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Synthesis of Acetylated Dihydropyrimidine Analogues Under Solvent Free Conditions and their Evaluation as Calcium Channel Blockers
One pot condensation of ethylacetoacetate with various para and ortho substituted aldehydes and urea or thiourea by SnCl2.2H2O affords eight different substituted 3,4-dihydropyrimidine ones/thiones. Further we prepared acetylated 3,4-dihydropyrimidine ones/thiones, on treatment of 3,4-dihydropyrimid...
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Published in: | Oriental journal of chemistry 2012-01, Vol.28 (2), p.1055-1059 |
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container_end_page | 1059 |
container_issue | 2 |
container_start_page | 1055 |
container_title | Oriental journal of chemistry |
container_volume | 28 |
creator | SATI, BHAWANA ELLAMMA, ELLAMMA SATI, HEMLATA NARGUND, L.V.G. KHAIDEM, SOMILA BHATT, PRAKASH CHANDRA SAKLANI, SARLA |
description | One pot condensation of ethylacetoacetate with various para and ortho substituted aldehydes and urea or thiourea by SnCl2.2H2O affords eight different substituted 3,4-dihydropyrimidine ones/thiones. Further we prepared acetylated 3,4-dihydropyrimidine ones/thiones, on treatment of 3,4-dihydropyrimidine ones/thiones with acetic anhydride using zinc chloride as a catalyst. Calcium channel blocker activity shows that synthesized compounds have moderate activity. |
doi_str_mv | 10.13005/ojc/280259 |
format | article |
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subjects | Aldehydes Anhydrides Calcium channel blockers Calcium chloride Calcium compounds Chemical synthesis Substitutes Zinc chloride |
title | Synthesis of Acetylated Dihydropyrimidine Analogues Under Solvent Free Conditions and their Evaluation as Calcium Channel Blockers |
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