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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324686Generated: October 27, 2026

Ethyl chloroformate → Cisapride (USP/INN)

https://huagongshe.com/reaction/324686

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
Reactant4-Amino-5-chloro-2-methoxybenzoic acidHCID 81626—
Reactant1-(3-(4-Fluorophenoxy)propyl)-3-methoxypiperidin-4-amineHCID 13677832—
SolventTriethylamineHCID 8471—
ProductCisapride (USP/INN)HCID 2769—

Reaction Steps

To a solution of 4-amino-5-chloro-2-methoxybenzoic acid (20.2 g) in MIK (250 ml) and triethyl amine (15.3 ml) was slowly dropped ethyl chloroformate (9.6 ml). The reaction mixture was stirred for 30 minutes at room temperature. To the formed mixed anhydride was then added intermediate 2 (28.2 g) and the reaction mixture was stirred for 2 hours at room temperature. Subsequently, the reaction mixture was washed with water (80 ml) and a NaOH solution (6.5% w/v, 50 ml). The organic layer was warmed to 65° C. and methanol (50 ml) and water (8.5 ml) were added. The solution was cooled slowly and stirred for 2 days during which crystallisation occurred, yielding cisapride having a cis/trans ratio higher than 99/1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218542B1
Source datasetuspto-grants-2001_04
ORD IDord-1ad2eecc9a7044a69e41c565dec8c602
Source noteuspto-grants-2001_04