HRID1690611

反应详情

EQUATION

反应方程式

HRID 1690611 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Sodium (0.35 g, 15.3 mmol) was dissolved in ethanol (8 mL) at room temperature. Once all the sodium was dissolved, guanidine hydrochloride (1.45 g, 15.3 mmol) was added and the mixture was stirred for 1 h. A white precipitate formed and was filtered off. The filtrate was evaporated under reduced pressure and a solution of ethyl 3-[4′-{[4-(dimethylamino)piperidin-1-yl]methyl}-2-(3-methoxy-propoxy)biphenyl-4-yl]propanoate (1.18 g, 2.4 mmol) and DMF (8 mL) was added at room temperature. After completion of the reaction, the mixture was poured into dichloromethane/brine (50/50). The aqueous layer was extracted three times with dichloromethane. The combined organic layers were washed with brine, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The residue was then dissolved in ethanol and HCl in diethyl ether (1N, 9 mL) was added. The mixture was evaporated and the residue was purified on reverse phase (C18) flash chromatography (H2O, HCl N/1000, acetonitrile, 100/0 to 80/20) to afford 0.51 g (42%) of the desired product as a white solid: mp=220° C.; 1H NMR (400 MHZ, d6-DMSO) δ 8.38 (bs, 4H), 7.52 (m, 4H), 7.25 (d, 1H), 7.02 (s, 1H), 6.89 (d, 1H), 4.29 (s, 2H), 4.08 (t, 2H), 3.56 (m, 4H), 3.40 (t, 2H), 3.20 (s, 3H), 2.90 (t, 2H), 2.80 (t, 2H), 2.71 (s, 3H), 2.70 (s, 3H), 2.21 (m, 4H), 1.80 (m, 2H).

WORKUP

后处理

  1. customA white precipitate formed
  2. filtrationwas filtered off
  3. customThe filtrate was evaporated under reduced pressure
  4. customAfter completion of the reaction
  5. extractionThe aqueous layer was extracted three times with dichloromethane
  6. washThe combined organic layers were washed with brine
  7. dry with materialdried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. customevaporated under reduced pressure
  10. dissolutionThe residue was then dissolved in ethanol
  11. additionHCl in diethyl ether (1N, 9 mL) was added
  12. customThe mixture was evaporated
  13. customthe residue was purified on reverse phase (C18) flash chromatography (H2O, HCl N/1000, acetonitrile, 100/0 to 80/20)