反応式
C([O:3][C:4]([C:6]1[C:7](=[O:18])[NH:8][N:9]=[C:10]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)[CH:11]=1)=O)C.O.[NH2:20][NH2:21]>C(O)C>[O:18]=[C:7]1[C:6]([C:4]([NH:20][NH2:21])=[O:3])=[CH:11][C:10]([C:12]2[CH:17]=[CH:16][N:15]=[CH:14][CH:13]=2)=[N:9][NH:8]1参加物
4
実験手順
10 g of 3-oxo-6-pyridin-4-yl-2,3-dihydro-pyridazine-4 -carboxylic acid ethyl ester are dissolved in 150 ml of ethanol, 4.2 ml of hydrazine hydrate is added and the mixture is refluxed for 5 hours. After cooling to room temperature, the solid is collected by filtration and dried in vacuo at 40° C.
後処理
- temperaturethe mixture is refluxed for 5 hours
- filtrationthe solid is collected by filtration
- customdried in vacuo at 40° C.
出典と根拠
- ORDレコード
- ord-b6617c3e1efe40648bbe980703bbf55d
- 出典データセット
- uspto-grants-2009_03
- 特許番号
- US07507734B2
関連ノート
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