Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1284564Generated: October 25, 2026

Water → N-(((1-(2-Naphthalenylmethyl)-4-piperidinyl)amino)carbonyl)benzamide

https://huagongshe.com/reaction/1284564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant2-BromomethylnaphthaleneHCID 70320—
Reactant4-BenzoylureidopiperidineHCID 12608582—
SolventDimethylformamideHCID 6228—
ProductN-(((1-(2-Naphthalenylmethyl)-4-piperidinyl)amino)carbonyl)benzamideHCID 72002—

Reaction Steps

4-Benzoylureidopiperidine (1.28 g, 0.005 m), 2-(bromomethyl)naphthalene (1.1 g, 0.005 m) and triethylamine (0.6 g, 0.006 m) in dimethylformamide (25 cm3) were stirred at room temperature for 23 hours. Water was added and the precipitated solid filtered off and washed well with water. The solid was suspended in warm ethanol, acidified with ethanolic HCl and then heated until all the solid had dissolved. The title compound crystallised and was collected as the hydrochloride salt, hemihydrate (1.6 g), m.p. 232°-234° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04563466
Source datasetuspto-grants-1986_01
ORD IDord-65eec61c6fdd4c09ba745fd6a339c7cf
Source noteuspto-grants-1986_01