Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | 4-Piperidinamine, 1-(2-(1H-indol-3-yl)ethyl)-, hydrate | HCID 215415 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-{1-[2-(1H-Indol-3-yl)ethyl]piperidin-4-yl}methanesulfonamide | HCID 22754838 | 105.7% |
반응 단계
To 3-[2-(4-Amino-1-piperidyl)ethyl]indole (1.307 g.) suspended in a solution of triethylamine (2 mls.) in dichloromethane (10 mls.) at room temperature with stirring was added methane sulphonyl chloride (0.570 g.) in dichloromethane (5 mls.). After stirring for 18 hours the solution was washed with water and the organic phase separated, dried and evaporated to yield the title compound (1.690 g.) as an oil. This was recrystallized from ethanolic hydrogen chloride as the hydrochloride salt (0.560 g., m.p. 241°-242° C.).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04131680 |
| 출처 데이터셋 | uspto-grants-1978_12 |
| ORD ID | ord-945371300be648fc962154efaeb99079 |
| 출처 메모 | uspto-grants-1978_12 |