| Literature DB >> 32786625 |
Molly V Campbell1, Alexei V Iretskii1, R Adam Mosey1.
Abstract
A multicomponent tandem assembly procedure for the synthesis of diverse C4-quaternary 3,4-dihydroquinazolines from amides, amines, and ketones has been developed. The one-pot reaction involves successive triflic anhydride mediated amide dehydration, ketimine addition, and Pictet-Spengler-like cyclization processes and affords products in up to 92% yield. Conversion of 3,4-dihydroquinazolines to the corresponding 1,4-dihydroquinazolines via a two-step N1 dealkylation and regioselective N3 functionalization protocol, including computational rationale for the observed regioselectivity, is also described.Entities:
Mesh:
Substances:
Year: 2020 PMID: 32786625 DOI: 10.1021/acs.joc.0c01308
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354