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PE20161427A1 - Inhibidores heteroarilo de syk - Google Patents

Inhibidores heteroarilo de syk

Info

Publication number
PE20161427A1
PE20161427A1 PE2016001619A PE2016001619A PE20161427A1 PE 20161427 A1 PE20161427 A1 PE 20161427A1 PE 2016001619 A PE2016001619 A PE 2016001619A PE 2016001619 A PE2016001619 A PE 2016001619A PE 20161427 A1 PE20161427 A1 PE 20161427A1
Authority
PE
Peru
Prior art keywords
methyl
syk
compounds
inhibitors
ona
Prior art date
Application number
PE2016001619A
Other languages
English (en)
Inventor
Fitzgerald Jennifer L Swantek
John Scott
Karen Parrish
Spencer Napier
David James Lamb
Jasna Klicic
Matthias Hoffmann
Georg Dahmann
Edward Walker
Clive Mccarthy
Original Assignee
Boehringer Ingelheim Int
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 Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of PE20161427A1 publication Critical patent/PE20161427A1/es

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems
    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A61K31/416—1,2-Diazoles condensed with carbocyclic ring systems, e.g. indazole
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/415—1,2-Diazoles
    • A61K31/4162—1,2-Diazoles condensed with heterocyclic ring systems
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    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
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    • A61K31/4353—Heterocyclic 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
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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    • A61K31/5375—1,4-Oxazines, e.g. morpholine
    • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
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Abstract

SE REFIERE A COMPUESTOS HETEROARILO DE FORMULA (1) DONDE A ES N O CH; D ES CH; E Y G SON C O N; T ES C; LOS ENLACES DOBLES DISCONTINUOS SON UN ENLACE SIMPLE O DOBLE; M ES -CH2-, -O-, -NH-, ENTRE OTROS; R3 ES METILO O ETILO; R1 ES ARILO C6-C10, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: (4R)-4-[(1R)-1-[6-(3,4-DIMETOXIFENIL)-2-METIL-PIRAZOLO[4,3-c]PIRIDIN-4-IL]OXIETIL]PIRROLIDIN-2-ONA; (4R)-4-[(1R)-1-[6-(1-TER-BUTILPIRAZOL-4-IL)-2-METIL-PIRAZOLO[4,3-c]PIRIDIN-4-IL]OXIETIL]PIRROLIDIN-2-ONA; ENTRE OTROS. TAMBIEN SE REFIERE A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS SON INHIBIDORES DE LA PROTEINA QUINASA SYK SIENDO UTILES EN EL TRATAMIENTO DE ASMA, EPOC, RINITIS ALERGICA
PE2016001619A 2014-03-19 2015-03-12 Inhibidores heteroarilo de syk PE20161427A1 (es)

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CN110183440A (zh) 2019-08-30
EP3119772B1 (en) 2019-05-22
MX2016011784A (es) 2016-12-02
TWI680967B (zh) 2020-01-01
US20170008896A1 (en) 2017-01-12
JP6416275B2 (ja) 2018-10-31
UA119667C2 (uk) 2019-07-25
IL247057A0 (en) 2016-09-29
MY185837A (en) 2021-06-12
AU2015233654B2 (en) 2018-12-06
US20160244446A1 (en) 2016-08-25
CA2942997A1 (en) 2015-09-24
ES2738416T3 (es) 2020-01-22
SI3119772T1 (sl) 2019-08-30
JP2017512778A (ja) 2017-05-25

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