PE57999A1 - S-atropisomeros de 3-heteroaril-4-(3h)-quinazolinonas - Google Patents

S-atropisomeros de 3-heteroaril-4-(3h)-quinazolinonas

Info

Publication number
PE57999A1
PE57999A1 PE1998000127A PE00012798A PE57999A1 PE 57999 A1 PE57999 A1 PE 57999A1 PE 1998000127 A PE1998000127 A PE 1998000127A PE 00012798 A PE00012798 A PE 00012798A PE 57999 A1 PE57999 A1 PE 57999A1
Authority
PE
Peru
Prior art keywords
alkyl
halo
formula
quinazolin
fluoro
Prior art date
Application number
PE1998000127A
Other languages
English (en)
Inventor
Keith Michael Devries
Jr Willard Mckowan Welch
Bertrand Leo Chenard
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 PE57999A1 publication Critical patent/PE57999A1/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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02Muscle relaxants, e.g. for tetanus or cramps
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • 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
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • C07D417/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10Spiro-condensed systems

Abstract

SE REFIERE A UN ATROPISOMERO DE FORMULA (Ia) DONDE UNO DE "A, B Y D" ES N Y EL RESTO ES CH, n ES 1-4, UN R5 DEBE ESTAR EN POSICION ORTO, ES ALQUILO C1-C6, HALOGENO, TRIFLUOROMETILO, AMINO(CH2)m, ENTRE OTROS; m ES CERO-4; R2 ES a)UN HETEROCICLO DE 6 MIEMBROS DE FORMULA (a) "N" ES N, "K, L Y M" ES C Y N, i)SOLO UNO "K, L Y M" ES N; ii)CUANDO "K, L Y M" ES N ESTA AUSENTE R15, R16 o R17; b)HETEROCICLO DE 5 MIEMBROS DE FORMULA (b), DONDE "T" ES CH, N ,NH, O o S Y AL MENOS UNO DE "P, Q o T" ES UN HETEROATOMO c)Ph2 DE FORMULA (c), R3 ES H, HALO, CN, NO2, ENTRE OTROS; R9 ES H, HALO, CF3, ALQUILO C1-C6, ENTRE OTROS; R10 ES H o HALO; R11 Y R14 SON INDEPENDIENTEMENTE H, HALO, CF3, ALQUILO C1-C6, ENTRE OTROS; R12 ES H, CN o HALO; R13 ES H, ALQUILO C1-C6, ALQUILO C1-C6-(CO), ENTRE OTROS, R15 ES H, CN, ALQUILO C1-C6, ENTRE OTROS; R16 ES H, CN, ALQUILO C1-C6, HALO, ENTRE OTROS; R17 ES H, CN, ALQUILO C1-C6. SON COMPUESTOS PREFERIDOS (S)-6-FLUORO-2-[2-(2-FLUOROFENIL)-VINIL]-3-(2-METIL-PIRIDIN-3-IL)-3H-QUINAZOLIN-4-ONA; (S)-2-{2-[6-FLUORO-3-(2-METILPIRIDIN-3-IL)-4-OXO-3,4-DIHIDRO-QUINAZOLIN-2-IL]-VINIL}-BENZONITRILO; ENTRE OTROS Y SUS SALES. EL COMPUESTO DE FORMULA (Ia) ANTAGONIZA AL RECEPTOR DE AMPA Y SE UTILIZA PARA TRATAR O PREVENIR DEFICITS CEREBRALES POSTERIORES A UNA CIRUGIA DE DESVIACION CARDIACA E INJERTOS, ATAQUE APOPLETICO
PE1998000127A 1997-02-28 1998-02-23 S-atropisomeros de 3-heteroaril-4-(3h)-quinazolinonas PE57999A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US3854097P 1997-02-28 1997-02-28

Publications (1)

Publication Number Publication Date
PE57999A1 true PE57999A1 (es) 1999-06-21

Family

ID=21900535

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1998000127A PE57999A1 (es) 1997-02-28 1998-02-23 S-atropisomeros de 3-heteroaril-4-(3h)-quinazolinonas

Country Status (40)

Country Link
US (1) US6380204B1 (es)
EP (1) EP0964860B1 (es)
JP (1) JP3299990B2 (es)
KR (1) KR20000075812A (es)
CN (1) CN1248254A (es)
AP (1) AP9801202A0 (es)
AR (1) AR011886A1 (es)
AT (1) ATE264854T1 (es)
AU (1) AU732448B2 (es)
BG (1) BG103687A (es)
BR (1) BR9807807A (es)
CA (1) CA2282279C (es)
CO (1) CO4950615A1 (es)
DE (1) DE69823339T2 (es)
DK (1) DK0964860T3 (es)
DZ (1) DZ2438A1 (es)
EA (1) EA001961B1 (es)
ES (1) ES2218801T3 (es)
GT (1) GT199800039A (es)
HN (1) HN1998000028A (es)
HR (1) HRP980108B1 (es)
HU (1) HUP0000935A3 (es)
ID (1) ID23435A (es)
IL (1) IL130897A0 (es)
IS (1) IS5141A (es)
MA (1) MA24485A1 (es)
NO (1) NO994178L (es)
NZ (1) NZ336627A (es)
OA (1) OA11088A (es)
PA (1) PA8446901A1 (es)
PE (1) PE57999A1 (es)
PL (1) PL335307A1 (es)
PT (1) PT964860E (es)
SK (1) SK113199A3 (es)
TN (1) TNSN98034A1 (es)
TR (1) TR199902094T2 (es)
TW (1) TW530055B (es)
UA (1) UA58536C2 (es)
WO (1) WO1998038187A1 (es)
ZA (1) ZA981665B (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6323208B1 (en) * 1997-09-05 2001-11-27 Pfizer Inc Atropisomers of 2,3-disubstituted-(5.6)-heteroaryl fused-pyrimidin-4-ones
JPH11279158A (ja) * 1998-02-09 1999-10-12 Pfizer Prod Inc キナゾリン―4―オン誘導体の製造方法
US6890930B1 (en) * 1999-09-28 2005-05-10 3-Dimensional Pharmaceuticals, Inc. Quinazolinones
US20080146562A1 (en) * 2003-08-08 2008-06-19 Ulysses Pharmaceutical Products Inc., Halogenated quinazolinyl nitrofurans as antibacterial agents
US7410974B2 (en) * 2003-08-08 2008-08-12 Ulysses Pharmaceutical Products, Inc. Halogenated Quinazolinyl nitrofurans as antibacterial agents
GB0416730D0 (en) 2004-07-27 2004-09-01 Novartis Ag Organic compounds
GB0507298D0 (en) 2005-04-11 2005-05-18 Novartis Ag Organic compounds
TWI409070B (zh) 2005-11-04 2013-09-21 Hydra Biosciences Inc 用於調節trpv3功能之化合物
AU2007303846B2 (en) * 2006-10-04 2011-03-10 Pfizer Products Inc. Pyrido[4,3-d]pyrimidin-4(3H)-one derivatives as calcium receptor antagonists
WO2008140750A1 (en) * 2007-05-10 2008-11-20 Hydra Biosciences Inc. Compounds for modulating trpv3 function
JP2012521994A (ja) * 2009-03-24 2012-09-20 ギリアード カリストガ エルエルシー 2−プリニル−3−トリル−キナゾリノン誘導体のアトロプ異性体および使用方法
JP5718323B2 (ja) * 2009-05-29 2015-05-13 メルク・シャープ・アンド・ドーム・コーポレーションMerck Sharp & Dohme Corp. 放射標識されたpde10阻害剤
US9216177B2 (en) 2011-02-28 2015-12-22 Drexel University Small molecular inhibitors of RAD51 recombinase and methods thereof
AU2021212754A1 (en) 2020-01-29 2022-08-04 Kamari Pharma Ltd. Compounds and compositions for use in treating skin disorders

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3748325A (en) 1970-04-06 1973-07-24 Karamchand Premchand Private Process for the preparation of quinazolinone derivatives
US4183931A (en) * 1977-09-08 1980-01-15 Research Corporation 2-Ketoalkyl-4(3H)-quinazolinones
WO1992013535A1 (en) * 1991-02-06 1992-08-20 Research Corporation Technologies, Inc. Anticonvulsant substituted quinazolones
CZ295565B6 (cs) 1996-05-15 2005-08-17 Pfizer Inc. 2,3-Disubstituované 4(3H)-chinazolinony, jejich použití a farmaceutické kompozice na jejich bázi
PT807633E (pt) * 1996-05-15 2003-02-28 Pfizer Novas pirimidin-4-onas substituidas em 2,3, e fundidas com heteroarilo em (5,6)

Also Published As

Publication number Publication date
PL335307A1 (en) 2000-04-10
NO994178D0 (no) 1999-08-27
AU732448B2 (en) 2001-04-26
OA11088A (en) 2002-03-15
EP0964860B1 (en) 2004-04-21
PT964860E (pt) 2004-07-30
NO994178L (no) 1999-08-27
HUP0000935A2 (hu) 2001-04-28
DE69823339T2 (de) 2005-05-12
CN1248254A (zh) 2000-03-22
BR9807807A (pt) 2000-02-22
ES2218801T3 (es) 2004-11-16
TR199902094T2 (xx) 1999-12-21
DZ2438A1 (fr) 2003-01-11
EP0964860A1 (en) 1999-12-22
HUP0000935A3 (en) 2002-04-29
EA001961B1 (ru) 2001-10-22
ATE264854T1 (de) 2004-05-15
AP9801202A0 (en) 1999-08-26
JP3299990B2 (ja) 2002-07-08
KR20000075812A (ko) 2000-12-26
TNSN98034A1 (fr) 2005-03-15
HN1998000028A (es) 1999-02-09
MA24485A1 (fr) 1998-10-01
ID23435A (id) 2000-04-20
CO4950615A1 (es) 2000-09-01
SK113199A3 (en) 2001-10-08
GT199800039A (es) 1999-08-13
NZ336627A (en) 2000-12-22
HRP980108B1 (en) 2004-10-31
EA199900689A1 (ru) 2000-02-28
DE69823339D1 (de) 2004-05-27
CA2282279A1 (en) 1998-09-03
DK0964860T3 (da) 2004-07-26
IL130897A0 (en) 2001-01-28
AU5775998A (en) 1998-09-18
AR011886A1 (es) 2000-09-13
CA2282279C (en) 2004-11-02
UA58536C2 (uk) 2003-08-15
HRP980108A2 (en) 1998-12-31
ZA981665B (en) 1999-08-17
BG103687A (en) 2000-06-30
WO1998038187A1 (en) 1998-09-03
US6380204B1 (en) 2002-04-30
PA8446901A1 (es) 2000-05-24
JP2000509732A (ja) 2000-08-02
TW530055B (en) 2003-05-01
IS5141A (is) 1999-07-30

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