Methylamine → 2-(4-Methyl-2H-phthalazin-1-on-2-yl)-N-methylethylamine hydrobromide
反応式
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[O:12])[N:4]([CH2:13][CH2:14][Br:15])[N:3]=1.[CH3:16][NH2:17]>C(O)C>[BrH:15].[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[C:5](=[O:12])[N:4]([CH2:13][CH2:14][NH:17][CH3:16])[N:3]=1参加物
4
実験手順
2-(4-Methyl-2H-phthalazin-1-on-2-yl)ethyl bromide (6.1 g) and methylamine (20 ml of 30% ethanolic methylamine) in ethanol (150 ml) were heated in a bomb at 100° for 2 hours. The solvent was removed and the residue triturated with ethyl acetate to give a yellow solid, which was recrystallised from ethanol to afford the title compound, yield 5.03 g, m.p. 219°-221°.
後処理
- customThe solvent was removed
- customthe residue triturated with ethyl acetate
- customto give a yellow solid, which
- customwas recrystallised from ethanol
出典と根拠
- ORDレコード
- ord-0bbadcf4dd9a4c6fb3f96ae94d9084ce
- 出典データセット
- uspto-grants-1991_02
- 特許番号
- US04990509
反応ノート
読み込み中…