IN2014DN08588A - - Google Patents
Info
- Publication number
- IN2014DN08588A IN2014DN08588A IN8588DEN2014A IN2014DN08588A IN 2014DN08588 A IN2014DN08588 A IN 2014DN08588A IN 8588DEN2014 A IN8588DEN2014 A IN 8588DEN2014A IN 2014DN08588 A IN2014DN08588 A IN 2014DN08588A
- Authority
- IN
- India
- Prior art keywords
- 1himidazol
- benzenamine
- trifluoromethyl
- safe
- prepare
- Prior art date
Links
- JGJYPPNLUXMOKO-UHFFFAOYSA-N 2-(pyrimidin-2-ylamino)benzamide Chemical class NC(=O)C1=CC=CC=C1NC1=NC=CC=N1 JGJYPPNLUXMOKO-UHFFFAOYSA-N 0.000 abstract 1
- WWTGXYAJVXKEKL-UHFFFAOYSA-N 3-(4-methylimidazol-1-yl)-5-(trifluoromethyl)aniline Chemical compound C1=NC(C)=CN1C1=CC(N)=CC(C(F)(F)F)=C1 WWTGXYAJVXKEKL-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- 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
- C07D233/56—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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C205/00—Compounds containing nitro groups bound to a carbon skeleton
- C07C205/07—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms
- C07C205/11—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings
- C07C205/12—Compounds containing nitro groups bound to a carbon skeleton the carbon skeleton being further substituted by halogen atoms having nitro groups bound to carbon atoms of six-membered aromatic rings the six-membered aromatic ring or a condensed ring system containing that ring being substituted by halogen atoms
-
- 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
- C07D233/56—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
- C07D233/61—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 with hydrocarbon radicals, substituted by nitrogen atoms not forming part of a nitro radical, attached to ring nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
The present invention provides an efficient, safe and cost effective way to prepare 5-(4-methyl-1Himidazol- l-yl)-3- (trifluoromethyl)-benzenamine which is a key intermediate for the preparation of substituted pyrimidinylaminobenzamides of formula (11).
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US68897605P | 2005-06-09 | 2005-06-09 | |
| PCT/US2006/022154 WO2006135640A2 (en) | 2005-06-09 | 2006-06-07 | Process for the synthesis of organic compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| IN2014DN08588A true IN2014DN08588A (en) | 2015-07-10 |
Family
ID=37149980
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IN8588DEN2014 IN2014DN08588A (en) | 2005-06-09 | 2006-06-07 | |
| IN8578DEN2014 IN2014DN08578A (en) | 2005-06-09 | 2006-06-07 |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| IN8578DEN2014 IN2014DN08578A (en) | 2005-06-09 | 2006-06-07 |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US7781597B2 (en) |
| EP (3) | EP1896426B1 (en) |
| JP (2) | JP5225078B2 (en) |
| KR (2) | KR101249199B1 (en) |
| CN (6) | CN102180796A (en) |
| AR (1) | AR057056A1 (en) |
| AT (1) | ATE540931T1 (en) |
| AU (3) | AU2006258050B2 (en) |
| BR (1) | BRPI0611683A2 (en) |
| CA (4) | CA2833394C (en) |
| DK (2) | DK2292607T3 (en) |
| ES (3) | ES2380489T3 (en) |
| GT (1) | GT200600202AA (en) |
| HU (1) | HUE028024T2 (en) |
| IN (2) | IN2014DN08588A (en) |
| JO (1) | JO2758B1 (en) |
| MX (1) | MX2007015609A (en) |
| MY (1) | MY146795A (en) |
| PE (3) | PE20070109A1 (en) |
| PL (3) | PL1896426T3 (en) |
| PT (3) | PT2292607E (en) |
| RU (1) | RU2446162C2 (en) |
| SI (2) | SI2292607T1 (en) |
| TW (1) | TWI380981B (en) |
| WO (1) | WO2006135640A2 (en) |
Families Citing this family (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4883296B2 (en) | 2004-03-05 | 2012-02-22 | 日産化学工業株式会社 | Isoxazoline-substituted benzamide compounds and pest control agents |
| MY146795A (en) * | 2005-06-09 | 2012-09-28 | Novartis Ag | Process for the synthesis of organic compounds |
| TW200803740A (en) | 2005-12-16 | 2008-01-16 | Du Pont | 5-aryl isoxazolines for controlling invertebrate pests |
| TWI412322B (en) | 2005-12-30 | 2013-10-21 | Du Pont | Isoxazolines for controlling invertebrate pests |
| JP5473906B2 (en) | 2007-06-13 | 2014-04-16 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | Isoxazoline insecticide |
| TWI430995B (en) | 2007-06-26 | 2014-03-21 | Du Pont | Naphthalene isoxazoline invertebrate pest control agents |
| JP6006471B2 (en) | 2007-06-27 | 2016-10-12 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニーE.I.Du Pont De Nemours And Company | Animal pest control methods |
| TWI649303B (en) | 2007-08-17 | 2019-02-01 | 杜邦股份有限公司 | Compound and method for preparing 4-acetyl-n-[2-oxo-2-[(2,2,2-trifluoroethyl)amino]ethyl]-1-naphthalenecarboxamide |
| AU2008308907B2 (en) | 2007-10-03 | 2014-08-14 | Corteva Agriscience Llc | Naphthalene isoxazoline compounds for control of invertebrate pests |
| TWI455919B (en) * | 2008-04-09 | 2014-10-11 | Du Pont | Method for preparing 3-trifluoromethylchalcone (CHALCONE) |
| EP2305667A3 (en) | 2008-07-17 | 2011-05-11 | Teva Pharmaceutical Industries Ltd. | Nilotinib intermediates and preparation thereof |
| EP2262793B1 (en) | 2008-11-05 | 2012-10-03 | Teva Pharmaceutical Industries Ltd. | Nilotinib hci crystalline forms |
| WO2010060074A1 (en) * | 2008-11-24 | 2010-05-27 | Teva Pharmaceutical Industries Ltd. | Preparation of nilotinib and intermediates thereof |
| US20110053968A1 (en) * | 2009-06-09 | 2011-03-03 | Auspex Pharmaceuticals, Inc. | Aminopyrimidine inhibitors of tyrosine kinase |
| UA108881C2 (en) | 2010-05-27 | 2015-06-25 | CRYSTAL FORM 4- $ 5- $ 3-CHLORINE-5- (TRIFLUOROMETHYL) PHENYL] -4,5-DIHYDRO-5- (TRIFLUORMETHYL) -3-ISOXAZOLYL] -N- $ 2-OXO-2 - $ 2,2 -TRIFLUOROTHYL) AMINO] ETHYL] -1-NAPHTHALINE CARBOXAMIDE | |
| DK2797927T3 (en) | 2011-12-30 | 2019-10-28 | Hanmi Pharm Ind Co Ltd | THIENO [3,2-d] PYRIMIDINE DERIVATIVES WHICH HAVE INHIBITORIAL ACTIVITY FOR PROTEINKINASE |
| CN102592837B (en) * | 2012-03-12 | 2014-01-15 | 河北师范大学 | Method for preparing polyaniline electrode doped with tetrachloride metal quaternary ammonium salt for supercapacitor |
| CN103694176B (en) | 2014-01-07 | 2015-02-18 | 苏州立新制药有限公司 | Preparation method of nilotinib intermediate |
| CN104592122B (en) * | 2014-12-09 | 2018-01-23 | 凯莱英医药集团(天津)股份有限公司 | The preparation method of 3 (base of 4 methyl 1H imidazoles 1) 5 (trifluoromethyl) aniline |
| CN105985293B (en) * | 2015-03-04 | 2018-04-03 | 埃斯特维华义制药有限公司 | The preparation method of AMN107 intermediate |
| EP3095782A1 (en) | 2015-05-18 | 2016-11-23 | Esteve Química, S.A. | New method for preparing 3-(4-methyl-1h-imidazol-1-yl)-5-(trifluoromethyl)benzenamine |
| CN107201532B (en) * | 2017-05-09 | 2019-08-27 | 吉林凯莱英医药化学有限公司 | The nitration method of aromatic compound |
| US11053220B2 (en) | 2018-01-01 | 2021-07-06 | Laurus Labs Ltd | Process for 3-(4-methyl-1H-imidazol-1-yl)-5-(trifluoromethyl) aniline |
| CN108530364B (en) | 2018-04-10 | 2020-01-21 | 江苏创诺制药有限公司 | Crystal form of 3- (4-methyl-1H-imidazole-1-yl) -5-trifluoromethyl aniline monohydrochloride and application thereof |
| JP7409696B2 (en) | 2018-06-15 | 2024-01-09 | ハンダ ファーマシューティカルズ インコーポレイテッド | Kinase inhibitor salts and compositions thereof |
| WO2020210174A2 (en) * | 2019-04-06 | 2020-10-15 | Trinapco, Inc. | Sulfonyldiazoles and n-(fluorosulfonyl)azoles, and methods of making the same |
| EP3904342A1 (en) | 2020-04-28 | 2021-11-03 | Grindeks, A Joint Stock Company | Process for the preparation of 3-(trifluoromethyl)-5-(4-methyl-1h-imidazole-1-yl)-benzeneamine hydrochloride |
| CN114751836B (en) * | 2021-02-23 | 2024-05-31 | 四川青木制药有限公司 | Synthesis method and intermediate of 3- (4-methyl-1H-imidazol-1-yl) -5- (trifluoromethyl) aniline |
| CN114853734A (en) * | 2022-06-14 | 2022-08-05 | 海南鑫开源医药科技有限公司 | A kind of preparation method of Nilotinib free base |
| CN116478319B (en) * | 2022-11-07 | 2025-07-01 | 华北电力大学 | Preparation method of an ionic covalent organic polymer and its application in adsorbing ReO4- in an alkaline environment |
| CN115626880B (en) * | 2022-11-15 | 2023-11-14 | 常州大学 | Synthesis method of 3-nitro-5-cyano benzotrifluoride |
| CN118108670B (en) * | 2023-12-28 | 2025-07-01 | 江苏希迪制药有限公司 | Purification method of nilotinib intermediate 3- (4-methyl-1H-imidazol-1-yl) -5- (trifluoromethyl) aniline |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SU1051076A1 (en) * | 1982-04-09 | 1983-10-30 | Алтайский политехнический институт | Process for preparing imidazole derivatives |
| GR851296B (en) * | 1984-05-29 | 1985-11-25 | Pfizer | |
| GB8413685D0 (en) * | 1984-05-29 | 1984-07-04 | Pfizer Ltd | Quinolone inotropic agents |
| GB8502267D0 (en) * | 1985-01-30 | 1985-02-27 | Pfizer Ltd | Quinolone inotropic agents |
| HN2001000008A (en) * | 2000-01-21 | 2003-12-11 | Inc Agouron Pharmaceuticals | AMIDA COMPOSITE AND PHARMACEUTICAL COMPOSITIONS TO INHIBIT PROTEINKINASES, AND THE INSTRUCTIONS FOR USE |
| GB0023383D0 (en) * | 2000-09-23 | 2000-11-08 | Synprotec Ltd | 3,5-Bis (Trifluormethyl)Benzene derivatives |
| AR037647A1 (en) | 2002-05-29 | 2004-12-01 | Novartis Ag | USED DIARILUREA DERIVATIVES FOR THE TREATMENT OF DEPENDENT DISEASES OF THE PROTEIN KINase |
| GB0215676D0 (en) * | 2002-07-05 | 2002-08-14 | Novartis Ag | Organic compounds |
| GB0222514D0 (en) * | 2002-09-27 | 2002-11-06 | Novartis Ag | Organic compounds |
| CN1939910A (en) * | 2004-12-31 | 2007-04-04 | 孙飘扬 | Amino-metadiazine compound and its salt, its preparation and pharmaceutical use |
| GT200600207A (en) * | 2005-06-09 | 2007-01-15 | Novartis Ag | PROCESS FOR THE SYNTHESIS OF ORGANIC COMPOUNDS |
| MY146795A (en) * | 2005-06-09 | 2012-09-28 | Novartis Ag | Process for the synthesis of organic compounds |
-
2006
- 2006-05-31 MY MYPI20062506A patent/MY146795A/en unknown
- 2006-06-06 JO JO2006161A patent/JO2758B1/en active
- 2006-06-07 AT AT06772447T patent/ATE540931T1/en active
- 2006-06-07 PE PE2006000628A patent/PE20070109A1/en not_active Application Discontinuation
- 2006-06-07 CN CN2011100581769A patent/CN102180796A/en active Pending
- 2006-06-07 WO PCT/US2006/022154 patent/WO2006135640A2/en active Application Filing
- 2006-06-07 EP EP06772447A patent/EP1896426B1/en active Active
- 2006-06-07 PT PT101719425T patent/PT2292607E/en unknown
- 2006-06-07 HU HUE10171941A patent/HUE028024T2/en unknown
- 2006-06-07 CN CN200680019924XA patent/CN101189212B/en not_active Expired - Fee Related
- 2006-06-07 JP JP2008515880A patent/JP5225078B2/en not_active Expired - Fee Related
- 2006-06-07 ES ES06772447T patent/ES2380489T3/en active Active
- 2006-06-07 CA CA2833394A patent/CA2833394C/en active Active
- 2006-06-07 PT PT101719417T patent/PT2266961E/en unknown
- 2006-06-07 RU RU2007148238/04A patent/RU2446162C2/en active
- 2006-06-07 MX MX2007015609A patent/MX2007015609A/en active IP Right Grant
- 2006-06-07 PE PE2010000467A patent/PE20100715A1/en not_active Application Discontinuation
- 2006-06-07 US US11/915,691 patent/US7781597B2/en active Active
- 2006-06-07 DK DK10171942.5T patent/DK2292607T3/en active
- 2006-06-07 IN IN8588DEN2014 patent/IN2014DN08588A/en unknown
- 2006-06-07 AU AU2006258050A patent/AU2006258050B2/en not_active Ceased
- 2006-06-07 PL PL06772447T patent/PL1896426T3/en unknown
- 2006-06-07 PL PL10171941T patent/PL2266961T3/en unknown
- 2006-06-07 EP EP10171941.7A patent/EP2266961B1/en active Active
- 2006-06-07 KR KR1020077028642A patent/KR101249199B1/en not_active Expired - Fee Related
- 2006-06-07 EP EP10171942.5A patent/EP2292607B1/en active Active
- 2006-06-07 PL PL10171942T patent/PL2292607T3/en unknown
- 2006-06-07 PT PT06772447T patent/PT1896426E/en unknown
- 2006-06-07 CN CN2011100581773A patent/CN102174020B/en not_active Expired - Fee Related
- 2006-06-07 AR ARP060102367A patent/AR057056A1/en unknown
- 2006-06-07 SI SI200631789T patent/SI2292607T1/en unknown
- 2006-06-07 ES ES10171941.7T patent/ES2558696T3/en active Active
- 2006-06-07 CN CN2011100581788A patent/CN102174021B/en not_active Expired - Fee Related
- 2006-06-07 CN CN2011100574125A patent/CN102180836B/en not_active Expired - Fee Related
- 2006-06-07 CN CN2011100572469A patent/CN102174019B/en not_active Expired - Fee Related
- 2006-06-07 CA CA2886482A patent/CA2886482C/en active Active
- 2006-06-07 IN IN8578DEN2014 patent/IN2014DN08578A/en unknown
- 2006-06-07 DK DK10171941.7T patent/DK2266961T3/en active
- 2006-06-07 SI SI200632010T patent/SI2266961T1/en unknown
- 2006-06-07 BR BRPI0611683-3A patent/BRPI0611683A2/en active Search and Examination
- 2006-06-07 KR KR1020127011979A patent/KR101283109B1/en not_active Expired - Fee Related
- 2006-06-07 CA CA2942046A patent/CA2942046A1/en not_active Abandoned
- 2006-06-07 PE PE2010000468A patent/PE20100716A1/en not_active Application Discontinuation
- 2006-06-07 CA CA2611280A patent/CA2611280C/en active Active
- 2006-06-07 ES ES10171942.5T patent/ES2465522T3/en active Active
- 2006-06-08 TW TW095120304A patent/TWI380981B/en not_active IP Right Cessation
-
2010
- 2010-07-12 US US12/834,295 patent/US8008504B2/en not_active Expired - Fee Related
- 2010-11-11 AU AU2010241374A patent/AU2010241374B2/en not_active Ceased
-
2011
- 2011-03-09 AU AU2011201044A patent/AU2011201044A1/en not_active Abandoned
-
2012
- 2012-05-17 GT GT200600202AK patent/GT200600202AA/en unknown
- 2012-09-21 JP JP2012208775A patent/JP2013035855A/en active Pending
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| IN2014DN08588A (en) | ||
| WO2009016462A3 (en) | Substituted bicyclolactam compounds | |
| WO2007085895A3 (en) | Fap inhibitors | |
| TW200626559A (en) | Anilino-pyrimidine analogs | |
| WO2007105058A8 (en) | Pyrazole compounds | |
| WO2007106192A3 (en) | Inhibitors of iap | |
| MX2007011023A (en) | 2- (4-0x0-4h-quinaz0lin-3-yl) acetamides and their use as vasopressin v3 antagonists. | |
| MX2010002938A (en) | (3-hydroxy-4-amino-butan-2-yl) -3- (2-thiazol-2-yl-pyrrolidine-1- carbonyl) benzamide derivatives and related compounds as beta-secretase inhibitors for treating. | |
| DK1696905T3 (en) | Substituted 2-aminotetralines for the prophylactic treatment of Morbus Parkinson | |
| TW200745039A (en) | Isotopically substituted pantoprazole | |
| EP1740559A4 (en) | 1,3,5-substituted phenyl derivative compounds useful as beta-secretase inhibitors for the treatment of alzheimer's disease | |
| WO2007062308A3 (en) | Homo- and heterocyclic compounds suitable as cetp inhibitors | |
| WO2007019191A3 (en) | Thiazolopyrimidine kinase inhibitors | |
| WO2005087724A3 (en) | Sulphonylpyrroles as hdac inhibitors | |
| GB0510143D0 (en) | Novel compounds A1 | |
| TW200624426A (en) | BACE inhibitors | |
| TW200710084A (en) | Process for the synthesis of organic compounds | |
| MY145788A (en) | Antitumoral dihydropyran-2-one compounds | |
| GB0521508D0 (en) | Organic compounds | |
| TNSN06260A1 (en) | Process for the preparation of tryptase inhibitors | |
| TW200619206A (en) | Chemokine-binding heterocyclic compound salts, and methods of use thereof | |
| NZ595579A (en) | 5-Difluoromethoxy-4-hydroxymethyl-1-methyl-3-trifluoromethyl-pyrazole / (5-(difluoromethoxy)-3-(trifluoromethyl)-1-methyl-1H-pyrazol-4-yl)methanol | |
| WO2008019030A8 (en) | Modified azole compounds as antiinfective agents | |
| MXPA02012400A (en) | Hetaryl-substituted heterocycles. | |
| RS20060195A (en) | Imidazopyridine-derivatives as inducible no-synthase inhibitors |