Hydrazine → 5-Hydroxy-6-methoxy-2H-phthalazin-1-one
反応式
O[CH:2]1[C:10]2[C:5](=[CH:6][CH:7]=[C:8]([O:12][CH3:13])[C:9]=2[OH:11])[C:4](=O)[O:3]1.[NH2:15][NH2:16]>C(O)C>[OH:11][C:9]1[C:8]([O:12][CH3:13])=[CH:7][CH:6]=[C:5]2[C:10]=1[CH:2]=[N:15][NH:16][C:4]2=[O:3]参加物
4
実験手順
A solution of 3,4-dihydroxy-5-methoxy-3H-isobenzofuran-1-one (6.63 g, 34 mmoles), prepared as described in example 57, in ethanol (60 ml) was added with 98% hydrazine (8.5 ml). The mixture was heated to clarity and after 5 minutes a precipitate formed and was filtered and treated with 1N HCl. The mother liquors were concentrated more times and the resultant solid fractions joined to give 4.65 g of the title compound (yield: 72%).
後処理
- temperatureThe mixture was heated to clarity and after 5 minutes a precipitate
- customformed
- filtrationwas filtered
- additiontreated with 1N HCl
- concentrationThe mother liquors were concentrated more times
出典と根拠
- ORDレコード
- ord-49376c41a8684afd9e87536e30d5fc7c
- 出典データセット
- uspto-grants-2002_12
- 特許番号
- US06492360B1
反応ノート
読み込み中…