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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533805Generated: November 4, 2026

Trifluoroacetic acid → HCID 70139538, compound

https://huagongshe.com/reaction/1533805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 70120934HCID 70120934—
SolventDichloromethaneHCID 6344—
ProductHCID 70139538HCID 7013953887.1%

Reaction Steps

To a solution of 4-[N-[1-[(tert-butyl)oxycarbonyl]-benzimidazol-4-yl]carbamoyl]-N-[2-[4,4-dimethyl(2,5-oxazolinyl)]phenyl]-3-methoxy-N-methylbenzamide (400 mg) in dichloromethane (10 ml) was added trifluoroacetic acid (4 ml). The mixture was stirred at ambient temperature for 3 hours. The reaction mixture was concentrated in vacuo and the residue was diluted with a mixture of chloroform and saturated aqueous sodium bicarbonate solution. The organic layer was separated and washed with water and brine. The solution was dried over magnesium sulfate and the solvent was evaporated in vacuo. The residue was purified by column chromatography (chloroform:methanol=100:3) to give 4-[N-(1H-benzimidazol-4-yl)carbamoyl]-N-[2-[4,4-dimethyl(2,5-oxazolinyl)]phenyl]-3-methoxy-N-methylbenzamide (290 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06207693B1
Source datasetuspto-grants-2001_03
ORD IDord-f2249b2e13fe4f35bbd0095259be1fda
Source noteuspto-grants-2001_03