Potassium Carbonate → N-(2,2-difluoroethyl)-6-((2R,6R)-2,6-dimethylmorpholino)-7-fluoro-5-formylbenzo[d]isoxazole-3-carboxamide

HRID 577943ノート

反応式

HRID 577943 の反応式
[F:1][CH:2]([F:20])[CH2:3][NH:4][C:5]([C:7]1[C:11]2[CH:12]=[C:13]([CH:18]=[O:19])[C:14](F)=[C:15]([F:16])[C:10]=2[O:9][N:8]=1)=[O:6].C(=O)([O-])[O-].[K+].[K+].[CH3:27][C@H:28]1[O:33][C@H:32]([CH3:34])[CH2:31][NH:30][CH2:29]1>C(#N)CCC.O.[Cl-].[Na+].O.C(OCC)(=O)C>[F:1][CH:2]([F:20])[CH2:3][NH:4][C:5]([C:7]1[C:11]2[CH:12]=[C:13]([CH:18]=[O:19])[C:14]([N:30]3[CH2:29][C@@H:28]([CH3:27])[O:33][C@H:32]([CH3:34])[CH2:31]3)=[C:15]([F:16])[C:10]=2[O:9][N:8]=1)=[O:6]

参加物

8

反応条件

温度
90 °C

実験手順

N-(2,2-Difluoroethyl)-6,7-difluoro-5-formylbenzo[d]isoxazole-3-carboxamide (Intermediate 243, 2.86 g, 9.86 mmol) was dissolved in butyronitrile (50 mL) and water (2.5 mL). Potassium carbonate (1.362 g, 9.86 mmol) and (2R,6R)-2,6-dimethylmorpholine (1.481 mL, 11.83 mmol) were added and the reaction was stirred at 90° C. for 4 hours. The crude reaction mixture was diluted with water, brine and ethyl acetate. The mixture was washed 2× with brine. The aqueous layer was back-extracted with ethyl acetate. The organic layers combined, dried over MgSO4 and concentrated. The residue was dissolved in DCM and purified by silica gel column chromatography using a gradient of DCM to ethyl acetate. Fractions were combined and concentrated to give the title compound.

後処理

  1. customThe crude reaction mixture
  2. washThe mixture was washed 2× with brine
  3. extractionThe aqueous layer was back-extracted with ethyl acetate
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated
  6. dissolutionThe residue was dissolved in DCM
  7. custompurified by silica gel column chromatography
  8. concentrationconcentrated

出典と根拠

ORDレコード
ord-7478b0cfc43d4f799e09f27716242dae
出典データセット
uspto-grants-2015_05
特許番号
US09040528B2

反応ノート

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