反应详情

1.0 g (0.004 mol) of 2-(2-methoxyethoxymethyl)-6-trifluoromethylnicotinic acid is dissolved in 10 ml of oxalyl chloride. Three drops of dimnethylformamide are added, and the mixture is stirred at room temperature for 1 hour. The mixture is then concentrated using a rotary evaporator, and the residue (2-(2-methoxyethoxymethyl)-6-trifluoromethylnicotinoyl chloride) is taken up in 10 ml of methylene chloride. At a temperature of 0° C., 0.84 ml (0.006 mol) of triethylamine and 0.45 g (0.004 mol) of 2,5dimethyl-2,4-dihydropyrazol-3one are added. After 2 hours at a temperature of 22° C., the solvent is removed using a vacuum rotary evaporator, and the residue that remains is dissolved in 10 ml of acetonitrile and, to rearrange the intermediate (2,5-dimethyl-2H-pyrazol-3-yl 2-(2-methoxyethoxymethyl)-6-trifluoromethylnicotinate), admixed with 0.1 ml of acetone cyanohydrin and 1.13 ml (0.008 mol) of triethylamine. The reaction solution is stirred at room temperature for four hours and then concentrated. The syrup that remains is chromatographed on silica gel. The viscous oil obtained by eluting with a mixture of toluene, ethyl alcohol, dioxane, triethylamine and water (100:40:20:20:5 parts by volume) is dissolved in ethyl acetate and washed successively with 10% hydrochloric acid and water. The organic solution is dried over Na2SO4 and concentrated, giving 0.93 g of (5-hydroxy-1,3-dimethyl-1H-pyrazol-4yl)-[2-(2-methoxyethoxymethyl)-6-trifluoromethylpyridin-3-yl]methanone in the form of a viscous oil.

1. additionThree drops of dimnethylformamide are added
2. concentrationThe mixture is then concentrated
3. customa rotary evaporator
4. waitAfter 2 hours at a temperature of 22° C.
5. customthe solvent is removed
6. customa vacuum rotary evaporator
7. dissolutionthe residue that remains is dissolved in 10 ml of acetonitrile
8. stirringThe reaction solution is stirred at room temperature for four hours
9. concentrationconcentrated
10. customThe syrup that remains is chromatographed on silica gel
11. customThe viscous oil obtained
12. washby eluting with a mixture of toluene, ethyl alcohol, dioxane, triethylamine and water (100:40:20:20:5 parts by volume)
13. dissolutionis dissolved in ethyl acetate
14. washwashed successively with 10% hydrochloric acid and water
15. dry with materialThe organic solution is dried over Na2SO4
16. concentrationconcentrated