KR840007724A - Agrohorticultural fungicides - Google Patents

Agrohorticultural fungicides Download PDF

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Publication number
KR840007724A
KR840007724A KR1019840000884A KR840000884A KR840007724A KR 840007724 A KR840007724 A KR 840007724A KR 1019840000884 A KR1019840000884 A KR 1019840000884A KR 840000884 A KR840000884 A KR 840000884A KR 840007724 A KR840007724 A KR 840007724A
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South Korea
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group
alkyl group
lower alkyl
hydrogen atom
general formula
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KR1019840000884A
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Korean (ko)
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요우지로(외 5) 히로다
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시미즈 야쓰오(외 1)
우베 고우산 가부시끼가이샤
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Publication of KR840007724A publication Critical patent/KR840007724A/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic 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
    • C07D233/56Heterocyclic 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

내용 없음.No content.

Description

농원예용 살균제Agrohorticultural fungicides

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (9)

일반식(I)Formula (I) 식중, R1기(단 R2는 저급알킬기, 씨크로알킬기, 페닐기 또는 저급알킬치환페닐기이고, 또한, R3는 수소원자 또는 저급알킬기이다) 또는기(단 m는 1 또는 2이고, n는 0 또는 1이다)를 나타내며, A는기(또 R4는 수소원자 또는 알킬기이다) 또는기(단 R5및 R6은 각각 독립하여 수소원자 또는 알킬기이다)를 나타내고, X는 할로겐원자, 저급알킬기 또는 저급알콕시기를 나타내고, 또 p는 0 또는 2이다)로 표시되는 이미다졸 화합물을 제조함에 있어서, 일반식(II)로 표시되는 화합물과,Wherein R 1 is (Wherein R 2 is a lower alkyl group, a cycloalkyl group, a phenyl group or a lower alkyl substituted phenyl group, and R 3 is a hydrogen atom or a lower alkyl group) or Where m is 1 or 2, n is 0 or 1, and A is (Wherein R 4 is a hydrogen atom or an alkyl group) or Preparing an imidazole compound represented by a group (wherein R 5 and R 6 are each independently a hydrogen atom or an alkyl group), X represents a halogen atom, a lower alkyl group or a lower alkoxy group, and p is 0 or 2; In the containing, the compound represented by the general formula (II), 이미다졸을 불활성 용매중에서 염기의 존재하에서 반응시키는 것을 특징으로 하는 이미다졸 화합물의 제조방법. 식중, R1, A, X 및 p는 상기에서 정의한 바와 같으며, Hal은 할로겐 원자이다.A method for producing an imidazole compound, characterized in that the imidazole is reacted in the presence of a base in an inert solvent. Wherein R 1 , A, X and p are as defined above and Hal is a halogen atom. 일반식(II)로 표시되는 화합물과 이미다졸의 몰비를 1:0.5부터 1:10로 반응시키는 것을 특징으로 하는 특허청구의 범위 제1항에 기재된 제조방법.The manufacturing method of Claim 1 which makes the molar ratio of the compound represented by General formula (II), and imidazole react from 1: 0.5 to 1:10. 반응용매가 아세톤, 메틸에틸케톤등의 케톤류, 아세토니트릴 N,N-디메틸포름아미드, N,N-디메틸 아세트아미드, 디메틸슬폭사이드, 디옥산, 테트라히드로후란인 것을 특징으로 하는 특허청구의 범위 제1항에 기재된 제조방법.The scope of the claims, wherein the reaction solvent is acetone, ketones such as methyl ethyl ketone, acetonitrile N, N-dimethylformamide, N, N-dimethyl acetamide, dimethylsulfoxide, dioxane, tetrahydrofuran The manufacturing method of Claim 1. 염기가 탄산칼륨, 탄산나트륨, 탄산수소나트륨 등의 알칼리금속의 탄산염, 트리에틸아민, 트리메틸아민피리딘, 코리딘(Collidine) 등의 피리딘류, 수산화나트륨, 수산화칼륨 등의 금속의 수산화물인 것을 특징으로 하는 특허청구의 범위 제1항에 기재된 제조방법.The base is a pyridine such as carbonates of alkali metals such as potassium carbonate, sodium carbonate and sodium hydrogen carbonate, triethylamine, trimethylamine pyridine, and corydine, hydroxides of metals such as sodium hydroxide and potassium hydroxide. The manufacturing method of Claim 1. 일반식(II)으로 표시되는 화합물과 염기의 몰비가 1:0.5부터 1:10로 반응시키는 것을 특징으로 하는 특허청구의 범위 제1항에 기재된 제조방법.The molar ratio of the compound represented by general formula (II) and a base is made to react from 1: 0.5 to 1:10, The manufacturing method of Claim 1 characterized by the above-mentioned. 반응온도가 0℃부터 140℃ 더욱 바람직하기는 20℃부터 100℃로 반응시키는 것을 특징으로 하는 특허청구의 범위 제1항에 기재된 제조방법.Reaction temperature is 0 degreeC-140 degreeC More preferably, it makes it react at 20 degreeC-100 degreeC, The manufacturing method of Claim 1 characterized by the above-mentioned. 반응압력이 1기압부터 5기압으로 반응시키는 것을 특징로 하는 특허청구의 범위 제1항에 기제된 제조방법.The production method according to claim 1, wherein the reaction pressure is reacted from 1 atmosphere to 5 atmospheres. 일반식General formula 식중, R1기(단, R2는 저급알킬기, 씨크로알킬기, 페닐기 또는 저급알킬치환페닐기이고, 또한, R3는 수소원자 또는 저급알킬기이다) 또는기(단 m는 1 또는 2이고, n는 0 또는 1이다)를 나타내며, A는기(또 R4는 수소원자 또는 알킬기이다) 또는기(단 R5및 R6은 각각 독립하여 수소원자 또는 알킬기이다)를 나타내고, X는 할로겐원자, 저급알킬기 또는 저급알콕시기를 나타내고, 또 알킬 p는 0,1 또는 2이다로 표시되는 이미다졸유도체를 유효성분로서 함유하는 것을 특징으로 하는 농원이용살균제.Wherein R 1 is (Wherein R 2 is a lower alkyl group, a cycloalkyl group, a phenyl group or a lower alkyl substituted phenyl group, and R 3 is a hydrogen atom or a lower alkyl group) or Where m is 1 or 2, n is 0 or 1, and A is (Wherein R 4 is a hydrogen atom or an alkyl group) or An imidazole derivative represented by a group (where R 5 and R 6 are each independently a hydrogen atom or an alkyl group), X represents a halogen atom, a lower alkyl group or a lower alkoxy group, and alkyl p is represented by 0, 1 or 2 Farm-use disinfectant, characterized in that it contains as an active ingredient. 일반식General formula 식중, R1기(단 R2는 저급알킬기씨크로알킬기, 페닐기 또는 저급알킬치활페닐기이고, 또한, R3는 수소원자 또는 저급알킬기이다)또는그(단 m는 1 또는 2이고, n는 0 또는 1이다)를 나타내며, A는기(또 R4는 수소원자 또는 알킬기이다) 또는기(단 R5및 은 R6각각 독립하여 수소원자 또는 알킬기이다)를 나타내고, X는 할로겐원자, 저급알킬기 또는 저급알콕시기를 나타내고, 또 p는 0 또는 2이다로 표시되는 이미다졸 화합물.Wherein R 1 is (Wherein R 2 is a lower alkyl group, a cycloalkyl group, a phenyl group or a lower alkyl substituted phenyl group, and R 3 is a hydrogen atom or a lower alkyl group) or Where m is 1 or 2, n is 0 or 1, and A is (Wherein R 4 is a hydrogen atom or an alkyl group) or An imidazole compound represented by a group (wherein R 5 and R 6 are each independently a hydrogen atom or an alkyl group), X represents a halogen atom, a lower alkyl group or a lower alkoxy group, and p is 0 or 2. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019840000884A 1983-02-23 1984-02-23 Agrohorticultural fungicides KR840007724A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP83-27754 1983-02-23
JP58027754A JPS59155304A (en) 1983-02-23 1983-02-23 Fungicide for agricultural and horticultural purposes

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KR840007724A true KR840007724A (en) 1984-12-10

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JP (1) JPS59155304A (en)
KR (1) KR840007724A (en)
BR (1) BR8400815A (en)
ES (1) ES529963A0 (en)
IT (1) IT1178861B (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007232036A (en) * 2006-02-28 2007-09-13 Shin Caterpillar Mitsubishi Ltd Cylinder cushion device
US9493451B2 (en) 2011-05-16 2016-11-15 Bionomics Limited Amine derivatives as potassium channel blockers

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ES8505660A1 (en) 1985-06-16
IT1178861B (en) 1987-09-16
JPH027563B2 (en) 1990-02-19
IT8467169A1 (en) 1985-08-22
JPS59155304A (en) 1984-09-04
ES529963A0 (en) 1985-06-16
IT8467169A0 (en) 1984-02-22
BR8400815A (en) 1984-10-02

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