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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889142Generated: October 30, 2026

Sodium Bicarbonate → Trifluoroacetic acid

https://huagongshe.com/reaction/1889142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant4-(1,3-Oxazol-5-yl)benzenesulphonyl chlorideHCID 2776415—
Reactant(S)-3-[(S)-2-Amino-1-(4-trifluoromethylphenoxy)ethyl]pyrrolidine-1-carboxylic Acid t-Butyl EsterHCID 67776985—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductTrifluoroacetic acidHCID 6422—
Product4-Oxazol-5-yl-N-[(S)-2-(S)-pyrrolidin-3-yl-2-(4-trifluoromethylphenoxy)ethyl]benzenesulfonamideHCID 67775858—

Reaction Steps

(S)-3-[(S)-2-Amino-1-(4-trifluoromethylphenoxy)ethyl]pyrrolidine-1-carboxylic acid t-butyl ester (35.0 mg, 0.093.5 μmol, 1.0 eq.) was dissolved in DCM (1.2 mL) and triethylamine (39.1 μL). A solution of 4-(1,3-oxazol-5-yl)benzenesulfonyl chloride (56.9 mg, 234 μmol, 2.5 eq.) in DCM (0.4 mL,) was then added. The resulting mixture was stirred for 1 hour at room temperature. Saturated sodium bicarbonate was then added (1 mL) and the mixture was diluted with DCM (2 mL). The organic layer was collected and concentrated under reduced pressure. The crude material was redissolved in 1.2 M of HCl in EtOH (1.9 mL) and stirred at room temperature overnight. The mixture was then concentrated under reduced pressure then redissolved in 1:1 AcOH/H2O (1.5 mL) and purified by preparative HPLC to yield the title compound as a TFA salt (20.1 mg). MS m/z: [M+H]+ calcd for C22H22F3N3O4S, 482.13. found 482.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501964B2
Source datasetuspto-grants-2013_08
ORD IDord-b8d32480e80446bdb227b93f8843470f
Source noteuspto-grants-2013_08