HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl chloroformate → Cisapride (USP/INN)
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl chloroformate | HCID 10928 | — |
| Reactant | 4-Amino-5-chloro-2-methoxybenzoic acid | HCID 81626 | — |
| Reactant | 1-(3-(4-Fluorophenoxy)propyl)-3-methoxypiperidin-4-amine | HCID 13677832 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Cisapride (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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218542B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-1ad2eecc9a7044a69e41c565dec8c602 |
| Source note | uspto-grants-2001_04 |