Methanesulfonic Acid → HCID 131724851、化合物
反応式
[CH3:1][S:2]([OH:5])(=[O:4])=[O:3].[CH3:6][N:7]([CH3:29])[CH:8]1[C:22]2=[CH:23][CH:19]([O:20][C:21]2=[O:24])[CH:18]2[CH:14]([O:15][C:16](=[O:26])[CH:17]2[CH3:25])[CH2:13][C:12]2([CH3:27])[CH:10]([O:11]2)[CH:9]1[OH:28]>CC(C)=O>[CH3:1][S:2]([O-:5])(=[O:4])=[O:3].[OH:28][CH:9]1[CH:8]([NH+:7]([CH3:6])[CH3:29])[C:22]2=[CH:23][CH:19]([O:20][C:21]2=[O:24])[CH:18]2[CH:14]([O:15][C:16](=[O:26])[CH:17]2[CH3:25])[CH2:13][C:12]2([CH3:27])[CH:10]1[O:11]2参加物
4
実験手順
A solution of methanesulphonic acid (0.1 mmol; 1 ml; 0.1N in acetone) is added to a solution of the compound of Example 5 (0.1 mmol; 34 mg) in acetone (2 ml). The precipitate is filtered, washed with acetone and dried under reduced pressure. 24 mg of the expected product is obtained in the form of a white powder. Melting point: 220° C.