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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2203086Generated: October 31, 2026

(5-Bromofuran-2-yl)methanol → 4-((5-Bromo-2-furyl)methoxy)-1-(2-cyclopropyl-1-methyl-1H-benzimidazol-6-yl)pyridin-2(1H)-one

https://huagongshe.com/reaction/2203086

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(5-Bromofuran-2-yl)methanolHCID 14595701—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant4-Chloro-1-(2-cyclopropyl-1-methyl-1h-benzimidazol-6-yl)-2(1h)-pyridinoneHCID 89690961—
SolventTolueneHCID 1140—
Product4-((5-Bromo-2-furyl)methoxy)-1-(2-cyclopropyl-1-methyl-1H-benzimidazol-6-yl)pyridin-2(1H)-oneHCID 12138625671.7%

Reaction Steps

To a solution of 4-chloro-1-(2-cyclopropyl-1-methyl-1H-benzimidazol-6-yl)pyridin-2(1H)-one (150 mg) and (5-bromo-2-furyl)methanol (177 mg) in toluene (2.0 ml) was added potassium tert-butoxide (112 mg) at 100° C., and the mixture was stirred for 30 min. The mixture was quenched with water (2 ml), and the precipitate was collected. The resulting solid was recrystallized from EtOH—H2O to give the title compound (158 mg) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365540B2
Source datasetuspto-grants-2016_06
ORD IDord-4cf1213d79e74e8db1fb311ed0041338
Source noteuspto-grants-2016_06