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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1643981Generated: November 3, 2026

Trifluoroacetic acid → HCID 66755470, compound

https://huagongshe.com/reaction/1643981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 66754949HCID 66754949—
SolventDichloromethaneHCID 6344—
ProductHCID 66755470HCID 6675547084.1%

Reaction Steps

A solution of (1-{2-[6-cyano-3-(4-methoxy-benzenesulfonyl)-2-oxo-2,3-dihydro-benzoimidazol-1-yl]-2-phenyl-acetyl}-piperidin-4-yl)-carbamic acid tert-butyl ester (254 mg, 0.39 mmol) in CH2Cl2 (5 mL) was treated with trifluoroacetic acid (5 mL). The reaction mixture was stirred at room temperature for 2 hours, concentrated in vacuo and co-evaporated the solvent with toluene (3×). The residue was dissolved in CH2Cl2 (30 mL) and treated with solid K2CO3. The reaction mixture was stirred at room temperature for 1 hour, filtered and concentrated in vacuo to afford 3-[2-(4-amino-piperidin-1-yl)-2-oxo-1-phenyl-ethyl]-1-(4-methoxy-benzenesulfonyl)-2-oxo-2,3-dihydro-1H-benzoimidazole-5-carbonitrile (179 mg, 83%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119676B2
Source datasetuspto-grants-2012_02
ORD IDord-3f12cb0dd39d4ce190179c6f8eceff4a
Source noteuspto-grants-2012_02