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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033741Generated: October 30, 2026

Water → 2-[(4-Difluoromethoxy-3-methyl-2-pyridyl)methylthio]benzimidazole

https://huagongshe.com/reaction/1033741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChlorodifluoromethaneHCID 6372—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 178431607HCID 178431607—
SolventDimethylformamideHCID 6228—
Product2-[(4-Difluoromethoxy-3-methyl-2-pyridyl)methylthio]benzimidazoleHCID 15230232—

Reaction Steps

In N,N-dimethylforamide (DMF) (100 ml) was dissolved 2-[(4-hydroxy-3-methyl-2-pyridyl)methylthio]benzimidazole (10.5 g). To the solution was added 1,8-diazabicyclo[5,4,0]undec-7-ene (DBU) (7.1 g), to which was introduced chlorodifluoromethane for 3 hours at room temperature. The reaction mixture was poured into water (500 ml), which was subjected to extraction with ethyl acetate. The ethyl acetate layer was washed with water and dried (MgSO4), then the solvent was distilled off. The residue was subjected to a silica gel column chromatography. From the portion eluted with chloroform-methanol (100:1, v/v), 2-[(4-difluoromethoxy-3-methyl-2-pyridyl)methylthio]benzimidazole was obtained (2.5 g, 20%). Recrystallization from ethyl acetate - hexane gave colorless needles, m.p. 99°-100° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312824
Source datasetuspto-grants-1994_05
ORD IDord-799d56d44e894c2bb11d33083a3da714
Source noteuspto-grants-1994_05