Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → 5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 4-Bromophenylhydrazine hydrochloride | HCID 12157 | — |
| 반응물 | 1,1-Dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylate | HCID 19936603 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | 5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indole | HCID 9905342 | 57% |
반응 단계
4-Bromophenylhydrazine hydrochloride (11.5 g) is solubilized in a solution of 1,1-dimethylethyl 4-[(2-oxopropyl)thio]piperidine-1-carboxylate (14 g, prepared in Example 11) in isopropanol (100 ml) under nitrogen. The solution is cooled to 0° C. and saturated with gaseous hydrogen chloride. After 4 hours at room temperature, the precipitate is filtered off, taken up in sodium hydroxide and extracted with ether and then with methylene chloride. The organic phases are combined, dried over sodium sulfate and concentrated. The solid obtained is taken up in the minimum amount of ether and recrystallized from xylene to give 5-bromo-2-methyl-3-(piperidin-4-ylthio)-1H-indole (9.5 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05418242 |
| 출처 데이터셋 | uspto-grants-1995_05 |
| ORD ID | ord-2f1d1b5dffd3455f9f2cc1fcb715958f |
| 출처 메모 | uspto-grants-1995_05 |