Sodium Hydroxide → (RS)-1-(5-methoxy-2,3-dihydro-1H-indol-2-ylmethyl)-4-(4-methyl-benzyl)-piperidin-4-ol

HRID 278439ノート

反応式

HRID 278439 の反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[N:8](S(C1C=CC(C)=CC=1)(=O)=O)[CH:7]([CH2:22][N:23]1[CH2:28][CH2:27][C:26]([CH2:30][C:31]3[CH:36]=[CH:35][C:34]([CH3:37])=[CH:33][CH:32]=3)([OH:29])[CH2:25][CH2:24]1)[CH2:6]2.[H-].COCCO[Al+]OCCOC.[Na+].[H-].[OH-].[Na+]>C1(C)C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]([CH2:22][N:23]1[CH2:28][CH2:27][C:26]([CH2:30][C:31]3[CH:32]=[CH:33][C:34]([CH3:37])=[CH:35][CH:36]=3)([OH:29])[CH2:25][CH2:24]1)[CH2:6]2

参加物

5

実験手順

To a solution of (RS)-1-[5-methoxy-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-indol-2-ylmethyl]-4-(4-methyl-benzyl)-piperidin-4-ol (300 mg, 0.576 mmol) in toluene (15 ml) was added sodium bis(2-methoxy-ethoxy) aluminium hydride (3.5 M in THF) (0.66 ml, 2.31 mmol), and the mixture refluxed 18 hr. After cooling, 2N NaOH was added to pH 14, the mixture was extracted with EtOAc (3x 25ml) and the combined extracts washed with satd. NaCl (25 ml), dried with (Na2SO4) then filtered and evaporated. The residue was chromatographed over SiO2 (Merck 230-400 mesh) eluting with EtOAc-cyclohexane-Et3N (9:10:1) to afford (RS)-1-(5-methoxy-2,3-dihydro-1H-indol-2-ylmethyl)-4-(4-methyl-benzyl)-piperidin-4-ol as a viscous yellow oil (158.4 mg, 0.433 mmol, 75%), MS: m/e=367.3 (M+H+).

後処理

  1. temperaturethe mixture refluxed 18 hr
  2. temperatureAfter cooling
  3. extractionthe mixture was extracted with EtOAc (3x 25ml)
  4. washthe combined extracts washed with satd
  5. dry with materialNaCl (25 ml), dried with (Na2SO4)
  6. filtrationthen filtered
  7. customevaporated
  8. customThe residue was chromatographed over SiO2 (Merck 230-400 mesh)
  9. washeluting with EtOAc-cyclohexane-Et3N (9:10:1)

出典と根拠

ORDレコード
ord-58771e84ee0b4e4a9a0978a11855d7c7
出典データセット
uspto-grants-2002_03
特許番号
US06359138B1

反応ノート

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