反応式
[NH2:1][C:2]1[C:7]([C:8]([OH:10])=O)=[CH:6][N:5]=[CH:4][CH:3]=1.[CH:11]([NH2:13])=O>>[N:1]1[C:2]2[CH:3]=[CH:4][N:5]=[CH:6][C:7]=2[C:8](=[O:10])[NH:13][CH:11]=1参加物
3
実験手順
Crude 4-amino nicotinic acid (2.72 g, 11.4 mmol) in formamide (20 mL) is heated to 170° C. for 12 h. The volatiles are distilled out under reduced pressure (0.8 mmHg). The residual solid is then purified on a medium pressure silica gel column, eluting with 10% MeOH in CHCl3 to give 3H-pyrido[4,3-d]pyrimidin-4-one (780 mg, 47%) as a whitish yellow solid. 1H NMR (DMSO) δ 12.64 (1H, brs), 9.28 (1H, s), 8.83 (1H, d, J=5.5 Hz), 8.30 (1H, s), 7.58 (1H, d, J=5.8 Hz).
後処理
- distillationThe volatiles are distilled out under reduced pressure (0.8 mmHg)
- customThe residual solid is then purified on a medium pressure silica gel column
- washeluting with 10% MeOH in CHCl3
出典と根拠
- ORDレコード
- ord-8e7572380b834a62a27cf7327625b916
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06521620B1
関連ノート
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