Sodium borohydride → (9b-morpholino-3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,9b-dihydro-3aH-chromeno[3,4-d]isoxazol-7-yl)methanol
反応式
[O:1]1[CH2:6][CH2:5][N:4]([C:7]23[C:34]4[CH:33]=[CH:32][C:31]([CH:35]=[O:36])=[CH:30][C:29]=4[O:28][CH2:27][CH:8]2[C:9]([C:12]2[O:16][N:15]=[C:14]([C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)[C:13]=2[C:23]([F:26])([F:25])[F:24])=[N:10][O:11]3)[CH2:3][CH2:2]1.[BH4-].[Na+]>CO>[O:1]1[CH2:2][CH2:3][N:4]([C:7]23[C:34]4[CH:33]=[CH:32][C:31]([CH2:35][OH:36])=[CH:30][C:29]=4[O:28][CH2:27][CH:8]2[C:9]([C:12]2[O:16][N:15]=[C:14]([C:17]4[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=4)[C:13]=2[C:23]([F:25])([F:26])[F:24])=[N:10][O:11]3)[CH2:5][CH2:6]1参加物
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of 9b-morpholino-3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,9b-dihydro-3aH-chromeno[3,4-d]isoxazole-7-carbaldehyde (Preparation 60F, 0.070 g, 0.140 mmol) in methanol (1.0 mL) at room temperature was added sodium borohydride (1.43 mg, 0.038 mmol). The reaction mixture was stirred at room temperature for 30 min. Methanol was removed under reduce pressure, and the residue was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded (9b-morpholino-3-(3-phenyl-4-(trifluoromethyl)isoxazol-5-yl)-4,9b-dihydro-3aH-chromeno[3,4-d]isoxazol-7-yl)methanol as a yellow oil. The product had an HPLC ret. time=2.83 min.−Column: Chromolith SpeedROD 4.6×50 mm (4 min.); Solvent A=10% MeOH, 90% H2O, 0.1% TFA; Solvent B=90% MeOH, 10% H2O, 0.1% TFA. LC/MS M+1=502.0.
後処理
- customMethanol was removed
- additionthe residue was diluted with dichloromethane
- washwashed with water
- dry with materialdried over anhydrous sodium sulfate
- concentrationConcentration under reduced pressure
出典と根拠
- ORDレコード
- ord-09a3e38745e749c9a34975d6aefad4ce
- 出典データセット
- uspto-grants-2015_12
- 特許番号
- US09216972B2
反応ノート
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