反応式
C(O[CH:4]=[C:5]([C:11]#[N:12])[C:6]([O:8][CH2:9][CH3:10])=[O:7])C.[Cl:13][C:14]1[C:15]([NH:21][NH2:22])=[N:16][CH:17]=[C:18]([Cl:20])[CH:19]=1>C(OC(O)C)C>[NH2:12][C:11]1[N:21]([C:15]2[C:14]([Cl:13])=[CH:19][C:18]([Cl:20])=[CH:17][N:16]=2)[N:22]=[CH:4][C:5]=1[C:6]([O:8][CH2:9][CH3:10])=[O:7]参加物
4
実験手順
16.9 g (0.1 mole) of ethyl ethoxymethylenecyanoacetate and 17.8 g (0.1 mole) of 3,5-dichloro-pyrid-2-ylhydrazine in 150 ml of ethoxyethanol are stirred at 80° C. for 5 hours and then at 120° C. for a further 2 hours. For working up, the solvent is removed in vacuo. 29.6 g (98% of theory) of 5-amino-1-(3,5-dichloro-pyrid-2-yl)-4-ethoxycarbonyl-pyrazole of melting point 98°-101° C. are obtained.
後処理
- customthe solvent is removed in vacuo
出典と根拠
- ORDレコード
- ord-c998c34efefb4ee99bb0ca2dbd3a393b
- 出典データセット
- uspto-grants-1988_09
- 特許番号
- US04772312
関連ノート
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