Urea as an Ammonia Surrogate in the Hantzsch’s Synthesis of Polyhydroquinolines / 1,4-dihydropyridines under Green Reaction Conditions

Author(s): G. Dhananjaya, Akula Raghunadh, P. Mahesh Kumar, S. Pulla Reddy, V. Narayana Murthy, Venkateswara Rao Anna*, Manojit Pal*

Journal Name: Letters in Organic Chemistry

Volume 18 , Issue 3 , 2021


Become EABM
Become Reviewer
Call for Editor

Graphical Abstract:


Abstract:

Synthesis of polyhydroquinolines via Hantzsch’s multicomponent reaction (MCR) involves the use of a hygroscopic and moderately toxic ammonium salt as one of the key reactants. In our effort, we have found urea as an effective ammonia surrogate when the MCR was performed in the presence of sulphonic acid-functionalized Wang resin (Wang-OSO3H) as a polymeric and recoverable acidic catalyst under green conditions. Urea is relatively less hygroscopic/toxic than the commonly used ammonium salts used in this MCR. The methodology afforded a range of polyhydroquinolines in good yields. Depending on the nature of reaction conditions employed, the MCR afforded Biginelli product or 1,4-DHPs when the use of 1,3-diketone was omitted.

Keywords: Urea, Hantzsch's reaction, Catalyst, Green reaction.

Rights & PermissionsPrintExport Cite as

Article Details

VOLUME: 18
ISSUE: 3
Year: 2021
Published on: 16 March, 2021
Page: [226 - 232]
Pages: 7
DOI: 10.2174/1570178617999200713144504
Price: $65

Article Metrics

PDF: 12