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PE20010523A1 - Procedimiento para preparar inhibidores de 5-lipoxigenasa que tienen sistemas anulares heterociclicos variados - Google Patents

Procedimiento para preparar inhibidores de 5-lipoxigenasa que tienen sistemas anulares heterociclicos variados

Info

Publication number
PE20010523A1
PE20010523A1 PE2000000886A PE0008862000A PE20010523A1 PE 20010523 A1 PE20010523 A1 PE 20010523A1 PE 2000000886 A PE2000000886 A PE 2000000886A PE 0008862000 A PE0008862000 A PE 0008862000A PE 20010523 A1 PE20010523 A1 PE 20010523A1
Authority
PE
Peru
Prior art keywords
procedure
phenyl
alkyl
heterociclic
varied
Prior art date
Application number
PE2000000886A
Other languages
English (en)
Inventor
Timothy Norris
Megan Elizabeth Hnatow
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 PE20010523A1 publication Critical patent/PE20010523A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/04Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/12Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P9/00Drugs for disorders of the cardiovascular system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/54Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
    • C07D233/56Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D249/00Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
    • C07D249/02Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
    • C07D249/081,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D309/00Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
    • C07D309/02Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D309/08Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Rheumatology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Hospice & Palliative Care (AREA)
  • Cardiology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyrane Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Catalysts (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION DE TETRAHIDRO-4-[3-(4-FLUOROFENIL)TIO]FENIL-2H-PIRAN-4-CARBOXAMIDA DE FORMULA 2.0.0; QUE COMPRENDE a)ESTABLECER UNA MEZCLA DE REACCION COMPUESTA POR 1)TETRAHIDRO-4-(3-BROMO- O YODO-FENIL)-2H-PIRAN-4-NITRILO 3.0.0; X ES Br O I; 2)4-FLUOROTIOFENOL 4.0.0; 3)EN UN DISOLVENTE TAL COMO ALCOHOL C2-C7; 4)EN PRESENCIA DE UNA BASE FUERTE M-O-R5; M ES Li, Na, K, Rb, Cs; R5 ES H, ALQUILO C1-C4; 5)EN PRESENCIA DE UN CATALIZADOR DE METAL DE TRANSICION QUE COMPRENDE UN COMPLEJO PALADIO; 6)EN PRESENCIA DE UN LIGANDO AUXILIAR PARA DICHO CATALIZADOR DE METAL DE TRANSICION QUE COMPRENDE UN COMPLEJO DE PALADIO, EL LIGANDO ES UN COMPUESTO AROMATICO 5.5.0, 5.5.1; W E Y SON P, N, O JUNTO CON R1, R2, R3, R4 SON HIDROGENOFOSFATO; m Y n SON 1-2; R1, R2, R3, R4 SON H, ALQUILO C1-C4, FENILO, NAFTILO, BIFENILO, ENTRE OTROS; ARIL1, ARIL2 SON FENILO, BIFENILO, ENTRE OTROS; p Y q SON 0-2; Z ES NR5, CH2; R5 ES H, ALQUILO C1-C4, ENTRE OTROS; b)CALENTAR LA MEZCLA DE REACCION POR 12 A 36 HORAS, OPCIONALMENTE SE AISLA EMPLEANDO TECNICAS DE SEPARACION. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION DE UN COMPUESTO 1.3.0, EL ANILLO CON N ES UN DIAZOL CONDENSADO OPCIONALMENTE SUSTITUIDO CON R7 Y R8; R7 Y R8 SON H, ALQUILO C1-C4, ENTRE OTROS. EL COMPUESTO ES UN INHIBIDOR DE 5-LIPOXIGENASA
PE2000000886A 1999-08-31 2000-08-29 Procedimiento para preparar inhibidores de 5-lipoxigenasa que tienen sistemas anulares heterociclicos variados PE20010523A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US15161099P 1999-08-31 1999-08-31

Publications (1)

Publication Number Publication Date
PE20010523A1 true PE20010523A1 (es) 2001-04-28

Family

ID=22539510

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2000000886A PE20010523A1 (es) 1999-08-31 2000-08-29 Procedimiento para preparar inhibidores de 5-lipoxigenasa que tienen sistemas anulares heterociclicos variados

Country Status (33)

Country Link
EP (1) EP1081144A3 (es)
JP (1) JP2001106686A (es)
KR (1) KR20010050274A (es)
CN (1) CN1286251A (es)
AP (1) AP2000001909A0 (es)
AR (1) AR022650A1 (es)
AU (1) AU5370200A (es)
BG (1) BG104730A (es)
BR (1) BR0003888A (es)
CA (1) CA2316748A1 (es)
CO (1) CO5180623A1 (es)
CZ (1) CZ20003159A3 (es)
EA (1) EA200000803A3 (es)
EE (1) EE200000513A (es)
GT (1) GT200000144A (es)
HR (1) HRP20000565A2 (es)
HU (1) HUP0003437A3 (es)
ID (1) ID27128A (es)
IL (1) IL138089A0 (es)
IS (1) IS5604A (es)
MA (1) MA26750A1 (es)
NO (1) NO20004312L (es)
NZ (1) NZ506633A (es)
OA (1) OA11451A (es)
PA (1) PA8499601A1 (es)
PE (1) PE20010523A1 (es)
PL (1) PL342280A1 (es)
SG (1) SG87145A1 (es)
SK (1) SK12862000A3 (es)
SV (1) SV2002000160A (es)
TN (1) TNSN00176A1 (es)
TR (1) TR200002530A2 (es)
UY (1) UY26315A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004112837A1 (ja) * 2003-05-23 2004-12-29 Hisamitsu Pharmaceutical Co., Inc. 非ステロイド系消炎鎮痛剤含有外用経皮製剤およびインターロイキン-1α生成抑制剤
US7674811B2 (en) 2006-03-14 2010-03-09 Ranbaxy Laboratories Limited 5-lipoxygenase inhibitors
CN103980312B (zh) * 2014-05-27 2016-09-07 广州大学 一种n杂环双膦配体及其合成方法
CN119630670A (zh) * 2023-08-16 2025-03-14 瑞雷拉公司 TNFα活性调节剂及其用途

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SK281577B6 (sk) * 1994-10-18 2001-05-10 Pfizer Inc. Heterocyklické zlúčeniny a farmaceutický prostriedok na ich báze

Also Published As

Publication number Publication date
HU0003437D0 (en) 2000-08-30
AU5370200A (en) 2001-03-08
AP2000001909A0 (en) 2000-09-30
CO5180623A1 (es) 2002-07-30
GT200000144A (es) 2002-02-20
HUP0003437A3 (en) 2002-08-28
ID27128A (id) 2001-03-01
BG104730A (en) 2001-09-28
UY26315A1 (es) 2001-04-30
PA8499601A1 (es) 2002-02-21
JP2001106686A (ja) 2001-04-17
SV2002000160A (es) 2002-01-23
NO20004312D0 (no) 2000-08-30
IL138089A0 (en) 2001-10-31
TNSN00176A1 (fr) 2005-11-10
OA11451A (en) 2003-12-08
IS5604A (is) 2001-03-01
EA200000803A2 (ru) 2001-04-23
HRP20000565A2 (en) 2001-06-30
CA2316748A1 (en) 2001-02-28
KR20010050274A (ko) 2001-06-15
SG87145A1 (en) 2002-03-19
PL342280A1 (en) 2001-03-12
TR200002530A2 (tr) 2001-04-20
SK12862000A3 (sk) 2002-02-05
CN1286251A (zh) 2001-03-07
EP1081144A2 (en) 2001-03-07
NO20004312L (no) 2001-03-01
HUP0003437A2 (hu) 2001-06-28
EE200000513A (et) 2001-04-16
BR0003888A (pt) 2001-12-11
NZ506633A (en) 2001-12-21
EP1081144A3 (en) 2001-04-11
EA200000803A3 (ru) 2001-06-25
AR022650A1 (es) 2002-09-04
CZ20003159A3 (cs) 2001-12-12
MA26750A1 (fr) 2004-12-20

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