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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217495Generated: November 1, 2026

Trifluoroacetic acid → Pyrrolidine-2-carboxylic acid (2'-tert-butylsulfamoyl-3-fluoro-biphenyl-4-yl)-amide

https://huagongshe.com/reaction/2217495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant2-(2'-tert-Butylsulfamoyl-3-fluoro-biphenyl-4-ylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 68806873—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductPyrrolidine-2-carboxylic acid (2'-tert-butylsulfamoyl-3-fluoro-biphenyl-4-yl)-amideHCID 86601536—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-(2′-tert-Butylsulfamoyl-3-fluoro-biphenyl-4-ylcarbamoyl)-pyrrolidine-1-carboxylic acid tert-butyl ester (1.3 g, 2.5 mmol) was dissolved in 40 mL DCM, cooled in an ice bath, added 10 mL trifluoroacetic acid, stirred at 0° C. for 30 minutes then at ambient temperature for one hour. Concentrated solution, redissolved in EtOAc (150 mL), washed with saturated NaHCO3 (2×100 mL), water (100 mL), brine (100 mL), dried with MgSO4, filtered and concentrated to yield title compound as a white solid. (1 g, 91%) APCI (AP−): 418.2 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07407974B2
Source datasetuspto-grants-2008_08
ORD IDord-d743b9584c6044c8aa7e6b7c995cb419
Source noteuspto-grants-2008_08