DK1711481T3 - Fremgangsmåde til fremstilling af 2-aminothiazol-5-aromatiske carboxamider som kinaseinhibitorer - Google Patents

Fremgangsmåde til fremstilling af 2-aminothiazol-5-aromatiske carboxamider som kinaseinhibitorer

Info

Publication number
DK1711481T3
DK1711481T3 DK05722772.0T DK05722772T DK1711481T3 DK 1711481 T3 DK1711481 T3 DK 1711481T3 DK 05722772 T DK05722772 T DK 05722772T DK 1711481 T3 DK1711481 T3 DK 1711481T3
Authority
DK
Denmark
Prior art keywords
aminothiazole
preparation
kinase inhibitors
aromatic carboxamides
carboxamides
Prior art date
Application number
DK05722772.0T
Other languages
English (en)
Other versions
DK1711481T4 (da
Inventor
Bang-Chi Chen
Roberto Droghini
Jean Lajeunesse
John D Dimarco
Michael Galella
Ramakrishnan Chidambaram
Original Assignee
Brystol Myers Squibb Company
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=34864498&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DK1711481(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Brystol Myers Squibb Company filed Critical Brystol Myers Squibb Company
Publication of DK1711481T3 publication Critical patent/DK1711481T3/da
Application granted granted Critical
Publication of DK1711481T4 publication Critical patent/DK1711481T4/da

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
    • C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
    • C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members 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
    • C07D277/56—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • 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
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and unsaturated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/42—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having nitrogen atoms of amino groups bound to the carbon skeleton of the acid part, further acylated
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Virology (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Thiazole And Isothizaole Compounds (AREA)
DK05722772.0T 2004-02-06 2005-02-04 Krystallinsk monohydrat som kinaseinhibitorer DK1711481T4 (da)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US54249004P 2004-02-06 2004-02-06
US62493704P 2004-11-04 2004-11-04
PCT/US2005/003728 WO2005077945A2 (en) 2004-02-06 2005-02-04 Process for preparing 2-aminothiazole-5-aromatic carboxamides as kinase inhibitors

Publications (2)

Publication Number Publication Date
DK1711481T3 true DK1711481T3 (da) 2010-04-19
DK1711481T4 DK1711481T4 (da) 2013-08-26

Family

ID=34864498

Family Applications (1)

Application Number Title Priority Date Filing Date
DK05722772.0T DK1711481T4 (da) 2004-02-06 2005-02-04 Krystallinsk monohydrat som kinaseinhibitorer

Country Status (27)

Country Link
EP (1) EP1711481B2 (da)
JP (2) JP5148115B2 (da)
KR (2) KR101310427B1 (da)
AR (1) AR047533A1 (da)
AT (1) ATE453630T1 (da)
AU (1) AU2005212405B2 (da)
BR (1) BRPI0507476B8 (da)
CA (1) CA2555291C (da)
CY (1) CY1109907T1 (da)
DE (1) DE602005018601D1 (da)
DK (1) DK1711481T4 (da)
ES (1) ES2337272T5 (da)
GE (1) GEP20094804B (da)
HK (1) HK1091835A1 (da)
HR (1) HRP20100166T4 (da)
IL (1) IL177280A (da)
IN (1) IN2014DN06567A (da)
NO (1) NO338049B1 (da)
NZ (1) NZ548613A (da)
PE (1) PE20050691A1 (da)
PL (1) PL1711481T5 (da)
PT (1) PT1711481E (da)
RU (1) RU2382039C2 (da)
SI (1) SI1711481T2 (da)
TW (1) TWI338004B (da)
WO (1) WO2005077945A2 (da)
ZA (1) ZA200606242B (da)

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US7652146B2 (en) 2004-02-06 2010-01-26 Bristol-Myers Squibb Company Process for preparing 2-aminothiazole-5-carboxamides useful as kinase inhibitors
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CN104341410A (zh) * 2013-08-09 2015-02-11 上海科胜药物研发有限公司 一种达沙替尼新晶型及其制备方法
CN103483289B (zh) * 2013-09-06 2016-01-27 浙江科源化工有限公司 一种2-氨基-n-(2-氯-6-甲基苯基)噻唑-5-甲酰胺的合成方法
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Also Published As

Publication number Publication date
GEP20094804B (en) 2009-10-26
HRP20100166T1 (hr) 2010-05-31
BRPI0507476B8 (pt) 2021-05-25
RU2006131591A (ru) 2008-03-20
DE602005018601D1 (de) 2010-02-11
NO338049B1 (no) 2016-07-25
JP5148115B2 (ja) 2013-02-20
ZA200606242B (en) 2008-01-08
NO20063780L (no) 2006-10-27
AR047533A1 (es) 2006-01-25
AU2005212405B2 (en) 2010-08-12
EP1711481B1 (en) 2009-12-30
SI1711481T2 (sl) 2013-10-30
ES2337272T5 (es) 2013-09-30
IN2014DN06567A (da) 2015-07-10
JP2012188446A (ja) 2012-10-04
IL177280A (en) 2013-09-30
ATE453630T1 (de) 2010-01-15
KR20060124692A (ko) 2006-12-05
EP1711481B2 (en) 2013-05-22
BRPI0507476A (pt) 2007-07-17
EP1711481A2 (en) 2006-10-18
WO2005077945A3 (en) 2006-05-18
PL1711481T5 (pl) 2013-10-31
DK1711481T4 (da) 2013-08-26
KR101310427B1 (ko) 2013-09-24
RU2382039C2 (ru) 2010-02-20
PT1711481E (pt) 2010-02-25
WO2005077945A2 (en) 2005-08-25
JP2007521340A (ja) 2007-08-02
BRPI0507476B1 (pt) 2020-12-08
NZ548613A (en) 2010-05-28
AU2005212405A1 (en) 2005-08-25
PL1711481T3 (pl) 2010-05-31
CY1109907T1 (el) 2014-09-10
IL177280A0 (en) 2006-12-10
PE20050691A1 (es) 2005-09-25
CA2555291A1 (en) 2005-08-25
HRP20100166T4 (en) 2013-09-30
ES2337272T3 (es) 2010-04-22
SI1711481T1 (sl) 2010-03-31
HK1091835A1 (en) 2007-01-26
TW200530205A (en) 2005-09-16
KR20120097424A (ko) 2012-09-03
CA2555291C (en) 2017-01-17
TWI338004B (en) 2011-03-01

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