KR890003783A - Herbicide - Google Patents

Herbicide Download PDF

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Publication number
KR890003783A
KR890003783A KR1019870008700A KR870008700A KR890003783A KR 890003783 A KR890003783 A KR 890003783A KR 1019870008700 A KR1019870008700 A KR 1019870008700A KR 870008700 A KR870008700 A KR 870008700A KR 890003783 A KR890003783 A KR 890003783A
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KR
South Korea
Prior art keywords
group
hydrogen
sulfonamide
substituted
thiazolotriazole
Prior art date
Application number
KR1019870008700A
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Korean (ko)
Inventor
스튜어트 게이츠 피터
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디.엘.리처
쉐링 애그로 케미칼스 리미티드
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
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Application filed by 디.엘.리처, 쉐링 애그로 케미칼스 리미티드 filed Critical 디.엘.리처
Priority to KR1019870008700A priority Critical patent/KR890003783A/en
Publication of KR890003783A publication Critical patent/KR890003783A/en

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Abstract

내용 없음No content

Description

제초제Herbicide

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

Claims (9)

하기 일반식(Ⅰ)로 표시되는 티아졸로트리아졸 술폰아미드.Thiazolotriazole sulfonamide represented by the following general formula (I). (Ⅰ) (Ⅰ) 상기 식중, R1및 R2는 서로 동일하거나 또는 상이한 것일 수 있으며, 각각 수소, 히드록시, 할로, 시아노, 치환 또는 비치환 알킬, 알콕시, 알케닐옥시, 알키닐옥시, 아릴, 아랄킬, 헤테로아릴 또는 카르바모일, 또는 기-CORα또는 -CORα(여기서, Rα는 수소 또는 알킬임)이거나, 또는 R1및 R2는 함께 탄소 원자수 3 또는 4개의 알킬렌 사슬이고, R3은 치환 또는 비치환 아릴, 헤테로시클릴 또는 벤즈헤테로시클릴기이고, R4는 수소, 알칼리 금속 원자, 암모늄 기, 치환 또는 비치환 알킬, 알케닐, 알키닐, 아실, 알콕시카르보닐 또는 아랄킬기, 헤테로시클릭기이거나 또는 하기 일반식(Ⅱ)의 기이다.Wherein R 1 and R 2 may be the same or different from each other, and each hydrogen, hydroxy, halo, cyano, substituted or unsubstituted alkyl, alkoxy, alkenyloxy, alkynyloxy, aryl, aralkyl, Heteroaryl or carbamoyl, or a group-COR α or -COR α , wherein R α is hydrogen or alkyl, or R 1 and R 2 together are an alkylene chain of 3 or 4 carbon atoms, R 3 is a substituted or unsubstituted aryl, heterocyclyl or benzheterocyclyl group, R 4 is hydrogen, an alkali metal atom, an ammonium group, a substituted or unsubstituted alkyl, alkenyl, alkynyl, acyl, alkoxycarbonyl or aralkyl group Or a heterocyclic group or a group of the following general formula (II). (Ⅱ) (Ⅱ) 상기 식중, R1및 R2는 상기 정의한 바와 같다.Wherein R 1 and R 2 are as defined above. 제 1 항에 있어서, R1이 수소이거나 또는 탄소 원자수 1 내지 6개의 비치환 알킬기인 티아졸리트리아졸 술폰아미드.The thiazolitriazole sulfonamide according to claim 1, wherein R 1 is hydrogen or an unsubstituted alkyl group having 1 to 6 carbon atoms. 제 1 항 또는 2 항에 있어서, R2가 수소이거나 또는 탄소 원자수 1 내지 6개의 비치환 알킬기인 티아졸리트리아졸 술폰아미드.The thiazolitriazole sulfonamide according to claim 1 or 2, wherein R 2 is hydrogen or an unsubstituted alkyl group having 1 to 6 carbon atoms. 제 1 항 내지 3항중 어느 하나의 항에 있어서, R3이 하나 이상의, 탄소 원자수 1 내지 4개의 알킬, 알콕시, 알코기카르보닐 또는 알킬티오(이들은 추가 치환될 수 있음), 할로겐 원자, 시아노기, 아미노술포닐기, 할로겐 원자 또는 니트로기에 의한 치환되는 페닐기인 티아졸로트리아졸 술폰아미드.4. A compound according to any one of claims 1 to 3, wherein R 3 is one or more alkyl, alkoxy, alkogicarbonyl or alkylthio having 1 to 4 carbon atoms (which may be further substituted), halogen atom, cya Thiazolotriazole sulfonamide which is a phenyl group substituted by a no group, an aminosulfonyl group, a halogen atom, or a nitro group. 제 1 항 내지 4항중 어느 하나의 항에 있어서, R4가 수소인 티아졸리트리아졸 술폰아미드.Thiazolitriazole sulfonamide according to any one of claims 1 to 4, wherein R 4 is hydrogen. 제 1 항 내지 5항중 어느 하나의 항에 있어서, R1및 R2가 각각 수소 또는 메틸이고, R이 하나 이상의, 탄소 원자수 1 내지 4개의 알킬, 알콕시, 알코기카르보닐 또는 알킬티오기, 할로겐 원자 또는 니트로기에 의한 치환되는 페닐기이고, R4가 수소인 티아졸로트라아졸 술폰아미드.The compound according to any one of claims 1 to 5, wherein R 1 and R 2 are each hydrogen or methyl, R is at least one alkyl, alkoxy, alcoholcarbonyl or alkylthio group having 1 to 4 carbon atoms, Thiazolotriazole sulfonamide which is a phenyl group substituted by a halogen atom or a nitro group, and R <4> is hydrogen. N-(2,6-디플루오로페닐)티아졸로[3,2-b][1,2,4]트리아졸-2-술폰아미드.N- (2,6-difluorophenyl) thiazolo [3,2-b] [1,2,4] triazole-2-sulfonamide. 적합한 담체 및(또는)계면 활성제와 함께 제 1항 내지 7항중 어느 하나의 항에 의한 이상의 화합물로 되는 제초 조성물.A herbicidal composition comprising the compound of any of the preceding claims together with a suitable carrier and / or surfactant. 하기 일반식(Ⅲ)의 티아졸로트리아졸 술포닐 할라이드를 염기 존재 하에서 구조식 R3R4NH의 아민과 반응시켜서 목적 화합물을 얻은, 제 1항에 의한 티아졸로트라아졸 술폰아미드의 제조 방법.A method for producing thiazolotriazole sulfonamide according to claim 1, wherein the thiazolotriazole sulfonyl halide of the general formula (III) is reacted with an amine of the formula R 3 R 4 NH in the presence of a base to obtain a target compound. (Ⅲ) (Ⅲ) 상기 식중, R1및 R2는 제 1항에서 정의한 바와 같고, Hal은 할로겐이며, R3및 R4는 제 1항에서 정의한 바와 같다.Wherein R 1 and R 2 are as defined in claim 1, Hal is halogen, and R 3 and R 4 are as defined in claim 1. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019870008700A 1987-08-08 1987-08-08 Herbicide KR890003783A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019870008700A KR890003783A (en) 1987-08-08 1987-08-08 Herbicide

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Application Number Priority Date Filing Date Title
KR1019870008700A KR890003783A (en) 1987-08-08 1987-08-08 Herbicide

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KR890003783A true KR890003783A (en) 1989-04-18

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100908990B1 (en) * 2001-07-07 2009-07-22 옥세아 게엠베하 Method of Making Aldehyde

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100908990B1 (en) * 2001-07-07 2009-07-22 옥세아 게엠베하 Method of Making Aldehyde

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