[ClH:1].[CH2:2]([N:4]([CH2:7][C:8]([O:10][CH:11]1[CH2:16][CH2:15][N:14]([C:17]2[S:18][C:19](/[CH:22]=[C:23](\[C:34]#[N:35])/[C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[C:26]([O:32][CH3:33])[CH:25]=3)=[CH:20][CH:21]=2)[CH2:13][CH2:12]1)=[O:9])[CH2:5][CH3:6])[CH3:3]>C(O)(C)C>[ClH:1].[CH2:2]([N:4]([CH2:7][C:8]([O:10][CH:11]1[CH2:12][CH2:13][N:14]([C:17]2[S:18][C:19](/[CH:22]=[C:23](\[C:34]#[N:35])/[C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[C:26]([O:32][CH3:33])[CH:25]=3)=[CH:20][CH:21]=2)[CH2:15][CH2:16]1)=[O:9])[CH2:5][CH3:6])[CH3:3]Isopropanol (10 mL) and 12N hydrochloric acid (59 μL) were added to Compound 103 (338 mg), and the mixture was heated for dissolution (external temperature: 80° C.). The solution was returned to room temperature, and allowed to stand overnight. The precipitated crystals were recovered through filtration, and the recovered crystals were recrystallized from isopropanol, to thereby yield the target product (yield: 254.5 mg, 70.0%).
読み込み中…