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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033740Generated: October 30, 2026

5-Fluoro-2-[(4-methoxy-3-methyl-2-pyridyl)methylthio]benzimidazole → HCID 178431608, compound

https://huagongshe.com/reaction/1033740

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-[(4-methoxy-3-methyl-2-pyridyl)methylthio]benzimidazoleHCID 19024498—
SolventHydrogen BromideHCID 260—
ProductHCID 178431608HCID 17843160862%

Reaction Steps

A solution of 5-fluoro-2-[(4-methoxy-3-methyl-2-pyridyl)methylthio]benzimidazole (5.5 g) in aqueous 47% HBr (50 ml) was heated for 24 hours under reflux. The reaction mixture was concentrated under reduced pressure. The residual oily substance was neutralized with a saturated aqueous solution of sodium hydrogencarbonate, to which was added ethyl acetate (50 ml) to give 5-fluoro-2-[(4-hydroxy-3-methyl-2-pyridyl)methylthio]benzimidazole (3.2 g, 62%). Recrystallization from ethanol afforded colorless needles, mp 232°-233° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312824
Source datasetuspto-grants-1994_05
ORD IDord-ffd857dc0bfe46479595f5a5ce73f935
Source noteuspto-grants-1994_05