Resolution of several racemic 3-hydroxy-1,4-benzodiazepin-2-ones by high-performance liquid chromatography on a chiral silica-bonded stationary phase.

Abstract:

:The resolution of four racemic 3-hydroxy-1,4-benzodiazepin-2-ones, widely used in therapeutics, by means of a chiral stationary phase is described. The chiral selector used is (S)-N-(3,5-dinitrobenzoyl)phenylalanine. This chiral stationary phase showed both good enantioselectivity and efficiency for the compounds. Elution times were in all cases shorter than those previously reported for such compounds on different stationary phases. Racemic oxazepam was used to evaluate the loading capacity of the chiral stationary phase.

journal_name

J Pharm Biomed Anal

authors

Oliveros L,Minguillon C,Billaud C

doi

10.1016/0731-7085(91)80100-n

subject

Has Abstract

pub_date

1992-10-01 00:00:00

pages

925-30

issue

10-12

eissn

0731-7085

issn

1873-264X

pii

0731-7085(91)80100-N

journal_volume

10

pub_type

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