KR980002028A - 벤질옥시 치환된 방향족 화합물 및 이를 이용한 균류 및 곤충제어방법 - Google Patents
벤질옥시 치환된 방향족 화합물 및 이를 이용한 균류 및 곤충제어방법 Download PDFInfo
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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- C07D261/08—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more 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
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- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- 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
- C07D409/04—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 directly linked by a ring-member-to-ring-member bond
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- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
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Abstract
하기 화학식(Ⅰ)의 살균성 및 살충성을 갖는 화합물.
단, 상기식에서 A는 N 혹은 CH ; V는 O 혹은 NH이며 ; m과 n은 m+n이 2가 되지 않도록 독립적으로 0 및 1이고 U 및 W는 독립적으로 O 혹은 N이며, U와 W가 모두 N인이고 n은 0, m은 1인 경우, 상기 1번째 원자와 5번째 원자사이의 결합은 이중결합이고 C3-C4원자사이의 결합은 단일 혹은 이중결합이며, n이 1이고 m이 0인 경우, 2번째와 3번째 원자 사이의 결합은 이중결합이며, C4-C5원자사이의 결합은 단일 혹은 이중결합이며 ; U는 O이고 W는 N이며, n=m=0인 경우, 1번째와 5번째 원자사이의 결합은 이중결합이고 C3-C4사이의 결합은 단일 혹은 이중결합이며; U는 N이고 W는 0, n=m=0인 경우, 2번째 원자와 3번째 원자사이의 결합은 이중결합이고 C4-C5사이의 결합은 단일 혹은 이중결합이며 ; X는 수소, 할로, (C1-C4)알킬 및 (C1-C4)알콕시로부터 독립적으로 선택되며 ; R은 수소, (C1-C12)알킬, 할로(C1-C12)알킬, (C2-C8)알케닐, (C2-C8)알키닐, (C1-C12)알콕시(C1-C12)알킬, (C3-C7)시클로알킬, (C3-C7)시클로알킬(C1-C4)알킬, 아릴, 아랄킬, 헤테로고리로부터 독립적으로 선택되며 ; R1은 수소, (C1-C8)알킬 및 아릴로부터 독립적으로 선택되고 ; Z는 (C1-C6)알킬, 할로(C1-C6)알킬, (C3-C7)시클로알킬, (C3-C7)시클로알킬(C1-C4)알킬, 아릴, 아랄킬로부터 선택된다.
Description
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Claims (20)
- 하기 화학식(Ⅰ)의 구조를 갖는 화합물.단, 상기식에서 A는 N 혹은 CH ; V는 O 혹은 NH이며 ; m과 n은 m+n이 2가 되지 않도록 독립적으로 0 및 1이고 U 및 W는 독립적으로 O 혹은 N이며, U와 W가 모두 N인이고 n은 0, m은 1인 경우, 상기 1번째 원자와 5번째 원자사이의 결합은 이중결합이고 C3-C4원자사이의 결합은 단일 혹은 이중결합이며, n이 1이고 m이 0인 경우, 2번째와 3번째 원자 사이의 결합은 이중결합이며, C4-C5원자사이의 결합은 단일 혹은 이중결합이며 ; U는 O이고 W는 N이며, n=m=0인 경우, 1번째와 5번째 원자사이의 결합은 이중결합이고 C3-C4사이의 결합은 단일 혹은 이중결합이며;U는 N이고 W는 0, n=m=0인 경우, 2번째 원자와 3번째 원자사이의 결합은 이중결합이고 C4-C5사이의 결합은 단일 혹은 이중결합이며 ; X는 수소, 할로, (C1-C4)알킬 및 (C1-C4)알콕시로부터 독립적으로 선택되며 ; R은 수소, (C1-C12)알킬, 할로(C1-C12)알킬, (C2-C8)알케닐, (C2-C8)알키닐, (C1-C12)알콕시(C1-C12)알킬, (C3-C7)시클로알킬, (C3-C7)시클로알킬(C1-C4)알킬, 아릴, 아랄킬, 헤테로고리로부터 독립적으로 선택되며 ; R1은 수소, (C1-C8)알킬 및 아릴로부터 독립적으로 선택되고 ; Z는 (C1-C6)알킬, 할로(C1-C6)알킬, (C3-C7)시클로알킬, (C3-C7)시클로알킬(C1-C4)알킬, 아릴, 아랄킬로부터 선택된다.
- 제1항에 있어서, 상기 A는 CH임을 특징으로 하는 화합물.
- 제1항에 있어서, 상기 A는 N임을 특징으로 하는 화합물.
- 제2항에 있어서, 상기 V는 0임을 특징으로 하는 화합물.
- 제3항에 있어서, 상기 V는 0, NH임을 특징으로 하는 화합물.
- 제4항에 있어서, 상기 부분은의 메타위치에 결합되며, R은 (C1-C12)알킬, 할로(C1-C12)알킬, 모노할로치환된 페닐, (C1-C4)알킬 치환된 페닐 및 트리할로치환된 페닐로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제6항에 있어서, U 및 W는 N이고 R1은 H, n=1, m=0이며 2번째 원자와 3번째 원자 사이의 결합은 이중 결합임을 특징으로 하는 화합물.
- 제7항에 있어서, Z는 (C1-C6)알킬, 페닐, 3-할로페닐, 4-할로페닐 및 4-(C1-C4)알킬페닐로부터 선택됨을 특징으로 하는 화합물.
- 제8항에 있어서, R은 (C1-C4)알킬, 할로(C1-C4)알킬, 페닐, 2-할로페닐, 3-할로페닐, 4-할로페닐, 2-(C1-C4)알킬페닐, 3-(C1-C4)알킬페닐 및 4-(C1-C4)알킬페닐로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제9항에 있어서, R은 2-플루오로페닐, 3-플루오로페닐 및 4-플루오로페닐로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제5항에 있어서, 상기 부분은에 대하여 메타위치이며, R은 (C1-C12)알킬, 할로(C1-C12)알킬, 모노할로치환된 페닐, (C1-C4)알킬 치환된 페닐 및 트리할로치환된 페닐로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제11항에 있어서, 상기 U 및 W는 N이고 R1은 H, n=1, m=0이며 2번째 원자와 3번째 원자 사이의 결합은 이중 결합임을 특징으로 하는 화합물.
- 제12항에 있어서, Z는 (C1-C6)알킬, 페닐, 3-할로페닐, 4-할로페닐 및 4-(C1-C4)알킬페닐로부터 선택됨을 특징으로 하는 화합물.
- 제13항에 있어서, R은 (C1-C4)알킬, 할로(C1-C4)알킬, 2-할로페닐, 3-할로페닐, 4-할로페닐, 2-(C1-C4)알킬페닐, 3-(C1-C4)알킬페닐 및 4-(C1-C4)알킬페닐로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 제14항에 있어서, R은 2-플루오로페닐, 3-플루오로페닐 및 4-플루오로페닐로 구성되는 그룹으로부터 선택됨을 특징으로 하는 화합물.
- 농경학적으로 수용가능한 캐리어와 청구범위 제1항의 화합물을 캐리어 대 화합물 99:1~1:4 중량비로 포함하는 식물성 병원(phytophathogenic)균류 제어용 살균조성물.
- 제16항에 있어서, 상기 농경학적으로 수용가능한 캐리어 대 화합물의 중량비는 10:1~1:3임을 특징으로 하는 조성물.
- 종자 서식처, 식물 혹은 토양에 청구범위 제1항의 화합물을 1ha당 0.005~50kg으로 적용함을 포함하는 식물성 병원(phytophathogenic)균류 제어방법.
- 제18항에 있어서, 상기 청구범위 제1항의 화합물을 1ha당 0.025~10kg으로 적용함을 특징으로 하는 방법.
- 청구범위 제1항의 화합물을 1ha당 0.005~10kg의 비율로 적용함을 포함하는 곤충 제어방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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US1919796P | 1996-06-06 | 1996-06-06 | |
US60/019,197 | 1996-06-06 |
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FR2773155B1 (fr) * | 1997-12-29 | 2000-01-28 | Rhone Poulenc Agrochimie | Nouveaux composes fongicides |
WO1999046246A1 (de) * | 1998-03-09 | 1999-09-16 | Basf Aktiengesellschaft | Hetarylsubstituierte benzylphenylether, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen und tierischen schädlingen |
US6734143B2 (en) | 2000-09-19 | 2004-05-11 | Dow Agrosciences Llc | 2-methoxyimino-2(pyridinyloxymethyl)phenyl acetamides useful as fungicides |
CN1305858C (zh) * | 2004-02-20 | 2007-03-21 | 沈阳化工研究院 | 取代唑类化合物及其制备与应用 |
CN100427481C (zh) | 2005-05-26 | 2008-10-22 | 沈阳化工研究院 | 一种芳基醚类化合物及其制备与应用 |
CN101119972B (zh) * | 2005-05-26 | 2011-04-13 | 中国中化集团公司 | 一种芳基醚类化合物及其制备与应用 |
TW200803740A (en) | 2005-12-16 | 2008-01-16 | Du Pont | 5-aryl isoxazolines for controlling invertebrate pests |
TWI412322B (zh) | 2005-12-30 | 2013-10-21 | Du Pont | 控制無脊椎害蟲之異唑啉 |
JP2008044880A (ja) * | 2006-08-15 | 2008-02-28 | Bayer Cropscience Ag | 殺虫性イソオキサゾリン類 |
ES2445651T3 (es) | 2007-06-13 | 2014-03-04 | E. I. Du Pont De Nemours And Company | Insecticidas de isoxazolina |
TWI430995B (zh) | 2007-06-26 | 2014-03-21 | Du Pont | 萘異唑啉無脊椎有害動物控制劑 |
ES2666187T3 (es) | 2007-06-27 | 2018-05-03 | E. I. Du Pont De Nemours And Company | Procedimiento de control de plagas en animales |
TWI461411B (zh) | 2007-08-17 | 2014-11-21 | Du Pont | 製備5-鹵烷基-4,5-二氫異唑衍生物之方法 |
JP5676262B2 (ja) | 2007-10-03 | 2015-02-25 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | 有害無脊椎生物の防除用ナフタレンイソキサゾリン化合物 |
TW201444787A (zh) | 2008-04-09 | 2014-12-01 | Du Pont | 製備3-三氟甲基查耳酮(chalcone)之方法 |
MY156670A (en) | 2010-05-27 | 2016-03-15 | Du Pont | Crystalline form of 4-[5-[3-chloro-5-(trifluoromethly)phenyl]-4,5-dihydro-5-(trifluoromethyl)-3-isoxazolyl]-n-[2-oxo-2-[(2,2,2-trifluoroethyl) amino]ethyl]-1-naphthalenecarboxamide |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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DE3875748T3 (de) * | 1987-02-09 | 2000-08-31 | Zeneca Ltd., London | Fungizide |
EP0335519A1 (en) * | 1988-03-31 | 1989-10-04 | Imperial Chemical Industries Plc | Insecticides |
US5185342A (en) * | 1989-05-17 | 1993-02-09 | Shionogi Seiyaku Kabushiki Kaisha | Alkoxyiminoacetamide derivatives and their use as fungicides |
DE4028391A1 (de) * | 1990-09-07 | 1992-03-12 | Basf Ag | (alpha)-arylacrylsaeurederivate, ihre herstellung und verwendung zur bekaempfung von schaedlingen und pilzen |
-
1997
- 1997-05-26 AU AU23609/97A patent/AU726670B2/en not_active Ceased
- 1997-05-26 AR ARP970102234A patent/AR007292A1/es unknown
- 1997-05-26 CA CA002206151A patent/CA2206151A1/en not_active Abandoned
- 1997-05-27 IL IL12091798A patent/IL120918A0/xx unknown
- 1997-05-29 MX MX9703980A patent/MX9703980A/es not_active IP Right Cessation
- 1997-05-30 ZA ZA9704771A patent/ZA974771B/xx unknown
- 1997-06-02 CZ CZ971697A patent/CZ169797A3/cs unknown
- 1997-06-03 AT AT97303765T patent/ATE224876T1/de not_active IP Right Cessation
- 1997-06-03 EP EP97303765A patent/EP0811614B1/en not_active Expired - Lifetime
- 1997-06-03 DE DE69715731T patent/DE69715731T2/de not_active Expired - Fee Related
- 1997-06-04 KR KR1019970023114A patent/KR100481810B1/ko not_active IP Right Cessation
- 1997-06-04 CO CO97030878A patent/CO4560333A1/es unknown
- 1997-06-04 TW TW086107658A patent/TW367224B/zh active
- 1997-06-05 JP JP9163351A patent/JPH1059944A/ja active Pending
- 1997-06-05 HU HU9701004A patent/HUP9701004A3/hu unknown
- 1997-06-05 TR TR97/00467A patent/TR199700467A2/xx unknown
- 1997-06-05 CN CN97112133A patent/CN1100761C/zh not_active Expired - Fee Related
- 1997-06-06 ID IDP971932A patent/ID17441A/id unknown
- 1997-06-06 BR BR9703487A patent/BR9703487A/pt not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
AU2360997A (en) | 1997-12-11 |
KR100481810B1 (ko) | 2005-09-20 |
TW367224B (en) | 1999-08-21 |
ID17441A (id) | 1997-12-24 |
ATE224876T1 (de) | 2002-10-15 |
DE69715731D1 (de) | 2002-10-31 |
AR007292A1 (es) | 1999-10-27 |
CN1100761C (zh) | 2003-02-05 |
CO4560333A1 (es) | 1998-02-10 |
EP0811614A1 (en) | 1997-12-10 |
JPH1059944A (ja) | 1998-03-03 |
IL120918A0 (en) | 1997-09-30 |
CN1175575A (zh) | 1998-03-11 |
HU9701004D0 (en) | 1997-07-28 |
DE69715731T2 (de) | 2003-02-06 |
AU726670B2 (en) | 2000-11-16 |
HUP9701004A2 (hu) | 1998-06-29 |
BR9703487A (pt) | 1999-01-05 |
CZ169797A3 (cs) | 1998-04-15 |
HUP9701004A3 (en) | 1999-03-01 |
ZA974771B (en) | 1997-12-08 |
EP0811614B1 (en) | 2002-09-25 |
MX9703980A (es) | 1997-12-31 |
TR199700467A2 (xx) | 1997-12-21 |
CA2206151A1 (en) | 1997-12-06 |
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