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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187809Generated: October 27, 2026

Hippuric Acid → 4-[(N-benzoylglycyl)amino]methyl-1-(4-chlorobenzyl)piperidine

https://huagongshe.com/reaction/2187809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHippuric AcidHCID 464—
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant{[1-(4-Chlorobenzyl)piperidin-4-yl]methyl}amineHCID 18426145—
SolventDichloromethaneHCID 6344—
Product4-[(N-benzoylglycyl)amino]methyl-1-(4-chlorobenzyl)piperidineHCID 18426192125%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 4-(aminomethyl)-1-(4-chlorobenzyl)piperidine (50 mg, 0.21 mmol) in CH2Cl2 (1 mL) was treated with hippuric acid (38 mg, 0.21 mmol), EDCI (48 mg, 0.24 mmol), HOBt (31 mg, 0.23 mmol) and Et3N (38 μL, 0.27 mmol). The reaction mixture was stirred for 16 h at 25° C., diluted with 1 mL of CH2Cl2, washed with 2 N aqueous NaOH solution (2×0.75 mL), dried (MgSO4) and concentrated. Chromatography (SiO2, 6 to 8% CH3OH/CH2Cl2 gradient elution) afforded 4-{(N-benzoylglycyl)amino)methyl-1-(compound No. 458) which was treated with TFA to give a TFA salt(105 mg, 97%): The purity was determined by RPLC/MS (85%); ESI/MS m/e 400 (M++H, C22H26ClN3O2)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410566B1
Source datasetuspto-grants-2002_06
ORD IDord-5a2dc793a2224f05a62d9771fb1d8491
Source noteuspto-grants-2002_06