Sodium hydride → 11beta-[4-[2-[2-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]ethoxy]ethoxy]phenyl]estra-4,9-diene-3,17-dione
反応式
Br[CH2:2][CH2:3][O:4][CH2:5][CH2:6][O:7][Si:8]([C:11]([CH3:14])([CH3:13])[CH3:12])([CH3:10])[CH3:9].[OH:15][C:16]1[CH:21]=[CH:20][C:19]([C@H:22]2[CH2:39][C@@:37]3([CH3:38])[C@@H:33]([CH2:34][CH2:35][C:36]3=[O:40])[C@H:32]3[C:23]2=[C:24]2[C:29]([CH2:30][CH2:31]3)=[CH:28][C:27](=[O:41])[CH2:26][CH2:25]2)=[CH:18][CH:17]=1.[H-].[Na+].[Cl-].[NH4+]>CN(C)C=O>[CH3:12][C:11]([Si:8]([CH3:10])([CH3:9])[O:7][CH2:6][CH2:5][O:4][CH2:3][CH2:2][O:15][C:16]1[CH:17]=[CH:18][C:19]([C@H:22]2[CH2:39][C@@:37]3([CH3:38])[C@@H:33]([CH2:34][CH2:35][C:36]3=[O:40])[C@H:32]3[C:23]2=[C:24]2[C:29]([CH2:30][CH2:31]3)=[CH:28][C:27](=[O:41])[CH2:26][CH2:25]2)=[CH:20][CH:21]=1)([CH3:14])[CH3:13]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
412 mg of the product obtained in Stage B in solution in 2 cm3 of dimethylformamide is added to 362 mg of a mixture containing 362 mg of 11beta-(4-hydroxyphenyl)4,9-estra-diene-3,17-dione, 4 cm3 of dimethylformamide and 55 mg of sodium hydride. Agitation is carried out for 3 hours at ambient temperature, an aqueous solution of ammonium chloride is added, followed by extraction with ethyl acetate, washing with salt water, drying and evaporating the solvent. After chromatography on silica (eluant: ethyl acetate-essence G 6-4), 400 mg of expected product is obtained.
後処理
- extractionfollowed by extraction with ethyl acetate
- washwashing with salt water
- customdrying
- customevaporating the solvent
出典と根拠
- ORDレコード
- ord-c8a6c5c2c6aa43678891bb1284b295a3
- 出典データセット
- uspto-grants-2003_07
- 特許番号
- US06596885B2
反応ノート
読み込み中…