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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2067943Generated: October 31, 2026

Sodium borohydride → [5-(2-Chloro-pyridin-4-ylethynyl)-3-(4-fluoro-phenyl)-2-methyl-3H-imidazol-4-yl]-methanol

https://huagongshe.com/reaction/2067943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(2-Chloro-pyridin-4-ylethynyl)-3-(4-fluoro-phenyl)-2-methyl-3H-imidazole-4-carbaldehydeHCID 86602966—
SolventMethanolHCID 887—
Product[5-(2-Chloro-pyridin-4-ylethynyl)-3-(4-fluoro-phenyl)-2-methyl-3H-imidazol-4-yl]-methanolHCID 11530240—

Reaction Steps

To a solution of 100 mg (0.29 mmol) 5-(2-Chloro-pyridin-4-ylethynyl)-3-(4-fluoro-phenyl)-2-methyl-3H-imidazole-4-carbaldehyde (example 26) in 5 ml of methanol were added at 0° C. 11 mg (0.29 mmol) of sodium borohydride, and the mixture was stirred for 1 h at 0° C. The reaction mixture was quenched with sat. NaHCO3− solution and evaporated. The residue was extracted with water and ethyl acetate. The combined organic extracts were dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel (heptane/ethyl acetate 1:1). The desired compound was obtained as a white solid (40 mg, 40%), MS: m/e=342.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293916B2
Source datasetuspto-grants-2012_10
ORD IDord-c6e7e0c8823344a38b139e628c0f4d96
Source noteuspto-grants-2012_10