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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280957Generated: October 27, 2026

Acetonitrile → benzamide, 2-amino-N-[2-[[(3R)-1-[(4-ethenylphenyl)methyl]-3-pyrrolidinyl]amino]-2-oxoethyl]-5-(trifluoromethyl)-

https://huagongshe.com/reaction/1280957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactantp-Vinylbenzyl chlorideHCID 74126—
Reactant(R)-3-[[N-(2-Amino-5-trifluoromethylbenzoyl)glycyl]amino]pyrrolidineHCID 54328411—
SolventChloroformHCID 6212—
Productbenzamide, 2-amino-N-[2-[[(3R)-1-[(4-ethenylphenyl)methyl]-3-pyrrolidinyl]amino]-2-oxoethyl]-5-(trifluoromethyl)-HCID 508869—

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of (R)-3-[{N-(2-amino-5-(trifluoromethyl)benzoyl)glycyl}amino]pyrrolidine (0.050 mmol), 4-vinylbenzyl chloride (9.9 mg, 0.065 mmol), peperidinomethylpolystyrene (60 mg), acetonitrile (1.0 mL) and chloroform (0.30 mL) was stirred at 50° C. for 12 h. The reaction mixture was cooled, loaded onto Varian™ SCX column and washed with CH3OH (15 mL). Product was eluted using 2 N NH3 in CH3OH (5 mL) and concentrated to afford (R)-3-[{N-(2-amino-5-(trifluoromethyl)benzoyl)glycyl}amino-]-(4-vinylbenzyl)pyrrolidine (compound No. 1701) (19.6 mg, 88%): The purity was determined by RPLC/MS (92%); ESI/MS m/e 547.2 (M++H, C23H25ClF3N4O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451842B1
Source datasetuspto-grants-2002_09
ORD IDord-39336786b8c04ce89cd231252775b021
Source noteuspto-grants-2002_09