PE20000174A1 - PYRIDINYLPYRIMIDINAMINES - Google Patents

PYRIDINYLPYRIMIDINAMINES

Info

Publication number
PE20000174A1
PE20000174A1 PE1999000018A PE00001899A PE20000174A1 PE 20000174 A1 PE20000174 A1 PE 20000174A1 PE 1999000018 A PE1999000018 A PE 1999000018A PE 00001899 A PE00001899 A PE 00001899A PE 20000174 A1 PE20000174 A1 PE 20000174A1
Authority
PE
Peru
Prior art keywords
alkyl
halogen
refers
compound
alcoxy
Prior art date
Application number
PE1999000018A
Other languages
Spanish (es)
Inventor
Peter Etimayer
Max Woisetschager
Volker Brinkmann
Christoph Heusser
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 GBGB9800522.6A external-priority patent/GB9800522D0/en
Priority claimed from GBGB9800520.0A external-priority patent/GB9800520D0/en
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of PE20000174A1 publication Critical patent/PE20000174A1/en

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

Abstract

SE REFIERE AL NUEVO USO DE PIRIDINILPIRIMIDINAMINAS DE FORMULA I; R1 ES HALOGENO, FENILO, ALQUILO; R2 ES H, HALO, ALQUILO, ALCOXI, TRIFLUOROMETILO, EN LA PREPARACION DE UN MEDICAMENTO PARA LA TERAPIA DE ENFERMEDADES MEDIADAS POR IgE (INMUNOGLOBULINA E). TAMBIEN SE REFIERE A UN COMPUESTO DE FORMULA Ib DONDE; R1`' ES HALOGENO CON UN NUMERO ATOMICO 17 o 35 Y R2'' ES H o ALCOXI O BIEN R1'' ES FENILO O ALQUILO, R2'' ES H, HALOGENO, ALQUILO, ALCOXI, TRIFLUOROMETILO. UN COMPUESTO PREFERIDO N-(3-METILFENIL)-N-[4-(2-METILPIRIDIN-4-IL)PIRIMIDIN-2-IL]AMINA. TAMBIEN SE REFIERE A UN PROCEDIMIENTO PARA LA PREPARACION. EL COMPUESTO I ACTUA COMO INHIBIDOR ESPECIFICO DE LA SINTESIS DE INMUNOGLOBULINA E (IgE) EN LOS LINFOCITOS B Y PUEDE SER UTIL PARA EL TRATAMIENTO DE ENFERMEDADES TAL COMO DERMATITIS ATOPICA, ASMA ALERGICA, CONJUNTIVITIS ALERGICA Y RINITIS ALERGICAREFERS TO THE NEW USE OF PYRIDINYLPYRIMIDINAMINES OF FORMULA I; R1 IS HALOGEN, PHENYL, ALKYL; R2 IS H, HALO, ALKYL, ALCOXY, TRIFLUOROMETHYL, IN THE PREPARATION OF A DRUG FOR THE THERAPY OF IgE-MEDIATED DISEASES (IMMUNOGLOBULIN E). ALSO REFERS TO A COMPOUND OF FORMULA Ib WHERE; R1` 'IS HALOGEN WITH AN ATOMIC NUMBER 17 or 35 AND R2' 'IS H or ALCOXI OR R1' 'IS PHENYL OR ALKYL, R2' 'IS H, HALOGEN, ALKYL, ALCOXY, TRIFLUOROMETHYL. A PREFERRED COMPOUND N- (3-METHYLPHENYL) -N- [4- (2-METHYLPYRIDIN-4-IL) PYRIMIDIN-2-IL] AMINE. IT ALSO REFERS TO A PROCEDURE FOR PREPARATION. COMPOUND I ACTS AS A SPECIFIC INHIBITOR OF THE SYNTHESIS OF IMMUNOGLOBULIN E (IgE) IN B LYMPHOCYTES AND MAY BE USEFUL FOR THE TREATMENT OF DISEASES SUCH AS ATOPIC DERMATITIS, ALLERGIC ASTHMA, ALLERGIC CONJUNCTIVITIS AND ALLERGIC RHINITIS

PE1999000018A 1998-01-12 1999-01-08 PYRIDINYLPYRIMIDINAMINES PE20000174A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9800522.6A GB9800522D0 (en) 1998-01-12 1998-01-12 Organic compounds
GBGB9800520.0A GB9800520D0 (en) 1998-01-12 1998-01-12 Organic compounds

Publications (1)

Publication Number Publication Date
PE20000174A1 true PE20000174A1 (en) 2000-03-17

Family

ID=26312926

Family Applications (1)

Application Number Title Priority Date Filing Date
PE1999000018A PE20000174A1 (en) 1998-01-12 1999-01-08 PYRIDINYLPYRIMIDINAMINES

Country Status (5)

Country Link
AR (1) AR014288A1 (en)
AU (1) AU2516199A (en)
CO (1) CO4940461A1 (en)
PE (1) PE20000174A1 (en)
WO (1) WO1999035140A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0025820D0 (en) * 2000-10-20 2000-12-06 Novartis Ag Organic compounds
US6890940B2 (en) 2001-06-29 2005-05-10 Kowa Co., Ltd. Bis(2-aryl-5-pyridyl) derivatives
US6706703B2 (en) 2001-06-29 2004-03-16 Kowa Co., Ltd. Bis(5-aryl-2-pyridyl) derivatives
AR038368A1 (en) 2002-02-01 2005-01-12 Novartis Ag N-PYRIMIDIN-2-IL-AMINAS SUBSTITUTED COMPOUNDS AS IGE INHIBITORS, A PHARMACEUTICAL COMPOSITION AND THE USE OF SUCH COMPOUNDS FOR THE PREPARATION OF A MEDICINAL PRODUCT
JP2012508723A (en) * 2008-11-14 2012-04-12 バイエル・クロップサイエンス・アーゲー Substituted (pyridyl) -azinylamine derivatives as plant protection agents

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3474817D1 (en) * 1983-09-01 1988-12-01 Boehringer Ingelheim Ltd Diazine-ethenylphenyl oxamic acids and esters and salts thereof
US5728708A (en) * 1993-10-01 1998-03-17 Novartis Corporation Pharmacologically active pyridine derivatives and processes for the preparation thereof
EP0672042B1 (en) * 1993-10-01 2006-05-03 Novartis AG Pharmacologically active pyrimidineamine derivatives and processes for the preparation thereof

Also Published As

Publication number Publication date
AU2516199A (en) 1999-07-26
AR014288A1 (en) 2001-02-07
CO4940461A1 (en) 2000-07-24
WO1999035140A1 (en) 1999-07-15

Similar Documents

Publication Publication Date Title
CY1105233T1 (en) 1,2,4-THIADIAZOLE CATION DERIVATIVES AS MELANOCORTIN RECEPTOR REGULATORS
NZ332477A (en) Tetrahydroisoquinoline derivatives as modulators of dopamine D3 receptors
PE20020467A1 (en) 1,4-DIHYDROPYRIDINE COMPOUNDS AS BRADYCININ ANTAGONISTS
BR0309522A (en) Pyridine compounds or salts thereof and herbicides containing them
EA200401172A1 (en) DERIVATIVES N- [PHENYL (PIPERIDIN-2-IL) METHYL] BENZAMIDE, METHOD OF THEIR RECEIVING AND THEIR USE IN THERAPY
EE9700283A (en) Benzimidazole compounds, pharmaceutical compositions containing said compounds and their use
NO20030471L (en) Carboxamide compounds and their use as antagonists for an 11CBY receptor
DK0842661T3 (en) Use of estrogen agonists and antagonists in the manufacture of a drug for the treatment of atherosclerosis, independent of lipid lowering
EE9700282A (en) Benzimidazole compounds, pharmaceutical compositions containing said compounds and their use
DE69616593D1 (en) PHENYLIMIDAZOLIDINE AND THEIR USE AS ANTI-ANDROGEN AGENT
DE60206164D1 (en) TRISUBSTITUTED-N - ((1S) -1,2,3,4-TETRAHYDRO-1-NAPHTHALENYL) BENZAMIDES INHIBITING P2X3 AND P2X2 / 3 CONTAINING RECEPTORS
CO4650183A1 (en) DERIVATIVES OF PIRROL
NO20022470D0 (en) pyrimidine
ID23053A (en) CARBOXAMIDE USED AS A 5-HT <IF> AGONIST
PE20000174A1 (en) PYRIDINYLPYRIMIDINAMINES
ATE369348T1 (en) CYCLIZED BENZAMIDE NEUROKININ ANTAGONISTS FOR USE IN THERAPY
TR200102585T2 (en) Biphenyl derivatives
DK1254905T3 (en) 4- (2-pyridyl) piperizines with 5HT7 receptor agonist activity
DE50304858D1 (en) N-'4- (2-IMINO-PYRROLIDIN-1-YL) PHENYL) ACETEMIDE AND CORRESPONDING PIPERIDINE DERIVATIVES AS FACTOR XA INHIBITORS FOR THE TREATMENT OF THROMBOEMBOLIC ILLNESSES
DE60121048D1 (en) PYRAZINOi1'2 ': 1,6öPYRIDOi3,4-BöINDOLDERIVATE
ATE191465T1 (en) CARBAMOYLCARBONIC ACID AMIDES
NZ333229A (en)
ATE287400T1 (en) 4-(PHENYLPIPERIDINE-4-YLIDENMETHYL) BENZAMIDE DERIVATIVES AND THE USE THEREOF FOR THE TREATMENT OF PAIN, ANXIETY OR GASTROINTESTINAL DISORDERS
DE60110233D1 (en) NEW N- (2-PHENYL-3-AMINOPROPYL) NAPHTAMIDE
ATE313528T1 (en) 4-(PHENYL(PIPERIDIN-4-YL)AMINO) BENZAMIDE DERIVATIVES AND THE USE THEREOF FOR THE TREATMENT OF PAIN, ANXIETY OR GASTROINTESTINAL DISORDERS

Legal Events

Date Code Title Description
FA Abandonment or withdrawal