## Abstract **BACKGROUND:** Mandelic acid enantiomers are important chiral analogs used for the resolution of racemic alcohols and amines. Rβ(β)βmandelic acid is a precursor for the production of semiβsynthetic penicillins and cephalosporins and also for the synthesis of various pharmaceuticals. P
Synergism of microwave irradiation and enzyme catalysis in synthesis of isoniazid
β Scribed by Ganapati D Yadav; Ashwini D Sajgure
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 2007
- Tongue
- English
- Weight
- 148 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0268-2575
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β¦ Synopsis
Abstract
Isoniazid is a useful antitubercular drug widely employed in combination therapy with rifampicin. The synthesis of isoniazid from ethyl isonicotinate and hydrazine hydrate was studied in nonβaqueous media via lipaseβcatalyzed hydrazinolysis under both conventional heating and microwave irradiation by using different supported lipases. Among three different commercial lipases used, namely Novozym 435 (Candida antarctica lipase), Lipozyme RM IM (Rhizomucor miehei lipase) and Lipozyme TL IM (Thermomyces lanuginosus lipase), Novozym 435 was found to be the most effective, with conversion of 54% for equimolar concentrations at 50 Β°C in 4 h. The rate of reaction as well as final conversion increased synergistically under microwave irradiation in comparison with conventional heating, which showed 36.4% conversion, even after 24 h, for the control experiment. Effects of various process parameters such as speed of agitation, catalyst loading, substrate concentration, product concentration and temperature were studied. A kinetic model is also described. Copyright Β© 2007 Society of Chemical Industry
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