2011
DOI: 10.1016/j.jiec.2011.02.031
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Synthesis of 1,4-dihydropyridine using microwave-assisted aza-Diels–Alder reaction and its application to Amlodipine

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Cited by 18 publications
(3 citation statements)
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“…The reaction of the bromo compound with 2-azidoethanol in the presence of the sodium hydride of the compound provided 8 in two steps yields good overall results. Finally, reduction of the azido group using zinc dust to the amine was achieved to give the desired amlodipine 9 with satisfactory results 17 .…”
Section: Amlodipin Synthesismentioning
confidence: 99%
“…The reaction of the bromo compound with 2-azidoethanol in the presence of the sodium hydride of the compound provided 8 in two steps yields good overall results. Finally, reduction of the azido group using zinc dust to the amine was achieved to give the desired amlodipine 9 with satisfactory results 17 .…”
Section: Amlodipin Synthesismentioning
confidence: 99%
“…(97) were prepared by an aza-Diels-Alder [4+2] cycloaddition strategy (Scheme 2.68) promoted by MW irradiation. The 1,4-dihydropyridine prepared (97) was converted further to antihypertensive drug Amlodipine (not shown here) [105].…”
Section: Diels-alder Cycloadditionsmentioning
confidence: 99%
“…A rapid synthesis of 1,4-dihydropyridine was achieved by microwave-assisted aza-Diels-Alder reaction (Lee and Kim, 2011). …”
mentioning
confidence: 99%