Hydrogen chloride-ethyl acetate → 5-[3-(4-Methoxyphenyl)propylidene]-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione hydrochloride
反応式
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH2:10][CH:11]=[C:12]2[S:16][C:15](=[O:17])[N:14]([CH2:18][CH2:19][CH2:20][CH2:21][S:22][C:23]3[N:28]4[CH:29]=[CH:30][N:31]=[C:27]4[CH:26]=[CH:25][CH:24]=3)[C:13]2=[O:32])=[CH:5][CH:4]=1.[ClH:33].C(OCC)(=O)C>CO>[ClH:33].[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([CH2:9][CH2:10][CH:11]=[C:12]2[S:16][C:15](=[O:17])[N:14]([CH2:18][CH2:19][CH2:20][CH2:21][S:22][C:23]3[N:28]4[CH:29]=[CH:30][N:31]=[C:27]4[CH:26]=[CH:25][CH:24]=3)[C:13]2=[O:32])=[CH:7][CH:8]=1参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
To a methanol solution of 1.08 g (2.3 mmol) of 5-[3-(4-methoxyphenyl)propylidene]-3-[4-(imidazo[1,2-a]pyridin-5-ylthio)butyl]thiazolidine-2,4-dione, 0.8 ml of 4N hydrochloric acid-ethyl acetate was added, followed by stirring. After the solvent was distilled off, the residue was dissolved in methanol and recrystallized from ether to yield 995 mg (85.6%, white crystal) of the desired product.
後処理
- distillationAfter the solvent was distilled off
- dissolutionthe residue was dissolved in methanol
- customrecrystallized from ether
出典と根拠
- ORDレコード
- ord-b7587759399b40118d1d0bcf4af57313
- 出典データセット
- uspto-grants-1998_11
- 特許番号
- US05840732
反応ノート
読み込み中…