KR850003722A - 이미다졸리논의 제조방법 - Google Patents
이미다졸리논의 제조방법 Download PDFInfo
- Publication number
- KR850003722A KR850003722A KR1019840007012A KR840007012A KR850003722A KR 850003722 A KR850003722 A KR 850003722A KR 1019840007012 A KR1019840007012 A KR 1019840007012A KR 840007012 A KR840007012 A KR 840007012A KR 850003722 A KR850003722 A KR 850003722A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- phenyl
- alkoxy
- hydrogen
- substituted
- Prior art date
Links
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 title 1
- -1 cyanomethyl Chemical group 0.000 claims 7
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 125000000217 alkyl group Chemical group 0.000 claims 4
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 239000001257 hydrogen Substances 0.000 claims 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 150000001875 compounds Chemical class 0.000 claims 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 2
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 2
- 229910052801 chlorine Inorganic materials 0.000 claims 2
- 239000000460 chlorine Substances 0.000 claims 2
- 229910052731 fluorine Inorganic materials 0.000 claims 2
- 239000011737 fluorine Substances 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 150000003839 salts Chemical class 0.000 claims 2
- 125000003944 tolyl group Chemical group 0.000 claims 2
- 125000004400 (C1-C12) alkyl group Chemical group 0.000 claims 1
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 claims 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- 125000006529 (C3-C6) alkyl group Chemical group 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 1
- 150000001204 N-oxides Chemical class 0.000 claims 1
- 239000002253 acid Substances 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000004849 alkoxymethyl group Chemical group 0.000 claims 1
- 125000003282 alkyl amino group Chemical group 0.000 claims 1
- 150000001408 amides Chemical class 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- 125000000068 chlorophenyl group Chemical group 0.000 claims 1
- 150000002431 hydrogen Chemical class 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 230000003287 optical effect Effects 0.000 claims 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D233/66—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 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
- C07D233/70—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (1)
- 일반식(Ⅱ)의 아미드로부터 물을 분리제거하고, 경우에 따라서는, Z가 수소인 생성된 화합물을 알킬화, 아실화, 설폰화, 산화 또는 염 형성시켜 일반식(Ⅰ)의 다른 화합물로 전환시킴을 특징으로 하여 일반식(Ⅰ)의 화합물, 그의 광학적 이성체(X와 Y가 서로 다른 경우), 그의 산부가염 및 N-옥사이드(A 가 질소인 경우)를 제조하는 방법.상기식에서, A는 N 또는 C-R4이고; B는 할로게노(C1-C2)알킬(여기서 할로겐은 불소, 염소 또는 브롬, 바람직하게 불소 또는 염소를 의미한다), (C1-(C4) 알콕시 메틸, 시아노메틸 또는 티오시아나토메틸이며; X가 (C1-(C4)알킬이고, Y가 (C1-C6)알킬, 시클로(C3-C3)알킬, (C2-C4)알케닐, (C2-C4)알키닐, 페닐 또는 벤질이거나; 또는 X와 Y가 그들이 결합되어 있는 탄소원자와 함께는 -CH3로 임의 치환되는 스피로시클로(C3-C6)알킬 그룹이고; Z는 수소, (C1-C4)알콕시카보닐로 치환될 수 있는(C1-C4)알킬, 또는 (C3-C4)알케닐, 프로파르길, -CO-R5또는 -SO2-R6이고; R1,R2,R3및 R4는 서로 독립적으로 수소, 할로겐, (C1-C4)알킬, (C1-C4)알콕시, (C1-C6)알콕시카보닐, 할로게노(C1-C6)알킬, 니트로, 시아노,페녹시, 또는 (C1-C2)알킬, (C1-C4)알콕시 또는 할로겐으로 임의 치환될 수 있는 페닐이며, 또한 상대적으로 O-위치에 있는 R1,R2,R3및 R4중 2개의 라디칼은 함께 그룹 -CH=CH-CH=CH-을 형성할 수도 있으며R5는 최대 2개까지의 (C1-C4)알콕시그룹 또는 최대 3개까지의 할로겐으로 임의 치환되는 (C1-C12) 알킬, 최대 2개의 할로겐 또는 하나의 메틸, 니트로 또는 메톡시그룹으로 치환될 수 있는 페닐, 또는 시클로(C3-C7)알킬, (C1-C4)알콕시, (C1-C4) 알콕시카보닐, 벤질옥시, 페녹시 또는 -NR7R8, 특히 (C1-C13)알킬이고; R6는 (C1-C4)알킬, CF3,CCl3, 페닐, 클로로페닐 또는 메틸페닐이며; R7은 수소 또는 (C1-C4)알킬이고; R8은 (C1-C4)알킬, 페닐 클로로페닐, 메틸페닐, 아미노 또는 모노-또는 디-(C1-C4)알킬아미노이다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19833340595 DE3340595A1 (de) | 1983-11-10 | 1983-11-10 | Imidazolinone, verfahren zu ihrer herstellung und ihre verwendung im pflanzenschutz |
DE???P3340595.6. | 1983-11-10 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR850003722A true KR850003722A (ko) | 1985-06-26 |
Family
ID=6213909
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019840007012A KR850003722A (ko) | 1983-11-10 | 1984-11-09 | 이미다졸리논의 제조방법 |
Country Status (14)
Country | Link |
---|---|
US (1) | US4614535A (ko) |
EP (1) | EP0144748A3 (ko) |
JP (1) | JPS60123475A (ko) |
KR (1) | KR850003722A (ko) |
CN (1) | CN85101424A (ko) |
AU (1) | AU3528884A (ko) |
BR (1) | BR8405750A (ko) |
DD (1) | DD231481A5 (ko) |
DE (1) | DE3340595A1 (ko) |
ES (1) | ES537502A0 (ko) |
HU (1) | HUT36341A (ko) |
IL (1) | IL73470A0 (ko) |
PH (1) | PH20098A (ko) |
ZA (1) | ZA848760B (ko) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4798619A (en) * | 1980-06-02 | 1989-01-17 | American Cyanamid Co. | 2-(2-imidazolin-2-yl)-pyridines and quinolines and use of said compounds as herbicidal agents |
GR861747B (en) * | 1985-07-25 | 1986-09-23 | Nissan Chemical Ind Ltd | Pyridine derivatives process for their production and herbicidal compositions |
CN86106435A (zh) * | 1985-09-24 | 1987-05-27 | 舍林股份公司 | 咪唑啉基衍生物,其制备方法和含有这类化合物的具有除草作用的制剂 |
GB2174395A (en) * | 1986-05-09 | 1986-11-05 | American Cyanimid Co | Herbicidal 2-(2-imidazolin-2-yl)pyridine derivatives |
EP0261705A1 (en) * | 1986-08-25 | 1988-03-30 | Shell Internationale Researchmaatschappij B.V. | Herbicidal imidazolinyl benzoic acids and derivatives |
DE3634887A1 (de) * | 1986-10-14 | 1988-04-21 | Bayer Ag | 2-(5-oxo-2-imidazolin-2-yl)-pyridin-derivate |
EP0303863A3 (en) * | 1987-08-17 | 1991-10-23 | American Cyanamid Company | Benzenesulfonyl carboxamide compounds, intermediate compounds and methods of preparation thereof and use of said compounds and intermediate compounds as herbicidal agents |
US5034532A (en) * | 1988-01-27 | 1991-07-23 | American Cyanamid Company | Method for the preparation of quinolyl and pyridyl substituted imidazolinones |
US5062881A (en) * | 1989-12-20 | 1991-11-05 | American Cyanamid Company | 2-(1-substituted-2-imidazolin-2-yl)benzoic and nicotinic acids and a method for their preparation |
US5270317A (en) * | 1990-03-20 | 1993-12-14 | Elf Sanofi | N-substituted heterocyclic derivatives, their preparation and the pharmaceutical compositions in which they are present |
IE910913A1 (en) * | 1990-03-20 | 1991-09-25 | Sanofi Sa | N-substituted heterocyclic derivates, their preparation¹and pharmaceutical compositions containing them |
US5076832A (en) * | 1990-07-20 | 1991-12-31 | Ici Americas Inc. | Certain 3-(substituted phenyl)-5-(substituted phenyl)-1-ethylimidazolidine-4-ones as herbicides |
US5108485A (en) * | 1990-08-31 | 1992-04-28 | American Cyanamid Company | Herbicidal 2-(2-imidazolin-2-yl)-benzazoles |
FR2677984B1 (fr) * | 1991-06-21 | 1994-02-25 | Elf Sanofi | Derives d'imidazoline n-substitues, leur preparation, les compositions pharmaceutiques en contenant. |
FR2706456B1 (fr) | 1993-06-18 | 1996-06-28 | Rhone Poulenc Agrochimie | Dérivés optiquement actifs de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
FR2685328B1 (fr) * | 1991-12-20 | 1995-12-01 | Rhone Poulenc Agrochimie | Derives de 2-imidazoline-5-ones et 2-imidazoline-5-thiones fongicides. |
US6002016A (en) * | 1991-12-20 | 1999-12-14 | Rhone-Poulenc Agrochimie | Fungicidal 2-imidazolin-5-ones and 2-imidazoline-5-thiones |
US6008370A (en) * | 1992-11-25 | 1999-12-28 | Rhone-Poulenc Agrochimie | Fungicidal-2-alkoxy/haloalkoxy-1-(mono- or disubstituted)amino-4,4-disubstituted-2-imidazolin-5-ones |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4125727A (en) * | 1976-10-18 | 1978-11-14 | American Cyanamid Company | Method of preparing imidazoisoindolediones |
IL55064A (en) * | 1977-08-08 | 1983-06-15 | American Cyanamid Co | 5,5-disubstituted-4-oxo-2-imidazolin-2-yl benzoic acid esters,their preparation and herbicidal compositions comprising them |
US4188487A (en) * | 1977-08-08 | 1980-02-12 | American Cyanamid Company | Imidazolinyl benzoic acids, esters and salts and their use as herbicidal agents |
IL55854A0 (en) * | 1978-01-09 | 1979-01-31 | American Cyanamid Co | Method for controlling the growth of plants by using imidazole derivatives |
-
1983
- 1983-11-10 DE DE19833340595 patent/DE3340595A1/de not_active Withdrawn
-
1984
- 1984-11-02 HU HU844076A patent/HUT36341A/hu unknown
- 1984-11-03 EP EP84113259A patent/EP0144748A3/de not_active Withdrawn
- 1984-11-08 US US06/669,620 patent/US4614535A/en not_active Expired - Fee Related
- 1984-11-08 DD DD84269265A patent/DD231481A5/de unknown
- 1984-11-08 PH PH31423A patent/PH20098A/en unknown
- 1984-11-08 ES ES537502A patent/ES537502A0/es active Granted
- 1984-11-09 ZA ZA848760A patent/ZA848760B/xx unknown
- 1984-11-09 BR BR8405750A patent/BR8405750A/pt unknown
- 1984-11-09 IL IL73470A patent/IL73470A0/xx unknown
- 1984-11-09 AU AU35288/84A patent/AU3528884A/en not_active Abandoned
- 1984-11-09 JP JP59235343A patent/JPS60123475A/ja active Pending
- 1984-11-09 KR KR1019840007012A patent/KR850003722A/ko not_active Application Discontinuation
-
1985
- 1985-04-01 CN CN198585101424A patent/CN85101424A/zh active Pending
Also Published As
Publication number | Publication date |
---|---|
US4614535A (en) | 1986-09-30 |
EP0144748A3 (de) | 1985-07-03 |
DD231481A5 (de) | 1986-01-02 |
HUT36341A (en) | 1985-09-30 |
CN85101424A (zh) | 1987-01-17 |
ES8600248A1 (es) | 1985-10-16 |
ZA848760B (en) | 1985-06-26 |
JPS60123475A (ja) | 1985-07-02 |
EP0144748A2 (de) | 1985-06-19 |
BR8405750A (pt) | 1985-09-17 |
PH20098A (en) | 1986-09-24 |
DE3340595A1 (de) | 1985-05-23 |
AU3528884A (en) | 1985-05-16 |
IL73470A0 (en) | 1985-02-28 |
ES537502A0 (es) | 1985-10-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |