Ethanolamine → 3-(2-Aminoethoxy)-6-chloropyridazine hydrochloride
反応式
[H-].[Na+].[NH2:3][CH2:4][CH2:5][OH:6].[Cl:7][C:8]1[N:9]=[N:10][C:11](Cl)=[CH:12][CH:13]=1>C1C=CC=CC=1>[ClH:7].[NH2:3][CH2:4][CH2:5][O:6][C:11]1[N:10]=[N:9][C:8]([Cl:7])=[CH:13][CH:12]=1参加物
5
実験手順
To a suspension of 4.2 g of 61% sodium hydride in 100 ml of benzene was added dropwise 6.2 g of 2-aminoethanol at room temperature. Then, 15 g of 3,6-dichloropyridazine was added, and the mixture was refluxed for 1 hour. After cooling, the reaction mixture was washed with water, and dried over magnesium sulfate. After evaporating the solvent, the residue was treated with hydrogen chrolide-ether solution to give 5.73 g of 3-(2-aminoethoxy)-6-chloropyridazine hydrochloride as crystals.
後処理
- temperaturethe mixture was refluxed for 1 hour
- temperatureAfter cooling
- washthe reaction mixture was washed with water
- dry with materialdried over magnesium sulfate
- customAfter evaporating the solvent
- additionthe residue was treated with hydrogen chrolide-ether solution
出典と根拠
- ORDレコード
- ord-5c6ef1edb3be4f9d8326bfb04e2e20ab
- 出典データセット
- uspto-grants-1986_07
- 特許番号
- US04599333
反応ノート
読み込み中…