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Efficient Niementowski synthesis of novel derivatives of 1,2,9,11-tetrasubstituted-7H-thieno[2',3':4,5]pyrimido[6,1-b]-quinazolin-7-one
Published:
30 November 2007
by MDPI
in The 11th International Electronic Conference on Synthetic Organic Chemistry
session Symposium on Microwave Assisted Synthesis
Abstract: Starting Starting from 5,6-disubstituted-3H-thieno[2,3-d]pyrimidin-4-ones, novel 1,2,9,11-tetrasubstituted-7H-thieno[2',3':4,5]pyrimido[6,1-b]quinazolin-7-ones could be reached in two steps through a von Niementowski reaction, which involves condensation of substituted anthranilic acids with a 4-chloro-5,6-disubstituted-3H-thieno[2,3-d] pyrimidines. Microwave irradiation in acetic acid media was used in order to improve reactions where conventional heating was limited.
Keywords: cyclization, fused thieno-[2,3-d]-pyrimidine, Microwave assisted synthesis, Sulphur heterocycles
