Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl chloroformate → Cisapride (USP/INN)
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl chloroformate | HCID 10928 | — |
| 반응물 | 4-Amino-5-chloro-2-methoxybenzoic acid | HCID 81626 | — |
| 반응물 | 1-(3-(4-Fluorophenoxy)propyl)-3-methoxypiperidin-4-amine | HCID 13677832 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | Cisapride (USP/INN) | HCID 2769 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06218542B1 |
| 출처 데이터셋 | uspto-grants-2001_04 |
| ORD ID | ord-1ad2eecc9a7044a69e41c565dec8c602 |
| 출처 메모 | uspto-grants-2001_04 |