New Approach for the Synthesis of Pyrido[1,2-a]pyrimidines
Author(s) -
Raghunath B. Toche,
Bhausaheb K. Ghotekar,
Muddassar A. Kazi,
Shivaraj P. Patil,
Madhukar N. Jachak
Publication year - 2008
Publication title -
scholarly research exchange
Language(s) - English
Resource type - Journals
eISSN - 1687-8302
pISSN - 1687-8299
DOI - 10.3814/2008/434329
Subject(s) - sodium ethoxide , yield (engineering) , chemistry , ethanol , condensation , phosphorus , sodium , organic chemistry , medicinal chemistry , combinatorial chemistry , materials science , physics , metallurgy , thermodynamics
A novel method was successfully demonstrated towards the synthesis of pyrido[1,2-a]pyrimidines having chloroethyl as an intractable side chain, through dihydrofuranone intermediates. The dihydrofuranone intermediates were synthesized by condensation of 2-aminopyridines with α -acetyl- γ -butyrolactone, which upon cyclization using phosphorus oxychloride or ethanol in sodium ethoxide furnished the pyrido[1,2-a]pyrimidines in good yield.
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