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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106771Generated: October 30, 2026

Hydrochloric Acid → HCID 178505025, compound

https://huagongshe.com/reaction/1106771

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 69352185HCID 69352185—
SolventAcetonitrileHCID 6342—
ProductHCID 178505025HCID 178505025—

Reaction Steps

A mixture of N-[3-(1-trityl-1H-imidazol-4-ylmethoxy)-phenyl]methanesulfonamide (0.63 g, from above) and 1N HCl (10 mL) in acetonitrile (10 mL) was stirred at room temperature overnight. The solvent was removed and the residue was brought to basic pH with saturated potassium carbonate solution. The mixture was extracted with dichloromethane, washed with brine and dried over sodium sulfate. After evaporation of the solvent, the residue was chromatographed on silica gel eluting with methanol (containing 2% NH4OH)/dichloromethane (7:93) to give N-[3-(1H-imidazol-4-ylmethoxy)-phenyl]methanesulfonamide. This was converted to N-[3-(1H-imidazol-4-ylmethoxy)-phenyl]methanesulfonamide oxalate salt, mp 178-180° C. by treating with 1M oxalic acid in ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057349
Source datasetuspto-grants-2000_05
ORD IDord-9187d0a58175406591259d99aaa6fb41
Source noteuspto-grants-2000_05