Hydrochloric Acid → (RS)-Toluene-4-sulfonic acid 5-methoxy-1-(toluene-4-sulfonyl)-2,3-dihydro-1H-indol-2-ylmethyl ester
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]([CH2:12][OH:13])[CH2:6]2.[C:14]1([CH3:24])[CH:19]=[CH:18][C:17]([S:20](Cl)(=[O:22])=[O:21])=[CH:16][CH:15]=1.C(N([CH2:30][CH3:31])CC)C.Cl>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:9](=[CH:10][CH:11]=1)[N:8]([S:20]([C:17]1[CH:18]=[CH:19][C:14]([CH3:24])=[CH:15][CH:16]=1)(=[O:22])=[O:21])[CH:7]([CH2:12][O:13][S:20]([C:17]1[CH:18]=[CH:19][C:30]([CH3:31])=[CH:15][CH:16]=1)(=[O:22])=[O:21])[CH2:6]2参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
(RS)-(5-methoxy-2,3-dihydro-1H-indol-2-yl)-methanol (100 mg, 0.46 mmol), p-toluenesulfonyl chloride (177 mg, 0.93 mmol), triethylamine (0.21 ml, 1.48 mmol) and N,N-dimethylamino pyridine (2 mg) were stirred for 18 hr at RT in CH2Cl2 (5 ml). 1N HCl (10 ml) was added, the mixture extracted with CH2Cl2 (2×25 ml) and the extracts washed with satd. NaCl solution (20 ml) and dried (Na2SO4). The crude material was chromatographed over SiO2 (Merck 230-400 mesh) eluting with EtOAc-cyclohexane-Et3N (9:10:1) to afford the title compound as a yellow oil (172.8 mg, 0.35 mmol, 76%), MS: m/e=488.0 (M+H+).
後処理
- extractionthe mixture extracted with CH2Cl2 (2×25 ml)
- washthe extracts washed with satd
- dry with materialNaCl solution (20 ml) and dried (Na2SO4)
- customThe crude material was chromatographed over SiO2 (Merck 230-400 mesh)
- washeluting with EtOAc-cyclohexane-Et3N (9:10:1)
出典と根拠
- ORDレコード
- ord-52b0b907ffca400bbd79314dd4b84bd8
- 出典データセット
- uspto-grants-2002_03
- 特許番号
- US06359138B1
反応ノート
読み込み中…