Ethanethiol → 2-(4-Hydroxyphenyl)benzo[b]thiophen-3-yl 4-[2-(1-Pyrrolidinyl)ethoxy]phenyl Ketone
反応式
COC.[N:4]1([CH2:9][CH2:10][O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([C:20]3[C:21]4[CH:36]=[CH:35][CH:34]=[CH:33][C:22]=4[S:23][C:24]=3[C:25]3[CH:30]=[CH:29][C:28]([O:31]C)=[CH:27][CH:26]=3)=[O:19])=[CH:14][CH:13]=2)[CH2:8][CH2:7][CH2:6][CH2:5]1.[Al+3].[Cl-].[Cl-].[Cl-].CCS>ClC(Cl)C>[N:4]1([CH2:9][CH2:10][O:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([C:20]3[C:21]4[CH:36]=[CH:35][CH:34]=[CH:33][C:22]=4[S:23][C:24]=3[C:25]3[CH:26]=[CH:27][C:28]([OH:31])=[CH:29][CH:30]=3)=[O:19])=[CH:14][CH:13]=2)[CH2:8][CH2:7][CH2:6][CH2:5]1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
By cleaving the methyl ether of 2-(4-methoxyphenyl)-benzo[b]thiophen-3-yl 4-[2-(1-pyrrolidinyl)ethoxy]phenyl ketone using AlCl3 (about 8 eq) and EtSH (about 10 eq) in dichloroethane at 0° C., the title compound was obtained in 33% yield as an oil following radial chromatography (SiO2; gradient of 2-10% MeOH in CH2Cl2).
後処理
- customat 0° C.
出典と根拠
- ORDレコード
- ord-96ebf036b74047f8ac2332bdf1d15fb2
- 出典データセット
- uspto-grants-2001_08
- 特許番号
- US06271227B1
反応ノート
読み込み中…