GT200600202AA - PROCESS FOR THE SYNTHESIS OF ORGANIC COMPOUNDS - Google Patents
PROCESS FOR THE SYNTHESIS OF ORGANIC COMPOUNDSInfo
- Publication number
- GT200600202AA GT200600202AA GT200600202AK GT200600202K GT200600202AA GT 200600202A A GT200600202A A GT 200600202AA GT 200600202A K GT200600202A K GT 200600202AK GT 200600202 K GT200600202 K GT 200600202K GT 200600202A A GT200600202A A GT 200600202AA
- Authority
- GT
- Guatemala
- Prior art keywords
- synthesis
- organic compounds
- methyl
- bencenamine
- pyrimidil
- Prior art date
Links
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
Abstract
LA PRESENTE INVENCIÓN PROPORCIONA UNA MANERA EFICIENTE, SEGURA Y EFECTIVA POR EL COSTO, PARA PREPARAR 5-(4-METIL -1H-IMIDAZOL-1-IL)-3- (TRIFLUORO-METIL)-BENCENAMINA, QUE ES UN INTERMEDIARIO CLAVE PARA LA PREPARACIÓN DE PIRIMIDIL-AMINO-BENZAMIDAS SUSTITUIDAS DE LA FÓRMULA IITHIS INVENTION PROVIDES AN EFFICIENT, SAFE AND EFFECTIVE WAY FOR THE COST, TO PREPARE 5- (4-METHYL -1H-IMIDAZOL-1-IL) -3- (TRIFLUORO-METHYL) -BENCENAMINE, WHICH IS A KEY INTERMEDIARY FOR PREPARATION OF PYRIMIDIL-AMINO-BENZAMIDES REPLACED OF FORMULA II
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US68897605P | 2005-06-09 | 2005-06-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
GT200600202AA true GT200600202AA (en) | 2014-06-09 |
Family
ID=37149980
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GT200600202AK GT200600202AA (en) | 2005-06-09 | 2012-05-17 | PROCESS FOR THE SYNTHESIS OF ORGANIC COMPOUNDS |
Country Status (25)
Country | Link |
---|---|
US (2) | US7781597B2 (en) |
EP (3) | EP1896426B1 (en) |
JP (2) | JP5225078B2 (en) |
KR (2) | KR101283109B1 (en) |
CN (6) | CN102174020B (en) |
AR (1) | AR057056A1 (en) |
AT (1) | ATE540931T1 (en) |
AU (3) | AU2006258050B2 (en) |
BR (1) | BRPI0611683A2 (en) |
CA (4) | CA2611280C (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) | PE20100716A1 (en) |
PL (3) | PL2266961T3 (en) |
PT (3) | PT1896426E (en) |
RU (1) | RU2446162C2 (en) |
SI (2) | SI2292607T1 (en) |
TW (1) | TWI380981B (en) |
WO (1) | WO2006135640A2 (en) |
Families Citing this family (30)
Publication number | Priority date | Publication date | Assignee | Title |
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ES2526614T3 (en) | 2004-03-05 | 2015-01-13 | Nissan Chemical Industries, Ltd. | Isoxazoline-substituted benzamide compound and harmful organisms control agent |
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 |
MX2009013469A (en) | 2007-06-13 | 2010-01-20 | Du Pont | Isoxazoline insecticides. |
TWI430995B (en) | 2007-06-26 | 2014-03-21 | Du Pont | Naphthalene isoxazoline invertebrate pest control agents |
MX368680B (en) | 2007-06-27 | 2019-10-11 | Du Pont | Animal pest control method. |
TWI461411B (en) | 2007-08-17 | 2014-11-21 | Du Pont | Method for preparing 5-haloalkyl-4,5-dihydroisoxazole derivatives |
MX2010003557A (en) | 2007-10-03 | 2010-04-12 | Du Pont | Naphthalene isoxazoline compounds for control of invertebrate pests. |
TWI455919B (en) * | 2008-04-09 | 2014-10-11 | Du Pont | Method for preparing 3-trifluoromethyl chalcones |
WO2010009402A2 (en) * | 2008-07-17 | 2010-01-21 | Teva Pharmaceutical Industries Ltd. | Nilotinib intermediates and preparation thereof |
ES2394258T3 (en) | 2008-11-05 | 2013-01-30 | Teva Pharmaceutical Industries Ltd. | Crystal forms of Nilotinib HCL |
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 |
CA2799963C (en) | 2010-05-27 | 2018-01-23 | E. I. Du Pont De Nemours And Company | Crystalline form of 4- [5 - [3 -chloro-5 - (trifluoromethyl) phenyl] -4,5 -dihydro-5 - (trifluoromethyl) -3 - isoxazolyl] -n- [2-0x0-2- [(2,2,2-trifluoroethyl)amino]ethyl] -1-naphthalenecarboxamide |
RU2705577C2 (en) | 2011-12-30 | 2019-11-08 | Ханми Фарм. Ко., Лтд. | THIENO[3,2-d]PYRIMIDINE DERIVATIVES WITH PROTEIN KINASE INHIBITORY ACTIVITY |
CN102592837B (en) * | 2012-03-12 | 2014-01-15 | 河北师范大学 | Method for preparing tetrachloride metal quaternary ammonium salt doped polyaniline electrode for super capacitor |
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 |
TWI815137B (en) | 2018-06-15 | 2023-09-11 | 漢達生技醫藥股份有限公司 | Crystalline of nilotinib lauryl sulfate salt |
CA3136189A1 (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 |
CN114751836A (en) * | 2021-02-23 | 2022-07-15 | 成都硕德药业有限公司 | Method for synthesizing 3- (4-methyl-1H-imidazole-1-yl) -5- (trifluoromethyl) aniline and intermediate thereof |
CN114853734A (en) * | 2022-06-14 | 2022-08-05 | 海南鑫开源医药科技有限公司 | Preparation method of nilotinib free base |
CN115626880B (en) * | 2022-11-15 | 2023-11-14 | 常州大学 | Synthesis method of 3-nitro-5-cyano benzotrifluoride |
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 |
GB8413685D0 (en) * | 1984-05-29 | 1984-07-04 | Pfizer Ltd | Quinolone inotropic agents |
NZ212209A (en) * | 1984-05-29 | 1988-08-30 | Pfizer | Quinolone derivatives and pharmaceutical compositions |
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 |
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2006
- 2006-05-31 MY MYPI20062506A patent/MY146795A/en unknown
- 2006-06-06 JO JO2006161A patent/JO2758B1/en active
- 2006-06-07 HU HUE10171941A patent/HUE028024T2/en unknown
- 2006-06-07 PT PT06772447T patent/PT1896426E/en unknown
- 2006-06-07 PE PE2010000468A patent/PE20100716A1/en not_active Application Discontinuation
- 2006-06-07 CN CN2011100581773A patent/CN102174020B/en active Active
- 2006-06-07 DK DK10171942.5T patent/DK2292607T3/en active
- 2006-06-07 JP JP2008515880A patent/JP5225078B2/en not_active Expired - Fee Related
- 2006-06-07 CA CA2611280A patent/CA2611280C/en active Active
- 2006-06-07 PL PL10171941T patent/PL2266961T3/en unknown
- 2006-06-07 CN CN2011100581769A patent/CN102180796A/en active Pending
- 2006-06-07 EP EP06772447A patent/EP1896426B1/en active Active
- 2006-06-07 CN CN2011100581788A patent/CN102174021B/en active Active
- 2006-06-07 PE PE2006000628A patent/PE20070109A1/en not_active Application Discontinuation
- 2006-06-07 WO PCT/US2006/022154 patent/WO2006135640A2/en active Application Filing
- 2006-06-07 CA CA2886482A patent/CA2886482C/en active Active
- 2006-06-07 CA CA2942046A patent/CA2942046A1/en not_active Abandoned
- 2006-06-07 PL PL06772447T patent/PL1896426T3/en unknown
- 2006-06-07 CA CA2833394A patent/CA2833394C/en active Active
- 2006-06-07 KR KR1020127011979A patent/KR101283109B1/en active IP Right Grant
- 2006-06-07 AU AU2006258050A patent/AU2006258050B2/en not_active Ceased
- 2006-06-07 DK DK10171941.7T patent/DK2266961T3/en active
- 2006-06-07 ES ES06772447T patent/ES2380489T3/en active Active
- 2006-06-07 CN CN2011100572469A patent/CN102174019B/en active Active
- 2006-06-07 ES ES10171941.7T patent/ES2558696T3/en active Active
- 2006-06-07 AR ARP060102367A patent/AR057056A1/en unknown
- 2006-06-07 PL PL10171942T patent/PL2292607T3/en unknown
- 2006-06-07 IN IN8588DEN2014 patent/IN2014DN08588A/en unknown
- 2006-06-07 SI SI200631789T patent/SI2292607T1/en unknown
- 2006-06-07 PE PE2010000467A patent/PE20100715A1/en not_active Application Discontinuation
- 2006-06-07 IN IN8578DEN2014 patent/IN2014DN08578A/en unknown
- 2006-06-07 US US11/915,691 patent/US7781597B2/en active Active
- 2006-06-07 CN CN200680019924XA patent/CN101189212B/en active Active
- 2006-06-07 AT AT06772447T patent/ATE540931T1/en active
- 2006-06-07 EP EP10171941.7A patent/EP2266961B1/en active Active
- 2006-06-07 SI SI200632010T patent/SI2266961T1/en unknown
- 2006-06-07 ES ES10171942.5T patent/ES2465522T3/en active Active
- 2006-06-07 MX MX2007015609A patent/MX2007015609A/en active IP Right Grant
- 2006-06-07 PT PT101719417T patent/PT2266961E/en unknown
- 2006-06-07 BR BRPI0611683-3A patent/BRPI0611683A2/en active Search and Examination
- 2006-06-07 KR KR1020077028642A patent/KR101249199B1/en active IP Right Grant
- 2006-06-07 PT PT101719425T patent/PT2292607E/en unknown
- 2006-06-07 EP EP10171942.5A patent/EP2292607B1/en active Active
- 2006-06-07 CN CN2011100574125A patent/CN102180836B/en active Active
- 2006-06-07 RU RU2007148238/04A patent/RU2446162C2/en active
- 2006-06-08 TW TW095120304A patent/TWI380981B/en not_active IP Right Cessation
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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
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2011
- 2011-03-09 AU AU2011201044A patent/AU2011201044A1/en not_active Abandoned
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2012
- 2012-05-17 GT GT200600202AK patent/GT200600202AA/en unknown
- 2012-09-21 JP JP2012208775A patent/JP2013035855A/en active Pending
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