KR860008166A - 카바모일이미다졸의 제조방법 - Google Patents
카바모일이미다졸의 제조방법 Download PDFInfo
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- KR860008166A KR860008166A KR1019860002337A KR860002337A KR860008166A KR 860008166 A KR860008166 A KR 860008166A KR 1019860002337 A KR1019860002337 A KR 1019860002337A KR 860002337 A KR860002337 A KR 860002337A KR 860008166 A KR860008166 A KR 860008166A
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- Prior art keywords
- halogen
- carbon atoms
- formula
- substituted
- alkyl
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- 125000000217 alkyl group Chemical group 0.000 claims 9
- 125000004432 carbon atom Chemical group C* 0.000 claims 8
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 6
- 125000004414 alkyl thio group Chemical group 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 6
- 125000003545 alkoxy group Chemical group 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical group 0.000 claims 5
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- CWJSHJJYOPWUGX-UHFFFAOYSA-N chlorpropham Chemical compound CC(C)OC(=O)NC1=CC=CC(Cl)=C1 CWJSHJJYOPWUGX-UHFFFAOYSA-N 0.000 claims 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims 3
- 125000000623 heterocyclic group Chemical group 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 claims 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 3
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
- VXPLXMJHHKHSOA-UHFFFAOYSA-N propham Chemical compound CC(C)OC(=O)NC1=CC=CC=C1 VXPLXMJHHKHSOA-UHFFFAOYSA-N 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PFKFTWBEEFSNDU-UHFFFAOYSA-N carbonyldiimidazole Chemical compound C1=CN=CN1C(=O)N1C=CN=C1 PFKFTWBEEFSNDU-UHFFFAOYSA-N 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Chemical group 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- YGYAWVDWMABLBF-UHFFFAOYSA-N Phosgene Chemical compound ClC(Cl)=O YGYAWVDWMABLBF-UHFFFAOYSA-N 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- -1 chlorine-substituted carbon atoms Chemical group 0.000 claims 1
- HCUYBXPSSCRKRF-UHFFFAOYSA-N diphosgene Chemical compound ClC(=O)OC(Cl)(Cl)Cl HCUYBXPSSCRKRF-UHFFFAOYSA-N 0.000 claims 1
- 125000001153 fluoro group Chemical group F* 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/04—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms
- C07D215/08—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, directly attached to the ring carbon atoms with acylated ring nitrogen atom
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- C—CHEMISTRY; METALLURGY
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- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/18—Halogen atoms or nitro radicals
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- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
- C07D215/26—Alcohols; Ethers thereof
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- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/36—Sulfur atoms
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- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
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- C07D219/00—Heterocyclic compounds containing acridine or hydrogenated acridine ring systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D219/00—Heterocyclic compounds containing acridine or hydrogenated acridine ring systems
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- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic 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
- C07D233/56—Heterocyclic 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
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- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (3)
- 일반식(Ⅱ)의 화합물을, 필요시 불활성 용매의 존재하에서, 구조식(Ⅲ)의 N,N'-카보닐디이미다졸과 반응시키거나 : 일반식(Ⅳ)의 화합물을, 필요시 불활성 용매의 존재하 및/또는 산결합제의 존재하에서, 구조식(Ⅴ)의 이미다졸과 반응시킴을 특징으로 하여 일반식(Ⅰ)의 카바모일이미다졸을 제조하는 방법.상기식에서, X는 할로겐, 저급알킬, 저급알콕시, 저급알킬티오, 할로겐-치환된 저급 알킬, 할로겐-치환된 저급 알콕시, 할로겐-치환된 저급 알킬티오, 니트로, 시아노, 저급 알킬설포닐, 저급 알킬설피닐, 할로겐-치환된 저급 알킬설포닐, 할로겐-치환된 저급 알킬설피닐, 페닐, 펜옥시 또는 페닐티오이고 n은 0,1,2 또는 3이며, Y1, Y2, Y3, Y4, Y5및 Y6는 각각 수소, 저급 알킬, 할로겐 또는 페닐이거나, Y2와 Y3가 함께는 헤테로사이클릭환내에 이중결합이 형성될 수 있도록 단일 결합을 형성할 수 있거나, Y4와 Y5가 함께는 테트라메틸렌 그룹을 형성할 수 있으며, 단, Y1, Y2, Y3, Y4, Y5및 Y6가 동시에 모두 수소는 아니어야 한다.
- 제1항에 있어서, X가 가 불소, 염소, 브롬, 탄소수 1 내지 4의 알킬, 탄소수 1 내지 4의 알콕시, 탄소수 1 내지 4의 알킬티오, 불소 및/또는 염소-치환된 탄소수 1 내지 4의 알킬, 불소 및/또는 염소-치환된 탄소수 1 내지 4의 알콕시, 불소 및/또는 염소 -치환된 탄소수 1 내지 4의 알킬티오, 니트로, 시아노, 탄소수 1 내지 4의 알킬설포닐, 탄소수 1 내지 4의 알킬설피닐, 탄소수 1 내지 4의 할로겐-치환된 알킬설포닐, 페닐, 펜옥시 또는 페닐티오이고 : n은 0,1 또는 2이며, Y1,Y2,Y3,Y4,Y5및 Y6는 각각 수소, 탄소수 1 내지 4의 알킬, 염소 또는 페닐이거나, Y2와 Y3가 함께는 헤테로 사이클릭환내에 이중결합이 형성되도록 단일 결합을 형성할 수 있거나, Y4와 Y5가 함께는 태트라메틸렌 그룹을 형성할 수 있으며, 단 Y1,Y2,Y3,Y4,Y5및 Y6가 동시에 모두 수소가 아닌 일반식(Ⅰ)의 화합물을 제조하는 방법.
- 일반식(Ⅱ)의 화합물을 구조식 COCl2의 포스겐 또는 구조식 ClCOOCCl3의 트리클로로메틸-클로로포르메이트와 반응시킴을 특징으로 하여, 일반식(Ⅳ)의 화합물을 제조하는 방법.상기식에서, X는 할로겐, 저급 알킬, 저급 알콕시, 저급 알킬티오, 할로겐-치환된 저급 알킬, 할로겐-치환된 저급 알콕시, 할로겐, 치환된 저급 알킬티오, 니트로, 시아노, 저급 알킬설포닐, 저급 알킬설피닐, 할로겐-치환된 저급 알킬설포닐, 할로겐-치환된 저급 알킬설피닐, 페닐, 펜옥시 또는 페닐티오이고 n은 0,1,2 또는 3이며 : Y1,Y2,Y3,Y4,Y5및 Y6는 각각 수소, 저급 알킬, 할로겐 또는 페닐이거나, Y2와 Y3가 함께는 헤테로사이클릭환내에 이중결합이 형성되도록 단일 결합을 형성할 수 있거나, Y4와 Y5가 함께는 테트라 메틸렌 그룹을 형성할 수 있으며 단, Y1,Y2,Y3,Y4,Y5및 Y6는 동시에 모두 수소는 아니어야 한다.※참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP66636 | 1985-04-01 | ||
| JP60066636A JPS61227506A (ja) | 1985-04-01 | 1985-04-01 | カルバモイルイミダゾ−ル類、その中間体、それらの製法並びに除草剤又は農園芸用殺菌剤 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR860008166A true KR860008166A (ko) | 1986-11-12 |
Family
ID=13321578
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019860002337A Withdrawn KR860008166A (ko) | 1985-04-01 | 1986-03-28 | 카바모일이미다졸의 제조방법 |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0198264A3 (ko) |
| JP (1) | JPS61227506A (ko) |
| KR (1) | KR860008166A (ko) |
| AU (1) | AU5423286A (ko) |
| BR (1) | BR8601429A (ko) |
| DK (1) | DK142686A (ko) |
| ES (1) | ES8800199A1 (ko) |
| HU (1) | HUT42269A (ko) |
| IL (1) | IL78304A0 (ko) |
| ZA (1) | ZA862324B (ko) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20020012116A (ko) * | 2000-08-05 | 2002-02-15 | 주정호 | 항암제로서 유용한 이미다졸릴우레아 유도체 및 그의제조방법 |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60222479A (ja) * | 1984-04-20 | 1985-11-07 | Nippon Tokushu Noyaku Seizo Kk | テトラヒドロキノリン―１―イルカルボニルイミダゾール誘導体、その製法並びに除草又は農園芸用殺菌剤 |
| JPS6160682A (ja) * | 1984-08-30 | 1986-03-28 | Nippon Tokushu Noyaku Seizo Kk | テトラヒドロキノリン−１−イルカルボニルイミダゾ−ル誘導体、その中間体、それらの製法並びに除草又は農園芸用殺菌剤 |
| DE3641343A1 (de) * | 1986-12-03 | 1988-06-16 | Hoechst Ag | Carbamoylimidazol-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| TW527355B (en) | 1997-07-02 | 2003-04-11 | Bristol Myers Squibb Co | Inhibitors of farnesyl protein transferase |
| NZ525928A (en) | 2000-10-30 | 2005-06-24 | Janssen Pharmaceutica Nv | Tripeptidyl peptidase inhibitors |
| JP2009536953A (ja) | 2006-05-11 | 2009-10-22 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Ｃｅｔｐ阻害剤としての１，２，３，４−テトラヒドロ−キノリン誘導体 |
| JP2009536954A (ja) | 2006-05-11 | 2009-10-22 | ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ | Ｃｅｔｐ阻害剤としての３，４−ジヒドロ−２ｈ−ベンゾ［１，４］オキサジンおよびチアジン誘導体 |
| RU2720237C2 (ru) | 2013-11-18 | 2020-04-28 | Форма Терапеутикс, Инк. | Композиции, содержащие бензопиперазин, в качестве ингибиторов бромодоменов вет |
| MX370535B (es) | 2013-11-18 | 2019-12-17 | Forma Therapeutics Inc | Compuestos de tetrahidroquinolina como inhibidores del bromodominio extra terminal y bromo (bet) y el uso de los mismos en el tratamiento de cáncer. |
| CN105330644B (zh) * | 2015-11-18 | 2017-12-19 | 中国农业大学 | （1,2,3,4‑四氢喹啉‑1‑基）（取代吡唑基）甲酮类化合物及其应用 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3308131A (en) * | 1962-12-06 | 1967-03-07 | Du Pont | Tertiary carbamyl triazoles |
| CH426821A (de) * | 1964-03-25 | 1966-12-31 | Siegfried Ag | Verfahren zur Herstellung neuer, basisch substituierter 5,5-Dialkylacridane |
| GB1154722A (en) * | 1965-07-08 | 1969-06-11 | Boots Pure Drug Co Ltd | 2,4,5-Tribromoimidazole Derivatives and Compositions thereof |
| US3830918A (en) * | 1972-05-17 | 1974-08-20 | Siegfried Ag | Method of treating parkinsonism and parkinsonoid syndromes |
| DE2408813A1 (de) * | 1974-02-23 | 1975-09-04 | Agfa Gevaert Ag | N-carbamoyloxypyridiniumsalze und verfahren zur herstellung derselben |
| JPS60222479A (ja) * | 1984-04-20 | 1985-11-07 | Nippon Tokushu Noyaku Seizo Kk | テトラヒドロキノリン―１―イルカルボニルイミダゾール誘導体、その製法並びに除草又は農園芸用殺菌剤 |
| JPS6160682A (ja) * | 1984-08-30 | 1986-03-28 | Nippon Tokushu Noyaku Seizo Kk | テトラヒドロキノリン−１−イルカルボニルイミダゾ−ル誘導体、その中間体、それらの製法並びに除草又は農園芸用殺菌剤 |
-
1985
- 1985-04-01 JP JP60066636A patent/JPS61227506A/ja active Pending
-
1986
- 1986-02-28 AU AU54232/86A patent/AU5423286A/en not_active Abandoned
- 1986-03-20 EP EP86103814A patent/EP0198264A3/de not_active Withdrawn
- 1986-03-26 DK DK142686A patent/DK142686A/da not_active Application Discontinuation
- 1986-03-27 ZA ZA862324A patent/ZA862324B/xx unknown
- 1986-03-28 IL IL78304A patent/IL78304A0/xx unknown
- 1986-03-28 KR KR1019860002337A patent/KR860008166A/ko not_active Withdrawn
- 1986-03-28 HU HU861318A patent/HUT42269A/hu unknown
- 1986-04-01 BR BR8601429A patent/BR8601429A/pt unknown
- 1986-04-01 ES ES553569A patent/ES8800199A1/es not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR20020012116A (ko) * | 2000-08-05 | 2002-02-15 | 주정호 | 항암제로서 유용한 이미다졸릴우레아 유도체 및 그의제조방법 |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0198264A2 (de) | 1986-10-22 |
| AU5423286A (en) | 1986-10-09 |
| JPS61227506A (ja) | 1986-10-09 |
| HUT42269A (en) | 1987-07-28 |
| IL78304A0 (en) | 1986-07-31 |
| ES8800199A1 (es) | 1987-10-16 |
| DK142686A (da) | 1986-10-02 |
| ZA862324B (en) | 1986-11-26 |
| BR8601429A (pt) | 1986-12-09 |
| EP0198264A3 (de) | 1987-08-19 |
| ES553569A0 (es) | 1987-10-16 |
| DK142686D0 (da) | 1986-03-26 |
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