p-(Trifluoromethoxy)phenyl isocyanate → HCID 86594050、化合物
反応式
[C:1]([O:5][C:6](=[O:24])[C:7]([S:10][C:11]1[CH:20]=[CH:19][C:18]2[CH2:17][CH:16]([NH:21][CH2:22][CH3:23])[CH2:15][CH2:14][C:13]=2[CH:12]=1)([CH3:9])[CH3:8])([CH3:4])([CH3:3])[CH3:2].[F:25][C:26]([F:38])([F:37])[O:27][C:28]1[CH:33]=[CH:32][C:31]([N:34]=[C:35]=[O:36])=[CH:30][CH:29]=1>C(Cl)Cl>[C:1]([O:5][C:6](=[O:24])[C:7]([S:10][C:11]1[CH:20]=[CH:19][C:18]2[CH2:17][CH:16]([N:21]([CH2:22][CH3:23])[C:35]([NH:34][C:31]3[CH:32]=[CH:33][C:28]([O:27][C:26]([F:25])([F:37])[F:38])=[CH:29][CH:30]=3)=[O:36])[CH2:15][CH2:14][C:13]=2[CH:12]=1)([CH3:9])[CH3:8])([CH3:2])([CH3:3])[CH3:4]参加物
4
実験手順
To a mixture of 2-(6-ethylamino-5,6,7,8-tetrahydronaphthalen-2-ylsulfanyl)-2-methylpropionic acid tert-butyl ester and borane complex (1.9 g; 5.2 mmol) dissolved in CH2Cl2 (15 mL) is added 4-trifluoromethoxyphenyl isocyanate (1.6 g; 7.8 mmol) and the reaction was stirred at RT for 18 h. The solvent was removed under reduced pressure and the crude residue was purified by flash chromatography (SiO2) eluting with a hexanes-EtOAc gradient to provide 1.66 g (58%) of 2-{6-[1-ethyl-3-(4-trifluoromethoxyphenyl)ureido]-5,6,7,8-tetrahydronaphthalen-2-ylsulfanyl}-2-methylpropionic acid tert butyl ester as a white foam.
後処理
- customThe solvent was removed under reduced pressure
- customthe crude residue was purified by flash chromatography (SiO2)
- washeluting with a hexanes-EtOAc gradient
出典と根拠
- ORDレコード
- ord-16437502459041d19a34cbe507dbe279
- 出典データセット
- uspto-grants-2008_04
- 特許番号
- US07351857B2
反応ノート
読み込み中…