1-Benzoyl-4-(4-methoxyphenyl)piperazine → 1-Benzoyl-4-(4-hydroxyphenyl)piperazine
反応式
COC1C=CC(N2CCN(CCC3C=CC=CC=3)CC2)=CC=1.[C:23]([N:31]1[CH2:36][CH2:35][N:34]([C:37]2[CH:42]=[CH:41][C:40]([O:43]C)=[CH:39][CH:38]=2)[CH2:33][CH2:32]1)(=[O:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[C:23]([N:31]1[CH2:32][CH2:33][N:34]([C:37]2[CH:38]=[CH:39][C:40]([OH:43])=[CH:41][CH:42]=2)[CH2:35][CH2:36]1)(=[O:30])[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1参加物
3
実験手順
Production Example 2 was repeated except that 1-(4-methoxyphenyl)-4-phenethylpiperazine was replaced with 1-benzoyl-4-(4-methoxyphenyl)piperazine (193 mg), and the resulting crude product was purified on TLC (developer, chloroform: acetone=4:1) to provide 1-benzoyl-4-(4-hydroxyphenyl)piperazine (141 mg).
後処理
- customthe resulting crude product was purified on TLC (developer, chloroform: acetone=4:1)
出典と根拠
- ORDレコード
- ord-eff20b8044ec47d8907dbb69c9bd52ff
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07449466B2
反応ノート
読み込み中…