Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086035Generated: October 26, 2026

Metoclopramide → HCID 14372582, compound

https://huagongshe.com/reaction/1086035

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMetoclopramideHCID 4168—
Reactant4-amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-methoxybenzamideHCID 10378510—
ProductHCID 14372582HCID 1437258289%

Reaction Steps

The general procedure of Preparation 1A was repeated except that the 4-amino-5-chloro-N-[2-(diethylamino)ethyl]-2-methoxybenzamide utilized therein was replaced by 4-amino-5-chloro-N-[2-(dimethylamino)ethyl]-2-methoxybenzamide (prepared according to U.K. Patent Specification 1,793,771). The solvent (DMF) was removed in vacuo, and the residue treated with water and methylene chloride saturated with carbon dioxide, concentrated, and the crude product isolated in 89% yield by extraction with ethanol. A sample was chromatographed on a silica gel column using methylene chloride (97), methanol (3), ammonia (0.3) solvent system. The appropriate fractions were combined and concentrated in vacuo. The residue was crystallized from methanol to give the title compound as a colorless solid, mp. 163°-165°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011992
Source datasetuspto-grants-1991_04
ORD IDord-5447ee2ae1194ef4b447c3ec9b75f254
Source noteuspto-grants-1991_04