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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13328Generated: October 26, 2026

5-benzyloxy-6-(2-fluorophenoxy)-2-pyrazin-2-yl-1H-benzimidazole → 5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazole

https://huagongshe.com/reaction/13328

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-benzyloxy-6-(2-fluorophenoxy)-2-pyrazin-2-yl-1H-benzimidazoleHCID 23145513—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178502593HCID 178502593—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product5-(2-fluorophenoxy)-6-hydroxy-2-pyrazin-2-yl-1H-benzimidazoleHCID 135697984—

Reaction Steps

500 mg of 20% palladium hydroxide-carbon catalyst was added to a suspension of 697 mg of 5-benzyloxy-6-(2-fluorophenoxy)-2-pyrazin-2-yl-1H-benzimidazole obtained in Example 250, in 10 ml of methanol and 10 ml of tetrahydrofuran, and the reaction liquid was stirred in a hydrogen atmosphere at room temperature for 1 hour. The catalyst was removed through filtration through Celite, the solvent was evaporated away under reduced pressure, and the residue was purified through silica gel column chromatography (developing solvent: ethyl acetate) to obtain the entitled compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-df04df0ea016440f827d8c46053bc877
Source noteuspto-grants-2010_06