AR016500A1 - Proceso para la preparacion de derivados de acido hidroxi-pirrolidinil-hidroxamico que son agonistas opiodes del kappa receptor e intermediarios utiles. - Google Patents

Proceso para la preparacion de derivados de acido hidroxi-pirrolidinil-hidroxamico que son agonistas opiodes del kappa receptor e intermediarios utiles.

Info

Publication number
AR016500A1
AR016500A1 ARP990102917A ARP990102917A AR016500A1 AR 016500 A1 AR016500 A1 AR 016500A1 AR P990102917 A ARP990102917 A AR P990102917A AR P990102917 A ARP990102917 A AR P990102917A AR 016500 A1 AR016500 A1 AR 016500A1
Authority
AR
Argentina
Prior art keywords
hydroxy
hydrogen
acid derivatives
hydroxamic acid
alkyloxy
Prior art date
Application number
ARP990102917A
Other languages
English (en)
Original Assignee
Pfizer Prod 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 Pfizer Prod Inc filed Critical Pfizer Prod Inc
Publication of AR016500A1 publication Critical patent/AR016500A1/es

Links

Classifications

    • 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
    • C07D207/04Heterocyclic 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 no double bonds between ring members or between ring members and non-ring members
    • C07D207/08Heterocyclic 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 no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
    • 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
    • C07D207/04Heterocyclic 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 no double bonds between ring members or between ring members and non-ring members
    • C07D207/10Heterocyclic 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 no 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
    • C07D207/12Oxygen or sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P23/00Anaesthetics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/04Centrally acting analgesics, e.g. opioids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/10Antioedematous agents; Diuretics
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Diabetes (AREA)
  • Pain & Pain Management (AREA)
  • Hematology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Rheumatology (AREA)
  • Anesthesiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrrole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Un método para preparar derivados de ácido hidroxámico de formula (I) y las sales de los mismos, donde A es hidrogeno, hidroxi, o OY donde Y es un grupoprotector hidroxi: Ar es fenilo opcionalmente substituido con uno o más (preferiblemente hasta tres) sustituyentes seleccionados de halo, hidroxi, C1-4 alquil,C1-4 alquiloxi, CF3, C1-4 alcoxi-C1-4 alquiloxi y carboxi-C1-4 alquiloxi; X es fenilo, naftil, bifenilo, indanil, benzofuranil, benzotiofenilo, 1-tetraluno-6-il, C1-4 alquilendioxi, piridil, furil, y tienil, estos grupos estando opcionalmente sustituidos con hasta tres sustituyentes seleccionados de halo, C1-4alquil, C1-4 alcoxi, hidroxi, NO2, CF3 y SO2CH3; y R3 es hidrogeno, C1-4 alquilo un grupo protector hidroxi. Compuestos Intermediarios utiles para prepararcompuestos de formula I son también provistos. Los derivados de ácido hidroxámico de fnormula (I), donde A es hidrogeno o hidroxi y R es hidrogeno o C1-4alquil, exhiben actividad agonista significativa hacia los receptoresopioides kappa. Estos agonistas son particularmente utiles como un agente analgésico enmamíferos, especialmente humanos. Ellos son también utiles como antiinflamatorios, diuréticos, anestésicos o agentes neuroprotectores, o un agente para eltratamiento de ataques cardíacos o enfermedades funcionales de los intestinos tales como dolor abdominal, para el tratamiento de un sujeto mamíferoespecialmente sujeto humano.
ARP990102917A 1998-08-24 1999-06-17 Proceso para la preparacion de derivados de acido hidroxi-pirrolidinil-hidroxamico que son agonistas opiodes del kappa receptor e intermediarios utiles. AR016500A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US9763398P 1998-08-24 1998-08-24

Publications (1)

Publication Number Publication Date
AR016500A1 true AR016500A1 (es) 2001-07-04

Family

ID=22264376

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP990102917A AR016500A1 (es) 1998-08-24 1999-06-17 Proceso para la preparacion de derivados de acido hidroxi-pirrolidinil-hidroxamico que son agonistas opiodes del kappa receptor e intermediarios utiles.

Country Status (18)

Country Link
US (1) US6031114A (es)
EP (1) EP0982297A3 (es)
JP (1) JP3245578B2 (es)
KR (1) KR100338916B1 (es)
CN (1) CN1245799A (es)
AR (1) AR016500A1 (es)
AU (1) AU4466599A (es)
BR (1) BR9902525A (es)
CA (1) CA2277242A1 (es)
HU (1) HUP9901944A3 (es)
ID (1) ID23462A (es)
IL (1) IL130429A0 (es)
IN (1) IN190844B (es)
PL (1) PL334144A1 (es)
RU (1) RU2163235C1 (es)
TR (1) TR199901546A3 (es)
YU (1) YU31499A (es)
ZA (1) ZA994285B (es)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1461317A2 (en) * 2001-04-30 2004-09-29 Pfizer Products Inc. Process for preparing hydroxypyrrolidinyl ethylamine compounds useful as kappa agonists
AU2003269399A1 (en) * 2002-11-01 2004-05-25 Pfizer Products Inc. Process for the preparation of pyrrolidinyl ethylamine compounds via a copper-mediated aryl amination
US7744750B2 (en) * 2005-11-17 2010-06-29 Exxonmobil Chemical Patents Inc. Process for reducing Bromine Index of hydrocarbon feedstocks
US8057664B2 (en) * 2005-11-17 2011-11-15 Exxonmobil Chemical Patents, Inc. Process for reducing bromine index of hydrocarbon feedstocks
US7517824B2 (en) * 2005-12-06 2009-04-14 Exxonmobil Chemical Company Process for steam stripping hydrocarbons from a bromine index reduction catalyst

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR0132001B1 (ko) * 1994-05-21 1998-04-17 강박광 신규한 치환된 이미다졸 유도체
IL117440A0 (en) * 1995-03-31 1996-07-23 Pfizer Pyrrolidinyl hydroxamic acid compounds and their production process
MX9701042A (es) * 1996-02-07 1998-05-31 Pfizer Compuestos del acido hidroxamico.
TNSN97092A1 (ar) * 1996-09-18 1999-12-31 Agouron Pharma مثبطات انزيم بروتيني فلزي وتركيبات صيدلانية تحتوي على تلك المثبتطات واستخدامها الصيدلاني وطرق ومركبات وسيطة مفيدة لتحضير التركيبات المذكورة.

Also Published As

Publication number Publication date
HU9901944D0 (en) 1999-08-30
HUP9901944A3 (en) 2001-10-29
IL130429A0 (en) 2000-06-01
KR20000016898A (ko) 2000-03-25
EP0982297A3 (en) 2001-08-01
JP2000072744A (ja) 2000-03-07
RU2163235C1 (ru) 2001-02-20
TR199901546A2 (xx) 2000-04-21
CN1245799A (zh) 2000-03-01
CA2277242A1 (en) 2000-02-24
IN190844B (es) 2003-08-23
ID23462A (id) 2000-04-27
EP0982297A2 (en) 2000-03-01
YU31499A (sh) 2002-11-15
ZA994285B (en) 2001-01-02
TR199901546A3 (tr) 2000-04-21
HUP9901944A2 (hu) 2000-06-28
JP3245578B2 (ja) 2002-01-15
US6031114A (en) 2000-02-29
KR100338916B1 (ko) 2002-05-30
AU4466599A (en) 2000-03-09
BR9902525A (pt) 2000-05-02
PL334144A1 (en) 2000-02-28

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