VERFAHREN ZUR HERSTELLUNG VON (3-CHLOR-4- FLUORPHENYL)-(4-FLUOR-4-ÄÄ(5METHYLPYRIMIDIN-2- YLMETHYL)AMINOÜMETHYLÜPIPERIDIN-1-YL)METHANON UND NEUE PYRIMIDINDERIVATZWISCHENPRODUKTE

Preparation of (3-chloro-4-fluorophenyl)-(4-fluoro-4-{[(5-methylpyrimidin-2-ylmethyl)amino]methyl}piperidinyl-1-yl)methanone (2) by reacting 5-methylpyrimidine-2-methylamine (1) with 1-(4-fluoro-3-chlorobenzoyl)-4-fluoro-4-(hydroxycyanomethyl)piperidine (3). Preparation of (3-chloro-4-fluorophenyl)-...

Full description

Saved in:
Bibliographic Details
Main Authors BRUNEL, SERGE, MAUREL, JEAN-LOUIS, VACHER, BERNARD
Format Patent
LanguageGerman
Published 15.07.2010
Online AccessGet full text

Cover

Loading…
More Information
Summary:Preparation of (3-chloro-4-fluorophenyl)-(4-fluoro-4-{[(5-methylpyrimidin-2-ylmethyl)amino]methyl}piperidinyl-1-yl)methanone (2) by reacting 5-methylpyrimidine-2-methylamine (1) with 1-(4-fluoro-3-chlorobenzoyl)-4-fluoro-4-(hydroxycyanomethyl)piperidine (3). Preparation of (3-chloro-4-fluorophenyl)-(4-fluoro-4-{[(5-methylpyrimidin-2-ylmethyl)amino]methyl}piperidinyl-1-yl)methanone (2) by reacting 5-methylpyrimidine-2-methylamine (1) with 1-(4-fluoro-3-chlorobenzoyl)-4-fluoro-4-(hydroxycyanomethyl)piperidine (3). Independent claims are included for the following: (1) 5-methylpyrimidine-2-methylamine (1) as new; and (2) three pyrimidine derivatives of formula (4) as new compounds. one or R 1and R 2H and the other is tert-butoxycarbonyl or benzyloxycarbonyl, or R 1and R 2together complete phthalimido. [Image] ACTIVITY : None given. MECHANISM OF ACTION : 5-Hydroxytryptamine agonist.
Bibliography:Application Number: AT20060793769T