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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 3885Generated: October 26, 2026

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

https://huagongshe.com/reaction/3885

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 numberUS04722930
Source datasetuspto-grants-1988_02
ORD IDord-b9ccee3c2bf64ab8b2bb177fb8f8050b
Source noteuspto-grants-1988_02