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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1988710Generated: October 31, 2026

Water → HCID 22380290, compound

https://huagongshe.com/reaction/1988710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl orthoformateHCID 31214—
ReactantSodium AzideHCID 33557—
ReactantHCID 22380213HCID 22380213—
SolventAcetic AcidHCID 176—
ProductHCID 22380290HCID 22380290—

Reaction Conditions

Temperature70 °C

Reaction Steps

1-Ethyl-2-{[2-(2,5-difluorophenyl)-pyrazol-3-yl]methyl}-5-amino-1H-benzimidazole (104 mg) is treated with triethylorthoformate (4 eq) in acetic acid (10 mL) at reflux for 4 h. After concentrating the solution, acetic acid is re-added, sodium azide (4 eq) added, and the mixture heated at 70° C. for 3 h. After cooling, water (15 mL) is added and the mixture concentrated. The residue is taken up in ethyl acetate, washed with aqueous sodium bicarbonate (2×) then saturated aqueous sodium chloride, dried (MgSO4), concentrated, and purified by preparative silica gel chromatography to give 1-ethyl-2-{[2-(2,5-difluorophenyl)-pyrazol-3-yl]methyl}-5-(1,2,3,4-tetrazol-1-yl)-1H-benzimidazole, which is converted to the hydrochloride salt in ethyl acetate. LCMS MH+ 395.018

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07642267B2
Source datasetuspto-grants-2010_01
ORD IDord-a3e20b18c21c41e48b7b3c1a6c142e4b
Source noteuspto-grants-2010_01