KR960037665A - 트리아진 유도체의 제조방법 - Google Patents
트리아진 유도체의 제조방법 Download PDFInfo
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- KR960037665A KR960037665A KR1019960011057A KR19960011057A KR960037665A KR 960037665 A KR960037665 A KR 960037665A KR 1019960011057 A KR1019960011057 A KR 1019960011057A KR 19960011057 A KR19960011057 A KR 19960011057A KR 960037665 A KR960037665 A KR 960037665A
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- C07C323/46—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and nitrogen atoms, not being part of nitro or nitroso groups, bound to the same carbon skeleton having at least one of the nitrogen atoms, not being part of nitro or nitroso groups, further bound to other hetero atoms
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- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D253/02—Heterocyclic compounds containing six-membered rings having three nitrogen atoms as the only ring hetero atoms, not provided for by group C07D251/00 not condensed with other rings
- C07D253/06—1,2,4-Triazines
- C07D253/065—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members
- C07D253/07—1,2,4-Triazines having three double bonds between ring members or between ring members and non-ring members with hetero atoms, or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
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- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/26—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract
본 발명의 목적은 트리아진 유도체를 편리하고 높은 수율로 제조하는 방법을 제공하는 것이다.
본 발명은 하기식(Ⅱ)로 표현되는 세미카르바존 유도체를 폐환 반응시키는 것으로 구성되는 하기 화학식(Ⅲ)으로 표현되는 1,2,4-트리아진-3-온 유도체의 제조방법에 관한 것이다.
〔상기 식 중, R1은 임의 치환된 탄화수소 잔기를 의미하고 ; X는 카르보닐기, 티오카르보닐기 또는 임의 치환된 메틸렌기를 의미하고 ; 점선은 이중결합이 임의 형성될 수도 있음을 의미하며 ; R2및 R3는 수소, 임의 치환된 탄화수소 잔기 또는 전자 당김기를 의미하고 ; R4는 임의 치환된 알킬기를 의미한다.
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (17)
- 하기 화학식(Ⅱ)로 나타낸 세미카르바존 유도체를 폐환 반응시킴을 특징으로 하는 하기 화학식(Ⅲ)으로 나타낸 1,2,4-트리아진-3-온 유도체의 제조방법.〔상기 식 중, R1은 임의 치환된 탄화수소 잔기를 의미하고 ; X는 카르보닐기, 티오카르보닐기 또는 임의 치환된 메틸렌기를 의미하고 ; 점선은 이중결합이 임의 형성될 수도 있음을 의미하며 ; R2및 R3는 수소, 임의 치환된 탄화수소 잔기 또는 전자 당김기를 의미하고 ; R4는 임의 치환된 알킬기를 의미한다.〕
- 제1항에 있어서, R1이 임의 치환된 페닐기임을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, 임의 치환된 페닐기가 3 및 4위치에서 치환된 페닐기 또는 3, 4 및 5위치에서 치환된 페닐기임을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, R4는 C1-4알킬이고 ; R2및 R3중의 하나는 수소이고 다른 것은 페닐임을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, R4가 메틸 또는 에틸임을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, 하기 일반식(Ⅰ) :〔상기 식 중, R1은 임의 치환된 탄화수소 잔기를 나타내고 ; R2및 R3은 수소, 임의 치환된 탄화수소 잔기 또는 전자 유인기를 나타낸다〕로 나타낸 히드라존 유도체를(R4O)2CHCH2NCO〔식 중, R4가 임의 치환된 알킬기를 나타낸다〕로 나타낸 디알콕시에틸 이소시아네이트와 반응시켜 제1항에 기재된 세미카르바존 유도체를 수득한 다음, 세미카르바존 유도체를 폐환 반응시킴을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, 1,2,4-트리아진-3-온 유도체의 생성을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, 1,2,4-트리아진-3-디온 유도체의 생성을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, 헥사히드로-1,2,4-트리아진-3-온 유도체의 생성을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, 2-〔4-(4-아세틸벤질)-3,5-디클로로페닐〕-4,5-디히드로-1,2,4-트리아진-3-(2H)온의 생성을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 제1항에 있어서, 2-{3,5-디클로로-4-〔4-(1-히드록시에틸)벤질)페닐}-4,5-디히드로-1,2,4-트리아진-3(2H)-온의 생성을 특징으로 하는 1,2,4-트리아진-3-온 유도체의 제조방법.
- 하기 화학식(Ⅱ)로 나타낸 세미카르바존 유도체 :〔상기 식 중, R1은 임의 치환된 탄화수소 잔기를 의미하고 ; R2및 R3은 수소, 임의 치환된 탄화수소 잔기 또는 전자 유인기를 나타내고 ; 및 R4는 임의 치환된 알킬기를 나타낸다〕.
- 제12항에 있어서, R1은 하기 화학식임을 특징으로 하는 세미카르바존 :〔상기 식 중, Ra는 아실, 임의 치환된 술파모일, 임의 치환된 카르바모일, 카르복실, 알콕시카르보닐, 임의 치환된 알킬 또는 임의 치환된 아미노기이며 ; A는 -CH- 또는 질소원자이며 ; Y'는 메틸렌, 시아노메틸렌, 카르보닐, 히드록시메틸렌, 황원자, 술피닐, 술포닐 또는 산소원자이며 ; Hal은 할로겐이고, Rb는 수소, 할로겐 또는 저급 알킬기이다〕.
- 제1항에 있어서, R1이 하기 화학식임을 특징으로 하는 세미카르바존 :〔상기 식 중, Ra는 아실, 임의 치환된 술파모일, 임의 치환된 카르바모일, 카르복실, 알콕시카르보닐, 임의 치환된 알킬 또는 임의 치환된 아미노기이며 ; A는 -CH- 또는 질소원자이며 ; Y'는 메틸렌, 시아노메틸렌, 카르보닐, 히드록시메틸렌, 황원자, 술피닐, 술포닐 또는 산소원자이고 ; Hal은 할로겐이고, Rb는 수소, 할로겐 또는 저급 알킬기이다〕
- 하기 화학식으로 표현되는 1,2,4-트리아진-3-온 유도체 :〔상기 식 중, Ra는 아실, 임의 치환된 술파모일, 임의 치환된 카르바모일, 카르복실, 알콕시카르보닐, 임의 치환된 알킬 또는 임의 치환된 아미노기이며 ; X'는 메틸렌 또는 카르보닐이다〕.
- 제15항에 있어서, 1,2,4-트리아진-3-온 유도체가 2-〔4-(4-아세틸벤질)-3,5-디클로로페닐〕-4,5-디히드로-1,2,4-트리아진-3(2H)-온임을 특징으로 하는 1,2,4-트리아진-3-온 유도체.
- 제15항에 있어서, 1,2,4-트리아진-3-온 유도체가 2-3,5-디클로로-4-〔4-(1-히드록시에틸)벤질)페닐-4,5-디히드로-1,2,4-트리아진-3(2H)-온임을 특징으로 하는 1,2,4-트리아진-3-온 유도체.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
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KR (1) | KR100433882B1 (ko) |
CN (1) | CN1062265C (ko) |
CA (1) | CA2174063A1 (ko) |
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EP0831088B1 (en) * | 1996-08-30 | 2002-11-27 | Takeda Schering-Plough Animal Health K.K. | 1,2,4-Triazine-3,5-dione derivatives as anticoccidial agents |
ID24224A (id) | 1997-07-10 | 2000-07-13 | Janssen Pharmaceutica Nv | Turunan-turunan 6-azaurasil sebagai inhibitor il-5 |
US6294536B1 (en) | 1997-08-29 | 2001-09-25 | Takeda Schering-Plough Animal Health K.K. | Triazine derivatives, their production and use |
EP0987265A1 (en) | 1998-09-18 | 2000-03-22 | Janssen Pharmaceutica N.V. | Interleukin-5 inhibiting 6-azauracil derivatives |
WO2000037451A1 (en) | 1998-12-18 | 2000-06-29 | Janssen Pharmaceutica N.V. | Il-5 inhibiting 6-azauracil derivatives |
US6787652B1 (en) | 1999-09-30 | 2004-09-07 | Pfizer, Inc. | 6-Azauracil derivatives as thyroid receptor ligands |
CN101265216B (zh) * | 2007-12-18 | 2012-06-27 | 重庆华邦胜凯制药有限公司 | 4-(取代乙氰基)-苯腙衍生物及其合成方法 |
CN104447597B (zh) * | 2014-10-26 | 2018-07-31 | 威海迪素制药有限公司 | 一种地克珠利的制备方法 |
CN113248453B (zh) * | 2021-06-28 | 2021-11-16 | 山东国邦药业有限公司 | 一种三嗪酮环的制备方法 |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU578708B2 (en) * | 1984-06-12 | 1988-11-03 | Fmc Corporation | Herbicidal 2-aryl-1,2,4-triazine-3,5(2h,4h)-diones and sulfuranalogs thereof |
US4631278A (en) * | 1984-08-01 | 1986-12-23 | Janssen Pharmaceutica N.V. | Anti-protozoal α-aryl-4-(4,5-dihydro-3,5-dioxo-1,2,4-triazin-2(3H)-yl)-benzeneacetonitrile derivatives, pharmaceutical compositions, and method of use therefor |
GB8602342D0 (en) * | 1986-01-30 | 1986-03-05 | Janssen Pharmaceutica Nv | 5 6-dihydro-2-(substituted phenyl)-1 2 4-triazine-3 5(2h 4h)-diones |
DE4120138A1 (de) * | 1991-06-19 | 1992-12-24 | Bayer Ag | Substituierte hexahydro-1,2,4-triazindione, verfahren zu ihrer herstellung, zwischenprodukte dafuer und ihre verwendung |
EP0476439A1 (de) * | 1990-09-18 | 1992-03-25 | Bayer Ag | Substituierte 1,2,4-Triazindione, Verfahren zu ihrer Herstellung, Zwischenprodukte dafür und ihre Verwendung |
TW403741B (en) * | 1993-10-15 | 2000-09-01 | Takeda Chemical Industries Ltd | Triazine derivative, production and use thereof |
-
1996
- 1996-04-04 EP EP96105485A patent/EP0737672B1/en not_active Expired - Lifetime
- 1996-04-04 DE DE69615601T patent/DE69615601T2/de not_active Expired - Fee Related
- 1996-04-12 CA CA002174063A patent/CA2174063A1/en not_active Abandoned
- 1996-04-12 CN CN96104625A patent/CN1062265C/zh not_active Expired - Fee Related
- 1996-04-12 KR KR1019960011057A patent/KR100433882B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CN1062265C (zh) | 2001-02-21 |
CA2174063A1 (en) | 1996-10-15 |
DE69615601D1 (de) | 2001-11-08 |
DE69615601T2 (de) | 2002-07-11 |
EP0737672A2 (en) | 1996-10-16 |
EP0737672B1 (en) | 2001-10-04 |
EP0737672A3 (en) | 1996-12-27 |
CN1140712A (zh) | 1997-01-22 |
KR100433882B1 (ko) | 2004-09-08 |
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