HRID1035749

反应详情

EQUATION

反应方程式

HRID 1035749 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
20 °C

PROCEDURE

实验过程

422 mg of zinc(0) are added to a solution of 240 mg of 5-{[6-(4-fluorophenyl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}-2-nitroaniline in 13 cm3 of acetic acid and the resulting mixture is stirred for 1 h at 20° C. 30 cm3 of water are then added to the reaction mixture, which is changed to an alkaline medium by adding 16 cm3 of an aqueous solution of ammonia at 28%. The mixture obtained is extracted with ethyl acetate. The resulting organic phase is washed successively with a saturated aqueous solution of sodium hydrogen carbonate and with a saturated aqueous solution of sodium chloride and is then dried over magnesium sulphate, filtered and evaporated to dryness. The residue is made into a paste in ether, filtered, and then dried under vacuum at 20° C. 479 mg of 4-{[6-(4-fluorophenyl)-7,8-dihydro[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}benzene-1,2-diamine are thus obtained, the characteristics of which are as follows:

WORKUP

后处理

  1. customThe mixture obtained
  2. extractionis extracted with ethyl acetate
  3. washThe resulting organic phase is washed successively with a saturated aqueous solution of sodium hydrogen carbonate and with a saturated aqueous solution of sodium chloride
  4. dry with materialis then dried over magnesium sulphate
  5. filtrationfiltered
  6. customevaporated to dryness
  7. filtrationfiltered
  8. customdried under vacuum at 20° C