rac-tert-butyl N-[(1r,4r)-4-formylcyclohexyl]carbamate → HCID 178489240、化合物

HRID 1012933

反応式

HRID 1012933 の反応式
[CH3:1][O:2][C:3]1[C:8]2[N:9]=[CH:10][S:11][C:7]=2[CH:6]=[CH:5][CH:4]=1.[Li]CCCC.[C:17]([O:21][C:22](=[O:32])[NH:23][CH:24]1[CH2:29][CH2:28][CH:27]([CH:30]=[O:31])[CH2:26][CH2:25]1)([CH3:20])([CH3:19])[CH3:18]>C1COCC1>[C:17]([O:21][C:22](=[O:32])[NH:23][C@H:24]1[CH2:25][CH2:26][C@H:27]([CH:30]([OH:31])[C:10]2[S:11][C:7]3[CH:6]=[CH:5][CH:4]=[C:3]([O:2][CH3:1])[C:8]=3[N:9]=2)[CH2:28][CH2:29]1)([CH3:20])([CH3:18])[CH3:19]

参加物

5

実験手順

To a solution of 4-methoxy-benzothiazole (1.65 g, 10 mmol) in THF (50 ml) was added dropwise n-BuLi (2.5M in hexanes, 4 ml) so that the temperature did not exceed −70° C. The brown solution was stirred at this temperature for 15 min before dropwise addition of a solution of (4-formyl-cyclohexyl)-carbamic acid tert-butyl ester (1.14 g, 5 mmol) in THF (10 ml). The temperature was kept below −70° C. The brown solution was then gradually allowed to reach RT (over 3 h). The reaction mixture was quenched with saturated NH4Cl solution and extracted with EtOAc. The organic layer was washed with brine and dried over MgSO4 and concentrated under reduced pressure. The product was crystallised from ether to give 1.04 g (53%) of a white solid.

後処理

  1. customdid not exceed −70° C
  2. customwas kept below −70° C
  3. customto reach RT
  4. custom(over 3 h)
  5. customThe reaction mixture was quenched with saturated NH4Cl solution
  6. extractionextracted with EtOAc
  7. washThe organic layer was washed with brine
  8. dry with materialdried over MgSO4
  9. concentrationconcentrated under reduced pressure
  10. customThe product was crystallised from ether

出典と根拠

ORDレコード
ord-728534994fab4e25b1ea419fa9a3127e
出典データセット
uspto-grants-2011_07
特許番号
US07981886B2

関連ノート

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