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Ethyl chloroformate → Cisapride (USP/INN)
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl chloroformate | HCID 10928 | — |
| 反応物 | 4-Amino-5-chloro-2-methoxybenzoic acid | HCID 81626 | — |
| 反応物 | 1-(3-(4-Fluorophenoxy)propyl)-3-methoxypiperidin-4-amine | HCID 13677832 | — |
| 溶媒 | Triethylamine | HCID 8471 | — |
| 生成物 | Cisapride (USP/INN) | HCID 2769 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06218542B1 |
| 出典データセット | uspto-grants-2001_04 |
| ORD ID | ord-1ad2eecc9a7044a69e41c565dec8c602 |
| 出典メモ | uspto-grants-2001_04 |