Sodium Hydroxide → 2-Chlorothieno[2,3-b]pyrazine-6-carboxylic acid
反応式
[Cl:1][C:2]1[N:7]=[C:6]2[CH:8]=[C:9]([C:11]([O:13]C)=[O:12])[S:10][C:5]2=[N:4][CH:3]=1.[OH-].[Na+]>C1COCC1.C(O)C.Cl>[Cl:1][C:2]1[N:7]=[C:6]2[CH:8]=[C:9]([C:11]([OH:13])=[O:12])[S:10][C:5]2=[N:4][CH:3]=1参加物
6
実験手順
To a solution of methyl 2-chlorothieno[3,2-b]pyrazine-6-carboxylate 22 (1.23 g, 5.38 mmol) in THF (10 mL) and ethanol (10 mL) was added a solution of 2N sodium hydroxide (13.45 mL, 26.9 mmol). The reaction was stirred at rt for 1 h. The reaction mixture was poured in 2N HCl solution and the resulting precipitate was collected, washed with water and dried to give crude 2-chlorothieno[3,2-b]pyrazine-6-carboxylic acid 23 (1.027 g, 89%). NMR (400 MHz, DMSO-d6) 8.18 (s, 1H), 8.90 (s, 1H).
後処理
- customthe resulting precipitate was collected
- washwashed with water
- customdried
出典と根拠
- ORDレコード
- ord-167a8d32dbdc4723a01e563dcb68ac35
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08669256B2
反応ノート
読み込み中…