PE20050470A1 - 5-arilpirimidinas como agentes anticancerigenos - Google Patents

5-arilpirimidinas como agentes anticancerigenos

Info

Publication number
PE20050470A1
PE20050470A1 PE2004000922A PE2004000922A PE20050470A1 PE 20050470 A1 PE20050470 A1 PE 20050470A1 PE 2004000922 A PE2004000922 A PE 2004000922A PE 2004000922 A PE2004000922 A PE 2004000922A PE 20050470 A1 PE20050470 A1 PE 20050470A1
Authority
PE
Peru
Prior art keywords
pyrimidin
chloro
compound
arylpyrimidines
cancer agents
Prior art date
Application number
PE2004000922A
Other languages
English (en)
Inventor
Nan Zhang
Semiramis Ayral-Kaloustian
Thai Nguyen
Original Assignee
Wyeth Corp
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 Wyeth Corp filed Critical Wyeth Corp
Publication of PE20050470A1 publication Critical patent/PE20050470A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/32One oxygen, sulfur or nitrogen atom
    • C07D239/42One nitrogen atom
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/24Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
    • C07D239/46Two or more oxygen, sulphur or nitrogen atoms
    • C07D239/48Two nitrogen 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
    • C07D401/02Heterocyclic 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
    • 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
    • C07D403/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/04Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

REFERIDA A UN COMPUESTO DE FORMULA II DONDE Z ES a O CICLOALQUILO C6-C8; R ES b; X ES Cl O Br, L1, L2, L3 Y L4 SON CADA UNO H, F, Cl, Br; A ES H, F, Cl, Br, ENTRE OTROS; R1 ES H O ALQUILO C1-C3; R5 ES CF3 O C2F5; W' ES -NHR6, -N(CN)R6 O ARILO C1-C6, ENTRE OTROS. TAMBIEN REFERIDA A UNA COMPOSICION FARMACEUTICA CUYOS COMPUESTOS PREFERIDOS SON: 4-CLORO-6-[(2,2,2-TRIFLUOROETIL)AMINO]-5-(2,4,6-TRIFLUORFENIL)PIRIMIDIN-2-IL(METIL)CIANAMIDA; N-{3-[4-(-CLORO-6-CICLOHEPTIL-2-PIRAZIN-2-ILPIRIMIDIN-5-IL)-3,5-DIFLUORFENOXI]PROPIL}-N-METILAMINA Y 2-(5-AZIDOPIRIDIN-2-IL)-6-CLORO-5-{4-[3-(DIMETILAMINO)PROPOXI]-2,6-DIFLUORFENIL}-N-(2,2,2-TRIFLUORETIL)PIRIMIDIN-4-AMINA; ENTRE OTROS. DICHO COMPUESTO ES UTIL EN TRATAMIENTO DE TUMORES CANCEROSOS DEBIDO A RESISTENCIA A FARMACOS MULTIPLES (MDR)
PE2004000922A 2003-09-24 2004-09-22 5-arilpirimidinas como agentes anticancerigenos PE20050470A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US50548703P 2003-09-24 2003-09-24

Publications (1)

Publication Number Publication Date
PE20050470A1 true PE20050470A1 (es) 2005-10-03

Family

ID=34393022

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2004000922A PE20050470A1 (es) 2003-09-24 2004-09-22 5-arilpirimidinas como agentes anticancerigenos

Country Status (24)

Country Link
US (1) US7524849B2 (es)
EP (1) EP1663241B1 (es)
JP (1) JP2007506746A (es)
KR (1) KR20060089215A (es)
CN (1) CN1871009A (es)
AR (1) AR045811A1 (es)
AT (1) ATE432077T1 (es)
AU (1) AU2004275733A1 (es)
BR (1) BRPI0414736A (es)
CA (1) CA2539235A1 (es)
CO (1) CO5690592A2 (es)
DE (1) DE602004021269D1 (es)
EC (1) ECSP066457A (es)
GT (1) GT200400188A (es)
IL (1) IL174305A0 (es)
MX (1) MXPA06003207A (es)
NO (1) NO20061319L (es)
PA (1) PA8613201A1 (es)
PE (1) PE20050470A1 (es)
RU (1) RU2006107578A (es)
SA (1) SA04250303A (es)
TW (1) TW200512198A (es)
WO (1) WO2005030216A1 (es)
ZA (1) ZA200602386B (es)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200637556A (en) * 2005-01-31 2006-11-01 Basf Ag Substituted 5-phenyl pyrimidines I in therapy
CN101193884A (zh) 2005-06-13 2008-06-04 惠氏公司 微管蛋白抑制剂和其制备方法
BRPI0612145A2 (pt) * 2005-06-13 2010-10-19 Wyeth Corp inibidor de tubulina e processo para sua preparação
WO2007110418A2 (de) * 2006-03-27 2007-10-04 Basf Se Substituierte 5-hetaryl-4-aminopyrimidine
CL2007002231A1 (es) * 2006-08-02 2008-04-11 Basf Ag Uso de compuestos derivados de 5-(het) arilpirimidina para combatir hongos daninos; compuestos derivados de 5-(het) arilpirimidina; agente fungicida; y agente farmaceutico.
TW200836741A (en) * 2007-01-11 2008-09-16 Basf Ag 2-substituted pyrimidines I in therapy
WO2009007187A1 (de) * 2007-07-09 2009-01-15 Basf Se Substituierte 5-hetarylpyrimidine
CN105001165B (zh) 2011-04-22 2020-06-23 西格诺药品有限公司 取代的二氨基嘧啶其组合物,和用其治疗的方法
US9649317B2 (en) 2012-09-19 2017-05-16 The Trustees Of The University Of Pennsylvania Heterocyclic compounds and their use for the treatment of neurodegenerative tauopathies
NZ715903A (en) 2014-01-30 2017-06-30 Signal Pharm Llc Solid forms of 2-(tert-butylamino)-4-((1r,3r,4r)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5-carboxamide, compositions thereof and methods of their use
JP6903577B2 (ja) 2014-12-16 2021-07-14 シグナル ファーマシューティカルズ,エルエルシー 皮膚におけるc−Jun N末端キナーゼの阻害の測定方法
JP6762940B2 (ja) 2014-12-16 2020-09-30 シグナル ファーマシューティカルズ,エルエルシー 2−(tert−ブチルアミノ)−4−((1R,3R,4R)−3−ヒドロキシ−4−メチルシクロヘキシルアミノ)−ピリミジン−5−カルボキサミドの製剤
US20180022710A1 (en) 2015-01-29 2018-01-25 Signal Pharmaceuticals, Llc Isotopologues of 2-(tert-butylamino)-4-((1r,3r,4r)-3-hydroxy-4-methylcyclohexylamino)-pyrimidine-5-carboxamide
CN107922287B (zh) 2015-07-24 2021-04-09 细胞基因公司 合成(1r,2r,5r)-5-氨基-2-甲基环己醇盐酸盐的方法和其中可用的中间体
WO2019169111A1 (en) 2018-03-02 2019-09-06 The Trustees Of The University Of Pennsylvania [1,2,4]triazolo[1,5-a]pyrimidine compounds and use in stabilizing microtubules
US20240150329A1 (en) * 2019-11-01 2024-05-09 Unimatec Co., Ltd. Fluorine-containing pyrimidine compound and manufacturing method for same
TW202132285A (zh) * 2019-11-13 2021-09-01 美商愛彼特生物製藥股份有限公司 經取代異吲哚啉基2,2’-聯嘧啶基化合物、其類似物及使用其之方法

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US147744A (en) * 1874-02-24 Improvement in locomotive-furnaces
US88096A (en) * 1869-03-23 t h a y e r
US116429A (en) * 1871-06-27 Improvement in dial-telegraph apparatus
US61889A (en) * 1867-02-05 Improvement in animal teaps
US69242A (en) * 1867-09-24 Calvin pepper
GB9700664D0 (en) 1997-01-14 1997-03-05 British Tech Group Anti-cancer agents
US6117876A (en) 1997-04-14 2000-09-12 American Cyanamid Company Fungicidal trifluorophenyl-triazolopyrimidines
WO1999055668A1 (fr) 1998-04-27 1999-11-04 Kumiai Chemical Industry Co., Ltd. Derives du 3-arylphenyl-sulfure, insecticides et acaricides
US6156925A (en) 1998-09-25 2000-12-05 American Cyanamid Company Process for the preparation of halogenated phenylmaloates
US5986135A (en) 1998-09-25 1999-11-16 American Cyanamid Company Fungicidal trifluoromethylalkylamino-triazolopyrimidines
CA2412010A1 (en) * 2000-06-13 2001-12-20 Basf Aktiengesellschaft Fungicidal 5-phenyl substituted 2-(cyanoamino) pyrimidines
US6670362B2 (en) 2000-09-20 2003-12-30 Pfizer Inc. Pyridazine endothelin antagonists
BR0207975A (pt) 2001-03-15 2004-06-15 Basf Ag Composto, processo para preparar 5 fenilpiridinas, produto intermediário, agente adequado para combater fungos nocivos fitopatogênicos, e, processo para combater fungos nocivos fitopatogênicos
ATE297390T1 (de) 2001-04-20 2005-06-15 Ciba Sc Holding Ag 4-amino-2-(2-pyridinyl)pyrimidine als mikrobizide wirksubstanzen
IL161893A0 (en) 2001-11-19 2005-11-20 Basf Ag 5-Phenylpyrimidines, agents comprising the same, method for production and use thereof
ATE428705T1 (de) 2002-02-21 2009-05-15 Basf Se 2-(2-pyridyl)-5-phenyl-6-aminopyrimidine, verfahren und zwischenprodukte zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen
AU2003214110A1 (en) 2002-03-15 2003-09-29 Ciba Specialty Chemicals Holding Inc. 4-aminopyrimidines and their use for the antimicrobial treatment of surfaces
KR101052482B1 (ko) 2002-11-21 2011-07-28 노바티스 백신즈 앤드 다이아그노스틱스 인코포레이티드 포스포티딜이노시톨(pi) 3-키나제 억제제인 2,4,6-삼치환피리미딘 및 암의 치료에서 이들의 사용

Also Published As

Publication number Publication date
AU2004275733A1 (en) 2005-04-07
SA04250303A (ar) 2005-12-03
ECSP066457A (es) 2006-09-18
PA8613201A1 (es) 2005-11-25
AR045811A1 (es) 2005-11-16
IL174305A0 (en) 2008-02-09
TW200512198A (en) 2005-04-01
US7524849B2 (en) 2009-04-28
KR20060089215A (ko) 2006-08-08
CO5690592A2 (es) 2006-10-31
RU2006107578A (ru) 2007-10-27
CA2539235A1 (en) 2005-04-07
ZA200602386B (en) 2009-03-25
EP1663241B1 (en) 2009-05-27
JP2007506746A (ja) 2007-03-22
NO20061319L (no) 2006-04-20
WO2005030216A1 (en) 2005-04-07
MXPA06003207A (es) 2006-06-23
US20050075357A1 (en) 2005-04-07
BRPI0414736A (pt) 2006-11-21
CN1871009A (zh) 2006-11-29
EP1663241A1 (en) 2006-06-07
GT200400188A (es) 2005-05-02
DE602004021269D1 (de) 2009-07-09
ATE432077T1 (de) 2009-06-15

Similar Documents

Publication Publication Date Title
PE20050470A1 (es) 5-arilpirimidinas como agentes anticancerigenos
RU2356903C2 (ru) C-6 модифицированные индазолилпирролотриазины
RU2433128C2 (ru) Новые пиримидиновые производные и их применение в терапии, а также применение пиримидиновых производных в изготовлении лекарственного средства для предупреждения и/или лечения болезни альцгеймера
RU2216545C2 (ru) Гетероарил-1-пиперидины и пиперазины, фармацевтическая композиция на их основе, способ лечения психозов и ослабления боли
RU2436776C2 (ru) ДИАРИЛАМИН-СОДЕРЖАЩИЕ СОЕДИНЕНИЯ, КОМПОЗИЦИИ И ИХ ПРИМЕНЕНИЕ В КАЧЕСТВЕ МОДУЛЯТОРОВ РЕЦЕПТОРОВ с-КIT
PE20050020A1 (es) DERIVADOS 4-(2-OXO-2,3-DIHIDRO-1-H-IMIDAZO[4,5-b]PIRIDIN-1-IL)-N-(2-OXO-AZEPAN-3-IL)PIPERIDINIL-1-CARBOXAMIDA SUSTITUIDOS COMO ANTAGONISTAS DEL RECEPTOR CGRP
PE20060374A1 (es) Inhibidores de cinasa heterociclicos fusionados
RU2437882C2 (ru) Производные имидазолидинона
PE20081530A1 (es) Nuevos compuestos 617
PE20080677A1 (es) Inhibidores de pirrolotriazina cinaza
PE20070108A1 (es) Control de parasitos en animales con derivados de n-[(feniloxi)fenil]-1,1,1-trifluorometansulfonamida y de n-[(fenilsulfanil)fenil]-1,1,1-trifluorometansulfonamida
PE20011291A1 (es) Combinacion sinergetica de derivados de benzodiazepina, agentes citotoxicos, citostaticos y antiproliferativos para el tratamiento del cancer
RU2008126391A (ru) Производные 1,5-замещенного индол-2-иламида
RU2436785C2 (ru) Гетеробициклические карбоксамиды в качестве ингибиторов киназ
PE20060501A1 (es) Compuestos de aminoheteroarilo enantiomericamente puros como inhibidores de proteina quinasa
RU2006146070A (ru) Циннамидное соединение
PE20060197A1 (es) Heterociclos biciclicos como inhibidores de cinasa
JP2007505878A5 (es)
PE20070218A1 (es) COMPUESTOS DE CICLOALQUILO AMINO-HIDANTOINA Y USO DE ESTOS PARA LA MODULACION DE ß-SECRETASA
JP2009513575A5 (es)
JP2013533317A5 (es)
JP2008543781A5 (es)
PE20100718A1 (es) Derivados triciclicos de 1, 4-dihidropiridina [b, e]-condensados como inhibidores de aurora quinasas
PE20050670A1 (es) Agentes antimigrana heterociclicos
PE20060150A1 (es) Antagonistas de cgrp seleccionados, composiciones farmaceuticas y procedimiento para su preparacion

Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed