反応式
[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2[CH2:11][CH:12](SC)[C:13](=[O:16])[NH:14][N:15]=2)[CH:5]=[C:6]([Cl:9])[C:7]=1[CH3:8].Cl>O>[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2[CH:11]=[CH:12][C:13](=[O:16])[NH:14][N:15]=2)[CH:5]=[C:6]([Cl:9])[C:7]=1[CH3:8]参加物
4
実験手順
A mixture of 6.06 g (0.02 mole) of 6-(3,5-dichloro-4-methylphenyl)-4-methylthio-4,5-dihydro-3(2H)pyridazinone, prepared as described in Example 1(d), 20 ml of water and 5.2 ml of concentrated hydrochloric acid was heated under reflux for 2 hours. The mixture was then cooled and the resulting crystals were collected by filtration, air-dried, washed with a small amount of ethyl acetate and again air-dried, to give 4.59 g (yield 90%) of the desired 6-(3,5-dichloro-4-methylphenyl)-3(2H)pyridazinone, melting at 254°-258° C.
後処理
- customprepared
- temperaturewas heated
- temperatureunder reflux for 2 hours
- temperatureThe mixture was then cooled
- filtrationthe resulting crystals were collected by filtration
- customair-dried
- washwashed with a small amount of ethyl acetate
- customagain air-dried
出典と根拠
- ORDレコード
- ord-aa0c7552c2b94ab48ee41aeca3d666de
- 出典データセット
- uspto-grants-1986_07
- 特許番号
- US04603201
関連ノート
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