Borane → HCID 20488239、化合物
反応式
[CH3:1][N:2]([CH3:18])[C:3]([C:5]1[C:10]([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:9][NH:8][C:7](=[O:17])[CH:6]=1)=O.B.[OH-].[Na+]>O1CCCC1>[CH3:18][N:2]([CH2:3][C:5]1[C:10]([C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=2)=[N:9][NH:8][C:7](=[O:17])[CH:6]=1)[CH3:1]参加物
実験手順
2,3-Dihydro-3-oxo-6-phenyl-5-pyridazinecarboxylic acid is treated with ethyl chloroformate, triethylamine, and dimethylamine according to the procedure of Example 3 to give N,N-dimethyl-2,3-dihydro-3-oxo-6-phenyl-5-pyridazinecarboxamide. A solution of this amide (12.5 g) in 400 ml of tetrahydrofuran is treated with 100 ml of 1 M borane in tetrahydrofuran and the resulting mixture is heated under reflux for 4 hours, then cooled and treated with 5% sodium hydroxide (100 ml) and heated under reflux for 1 hour. The tetrahydrofuran is removed on the rotary evaporator and the pH of the residual liquid is adjusted with acetic acid followed by ammonium hydroxide to 10. The product is extracted into dichloromethane and the dichloromethane is filtered and concentrated on the rotary evaporator. The residue is chromatographed on silica gel with 2% methanol and chloroform to give 5-(dimethylaminomethyl)-6-phenyl-3(2H)-pyridazinone.
後処理
- temperaturethe resulting mixture is heated
- temperatureunder reflux for 4 hours
- temperaturecooled
- temperatureheated
- temperatureunder reflux for 1 hour
- customThe tetrahydrofuran is removed on the rotary evaporator
- extractionThe product is extracted into dichloromethane
- filtrationthe dichloromethane is filtered
- concentrationconcentrated on the rotary evaporator
- customThe residue is chromatographed on silica gel with 2% methanol and chloroform
出典と根拠
- ORDレコード
- ord-4a088dbc6f2c40879c7548761859377e
- 出典データセット
- uspto-grants-1983_09
- 特許番号
- US04404203
反応ノート
読み込み中…