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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 133594Generated: October 30, 2026

Triethylamine → 4-[(glycylamino)methyl]-1-[4-(N-phenylcarbamoyl)benzyl]piperidine

https://huagongshe.com/reaction/133594

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(chloromethyl)-N-phenylbenzamideHCID 11413905—
Reactant4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidineHCID 54359471—
SolventAcetonitrileHCID 6342—
Product4-[(glycylamino)methyl]-1-[4-(N-phenylcarbamoyl)benzyl]piperidineHCID 1842622830.2%

Reaction Steps

An acetonitrile (100 mL) solution of 4-(N-phenylcarbamoyl)benzyl chloride (800 mg, 3.26 mmol) was dropped into a mixture of 4-[[N-(9-fluorenylmethyloxycarbonyl)glycyl]aminomethyl]piperidine (1.27 g, 2.96 mmol) with triethylamine (1.25 mL, 8.88 mmol), KI (50 mg, 0.30 mmol) and acetonitrile (200 mL). The resulting mixture was stirred at room temperature for 19 hours and stirred at 60° C. for another 5 hours. After concentrating, the obtained crude product was purified by column chromatography (SiO2, 5% methanol/dichloromethane-triethylamine/methanol/dichloromethane=2:2:96) to provide 4-[(glycylamino)methyl]-1-[4-(N-phenylcarbamoyl)benzyl]piperidine (340 mg, 30%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07390830B1
Source datasetuspto-grants-2008_06
ORD IDord-0f213beb0cf7442493f52ba91697ded6
Source noteuspto-grants-2008_06