KR940007016A - 축합헤테로사이클 유도체 및 그것을 함유한 농업용 또는 원예용 살균제 - Google Patents
축합헤테로사이클 유도체 및 그것을 함유한 농업용 또는 원예용 살균제 Download PDFInfo
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- KR940007016A KR940007016A KR1019930017947A KR930017947A KR940007016A KR 940007016 A KR940007016 A KR 940007016A KR 1019930017947 A KR1019930017947 A KR 1019930017947A KR 930017947 A KR930017947 A KR 930017947A KR 940007016 A KR940007016 A KR 940007016A
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Abstract
본 발명은 하기 구조식으로 표시되는 축합헤테로싸이클 유도체
(상기 구조식에서 R1은 저급알킬기, 알케닐기등을 표시하고, R2, R3, R4, R5, 및 R6는 각각 수소원자, 저급알킬등을 표시하고, W는 -OC(O)-, -SC(O)-,등을 표시하고, Z는 2-인돌일기을 표시한다)를 제공하는 것이다. 또한 본 발명은 살균제로서 효과가 있는 것으로 알려진 축합유도체를 함유하는 농업용 및 원예용 살균제를 제공하는 것이다. 본 발명에 따른 농업용 또는 원예용 살균제를 비균, 광합성식물엔 해가 없이 노균병 및 잎마름병에 뛰어난 살균효과를 나타낸다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (8)
- 하기 구조식으로 표시되는 축합헤테로싸이클 유도체상기 구조식에서 R1은 할로겐원자, 시아노기, 및 메톡시기중에서 선택된 적어도 하나 이상의 치환기를 선택적으로 가진 C1∼C6알킬기, C2∼C6알케닐기, C2∼C6알키닐기 적어도 하나이상의 메틸기를 선택적으로 가진 C3∼C8 사이클로알케닐기, 적어도 하나이상의 메틸기를 선택적으로 가진 C2∼C6사이클릭에테르기, 메틸기, 메톡시기, 및 니트로기로 구성되는 기중에서 선택된 적어도 하나이상의 치환기를 선택적으로 가진 C7∼C10아랄킬기, 할로겐원자, 메틸기, 메톡시기, 니트로기, 및 메톡시카르보닐기중에서 선택된 적어도 하나이상의 치환기를 선택적으로 가진 페닐기, 디메틸아미노기 또는 에톡시 카르보닐기를 표시하고, R2, R3, R4, R5및 R6는 각각 수소원자, 적어도 하나이상의 할로겐기를 선택적으로 가진 C1-C6알킬기, C3-C6사이클로알킬기, C7-C10아랄킬기; 페닐기, 시아노기, 아실기, C1∼C6알콕시기, 또는 C1∼C6알콕시카르보닐기를 표시하고, R2는 R3와 함께 C3-C6알킬고리를 형성해도 되며, Z는 다음 구조식으로 표시된다;상기 구조식에서 X는 구조식에서 R1은 적어도 하나이상의 할로겐원자를 선택적으로 가진 C1∼C6알킬기, C2∼C6알키닐기, 메톡시기, 트리플루오로메톡시기, 하이드록실기, 메톡시카르보닐기, 메탈카르보닐옥시기, 아미노기, 디메틸아미노기, 니트로기, 메틸티오기, 메틸설피닐기, 메틸설포닐기, 페닐기, 아세틸기, 포르밀기, 또는 시아노기를 표시하고, n은 1,2 또는 3의 정수이고; A는 O,S,N, 또는 다음 구조식으로 표시되고,상기 구조식에서, R7은 수소원자, 메틸기, 아세틸기 또는 벤조일기를 나타내며; W는 -C(0)-, -SO2-, -NHC(O)-, -N(CH3)C(O)-, -OC(O)-, -SC(O)-, -OC(S)- 또는 -SC(S)-를 표시한다.
- 제1항에 있어서, 상기 구조식에서 R1은 C2∼C6 곧거나 또는 분기된 알킬기, C3 곧거나 또는 분기된 알케닐기, C5-C6사이클로알키기, 또는 페닐기를 표시하고, R2는 수소원자를 표시하고, R3는 에틸기, 이소프로필기, 또는 sec-부틸기를 표시하고, R4는 수소원자, 메틸기, 에틸기, 또는 페닐기를 표시하고, R5는 수소원자, 또는 메틸기를 표시하고, R6는 수소원자를 표시하고, Z는 벤조퓨란기, 벤조티오펜기, 인돌기, 또는 2,3-디하이드로벤조퓨란기등의 치환된 헤테로사이클기를 표시하며, 상기 2,3-디하이드로벤조퓨란은 플로우드 원자, 클로로원자, 니트로원자, 시아노기, 및 메틸기등 중에서 선택된 하나 또는 두개의 치환기를 가지는 것이며, W는 -OC(O)-를 표시하며 아미노산이 L-이성체인 것을 특징으로 하는 축합헤테로사이클 유도체.
- 제1항에 있어서, 상기 구조식에서 R1은 이소프로필기 tert-부틸기, sec-부틸기, 사이클로펜틸기, 이소프로페닐기, 또는 페닐기를 표시하고, R2는 수소원자를 표시하고, R3는 에틸기, 이소프로필기, 또는 sec-부틸기를 표시하고, R4는 메틸기를 표시하고, R6는 수소원자를 표시하고, R6는 수소원자를 표시하고, Z는 벤조퓨란기 또는 벤조티오펜기등의 치환 헤테로사이클로를 표시하고, 상기 벤조티오펜기는 플루오르원소, 클로로원소, 니트로기, 시아노기 및 메틸기로 구성된 기에서 선택된 하나 또는 두개의 치환기를 가지며, W는 -OC(CO)-를 표시하며, 아미노산은 L-이성체인 것을 특징으로 하는 축합헤테로싸이클 유도체.
- 제1항에 있어서, 상기 유도체에 N1-[1-(5-클로로-2-벤조프라닐)에틸]-N2-사이클로펜틸톡시카르보닐-L-발린아마이드, N1-[1-(5-클로로-2-벤조프라닐)에틸-N2-이소프로필옥시카르보닐-L-발린아마이드, N1-[1-(5-클로로-2-벤조프라닐)에틸]-N2-이소프로필옥시카르보닐-L-발린아마이드, N2-이소프로필옥시카르보닐-N1-[1-(5-니트로-2-벤조(퓨라닐)에틸]-L-빌린아마이드, N1-[1-(5-플루오르-2-벤조[b]티에닐)에틸]-N2-이소프로필옥시카르보닐-L-발린아마니드, N1-[1-(6-플루오르-2-벤조[b]테이닐)에틸]-N2-이소프로필옥시카르보닐-L-발린아마이드 또는 N1-[1-(5-클로로-2-벤조퓨라닐)에틸]-L-발린아마이드 N2-sec-부틸시카르보닐-N′-[1-(5-클로로-2-벤조프라닐)에틸]-L-발란아마이드 또는 N1-[1-(5-클로로-2-벤조퓨라닐)에틸]-N2-페녹시카르보닐-L-발란아마이드를 포함하는 것을 특징으로 하는 축합헤테로싸이클 유도체.
- 하기 구조식으로 표시되는 축합헤테로싸이클 유도체의 제조방법에 있어서,(상기 구조식에서, R1, R2, R3, R4, R5, R6, W 및 Z는 제1항에 정의된 것과 동일함) 하기 구조식으로 표시되는 아미노산 유도체.(상기에서, R1, R2, R3, 및 W는 제1항에서와 동일함)를 반응시키거나 또는 다음 구조식로 표시되는 아민유도체.(상기에서, R4, R5, R6및 Z는 제1항에서 정의된 것과 동일함)의 동량이상으로 활성화 되는 아미노산 유도체와 반응시키는 단계로 구성된 것을 특징으로 축합헤테로싸이클 유도체의 제조방법.
- 하기 구조식으로 표시되는 축합헤테로싸이클 유도체의 제조방법에 있어서,(상기 구조식에서, R1, R2, R3, R4, R5, R6, W 및 Z는 제1항에 정의된 것과 동일함) 하기 구조식으로 표시되는 아민유도체.(상기 구조식에서 R1, R2, R3, R4, R5, R6, W 및 Z는 제1항에 정의된 것과 동일함)와 반응시키거나, 또는 하기구조식으로 표시되는R1-W-Y(상기에서 R1및 W는 제1항에서 정의된 것과 동일하며, Y는 할로겐원자, 또는 R1OC(O)O-또는 R1C(O)O-로 표시됨)화합물의 동량이상으로 가지며 비유기산 또는 유기산을 가진 아민유도체의 염과 반응시키는 단계로 구성된 것을 특징으로 하는 축합헤테로싸이클 유도체 제조방법.
- 살균제 및 희석제로서의 효과를 가진 제1항에서 설명된 축합헤테로싸이클 유도체의 효과량을 함유하는 것을 특징으로 하는 농업용 또는 원예용 살균제.
- 식물에 대해 살균제로서의 효과를 가진 제1항에서 설명된 축합헤테로싸이클 유도체의 효과량을 투여하는 단계로 구성된 것을 특징으로 하는 농업 또는 원예의 비균 및 광합성식물에 해를 끼치는 균의 예방방법.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
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JP26271892 | 1992-09-07 | ||
JP92-262718 | 1992-09-07 | ||
JP3111793 | 1993-01-28 | ||
JP93-031117 | 1993-01-28 | ||
JP93-208258 | 1993-07-30 | ||
JP20825893A JP3283114B2 (ja) | 1992-09-07 | 1993-07-30 | 縮合ヘテロ環誘導体及び農園芸用殺菌剤 |
Publications (2)
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KR940007016A true KR940007016A (ko) | 1994-04-26 |
KR0139185B1 KR0139185B1 (ko) | 1998-05-15 |
Family
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KR1019930017947A KR0139185B1 (ko) | 1992-09-07 | 1993-09-07 | 축합 헤테로 고리형 유도체, 이의 제조방법 및 이를 함유한 농원예용 살균제 |
Country Status (7)
Country | Link |
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US (1) | US5348976A (ko) |
EP (1) | EP0587110B1 (ko) |
JP (1) | JP3283114B2 (ko) |
KR (1) | KR0139185B1 (ko) |
CN (3) | CN1036195C (ko) |
DE (1) | DE69315774T2 (ko) |
RU (1) | RU2098408C1 (ko) |
Families Citing this family (18)
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FR2701480B1 (fr) * | 1993-02-15 | 1995-05-24 | Sanofi Elf | Composés à groupe sulfamoyle et amidino, leur procédé de préparation et les compositions pharmaceutiques les contenant. |
DE69406083T2 (de) * | 1993-04-28 | 1998-02-26 | Ihara Chemical Ind Co | Aminosäureamide, bakterizide für gartenbau und landwirtschaft sowie herstellungverfahren |
HU223083B1 (hu) * | 1994-06-28 | 2004-03-29 | Bayer Ag. | Fungicid hatású aminosavszármazékok, eljárás előállításukra és alkalmazásuk |
DE19501175A1 (de) * | 1994-06-28 | 1996-01-04 | Bayer Ag | Aminosäure-Derivate |
US5554641A (en) * | 1995-03-20 | 1996-09-10 | Horwell; David C. | Nonpeptides as tachykinin antagonists |
US6034256A (en) * | 1997-04-21 | 2000-03-07 | G.D. Searle & Co. | Substituted benzopyran derivatives for the treatment of inflammation |
US6077850A (en) | 1997-04-21 | 2000-06-20 | G.D. Searle & Co. | Substituted benzopyran analogs for the treatment of inflammation |
GB9723407D0 (en) | 1997-11-05 | 1998-01-07 | Ciba Geigy Ag | Organic compounds |
US6395897B1 (en) | 1999-03-02 | 2002-05-28 | Boehringer Ingelheim Pharmaceuticals, Inc. | Nitrile compounds useful as reversible inhibitors of #9 cathepsin 5 |
EP1452522A3 (en) * | 1999-03-15 | 2005-02-09 | Axys Pharmaceuticals, Inc. | Novel compounds and compositions as protease inhibitors |
US6420364B1 (en) | 1999-09-13 | 2002-07-16 | Boehringer Ingelheim Pharmaceuticals, Inc. | Compound useful as reversible inhibitors of cysteine proteases |
GB0003111D0 (en) | 2000-02-10 | 2000-03-29 | Novartis Ag | Organic compounds |
US20050261347A1 (en) * | 2003-10-24 | 2005-11-24 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
US7435837B2 (en) * | 2003-10-24 | 2008-10-14 | Wyeth | Dihydrobenzofuranyl alkanamine derivatives and methods for using same |
AR056320A1 (es) * | 2005-04-22 | 2007-10-03 | Wyeth Corp | Derivados de cromano y cromeno, procesos de obtencion, composiciones farmaceuticas y usos de los mismos |
CN102452959A (zh) * | 2010-10-20 | 2012-05-16 | 中国农业科学院植物保护研究所 | 取代的缬氨酰胺衍生物及其制备 |
CN105037208B (zh) * | 2015-06-18 | 2017-06-06 | 南开大学 | 一种n‑(1‑甲基‑2‑取代乙基)缬氨酰胺氨基甲酸酯衍生物及应用 |
CN105037207B (zh) * | 2015-06-18 | 2017-05-17 | 南开大学 | 一种(异)亮氨酰胺氨基甲酸酯衍生物及应用 |
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DE3410925A1 (de) * | 1984-03-24 | 1985-10-03 | Basf Ag, 6700 Ludwigshafen | N-((2,3-dihydrobenzofuran)-2-yl)-azolylharnstoffe und diese enthaltende fungizide |
JPS6145A (ja) * | 1984-06-09 | 1986-01-06 | Kaken Pharmaceut Co Ltd | N‐(4‐tert‐ブチルベンジル)‐N‐メチル‐1‐ナフチルメチルアミンおよびそれを有効成分とする抗真菌剤 |
CH672311A5 (ko) * | 1985-09-14 | 1989-11-15 | Sandoz Ag | |
DE3915755A1 (de) * | 1989-05-13 | 1990-11-29 | Bayer Ag | Fungizide mittel sowie substituierte aminosaeureamid-derivate und deren herstellung |
DE3936298A1 (de) * | 1989-11-01 | 1991-05-02 | Bayer Ag | Substituierte aminosaeureamid-derivate deren herstellung und verwendung |
DE4029472C1 (ko) * | 1990-09-17 | 1991-10-24 | Schuetz-Werke Gmbh & Co Kg, 5418 Selters, De | |
DE4030062A1 (de) * | 1990-09-22 | 1992-03-26 | Bayer Ag | Substituierte aminosaeureamid-derivate deren herstellung und verwendung |
EP0493683A1 (en) * | 1990-12-20 | 1992-07-08 | American Cyanamid Company | Fungicidal amino acid amides |
US5134140A (en) * | 1991-06-21 | 1992-07-28 | American Home Products Corporation | Psychotropic benzofuran derivatives |
-
1993
- 1993-07-30 JP JP20825893A patent/JP3283114B2/ja not_active Expired - Fee Related
- 1993-09-06 RU RU9393051174A patent/RU2098408C1/ru not_active IP Right Cessation
- 1993-09-07 DE DE69315774T patent/DE69315774T2/de not_active Expired - Fee Related
- 1993-09-07 CN CN93119072A patent/CN1036195C/zh not_active Expired - Fee Related
- 1993-09-07 US US08/117,284 patent/US5348976A/en not_active Expired - Lifetime
- 1993-09-07 EP EP93114325A patent/EP0587110B1/en not_active Expired - Lifetime
- 1993-09-07 KR KR1019930017947A patent/KR0139185B1/ko not_active IP Right Cessation
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1996
- 1996-07-30 CN CN96111473A patent/CN1062264C/zh not_active Expired - Fee Related
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Also Published As
Publication number | Publication date |
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DE69315774D1 (de) | 1998-01-29 |
EP0587110A3 (en) | 1994-05-25 |
CN1149054A (zh) | 1997-05-07 |
CN1062270C (zh) | 2001-02-21 |
EP0587110B1 (en) | 1997-12-17 |
CN1036195C (zh) | 1997-10-22 |
US5348976A (en) | 1994-09-20 |
DE69315774T2 (de) | 1998-05-07 |
JPH06279405A (ja) | 1994-10-04 |
EP0587110A2 (en) | 1994-03-16 |
CN1086810A (zh) | 1994-05-18 |
CN1062264C (zh) | 2001-02-21 |
KR0139185B1 (ko) | 1998-05-15 |
JP3283114B2 (ja) | 2002-05-20 |
CN1154964A (zh) | 1997-07-23 |
RU2098408C1 (ru) | 1997-12-10 |
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