KR920000709A - O-벤질옥심 에테르 및 그를 함유하는 농작물 보호제 - Google Patents

O-벤질옥심 에테르 및 그를 함유하는 농작물 보호제 Download PDF

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KR920000709A
KR920000709A KR1019910010704A KR910010704A KR920000709A KR 920000709 A KR920000709 A KR 920000709A KR 1019910010704 A KR1019910010704 A KR 1019910010704A KR 910010704 A KR910010704 A KR 910010704A KR 920000709 A KR920000709 A KR 920000709A
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substituted
unsubstituted
alkyl
same
alkoxy
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KR1019910010704A
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KR100200466B1 (ko
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브란트 지그베르트
카르도르프 우베
키르스트겐 라인하르트
무엘러 베른트
오베르도르프 클라우스
사우터 후베르트
로렌쯔 기젤라
암메르만 에베르하르트
쿠에나스트 크리스토프
하르로이스 알브레크트
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바르쯔, 비텐베르그
바스프 악티엔게젤샤프트
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Priority claimed from DE4020388A external-priority patent/DE4020388A1/de
Priority claimed from DE4020384A external-priority patent/DE4020384A1/de
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  • Pest Control & Pesticides (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pyrane Compounds (AREA)
  • Indole Compounds (AREA)
  • Polyesters Or Polycarbonates (AREA)

Abstract

내용 없음

Description

0-벤질옥심 에테르 및 그를 함유하는 농작물 보호제
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음

Claims (8)

  1. 하기 일반식(I)의 O-벤질옥심 에테르.
    상기 식 중, X는 CH2, CH-Cl-C4-알킬. CH-Cl-C4-알록시. CH-C1-C4-알킬티오 또는 N-Cl-C4-알콕시기이고, Y는 0, 5또는 NR5이고, R1R2및 R5는 각각 H또는 Cl-C4-알킬기이고, Z1및 Z2는 동일 또는 상이한 것으로서, 각각 H, 할로겐, 메틸, 메톡시 또는 시아노기이고, R3및 R4는 동일 또는 상이한 것으로서,각각 수소, 시아노, 직쇄 또는 분지쇄형의 Cl-Cl0-알킬, Cl-C4-할로알킬, C3-C6-시클로알킬, C3-C6-할로시클로알릴, C3-C6-시클로알킬-Cl-C4-알킬, Cl-C4-알콕시-Cl-C4-알킬, Cl-C4-알킬티오-C1-C4-알킬, 아릴티오-Cl-C4-알킬, C2-C6-알케닐, C3-C6-할로알케닐, C3-C6-시클로알케닐, C1-C4할로시클로알케닐, C2-C6-알키닐, Cl-C6-알콕시, Cl-C6-할로알콕시, Cl-C4-알킬티오, 벤질티오-알킬카르카닐, 치환되거나 비치환된 궤닐카르보닐, 치환되거나 비치환된 벤질카르보닐, Cl-C4-알콕시카르보닐, 치환되거나 비치환된 페녹시카르보닐, 치환되거나 비치환된 벤질옥시카르보닐, 치환되거나 비치환된 아릴, 치환되거나 비치환된 아릴옥시, 치환되거나 비치환된 아릴티오, 치환되거나 비치환된 아릴-Cl-C4-알킬, 치환되거나, 비치환된 아릴-C1-C4-알케닐, 치환되거나 비치환된 아릴옥시-Cl-C4-알킬, 치환되거나 비치환된 아릴티오-Cl-C4-알킬, 치환되거나 비치환된 헤트아릴, 치환되거나 비치환된 혜트아릴옥시, 치환되거나, 비치환된 헤트아릴티오, 치환되거나 비치환된 헤테로아릴-Cl-C4-알킬, 치환되거나 비치환된 헤트아릴 -C1-C4-알케닐, 치환되거나 비치환된 헤트아릴옥시 -Cl-C4-알킬, 치환되거나 비치환된 혜테로시클릴.치환되거나 비치환된 헤테로시클릴옥시, N(R6)2(여기서, R6은 동일 또는 상이란 것으로서, 각각 H C1-C6-알킬또는 치환되거나 비치환된 페닐기 임) 또는 -C0-N (R7)2, (여기서, R7은 동일 또는 상이한 것으로서, 각각 H 또는Cl-C4-알킬임)이고, 치환되거나 비치환됨이 의미하는 치환기는 수소외에 할로겐. 시아노, 니트로, C1-C4-알킬, C1-C4-알콕시, C1-C4-할로알힐, C1-C4-할로알콕시, Cl-C10-알콕시미노-Cl-C2-알킬. 아릴,아릴옥시, 벤질옥시, 헤트아릴, 헤트아릴옥시, C3-C6-시플로알킬, 헤테로시클릴 또는 헤테로시클릴옥시기이며, R3및 R5는 함게, 상기 치환기에 의해 치환될 수 있는 카르보시클릭 또는 헤테로시를릭 고리를 형성할 수 있고, R3또는 R4가 할로겐이거나, 또는
    (식 중, n은 1 내지 4의 정수이고, R8또는, n〉1일 경우 R8들은 동일 또는 상이한 것으로서, 각각 H 할로겐,시아노, 니트로, 치환되거나 비치환된 Cl-C4-알킬, Cl-C4-알콕시, Cl-C4-할로알킬, Cl-C4-할로알콕시, 아릴, 아릴옥시, 벤질옥시, 헤트아릴 또는 헤트아릴옥시기임)일 수 있다.
  2. 하기 일반식 (Ⅱ)의 0-벤질옥심 에테르.
    상기 식 중 R3내지 R6기는 제1항에 정의한 바와 동일하다.
  3. 하기 일박식(Ⅲ)의 0-벤질옥심 에테르.
    상기식중 R3내지 R8기는 제1항에서 정의한 바와 동일하다.
  4. 1항에 있어서, X는NOCH3또는NOC2H5이고, Y는0이고, R1은C1-C4-알킬기이고, R3는H또는C1-C2-알킬기이고, R3및 R5는 동일 또는 상이한 것으로서 각각수소, 시아노, 직쇄 또는 분지쇄형의 Cl-C10-알킬 Cl-C4-할로알킬, C3-C6-시클로알킬, C3-C6-할로시클로알킬, C3-C6-시클로알킬-Cl-C4-알킬, C1-C4-알콕시 -Cl-C4-알킬, C1-C6-알킬티오-Cl-C4-알킬, 아릴티오-C1-C6-알킬, C2-C6-알케닐, C2-C5-알키닐, C2-C4-할로알케닐, Cl-C6-알콕시, Cl-C6-알킬티오, Cl-C4-알킬카르보닐, Cl-C4-알콕시카르보닐, 치환되거나 비치환된 아릴,, 치환되거나 비치환된 아릴옥시, 치환되거나, 비치환된 아릴티오 치환되거나, 비치환된 아릴-C1-C4-알킬, 치환되거나 비치환된 아릴-C2-C4-알케닐, 치환되거나 비치환된 헤트아릴, 치환되거나 비치환된 헤트아릴옥시, 치환되거나, 비치환된 헤트아릴티오, 치환되거나 비치환된 헤테로시클릴, N(R6)2(여기서, R6은 동일 또는 상이한 것으로서, 각각 H, C1-C6-알킬 C3-C6-시클로알킬 또는 치환되거나 비치환된 페닐임) , -CO-N (R7)2(여기서, R7은 동일 또는 상이한 것으로서, 각각 H또는 C1-C4-알킬임) 이고, 치환되거나 비치환됨이 의미하는 치환기는 제 1항에서 기재한 바와 동일하고, R3및 R4는 함께 상기치환되거나 비치환됨이 외미하는 치환기에 의해 치환될 수 있는 카르보시클릭 또는 헤테로시클릭기를 형성하거나, R3또는 R4가 할로겐일 수 있으며, Z1및 Z2는 각각 수소인 것을 특징으로 하는 화합물
  5. 불활성 담체 및 살진균 유효량의 하기 일반식(I)의 0-벤질옥심 에테르를 함유하는 살진균제.
    상기 식에서, X는 CH2, CH-C1-C4-알킬, CH-Cl-C4-알콕시, CH-Cl-C4-알킬티오 또는 N-Cl-C4-알콕시기이고, Y는 0, S 또는 NR5이고, R1,R2및 R5는 각각 H또는 Cl-C4-알킬기이고, Z1및 Z2는 동일 또는 상이한 것으로서, 각각 H 할로겐, 메틸, 메톡시 또는 시아노기이고, R3및 R4는 동일 또는 상이한 것으로서, 각각 수소. 시아노, 직쇄 또는 분지쇄형의 C1-C10-알킬, Cl-C4-할로알킬, C3-C6-시클로알킬, C3-C6-할로시클로알킬, C3-C6-시클로알킬-Cl-C4-알킬, Cl-C4-알콕시-Cl-C4-알킬, Cl-C4-알킬티오-Cl-C4-알킬, 아릴티오-Cl-C4-알킬. C2-C6-알케닐, C2-C5-할로알케닐, C3-C6-시클로알케닐, C3-C6-할로시클로알케닐, C3-C6-알키닐, Cl-C6-알콕시. Cl-C4-할로알콕시, Cl-C4-알킬티오 벤질티오 C1-C4-알킬카르보닐, 치환되거나 비치환된 페닐카르보닐, 치환되거나 비치환된 벤질카르보닐, Cl-C4-알록시 카르보닐, 치환되거나 비치환된 페녹시카르보닐, 치환되거나 비치환된 벤질옥시카르보닐, 치환되거나 비치환된아릴, 치환되거나 비치환된 아릴옥시, 치환되거나 비치환된 아릴티오, 치환되거나 비치환된 아릴-C1-C4-알킬, 치환되거나, 비치환된 아릴-C1-C4-알케닐. 치환되거나 비치환된 아릴옥시-C1-C4-알킬, 치환되거나 비치환된 아릴티오-C1-C4-알킬, 치환되거나 비치환된 헤트아릴, 치환되거나 비치환된 헤트아릴옥시, 치환되거나, 비치환된 헤트아릴티오, 치환되거나 비치환된 헤테로아릴-C1-C4-알킬, 치환되거나 비치환된 헤트아릴 -C2-C4-알케닐, 치환되거나 비치환된 헤트아릴옥시-Cl-C4-알킬, 치환되거나 비치환된 헤테로시클릴, 치환되거나 비치환된 헤테로시클릴옥시, N(R6)2(여기서, R6은 동일 또는 상이한 것으로서, 각각H, C1-C6-알킬 또는 치환되거나 비치환된 페닐기잉) 또는 -CO-N (R7)2(여기서, R7은 동일 또는 상이한 것으로서, 각각 H 또는C1-C4-알킬임)이고. 치환되거나 비치환됨이 의미하는 치환기는 수소외에 할로겐, 시아노, 니트로, Cl-C4-알킬, C1-C4-알폭시, C1-C4-할로알킬, Cl-C4-할로알콕시. Cl-C10-알콕시미노-Cl-Cl-알킬, 아릴,아릴옥시, 벤질옥시, 헤트아릴, 헤트아릴옥시, C3-C6-시클로알킬, 헤테로시클릭 또는 헤테로시클릴옥시기이며, R3및 R4는 함께, 상기 치환기에 의해 치환될 수 있는 카르보시클릭 또는 헤테로시클릭 고리를 형성할 수 있고, R3또는 R4가 할로겐이거나, 또는
    (식 중, n은 1 내지 4의 정수이고, R8또는. n〉1일 경우 R8들은 동일 또는 상이한 것으로서. 각각 H, 할로겐,시아노, 니트로, 치환되거나 비치환된 C1-C4-알킬, C1-C4-알콕시, C1-C4-할로알킬, C1-C4-할로알콕시, 아릴, 아릴옥시, 벤질옥시, 헤트아릴 또는 헤트아릴옥시기임)일 수 있다.
  6. 진균, 또는 진균공격의 위험이 있는 개체, 식물 또는 종자, 또는 토양을 살진균 유효량의 하기 일반식(I)의 화합물로 처리하는 것을 특징으로 하는 진균 박멸 방법.
    상기 식에서. X는 CH2. CH-Cl-C4-알킬, CH-Cl-C4-알콕시, CH-Cl-C4-알킬티오 또는 N-Cl-C4-알콕시기이고, Y는 0, 5 또는 NR5이고, R1,R2및 R5는 각각 H또는 C1-C5-알킬기이고, Z1및 Z2는 동일 또는 상이한 것으로서, 각각 H, 할로겐, 메틸, 메톡시 또는 시아노기이고, R3및 R4는 동일 또는 상이한 것으로서, 각각 수소, 시아노, 직쇄 또는 분지쇄형의 Cl-C10-알킬, Cl-C4-할로알킬, C3-C6-시클로알킬, C3-C6-할로시클로알킬, C3-C6-시클로알킬-Cl-C4-알킬, Cl-C4-알콕시 -Cl-C4-알킬, Cl-C4-알킬티오-Cl-C4-알킬, 아릴티오-Cl-C4-알킬, C2-C6-알케닐. C2-C5-할로알케닐, C3-C6-시클로알케닐. C3-C6-할로시클로알케닐, C2-C6-알키닐, Cl-C6-알콕시, Cl-C6-할로알콕시, C1-C4-알킬티오, 벤질티오, C1-C4-알킬카르보닐, 치환되거나 비치환된 페닐카르보닐, 치환되거나 비치환된 벤질카르보닐, C1-C4-알콕시 카르보닐, 치환되거나 비치환된 페녹시카르보닐, 치환되거나 비치환된 벤질옥시카르보닐, 치환되거나 비치환된 아릴, 치환되거나 비치환된 아릴옥시, 치환되거나 비치환된 아릴티오, 치환되거나 비치환된 아릴-Cl-C4-알킬, 치환되거나, 비치환된 아릴-C2-C4-알케닐, 치환되거나 비치환된 아릴옥시-Cl-C4-알킬, 치환되거나 비치환된 아릴티오-Cl-C4-알킬, 치환되거나 비치환된 헤트아릴. 치환되거나 비치환된 헤트아릴옥시, 치환되거나, 비치환된 헤트아릴티오, 치환되거나 비치환된 헤테로아릴-Cl-C4-알킬, 치환되거나 비치환된 헤트아릴 -C2-C4-알케닐, 치환되거나 비치환된 헤트아릴옥시-Cl-C4-알킬, 치환되거나 비치환된 헤테로시클릴, 치환되거나 비치환된 헤테로시클릴옥시, N(R7)2(여기서, R6은 동일 또는 상이한 것으로서, 각각H. C1-C6-알킬 또는 치환되거나 비치환된 페닐기임) 또는 -CO-N (R7)2(여기서, R7은 동일 또는 상이한 것으로서, 각각 H 또는Cl-C4-알킬임)이고, 치환되거나 비치환됨이 의미하는 치환기는 수소외에 할로겐, 시아노, 니트로. Cl-C4-알릴, Cl-C4-알록시, Cl-C4-할로알킬, C1-C4-할로알콕시, C1-Cl0-알콕시미노-Cl-C2-알킬, 아릴,아릴옥시, 벤질옥시. 헤트아릴, 헤트아릴옥시, C3-C6-시클로알킬, 헤테로시클릴 또는 헤테로시클릴옥시기이며, R3및 R4는 함께, 상기 치환기에 의해 치환될 수 있는 카르보시클릭 또는 헤테로시클릭 고리를 형성할 수 있고. R3또는 R5가 할로겐이거나, 또는
    (식 중, n은 1 내지 4의 정수이고, R8또는, n〉1일 경우 R8들은 동일 또는 상이한 것으로서, 각각 H, 할로겐,시아노, 니트로, 치환되거나 비치환된 Cl-C4-알킬, Cl-C4-알콕시, Cl-C4-할로알킬, Cl-C4-할로알콕시, 아릴, 아릴옥시, 벤질옥시, 헤트아릴 또는 헤트아릴옥시기임)일 수 있다.
  7. 제1항에 있어서. R1이 메틸기이고, R2가 H이고, R3가 CN이고, R4가 CH-OCH3이고, Y가 0이고,Z1및 Z2가 수소인 것을 특징으로 하는 화합물.
  8. 제1항에 있어서, R1이 메틸기이고, R2가 H이고, R3가 CN이고, R4가 시클로프로필기이고, X가 N-OCH3이고, Y가 0이고, Z1및 Z2가 수소인 것을 특징으로 하는 화합물.
    ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
KR1019910010704A 1990-06-27 1991-06-26 오-벤질옥심 에테르 및 그를 함유하는 농작물 보호제 KR100200466B1 (ko)

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AU2021266044A1 (en) 2020-04-28 2022-11-24 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution F129L in the mitochondrial cytochrome b protein conferring resistance to Qo inhibitors IV
WO2021219386A1 (en) 2020-04-28 2021-11-04 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors i
EP3903583A1 (en) 2020-04-28 2021-11-03 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors iii
JP2023527959A (ja) 2020-04-28 2023-07-03 ビーエーエスエフ ソシエタス・ヨーロピア ミトコンドリアチトクロムｂタンパク質中にＱｏ阻害剤ＩＩＩに対して耐性を付与するアミノ酸置換Ｆ１２９Ｌを含む植物病原性菌類を駆除するためのストロビルリン型化合物の使用
AU2021288898A1 (en) 2020-06-10 2023-01-19 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution F129L in the mitochondrial cytochrome b protein conferring resistance to Qo inhibitors V
EP3945089A1 (en) 2020-07-31 2022-02-02 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors v
EP4178943A1 (en) * 2020-07-08 2023-05-17 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors vi
EP3939961A1 (en) 2020-07-16 2022-01-19 Basf Se Strobilurin type compounds and their use for combating phytopathogenic fungi
EP3970494A1 (en) 2020-09-21 2022-03-23 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors viii
BR112023002312A2 (pt) 2020-08-11 2023-03-21 Basf Se Uso de compostos, métodos para combater fungos fitopatogênicos, compostos, composições agroquímicas e uso de pelo menos um composto de fórmula i
WO2023072671A1 (en) 2021-10-28 2023-05-04 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors ix
WO2023072670A1 (en) 2021-10-28 2023-05-04 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors x
EP4242199A1 (en) 2022-03-07 2023-09-13 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors xii
EP4242198A1 (en) 2022-03-07 2023-09-13 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors xiv
EP4361126A1 (en) 2022-10-24 2024-05-01 Basf Se Use of strobilurin type compounds for combating phytopathogenic fungi containing an amino acid substitution f129l in the mitochondrial cytochrome b protein conferring resistance to qo inhibitors xv

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IL98626A0 (en) 1992-07-15
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US5387607A (en) 1995-02-07
CA2045725A1 (en) 1991-12-28
JPH04261147A (ja) 1992-09-17
EP0669319A3 (de) 1996-03-27
US6316459B1 (en) 2001-11-13
KR100200466B1 (ko) 1999-06-15
US5194662A (en) 1993-03-16
EP0463488B2 (de) 2004-04-21
AU7929691A (en) 1993-01-28
EP0669319A2 (de) 1995-08-30
US5563168A (en) 1996-10-08
DK0463488T3 (da) 1998-01-12
US6326399B1 (en) 2001-12-04
ATE161007T1 (de) 1997-12-15
ES2120100T3 (es) 1998-10-16
DE59108900D1 (de) 1998-01-22
HUT58692A (en) 1992-03-30
HU209642B (en) 1994-09-28
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DK0669319T3 (da) 1999-02-08
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DK0463488T4 (da) 2004-05-10
IL98626A (en) 1995-11-27
HU912143D0 (en) 1991-12-30
EP0669319B1 (de) 1998-09-02
ATE170511T1 (de) 1998-09-15
AU652159B2 (en) 1994-08-18
GR3026148T3 (en) 1998-05-29
SK280842B6 (sk) 2000-08-14
JP3009505B2 (ja) 2000-02-14
US5292759A (en) 1994-03-08
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EP0463488A1 (de) 1992-01-02
CS196691A3 (en) 1992-02-19

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