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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248905Generated: October 25, 2026

Ammonia → 1-(Pyrid-2-oyl)-3-[1-(naphth-2-ylmethyl)piperid-4-yl]urea

https://huagongshe.com/reaction/248905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthyl 2-pyridinecarboxylateHCID 17307—
ReactantSodiumHCID 5360545—
Reactant[1-(Naphth-2-ylmethyl)piperid-4-yl]ureaHCID 13145794—
Product1-(Pyrid-2-oyl)-3-[1-(naphth-2-ylmethyl)piperid-4-yl]ureaHCID 1976239832.5%

Reaction Steps

Sodium (0.1 g, 4.35 mmol) in liquid ammonia (100-150 cm3) was stirred until the blue colour was discharged. A bomb was charged with [1-(naphth-2-ylmethyl)piperid-4-yl]urea (0.83 g, 2.93 mmol) and the liquid ammonia solution was added. The mixture was stirred at room temperature for 2 days then the bomb was cooled to -78° C., and ethyl picolinate (0.6 g, 3.97 mmol) was added. Stirring was continued for 3 hours at room temperature then the ammonia was allowed to evaporate and the gummy residue triturated with water then ethyl acetate. The ethyl acetate suspension was filtered to give recovered [1-(naphth-2-ylmethyl)piperid-4-yl]urea (0.33 g). The filtrate was evaporated and the residue chromatographed on silica eluting with chloroform then chloroform: ethyl acetate 4:1 to give the title compound (0.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212179
Source datasetuspto-grants-1993_05
ORD IDord-e71edb4f34674b9db43252afc220840c
Source noteuspto-grants-1993_05