反応式
C(=O)(O)[O-].[Na+].Cl[C:7]([O:9][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:8].O1CCCC1.[F:22][C:23]1[CH:24]=[C:25]([C@H:31]2[NH:36][C@@H:35]([C@H:37]([OH:39])[CH3:38])[CH2:34][O:33][CH2:32]2)[CH:26]=[C:27]([F:30])[C:28]=1[F:29]>C(OCC)(=O)C.O>[CH2:10]([O:9][C:7]([N:36]1[C@H:31]([C:25]2[CH:24]=[C:23]([F:22])[C:28]([F:29])=[C:27]([F:30])[CH:26]=2)[CH2:32][O:33][CH2:34][C@@H:35]1[C@H:37]([OH:39])[CH3:38])=[O:8])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
Saturated sodium bicarbonate aqueous solution (20 mL) and benzyl chloroformate (1.31 mL) were added to a tetrahydrofuran (20 mL) solution of (R)-1-[(3R,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]ethanol (2 g). After stirring the reaction solution for 16 hours at room temperature, additional benzyl chloroformate (1.33 mL) was added, and the resultant was further stirred for 20 hours. Water and ethyl acetate were added, and the organic layer was partitioned. The organic layer was washed with brine and dried over anhydrous magnesium sulfate, and the solvent was removed under a vacuum. The residue was purified by silica gel column chromatography (heptane/ethyl acetate), and the title compound (880 mg) was obtained. The physical property values are as follows.
後処理
- stirringthe resultant was further stirred for 20 hours
- customthe organic layer was partitioned
- washThe organic layer was washed with brine
- dry with materialdried over anhydrous magnesium sulfate
- customthe solvent was removed under a vacuum
- customThe residue was purified by silica gel column chromatography (heptane/ethyl acetate)
出典と根拠
- ORDレコード
- ord-c0d90e89cdf742cb928f5520b1f6b064
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US08008293B2
関連ノート
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