Hydrochloric Acid → 2-Methyl-1-phenylpiperaZine hydrochloride
反応式
[CH3:1][CH:2]1[N:7]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH2:6][CH2:5][N:4](C(OC(C)(C)C)=O)[CH2:3]1.[ClH:21]>C(OCC)(=O)C>[ClH:21].[C:8]1([N:7]2[CH2:6][CH2:5][NH:4][CH2:3][CH:2]2[CH3:1])[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1参加物
4
実験手順
(±)-tert-Butyl 3-methyl-4-phenylpiperazine-1-carboxylate (142 mg) was dissolved in 4N hydrogen chloride in ethyl acetate (5 ml). After stirring for 15 minutes, the solvent was removed under reduced pressure to give the title compound as a slightly yellow solid.
後処理
- customthe solvent was removed under reduced pressure
出典と根拠
- ORDレコード
- ord-bad87fa887ec45f383499b68be82f86c
- 出典データセット
- uspto-grants-2004_11
- 特許番号
- US06825200B1
反応ノート
読み込み中…