, (C1-C4)알킬, (C1-C4)알콕시 및 -HC=CH-CH=CH-에서 독립적으로 선택되어 나프틸 고리를 형성하고 ; R2는 하이드로겐, (C1-C12)알킬, (C1-C12)알콕시, 할로(C1-C12)알킬, 할로(C1-C12)알콕시, 히드록시(C1-C12)알킬, (C1-C12)알콕시(C1-C12)알킬, (C1-C12)알콕시카보닐(C1-C12)알킬, (C2-C8)알케닐, 할로(C2-C8)알케닐, (C3-C10)알키닐, 할로(C3-C10)알키닐, (C3-C7)시클로알킬, (C3-C7)시클로알킬(C1-C4)알킬, 에폭시(C1-C12)알킬, PO(OR1)2(C1-C12)알킬, R1S(O)2,(C1-C12)알킬, (R1)3Si(C1-C12)알킬, 아릴, 아릴옥시, (C1-C12)알킬, 아릴카보닐(C1-C12)알킬, 아랄킬, 아릴알케닐, 헤테로사이클릭, 헤테로사이클릭(C1-C12)알킬, N-모르폴리노(C1-C12)알킬, N-피페리디닐(C1-C12)알킬로부터 독립적으로 선택되고 ; R1은 (C1-C12)알킬, (C2-C8)알케닐 및 아릴로부터 독립적으로 선택되고 ; R4및 R5는 하이드로겐, 할로 (C1-C8)알킬, (C1-C8)알콕시, 시아노, 할로(C1-C12)알킬, (C2-C8)알케닐, (C3-C10)알키닐, 아릴 및 아랄킬로부터 독립적으로 선택되고 ; R6은 (C1-C12)알킬레닐 및 (C2-C12)알케니레닐로부터 독립적으로 선택된다.
- 제1항에 있어서, R4및 R5와 결합된 탄소사이의 고리 결합은 이중 결합임을 특징으로 하는 화합물.
- 제2항에 있어서, 상기 A는 CH임을 특징으로 하는 화합물.
- 제2항에 있어서, 상기 A는 N임을 특징으로 하는 화합물.
- 제3항에 있어서, 상기 V는 O임을 특징으로 하는 화합물.
- 제4항에 있어서, 상기 V는 O임을 특징으로 하는 화합물.
- 제5항에 있어서, 상기 R4및 R5는 하이드로겐이고,부분은 Y에 대한 메타이며, 그리고, R2는 (C1-C12)알킬, (C2-C8)알케닐, 할로(C1-C12)알킬, 및 할로(C2-C8)알케닐로부터 선택됨을 특징으로 하는 화합물.
- 제7항에 있어서, 상기 n=0이고, X는 하이드로겐이고 R2는 에틸, 프로필, 부틸, 비닐, 아릴, 클로로에틸, 플루오로에틸 및 치환된 벤질로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제8항에 있어서, 상기 R2은 할로치환된 벤질, (C1-C4)알킬치환된 벤질, 트리할로치환된 벤질 및 시아노 치환된 벤질로부터 선택됨을 특징으로 하는 화합물.
- 제9항에 있어서, 상기 R2는 2-클로로벤질, 3-클로로벤질, 4-클로로벤질, 2-플루오로벤질, 3-플루오로벤질, 4-플루오로벤질, 2-시아노벤질, 3-시아노벤질, 4-시아노벤질 및 4-트리플루오로메틸벤질로부터 선택됨을 특징으로 하는 화합물.
- 제6항에 있어서, 상기 R4및 R5는 하이드로겐이고, 상기부분은 Y에 대한 메타이고, R2는 (C1-C12)알킬, (C2-C8)알케닐, 할로(C1-C12)알킬, 할로(C2-C8)알케닐 및 아랄킬로부터 선택됨을 특징으로 하는 화합물.
- 제11항에 있어서, 상기 n=0이고, X는 하이드로겐이고 R2는 에틸, 프로필, 부틸, 비닐, 알릴, 클로로에틸, 플루오로에틸 및 치환된 벤질로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제12항에 있어서, 상기 R2는 할로치환된 벤질, (C1-C4)알킬치환된 벤질 및 트리할로치환된 벤질 및 시아노치환된 벤질로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제13항에 있어서, 상기 R2는 2-클로로벤질, 3-클로로벤질, 4-클로로벤질, 2-플루오로벤질, 3-플루오로벤질, 4-플루오로벤질, 2-시아노벤질, 3-시아노벤질, 4-시아노벤질 및 4-트리플루오로메틸벤질로부터 선택됨을 특징으로 하는 화합물.
- 농경학적으로 수용가능한 캐리어와 제1항의 화합물를 포함하고, 상기 혼합물에 대한 상기 화합물의 비가 99 : 1∼1 : 4인 식물 균을 방제하기 위한 살균 조성물.
- 제15항에 있어서, 상기 화합물에 대한 농학적으로 적합한 캐리어의 비는 10 : 1∼1:3임을 특징으로 하는 조성물.
- 제1항의 화합물을 헥타르당 0.005∼50kg의 비로 방제가 필요한 서식지에 적용함을 포함하는 식물 균방제 방법.
- 제17항에 있어서, 제1항의 화합물을 헥타르당 0.025∼10kg의 비로 사용함을 특징으로 하는 방법.
- 제1항에 화합물 헥타르당 0.005∼10kg의 비로 곤충의 거주지에 적용함을 포함하는 곤충 방제 방법.
- 제19항에 있어서, 상기 화합물을 헥타르당 0.01∼1kg의 비로 적용함을 특징으로 하는 방법.※ 참고사항 : 최초출원 내용에 의하여 공개되는 것임.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/426,514 | 1995-04-21 | ||
| US08/426,514 US5635494A (en) | 1995-04-21 | 1995-04-21 | Dihydropyridazinones and pyridazinones and their use as fungicides and insecticides |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| KR960037663A true KR960037663A (ko) | 1996-11-19 |
| KR100430695B1 KR100430695B1 (ko) | 2004-07-30 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019960011980A KR100430695B1 (ko) | 1995-04-21 | 1996-04-19 | 디하이드로피리다지논과피리다지논화합물,이를포함하는조성물및이를이용한균방제방법 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US5635494A (ko) |
| EP (1) | EP0738716A3 (ko) |
| JP (1) | JPH08291147A (ko) |
| KR (1) | KR100430695B1 (ko) |
| CN (1) | CN1124267C (ko) |
| AR (2) | AR001656A1 (ko) |
| AU (1) | AU713334B2 (ko) |
| BR (1) | BR9602004A (ko) |
| CA (1) | CA2174296A1 (ko) |
| CO (1) | CO4650121A1 (ko) |
| CZ (1) | CZ110696A3 (ko) |
| HU (1) | HUP9601035A3 (ko) |
| IL (1) | IL117865A0 (ko) |
| NZ (1) | NZ286342A (ko) |
| TR (1) | TR199600328A2 (ko) |
| TW (1) | TW499294B (ko) |
| ZA (1) | ZA963140B (ko) |
Families Citing this family (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL115889A0 (en) * | 1994-11-14 | 1996-01-31 | Rohm & Haas | Pyridazinones and their use as fungicides |
| US6121251A (en) * | 1996-10-11 | 2000-09-19 | Rohm And Haas Company | Dihydropyridazinones and pyridazinones and their use as fungicides and insecticides |
| CA2317778A1 (en) | 1999-09-29 | 2001-03-29 | Vivienne E. Harris | Synergistic insecticidal formulations of pyridaben and strobilurins |
| WO2001022817A1 (en) * | 1999-09-29 | 2001-04-05 | Basf Corporation | Pyridaben compounds for fungicidal uses |
| US6734143B2 (en) | 2000-09-19 | 2004-05-11 | Dow Agrosciences Llc | 2-methoxyimino-2(pyridinyloxymethyl)phenyl acetamides useful as fungicides |
| PT1928454E (pt) | 2005-05-10 | 2014-12-04 | Intermune Inc | Derivativos da piridona para modulação do sistema de proteína quinase ativada pelo stress |
| DE102006037478A1 (de) | 2006-08-10 | 2008-02-14 | Merck Patent Gmbh | 2-(Heterocyclylbenzyl)-pyridazinonderivate |
| DE102007025717A1 (de) | 2007-06-01 | 2008-12-11 | Merck Patent Gmbh | Arylether-pyridazinonderivate |
| DE102007025718A1 (de) | 2007-06-01 | 2008-12-04 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102007032507A1 (de) | 2007-07-12 | 2009-04-02 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102007038957A1 (de) | 2007-08-17 | 2009-02-19 | Merck Patent Gmbh | 6-Thioxo-pyridazinderivate |
| DE102007041115A1 (de) | 2007-08-30 | 2009-03-05 | Merck Patent Gmbh | Thiadiazinonderivate |
| DE102007061963A1 (de) * | 2007-12-21 | 2009-06-25 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102008019907A1 (de) | 2008-04-21 | 2009-10-22 | Merck Patent Gmbh | Pyridazinonderivate |
| JP5627574B2 (ja) | 2008-06-03 | 2014-11-19 | インターミューン， インコーポレイテッド | 炎症性および線維性疾患を治療するための化合物および方法 |
| DE102008062826A1 (de) | 2008-12-23 | 2010-07-01 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102009003954A1 (de) | 2009-01-07 | 2010-07-08 | Merck Patent Gmbh | Pyridazinonderivate |
| DE102009004061A1 (de) | 2009-01-08 | 2010-07-15 | Merck Patent Gmbh | Pyridazinonderivate |
| US8772290B2 (en) | 2010-04-21 | 2014-07-08 | Oscotech Inc. | Alpha-arylmethoxyacrylate derivative, preparation method thereof, and pharmaceutical composition containing same |
| WO2013097052A1 (en) | 2011-12-30 | 2013-07-04 | Abbott Laboratories | Bromodomain inhibitors |
| AR092742A1 (es) | 2012-10-02 | 2015-04-29 | Intermune Inc | Piridinonas antifibroticas |
| EP2958726B1 (en) | 2013-02-22 | 2019-07-10 | Velcro Bvba | Touch fastener structures |
| CN103951612A (zh) * | 2014-03-11 | 2014-07-30 | 浙江工业大学 | 一种肟醚乙酸酯类化合物及其制备方法与应用 |
| CA2943363A1 (en) | 2014-04-02 | 2015-10-08 | Intermune, Inc. | Anti-fibrotic pyridinones |
| RU2741808C2 (ru) | 2016-04-15 | 2021-01-28 | Эббви Инк. | Ингибиторы бромодомена |
| WO2023276813A1 (ja) * | 2021-06-28 | 2023-01-05 | 日本曹達株式会社 | ピリダジノン化合物並びに農園芸用殺菌剤、殺線虫剤、および医療用・動物用抗真菌剤 |
| CN118047724A (zh) * | 2022-11-17 | 2024-05-17 | 沈阳中化农药化工研发有限公司 | 一种哒嗪酮衍生物及其用途 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4052395A (en) * | 1975-09-11 | 1977-10-04 | Sankyo Company Limited | Agricultural fungicidal compositions containing 6-(substituted phenyl)-pyridazinones and said pyridazinones |
| JPS5826802A (ja) * | 1981-08-10 | 1983-02-17 | Sankyo Co Ltd | 農園芸用殺菌剤 |
| NZ213630A (en) * | 1984-10-19 | 1990-02-26 | Ici Plc | Acrylic acid derivatives and fungicidal compositions |
| DE3545319A1 (de) * | 1985-12-20 | 1987-06-25 | Basf Ag | Acrylsaeureester und fungizide, die diese verbindungen enthalten |
| GB8617648D0 (en) * | 1986-07-18 | 1986-08-28 | Ici Plc | Fungicides |
| DE3705389A1 (de) * | 1987-02-20 | 1988-09-01 | Basf Ag | Substituierte crotonsaeureester und diese enthaltende fungizide |
| EP0283271A3 (en) * | 1987-03-17 | 1990-04-25 | Ube Industries, Ltd. | Pyridazinone derivative, process for producing thereof and insecticide, acaricide and fungicide containing said derivative as active ingredient |
| DE3821503A1 (de) * | 1988-06-25 | 1989-12-28 | Basf Ag | (alpha)-aryl-acrylsaeureester und diese enthaltende fungizide |
| ATE169616T1 (de) * | 1988-11-21 | 1998-08-15 | Zeneca Ltd | Zwischenverbindungen zur herstellung von fungiziden |
| ES2097583T3 (es) * | 1989-05-17 | 1997-04-01 | Shionogi & Co | Procedimiento de preparacion de derivados de alcoxiiminoacetamida y un intermediario de este procedimiento. |
| ES2110421T5 (es) * | 1990-06-27 | 2004-12-01 | Basf Aktiengesellschaft | O-bencil-oximeteres y los agentes protectores de las plantas que contienen estos compuestos. |
| ES2131506T3 (es) * | 1990-09-21 | 1999-08-01 | Rohm & Haas | Dihidropiridacinonas y piridacinonas como fungicidas. |
| JPH06504538A (ja) * | 1991-01-30 | 1994-05-26 | ゼネカ・リミテッド | 殺菌剤 |
| DE4142191A1 (de) * | 1991-12-20 | 1993-06-24 | Bayer Ag | Verfahren zur herstellung von 3-alkoxy-acrylestern |
| DE4305502A1 (de) * | 1993-02-23 | 1994-08-25 | Basf Ag | Ortho-substituierte 2-Methoxyiminophenylessigsäuremethylamide |
-
1995
- 1995-04-21 US US08/426,514 patent/US5635494A/en not_active Expired - Fee Related
-
1996
- 1996-04-09 IL IL11786596A patent/IL117865A0/xx unknown
- 1996-04-09 AU AU50550/96A patent/AU713334B2/en not_active Ceased
- 1996-04-09 EP EP96302488A patent/EP0738716A3/en not_active Withdrawn
- 1996-04-10 NZ NZ286342A patent/NZ286342A/en unknown
- 1996-04-16 CA CA002174296A patent/CA2174296A1/en not_active Abandoned
- 1996-04-17 TW TW085104563A patent/TW499294B/zh not_active IP Right Cessation
- 1996-04-17 CZ CZ961106A patent/CZ110696A3/cs unknown
- 1996-04-18 AR AR33621296A patent/AR001656A1/es unknown
- 1996-04-19 TR TR96/00328A patent/TR199600328A2/xx unknown
- 1996-04-19 BR BR9602004A patent/BR9602004A/pt not_active Application Discontinuation
- 1996-04-19 AR AR33622896A patent/AR001667A1/es unknown
- 1996-04-19 JP JP8120852A patent/JPH08291147A/ja active Pending
- 1996-04-19 CO CO96019024A patent/CO4650121A1/es unknown
- 1996-04-19 HU HU9601035A patent/HUP9601035A3/hu unknown
- 1996-04-19 ZA ZA963140A patent/ZA963140B/xx unknown
- 1996-04-19 KR KR1019960011980A patent/KR100430695B1/ko not_active IP Right Cessation
- 1996-04-19 CN CN96104596A patent/CN1124267C/zh not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| NZ286342A (en) | 1998-04-27 |
| HU9601035D0 (en) | 1996-06-28 |
| CA2174296A1 (en) | 1996-10-22 |
| BR9602004A (pt) | 1998-04-07 |
| KR100430695B1 (ko) | 2004-07-30 |
| HUP9601035A3 (en) | 1999-04-28 |
| TW499294B (en) | 2002-08-21 |
| EP0738716A3 (en) | 1998-12-30 |
| CN1124267C (zh) | 2003-10-15 |
| IL117865A0 (en) | 1996-08-04 |
| HUP9601035A2 (en) | 1997-04-28 |
| AR001667A1 (es) | 1997-11-26 |
| AU5055096A (en) | 1996-10-31 |
| US5635494A (en) | 1997-06-03 |
| AR001656A1 (es) | 1997-11-26 |
| JPH08291147A (ja) | 1996-11-05 |
| EP0738716A2 (en) | 1996-10-23 |
| CZ110696A3 (en) | 1996-11-13 |
| AU713334B2 (en) | 1999-12-02 |
| CN1143637A (zh) | 1997-02-26 |
| TR199600328A2 (tr) | 1996-11-21 |
| CO4650121A1 (es) | 1998-09-03 |
| ZA963140B (en) | 1996-10-21 |
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