反应详情

0.6 cm3 of acetic acid and 145 mg of iron(0) are added to a mixture of 146 mg of 5-{[6-(4-fluorophenyl)[1,2,4]triazolo[4,3-b]pyridazin-3-yl]sulphanyl}-2-nitroaniline in 7 cm3 of methanol. The reaction mixture is then stirred at reflux for 5 h 15 and then overnight at 20° C. before the addition of 10 cm3 of a 5N aqueous solution of sodium hydroxide and 10 cm3 of demineralized water. The mixture obtained is extracted with 2×30 cm3 of ethyl acetate. The combined organic phases are washed with 20 cm3 of water and then dried over magnesium sulphate and concentrated to dryness. The beige solid obtained is taken up in diethyl ether, spin-filter-dried, and then dried under vacuum. 71 mg of 4-{[6-(4-fluorophenyl)[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:

1. temperatureat reflux for 5 h 15
2. customThe mixture obtained
3. extractionis extracted with 2×30 cm3 of ethyl acetate
4. washThe combined organic phases are washed with 20 cm3 of water
5. dry with materialdried over magnesium sulphate
6. concentrationconcentrated to dryness
7. customThe beige solid obtained
8. customspin-filter-dried
9. customdried under vacuum