ECSP045213A - Aminas de fenilpirimidina como inhibidores ige - Google Patents

Aminas de fenilpirimidina como inhibidores ige

Info

Publication number
ECSP045213A
ECSP045213A EC2004005213A ECSP045213A ECSP045213A EC SP045213 A ECSP045213 A EC SP045213A EC 2004005213 A EC2004005213 A EC 2004005213A EC SP045213 A ECSP045213 A EC SP045213A EC SP045213 A ECSP045213 A EC SP045213A
Authority
EC
Ecuador
Prior art keywords
phenyl pyrimidine
ige inhibitors
pyrimidine amines
amines
phenyl
Prior art date
Application number
EC2004005213A
Other languages
English (en)
Inventor
Murty Bulusu
Peter Ettmayer
Klaus Weigand
Max Woisetschalaeger
Original Assignee
Novartis Ag
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
Priority claimed from GB0202381A external-priority patent/GB0202381D0/en
Priority claimed from GB0221953A external-priority patent/GB0221953D0/en
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of ECSP045213A publication Critical patent/ECSP045213A/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
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • A61P37/06Immunosuppressants, e.g. drugs for graft rejection
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/08Antiallergic agents
    • 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
    • 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links
    • 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
    • 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
    • C07D405/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Transplantation (AREA)
  • Pulmonology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Una amina, la cual se sustituye por pirimidina sustituida por fenilo; y fenilo; y un tercer sustituyente y su uso como una preparación farmacéutica.
EC2004005213A 2002-02-01 2004-07-30 Aminas de fenilpirimidina como inhibidores ige ECSP045213A (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0202381A GB0202381D0 (en) 2002-02-01 2002-02-01 Organic compounds
GB0221953A GB0221953D0 (en) 2002-09-20 2002-09-20 Organic compounds

Publications (1)

Publication Number Publication Date
ECSP045213A true ECSP045213A (es) 2004-09-28

Family

ID=27665364

Family Applications (1)

Application Number Title Priority Date Filing Date
EC2004005213A ECSP045213A (es) 2002-02-01 2004-07-30 Aminas de fenilpirimidina como inhibidores ige

Country Status (23)

Country Link
US (2) US20050119255A1 (es)
EP (1) EP1474146B1 (es)
JP (1) JP4393198B2 (es)
KR (1) KR20040081159A (es)
CN (2) CN1622807A (es)
AR (1) AR038368A1 (es)
AT (1) ATE406165T1 (es)
AU (1) AU2003206810B2 (es)
BR (1) BR0307379A (es)
CA (1) CA2471883C (es)
DE (1) DE60323205D1 (es)
EC (1) ECSP045213A (es)
ES (1) ES2312749T3 (es)
IL (1) IL162766A0 (es)
MX (1) MXPA04007395A (es)
NO (1) NO20043610L (es)
NZ (1) NZ534229A (es)
PE (1) PE20030983A1 (es)
PL (1) PL370666A1 (es)
PT (1) PT1474146E (es)
RU (1) RU2004126614A (es)
TW (1) TW200302728A (es)
WO (1) WO2003063871A1 (es)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20050014753A1 (en) * 2003-04-04 2005-01-20 Irm Llc Novel compounds and compositions as protein kinase inhibitors
CA2533474A1 (en) * 2003-07-30 2005-02-10 Shudong Wang 2-aminophenyl-4-phenylpyrimidines as kinase inhibitors
EP1679309A4 (en) * 2003-10-24 2007-03-28 Ono Pharmaceutical Co ANTISTRESS MEDICAMENT AND ITS MEDICAL USE
JP2009509995A (ja) * 2005-09-29 2009-03-12 ノバルティス アクチエンゲゼルシャフト 免疫寛容を増強するためのフェニル−(4−フェニル−ピリミジン−2−イル)−アミン
CA2696321A1 (en) 2007-08-15 2009-02-19 Cytokinetics, Incorporated Certain chemical entities, compositions, and methods
US11608329B2 (en) 2019-12-20 2023-03-21 Ikena Oncology, Inc. Aryl hydrocarbon receptor (AHR) agonists and uses thereof

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1185039A (en) 1966-03-31 1970-03-18 Ici Ltd Pyrimidine Derivatives and Compositions containing them
GB2001069B (en) 1977-07-12 1982-01-20 Scras Pyrimidine derivatives
AU5319479A (en) 1978-12-22 1980-06-26 Ici Australia Limited Pyrimidinyl amino phenoxy carboxylate derivatives
US4351939A (en) * 1980-10-16 1982-09-28 Mead Johnson & Company Spiro-quaternary ammonium halides and N-(2-pyrimidinyl)piperazinylalkylazaspiroalkanedione process
DE3270906D1 (en) * 1982-01-14 1986-06-05 Merck Patent Gmbh Liquid crystal mixtures
FR2536071B1 (fr) 1982-11-12 1986-07-11 Sanofi Sa Sels acides de 2-piperazinopyrimidine, procede pour leur preparation et compositions pharmaceutiques en contenant
FR2547821B1 (fr) * 1983-06-24 1985-12-06 Sanofi Sa Sel de 2-piperazinopyrimidine, procede pour sa preparation et compositions pharmaceutiques en contenant
US4659363A (en) 1983-07-25 1987-04-21 Ciba-Geigy Corporation N-(2-nitrophenyl)-2-aminopyrimidine derivatives, the preparation and use thereof
EP0164204A1 (en) 1984-05-12 1985-12-11 FISONS plc Novel pharmaceutically useful pyrimidines
ATE60591T1 (de) * 1984-06-25 1991-02-15 Ciba Geigy Ag Pyrimidinderivate wirksam als schaedlingsbekaempfungsmittel.
ATE135699T1 (de) 1986-01-13 1996-04-15 American Cyanamid Co 4,5,6-substituierte 2-pyrimidinamine
DE3614060A1 (de) 1986-04-23 1987-10-29 Schering Ag Pyrimidin-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
US4868183A (en) 1986-07-21 1989-09-19 Otsuka Pharmaceutical Factory, Inc. N-pyrazinyl substituted P-aminophenols
DE3788494D1 (de) * 1986-10-13 1994-01-27 Ciba Geigy Harnstoffe.
US4826990A (en) 1987-09-30 1989-05-02 American Home Products Corporation 2-aryl substituted heterocyclic compounds as antiallergic and antiinflammatory agents
US4966622A (en) * 1988-04-12 1990-10-30 Ciba-Geigy Corporation N-phenyl-N-pyrimidin-2-ylureas
ES2058589T3 (es) * 1988-04-12 1994-11-01 Ciba Geigy Ag Ureas.
US4973690A (en) * 1988-04-12 1990-11-27 Ciba-Geigy Corporation Novel ureas
JPH02308248A (ja) * 1989-05-24 1990-12-21 Fuji Photo Film Co Ltd アミノピリミジン系色素形成カプラーおよび該カプラーを含有するハロゲン化銀カラー写真感光材料
US5521184A (en) * 1992-04-03 1996-05-28 Ciba-Geigy Corporation Pyrimidine derivatives and processes for the preparation thereof
US5516775A (en) * 1992-08-31 1996-05-14 Ciba-Geigy Corporation Further use of pyrimidine derivatives
AU693114B2 (en) 1993-10-01 1998-06-25 Novartis Ag Pharmacologically active pyrimidineamine derivatives and processes for the preparation thereof
EP0672035A1 (en) 1993-10-01 1995-09-20 Novartis AG Pyrimidineamine derivatives and processes for the preparation thereof
KR100330553B1 (ko) 1993-10-01 2002-11-27 노파르티스 아게 약물학적활성피리딘유도체및그의제조방법
CA2174080A1 (en) * 1993-10-12 1995-04-20 Paul Edward Aldrich 1n-alkyl-n-arylpyrimidinamines and derivatives thereof
AU688087B2 (en) 1994-08-13 1998-03-05 Yuhan Corporation Novel pyrimidine derivatives and processes for the preparation thereof
GB9523675D0 (en) 1995-11-20 1996-01-24 Celltech Therapeutics Ltd Chemical compounds
WO1998024782A2 (en) 1996-12-05 1998-06-11 Amgen Inc. Substituted pyrimidine compounds and their use
DK0976745T3 (da) * 1997-03-26 2003-10-27 Taisho Pharmaceutical Co Ltd 4-tetrahydropyridylpyrimidinderivat
IN188411B (es) 1997-03-27 2002-09-21 Yuhan Corp
US6440965B1 (en) 1997-10-15 2002-08-27 Krenitsky Pharmaceuticals, Inc. Substituted pyrimidine derivatives, their preparation and their use in the treatment of neurodegenerative or neurological disorders of the central nervous system
PE20000174A1 (es) * 1998-01-12 2000-03-17 Novartis Ag Piridinilpirimidinaminas
AU742641B2 (en) * 1998-01-28 2002-01-10 Shionogi & Co., Ltd. Novel tricyclic compound
CZ299380B6 (cs) 1998-03-27 2008-07-09 Janssen Pharmaceutica N. V. Pyrimidinová sloucenina, použití této slouceniny pro prípravu léciva, farmaceutický prostredek tutoslouceninu obsahující, zpusob prípravy tohoto prostredku a uvedené slouceniny a kombinace a produktuvedenou slouceninu obsahující
TWI241298B (en) 1998-09-25 2005-10-11 Mitsubishi Chem Corp Pyrimidone derivatives
CZ20011466A3 (cs) * 1998-11-17 2001-09-12 Kumiai Chemical Industry Co., Ltd. Deriváty pyrimidinylbenzimidazolu, triazinylbenzimidazolu, anilinpyrimidinu nebo anilintriazinu a je obsahující zemědělské a zahradnické fungicidy
GB9828511D0 (en) 1998-12-24 1999-02-17 Zeneca Ltd Chemical compounds
ATE365158T1 (de) 1999-04-28 2007-07-15 Inst Med Molecular Design Inc Pyrimidincarbonsäurederivate
GB9914258D0 (en) 1999-06-18 1999-08-18 Celltech Therapeutics Ltd Chemical compounds
GB0003224D0 (en) 2000-02-11 2000-04-05 Glaxo Group Ltd Chemical compounds

Also Published As

Publication number Publication date
PT1474146E (pt) 2008-12-05
RU2004126614A (ru) 2005-05-27
KR20040081159A (ko) 2004-09-20
TW200302728A (en) 2003-08-16
US20070281956A1 (en) 2007-12-06
PE20030983A1 (es) 2004-01-26
JP4393198B2 (ja) 2010-01-06
MXPA04007395A (es) 2005-06-17
US7759357B2 (en) 2010-07-20
NZ534229A (en) 2005-04-29
ATE406165T1 (de) 2008-09-15
ES2312749T3 (es) 2009-03-01
DE60323205D1 (en) 2008-10-09
EP1474146B1 (en) 2008-08-27
PL370666A1 (en) 2005-05-30
AR038368A1 (es) 2005-01-12
BR0307379A (pt) 2004-12-28
CA2471883A1 (en) 2003-08-07
US20050119255A1 (en) 2005-06-02
EP1474146A1 (en) 2004-11-10
CN1622807A (zh) 2005-06-01
CN101684097A (zh) 2010-03-31
JP2005516051A (ja) 2005-06-02
NO20043610L (no) 2004-10-05
AU2003206810B2 (en) 2006-06-29
IL162766A0 (en) 2005-11-20
CA2471883C (en) 2010-12-07
WO2003063871A1 (en) 2003-08-07

Similar Documents

Publication Publication Date Title
CR7728A (es) Nuevas quinazolinas espirocondensadas y su uso como inhibidores de la fosfodiesterasa
LTC1663240I2 (lt) Pirimidino deriniai, turintys nnrti su rt slopikliais
ATE405570T1 (de) Hiv-integrase-inhibitoren: cyclische pyrimidinonverbindung
EA200501928A1 (ru) Пирролодигидроизохинолины как ингибиторы pde10
DK1761505T3 (da) Pyrimidin-urinstof-derivater som kinaseinhibitorer
ECSP077271A (es) Derivados de pirimidina
DE602004012154D1 (de) Pyridoä2,3-düpyrimidin-2,4-diamine als pde-2-inhibitoren
DE60313872D1 (de) Pyrazoloä1,5-aüpyrimidine als hemmstoffe cyclin-abhängiger kinasen
DK1763517T3 (da) Pyrimidinderivater som 11beta-HSD1-inhibitorer
DK1492785T3 (da) 2-hydroxy-3-heteroarylindol-derivater som GSK3-inhibitorer
DK1483265T3 (da) Purinderivater som kinaseinhibitorer
ECSP077259A (es) Derivados de pirimidina
BRPI0608886B8 (pt) derivados de n-sulfonilpirróis e seus usos
EA200700142A1 (ru) Замещенные гетероциклом циклические производные мочевины, их получение и их фармацевтическое применение в качестве ингибиторов киназы
CR8418A (es) Biaril sulfonamidas y metodos para su uso
DK1682530T3 (da) Pyrrolsubstituerede indoler som inhibitorer af PAI-1
DK1789390T3 (da) Pyridyl-inhibitorer af hedgehog-signalering
DK1480644T3 (da) Heterocykliske forbindelser, der er aktive som inhibitorer af beta-lactamaser
SV2006002232A (es) Inhibidores bace ref. x-16940
NO20050665L (no) Pyrrolidonderivater som MAOE inhibitoere
UY29213A1 (es) Derivados de quinolina e isoquinolina 5-sustitiuidos, un procedimiento para su preparación y su uso como inhibidores de la inflamación
PA8657801A1 (es) Aminalcoholes triciclicos, procedimientos para su preparacion
DK1745009T3 (da) Heteroarylsubstituerede cyklohexyl-1,4-diamin-derivater
DK1711177T3 (da) 1H-thieno-2,3-c-pyrazolderivater, der er egnede som kinase-I-inhibitorer
NO20061317L (no) Imidazopyridinderivater som induserbare NO-syntaseinhibatorer