KR20120066067A - 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법 - Google Patents

5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법 Download PDF

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Publication number
KR20120066067A
KR20120066067A KR1020127011980A KR20127011980A KR20120066067A KR 20120066067 A KR20120066067 A KR 20120066067A KR 1020127011980 A KR1020127011980 A KR 1020127011980A KR 20127011980 A KR20127011980 A KR 20127011980A KR 20120066067 A KR20120066067 A KR 20120066067A
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KR
South Korea
Prior art keywords
lower alkyl
formula
phenyl
methyl
synthesis
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Ceased
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KR1020127011980A
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English (en)
Korean (ko)
Inventor
조셉 맥케나
웬-충 시에
Original Assignee
노파르티스 아게
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Publication of KR20120066067A publication Critical patent/KR20120066067A/ko
Ceased legal-status Critical Current

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    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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
    • C07D401/14—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 three or more hetero rings

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Steroid Compounds (AREA)
KR1020127011980A 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법 Ceased KR20120066067A (ko)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US68897705P 2005-06-09 2005-06-09
US60/688,977 2005-06-09
US70559005P 2005-08-04 2005-08-04
US60/705,590 2005-08-04

Related Parent Applications (1)

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KR1020077028638A Division KR101216249B1 (ko) 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법

Related Child Applications (1)

Application Number Title Priority Date Filing Date
KR1020137025659A Division KR101514593B1 (ko) 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법

Publications (1)

Publication Number Publication Date
KR20120066067A true KR20120066067A (ko) 2012-06-21

Family

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Family Applications (3)

Application Number Title Priority Date Filing Date
KR1020127011980A Ceased KR20120066067A (ko) 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법
KR1020077028638A Expired - Lifetime KR101216249B1 (ko) 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법
KR1020137025659A Expired - Lifetime KR101514593B1 (ko) 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법

Family Applications After (2)

Application Number Title Priority Date Filing Date
KR1020077028638A Expired - Lifetime KR101216249B1 (ko) 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법
KR1020137025659A Expired - Lifetime KR101514593B1 (ko) 2005-06-09 2006-06-07 5-(메틸-1ｈ-이미다졸-1-일)-3-(트리플루오로메틸)-벤젠아민의 합성 방법

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US (2) US8124763B2 (cg-RX-API-DMAC10.html)
EP (1) EP1924574B1 (cg-RX-API-DMAC10.html)
JP (1) JP5118024B2 (cg-RX-API-DMAC10.html)
KR (3) KR20120066067A (cg-RX-API-DMAC10.html)
AR (1) AR053890A1 (cg-RX-API-DMAC10.html)
AT (1) ATE487709T1 (cg-RX-API-DMAC10.html)
AU (1) AU2006258051B2 (cg-RX-API-DMAC10.html)
BR (1) BRPI0611663A2 (cg-RX-API-DMAC10.html)
CA (1) CA2610105C (cg-RX-API-DMAC10.html)
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DE (1) DE602006018156D1 (cg-RX-API-DMAC10.html)
DK (1) DK1924574T3 (cg-RX-API-DMAC10.html)
EC (1) ECSP077982A (cg-RX-API-DMAC10.html)
EG (1) EG25039A (cg-RX-API-DMAC10.html)
GT (1) GT200600217A (cg-RX-API-DMAC10.html)
IL (1) IL187421A (cg-RX-API-DMAC10.html)
JO (1) JO2636B1 (cg-RX-API-DMAC10.html)
MA (1) MA29599B1 (cg-RX-API-DMAC10.html)
MX (1) MX2007015423A (cg-RX-API-DMAC10.html)
MY (1) MY147436A (cg-RX-API-DMAC10.html)
NO (1) NO340743B1 (cg-RX-API-DMAC10.html)
NZ (1) NZ563740A (cg-RX-API-DMAC10.html)
PE (1) PE20070015A1 (cg-RX-API-DMAC10.html)
PL (1) PL1924574T3 (cg-RX-API-DMAC10.html)
PT (1) PT1924574E (cg-RX-API-DMAC10.html)
RU (1) RU2444520C2 (cg-RX-API-DMAC10.html)
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Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GT200600316A (es) * 2005-07-20 2007-04-02 Sales de 4-metilo-n-(3-(4-metilo-imidazol-1-ilo)-5-trifluorometilo-fenilo)-3-(4-piridina-3-ilo-pirimidina-2-iloamino)- benzamida.
US8242271B2 (en) 2007-06-04 2012-08-14 Avila Therapeutics, Inc. Heterocyclic compounds and uses thereof
EP2305667A3 (en) 2008-07-17 2011-05-11 Teva Pharmaceutical Industries Ltd. Nilotinib intermediates and preparation thereof
HRP20120793T1 (hr) 2008-11-05 2012-12-31 Teva Pharmaceutical Industries Ltd. Kristalni oblici nilotinib hci
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
JO3634B1 (ar) 2009-11-17 2020-08-27 Novartis Ag طريقة لعلاج اضطرابات تكاثرية وحالات مرضية أخرى متوسطة بنشاط كيناز bcr-abl، c-kit، ddr1، ddr2، أو pdgf-r
JP5841234B2 (ja) 2011-03-31 2016-01-13 ザ プロクター アンド ギャンブルカンパニー フケ／脂漏性皮膚炎の治療に有効な皮膚活性剤を特定及び評価するためのシステム、モデル、及び方法
AR086913A1 (es) * 2011-06-14 2014-01-29 Novartis Ag 4-metil-3-[[4-(3-piridinil)-2-pirimidinil]-amino]-n-[5-(4-metil-1h-imidazol-1-il)-3-(trifluoro-metil)-fenil]-benzamida amorfa, forma de dosificacion que la contiene y metodo para prepararlas
GB2514285B (en) 2012-02-13 2018-07-18 Grindeks Jsc Intermediates for a novel process of preparing imatinib and related tyrosine kinase inhibitors
MX2014014898A (es) 2012-06-06 2015-03-04 Procter & Gamble Sistemas y metodos de identificacion de agentes cosmeticos para composiciones para el cuidado del cabello/cuero cabelludo.
WO2015092624A1 (en) 2013-12-16 2015-06-25 Ranbaxy Laboratories Limited Nilotinib mono-oxalate and its crystalline form
CN103694176B (zh) 2014-01-07 2015-02-18 苏州立新制药有限公司 尼洛替尼中间体的制备方法
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
CN111683976B (zh) 2018-02-05 2022-11-18 生物辐射实验室股份有限公司 具有阴离子交换-疏水混合模式配体的色谱树脂
TWI787523B (zh) 2018-06-15 2022-12-21 漢達生技醫藥股份有限公司 達沙替尼十二烷基硫酸鹽之結晶
JP2020007240A (ja) * 2018-07-04 2020-01-16 住友化学株式会社 ベンズアミド化合物の製造方法

Family Cites Families (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5136082A (en) * 1990-08-03 1992-08-04 Himont Incorporated Process for preparing organic esters and amides and catalyst system therefor
AU5539294A (en) 1992-12-24 1994-07-19 Hemagen/Pfc Fluorocarbon emulsions
TW406020B (en) 1993-09-29 2000-09-21 Bristol Myers Squibb Co Stabilized pharmaceutical composition and its method for preparation and stabilizing solvent
US5597829A (en) 1994-05-09 1997-01-28 Bionumerik Pharmaceuticals, Inc. Lactone stable formulation of camptothecin and methods for uses thereof
US5726181A (en) 1995-06-05 1998-03-10 Bionumerik Pharmaceuticals, Inc. Formulations and compositions of poorly water soluble camptothecin derivatives
US6323366B1 (en) 1997-07-29 2001-11-27 Massachusetts Institute Of Technology Arylamine synthesis
AR013261A1 (es) 1997-08-01 2000-12-13 Smithkline Beecham Corp Formulaciones farmaceuticas para analogos de camptotecina en capsula de gelatina
US20030059465A1 (en) 1998-05-11 2003-03-27 Unger Evan C. Stabilized nanoparticle formulations of camptotheca derivatives
US6395916B1 (en) 1998-07-10 2002-05-28 Massachusetts Institute Of Technology Ligands for metals and improved metal-catalyzed processes based thereon
DK1044977T3 (da) 1999-03-09 2002-07-08 Sigma Tau Ind Farmaceuti Camptothecinderivater med antitumoraktivitet
IT1306129B1 (it) 1999-04-13 2001-05-30 Sigma Tau Ind Farmaceuti Esteri della l-carnitina o di alcanoil l-carnitine utilizzabili comelipidi cationici per l'immissione intracellulare di composti
DE19926056B4 (de) 1999-06-08 2004-03-25 Gkss-Forschungszentrum Geesthacht Gmbh Einrichtung zur Analyse atomarer und/oder molekularer Elemente mittels wellenlängendispersiver, röntgenspektrometrischer Einrichtungen
GB9918885D0 (en) 1999-08-10 1999-10-13 Pharmacia & Upjohn Spa Pharmaceutical formulations in hydroxypropymethycellulose capsules
GB9925127D0 (en) 1999-10-22 1999-12-22 Pharmacia & Upjohn Spa Oral formulations for anti-tumor compounds
US20040009229A1 (en) 2000-01-05 2004-01-15 Unger Evan Charles Stabilized nanoparticle formulations of camptotheca derivatives
US20020150615A1 (en) 2001-02-12 2002-10-17 Howard Sands Injectable pharmaceutical composition comprising microdroplets of a camptothecin
US6629598B2 (en) 2001-08-10 2003-10-07 Vinod K. Narula Flexible ribbed splint system
US6653319B1 (en) 2001-08-10 2003-11-25 University Of Kentucky Research Foundation Pharmaceutical formulation for poorly water soluble camptothecin analogues
WO2003032906A2 (en) 2001-10-15 2003-04-24 Crititech, Inc. Delivery of poorly soluble drugs
US20060078618A1 (en) 2001-12-11 2006-04-13 Constantinides Panayiotis P Lipid particles and suspensions and uses thereof
JP2003267891A (ja) 2002-03-13 2003-09-25 Mitsubishi-Kagaku Foods Corp Ｗ／ｏ／ｗ型エマルション製剤
US7202367B2 (en) 2002-05-31 2007-04-10 Rhodia Chimie Process for arylating or vinylating or alkynating a nucleophilic compound
CZ294371B6 (cs) 2002-06-10 2004-12-15 Pliva - Lachema, A. S. Stabilizovaná farmaceutická kompozice na bázi polyoxyethylovaného ricinového oleje a způsob její přípravy
EP1393719A1 (en) 2002-08-23 2004-03-03 Munich Biotech AG Camptothecin-carboxylate formulations
GB0215676D0 (en) 2002-07-05 2002-08-14 Novartis Ag Organic compounds
JP4426749B2 (ja) 2002-07-11 2010-03-03 株式会社産学連携機構九州 Ｏ／ｗ型エマルション製剤
US20040171560A1 (en) 2002-12-23 2004-09-02 Dabur Research Foundation Stabilized pharmaceutical composition
JP2006199590A (ja) 2003-09-04 2006-08-03 Nano Career Kk 水溶性の塩基性薬物内包ナノ粒子含有組成物
CA2543722C (en) 2003-10-29 2011-01-04 Sonus Pharmaceuticals, Inc. Tocopherol-modified therapeutic drug compounds
DK1694242T3 (da) 2003-12-17 2014-06-30 Bionumerik Pharmaceuticals Inc Fremgangsmåde til fremstilling af farmaceutiske 7-(2-trimethylsilylethyl)camptothecinpræparater
GT200500310A (es) 2004-11-19 2006-06-19 Compuestos organicos

Also Published As

Publication number Publication date
ATE487709T1 (de) 2010-11-15
AU2006258051A1 (en) 2006-12-21
EP1924574B1 (en) 2010-11-10
GT200600217A (es) 2007-03-28
RU2007148231A (ru) 2009-07-20
TW200726756A (en) 2007-07-16
US8124763B2 (en) 2012-02-28
MA29599B1 (fr) 2008-07-01
KR20080022093A (ko) 2008-03-10
KR101514593B1 (ko) 2015-04-22
JO2636B1 (en) 2012-06-17
CA2610105A1 (en) 2006-12-21
WO2006135641A2 (en) 2006-12-21
JP5118024B2 (ja) 2013-01-16
NZ563740A (en) 2011-03-31
JP2008545786A (ja) 2008-12-18
HK1117524A1 (en) 2009-01-16
US20120116081A1 (en) 2012-05-10
DE602006018156D1 (de) 2010-12-23
CY1111428T1 (el) 2015-08-05
US20080188656A1 (en) 2008-08-07
TNSN07463A1 (en) 2009-03-17
ECSP077982A (es) 2008-01-23
CA2610105C (en) 2014-03-25
NO20080157L (no) 2008-01-09
NO340743B1 (no) 2017-06-12
PE20070015A1 (es) 2007-02-06
RU2444520C2 (ru) 2012-03-10
AR053890A1 (es) 2007-05-23
MY147436A (en) 2012-12-14
PL1924574T3 (pl) 2011-04-29
MX2007015423A (es) 2008-02-21
EG25039A (en) 2011-07-06
US8946416B2 (en) 2015-02-03
KR101216249B1 (ko) 2012-12-28
AU2006258051B2 (en) 2010-09-09
EP1924574A2 (en) 2008-05-28
DK1924574T3 (da) 2011-02-14
TWI430999B (zh) 2014-03-21
PT1924574E (pt) 2011-02-08
IL187421A0 (en) 2008-02-09
SA06270147B1 (ar) 2009-12-22
BRPI0611663A2 (pt) 2010-09-28
WO2006135641A3 (en) 2007-03-29
KR20130118394A (ko) 2013-10-29
SI1924574T1 (sl) 2011-02-28
IL187421A (en) 2011-11-30

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