HRID1809083

反应详情

EQUATION

反应方程式

HRID 1809083 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

(2-Bromo-5-ethyl-thiophen-3-yl)-piperidin-1-yl-methanone (0.1 g, 0.33 mmol) was dissolved in DMF (3 mL). Zinc cyanide (0.34 mmol) and tetrakis-(triphenylphosphine) palladium (0) (0.017 mmol) were added and the reaction mixture heated at 100° C. for 4 hours. The mixture was cooled to ambient temperature and the reaction quenched with a mixture of 5% aqueous sodium thiosulphate and saturated aqueous potassium carbonate (1:1, 5 mL) and extracted with diethyl ether. The organic solution was dried over magnesium sulphate, filtered and the solvent removed. The product was purified by HPLC, eluting with 20%-95% acetonitrile in water (0.1% formic acid) over 30 minutes. The fractions containing the desired product were concentrated under vacuum and freeze-dried to give the title compound (0.26 mg). LCMS m/z 249.14 [M+H]+ RT=9.75 min (Analytical Method 1). 1H NMR (400 MHz, CHCl3-d): δ 6.85 (t, 1H), 3.70 (m, 2H), 3.4 (m, 2H), 2.9 (m, 2H), 1.7 (m, 4H), 1.6 (s, 2H), 1.3 (t, 3H).

WORKUP

后处理

  1. temperatureThe mixture was cooled to ambient temperature
  2. customthe reaction quenched with a mixture of 5% aqueous sodium thiosulphate and saturated aqueous potassium carbonate (1:1, 5 mL)
  3. extractionextracted with diethyl ether
  4. dry with materialThe organic solution was dried over magnesium sulphate
  5. filtrationfiltered
  6. customthe solvent removed
  7. customThe product was purified by HPLC
  8. washeluting with 20%-95% acetonitrile in water (0.1% formic acid) over 30 minutes
  9. additionThe fractions containing the desired product
  10. concentrationwere concentrated under vacuum
  11. customfreeze-dried