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Methanol → HCID 118024054, 화합물

HRID 2171790
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HRID 2171790 반응식
[CH:1]1([C:7]2[S:19][C:10]3[N:11]=[C:12]([CH3:18])[N:13]=[C:14](/[CH:15]=[CH:16]\[OH:17])[C:9]=3[CH:8]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CO.[BH4-].[Na+]>O>[CH:1]1([C:7]2[S:19][C:10]3[N:11]=[C:12]([CH3:18])[N:13]=[C:14]([CH2:15][CH2:16][OH:17])[C:9]=3[CH:8]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 887MethanolHCID 4311764Sodium borohydrideHCID 136951116HCID 136951116, 화합물

생성물 1

HCID 118024054HCID 118024054, 화합물수율 72.7%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

To a mixture of (Z)-2-(6-cyclohexyl-2-methylthieno[2,3-d]pyrimidin-4-yl)ethenol (430 mg) and MeOH (10 mL) was added NaBH4 (65 mg) in small divided portions, followed by stirring for 15 minutes. To the reaction mixture was added water, followed by extraction with EtOAc. The organic layer was washed sequentially with a saturated aqueous NH4Cl solution and brine, and dried over Na2SO4, and the residue was purified by silica gel column (hexane/EtOAc) to obtain 2-(6-cyclohexyl-2-methylthieno[2,3-d]pyrimidin-4-yl)ethanol (315 mg).

후처리

  1. extractionfollowed by extraction with EtOAc
  2. washThe organic layer was washed sequentially with a saturated aqueous NH4Cl solution and brine
  3. dry with materialdried over Na2SO4
  4. customthe residue was purified by silica gel column (hexane/EtOAc)

출처 및 근거

ORD 기록
ord-bd71cf25f16f4ce1923e3a50ee7536d7
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09051339B2

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