Acetic Acid → Aptazapine
反応式
[CH3:1][N:2]1[C:19](=O)[C:18](=O)[N:5]2[C:6]3[CH:17]=[CH:16][CH:15]=[CH:14][C:7]=3[CH2:8][N:9]3[CH:13]=[CH:12][CH:11]=[C:10]3[CH:4]2[CH2:3]1.C(O)(=O)C>O1CCCC1.B#B>[CH3:1][N:2]1[CH2:19][CH2:18][N:5]2[C:6]3[CH:17]=[CH:16][CH:15]=[CH:14][C:7]=3[CH2:8][N:9]3[CH:13]=[CH:12][CH:11]=[C:10]3[CH:4]2[CH2:3]1参加物
5
実験手順
To the suspension of 12.8 g of 2-methyl-3,4-dioxo-1,3,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine in 460 ml of tetrahydrofuran, 200 ml of 1-molar diborane in tetrahydrofuran are added while stirring and cooling with ice. The mixture is refluxed for one hour, again cooled and combined with 25 ml of acetic acid. It is evaporated, the residue taken up in 50 ml of 30% aqueous sodium hydroxide and the mixture extracted with methylene chloride. The extract is dried, evaporated, the residue dissolved in diethyl ether, the solution filtered and the filtrate evaporated, to yield the 2-methyl-1,3,4,14b-tetrahydro-10H-pyrazino[1,2-a]pyrrolo[2,1-c][1,4]benzodiazepine.
後処理
- additionare added
- temperaturecooling with ice
- temperatureThe mixture is refluxed for one hour
- temperatureagain cooled
- customIt is evaporated
- extractionthe mixture extracted with methylene chloride
- customThe extract is dried
- customevaporated
- dissolutionthe residue dissolved in diethyl ether
- filtrationthe solution filtered
- customthe filtrate evaporated
出典と根拠
- ORDレコード
- ord-d905523a2c1e4d0d9da26b1c5869361f
- 出典データセット
- uspto-grants-1982_12
- 特許番号
- US04362666
反応ノート
読み込み中…