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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058291Generated: November 1, 2026

1-(2-hydroxy-2-phenyl-3,3,3-trifluoropropanoyl)-N-(2-tert-butyloxycarbonylaminomethyl-5-chlorobenzyl)-L-prolinamide → 1-(2-Hydroxy-2-phenyl-3,3,3-trifluoropropanoyl)-N-(2-aminomethyl-5-chlorobenzyl)-L-prolinamide

https://huagongshe.com/reaction/1058291

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-hydroxy-2-phenyl-3,3,3-trifluoropropanoyl)-N-(2-tert-butyloxycarbonylaminomethyl-5-chlorobenzyl)-L-prolinamideHCID 69938810—
SolventEthyl AcetateHCID 8857—
Product1-(2-Hydroxy-2-phenyl-3,3,3-trifluoropropanoyl)-N-(2-aminomethyl-5-chlorobenzyl)-L-prolinamideHCID 59038214—

Reaction Conditions

Temperature0 °C

Reaction Steps

1-(2-Hydroxy-2-phenyl-3,3,3-trifluoropropanoyl)-N-(2-tert-butyloxycarbonylaminomethyl-5-chlorobenzyl)-L-prolinamide from step 3 (more polar isomer, 8.5 mg, 0.015 mmol) was dissolved in EtOAc (20 mL) and cooled with stirring to 0° C. Into this solution was bubbled in HCl gas for 5 min. The resulting solution was stirred at 0° C. for 30 min. The hydrochloride salt of the title compound was obtained as a white crystalline solid after concentrating the reaction in vacuo (HPLC RT=2.78 min, method A; LC-MS m/z=470.1; 1H NMR, 400 MHz, CD3OD, 7.54 ppm (m, 3H), 7.44 ppm (d, 1H), 7.42 ppm (m, 1H), 4.5 ppm (d, 1H), 4.4 ppm (m, 2H), 4.3 ppm (m, 2H), 3.75 ppm (m, 1H), 2.7 pm (m, 1H), 2.1 ppm (m, 1H), 1.7 ppm (m, 3H)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06515011B2
Source datasetuspto-grants-2003_02
ORD IDord-7965f0f3cb404c7495d318794e5b91df
Source noteuspto-grants-2003_02