HRID83141

反应详情

EQUATION

反应方程式

HRID 83141 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

To a solution of 6-(5-methyl-3-phenyl-isoxazol-4-ylmethoxy)-nicotinic acid (100 mg, 0.32 mmol) in DMF (2 mL) were added 2-(1H-benzotriazole-1-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate (114 mg, 0.35 mmol), N,N-diisopropyl ethyl amine (275 μL, 1.6 mmol) and 1-methylpiperidin-4-amine (41 mg, 0.35 mmol). The resulting reaction mixture was stirred overnight at room temperature. Concentration and purification by preparative HPLC on reversed phase eluting with acetonitrile/water [0.1% aq NH3 (25%)]. Then the residue was partitioned with ethyl acetate and water, the organic extract was washed with aqueous sodium hydrogen carbonate (saturated) dried over sodium sulfate and concentrated to afford the title compound (94 mg, 72%) which was obtained as a white solid. MS: m/e=407.5 [M+H]+.

WORKUP

后处理

  1. customThe resulting reaction mixture
  2. concentrationConcentration and purification by preparative HPLC on reversed phase
  3. washeluting with acetonitrile/water [0.1% aq NH3 (25%)]
  4. customThen the residue was partitioned with ethyl acetate and water
  5. extractionthe organic extract
  6. washwas washed with aqueous sodium hydrogen carbonate (saturated)
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated