PE20070015A1 - Proceso para la sintesis de compuestos pirimidinilaminobenzamidas - Google Patents

Proceso para la sintesis de compuestos pirimidinilaminobenzamidas

Info

Publication number
PE20070015A1
PE20070015A1 PE2006000631A PE2006000631A PE20070015A1 PE 20070015 A1 PE20070015 A1 PE 20070015A1 PE 2006000631 A PE2006000631 A PE 2006000631A PE 2006000631 A PE2006000631 A PE 2006000631A PE 20070015 A1 PE20070015 A1 PE 20070015A1
Authority
PE
Peru
Prior art keywords
methyl
alkyl
phenyl
compounds
formula
Prior art date
Application number
PE2006000631A
Other languages
English (en)
Inventor
Joseph Mckenna
Wen-Chung Shieh
Original Assignee
Novartis Ag
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of PE20070015A1 publication Critical patent/PE20070015A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/14Heterocyclic 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

Landscapes

  • 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)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Steroid Compounds (AREA)

Abstract

SE REFIERE A UN PROCESO DE PREPARACION DE COMPUESTOS DE LA FORMULA (I) DONDE R1 ES ARILO(C6-C14) OPCIONALMENTE SUSTITUIDO CON HALOGENO, ALQUILO(C1-C6), FENILO, NITRO, ENTRE OTROS; R2 ES H, ALQUILO(C1-C6) O ARILO(C6-C14); R4 ES H, HALOGENO O ALQUILO(C1-C6); UN COMPUESTO PREFERIDO ES 4-METIL-3-[[4-(3-PIRIDINIL)-2-PIRIMIDINIL]-AMINO]-N-[5-(4-METIL-1H-IMIDAZOL-1-IL)-3-(TRIFLUORO-METIL)-FENIL]-BENZAMIDA. DICHO PROCESO COMPRENDE: A) HACER REACCIONAR EL COMPUESTO DE FORMULA (II) CON EL COMPUESTO DE FORMULA R1-NH-R2 TAL COMO 5-(4-METIL-1H-IMIDAZOL-1-IL)-3-(TRIFLUORO-METIL)-BENCENAMINA, DONDE R3 ES ALQUILO(C1-C6), FENILO OPCIONALMENTE SUSTITUIDO O FENIL-ALQUILO(C1-C6), DICHA REACCION SE CATALIZA CON UNA BASE TAL COMO HIDRURO DE METAL, BIS-(TRIMETIL-SILIL)-AMIDA DE METAL, DIALQUIL-AMIDA DE LITIO, TERBUTOXIDO DE POTASIO, ENTRE OTROS, EN UN SOLVENTE ORGANICO TAL COMO TETRAHIDROFURANO, DIMETIL-FORMAMIDA, TOLUENO O N-METIL-PIRROLIDONA. EL PROCESO SE LLEVA A CABO A UNA TEMPERATURA DE -50°C A 50°C. DICHOS COMPUESTOS SON INHIBIDORES DE QUINASAS DE TIROSINA SIENDO UTILES EN EL TRATAMIENTO DE ENFERMEDADES NEOPLASICAS TAL COMO LEUCEMIA
PE2006000631A 2005-06-09 2006-06-07 Proceso para la sintesis de compuestos pirimidinilaminobenzamidas PE20070015A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US68897705P 2005-06-09 2005-06-09
US70559005P 2005-08-04 2005-08-04

Publications (1)

Publication Number Publication Date
PE20070015A1 true PE20070015A1 (es) 2007-02-06

Family

ID=37091153

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2006000631A PE20070015A1 (es) 2005-06-09 2006-06-07 Proceso para la sintesis de compuestos pirimidinilaminobenzamidas

Country Status (32)

Country Link
US (2) US8124763B2 (es)
EP (1) EP1924574B1 (es)
JP (1) JP5118024B2 (es)
KR (3) KR101514593B1 (es)
AR (1) AR053890A1 (es)
AT (1) ATE487709T1 (es)
AU (1) AU2006258051B2 (es)
BR (1) BRPI0611663A2 (es)
CA (1) CA2610105C (es)
CY (1) CY1111428T1 (es)
DE (1) DE602006018156D1 (es)
DK (1) DK1924574T3 (es)
EC (1) ECSP077982A (es)
EG (1) EG25039A (es)
GT (1) GT200600217A (es)
HK (1) HK1117524A1 (es)
IL (1) IL187421A (es)
JO (1) JO2636B1 (es)
MA (1) MA29599B1 (es)
MX (1) MX2007015423A (es)
MY (1) MY147436A (es)
NO (1) NO340743B1 (es)
NZ (1) NZ563740A (es)
PE (1) PE20070015A1 (es)
PL (1) PL1924574T3 (es)
PT (1) PT1924574E (es)
RU (1) RU2444520C2 (es)
SA (1) SA06270147B1 (es)
SI (1) SI1924574T1 (es)
TN (1) TNSN07463A1 (es)
TW (1) TWI430999B (es)
WO (1) WO2006135641A2 (es)

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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
WO2013120852A1 (en) 2012-02-13 2013-08-22 Grindeks, A Joint Stock Company Intermediates for a novel process of preparing imatinib and related tyrosine kinase inhibitors
US9920357B2 (en) 2012-06-06 2018-03-20 The Procter & Gamble Company Systems and methods for identifying cosmetic agents for hair/scalp care compositions
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
US11666888B2 (en) 2018-02-05 2023-06-06 Bio-Rad Laboratories, Inc. Chromatography resin having an anionic exchange-hydrophobic mixed mode ligand
JP7409696B2 (ja) 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 キナーゼ阻害剤の塩およびその組成物
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

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Also Published As

Publication number Publication date
JP5118024B2 (ja) 2013-01-16
MX2007015423A (es) 2008-02-21
ECSP077982A (es) 2008-01-23
DE602006018156D1 (de) 2010-12-23
JP2008545786A (ja) 2008-12-18
TNSN07463A1 (en) 2009-03-17
PT1924574E (pt) 2011-02-08
DK1924574T3 (da) 2011-02-14
KR101514593B1 (ko) 2015-04-22
KR20080022093A (ko) 2008-03-10
CY1111428T1 (el) 2015-08-05
WO2006135641A3 (en) 2007-03-29
GT200600217A (es) 2007-03-28
EP1924574A2 (en) 2008-05-28
MY147436A (en) 2012-12-14
EP1924574B1 (en) 2010-11-10
NO340743B1 (no) 2017-06-12
BRPI0611663A2 (pt) 2010-09-28
NZ563740A (en) 2011-03-31
MA29599B1 (fr) 2008-07-01
AU2006258051B2 (en) 2010-09-09
EG25039A (en) 2011-07-06
AR053890A1 (es) 2007-05-23
PL1924574T3 (pl) 2011-04-29
IL187421A0 (en) 2008-02-09
CA2610105A1 (en) 2006-12-21
WO2006135641A2 (en) 2006-12-21
SI1924574T1 (sl) 2011-02-28
US20120116081A1 (en) 2012-05-10
KR20130118394A (ko) 2013-10-29
CA2610105C (en) 2014-03-25
US8124763B2 (en) 2012-02-28
HK1117524A1 (en) 2009-01-16
KR20120066067A (ko) 2012-06-21
AU2006258051A1 (en) 2006-12-21
SA06270147B1 (ar) 2009-12-22
RU2007148231A (ru) 2009-07-20
TWI430999B (zh) 2014-03-21
NO20080157L (no) 2008-01-09
US8946416B2 (en) 2015-02-03
JO2636B1 (en) 2012-06-17
ATE487709T1 (de) 2010-11-15
TW200726756A (en) 2007-07-16
IL187421A (en) 2011-11-30
RU2444520C2 (ru) 2012-03-10
KR101216249B1 (ko) 2012-12-28
US20080188656A1 (en) 2008-08-07

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