Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
6-Nitroindoline → 1-(1-Methyl(4-piperidyl))-6-nitroindoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 6-Nitroindoline | HCID 29757 | — |
| 반응물 | 1-Methyl-4-piperidone | HCID 74049 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Sodium triacetoxyborohydride | HCID 5049666 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 용매 | 1,1-Dichloroethane | HCID 6365 | — |
| 생성물 | 1-(1-Methyl(4-piperidyl))-6-nitroindoline | HCID 18796623 | — |
반응 단계
6-Nitroindoline (5 g) was dissolved in 200 mL of dichloroethane, N-methyl-4-piperidone (5 g) was added to the mixture, followed by 12 g NaBH(OAc)3 and 1 mL of glacial AcOH. The mixture was stirred at RT overnight. Saturated NaHCO3 solution (200 mL) was added to the reaction mixture and stirred for 1 h. The resulting mixture was separated by separation funnel, the organic layer was extracted once with saturated NaHCO3 solution and once with brine. The resulting organic layer was dried over MgSO4, filtered and concentrated in vacuo. The crude material was purified by flash chromatography on silica gel with 2:1 EtOAc:MeOH to afford an orange oil. MS: 262 (M+1). Calc'd. for C14H19N3O2—261.32.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08642624B2 |
| 출처 데이터셋 | uspto-grants-2014_02 |
| ORD ID | ord-7d1fd85e774f4ec59f2291df1b4171fd |
| 출처 메모 | uspto-grants-2014_02 |