Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261055Generated: October 27, 2026

Dicyclohexylcarbodiimide → N-(1-cyclohexylmethylpiperid-4-yl)-2-methoxy-4-acetamido-5-chlorobenzamide hydrochloride monohydrate

https://huagongshe.com/reaction/261055

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-(Cyclohexylmethyl)piperidin-4-amineHCID 6496941—
Reactant4-Acetamido-5-chloro-2-methoxybenzoic acidHCID 10988496—
SolventDichloromethaneHCID 6344—
ProductN-(1-cyclohexylmethylpiperid-4-yl)-2-methoxy-4-acetamido-5-chlorobenzamide hydrochloride monohydrateHCID 20395819119.2%

Reaction Steps

N,N'-dicyclohexylcarbodiimide (10.3 g; 0.05 moles) and 1-cyclohexylmethyl-4-aminopiperidine (9.8 g; 0.05 moles) were added successively to a solution of 2-methoxy-4-acetamido-5-chlorobenzoic acid (12.1 g; 0.05 moles) in methylene chloride (250 ml). After stirring overnight at room temperature, the insoluble N,N'-dicyclohexylurea was filtered off, the solution was washed with water, dried (Na2SO4) and the solvent removed in vacuo. The residue was recrystallized and the product converted into its hydrochloride to give 14.2 g of N-(1-cyclohexylmethylpiperid-4-yl)-2-methoxy-4-acetamido-5-chlorobenzamide hydrochloride monohydrate, m.p. 219°-221° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04163789
Source datasetuspto-grants-1979_08
ORD IDord-9e62b10c89f644c49f4826dcc4b17295
Source noteuspto-grants-1979_08