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AR057855A1 - Derivados de pirazina y composicion farmaceutica - Google Patents

Derivados de pirazina y composicion farmaceutica

Info

Publication number
AR057855A1
AR057855A1 ARP060104815A ARP060104815A AR057855A1 AR 057855 A1 AR057855 A1 AR 057855A1 AR P060104815 A ARP060104815 A AR P060104815A AR P060104815 A ARP060104815 A AR P060104815A AR 057855 A1 AR057855 A1 AR 057855A1
Authority
AR
Argentina
Prior art keywords
alkyl
alkoxy
compounds
aminoalkyl
haloalkyl
Prior art date
Application number
ARP060104815A
Other languages
English (en)
Original Assignee
Pfizer Ltd
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 Ltd filed Critical Pfizer Ltd
Publication of AR057855A1 publication Critical patent/AR057855A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D403/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/4965Non-condensed pyrazines
    • A61K31/497Non-condensed pyrazines containing further heterocyclic rings
    • 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
    • A61P25/02Drugs for disorders of the nervous system for peripheral neuropathies
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Anesthesiology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Medicines Containing Plant Substances (AREA)

Abstract

La presente se refiere a compuestos, a intermediarios utiles en su preparacion y a composiciones que contienen dichos compuestos. Estos compuestos resultan utiles para el tartamiento de dolor. Reivindicacion 1: Un compuesto de formula (1) o una sal o solvato farmacéuticamente aceptable del mismo, en a que R1 es un grupo heteroarilo de 5 miembros que comprende (a) de 1 a 4 átomos de N o (b) un átomo de O o S y 0, 1 o 2 átomos de N, opcionalmente sustituido con uno o más sustituyentes seleccioandos cada uno independientemente de alquilo C1-4, alcoxi C1-4, haloalquilo C1-4, alcoxi C1-4-alquilo C1-4, aminoalquilo C1-4, amino, alquil C1-4-amino, di(alquil C1-4)amino, alquil C1-4-aminoalquilo C1-4 y di(alquil C1-4)aminoalquilo C1-4; con la condicion de que R1 no sea imidazolilo, oxazolilo o 1,2,4-triazolilo; Ar es como en las formulas (2) en las que la flecha indica el punto de union al anillo de pirazina; y cada R2 se selecciona independientemente de H, alquilo C1-4, alcoxi C1- 4, haloalquilo C1-4, haloalcoxi C1-4, ciano y halo.
ARP060104815A 2005-11-04 2006-11-02 Derivados de pirazina y composicion farmaceutica AR057855A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US73366205P 2005-11-04 2005-11-04

Publications (1)

Publication Number Publication Date
AR057855A1 true AR057855A1 (es) 2007-12-19

Family

ID=37890558

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP060104815A AR057855A1 (es) 2005-11-04 2006-11-02 Derivados de pirazina y composicion farmaceutica

Country Status (27)

Country Link
US (1) US7572797B2 (es)
EP (1) EP1945630B1 (es)
JP (1) JP2009514937A (es)
KR (1) KR20080066073A (es)
CN (1) CN101356169A (es)
AP (1) AP2008004468A0 (es)
AR (1) AR057855A1 (es)
AT (1) ATE525372T1 (es)
AU (1) AU2006310215A1 (es)
BR (1) BRPI0618129A2 (es)
CA (1) CA2624621C (es)
CR (1) CR9954A (es)
DO (1) DOP2006000243A (es)
EA (1) EA200801011A1 (es)
EC (1) ECSP088412A (es)
ES (1) ES2371932T3 (es)
GT (1) GT200600475A (es)
IL (1) IL191059A0 (es)
MA (1) MA29926B1 (es)
NL (1) NL2000284C2 (es)
NO (1) NO20082496L (es)
PE (1) PE20070715A1 (es)
TN (1) TNSN08196A1 (es)
TW (1) TW200804353A (es)
UY (1) UY29893A1 (es)
WO (1) WO2007052123A2 (es)
ZA (1) ZA200803671B (es)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0934061B3 (en) 1996-07-24 2015-01-21 Warner-Lambert Company LLC Isobutylgaba and its derivatives for the treatment of pain
EP1741708A1 (en) * 2005-06-28 2007-01-10 Sanofi-Aventis Deutschland GmbH Heteroaryl-substituted amides comprising an unsaturated or cyclic linker group, and their use as pharmaceuticals
GB2431927B (en) 2005-11-04 2010-03-17 Amira Pharmaceuticals Inc 5-Lipoxygenase-activating protein (FLAP) inhibitors
US8399666B2 (en) 2005-11-04 2013-03-19 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
US7977359B2 (en) 2005-11-04 2011-07-12 Amira Pharmaceuticals, Inc. 5-lipdxygenase-activating protein (FLAP) inhibitors
US20100227872A1 (en) * 2007-05-03 2010-09-09 Mark Ian Kemp Pyrazine derivatives
GEP20125379B (en) 2007-05-03 2012-01-10 Pfizer Ltd 2 -pyridine carboxamide derivatives as sodium channel modulators
US8614255B2 (en) * 2007-08-21 2013-12-24 Civitas Therapeutics, Inc. Pulmonary pharmaceutical formulations
KR101578235B1 (ko) 2007-12-10 2015-12-16 노파르티스 아게 유기 화합물
RU2010137862A (ru) 2008-02-13 2012-03-20 ЭЙСАЙ Ар энд Ди МЕНЕДЖМЕНТ КО., ЛТД. (JP) Производное бициклоамина
US20110160249A1 (en) 2008-05-23 2011-06-30 Schaab Kevin Murray 5-lipoxygenase-activating protein inhibitor
US8546431B2 (en) 2008-10-01 2013-10-01 Panmira Pharmaceuticals, Llc 5-lipoxygenase-activating protein (FLAP) inhibitors
US10703722B2 (en) 2010-04-27 2020-07-07 Calcimedica, Inc. Compounds that modulate intracellular calcium
WO2013059677A1 (en) * 2011-10-19 2013-04-25 Calcimedica, Inc. Compounds that modulate intracellular calcium
KR102090944B1 (ko) * 2012-04-25 2020-03-19 라퀄리아 파마 인코포레이티드 Ttx-s 차단제로서의 피롤로피리디논 유도체
EP3070085B1 (en) 2013-02-04 2019-01-09 Janssen Pharmaceutica NV Flap modulators
TWI644899B (zh) 2013-02-04 2018-12-21 健生藥品公司 Flap調節劑
US10428029B2 (en) 2014-09-10 2019-10-01 Epizyme, Inc. Isoxazole carboxamide compounds
CA2978007A1 (en) 2015-02-27 2016-09-01 Calcimedica, Inc. Pancreatitis treatment
JP6738575B2 (ja) * 2015-08-07 2020-08-12 カルシメディカ,インク. 脳卒中および外傷性脳損傷の処置のためのcracチャネル阻害剤の使用
GB201801128D0 (en) 2018-01-24 2018-03-07 Univ Oxford Innovation Ltd Compounds
EP4243813A4 (en) 2020-11-13 2024-07-17 Calcimedica, Inc. IMPROVED SYNTHESIS OF CRAC CHANNEL INHIBITORS

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MA26473A1 (fr) * 1997-03-01 2004-12-20 Glaxo Group Ltd Composes pharmacologiquement actifs.
MXPA04004714A (es) * 2001-11-21 2004-08-19 Upjohn Co Derivados de aril 1,4-pirazina sustituidos.
US20030187026A1 (en) 2001-12-13 2003-10-02 Qun Li Kinase inhibitors
KR20060123208A (ko) * 2003-10-27 2006-12-01 아스테라스 세이야쿠 가부시키가이샤 피라진 유도체 및 이의 약학적 용도
WO2006047504A1 (en) * 2004-10-22 2006-05-04 Janssen Pharmaceutica, N.V. Aromatic amides as inhibitors of c-fms kinase

Also Published As

Publication number Publication date
UY29893A1 (es) 2007-06-29
NO20082496L (no) 2008-07-24
ZA200803671B (en) 2009-03-25
CA2624621A1 (en) 2007-05-10
ECSP088412A (es) 2008-05-30
ATE525372T1 (de) 2011-10-15
US7572797B2 (en) 2009-08-11
NL2000284A1 (nl) 2007-05-07
US20070105872A1 (en) 2007-05-10
CN101356169A (zh) 2009-01-28
TNSN08196A1 (fr) 2009-10-30
PE20070715A1 (es) 2007-08-11
DOP2006000243A (es) 2007-05-31
EA200801011A1 (ru) 2009-02-27
WO2007052123A3 (en) 2007-07-12
AP2008004468A0 (en) 2008-06-30
IL191059A0 (en) 2008-12-29
TW200804353A (en) 2008-01-16
AU2006310215A1 (en) 2007-05-10
BRPI0618129A2 (pt) 2011-08-16
ES2371932T3 (es) 2012-01-11
WO2007052123A2 (en) 2007-05-10
EP1945630A2 (en) 2008-07-23
GT200600475A (es) 2007-07-06
MA29926B1 (fr) 2008-11-03
CR9954A (es) 2008-05-28
JP2009514937A (ja) 2009-04-09
EP1945630B1 (en) 2011-09-21
NL2000284C2 (nl) 2007-09-28
KR20080066073A (ko) 2008-07-15
CA2624621C (en) 2010-11-30

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