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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407997Generated: October 29, 2026

Hydrochloric Acid → (S)-3-amino-1-(1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)piperidin-4-yl)pyrrolidin-2-one

https://huagongshe.com/reaction/407997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant(S)-tert-butyl 1-(1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-ylcarbamateHCID 67469801—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
Product(S)-3-amino-1-(1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)piperidin-4-yl)pyrrolidin-2-oneHCID 67469689100%

Reaction Steps

To a solution of (S)-tert-butyl 1-(1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)piperidin-4-yl)-2-oxopyrrolidin-3-ylcarbamate (4 g, 8.6 mmol) in EtOAc (20 mL) was added HCl in isopropanol (5-6 M, 16 mL) and the reaction was stirred overnight at ambient temperature. The reaction was concentrated under vacuum and the material dissolved in water (about 20 mL). The aqueous layer was basified to about pH 12 using NaOH (1 N) and the aqueous layer extracted with DCM (150 mL). The organic layer was washed with brine (30 mL), dried over MgSO4, filtered and concentrated under vacuum to give (S)-3-amino-1-(1-(3-chloro-5-(trifluoromethyl)pyridin-2-yl)piperidin-4-yl)pyrrolidin-2-one (3.1 g, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754226B2
Source datasetuspto-grants-2014_06
ORD IDord-312c7eb2dd924d7e87dafb7e9c620211
Source noteuspto-grants-2014_06