Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 559359생성일: 2026년 10월 24일
Acetic Acid → 4-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-3-methyl-1-(4-piperidin-1-yl-butyl)-piperazin-2-one
https://huagongshe.com/ko/reaction/559359
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | Borane;pyridine | HCID 2723995 | — |
| 반응물 | Sodium periodate | HCID 23667635 | — |
| 반응물 | 4-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-3-methyl-1-pent-4-enyl-piperazin-2-one | HCID 66999276 | — |
| 반응물 | 4-{4-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-2-oxo-piperazin-1-yl}-butyraldehyde | HCID 87231749 | — |
| 촉매 | Osmium Tetroxide | HCID 30318 | — |
| 용매 | 1,2-Dichloroethane | HCID 11 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Propan-2-one--water (1/1) | HCID 18366337 | — |
| 생성물 | 4-[(E)-3-(3,4-Dichloro-phenyl)-acryloyl]-3-methyl-1-(4-piperidin-1-yl-butyl)-piperazin-2-one | HCID 57550391 | 11% |
반응 단계
Sodium metaperiodate (310 mg, 1.45 mmol) and osmium(VIII) oxide (2.5% solution in tert-butylalcohol, 49 μl, 48 μmol) were added at 0° C. to a solution of 4-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-3-methyl-1-pent-4-enyl-piperazin-2-one (intermediate 20; 184 mg, 0.48 mmol) in acetone/water 1:1 (10 ml). The reaction mixture was stirred at 0° C. for 30 min, then allowed to reach room temperature over 45 min, then partitioned between ethyl acetate and water. The organic layer was washed with brine, dried (MgSO4), and evaporated. The crude aldehyde intermediate [4-{-4-[(E)-3-(3,4-dichloro-phenyl)-acryloyl]-3-methyl-2-oxo-piperazin-1-yl}-butyraldehyde] and piperidine (33 mg, 0.39 mmol) were dissolved in 1,2-dichloroethane (1.5 ml), then a freshly prepared solution of pyridine borane complex (8 M in pyridine, 71 μl, 0.78 mmol) and acetic acid (69 mg, 1.16 mmol) in ethanol (1.5 ml) was added dropwise at room temperature. The reaction mixture was stirred overnight, then 25%. aq. ammonium hydroxide solution (0.16 ml) was added, and volatile material was removed by rotary evaporation. The residue was purified by chromatography (SiO2; CH2Cl2/MeOH/NH4OH 90:10:0.25) to afford the title compound (15 mg, 11%). Light yellow solid, MS (ISP)=452.1 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08063042B2 |
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| 출처 데이터셋 | uspto-grants-2011_11 |
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| ORD ID | ord-4a2f1bcaef924f159a2086988fb27dc5 |
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| 출처 메모 | uspto-grants-2011_11 |
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