Ammonium Chloride → 9H-fluoren-9-ylmethyl (3S,5R)-3-hydroxymethyl-5-(3,4,5-trifluorophenyl)morpholine-4-carboxylate
反応式
Cl[C:2]([O:4][CH2:5][CH:6]1[C:18]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:12]2[C:7]1=[CH:8][CH:9]=[CH:10][CH:11]=2)=[O:3].[F:19][C:20]1[CH:21]=[C:22]([C@H:28]2[NH:33][C@@H:32]([CH2:34][OH:35])[CH2:31][O:30][CH2:29]2)[CH:23]=[C:24]([F:27])[C:25]=1[F:26].C(=O)(O)[O-].[Na+].[Cl-].[NH4+]>ClCCl>[OH:35][CH2:34][C@H:32]1[CH2:31][O:30][CH2:29][C@@H:28]([C:22]2[CH:21]=[C:20]([F:19])[C:25]([F:26])=[C:24]([F:27])[CH:23]=2)[N:33]1[C:2]([O:4][CH2:5][CH:6]1[C:18]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[C:12]2[C:7]1=[CH:8][CH:9]=[CH:10][CH:11]=2)=[O:3]参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
9-Fluorenylmethyl chloroformate (327 mg) was added to a mixed solution of [(3S,5R)-5-(3,4,5-trifluorophenyl)morpholin-3-yl]methanol (250 mg) in dichloromethane (5 mL) and a saturated sodium bicarbonate solution (5 mL), and the reaction solution was stirred at room temperature for six hours. Dichloromethane and a saturated ammonium chloride solution were added to the reaction solution, and the organic layer was separated. The resulting organic layer was dried over magnesium sulfate and then concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent: heptane->heptane:ethyl acetate=2:1) to obtain 470 mg of the title compound. The property values of the compound are as follows.
後処理
- customthe organic layer was separated
- dry with materialThe resulting organic layer was dried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was purified by silica gel chromatography (elution solvent: heptane->heptane:ethyl acetate=2:1)
出典と根拠
- ORDレコード
- ord-8bf7ad4ff91b48c19369939401fb287a
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08048878B2
反応ノート
読み込み中…