Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1379197생성일: 2026년 10월 27일
Acetyl chloride → (2R)-4-acetyl-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-yl-methyl) piperazine
https://huagongshe.com/reaction/1379197
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Acetyl chloride | HCID 6367 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-ylmethyl)piperazine | HCID 10972505 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (2R)-4-acetyl-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-yl-methyl) piperazine | HCID 86751297 | — |
반응 단계
To a stirred mixture of (2R)-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-yl-methyl)piperazine (0.15 g) and potassium carbonate (0.14 g) in dimethylformamide (10 ml) was added acetyl chloride (0.04 ml) at room temperature. After being stirred for 3 hours, the reaction mixture was quenched with water (50 ml) and extracted with dichloromethane (50 ml). The organic layer was washed with aqueous sodium bicarbonate solution and brine, and dried over magnesium sulfate. After evaporation of the solvent, the residue was purified on a silica gel column (10 g) eluting with a mixture of dichloromethane and methanol (20:1). The fractions containing object compound were collected and evaporated under reduced pressure. To the resulting oily product was added a mixed solvent of ethyl ether and diisopropyl ether, and the mixture was concentrated under reduced pressure. The obtained powder was collected by filtration and dried in vacuo to give (2R)-4-acetyl-1-[3,5-bis(trifluoromethyl)benzoyl]-2-(1H-indol-3-yl-methyl)piperazine (0.09 g) as a powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05670505 |
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| 출처 데이터셋 | uspto-grants-1997_09 |
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| ORD ID | ord-a3bfa9d9d24a4237a11e995e5ecf47fc |
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| 출처 메모 | uspto-grants-1997_09 |
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