HRID1431095

反应详情

EQUATION

反应方程式

HRID 1431095 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

3

CONDITIONS

反应条件

温度
100 °C

PROCEDURE

实验过程

In a 250 mL round-bottomed flask, 5-(ethylsulfonyl)pyridin-2-amine (183 mg, 983 μmol), 4-bromo-6-chloro-2-methylpyridazin-3(2H)-one (263 mg, 1.18 mmol), xantphos (85.3 mg, 147 μmol) and Cs2CO3 (960 mg, 2.95 mmol) were combined with dioxane (10 mL) to give a light brown suspension. The flask was evacuated and filled with argon. Pd2(dba)3 (45.0 mg, 49.1 μmol) was added and the reaction mixture was stirred at 100° C. for 20 h under argon. Cooled to 25° C. and diluted with DCM. The reaction mixture was filtered through celite and the filter cake was washed with DCM until clear. The filtrate was concentrated and purified by flash chromatography (silica gel, 40 g, 0% to 2% MeOH in DCM) to afford 0.323 g (25%) of the title compound as a tan powder. (M+H)+=329/331 m/e. 1H NMR (300 MHz, DMSO-d6) δ: 10.18 (s, 1H), 8.78 (d, J=2.3 Hz, 1H), 8.12 (dd, J=8.9, 2.5 Hz, 1H), 7.74 (d, J=9.1 Hz, 1H), 3.69 (s, 3H), 3.32 (q, J=7.4 Hz, 2H), 1.11 (t, J=7.4 Hz, 3H).

WORKUP

后处理

  1. customto give a light brown suspension
  2. customThe flask was evacuated
  3. additionfilled with argon
  4. temperatureCooled to 25° C.
  5. filtrationThe reaction mixture was filtered through celite
  6. washthe filter cake was washed with DCM until clear
  7. concentrationThe filtrate was concentrated
  8. custompurified by flash chromatography (silica gel, 40 g, 0% to 2% MeOH in DCM)