Method of preparing phenoxy alkanoic, alkenoic, and alkynoic acids and salts thereof via a dicarboxylate intermediate
View Patent ↗The present invention relates to a method of preparing a phenoxy alkanoic, alkenoic, or alkynoic acid or a salt thereof from a phenoxy containing compound via a dicarboxylate intermediate. The phenoxy alkanoic, alkenoic, and alkynoic acids and salts thereof prepared by this method are suitable for use in composition for delivering active agents via oral or other routes of administration to animals. Furthermore, the present invention relates to phenoxy dicarboxylic acids and their salts for delivering active agents, such as biologically or chemically active agents, to a target.
1. A method of preparing an alkylated phenoxy containing compound from a phenoxy containing compound, the method comprises the steps of (a) alkylating the phenoxy containing compound with a dicarboxylate alkylating agent to form a dicarboxylated phenoxy containing compound, and (b) decarboxylating the dicarboxylated phenoxy containing compound to form the alkylated phenoxy containing compound,
wherein the dicarboxylate alkylating agent has the formula
wherein
R 7 is a linear or branched C 7 -C 12 alkylene;
R 7 is optionally substituted with C 1 -C 4 alkyl, C 1 -C 4 alkenyl, oxygen, nitrogen, sulfur, halogen, —OH, C 1 -C 4 alkoxy, aryl, heteraryl, or vinyl;
R 7 is optionally interrupted with aryl, heteroaryl, vinyl, oxygen, nitrogen, or sulfur;
R 8 and R 11 are independently C 1 -C 4 alkyl or C 1 -C 4 haloalkyl; and
X is a suitable leaving group.
2. The method of claim 1 , wherein the molar ratio of phenoxy containing compound to dicarboxylate alkylating agent is from about 1:1 to about 1:0.5.
3. The method of claim 1 , wherein the alkylating step is performed in the presence of a base.
4. The method of claim 3 , wherein the molar ratio of base to phenoxy containing compound is greater than 1.
5. The method of claim 4 , wherein the base is pyridine, picoline, tetramethylguanidine, triethylamine, diisopropylethylamine, sodium bicarbonate, potassium bicarbonate, sodium carbonate, potassium carbonate, or any combination of any of the foregoing.
6. The method of claim 5 , wherein the base is sodium carbonate.
7. The method of claim 1 , wherein the alkylating step is performed at a temperature of from about 40 to about 80° C.
8. The method of claim 7 , wherein the alkylating step is performed at a temperature of from about 60 to about 80° C.
9. The method of claim 1 , further comprising hydrolyzing one or more carboxyl moieties of the alkylated phenoxy carboxylic acid compound after step (a) to form the free acid of the alkylated phenoxy carboxylic acid compound.
10. The method of claim 9 , wherein the decarboxylating step is performed after the hydrolyzing step.
11. The method of claim 1 , wherein decarboxylating comprises heating the dicarboxylated phenoxy containing compound in an organic solvent to a temperature ranging from about 140 to about 200° C.
12. The method of claim 11 , wherein the organic solvent has a boiling point of at least about 110° C.
13. The method of claim 11 , wherein the organic solvent is selected from xylenes, toluene, heptane, dimethyl acetamide, dimethyl formamide, methyl sulfoxide, isoparaffins, and any combination of any of the foregoing.
14. A method of preparing an alkylated phenoxy containing compound from a dicarboxylated phenoxy containing compound comprising the step of decarboxylating and hydrolyzing the dicarboxylated phenoxy containing compound to form the alkylated phenoxy containing compound, wherein the dicarboxylated phenoxy containing compound has the formula
where
R 1 , R 2 , R 3 , and R 4 are independently H, —OH, halogen, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 alkoxy, —C(O)R 12 , —NO 2 , —NR 9 R 10 , or —N + R 9 R 10 R 13 (R 14 ) − ;
R 5 is H, —OH, —NO 2 , halogen, —CF 3 , —R 15 R 16 , —N + R 15 R 16 R 17 (R 18 ) − , amide, C 1 -C 12 alkoxy, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, carbamate, carbonate, urea, or —C(O)R 19 ;
R 7 is a linear or branched C 1 -C 20 alkylene, C 2 -C 20 alkenylene, or C 2 -C 20 alkynylene;
R 7 is optionally substituted with C 1 -C 4 alkyl, C 1 -C 4 alkenyl, oxygen, nitrogen, sulfur, halogen, —OH, C 1 -C 4 alkoxy, aryl, heteraryl, or vinyl;
R 7 is optionally interrupted with aryl, heteroaryl, vinyl, oxygen, nitrogen, or sulfur;
R 8 and R 11 are independently C 1 -C 4 alkyl or C 1 -C 4 haloalkyl;
R 9 , R 10 , and R 13 are independently H or C 1 -C 10 alkyl;
R 12 is H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, or —NH 2 ;
R 14 and R 18 are independently a halide, hydroxide, sulfate, tetrafluoroborate, or phosphate;
R 15 , R 16 , and R 17 are independently H, C 1 -C 10 alkyl, C 1 -C 10 alkyl substituted with —COOH, C 2 -C 12 alkenyl, C 2 -C 12 alkenyl substituted with —COOH, —C(O)R 20 ;
R 19 is —H, C 1 -C 6 alkyl, or C 2 -C 12 alkenyl; and
R 20 is —OH, C 1 -C 10 alkyl, or C 2 -C 12 alkenyl,
wherein at least one of R 1 , R 2 , R 3 , R 4 and R 5 is —OH or alkoxy.
15. The method of claim 1 , wherein R 7 is a linear or branched C 7 -C 9 alkylene.
16. A method of preparing an alkylated phenoxy containing compound from a phenoxy containing compound, the method comprises the steps of (a) alkylating the phenoxy containing compound with a dicarboxylate alkylating agent to form a dicarboxylated phenoxy containing compound, and (b) decarboxylating the dicarboxylated phenoxy containing compound to form the alkylated phenoxy containing compound,
wherein the phenoxy containing compound has the formula
wherein
R 1 , R 2 , R 3 , and R 4 are independently H, —OH, halogen, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 alkoxy, —C(O)R 12 , —NO 2 , —NR 9 R 10 , or —N + R 9 R 10 R 13 (R 14 ) − ;
R 5 is H, —OH, —NO 2 , halogen, —CF 3 , —R 15 R 16 , —N + R 15 R 16 R 17 (R 18 ) − , amide, C 1 -C 12 alkoxy, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, carbamate, carbonate, urea, or —C(O)R 19 ;
R 6 is a leaving group;
R 9 , R 10 , and R 13 are independently H or C 1 -C 10 alkyl;
R 12 is H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, or —NH 2 ;
R 14 and R 18 are independently a halide, hydroxide, sulfate, tetrafluoroborate, or phosphate;
R 15 , R 16 , and R 17 are independently H, C 1 -C 10 alkyl, C 1 -C 10 alkyl substituted with —COOH, C 2 -C 12 alkenyl, C 2 -C 12 alkenyl substituted with —COOH, —C(O)R 20 ;
R 19 is —H, C 1 -C 6 alkyl, or C 2 -C 12 alkenyl; and
R 20 is —OH, C 1 -C 10 alkyl, or C 2 -C 12 alkenyl,
wherein at least one of R 1 , R 2 , R 3 , R 4 and R 5 is —OH or alkoxy.
17. The method of claim 16 , wherein the dicarboxylate phenoxy containing compound has the formula
where
R 1 , R 2 , R 3 , and R 4 are independently H, —OH, halogen, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 alkoxy, —C(O)R 12 , —NO 2 , —NR 9 R 10 , or —N + R 9 R 10 R 13 (R 14 )—;
R 5 is H, —OH, —NO 2 , halogen, —CF 3 , —R 15 R 16 , —N + R 15 R 16 R 17 (R 18 ) − , amide, C 1 -C 12 alkoxy, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, carbamate, carbonate, urea, or —C(O)R 19 ;
R 7 is a linear or branched, C 1 -C 20 alkylene, C 2 -C 20 alkenylene, or C 2 -C 20 alkynylene;
R 7 is optionally substituted with C 1 -C 4 alkyl, C 1 -C 4 alkenyl, oxygen, nitrogen, sulfur, halogen, —OH, C 1 -C 4 alkoxy, aryl, heteraryl, or vinyl;
R 7 is optionally interrupted with aryl, heteroaryl, vinyl, oxygen, nitrogen, or sulfur;
R 8 and R 11 are independently C 1 -C 4 alkyl or C 1 -C 4 haloalkyl;
R 9 , R 10 , and R 13 are independently H or C 1 -C 10 alkyl;
R 12 is H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, or —NH 2 ;
R 14 and R 18 are independently a halide, hydroxide, sulfate, tetrafluoroborate, or phosphate;
R 15 , R 16 , and R 17 are independently H, C 1 -C 10 alkyl, C 1 -C 10 alkyl substituted with —COOH, C 2 -C 12 alkenyl, C 2 -C 12 alkenyl substituted with —COOH, —C(O)R 20 ;
R 19 is —H, C 1 -C 6 alkyl, or C 2 -C 12 alkenyl; and
R 20 is —OH, C 1 -C 10 alkyl, or C 2 -C 12 alkenyl,
wherein at least one of R 1 , R 2 , R 3 , R 4 and R 5 is —OH or alkoxy.
18. The method of claim 16 , wherein the alkylated phenoxy containing compound has the formula
where
R 1 , R 2 , R 3 , and R 4 are independently H, —OH, halogen, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, C 1 -C 4 alkoxy, —C(O)R 12 , —NO 2 , —NR 9 R 10 , or —N + R 9 R 10 R 13 (R 14 ) − ;
R 5 is H, —OH, —NO 2 , halogen, —CF 3 , —R 15 R 16 , —N + R 15 R 16 R 17 (R 18 ) − , amide, C 1 -C 12 alkoxy, C 1 -C 12 alkyl, C 2 -C 12 alkenyl, carbamate, carbonate, urea, or —C(O)R 19 ;
R 7 is a linear or branched, C 1 -C 20 alkylene, C 2 -C 20 alkenylene, or C 2 -C 20 alkynylene;
R 7 is optionally substituted with C 1 -C 4 alkyl, C 1 -C 4 alkenyl, oxygen, nitrogen, sulfur, halogen, —OH, C 1 -C 4 alkoxy, aryl, heteraryl, or vinyl;
R 7 is optionally interrupted with aryl, heteroaryl, vinyl, oxygen, nitrogen, or sulfur;
R 9 , R 10 , and R 13 are independently H or C 1 -C 10 alkyl;
R 12 is H, C 1 -C 4 alkyl, C 2 -C 4 alkenyl, or —NH 2 ;
R 14 and R 18 are independently a halide, hydroxide, sulfate, tetrafluoroborate, or phosphate;
R 15 , R 16 , and R 17 are independently H, C 1 -C 10 alkyl, C 1 -C 10 alkyl substituted with —COOH, C 2 -C 12 alkenyl, C 2 -C 12 alkenyl substituted with —COOH, —C(O)R 20 ;
R 19 is —H, C 1 -C 6 alkyl, or C 2 -C 12 alkenyl; and
R 20 is —OH, C 1 -C 10 alkyl, or C 2 -C 12 alkenyl,
wherein at least one of R 1 , R 2 , R 3 , R 4 and R 5 is —OH or alkoxy.