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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280949Generated: October 26, 2026

Triethylamine → (R)-1-(4-chlorobenzyl)-3-[[N-(4-dimethylaminobenzoyl)glycyl]amino]pyrrolidine

https://huagongshe.com/reaction/1280949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Dimethylamino)benzoic acidHCID 12092—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant(R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidineHCID 54551710—
SolventChloroformHCID 6212—
Product(R)-1-(4-chlorobenzyl)-3-[[N-(4-dimethylaminobenzoyl)glycyl]amino]pyrrolidineHCID 69215736—

Reaction Steps

A solution of (R)-1-(4-chlorobenzyl)-3-(glycylamino)pyrrolidine (13.8 mg, 0.052 mmol) in CHCl3 (2 mL) was treated with Et3N (0.021 mL, 0.15 mmol), 4-(dimethylamino)benzoic acid (10 mg, 0.061 mmol), EDCI (10.2 mg, 0.053 mmol) and HOBt (7.5 mg, 0.055 mmol). The reaction mixture was stirred at room temperature for 16 h. The solution was washed with 2 N aqueous NaOH solution (2 mL×2) and brine (2 mL), and dried by filtration through a PTFE membrane using CH2Cl2 (3 mL). Concentration afforded the desired material (compound No. 952) (24.9 mg, quant): The purity was determined by RPLC/MS (91%); ESI/MS m/e 415.0 (M++H, C22H27ClN4O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451842B1
Source datasetuspto-grants-2002_09
ORD IDord-c1216aed88664c66a1c17263040677a0
Source noteuspto-grants-2002_09