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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133587Generated: October 25, 2026

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

https://huagongshe.com/reaction/133587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHippuric AcidHCID 464—
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

Hippuric acid (38 mg, 0.21 mmol), EDCI (48 mg, 0.24 mmol), HOBt (31 mg, 0.23 mmol) and triethylamine (38 μL, 0.27 mmol) were added to a dichloromethane (1 mL) solution of 4-(aminomethyl)-1-(4-chlorobenzyl)piperidine (50 mg, 0.21 mmol). The resulting reaction mixture was shaken at 25° C. for 16 hours, then diluted with 1 mL of dichloromethane, washed with a 2 M aqueous solution of NaOH (0.75 mL×2), dried (over MgSO4), concentrated and purified by chromatography (SiO2, 6-8% methanol/dichloromethane) to thereby afford 4-[(N-benzoylglycyl)amino]methyl-1-(4-chlorobenzyl)piperidine (Compd. No. 458). The resulting compound was treated with TFA to provide 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 numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-417eb02fb1774d4c84ec57fe787b3474
Source noteuspto-grants-2008_06