Trifluoroacetic acid → 2-(2-(4-(4-(Hydroxycarbonylmethoxy)phenoxy)phenyl)-acetylamino)benzoic acid methyl ester
反応式
C(O)(C(F)(F)F)=O.[CH3:8][O:9][C:10](=[O:43])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[NH:17][C:18](=[O:42])[CH2:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][C:27]2[CH:32]=[CH:31][C:30]([O:33][CH2:34][C:35]([O:37]C(C)(C)C)=[O:36])=[CH:29][CH:28]=2)=[CH:22][CH:21]=1>>[CH3:8][O:9][C:10](=[O:43])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[NH:17][C:18](=[O:42])[CH2:19][C:20]1[CH:25]=[CH:24][C:23]([O:26][C:27]2[CH:28]=[CH:29][C:30]([O:33][CH2:34][C:35]([OH:37])=[O:36])=[CH:31][CH:32]=2)=[CH:22][CH:21]=1参加物
3
実験手順
TFA (4 ml) was added to 2-(2-(4-(4-(t-butoxycarbonylmethoxy)-phenoxy)phenyl)acetylamino)benzoic acid methyl ester produced by the Example 27 and the mixture was stirred for 2 hours at room temperature. After the reaction, TFA was distilled out under reduced pressure and the product was dissolved in ethyl acetate. The organic layer was washed with water and dried with anhydrous magnesium sulfate, and the solvent was distilled out under reduced pressure to quantitatively obtain the subject compound (164 mg). The result of 1H-NMR was consistent with the above structure.