GB1419789A - 2-trifluoromethyl-4-quinolinols - Google Patents
2-trifluoromethyl-4-quinolinolsInfo
- Publication number
- GB1419789A GB1419789A GB3043974A GB3043974A GB1419789A GB 1419789 A GB1419789 A GB 1419789A GB 3043974 A GB3043974 A GB 3043974A GB 3043974 A GB3043974 A GB 3043974A GB 1419789 A GB1419789 A GB 1419789A
- Authority
- GB
- United Kingdom
- Prior art keywords
- trifluoromethyl
- alkyl
- halogen
- quinolinols
- ethyl
- 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.)
- Expired
Links
- SUNAMHNJYSQUPL-UHFFFAOYSA-N 2-(trifluoromethyl)-1h-quinolin-4-one Chemical class C1=CC=C2NC(C(F)(F)F)=CC(=O)C2=C1 SUNAMHNJYSQUPL-UHFFFAOYSA-N 0.000 title abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical class 0.000 abstract 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- CKUFLXIDNIXAEK-UHFFFAOYSA-N 3-methyl-6-nitro-2,8-bis(trifluoromethyl)-1H-quinolin-4-one Chemical compound [N+](=O)([O-])C=1C=C2C(=C(C(=NC2=C(C1)C(F)(F)F)C(F)(F)F)C)O CKUFLXIDNIXAEK-UHFFFAOYSA-N 0.000 abstract 1
- DKYMVJNAPJUIDZ-UHFFFAOYSA-N 6,8-dichloro-3-methyl-2-(trifluoromethyl)-1h-quinolin-4-one Chemical compound C1=C(Cl)C=C2C(=O)C(C)=C(C(F)(F)F)NC2=C1Cl DKYMVJNAPJUIDZ-UHFFFAOYSA-N 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-M Butyrate Chemical compound CCCC([O-])=O FERIUCNNQQJTOY-UHFFFAOYSA-M 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 229910052783 alkali metal Inorganic materials 0.000 abstract 1
- 150000001340 alkali metals Chemical class 0.000 abstract 1
- -1 alkylamine salts Chemical class 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 150000001448 anilines Chemical class 0.000 abstract 1
- 230000005494 condensation Effects 0.000 abstract 1
- 238000009833 condensation Methods 0.000 abstract 1
- WBABTXDYXLMRPM-NTMALXAHSA-N ethyl (z)-3-anilino-4,4,4-trifluorobut-2-enoate Chemical compound CCOC(=O)\C=C(C(F)(F)F)/NC1=CC=CC=C1 WBABTXDYXLMRPM-NTMALXAHSA-N 0.000 abstract 1
- OCJKUQIPRNZDTK-UHFFFAOYSA-N ethyl 4,4,4-trifluoro-3-oxobutanoate Chemical compound CCOC(=O)CC(=O)C(F)(F)F OCJKUQIPRNZDTK-UHFFFAOYSA-N 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
Classifications
-
- 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
- C07D215/233—Oxygen atoms attached in position 2 or 4 only one oxygen atom which is attached in position 4
-
- 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
-
- 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
- C07D215/36—Sulfur atoms
-
- 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
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
1419789 2 - Trifluoromethyl - 4 - quinolinols PFIZER Inc 11 Jan 1973 [2 Aug 1972] 30439/74 Divided out of 1419788 Heading C2C 2 - Trifluoromethyl - 4 - quinolinols of general formula or the alkali metal, ammonia and alkylamine salts thereof, wherein R 1 is H, halogen or C 1-4 alkyl; each of R 2 and R 3 is CN, NO 2 , CF 3 , C 1-5 acyl, S(O)R 4 , S(O) 2 R 4 , SO 2 NR 4 R 5 or CONR 4 R 5 in which R 4 and R 5 are each C 1-4 alkyl or R 2 is H, halogen or C 1-4 alkyl and R 3 is halogen or C 1-4 alkyl with the provisos that (a) when both R 1 and R 2 are H, R 3 is not a 6- or 8-position substituent and (b) when each of R 2 and R 3 is halogen or CH 3 and R 1 is H, R 2 and R 3 are not 6- and 8-position substituents, are prepared by condensation of the appropriate aniline derivative with ethyl 3-keto, 4,4,4-trifluorobutyrate or the appropriate ethyl-2-alkyl-3- keto-4,4,4-trifluoro butyrate in polyphosphonic acid at 100-200‹ C. Alternatively, the intermediate ethyl 3-anilino-trifluorocrotonate can be isolated and cyclized by heating in a suitable solvent at about 250‹ C. The 2-trifluoromethyl- 4-quinolinols in which R 1 = H can be chlorinated or brominated in the 3-position by reaction with SOCl 2 , Cl 2 or Br 2 . Amongst numerous examples compounds 6,8-dichloro-3-methyl-2- trifluoromethyl - 4 - quinolinol and 6 - nitro - 3- methyl - 2,8 - bis - (trifluoromethyl) - 4 - quinolinol are prepared. Herbicidal compositions comprise compounds of the above general formula and a carrier.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27731572A | 1972-08-02 | 1972-08-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1419789A true GB1419789A (en) | 1975-12-31 |
Family
ID=23060321
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB3043974A Expired GB1419789A (en) | 1972-08-02 | 1973-01-11 | 2-trifluoromethyl-4-quinolinols |
| GB162573A Expired GB1419788A (en) | 1972-08-02 | 1973-01-11 | Herbicidal method using 2-trifuluromethyl-4-quinolinols |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB162573A Expired GB1419788A (en) | 1972-08-02 | 1973-01-11 | Herbicidal method using 2-trifuluromethyl-4-quinolinols |
Country Status (1)
| Country | Link |
|---|---|
| GB (2) | GB1419789A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8697673B2 (en) | 2011-03-31 | 2014-04-15 | Pfizer Inc. | Bicyclic pyridinones |
| US8916564B2 (en) | 2012-09-21 | 2014-12-23 | Pfizer Inc. | Substituted pyrido[1,2-a]pyrazines for the treatment of neurodegenerative and neurological disorders |
| US9765073B2 (en) | 2015-02-03 | 2017-09-19 | Pfizer Inc. | Cyclopropabenzofuranyl pyridopyrazinediones |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3210979A1 (en) * | 1982-03-25 | 1983-09-29 | Basf Ag, 6700 Ludwigshafen | 3-CHLORINE-8-CYANO-CHINOLINE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE FOR COMBATING UNWANTED PLANT GROWTH |
| DE3229175A1 (en) * | 1982-08-05 | 1984-02-09 | Basf Ag, 6700 Ludwigshafen | 3,7-DICHLOR-8-CHINOLINE DERIVATIVES |
| FR2680510B1 (en) * | 1991-08-20 | 1995-06-23 | Roussel Uclaf | NEW NITROGEN BICYCLIC DERIVATIVES, THEIR PREPARATION PROCESS, THE NEW INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| FR2684671B1 (en) * | 1991-11-20 | 1995-05-19 | Roussel Uclaf | NEW QUINOLEIN DERIVATIVES, THEIR PREPARATION AND INTERMEDIATE PROCESSES AND THEIR APPLICATION AS MEDICAMENTS. |
| FR2680509B1 (en) * | 1991-08-20 | 1995-07-28 | Roussel Uclaf | NITROGEN BICYCLIC DERIVATIVES SUBSTITUTED BY A RADICAL BENZYL, THEIR PREPARATION PROCESS, THE INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE COMPOSITIONS CONTAINING THEM. |
| JP3531944B2 (en) * | 1991-02-07 | 2004-05-31 | アベンティス・ファーマ・ソシエテ・アノニム | Novel benzyl group-substituted nitrogen-based bicyclic derivative and method for producing the same |
| FR2672597B1 (en) * | 1991-02-07 | 1995-05-19 | Roussel Uclaf | NEW N-SUBSTITUTED QUINOLEIN DERIVATIVES, THEIR PREPARATION PROCESS, THE NEW INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| FR2672595B1 (en) * | 1991-02-07 | 1995-05-19 | Roussel Uclaf | NOVEL NITROGEN BICYCLIC DERIVATIVES SUBSTITUTED BY A RADICAL BENZYL, THEIR PREPARATION PROCESS, THE NEW INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS. |
| FR2672596B1 (en) * | 1991-02-07 | 1995-07-13 | Roussel Uclaf | NEW NITROGEN BICYCLIC DERIVATIVES, THEIR PREPARATION PROCESS, THE NEW INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
| FR2680511B1 (en) * | 1991-08-20 | 1995-05-19 | Roussel Uclaf | N-SUBSTITUTED QUINOLEIN DERIVATIVES, THEIR PREPARATION PROCESS, INTERMEDIATES OBTAINED, THEIR APPLICATION AS MEDICAMENTS AND THE COMPOSITIONS CONTAINING THEM. |
| IL100555A (en) * | 1991-02-07 | 2000-08-31 | Hoechst Marion Roussel Inc | N-substituted quinoline derivatives their preparation their use for the preparation of medicaments and the pharmaceutical compositions containing them |
| MX9200299A (en) * | 1991-02-07 | 1992-12-01 | Roussel Uclaf | NEW NITROGENATED BICYCLE DERIVATIVES, THEIR PROCEDURE FOR PREPARING THE NEW INTERMEDIATE COMPOUNDS OBTAINED THEIR APPLICATION AS MEDICINES AND THE PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM. |
| FR3132613B1 (en) * | 2022-02-17 | 2025-02-28 | Ecole Polytech | Use of chromene or chroman derivatives as herbicidal agents |
-
1973
- 1973-01-11 GB GB3043974A patent/GB1419789A/en not_active Expired
- 1973-01-11 GB GB162573A patent/GB1419788A/en not_active Expired
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8697673B2 (en) | 2011-03-31 | 2014-04-15 | Pfizer Inc. | Bicyclic pyridinones |
| US9067934B2 (en) | 2011-03-31 | 2015-06-30 | Pfizer Inc. | Bicyclic pyridinones |
| US8916564B2 (en) | 2012-09-21 | 2014-12-23 | Pfizer Inc. | Substituted pyrido[1,2-a]pyrazines for the treatment of neurodegenerative and neurological disorders |
| US9193726B2 (en) | 2012-09-21 | 2015-11-24 | Pfizer Inc. | Substituted pyrido[1,2-a]pyrazines for the treatment of neurodegenerative and neurological disorders |
| US9751877B2 (en) | 2012-09-21 | 2017-09-05 | Pfizer Inc. | Substituted pyrido[1,2-a]pyrazines for the treatment of neurodegenerative and neurological disorders |
| US9765073B2 (en) | 2015-02-03 | 2017-09-19 | Pfizer Inc. | Cyclopropabenzofuranyl pyridopyrazinediones |
Also Published As
| Publication number | Publication date |
|---|---|
| GB1419788A (en) | 1975-12-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed | ||
| PCNP | Patent ceased through non-payment of renewal fee |