反応式
[N+:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[NH:9][N:8]=[C:7]2[NH2:13])([O-:3])=[O:2].[C:14](OC(=O)C)(=[O:16])[CH3:15].[OH2:21].N1[CH:27]=[CH:26]C=CC=1>>[C:14]([N:9]1[C:10]2[C:6](=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:12][CH:11]=2)[C:7]([NH:13][C:26](=[O:21])[CH3:27])=[N:8]1)(=[O:16])[CH3:15]参加物
5
実験手順
The product from Step (a) above (3.6 g, 20.2 mmol) was dissolved in pyridine (30 mL), acetic anhydride (4.15 mL, 44 mmol) was added and the mixture was stirred overnight at rt. The red solution was pouted into H2O and the resulting solid was filtered to give the title compunt as a red solid (4.8 g, 91%). NMR 1H NMR (400 MHz, DMSO-D6) δ 11.21 (br s, 1H), 9.08 (s, 1H), 8.46 (s, 2H), 2.51 (s, 3H), 2.23 (s, 3H) (MS m/z 263.2.0 [M+H]+
後処理
- filtrationthe resulting solid was filtered
出典と根拠
- ORDレコード
- ord-1a43f481a3d64d9fbdc7114267fb6e72
- 出典データセット
- uspto-grants-2009_07
- 特許番号
- US07560467B2
関連ノート
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