Preparation methods of azoxystrobin and its analogs
Preparation method of a compound of general formula (I) comprises the following steps: (1) a compound of general formula (II) reacts with a formylating agent in an aprotic solvent at a temperature between −20° C. and 200° C. in the presence of a Lewis acid, then an organic base is added to promote the reaction to obtain an intermediate product; (2) the above intermediate product reacts with a methylating agent in the presence of an alkali at a temperature between −20° C. and 100° C. to obtain the compound of formula (I).
1. A method for preparing a compound of general formula (I),
wherein R 1 is 6-(2-cyanophenoxypyrimidin)-4-yl or pyrimidin-4-yl substituted by a halogen atom at site 6, the method comprising the steps of:
(1) reacting a compound of general formula (II) with a formylating agent in an aprotic solvent in the presence of a Lewis acid at a temperature ranging from −20° C. to 200° C., and adding an organic base to promote the reaction so that an intermediate product is obtained,
wherein R 1 has the same definition as R 1 in general formula (I);
(2) isolating the intermediate product produced by step 1;
(3) reacting the isolated intermediate product obtained in step (2) with a methylating agent in the presence of an alkali at a temperature ranging from −20° C. to 100° C. to obtain the compound of general formula (I).
2. A method according to claim 1 , wherein the Lewis acid is selected from the group consisting of titanium tetrachloride, aluminum trichloride, methylaluminum chloride, tin chloride, ferric chloride, zinc chloride, boron trifluoride ethyl ether and combinations thereof.
3. A method according to claim 1 , wherein the organic base includes amine and metal alkoxide.
4. A method according to claim 3 , wherein the organic base is a tertiary amine.
5. A method according to claim 1 , wherein the formylating agent includes methyl formate, ethyl formate, trimethyl orthoformate, triethyl orthoformate, and combinations thereof.
6. A method according to claim 1 , wherein the alkali is comprised of sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, sodium bicarbonate, potassium bicarbonate, sodium methoxide, sodium ethoxide, sodium tertiary butoxide and combinations thereof.
7. A method according to claim 1 , wherein the methylating agent is comprised of dimethyl sulfate, trimethyl orthoformate, chloromethane, bromomethane, iodomethane and combinations thereof.
8. A method according to claim 1 , wherein the step (1) is conducted at a temperature ranging from −20° C. to 100° C.
9. A method according to claim 1 , wherein the aprotic solvent is comprised of a halogenated hydrocarbon, benzene, saturated hydrocarbon, dimethyl sulfoxide and combination thereof.
10. A method according to claim 1 , wherein the methylation reaction in step (3) is conducted in a solvent selected from the group consisting of benzene, toluene, chlorobenzene, dichloromethane, dichloroethane, methanol, ethanol, butanol, ethyl ether, 1,2-dimethoxyethane, tetrahydrofuran, acetone, methyl ethyl ketone, methyl isobutyl ketone, ethyl acetate, isopropyl acetate, propyl acetate, butyl acetate and combinations thereof.
11. The method of claim 4 wherein the tertiary amine is selected from the group of trimethyl amine, triethyl amine, tributyl amine, diisopropylethyl amine and combinations thereof.
12. The method of claim 8 wherein the temperature of step (1) is between −10° C. and 50° C.
13. The method of claim 12 wherein the temperature of step (1) is between −5° C. and 5° C.
14. The method of claim 1 wherein the temperature of step (3) is between −10° C. and 80° C.
15. The method of claim 14 wherein the temperature of step (3) is between 10° C. and 60° C.