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Synthesis of [9, 10-dihydro-9-(4-methylaminobutyl)-9, 10-propanoanthracene] using Diels–Alder cycloaddition
Journal article   Open access  Peer reviewed

Synthesis of [9, 10-dihydro-9-(4-methylaminobutyl)-9, 10-propanoanthracene] using Diels–Alder cycloaddition

Adel Al-Saeedi, Usama Karama and Mazahar Farooqui
Journal of Saudi Chemical Society, Vol.20(4), pp.428-431
07/2016

Abstract

Antidepressant Cycloaddition Homolog Maprotiline Synthesis
The synthesis of [9, 10-dihydro-9-(4-methylaminobutyl)-9, 10-propanoanthracene] (2) as a homolog of the antidepressant [9, 10-dihydro-9-(3-methylaminopropyl)-9, 10-ethanoanthracene] (1) is described in the present paper. The key intermediate [9, 10-dihydro (4-pentyl)-9, 10- propanoanthracene-12-one] (7) is successfully synthesized by using the reaction of α-bromoacrolein with 9-pent-4-enyl-anthracene (4) followed by ring expansion and samarium diiodide deoxygenation.
url
https://doi.org/10.1016/j.jscs.2013.03.001View
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