Hydrochloric Acid → 1-(3-Phenylpropyl)-1,4-diazepane dihydrochloride
反応式
[C:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH2:16][CH2:15][CH2:14][N:13](C(OC(C)(C)C)=O)[CH2:12][CH2:11]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:24]>C(O)C>[ClH:24].[ClH:24].[C:1]1([CH2:7][CH2:8][CH2:9][N:10]2[CH2:16][CH2:15][CH2:14][NH:13][CH2:12][CH2:11]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
4
実験手順
To 5.41 g (5.41 g (16.99 mmol.) of tert-butyl 4-(3-phenylpropan-1-yl)-2,3,5,6-tetrahydro-7H-1,4-diazepine-1-carboxylate was added, at room temperature, 5 ml (60 mmol.) of 12N hydrochloric acid. The mixture was stirred for 2 hours. To the reaction system was added ethanol, then the solvent was distilled off under reduced pressure to give the object compound as a pale yellow amorphous product. The yield was 5.65 g (100%).
後処理
- distillationthe solvent was distilled off under reduced pressure
- customto give the object compound as a pale yellow amorphous product
出典と根拠
- ORDレコード
- ord-93d64ea0f2804ca5aff7510c7e20c2b8
- 出典データセット
- uspto-grants-2001_05
- 特許番号
- US06235731B1
反応ノート
読み込み中…