2,4-Difluoroaniline → 5-Bromo-N-(2,4-difluorophenyl)-2-fluoronicotinamide

HRID 1986095ノート

反応式

HRID 1986095 の反応式
[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

7

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

  1. temperatureAfter cooling
  2. customthe solvent was removed under reduced pressure
  3. dissolutionThe residue was dissolved in 2.0 mL of DCM and to it
  4. stirringThe mixture was stirred at room temperature for 2 h
  5. customThe organic layer was separated
  6. extractionthe aqueous layer was extracted with EtOAc
  7. washThe combined organic layers were washed with brine
  8. dry with materialdried over MgSO4
  9. filtrationAfter filtration and concentration in vacuo
  10. 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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