反応式
[Cl:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[N:14]=[C:13]([C:15]([F:18])([F:17])[F:16])[C:12](C(O)=O)=[CH:11][N:10]=2)[CH:5]=[CH:6][CH:7]=1.C([N:24](CC)CC)C.C1(P(N=[N+]=[N-])(C2C=CC=CC=2)=O)C=CC=CC=1.[C:46](=[O:49])([O-])[OH:47].[Na+].[C:51](O)([CH3:54])([CH3:53])[CH3:52]>>[Cl:1][C:2]1[CH:3]=[C:4]([NH:8][C:9]2[N:14]=[C:13]([C:15]([F:16])([F:17])[F:18])[C:12]([NH:24][C:46](=[O:49])[O:47][C:51]([CH3:54])([CH3:53])[CH3:52])=[CH:11][N:10]=2)[CH:5]=[CH:6][CH:7]=1参加物
反応条件
- 温度
- 90 °C
実験手順
To a mixture of 2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidine-5-carboxylic acid (307 mg), triethylamine (162 μL), and tert-butyl alcohol (9 mL) was added diphenylphosphorylazide (250 μL), followed by stirring at 90° C. for 7 hours. To the reaction mixture was added a saturated aqueous sodium hydrogen carbonate solution (50 mL), followed by extraction with ethyl acetate (50 mL), and then the extract was washed with saturated brine (30 mL). The organic layer was dried over anhydrous magnesium sulfate and then concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate) to obtain tert-butyl {2-[(3-chlorophenyl)amino]-4-(trifluoromethyl)pyrimidin-5-yl}carbamate (270 mg) as a pale yellow powder.
後処理
- extractionfollowed by extraction with ethyl acetate (50 mL)
- washthe extract was washed with saturated brine (30 mL)
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
- customthe obtained residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate)
出典と根拠
- ORDレコード
- ord-cc9395f6678a4328bd0405ccf8eb2dbe
- 出典データセット
- uspto-grants-2013_09
- 特許番号
- US08524727B2
関連ノート
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