Hydrochloric Acid → HCID 68413743、化合物
反応式
[NH2:1][C:2]([CH3:39])([CH3:38])[C:3]([NH:5][C@H:6]([CH2:34][CH:35]([CH3:37])[CH3:36])[C:7]([NH:9][CH:10]1[CH2:19][C:18]2[C:13](=[C:14]([N:20]3[C:24](=[O:25])[CH2:23][CH2:22][C:21]3=[O:26])[CH:15]=[CH:16][CH:17]=2)[N:12]([CH2:27][C:28]2[CH:32]=[CH:31][S:30][CH:29]=2)[C:11]1=[O:33])=[O:8])=[O:4].[ClH:40]>C(O)C>[ClH:40].[NH2:1][C:2]([CH3:38])([CH3:39])[C:3]([NH:5][C@H:6]([CH2:34][CH:35]([CH3:36])[CH3:37])[C:7]([NH:9][CH:10]1[CH2:19][C:18]2[C:13](=[C:14]([N:20]3[C:21](=[O:26])[CH2:22][CH2:23][C:24]3=[O:25])[CH:15]=[CH:16][CH:17]=2)[N:12]([CH2:27][C:28]2[CH:32]=[CH:31][S:30][CH:29]=2)[C:11]1=[O:33])=[O:8])=[O:4]参加物
4
実験手順
(2R)-2-(2-Amino-2-methylpropanamido)-N-(8-(2,5-dioxopyrrolidin-1-yl)-2-oxo-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-yl)-4-methylpentanamide (14 mg) was dissolved in ethanol (1 mL), and concentrated hydrochloric acid (35% aqueous hydrochloric acid solution) (25 μL) was added thereto. The solvent was evaporated under reduced pressure, whereby the title compound (16 mg) was yielded.
後処理
- custom