[C:1]([CH:5]=P(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)([O:3][CH3:4])=[O:2].[CH:25]([C:27]1[C:36]2[O:37][C:38]3([C:48]([CH3:50])([CH3:49])[C:47]4[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=4)[N:41]3[CH3:51])[CH:39]=[N:40][C:35]=2[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=1)=O>ClCCl>[CH3:4][O:3][C:1]([CH:5]=[CH:25][C:27]1[C:36]2[O:37][C:38]3([C:48]([CH3:50])([CH3:49])[C:47]4[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=4)[N:41]3[CH3:51])[CH:39]=[N:40][C:35]=2[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=1)=[O:2]0.34 g (1 mmol) of carbomethoxymethylene triphenylphosphorane and 0.36 g (1 mmol) of the compound of Example 1 are heated to reflux in 20 ml of dichloromethane for 18 hours. The solvent is evaporated off. The product is purified on a silica column (80/20 pentane/ethyl acetate eluent).
Loading…