Methanol → 6-(2,6-Dimethoxypyridin-3-yl)-9-ethoxy-8-methoxy-1,2,3,4,4a,10b-hexahydrophenanthridin-2-ol

HRID 1675803Notes

Reaction equation

HRID 1675803 reaction equation
[CH3:1][O:2][C:3]1[C:8]([C:9]2[C:22]3[C:17](=[CH:18][C:19]([O:25][CH2:26][CH3:27])=[C:20]([O:23][CH3:24])[CH:21]=3)[CH:16]3[CH:11]([CH2:12][CH2:13][CH:14]([O:28]C(=O)C)[CH2:15]3)[N:10]=2)=[CH:7][CH:6]=[C:5]([O:32][CH3:33])[N:4]=1.CO.C(=O)([O-])[O-].[Cs+].[Cs+]>ClCCl>[CH3:1][O:2][C:3]1[C:8]([C:9]2[C:22]3[C:17](=[CH:18][C:19]([O:25][CH2:26][CH3:27])=[C:20]([O:23][CH3:24])[CH:21]=3)[CH:16]3[CH:11]([CH2:12][CH2:13][CH:14]([OH:28])[CH2:15]3)[N:10]=2)=[CH:7][CH:6]=[C:5]([O:32][CH3:33])[N:4]=1

Participants

5

Procedure

423 mg of acetic acid (2RS,4aRS, 10bRS)-6-(2,6-dimethoxy-pyridin-3-yl)-9-ethoxy-8-methoxy-1,2,3,4,4a,10b-hexahydro-phenanthridin-2-yl ester (Example 18) dissolved in 1 ml of dichloromethane and 9 ml of methanol are added to 152 mg of cesium carbonate and the solution stirred for 19 h. The reaction mixture is adsorbed to silica gel and purified by flash chromatography to give 229 mg of the title compound as a colourless foam.

Workup

  1. custompurified by flash chromatography

Sources & evidence

ORD record
ord-70e075092a684963a01666bed1348ef4
Source dataset
uspto-grants-2011_08
Patent number
US08003798B2

Reaction notes

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