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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486406Generated: October 25, 2026

Benzimidazole → 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-benzimidazole

https://huagongshe.com/reaction/486406

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzimidazoleHCID 5798—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(4-(4-Bromobutyl)piperazin-1-yl)pyrimidineHCID 14726843—
SolventDimethylformamideHCID 6228—
Product1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl}-1H-benzimidazoleHCID 9819148—

Reaction Steps

A mixture of 6 g (20 mmol) of 2-[4-(4-bromobutyl)-1-piperazinyl]-pyrimidine, 2.36 g (20 mmol) of benzimidazole and 4.1 g (30 mmol) of potassium carbonate in 60 ml of dimethylformamide is refluxed for 14 hours. The reaction mixture is evaporated under vacuum, chloroform is added, the mixture is washed with water, dried over sodium sulphate and evaporated under vacuum and 4.8 g of 1-{4-[4-(2-pyrimidinyl)-1-piperazinyl]-butyl}-1H-benzimidazole are obtained, which may be recrystallised from ethyl ether, with a melting point of 85°- 88° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292739
Source datasetuspto-grants-1994_03
ORD IDord-5e633289eb194f449b57f05e553b1430
Source noteuspto-grants-1994_03