HRID1070661

反应详情

EQUATION

反应方程式

HRID 1070661 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
-75 °C

PROCEDURE

实验过程

4-((4-Bromo-5-chloro-2-thienyl)methyl)morpholine (Preparation 62, 7.65 g) is dissolved in diethyl ether (75 mL) and is cooled to −75° C. A solution of n-butyllithium (2.5 M in hexane, 11.0 mL) is added via addition funnel, maintaining the temperature below −68° C. The reaction is stirred for 15 minutes at −70° C. and allowed to warm to 0° C. A solution of N-methoxy-N-methylacetamide (3.09 g) in ether (5 mL) is added via addition funnel, maintaining the temperature below 5° C. The reaction is stirred at 0° C. for 1 h and allowed to warm to rt. The reaction is quenched with saturated aq. NH4Cl solution (50 mL) and made basic with sat. aq. NaHCO3. The mixture is extracted with ethyl acetate (3×125 mL). The combined organic layers are washed with sat. NaHCO3 (2×100 mL) and brine (50 mL). The combined aqueous washes are back-extracted with ethyl acetate (100 mL). The organic layers are combined, dried (Na2SO4), and concentrated in vacuo to a yellow oil. The crude product is chromatographed, eluting with 25% ethyl acetate/heptane to afford 2.42 g (37%) of the title compound. Physical characteristics: 1H NMR (400 MHz, DMSO-d6) δ7.33, 3.64, 3.58, 2.51; IR (liq.) 2854, 2809, 1673, 1456, 1372, 1351, 1328, 1243, 1212, 1165, 1118, 1034, 1008, 867, 618 cm−1; HRMS (FAB) m/z 260.0506 (C11H14ClNO2S+H). Anal. Found: C, 50.77; H, 5.51; N, 5.35; Cl, 13.24; S, 12.00.

WORKUP

后处理

  1. temperaturemaintaining the temperature below −68° C
  2. temperatureto warm to 0° C
  3. temperaturemaintaining the temperature below 5° C
  4. stirringThe reaction is stirred at 0° C. for 1 h
  5. temperatureto warm to rt
  6. customThe reaction is quenched with saturated aq. NH4Cl solution (50 mL)
  7. extractionThe mixture is extracted with ethyl acetate (3×125 mL)
  8. washThe combined organic layers are washed with sat. NaHCO3 (2×100 mL) and brine (50 mL)
  9. extractionThe combined aqueous washes are back-extracted with ethyl acetate (100 mL)
  10. dry with materialdried (Na2SO4)
  11. concentrationconcentrated in vacuo to a yellow oil
  12. customThe crude product is chromatographed
  13. washeluting with 25% ethyl acetate/heptane