Please use this identifier to cite or link to this item: http://nopr.niscpr.res.in/handle/123456789/16579
Title: 9+9+9Synthesis of N,N'-bis(4-methyloxazol-5-yl)-urea as the key building block of 1,3-bis(4-methyloxazol-5-yl)xanthine towards an improved bronchodilator
Authors: Ray, Sibdas
Ghosh, Sukla
Issue Date: Aug-1999
Publisher: NISCAIR-CSIR, India
Abstract: 4-Methyloxazole-5-carboxylic acid 2 is converted to 4-methyloxazol-5-yl carboxazide 3 in a one-pot reaction with ethyl chloroformate and triethylamine in cold followed by treatment with sodium azide. 3 is transformed to 4-methyloxazol-5-yl isocyanate 4 by heating in dry benzene. 4, on reaction with aqueous sodium hydroxide in the presence of benzyltriethylammonium chloride and dichloromethane furnish N,N'-bis(4-methyloxazol-5-yl)urea 5, as the key building block of the theophylline analogue, 1,3-bis(4- methyloxazol-5-yl)xanthine, a possible improved bronchodialator. 13C NMR spectral intricacies of the oxazole ring system as an electron withdrawing unit have been discussed.
Page(s): 986-988
Appears in Collections:IJC-B Vol.38B(08) [August 1999]

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