ECSP11011415A - Piperidinas sustituidas como antagonistas de ccr3. - Google Patents

Piperidinas sustituidas como antagonistas de ccr3.

Info

Publication number
ECSP11011415A
ECSP11011415A EC2011011415A ECSP11011415A ECSP11011415A EC SP11011415 A ECSP11011415 A EC SP11011415A EC 2011011415 A EC2011011415 A EC 2011011415A EC SP11011415 A ECSP11011415 A EC SP11011415A EC SP11011415 A ECSP11011415 A EC SP11011415A
Authority
EC
Ecuador
Prior art keywords
ccr3
antigonist
piperidins
replaced
present
Prior art date
Application number
EC2011011415A
Other languages
English (en)
Inventor
Jean C Califano
James J Napier
Original Assignee
Abbott Lab
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 Abbott Lab filed Critical Abbott Lab
Publication of ECSP11011415A publication Critical patent/ECSP11011415A/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • C07D239/545Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals with other hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/52Two oxygen atoms
    • C07D239/54Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C07C303/40Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids by reactions not involving the formation of sulfonamide groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/01Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms
    • C07C311/02Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C311/08Sulfonamides having sulfur atoms of sulfonamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atom of at least one of the sulfonamide groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/0803Compounds with Si-C or Si-Si linkages
    • C07F7/081Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
    • C07F7/0812Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Virology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Oncology (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Objeto de la presente invención son compuestos novedosos sustituidos de la fórmula 1,en la que A, R1, R2, R3 y R4 se definen como en la descripción. Otro objeto de la presente invención es proporcionar antagonistas de CCR3, más particularmente proporcionar composiciones farmacéuticas que comprenden un vehículo farmacéuticamente aceptable y una cantidad terapéuticamente eficaz de al menos uno de los compuestos de la presente invención o una sal farmacéuticamente aceptable del mismo.
EC2011011415A 2009-03-24 2011-08-24 Piperidinas sustituidas como antagonistas de ccr3. ECSP11011415A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16270509P 2009-03-24 2009-03-24
US31671310P 2010-03-23 2010-03-23

Publications (1)

Publication Number Publication Date
ECSP11011415A true ECSP11011415A (es) 2011-11-30

Family

ID=42136100

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2011011415A ECSP11011415A (es) 2009-03-24 2011-08-24 Piperidinas sustituidas como antagonistas de ccr3.

Country Status (24)

Country Link
EP (1) EP2411372B1 (es)
JP (1) JP5744003B2 (es)
KR (1) KR101665955B1 (es)
CN (1) CN102361858B (es)
AU (1) AU2010229975B2 (es)
BR (1) BRPI1009854A2 (es)
CA (1) CA2753825C (es)
CL (1) CL2011002278A1 (es)
CO (1) CO6450678A2 (es)
CR (1) CR20110524A (es)
DO (1) DOP2011000297A (es)
EC (1) ECSP11011415A (es)
ES (1) ES2488821T3 (es)
GT (1) GT201100241A (es)
HK (1) HK1166798A1 (es)
IL (1) IL214858A (es)
MX (1) MX2011010049A (es)
MY (1) MY169288A (es)
NZ (1) NZ594923A (es)
PE (1) PE20120519A1 (es)
RU (1) RU2524573C2 (es)
SG (1) SG174211A1 (es)
WO (1) WO2010111348A1 (es)
ZA (1) ZA201106511B (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX338725B (es) 2010-07-16 2016-04-28 Abbvie Bahamas Ltd Ligando de fosfina para reacciones cataliticas.
US9255074B2 (en) 2010-07-16 2016-02-09 Abbvie Inc. Process for preparing antiviral compounds
AU2011278927B2 (en) 2010-07-16 2015-05-21 Abbvie Ireland Unlimited Company Process for preparing antiviral compounds
US8975443B2 (en) 2010-07-16 2015-03-10 Abbvie Inc. Phosphine ligands for catalytic reactions
TWI558400B (zh) * 2011-03-18 2016-11-21 艾伯維有限公司 苯基尿嘧啶化合物之調配物
US20160375017A1 (en) 2015-06-26 2016-12-29 Abbvie Inc. Solid Pharmaceutical Compositions for Treating HCV

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1219626B1 (en) * 1999-09-20 2005-06-01 Fuji Photo Film Co., Ltd. Compounds for fluorescence labeling
EP1218401B1 (de) * 1999-09-22 2004-06-16 Aventis Pharma Deutschland GmbH 4-benzylaminochinoline konjugate mit gallensaeure und ihre heteroanalogen, verfahren zu ihrer herstellung, diese verbindungen enthaltende arzneimittel und deren anwendung
DE10051981A1 (de) * 2000-10-20 2002-05-02 Bayer Ag Substituierte Phenyluracile
WO2007138242A1 (en) * 2006-05-30 2007-12-06 Arrow Therapeutics Limited Biphenyl derivatives and their use in treating hepatitis c
KR101552474B1 (ko) * 2007-09-17 2015-09-11 애브비 바하마스 리미티드 C형 간염 치료용 우라실 또는 티민 유도체
CN105693626A (zh) * 2007-09-17 2016-06-22 艾伯维巴哈马有限公司 治疗丙型肝炎的尿嘧啶或胸腺嘧啶衍生物
BRPI0916233A2 (pt) * 2008-07-23 2018-03-13 F.Hoffman-La Roche Ag compostos heterocíclicos antivirais

Also Published As

Publication number Publication date
CN102361858B (zh) 2014-07-23
CO6450678A2 (es) 2012-05-31
NZ594923A (en) 2013-11-29
PE20120519A1 (es) 2012-06-03
JP5744003B2 (ja) 2015-07-01
EP2411372A1 (en) 2012-02-01
CA2753825A1 (en) 2010-09-30
RU2011142757A (ru) 2013-04-27
CA2753825C (en) 2017-10-17
WO2010111348A1 (en) 2010-09-30
AU2010229975A1 (en) 2011-09-29
MX2011010049A (es) 2011-10-11
IL214858A (en) 2015-05-31
SG174211A1 (en) 2011-10-28
MY169288A (en) 2019-03-21
JP2012521990A (ja) 2012-09-20
GT201100241A (es) 2015-08-19
KR20110137372A (ko) 2011-12-22
HK1166798A1 (en) 2012-11-09
AU2010229975B2 (en) 2015-05-21
IL214858A0 (en) 2011-11-30
CR20110524A (es) 2012-01-19
CN102361858A (zh) 2012-02-22
BRPI1009854A2 (pt) 2015-08-25
ES2488821T3 (es) 2014-08-29
RU2524573C2 (ru) 2014-07-27
KR101665955B1 (ko) 2016-10-13
ZA201106511B (en) 2012-05-30
DOP2011000297A (es) 2011-10-15
EP2411372B1 (en) 2014-07-23
CL2011002278A1 (es) 2012-03-09

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