Process for preparing (R) salbutamol

The present invention relates to an improved process for preparing levosalbutamol or the pharmacologically acceptable salts thereof on an industrial scale, using asymmetric hydrogenation as the key step and optionally a special sequence of subsequent steps, using rhodium as catalyst and a chiral bid...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: KREYE PAUL, LENHART ALFONS, KLINGLER FRANZ DIETRICH
Format: Patent
Sprache:eng
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Beschreibung
Zusammenfassung:The present invention relates to an improved process for preparing levosalbutamol or the pharmacologically acceptable salts thereof on an industrial scale, using asymmetric hydrogenation as the key step and optionally a special sequence of subsequent steps, using rhodium as catalyst and a chiral bidentate phosphine ligand such as (2R, 4R)-4-(dicyclohexylphosphino)-2-(diphenyl-phosphino-methyl)-N-methyl-aminocarbonyl-pyrrolidine as catalyst system.