PA8516201A1 - Derivados de pirrol - Google Patents

Derivados de pirrol

Info

Publication number
PA8516201A1
PA8516201A1 PA20018516201A PA8516201A PA8516201A1 PA 8516201 A1 PA8516201 A1 PA 8516201A1 PA 20018516201 A PA20018516201 A PA 20018516201A PA 8516201 A PA8516201 A PA 8516201A PA 8516201 A1 PA8516201 A1 PA 8516201A1
Authority
PA
Panama
Prior art keywords
rent
hydrogen
compounds
arilo
aryl
Prior art date
Application number
PA20018516201A
Other languages
English (en)
Inventor
Brian William Dymock
Philip Stephen Jones
John Herbert Merrett
Martin John Pirratt
Original Assignee
Hoffmann La Roche
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 Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PA8516201A1 publication Critical patent/PA8516201A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • 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
    • C07D401/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms
    • 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
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/04Immunostimulants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
    • C07D207/36Oxygen or sulfur atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/06Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic 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
    • C07D417/02Heterocyclic 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
    • C07D417/06Heterocyclic 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 carbon chain containing only aliphatic carbon atoms

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Immunology (AREA)
  • Virology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • AIDS & HIV (AREA)
  • Molecular Biology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyrrole Compounds (AREA)

Abstract

EL INVENTO ESTA RELACIONADO CON NOVELES DERIVADOS DE PIRROL, UN PROCESO PARA SU FABRICACION, COMPOSICIONES FARMACEUTICAS Y EL USO DE DICHOS COMPUESTOS EN MEDICINA. ESPECIFICAMENTE, LOS COMPUESTO DE LA FORMULA I SON INHIBIDORES DE LA ENCIMA DE TRANSCRIPTASE INVERSA DEL VIRUS DE INMUNODEFICIENCIA HUMANA QUE SE ENCUENTRA INVOLUCRADO EN LA REPLICA VIRAL. CONSECUENTEMENTE, LOS COMPUESTOS DE ESTE INVENTO PUEDEN SER USADOS PROVECHOSAMENTE COMO AGENTES TERAPEUTICOS PARA EL PROCESO MEDIADO DEL VIH. EL INVENTO DESCRIBE COMPUESTOS NOVELES DE LA FORMULA I EN DONDE R1 ES ALQUILO, CICLOALQUILO, ARILO O HETEROCICLICO; R2 ES ALQUILO, CICLOALQUILO, ARILO O HETEROCICLILO; R3 ES HIDROGENO, ALQUILO, CICLOALQUILO, ARILO O HETEROCICLICO; R4 ES HIDROGENO, ALQUILO, CARBOXILO, C(=O)R, CONR'R", CIANO O ALQUENILO, DONDE R ES HIDROGENO, ALQUILO, ALCOXI, TRIFLUOROMETILO, METILO-OXI-CARBONILO O ETILO-OXI,CARBONILO, Y DONDE R' Y R", SON IDEPENDIENTEMENTES UNO DEL OTRO, HIDROGENO, ALQUILO O ARILO; R5 ES ALQUILO, ARILO O UN GRUPO -Z-C(=O)R'", DONDE Z ES UN ENLACE SIMPLE O -CH=CH, Y DONDE R'" ES HIDROGENO O ALQUILO; X REPRESENTA S, S(O), S(O)2, O, N(ALQUILO) O X-R2 EN FORMA CONJUNTA REPRESENTA CH2-ARILO O CH2-HETEROCICLILO; Y SIEMPRE QUE SOLO UNO DE R3 Y R4 SEA HIDROGENO Y EL ALQUILO EN R3 NO SEA CF3; Y ESTERES HIDROLIZABLES O LOS ETERES DE LOS MISMOS O UNA SAL DE LA MISMA FARMACEUTICAMENTE ACEPTABLE DE LOS MISMOS.
PA20018516201A 2000-07-04 2001-05-04 Derivados de pirrol PA8516201A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0016453.3A GB0016453D0 (en) 2000-07-04 2000-07-04 Pyrrole derivatives

Publications (1)

Publication Number Publication Date
PA8516201A1 true PA8516201A1 (es) 2002-07-30

Family

ID=9895031

Family Applications (1)

Application Number Title Priority Date Filing Date
PA20018516201A PA8516201A1 (es) 2000-07-04 2001-05-04 Derivados de pirrol

Country Status (17)

Country Link
US (1) US6737429B2 (es)
EP (1) EP1301481A1 (es)
JP (1) JP2004502674A (es)
KR (1) KR100549884B1 (es)
CN (1) CN1440385A (es)
AR (1) AR028602A1 (es)
AU (2) AU2001263874B2 (es)
BR (1) BR0112241A (es)
CA (1) CA2412270A1 (es)
EC (1) ECSP014109A (es)
GB (1) GB0016453D0 (es)
GT (1) GT200100111A (es)
MX (1) MXPA02012409A (es)
PA (1) PA8516201A1 (es)
PE (1) PE20020269A1 (es)
UY (1) UY26720A1 (es)
WO (1) WO2002002524A1 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1405849A1 (en) * 2002-10-04 2004-04-07 Corning Incorporated Halogenated styrene compounds and low-absorption-loss polymers obtainable therefrom
CN101837125B (zh) * 2003-12-26 2014-02-26 萩原正敏 Sr蛋白质的磷酸化控制方法以及以包含sr蛋白质活性控制剂的试剂为有效成分的抗病毒剂
ES2402362T3 (es) 2004-09-30 2013-05-03 Takeda Pharmaceutical Company Limited Inhibidores de la bomba de protones
TW200628446A (en) * 2004-12-14 2006-08-16 Takeda Pharmaceuticals Co Substituted pyrrole derivative
EP1838679A1 (en) * 2005-01-06 2007-10-03 Pfizer Limited Imidazole derivatives as enzyme reverse transcriptase modulators
PE20110009A1 (es) 2005-08-30 2011-01-31 Takeda Pharmaceutical Derivados de pirrol como inhibidores de la secrecion acida
US20100113421A1 (en) * 2006-10-06 2010-05-06 Williams Theresa M Non-nucleoside reverse transcriptase inhibitors
CN101677977A (zh) * 2006-11-10 2010-03-24 欣达克斯制药公司 用于治疗癌症的ERα+配体和组蛋白脱乙酰化酶抑制剂组合
US8933105B2 (en) 2007-02-28 2015-01-13 Takeda Pharmaceutical Company Limited Pyrrole compounds
WO2009015180A2 (en) * 2007-07-23 2009-01-29 Syndax Pharmaceuticals, Inc. Novel compounds and methods of using them
EP2179329A1 (en) * 2007-10-16 2010-04-28 Nikon Corporation Illumination optical system, exposure apparatus, and device manufacturing method
WO2009067453A1 (en) * 2007-11-19 2009-05-28 Syndax Pharmaceuticals, Inc. Combinations of hdac inhibitors and proteasome inhibitors
US8969387B2 (en) 2008-08-27 2015-03-03 Takeda Pharmaceutical Company Limited Pyrrole compounds
GB0823001D0 (en) * 2008-12-17 2009-01-28 Syngenta Participations Ag Thiophene,furan and pyrrole derivatives with plant growth regulating properties
CN101775011B (zh) * 2009-01-13 2013-07-31 中国人民解放军军事医学科学院毒物药物研究所 N-取代苯基-3-甲烯杂环芳烃-2,5-二甲基吡咯类化合物及其抗hiv/aids的应用
JP2023503062A (ja) * 2019-11-19 2023-01-26 ニューヨーク ブラッド センター インコーポレイテッド Hivにおける治療活性を有する置換複素環

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3644631A (en) * 1969-05-13 1972-02-22 Endo Lab Therapeutic methods utilizing aryl pyrrol-3-yl ketones
US4282242A (en) * 1980-03-07 1981-08-04 Pfizer Inc. Antidiabetic pyrrolecarboxylic acids
US4347186A (en) * 1980-10-20 1982-08-31 Syntex (U.S.A.) Inc. Process for preparing 5-aroyl 1,2-dihydro-3-H pyrrolo[1,2-a]pyrrole-1-carboxylic acids and novel intermediates therein
EP0674631B1 (en) * 1992-12-17 1999-12-08 Pfizer Inc. Substituted pyrazoles as crf antagonists
KR100263429B1 (ko) * 1994-06-06 2000-08-01 디. 제이. 우드 코르티코트로핀-방출 인자(crf) 길항 활성을 갖는 치환된 피라졸
TW406075B (en) * 1994-12-13 2000-09-21 Upjohn Co Alkyl substituted piperidinyl and piperazinyl anti-AIDS compounds
US6417202B1 (en) * 1996-07-11 2002-07-09 Pfizer Inc. Pyridylpyrrole compounds useful as interleukin-and TNF antagonists
DE19963174A1 (de) * 1999-12-27 2001-07-12 Gruenenthal Gmbh Substituierte Pyrrol-Mannichbasen

Also Published As

Publication number Publication date
GT200100111A (es) 2002-03-18
KR100549884B1 (ko) 2006-02-06
US20020032221A1 (en) 2002-03-14
AR028602A1 (es) 2003-05-14
JP2004502674A (ja) 2004-01-29
MXPA02012409A (es) 2003-04-25
BR0112241A (pt) 2003-06-24
KR20030014321A (ko) 2003-02-15
EP1301481A1 (en) 2003-04-16
WO2002002524A1 (en) 2002-01-10
US6737429B2 (en) 2004-05-18
PE20020269A1 (es) 2002-04-08
CN1440385A (zh) 2003-09-03
CA2412270A1 (en) 2002-01-10
ECSP014109A (es) 2002-02-25
GB0016453D0 (en) 2000-08-23
AU2001263874B2 (en) 2006-10-19
AU6387401A (en) 2002-01-14
UY26720A1 (es) 2001-11-30

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