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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660012Generated: October 31, 2026

N-(2-Aminoethyl)piperidine → N-[piperidino ethyl]-7-chloro-1,4-benzodioxane-5-carboxamide hydrochloride

https://huagongshe.com/reaction/1660012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
Reactant7-Chloro-1,4-benzodioxane-5-carbonyl chlorideHCID 20544703—
SolventMethyl Ethyl KetoneHCID 6569—
ProductN-[piperidino ethyl]-7-chloro-1,4-benzodioxane-5-carboxamide hydrochlorideHCID 70549227129%

Reaction Steps

150 ml of methyl ethyl ketone and 22 g of N-(aminoethyl)-piperidine were introduced into a 500 ml balloon flask provided with an agitator and a thermometer. The mixture was cooled and then a suspension of 35 g of 7-chloro-1,4-benzodioxane-5-carbonyl chloride in 200 ml of methyl ethyl ketone was added at a temperature of from 15°-20° C. After agitation the crystals formed were dried off and then washed with methyl ethyl ketone. 35 g of N-[piperidino ethyl]-7-chloro-1,4-benzodioxane-5-carboxamide hydrochloride was produced (M.P.: 192° C.; yield: 64.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04306072
Source datasetuspto-grants-1981_12
ORD IDord-0d784bba41e7487a9090c873b5be549d
Source noteuspto-grants-1981_12