Methanol → (+/-)-3,4-bis-cyclopropylmethoxy-N-[(1RS,2RS,5RS)-2-(3,4-dimethoxyphenyl)-5-hydroxycyclohexyl]benzamide

HRID 30071ノート

反応式

HRID 30071 の反応式
[CH:1]1([CH2:4][O:5][C:6]2[CH:7]=[C:8]([CH:29]=[CH:30][C:31]=2[O:32][CH2:33][CH:34]2[CH2:36][CH2:35]2)[C:9]([NH:11][CH:12]2[CH:18]([C:19]3[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[C:21]([O:27][CH3:28])[CH:20]=3)[CH2:17][CH:16]3[CH:14]([O:15]3)[CH2:13]2)=[O:10])[CH2:3][CH2:2]1.[BH4-].[Na+].CO.O>C(O)(C)(C)C.C(OCC)(=O)C>[CH:1]1([CH2:4][O:5][C:6]2[CH:7]=[C:8]([CH:29]=[CH:30][C:31]=2[O:32][CH2:33][CH:34]2[CH2:35][CH2:36]2)[C:9]([NH:11][CH:12]2[CH2:13][CH:14]([OH:15])[CH2:16][CH2:17][CH:18]2[C:19]2[CH:24]=[CH:23][C:22]([O:25][CH3:26])=[C:21]([O:27][CH3:28])[CH:20]=2)=[O:10])[CH2:2][CH2:3]1

参加物

7

実験手順

16.5 g of (±)-3,4-bis-cyclopropylmethoxy-N-[(3RS,4RS)-4-(3,4-dimethoxyphenyl)-7-oxabicyclo[4.1.0]-hept-3-yl]benzamide (compound E1) are dissolved in 500 ml of tert-butanol, 5.0 g of sodium borohydride are added and the reaction mixture is heated to boiling. After slow addition of 70 ml of methanol, the reaction mixture is cooled and treated with 200 ml of water and 150 ml of ethyl acetate. The organic phase is dried using sodium sulfate, concentrated and the residue is chromatographed on silica gel using a mixture of petroleum ether/ethyl acetate in the ratio 1/2. 11.3 g of the title compound are obtained.

後処理

  1. temperaturethe reaction mixture is heated to boiling
  2. temperaturethe reaction mixture is cooled
  3. customThe organic phase is dried
  4. concentrationconcentrated
  5. customthe residue is chromatographed on silica gel using
  6. additiona mixture of petroleum ether/ethyl acetate in the ratio 1/2

出典と根拠

ORDレコード
ord-887b89fa857b4adb9f116c835ffbcbb4
出典データセット
uspto-grants-2008_09
特許番号
US07423046B2

反応ノート

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