1-Benzylpiperazine → 1-Benzyl-4-(benzothiophen-2-yl)piperazine
反応式
S[C:2]1[S:3][C:4]2[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=2[CH:6]=1.[CH2:11]([N:18]1[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]1)[C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1>C1(C)C=CC=CC=1>[CH2:11]([N:18]1[CH2:23][CH2:22][N:21]([C:2]2[S:3][C:4]3[CH:10]=[CH:9][CH:8]=[CH:7][C:5]=3[CH:6]=2)[CH2:20][CH2:19]1)[C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1参加物
4
実験手順
To a solution of 2-mercaptobenzothiophene (1.8 g, 10.8 mmol) in toluene under nitrogen was added N-benzylpiperazine (1.88 ml, 10.8 mmol) and the mixture heated at reflux for 1.5 h. Left to cool, concentrated in vacuo and product recrystallised from diethyl ether-hexane to yield the title compound (1.55 g), m.p. 160°-161° C.
後処理
- temperaturethe mixture heated
- temperatureat reflux for 1.5 h
- waitLeft
- temperatureto cool
- concentrationconcentrated in vacuo and product
- customrecrystallised from diethyl ether-hexane
出典と根拠
- ORDレコード
- ord-1752c34019b44edc9e735b4d3cbefc7f
- 出典データセット
- uspto-grants-1998_08
- 特許番号
- US05792768
反応ノート
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