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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280979Generated: October 26, 2026

Methanol → 3-[[N-[3-trifluoromethylbenzoyl]glycyl]aminomethyl]-1-(4-chlorobenzyl)pyrrolidine

https://huagongshe.com/reaction/1280979

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant3-(Trifluoromethyl)benzoyl chlorideHCID 75257—
Reactant1-(4-Chlorobenzyl)-3-[(glycylamino)methyl]pyrrolidineHCID 18426257—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product3-[[N-[3-trifluoromethylbenzoyl]glycyl]aminomethyl]-1-(4-chlorobenzyl)pyrrolidineHCID 18426181—

Reaction Steps

A solution of 3-(trifluoromethyl)benzoyl chloride (0.058 mmol) in dichloromethane (0.2 mL) was added to a mixture of 1-(4-chlorobenzyl)-3-{(glycylamino)methyl}pyrrolidine (0.050 mmol) and peperidinomethylpolystyrene (60 mg) in chloroform (0.2 mL) and dichloromethane (1 mL). After the reaction mixture was stirred at room temperature for 2.5 h, methanol (0.30 mL) was added and the mixture was stirred at room temperature for 1 h. The reaction mixture was loaded onto Varian™ SCX column, and washed with CH3OH (15 mL). Product was eluted off using 2 N NH3 in CH3OH (5 mL) and concentrated to afford (3-[{N-(3-trifluoromethylbenzoyl)glycyl}aminomethyl]-1-(4-chlorobenzyl)pyrrolidine (Compound No. 1463) (22.4 mg, 99%): The purity was determined by RPLC/MS (97%); ESIJMS m/e 454.2 (M++H, C22H23ClF3N3O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451842B1
Source datasetuspto-grants-2002_09
ORD IDord-21734d6f8337480cae67743698fe521d
Source noteuspto-grants-2002_09