Three-component one-pot construction of 2-aryl-3-benzylbenzo[4,5]imidazo[1,2- <i>a</i> ]pyrimidines using solid calcium carbide as an alkyne source

A concise method for the construction of 2-aryl-3-benzylbenzo[4,5]imidazo[1,2-<i>a</i>]pyrimidines using solid calcium carbide as an alkyne source, 2-aminobenzimidazoles, and (hetero)aromatic aldehydes as substrates through one-pot three-component procedure is described. The target products were effectively obtained through A<sup>3</sup> coupling, 6-<i>endo-dig</i> cyclization, isomerization, and dehydration cascade processes. The salient features of this protocol are the use of an inexpensive, abundant and easy-to-handle solid alkyne source instead of flammable and explosive gaseous acetylene, low-cost catalyst, wide functional tolerance, satisfactory yield, and simple workup procedure. The reactions can also be carried out on a gram scale.

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Publication Details

Journal
Synthetic Communications
Published
2025-02-16
DOI
https://doi.org/10.1080/00397911.2025.2466015
Citations
3
Primary Topic
Synthesis and bioactivity of alkaloids
Type
article
Field-Weighted Citation Impact
2.42
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article

Three-component one-pot construction of 2-aryl-3-benzylbenzo[4,5]imidazo[1,2- a ]pyrimidines using solid calcium carbide as an alkyne source

Jinhui Yang, Zheng Li, Botao Wang, Zhiqiang Wang et al.
3 citations
Synthetic Communications
Synthesis and bioactivity of alkaloids
2.42
article

Three-component one-pot construction of 2-aryl-3-benzylbenzo[4,5]imidazo[1,2- a ]pyrimidines using solid calcium carbide as an alkyne source

Jinhui Yang, Zheng Li, Botao Wang, Zhiqiang Wang, Jiao Wang
article en
3 citations

Abstract

A concise method for the construction of 2-aryl-3-benzylbenzo[4,5]imidazo[1,2-<i>a</i>]pyrimidines using solid calcium carbide as an alkyne source, 2-aminobenzimidazoles, and (hetero)aromatic aldehydes as substrates through one-pot three-component procedure is described. The target products were effectively obtained through A<sup>3</sup> coupling, 6-<i>endo-dig</i> cyclization, isomerization, and dehydration cascade processes. The salient features of this protocol are the use of an inexpensive, abundant and easy-to-handle solid alkyne source instead of flammable and explosive gaseous acetylene, low-cost catalyst, wide functional tolerance, satisfactory yield, and simple workup procedure. The reactions can also be carried out on a gram scale.

Synthetic CommunicationsVol. 55(6)
Ningxia University (CN), Northwest Normal University (CN)
Openalex Percentile: Top 13%
Synthesis and bioactivity of alkaloids
2.42
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