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PE20110545A1 - Compuestos de triazolopiridina como inhibidores de jak - Google Patents

Compuestos de triazolopiridina como inhibidores de jak

Info

Publication number
PE20110545A1
PE20110545A1 PE2010001173A PE2010001173A PE20110545A1 PE 20110545 A1 PE20110545 A1 PE 20110545A1 PE 2010001173 A PE2010001173 A PE 2010001173A PE 2010001173 A PE2010001173 A PE 2010001173A PE 20110545 A1 PE20110545 A1 PE 20110545A1
Authority
PE
Peru
Prior art keywords
pyridin
phenyl
triazolo
compounds
jak inhibitors
Prior art date
Application number
PE2010001173A
Other languages
English (en)
Inventor
Bing-Yan Zhu
Michael Siu
Steven R Magnuson
Richard Pastor
He Haiying
Xiao Yisong
Xu Xing
Zhao Junping
Wendy Liu
Christopher A Hurley
Joseph P Lyssikatos
Jun Liang
Zheng Jifu
Original Assignee
Genentech Inc
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 Genentech Inc filed Critical Genentech Inc
Publication of PE20110545A1 publication Critical patent/PE20110545A1/es

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    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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    • A61K31/33Heterocyclic compounds
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    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
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    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

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Abstract

SE REFIERE A COMPUESTOS DERIVADOS DE TRIAZOLPIRIDINA DE FORMULA (I) DONDE R1 ES H, FENILO, C(O)ORa, ENTRE OTROS, DONDE Ra ES H, ALQUILO(C1-C6), CICLOALQUILO(C3-C6), ENTRE OTROS; R2 ES FENILO, HETEROARILO O HETEROCICLILO; R3, R4 Y R5 SON CADA UNO H, CH3, OCH3, CF3, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N-PIPERIDIN-4-IL-4-[8-(3-TRIFLUOROMETIL-ENIL)-[1,2,4]TRIAZOLO[1,5-a]PIRIDIN-2-ILAMINO]-BENZAMIDA; [8-(3-METOXI-ENIL)-[1,2,4]TRIAZOLO[1,5-a]PIRIDIN-2-IL]-(2-METIL-PIRIDIN-4-IL)-AMINA; (3,5-DIFLUORO-FENIL)-[8-(3-METOXI-FENIL)-[1,2,4]TRIAZOLO[1,5-a]PIRIDIN-2-IL]-AMINA; ENTRE OTROS. SE REFIERE TAMBIEN A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LAS QUINASAS DE JANUS COMO JAK2 SIENDO UTILES EN EL TRATAMIENTO DE CANCER, DIABETES, ESCLEROSIS MULTIPLE, PSORIASIS, POLICITEMIA VERA
PE2010001173A 2008-06-20 2009-06-19 Compuestos de triazolopiridina como inhibidores de jak PE20110545A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US7450608P 2008-06-20 2008-06-20

Publications (1)

Publication Number Publication Date
PE20110545A1 true PE20110545A1 (es) 2011-08-18

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PE2010001173A PE20110545A1 (es) 2008-06-20 2009-06-19 Compuestos de triazolopiridina como inhibidores de jak

Country Status (15)

Country Link
US (4) US20100048557A1 (es)
EP (1) EP2288260A4 (es)
JP (1) JP5512665B2 (es)
KR (1) KR20110033223A (es)
CN (1) CN102131389A (es)
AU (1) AU2009259853A1 (es)
BR (1) BRPI0910021A2 (es)
CA (1) CA2727036C (es)
IL (1) IL209763A0 (es)
MX (1) MX2010014005A (es)
PE (1) PE20110545A1 (es)
RU (1) RU2560153C2 (es)
SG (1) SG178812A1 (es)
WO (1) WO2009155551A1 (es)
ZA (1) ZA201008957B (es)

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