IN2014CN04065A - - Google Patents

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IN2014CN04065A
IN2014CN04065A IN4065CHN2014A IN2014CN04065A IN 2014CN04065 A IN2014CN04065 A IN 2014CN04065A IN 4065CHN2014 A IN4065CHN2014 A IN 4065CHN2014A IN 2014CN04065 A IN2014CN04065 A IN 2014CN04065A
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India
Prior art keywords
methods
syk kinase
kinase activity
compounds
inhibiting
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Inventor
Yonghong Song
Qing Xu
Zhaozhong J Jia
Brian Kane
Shawn M Bauer
Anjali Pandey
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Portola Pharm Inc
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Publication of IN2014CN04065A publication Critical patent/IN2014CN04065A/en

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    • C07D241/00Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
    • C07D241/02Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
    • C07D241/10Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D241/14Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having 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
    • C07D241/24Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D241/26Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms
    • C07D241/28Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with nitrogen atoms directly attached to ring carbon atoms in which said hetero-bound carbon atoms have double bonds to oxygen, sulfur or nitrogen atoms
    • AHUMAN NECESSITIES
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    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
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    • 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
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    • C07DHETEROCYCLIC COMPOUNDS
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    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
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    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
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Abstract

Provided are pyrazine compounds for inhibiting of Syk kinase intermediates used in making such compounds methods for their preparation pharmaceutical compositions thereof methods for inhibition Syk kinase activity and methods for treating conditions mediated at least in part by Syk kinase activity.
IN4065CHN2014 2011-11-23 2012-11-23 IN2014CN04065A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201161563466P 2011-11-23 2011-11-23
PCT/US2012/066468 WO2013078466A1 (en) 2011-11-23 2012-11-23 Pyrazine kinase inhibitors

Publications (1)

Publication Number Publication Date
IN2014CN04065A true IN2014CN04065A (en) 2015-09-04

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ID=48427516

Family Applications (1)

Application Number Title Priority Date Filing Date
IN4065CHN2014 IN2014CN04065A (en) 2011-11-23 2012-11-23

Country Status (18)

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US (2) US9359308B2 (en)
EP (1) EP2782579B1 (en)
JP (1) JP6039683B2 (en)
KR (1) KR102019530B1 (en)
CN (1) CN104066431B (en)
AU (1) AU2012340555B2 (en)
BR (1) BR112014012396B1 (en)
CA (2) CA2856301C (en)
CL (1) CL2014001346A1 (en)
CO (1) CO6990735A2 (en)
EA (1) EA026939B1 (en)
HK (1) HK1201460A1 (en)
IL (1) IL232701A (en)
IN (1) IN2014CN04065A (en)
MX (1) MX363551B (en)
SG (2) SG11201402570QA (en)
WO (1) WO2013078466A1 (en)
ZA (1) ZA201403651B (en)

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BR112014012396B1 (en) 2011-11-23 2020-08-25 Portola Pharmaceuticals, Inc pyrazine kinase inhibitors, composition, in vitro method for inhibiting kinase syk or signal transduction pathway, use of said inhibitors and kit
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US9775839B2 (en) 2014-03-13 2017-10-03 Merck Sharp & Dohme Corp. 2-pyrazine carboxamides as spleen tyrosine kinase inhibitors
CZ306322B6 (en) 2014-12-17 2016-11-30 Univerzita Karlova v Praze, Farmaceutická fakulta v Hradci Králové Substituted 2-(2-phenylhydrazinyl)pyrazine, process of its preparation, its use and pharmaceutical composition containing thereof
US20180305348A1 (en) * 2015-06-02 2018-10-25 Pharmacyclics Llc Inhibitors of brutons tyrosine kinase
WO2019237125A1 (en) * 2018-06-08 2019-12-12 The General Hospital Corporation Inhibitors of prolyl-trna-synthetase
CN112047899A (en) * 2020-10-19 2020-12-08 成都睿智化学研究有限公司 Method for synthesizing 3-substituted aminobenzo [ c ] isothiazole derivative
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