Sodium borohydride → 3-(4-hydroxycyclohexyl)-2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(1-methyl-1H-pyrazol-3-yl)propionamide

HRID 14991노트

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HRID 14991 반응식
[CH3:1][N:2]1[C:15]2[CH:14]=[C:13]([CH:16]([CH2:26][CH:27]3[CH2:32][CH2:31][C:30](=[O:33])[CH2:29][CH2:28]3)[C:17]([NH:19][C:20]3[CH:24]=[CH:23][N:22]([CH3:25])[N:21]=3)=[O:18])[CH:12]=[CH:11][C:10]=2[S:9](=[O:35])(=[O:34])[C:8]2[C:3]1=[CH:4][CH:5]=[CH:6][CH:7]=2.[BH4-].[Na+]>CO>[OH:33][CH:30]1[CH2:31][CH2:32][CH:27]([CH2:26][CH:16]([C:13]2[CH:12]=[CH:11][C:10]3[S:9](=[O:35])(=[O:34])[C:8]4[C:3](=[CH:4][CH:5]=[CH:6][CH:7]=4)[N:2]([CH3:1])[C:15]=3[CH:14]=2)[C:17]([NH:19][C:20]2[CH:24]=[CH:23][N:22]([CH3:25])[N:21]=2)=[O:18])[CH2:28][CH2:29]1

참가 물질

4

실험 절차

50 mg of 2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(1-methyl-1H-pyrazol-3-yl)-3-(4-oxocyclohexyl)propionamide are suspended in 20 ml of methanol, and 3.8 mg of sodium borohydride are added at room temperature. The mixture is stirred at room temperature for another hour. During the duration of the reaction, a clear solution slowly forms. The methanol is removed under reduced pressure, and the residue is extracted with ethyl acetate and water. The organic phase is washed twice with water and then dried over MgSO4 and concentrated under reduced pressure. The residue is lyophilized. This gives 42 mg of 3-(4-hydroxycyclohexyl)-2-(10-methyl-5,5-dioxo-5,10-dihydrophenothiazin-2-yl)-N-(1-methyl-1H-pyrazol-3-yl)propionamide as a white amorphous solid.

후처리

  1. customDuring the duration of the reaction
  2. customThe methanol is removed under reduced pressure
  3. extractionthe residue is extracted with ethyl acetate and water
  4. washThe organic phase is washed twice with water
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-259e2f79c5ee4441b6af173430a08c49
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07732440B2

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