Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1992474생성일: 2026년 10월 26일
Cesium carbonate → (4-Benzenesulfonyl-piperazin-1-yl)-[1-isopropyl-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone
https://huagongshe.com/reaction/1992474
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | Isopropyl methanesulfonate | HCID 13551 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | (4-Benzenesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone | HCID 68535846 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | (4-Benzenesulfonyl-piperazin-1-yl)-[1-isopropyl-5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone | HCID 68536609 | 39% |
반응 단계
A suspension of 0.20 g (0.38 mmol) (4-benzenesulfonyl-piperazin-1-yl)-[5-(4-isopropyl-piperazine-1-carbonyl)-1H-indol-2-yl]-methanone (example 13), 0.25 g (0.77 mmol) caesium carbonate and isopropyl methanesulfonate in 4 mL acetonitrile was heated 16 h under reflux. After cooling to room temperature, the mixture was poured into saturated aqueous sodium bicarbonate solution and the phases were separated. The aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over magnesium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silica gel with dichloromethane:methanol (19:1 v/v) as eluant to afford 0.85 g (39%) of the desired compound as a light brown foam. MS (ISP): 566.4 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07648979B2 |
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| 출처 데이터셋 | uspto-grants-2010_01 |
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| ORD ID | ord-4d7750247d5b4b7ea20b23d2787e9dd9 |
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| 출처 메모 | uspto-grants-2010_01 |
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