HRID2055311

反应详情

EQUATION

反应方程式

HRID 2055311 的结构方程式

PROCEDURE

实验过程

5,5-Dioxo-2-aminodibenzothiophene (J Med Chem, (1994), 37 (13), 2085-9; 115 mg, 0.5 mmol) was dissolved in DMF (2.0 ml) and 3-(pyridin-4-yl)propionic acid (Method 1; 75 mg, 0.5 mmol) was added in one portion followed by EDAC (115 mg, 0.5 mmol) and the resultant mixture was stirred for 72 hours at ambient temperature. It was then poured onto water (50 ml) and extracted with DCM (2×50 ml), dried and evaporated in vacuo. The residue thus obtained was purified by chromatography (Bond Elut column) eluted with 0-0.5% methanol in DCM to give the product as a colourless solid (31.8 mg). NMR 10.52 (brs, 1H), 8.46 (d, 2H), 8.32 (d, 1H), 7.97 (d, 1H), 7.94 (d, 1H), 7.88 (d, 1H), 7.76 (d, 1H), 7.70 (t, 1H), 7.64 (t, 1H), 7.26 (d, 2H), 2.93 (t, 2H), 2.75 (t, 2H); m/z 365.

WORKUP

后处理

  1. additionIt was then poured onto water (50 ml)
  2. extractionextracted with DCM (2×50 ml)
  3. customdried
  4. customevaporated in vacuo
  5. customThe residue thus obtained
  6. customwas purified by chromatography (Bond Elut column)
  7. washeluted with 0-0.5% methanol in DCM