HRID1878762

反应详情

EQUATION

反应方程式

HRID 1878762 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
23 °C

PROCEDURE

实验过程

A mixture of 6-phenyl-3(2h)-pyridazinone (306 mg, 1.78 mmol), 1-(2-bromo-ethyl)-4-fluoro-benzene (397 μl, 1.95 mmol), and potassium carbonate, −325 mesh (614 mg, 4.44 μmol) in DMF (5 mL) was stirred for 3 days at 23° C. The mixture was partitioned between CH2Cl2 (30 mL) and 5% NaHCO3 (15 mL). The aqueous was further extracted with CH2Cl2 (2×5 mL) and the combined organics was dried over MgSO4, and concentrated under reduced pressure To give a clear oil. MS (ESI pos. ion) m/z (MH+): 295. Calc'd exact mass for C18H15FN2O: 294. 1H NMR (400 MHz, Chloroform-d) δ ppm 3.16 (t, J=7.53 Hz, 2 H) 4.47 (t, J=7.78 Hz, 2 H) 6.88-7.06 (m, 3 H) 7.15-7.25 (m, 2 H) 7.35-7.53 (m, 3 H) 7.59-7.74 (m, 3 H). 13C NMR (101 MHz, Chloroform-d) δ ppm 32.60, 52.08, 114.07, 114.28, 124.73, 127.81, 128.32, 128.89, 129.01, 129.20, 129.27, 132.63, 132.67, 133.57, 143.32, 158.60, 159.33, 161.76.

WORKUP

后处理

  1. customThe mixture was partitioned between CH2Cl2 (30 mL) and 5% NaHCO3 (15 mL)
  2. extractionThe aqueous was further extracted with CH2Cl2 (2×5 mL)
  3. dry with materialthe combined organics was dried over MgSO4
  4. concentrationconcentrated under reduced pressure
  5. customTo give a clear oil