KR970042520A - 트리아졸 유도체 및 이의 용도 - Google Patents
트리아졸 유도체 및 이의 용도 Download PDFInfo
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Abstract
하기 화학식 1 로 나타낸 트리아졸 유도체, 활성성분으로 트리아졸 유도체를 함유하는 살충제 및 살진드기제, 및 곤충 및 진드기 방제 방법이 개시되어 있다.
[식중, R1은 수소원자, 저급 알킬기, 할로겐 원자, 1-피롤릴기, 화학식NR2R3로 나타낸기(식중, R2 및 R3 은 동일하거나 상이하며, 각각은 수소원자, 알킬기, 시클로알킬기, 알콕시알킬기, 알킬티오카르보닐기, 알콕시카르보닐술페닐기, 알킬티오기, 알킬술포닐기, 치환 페닐기, 알콕시카르보닐기, 비치환 또는 알콕시-치환 알카노일기, 포화 헤테로시클릭 고리, 또는 하기 화학식 :
이고 (식중, R2' 및 R3' 는 동일하거나 상이하고, 각각은 알킬기, 알콕시카르보닐기, 알콕시카르보닐-치환 알킬기이며, 또는 R2' 및 R3'은 상호 결합하여 함산소알킬렌기를 형성한다) 또는 R2및 R3은 상호결합하여 NR2R3로 나타낸 비치환 또는 치환된 함질소 포화 헤테로시클릭기고리를 형성한다) 또는 화학식 N=CR4R6로 나타낸 기(식중, R4는 수소원자, 알킬기 또는 비치환 또는 치환된 페닐기이고, R6은 수소원자, 알킬기, 알콕시기 또는 디알킬아미노기이다) 이고; R5는 1 종이상의 할로겐원자로 치환된 메틸기 또는 1 종이상의 할로겐원자로 치환된 에틸기이며; n은 0, 1 또는 2 이고 ; Y는 질소 원자 또는 화학식 CX2로 나타낸 기이며(식중, X2는 이후에 정의된바와 같다); X1및 X2은 동일하거나 상이하고, 각각은 할로겐원자, 니트로기 또는 시아노기이다.]
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Claims (17)
- 하기 화학식 1로 나타낸 트리아졸 유도체.<화학식 1>[식중, R1은 수소원자, 저급 알킬기, 할로겐 원자, 1-피롤릴기, 화학식NR2R3로 나타낸기(식중, R2및 R3은 동일하거나 상이하며, 각각은 수소원자, 알킬기, 시클로알킬기, 알콕시알킬기, 알킬티오카르보닐기, 알콕시카르보닐술페닐기, 알킬티오기, 알킬술포닐기, 치환 페닐기, 알콕시카르보닐기, 비치환 또는 알콕시-치환 알카노일기, 포화 헤테로시클릭 고리, 또는 하기 화학식 :이고 (식중, R2' 및 R3' 는 동일하거나 상이하고, 각각은 알킬기, 알콕시카르보닐기, 알콕시카르보닐-치환 알킬기이며, 또는 R2' 및 R3'은 상호 결합하여 함산소알킬렌기를 형성한다) 또는 R2및 R3은 상호결합하여 NR2R3로 나타낸 비치환 또는 치환된 함질소 포화 헤테로시클릭기고리를 형성한다) 또는 화학식 N=CR4R6로 나타낸 기(식중, R4는 수소원자, 알킬기 또는 비치환 또는 치환된 페닐기이고; R6은 수소원자, 알킬기, 알콕시기 또는 디알킬아미노기이다) 이고; R5는 1 종이상의 할로겐원자로 치환된 메틸기 또는 1 종이상의 할로겐원자로 치환된 에틸기이며; n은 0, 1 또는 2 이고 ; Y는 질소 원자 또는 화학식 CX2로 나타낸 기이며(식중, X2는 이후에 정의된바와 같다); X1및 X2은 동일하거나 상이하고, 각각은 할로겐원자, 니트로기 또는 시아노기이다.]
- 제 1 항에 있어서, R5는 화학식 CF2Z [식중, Z 는 할로겐원자, 수소원자, 메틸기, 디틀루오로메틸기, 트리플루오로메틸기 또는 브로모디플루오로메틸기를 나타낸다]로 나타낸 기인 트리아졸 유도체.
- 제 1 항에 있어서, R5는 트리플루오로메틸기, 디플루오로메틸기, 클로로디플루오로메틸기, 브로모디플루오로메틸기, 1,1,2,2-테트라플푸오로에틸기, 2,2,2-트리플루오로에틸기, 펜타플루오로에틸기, 1,1-디플루오로에틸기 또는 2-브로모-1,1,2,2-테트라플루오로에틸기인 트리아졸 유도체.
- 제 1 항에 있어서, R5는 트리플루오로메틸기인 트리아졸 유도체.
- 제 1 항에 있어서, R2또는 R3으로 나타낸 포화 레테로시클릭 고리는 2-테트라히드로피라닐기인 트리아졸 유도체.
- 제 1 항에 있어서, NR2R3로 나타낸 치환 포화 헤테로시클릭 고리의 치환제는 알킬기, 할로겐원자, 알콕시기, 히드록실기, 메르캅토기, 알콕시카르보닐기, 옥소기 및 아실옥시기로 구성된 군으로부터 선택된 1 종이상의 것인 트리아졸 유도체.
- 제 1 항에 있어서, NR2R3로 나타낸 비치환 또는 치환된 함질소 포화 헤테로시클릭기 고리는 아지리딘고리, 아제티딘고리, 피롤리딘고리, 모르폴린고리, 티오모르폴린고리, 이소티아졸리딘고리, 1,3-옥사조리딘고리 및 1,3-티아졸리딘고리로 구성된 군으로부터 선택된 1 종이상의 것인 트리아졸 유도체.
- 제 1 항에 있어서, R4로 나타낸 치환 페닐기중의 치환제는 히드록실시, 알콕시기, 알킬기, 니트로기, 할로겐원자, 페닐기, 페녹시기, 알킬티오기, 아미노기, 카르복실기, 시아노기, 알콕시카르보닐기 및 아실옥시기로 구성된 군으로부터 선택된 1 종이상의 것인 트리아졸 유도체.
- 제 1 내지 4 항중 어느 한 항에 있어서, R1은 수소원자, 메틸기 또는 화학식 NR2R3으로 나타낸 기인 트리아졸 유도체.
- 제 9 항에 있어서, R2는 수소원자, 알카노일기 또는 알콕시가르보닐기이고 R3은 수소원자, 알킬기, 시클로알킬기, 알콕시카르보닐기, 알콕시카르보닐술페닐기, 알콕시알킬기 또는 화학식:인 트리아졸 유도체.
- 제 1 내지 4 항중 어느 한 항에 있어서, Y는 화학식 CX2로 나타낸기인 트리아졸 유도체.
- 제 1 내지 4 항중 어느 한 항에 있어서, n 는 0 인 트리아졸 유도체.
- 제 1 내지 4 항중 어느 한 항에 있어서, R1은 수소원자, 메틸기 또는 화학식 NR2R3로 나타낸 기이고, R2는 수소원자이며, R3은 수소원자, 알킬기, 시클로알킬기 또는 알콜시알킬기이고, Y는 화학식 CX2으로 나타낸 기이며 n 은 0 인 트리아졸 유도체.
- 제 1 항의 트리아졸 유도체를 활성성분으로 함유하는 살충제 또는 살진드기제.
- 유효량의 제 1 항의 트리아졸 유도체를 곤충 및 진드기, 또는 곤충또는 진드기가 서식하는 장소에 적용하는 것을 특징으로하는, 곤충 및 진드기 방제방법.
- 살충제 또는 살진드기제로 사용되는 제 1 항의 트리아졸 유도체.
- 제 1 항에 있어서, R1은 수소원자, 메틸기 또는 화학식 NR2R3(식중, R2및 R3는 동일하거나 상이하며 수소원자 또는 알킬기이다)로 나타낸기 또는 N=CHR4(식중, R4는 비치환 또는 치환 페닐기이다)로 나타낸기이고 R5는 1 종이상의 할로겐원자로 치환된 트리아졸 유도체.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP33346395 | 1995-12-21 | ||
JP95-333463 | 1995-12-21 | ||
JP96-260917 | 1996-10-01 | ||
JP26091796 | 1996-10-01 |
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KR970042520A true KR970042520A (ko) | 1997-07-24 |
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KR1019960069486A KR970042520A (ko) | 1995-12-21 | 1996-12-21 | 트리아졸 유도체 및 이의 용도 |
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US (1) | US5756522A (ko) |
EP (1) | EP0780381A1 (ko) |
KR (1) | KR970042520A (ko) |
CN (1) | CN1165818A (ko) |
AR (1) | AR005142A1 (ko) |
AU (1) | AU701981B2 (ko) |
BR (1) | BR9606147A (ko) |
MX (1) | MX9700179A (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
ES2179254T3 (es) | 1996-11-04 | 2003-01-16 | Bayer Cropscience Sa | 1-poliarilpirazoles plaguicidas. |
JPH10236905A (ja) * | 1997-02-25 | 1998-09-08 | Sumitomo Chem Co Ltd | 衣料害虫防除剤 |
ZA989421B (en) * | 1997-10-31 | 1999-04-21 | Sumitomo Chemical Co | Heterocyclic compounds |
AU2611200A (en) * | 1999-01-14 | 2000-08-01 | Monsanto Technology Llc | Triazole sulfones having herbicidal activity |
US6362342B1 (en) | 1999-06-29 | 2002-03-26 | Lion Bioscience Ag | Triazole compounds and methods of making same |
US20030109187A1 (en) * | 2001-12-10 | 2003-06-12 | Cantrell Larry J. | Treated fabric and method and apparatus for producing same |
JP2006265209A (ja) * | 2005-03-25 | 2006-10-05 | Bayer Cropscience Ag | 殺虫性アニリノトリアゾール類 |
JP6140446B2 (ja) * | 2009-08-20 | 2017-05-31 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH | 殺ダニ剤および殺虫剤としての3−トリアゾリルフェニル置換スルフィド誘導体 |
CN106349236B (zh) * | 2016-07-28 | 2018-11-16 | 中国农业大学 | 1h-1,2,4-三唑脒类化合物及其制备方法和应用 |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
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GB1121211A (en) | 1966-04-19 | 1968-07-24 | Ilford Ltd | Benzimidazole dyes |
US3888932A (en) | 1972-03-14 | 1975-06-10 | Rohm & Haas | Herbicidal 4-trifluoromethyl-4-nitrodiphenyl ethers |
US3928416A (en) | 1972-03-14 | 1975-12-23 | Rohm & Haas | Herbicidal 4-trifluoromethyl-4{40 nitrodiphenyl ethers |
SE396748B (sv) | 1975-02-21 | 1977-10-03 | Astra Laekemedel Ab | Forfarande for framstellning av 3-fenyl-sek -butylaminderivat |
US4181041A (en) | 1977-04-18 | 1980-01-01 | Clark Equipment Company | Dual path, dual range transmission |
GB2002368A (en) | 1977-08-12 | 1979-02-21 | Ici Ltd | Herbicidal 2-(4-Alkoxyphenyloxy) pyridine compounds |
GB2055293A (en) | 1979-07-18 | 1981-03-04 | Ici Ltd | Herbicides |
EP0034402B1 (en) | 1980-02-05 | 1984-08-29 | Imperial Chemical Industries Plc | Method of preparing fluorine-substituted diphenyl ether derivatives and fluorine-substituted halogeno benzene derivatives for use therein |
US4480102A (en) | 1982-07-23 | 1984-10-30 | The Dow Chemical Company | 2,3-Difluoro-5-(trifluoromethyl)pyridine and methods of making and using the same |
DE3545570A1 (de) | 1985-12-21 | 1987-06-25 | Hoechst Ag | Neue pyridin-derivate und deren n-oxide, verfahren zu ihrer herstellung und ihre verwendung als zwischenprodukte |
DE3869167D1 (de) * | 1987-03-27 | 1992-04-23 | Kumiai Chemical Industry Co | Phenyltriazol-derivate und insectizid. |
JPH01230562A (ja) | 1987-03-27 | 1989-09-14 | Kumiai Chem Ind Co Ltd | フェニルトリアゾール誘導体及び殺虫剤 |
JPH0242423A (ja) * | 1988-03-11 | 1990-02-13 | Fuji Photo Film Co Ltd | 非線形光学材料および光波長変換方法 |
JP2729810B2 (ja) | 1988-09-27 | 1998-03-18 | クミアイ化学工業株式会社 | フェニルトリアゾール誘導体及び殺虫剤 |
JPH0291062A (ja) * | 1988-09-27 | 1990-03-30 | Kumiai Chem Ind Co Ltd | トリアゾール誘導体及び殺虫剤 |
GB9006479D0 (en) | 1989-04-17 | 1990-05-23 | Ici Plc | Novel compounds |
US5008396A (en) | 1989-11-06 | 1991-04-16 | Dowelanco | Process for the preparation of 5-amino-3-chlorosulfonyl-1,2,4-triazole |
DE4343528A1 (de) * | 1993-12-16 | 1995-06-22 | Schering Ag | Zweifach heterocyclisch substituierte Benzole und Pyridine, Verfahren zu ihrer Herstellung und ihre Verwendung als Schädlingsbekämpfungsmittel |
JPH07258227A (ja) * | 1994-03-25 | 1995-10-09 | Kumiai Chem Ind Co Ltd | フェニルトリアゾール誘導体及び殺虫剤 |
-
1996
- 1996-12-19 AU AU75443/96A patent/AU701981B2/en not_active Ceased
- 1996-12-19 EP EP96120534A patent/EP0780381A1/en not_active Withdrawn
- 1996-12-19 AR ARP960105769A patent/AR005142A1/es unknown
- 1996-12-20 BR BR9606147A patent/BR9606147A/pt active Search and Examination
- 1996-12-20 US US08/772,086 patent/US5756522A/en not_active Expired - Fee Related
- 1996-12-21 KR KR1019960069486A patent/KR970042520A/ko not_active Application Discontinuation
- 1996-12-21 CN CN96123830A patent/CN1165818A/zh active Pending
-
1997
- 1997-01-07 MX MX9700179A patent/MX9700179A/es unknown
Also Published As
Publication number | Publication date |
---|---|
CN1165818A (zh) | 1997-11-26 |
AR005142A1 (es) | 1999-04-14 |
AU701981B2 (en) | 1999-02-11 |
EP0780381A1 (en) | 1997-06-25 |
MX9700179A (es) | 1997-12-31 |
AU7544396A (en) | 1997-06-26 |
US5756522A (en) | 1998-05-26 |
BR9606147A (pt) | 1998-09-01 |
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