反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([C:11]([O:13]C)=O)[N:2]=1.[NH2:15][NH2:16]>C(O)C>[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[C:3]([C:11]([NH:15][NH2:16])=[O:13])[N:2]=1参加物
4
実験手順
To a solution of methyl isoquinoline-3-carboxylate (10 g, 53.42 mmol) in ethanol (100 mL) was added hydrazine (17.1 g). The reaction mixture was refluxed for 30 min and concentrated under high vacuum to remove hydrazine. The resulting residue was triturated with ethanol (20 mL) to give isoquinoline-3-carbohydrazide (8.6 g, 86%). LRMS (M+H+) m/z 188.1.
後処理
- temperatureThe reaction mixture was refluxed for 30 min
- concentrationconcentrated under high vacuum
- customto remove hydrazine
- customThe resulting residue was triturated with ethanol (20 mL)
出典と根拠
- ORDレコード
- ord-4011f0480f4e446aa3625771427965f9
- 出典データセット
- uspto-grants-2014_06
- 特許番号
- US08759374B2
関連ノート
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