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

HRID 220103Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 220103
[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

Komponenten

7

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-e17d2cb1e00f4610a2505c89e51744cc
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08202880B2

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