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Regioselective Synthesis of Novel Functionalized Pyrano[2',3':4,5]pyrimido[1,6-b][1,2,4,5]triazaphosphepines
Journal article   Peer reviewed

Regioselective Synthesis of Novel Functionalized Pyrano[2',3':4,5]pyrimido[1,6-b][1,2,4,5]triazaphosphepines

T. E. Ali, M. A. Assiri, I. S. Yahia, H. Y. Zahran, M. H. Meselhy and M. S. A. Hussien
Russian journal of organic chemistry, Vol.57(1), pp.79-84
01/01/2021

Abstract

Chemistry Chemistry, Organic Physical Sciences Science & Technology
The reactions of 6-acetyl- 3-amino-4- imino-7-methyl-5-phenyl-3,5-dihydro-4H-pyrano[2,3-d]pyrimi dine with triethyl phosphite and some electrophilic reagents, namely 1,2-dibromoethane, oxalyl chloride, chloroacetyl chloride, and ethyl chloroacetate, were studied. These one-pot three-component reactions regioselectively afforded four new 11-acetyl-2-ethoxy-10-methyl-12- phenylpyrano[2',3':4,5]pyrimido[1,6-b][1,2,4,5.5]triazaphosphepin-2-ones in 69-73% yields.

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