KR860001072A - 치환된 5-아미노-1- 페닐피라졸의 제조방법 - Google Patents
치환된 5-아미노-1- 페닐피라졸의 제조방법 Download PDFInfo
- Publication number
- KR860001072A KR860001072A KR1019850005067A KR850005067A KR860001072A KR 860001072 A KR860001072 A KR 860001072A KR 1019850005067 A KR1019850005067 A KR 1019850005067A KR 850005067 A KR850005067 A KR 850005067A KR 860001072 A KR860001072 A KR 860001072A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- methyl
- same
- radical
- hydrogen
- Prior art date
- Legal status (The legal status 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 status listed.)
- Ceased
Links
- ZVNYYNAAEVZNDW-UHFFFAOYSA-N 2-phenylpyrazol-3-amine Chemical class NC1=CC=NN1C1=CC=CC=C1 ZVNYYNAAEVZNDW-UHFFFAOYSA-N 0.000 title claims 4
- 238000000034 method Methods 0.000 title claims 2
- -1 nitro , Hydroxyl Chemical group 0.000 claims 40
- 229910052739 hydrogen Inorganic materials 0.000 claims 12
- 239000001257 hydrogen Substances 0.000 claims 12
- 125000000217 alkyl group Chemical group 0.000 claims 11
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000004432 carbon atom Chemical group C* 0.000 claims 8
- 125000004093 cyano group Chemical group *C#N 0.000 claims 8
- 125000001188 haloalkyl group Chemical group 0.000 claims 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 7
- 125000003342 alkenyl group Chemical group 0.000 claims 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 7
- 125000002496 methyl group Chemical class [H]C([H])([H])* 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- 239000001301 oxygen Substances 0.000 claims 7
- 125000001424 substituent group Chemical group 0.000 claims 7
- 239000011593 sulfur Chemical group 0.000 claims 7
- 229910052717 sulfur Chemical group 0.000 claims 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 5
- 229910052801 chlorine Inorganic materials 0.000 claims 5
- 239000000460 chlorine Substances 0.000 claims 5
- 229910052736 halogen Inorganic materials 0.000 claims 5
- 150000002367 halogens Chemical class 0.000 claims 5
- 150000002431 hydrogen Chemical class 0.000 claims 5
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 5
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 4
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 4
- 229910052794 bromium Inorganic materials 0.000 claims 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 4
- 125000001495 ethyl group Chemical class [H]C([H])([H])C([H])([H])* 0.000 claims 4
- 229910052731 fluorine Inorganic materials 0.000 claims 4
- 239000011737 fluorine Substances 0.000 claims 4
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 claims 4
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 3
- 125000000304 alkynyl group Chemical group 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 3
- 239000003085 diluting agent Substances 0.000 claims 3
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims 3
- 125000000547 substituted alkyl group Chemical group 0.000 claims 3
- JVVRJMXHNUAPHW-UHFFFAOYSA-N 1h-pyrazol-5-amine Chemical compound NC=1C=CNN=1 JVVRJMXHNUAPHW-UHFFFAOYSA-N 0.000 claims 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims 2
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 125000005089 alkenylaminocarbonyl group Chemical group 0.000 claims 2
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 claims 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 2
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 2
- 125000003282 alkyl amino group Chemical group 0.000 claims 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims 2
- 125000004414 alkyl thio group Chemical group 0.000 claims 2
- 125000005095 alkynylaminocarbonyl group Chemical group 0.000 claims 2
- 125000005225 alkynyloxycarbonyl group Chemical group 0.000 claims 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims 2
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 claims 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 2
- 239000003054 catalyst Substances 0.000 claims 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 2
- 150000001875 compounds Chemical class 0.000 claims 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 2
- 125000004663 dialkyl amino group Chemical group 0.000 claims 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 claims 2
- 125000004772 dichloromethyl group Chemical group [H]C(Cl)(Cl)* 0.000 claims 2
- 125000006260 ethylaminocarbonyl group Chemical group [H]N(C(*)=O)C([H])([H])C([H])([H])[H] 0.000 claims 2
- 125000005843 halogen group Chemical group 0.000 claims 2
- 239000011630 iodine Substances 0.000 claims 2
- 229910052740 iodine Inorganic materials 0.000 claims 2
- 125000001449 isopropyl group Chemical class [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 2
- 125000004123 n-propyl group Chemical class [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000001478 1-chloroethyl group Chemical group [H]C([H])([H])C([H])(Cl)* 0.000 claims 1
- 125000005999 2-bromoethyl group Chemical group 0.000 claims 1
- 125000001340 2-chloroethyl group Chemical group [H]C([H])(Cl)C([H])([H])* 0.000 claims 1
- 125000001627 3 membered heterocyclic group Chemical group 0.000 claims 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims 1
- 239000004606 Fillers/Extenders Substances 0.000 claims 1
- 229940100198 alkylating agent Drugs 0.000 claims 1
- 239000002168 alkylating agent Substances 0.000 claims 1
- 125000001769 aryl amino group Chemical group 0.000 claims 1
- 125000005110 aryl thio group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 239000011230 binding agent Substances 0.000 claims 1
- 125000005997 bromomethyl group Chemical group 0.000 claims 1
- 125000000480 butynyl group Chemical group [*]C#CC([H])([H])C([H])([H])[H] 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 1
- 238000007796 conventional method Methods 0.000 claims 1
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000001559 cyclopropyl group Chemical class [H]C1([H])C([H])([H])C1([H])* 0.000 claims 1
- 125000004774 dichlorofluoromethyl group Chemical group FC(Cl)(Cl)* 0.000 claims 1
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 1
- 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims 1
- 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 claims 1
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims 1
- 125000006341 heptafluoro n-propyl group Chemical group FC(F)(F)C(F)(F)C(F)(F)* 0.000 claims 1
- 239000004009 herbicide Substances 0.000 claims 1
- 125000005842 heteroatom Chemical group 0.000 claims 1
- 150000002576 ketones Chemical class 0.000 claims 1
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims 1
- UCFFGYASXIPWPD-UHFFFAOYSA-N methyl hypochlorite Chemical compound COCl UCFFGYASXIPWPD-UHFFFAOYSA-N 0.000 claims 1
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims 1
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 1
- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- 150000003254 radicals Chemical class 0.000 claims 1
- 229920006395 saturated elastomer Polymers 0.000 claims 1
- 125000003107 substituted aryl group Chemical group 0.000 claims 1
- 125000005346 substituted cycloalkyl group Chemical group 0.000 claims 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 1
- 125000006337 tetrafluoro ethyl group Chemical group 0.000 claims 1
- 125000006000 trichloroethyl group Chemical group 0.000 claims 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 claims 1
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 1
- 210000003708 urethra Anatomy 0.000 claims 1
Classifications
-
- 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
- C07D231/14—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 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
- C07D231/38—Nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEP3426424.8 | 1984-07-18 | ||
| DE3426424A DE3426424A1 (de) | 1984-07-18 | 1984-07-18 | Substituierte 5-amino-1-phenylpyrazole |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR860001072A true KR860001072A (ko) | 1986-02-22 |
Family
ID=6240927
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1019850005067A Ceased KR860001072A (ko) | 1984-07-18 | 1985-07-16 | 치환된 5-아미노-1- 페닐피라졸의 제조방법 |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US4740232A (enExample) |
| EP (1) | EP0173821B1 (enExample) |
| JP (1) | JPS6136267A (enExample) |
| KR (1) | KR860001072A (enExample) |
| AT (1) | ATE40119T1 (enExample) |
| AU (1) | AU574204B2 (enExample) |
| BR (1) | BR8503419A (enExample) |
| DD (1) | DD238909A5 (enExample) |
| DE (2) | DE3426424A1 (enExample) |
| DK (1) | DK325985A (enExample) |
| ES (3) | ES8609268A1 (enExample) |
| GR (1) | GR851758B (enExample) |
| HU (1) | HU198609B (enExample) |
| IL (1) | IL75809A (enExample) |
| NZ (1) | NZ212737A (enExample) |
| TR (1) | TR22440A (enExample) |
| ZA (1) | ZA855386B (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3520331A1 (de) * | 1985-06-07 | 1986-12-11 | Bayer Ag, 5090 Leverkusen | 1-aryl-5-alkoximinoalkylamino-pyrazole |
| DE3539844A1 (de) | 1985-11-09 | 1987-05-14 | Bayer Ag | Substituierte 5-amino-1-aryl-pyrazole |
| DE3707686A1 (de) * | 1987-03-11 | 1988-09-22 | Bayer Ag | 4-cyano-1-aryl-pyrazole |
| DE3712072A1 (de) * | 1987-04-09 | 1988-10-20 | Bayer Ag | 1-aralkylpyrazole |
| US5360910A (en) * | 1991-04-30 | 1994-11-01 | Rhone-Poulenc Ag Company | Pesticidal 1-aryl-5-(substituted alkylideneimino)pyrazoles |
| IL101702A (en) * | 1991-04-30 | 1996-03-31 | Rhone Poulenc Agrochimie | 1-aryl-5-(substituted alkylideneimino)-pyrazoles process for their preparation and arthropodicidal nematodicidal helminthicidal and protozoocidal compositions containing them |
| US5236938A (en) * | 1991-04-30 | 1993-08-17 | Rhone-Poulenc Inc. | Pesticidal 1-aryl-5-(substituted alkylideneimino)pyrazoles |
| SE517612C2 (sv) * | 1995-12-20 | 2002-06-25 | Rhone Poulenc Agrochimie | Användning av 5-amino-4-etylsulfinyl-1-arylpyrazol föreningar som pesticider |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| HU187320B (en) * | 1980-02-26 | 1985-12-28 | May & Baker Ltd | Herbicides consisting of n-phenyl derivates and process for production of n-phenyl-pirasole derivates |
| MA19540A1 (fr) * | 1981-07-17 | 1983-04-01 | May & Baker Ltd | Derives du n-phenylpyrazole |
| DE3129429A1 (de) * | 1981-07-25 | 1983-02-10 | Basf Ag, 6700 Ludwigshafen | 5-amino-1-phenyl-pyrazol-4-carbonsaeurederivate, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses |
| MA19840A1 (fr) * | 1982-07-15 | 1984-04-01 | May & Baker Ltd | Alcoylamino n-phenyl pyrazole et n-phenyl pyrazole lactames herbicides . |
| GB2123420B (en) * | 1982-07-15 | 1986-03-26 | May And Barker Limited | Herbicidal n-phenylpyrazole derivatives |
| DE3420985A1 (de) * | 1983-10-15 | 1985-04-25 | Bayer Ag, 5090 Leverkusen | Substituierte 5-acylamino-1-phenylpyrazole |
-
1984
- 1984-07-18 DE DE3426424A patent/DE3426424A1/de not_active Withdrawn
-
1985
- 1985-07-08 DE DE8585108420T patent/DE3567646D1/de not_active Expired
- 1985-07-08 AT AT85108420T patent/ATE40119T1/de not_active IP Right Cessation
- 1985-07-08 EP EP85108420A patent/EP0173821B1/de not_active Expired
- 1985-07-11 US US06/754,048 patent/US4740232A/en not_active Expired - Fee Related
- 1985-07-12 AU AU44883/85A patent/AU574204B2/en not_active Ceased
- 1985-07-15 NZ NZ212737A patent/NZ212737A/en unknown
- 1985-07-15 IL IL75809A patent/IL75809A/xx unknown
- 1985-07-16 KR KR1019850005067A patent/KR860001072A/ko not_active Ceased
- 1985-07-16 DD DD85278632A patent/DD238909A5/de not_active IP Right Cessation
- 1985-07-16 ES ES545254A patent/ES8609268A1/es not_active Expired
- 1985-07-16 GR GR851758A patent/GR851758B/el unknown
- 1985-07-17 HU HU852750A patent/HU198609B/hu not_active IP Right Cessation
- 1985-07-17 TR TR32477/85A patent/TR22440A/xx unknown
- 1985-07-17 BR BR8503419A patent/BR8503419A/pt unknown
- 1985-07-17 DK DK325985A patent/DK325985A/da not_active Application Discontinuation
- 1985-07-17 ZA ZA855386A patent/ZA855386B/xx unknown
- 1985-07-18 JP JP15710085A patent/JPS6136267A/ja active Pending
-
1986
- 1986-04-01 ES ES553561A patent/ES8703431A1/es not_active Expired
- 1986-04-01 ES ES553560A patent/ES8703430A1/es not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6136267A (ja) | 1986-02-20 |
| ES8703430A1 (es) | 1987-02-16 |
| ES553561A0 (es) | 1987-02-16 |
| ES545254A0 (es) | 1986-07-16 |
| ATE40119T1 (de) | 1989-02-15 |
| HUT38505A (en) | 1986-06-30 |
| NZ212737A (en) | 1987-11-27 |
| DE3426424A1 (de) | 1986-01-23 |
| ES8609268A1 (es) | 1986-07-16 |
| ES8703431A1 (es) | 1987-02-16 |
| EP0173821A1 (de) | 1986-03-12 |
| GR851758B (enExample) | 1985-11-26 |
| DD238909A5 (de) | 1986-09-10 |
| IL75809A (en) | 1989-10-31 |
| TR22440A (tr) | 1987-06-26 |
| BR8503419A (pt) | 1986-04-08 |
| EP0173821B1 (de) | 1989-01-18 |
| ZA855386B (en) | 1986-07-30 |
| IL75809A0 (en) | 1985-11-29 |
| DE3567646D1 (en) | 1989-02-23 |
| HU198609B (en) | 1989-11-28 |
| AU4488385A (en) | 1986-01-23 |
| DK325985D0 (da) | 1985-07-17 |
| DK325985A (da) | 1986-01-19 |
| ES553560A0 (es) | 1987-02-16 |
| US4740232A (en) | 1988-04-26 |
| AU574204B2 (en) | 1988-06-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PA0109 | Patent application |
Patent event code: PA01091R01D Comment text: Patent Application Patent event date: 19850716 |
|
| PG1501 | Laying open of application | ||
| A201 | Request for examination | ||
| PA0201 | Request for examination |
Patent event code: PA02012R01D Patent event date: 19890920 Comment text: Request for Examination of Application Patent event code: PA02011R01I Patent event date: 19850716 Comment text: Patent Application |
|
| E902 | Notification of reason for refusal | ||
| PE0902 | Notice of grounds for rejection |
Comment text: Notification of reason for refusal Patent event date: 19910530 Patent event code: PE09021S01D |
|
| E601 | Decision to refuse application | ||
| PE0601 | Decision on rejection of patent |
Patent event date: 19910904 Comment text: Decision to Refuse Application Patent event code: PE06012S01D Patent event date: 19910530 Comment text: Notification of reason for refusal Patent event code: PE06011S01I |