2,4-Difluoroaniline → 5-Bromo-N-(2,4-difluorophenyl)-2-fluoronicotinamide
反応式
[Br:1][C:2]1[CH:3]=[N:4][C:5]([F:11])=[C:6]([CH:10]=1)[C:7]([OH:9])=O.C(Cl)(C(Cl)=O)=O.[F:18][C:19]1[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:20]=1[NH2:21]>C1COCC1.C(Cl)Cl.O>[Br:1][C:2]1[CH:3]=[N:4][C:5]([F:11])=[C:6]([CH:10]=1)[C:7]([NH:21][C:20]1[CH:22]=[CH:23][C:24]([F:26])=[CH:25][C:19]=1[F:18])=[O:9]参加物
反応条件
- 温度
- 40 °C
実験手順
To a solution of 5-bromo-2-fluoronicotinic acid (55 mg, 0.25 mmol) in a mixture of 2.0 mL of THF and 5.0 mL of DCM was added (COCl)2 (0.13 mL, 1.5 mmol). The mixture was stirred at room temperature for 1 h and at 40° C. overnight. After cooling, the solvent was removed under reduced pressure. The residue was dissolved in 2.0 mL of DCM and to it were added 2,4-difluoroaniline (0.05 mL, 0.5 mmol) and 0.1 mL of TEA. The mixture was stirred at room temperature for 2 h and diluted with H2O. The organic layer was separated and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with brine and dried over MgSO4. After filtration and concentration in vacuo, the residue was purified on preparative (RP) HPLC to give the desired product (60 mg, 73% yield). MS(ESI+) m/z 331.18, 333.18 (M+H)+.
後処理
- temperatureAfter cooling
- customthe solvent was removed under reduced pressure
- dissolutionThe residue was dissolved in 2.0 mL of DCM and to it
- stirringThe mixture was stirred at room temperature for 2 h
- customThe organic layer was separated
- extractionthe aqueous layer was extracted with EtOAc
- washThe combined organic layers were washed with brine
- dry with materialdried over MgSO4
- filtrationAfter filtration and concentration in vacuo
- customthe residue was purified on preparative (RP) HPLC
出典と根拠
- ORDレコード
- ord-7c1a82c56ab7401e826aa28fb4a2624a
- 出典データセット
- uspto-grants-2009_06
- 特許番号
- US07547782B2
反応ノート
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