PE20000174A1 - PYRIDINYLPYRIMIDINAMINES - Google Patents
PYRIDINYLPYRIMIDINAMINESInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic 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
- C07D401/02—Heterocyclic 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
- C07D401/04—Heterocyclic 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
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)
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)
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 |
-
1999
- 1999-01-08 PE PE1999000018A patent/PE20000174A1/en not_active Application Discontinuation
- 1999-01-08 WO PCT/EP1999/000060 patent/WO1999035140A1/en active Application Filing
- 1999-01-08 AU AU25161/99A patent/AU2516199A/en not_active Abandoned
- 1999-01-11 AR ARP990100084A patent/AR014288A1/en unknown
- 1999-01-12 CO CO99001220A patent/CO4940461A1/en unknown
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 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |