反応式
[H-].[Na+].[F:3][CH:4]([C:10]([O:12]CC)=O)[C:5]([O:7]CC)=O.Br.[O:16]1[CH2:21][CH2:20][N:19]([C:22]([NH2:24])=[NH:23])[CH2:18][CH2:17]1>CCO>[F:3][C:4]1[C:5]([OH:7])=[N:23][C:22]([N:19]2[CH2:20][CH2:21][O:16][CH2:17][CH2:18]2)=[N:24][C:10]=1[OH:12]参加物
実験手順
Sodium hydride (60% in oil, 3.9 g, 96.5 mmol) was washed with hexanes in a round bottom flask under argon and cooled with an ice water bath. EtOH (100 mL) was slowly added. The resulting mixture was warmed to RT and stirred for 30 minutes. To the base mixture, diethyl 2-fluoromalonate (5.7 g, 32.2 mmol) was added, followed by morpholinoformamidine hydrobromide (6.8 g, 32.2 mmol). The mixture was heated to 90-95° C. with stirring under argon. After 12 hours, the reaction was cooled to room temperature and the EtOH was removed in vacuo. The resulting white solid was dissolved in water (25 mL) and acidified with conc. HCl to pH=3-4. A white precipitate formed which was collected on a Büchner filter, washed with water (2×50 mL), air dried on the filter, and dried in vacuo to give 5-fluoro-2-morpholinopyrimidine-4,6-diol (0.87 g, 12%). LC/MS (m/z): 216.0 (MH+), Rt 0.63 minutes.
後処理
- temperaturecooled with an ice water bath
- temperatureThe mixture was heated to 90-95° C.
- stirringwith stirring under argon
- waitAfter 12 hours
- temperaturethe reaction was cooled to room temperature
- customthe EtOH was removed in vacuo
- dissolutionThe resulting white solid was dissolved in water (25 mL)
- customA white precipitate formed which
- customwas collected on a Büchner
- filtrationfilter
- washwashed with water (2×50 mL), air
- customdried on the filter
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-92357aa0b697475ebba744cb2772c7e3
- 出典データセット
- uspto-grants-2013_10
- 特許番号
- US08563549B2
関連ノート
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