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  • Efficient oxidizing methods for the synthesis of oxandrolone intermediates.

Efficient oxidizing methods for the synthesis of oxandrolone intermediates.

Chemical & pharmaceutical bulletin (2004-08-12)
Sandeep K Ginotra, Bhupender S Chhikara, Manish Singh, Ramesh Chandra, Vibha Tandon
ABSTRACT

Mild, efficient and eco-friendly oxidation of 17alpha-methylandrostan-3beta-17beta-diol (1) has been studied with three different reagents viz. pentavalent iodine reagent 2-iodoxy benzoic acid (IBX) in DMSO at 65 degrees C, sodium hypochlorite and H2O2/Na2WO4 under phase transfer conditions to give 17beta-hydroxy-17alpha-methylandrostan-3-one (mestanolone 2), a drug intermediate as oxidized product. The H2O2/Na2WO4/PTC gave mestanolone in high yield and purity whereas sodium hypochlorite/PTC system yielded some chlorinated material along with the mestanolone. However, 1 with 2.5 equivalent of IBX gave 17beta-hydroxy-17alpha-methyl-Delta1-androsten-3-one (3) under the similar reaction conditions in good yield and single step reaction.

MATERIALS
Product Number
Brand
Product Description

Supelco
17α-Methylandrostan-17β-ol-3-one, analytical standard