Patent Application
20210078941
This application claims priority of Chinese patent application submitted to the Chinese Patent Office on Sep. 7, 2017, with the application number 201710800788.8, and entitled “Preparation Method For Substituted Phenylacetic Acid Derivatives”. All of its contents are incorporated in this application by reference.
The invention belongs to the field of pharmaceutical manufacturing in reference to a preparation method of substituted phenylacetic acid derivatives, specifically relates to 2-(4-((2-oxocyclopentyl)methyl)phenyl)propanoic acid.
Substituted phenylacetic acid derivatives are disclosed in U.S. Pat. No. 4,161,538, with good pharmaceutical activity of anti-inflammatory, analgesic and antipyretic. the structure is shown as follows:
When A is oxygen and n=1 meanwhile and R is methyl group, in the above general formula structure, the representative substituted phenylacetic acid is loxoprofen. The structure is shown as follows:
Loxoprofen is a non-steroidal anti-inflammatory type drug of with propionic acid moiety. The propionic acid derivatives drug family also include ibuprofen and naproxen et al. The loxoprofen has been launched in Brazil, Mexico and Japan in the form of sodium salt wherein honored by Sankyo. The trade names of the loxoprofen sodium in Japan, Argentina and India are Loxonin, Oxeno and Loxomac respectively. Loxoprofen sodium is used for oral administration in these countries, and the injection administration form is approved to sell in Japan in January 2006.
In the U.S. Pat. No. 4,161,538, it disclosed the following synthetic route to prepare loxoprofen, wherein n=1, R1 represents methyl group.
In the U.S. Pat. No. 5,681,979, it disclosed the compound with the following formula:
However, this formula was not used for the preparation of loxoprofen in this patent.
Owing to the good medical prospects of loxoprofen sodium, it is necessary to develop more excellent process for the preparation of loxoprofen.
The present invention provides a synthetic process of substituted phenylacetic acid derivatives including loxoprofen. The novel process can synthesize the substituted phenylacetic acid and its derivatives in low-cost and high yield.
Firstly, the present invention provides an intermediate compound of general formula G and G1:
wherein R1 is hydrogen or short chain alkyl groups; R2 is halogen, CN, OH, —CH2OH, —CHO, CH3NO2, ester group, —NR4R5, OTf, OTs, OMs, —C═CR6, or —C≡CR7, wherein R4, R5, R6, R7 are short chain alkyl groups; Z is cyclopentanone group and its precursor form selected from
R3 is short chain alkyl groups; The definition of L2 is same with R2. L3 is a suitable leaving group selected from halogen, OH, OMs, OTs, OTf and the like, or organometallic groups.
Secondly, the invention further provides a method for preparing general formula G and G1 compounds by the reaction of 1,4-di-halobenzyl compounds or disubstituted benzyl compounds with the precursor form of cyclopentanone group. The reaction scheme is shown as follows:
Wherein X is halogen, L1 is a suitable leaving group selected from halogen, OH, OMs, OTs, OTf and the like; L2 is same with the definition of R2; Z represents cyclopentanone group and the precursor form of cyclopentanone group, the precursor form is
L3 is a suitable leaving group selected from halogen, OH, OMs, OTs, OTf and the like, or organometallic groups.
The preparation of above disubstituted benzyl compounds is carried out starting from 1,4-di-halobenzyl compounds or 1,4-dihydroxylbenzyl alcohol. The reaction scheme is shown as follows:
Wherein X is halogen, R3 is short chain alkyl groups, L1 or L2 is a suitable leaving group selected from OMs, OTs, OTf, CH3NO2, —CN, —C≡C or
the reaction is shown as follows
Wherein X is halogen, R3 is short chain alkyl groups.
The above formula G and formula G1 for the preparation of loxoprofen include the decarboxylation step.
The sequence of the decarboxylation step can be the first step, the second step or the third step, which means that the sequence is changeable, and it is the best sequence that the decarboxylation ahead of the cyanation step.
The above formula G and formula G1 for the preparation of loxoprofen include the step of transforming the precursor form of cyclopentanone group to cyclopentanone. The sequence of the transformation step can be the first step, the second step or the third step.
The invention further provides compound of formula III, the structure is shown as follows:
Wherein R1 is H or short chain alkyl groups; R2 is the group selected from halogen, —CN, —OH, —CH2OH, —CHO, CH3NO2, ester groups, —NR4R5, OTf, OTs, OMs, —C═CR6, —C≡CR7 and the like, wherein R4, R5, R6, R7 is alkyl groups; R3 is short chain alkyl groups.
In above formula III, when R1 is H, R2 is halogen, the formula of the compound is shown as follows:
The definition of R3 is the same as above.
The above compound of formula III-1 is prepared by the reaction of 1,4-bis(halomethyl)benzene and alkyl 2-oxocyclopentanecarboxylate, the reaction is shown as follows:
Wherein X is halogen, R1 is H, the definition of R3 is the same as above.
In above formula III, when R1 is H, R2 is OH, the formula of the compound is shown as follows:
The above compound of formula III-1′ is prepared by the reaction of 1,4-phenylenedimethanol and alkyl 2-oxocyclopentanecarboxylate, the reaction is shown as follows:
The definition of R3 is the same as above.
In the above formula III, R2 can be prepared from compound of formula III-1 and compound of formula III-1′. Alternatively, treatment of 1,4-phenylenedimethanol or 1,4-bis(halomethyl)benzene with sulfonation, amination or homocoupling reaction, then proceeding substitution. Or it can be prepared by Grignard reaction, and further react with carbon dioxide. The sulfonation reaction is shown as follows:
In above formula III, when R2 is cyano group, the formula of the compound is shown as follows:
Wherein the definition of R3 is the same as above.
The above compound of formula III-2 is prepared by the cyanation reaction of formula III-1, the reaction is shown as follows:
Wherein the definition of R3 is the same as above.
In above formula III, when R1 is short chain alkyl group, the formula of the compound is shown as follows:
Wherein the definition of R3 is the same as above.
The above compound of formula III-3 is prepared by alkylation of formula III-2, the reaction is shown as follows:
Wherein the definition of R1 and R3 are the same as above.
In addition, the above three steps such as {circle around (1)} substitution reaction of alkyl 2-oxocyclopentanecarboxylate, {circle around (2)} cyanation reaction, {circle around (3)} alkylation reaction, the reaction sequence can adopt in any sequence. For example, the sequence can be {circle around (1)}{circle around (2)}{circle around (3)}, {circle around (1)}{circle around (3)}{circle around (2)}, {circle around (3)}{circle around (2)}{circle around (1)}, {circle around (2)}{circle around (1)}{circle around (3)} or {circle around (2)}{circle around (3)}{circle around (1)}.
When the reaction sequence is {circle around (3)}{circle around (2)}{circle around (1)}, the reaction is shown as follows:
Wherein X is halogen, the definition of R1 and R3 are the same as above.
When the reaction sequence is {circle around (2)}{circle around (3)}{circle around (1)}, the reaction is shown as follows:
Wherein X is halogen, the definition of R1 and R3 are the same as above.
In the present invention, the substitution of alkyl 2-oxocyclopentanecarboxylate is carried out under base condition, the base is potassium carbonate, sodium carbonate, sodium alkoxide and the like.
In the present invention, the cyanation reaction is proceeded by using common cyanating reagent, such as NaCN, KCN, CuCN2 and the like.
In the present invention, the alkylation reaction is proceeded by using common alkylating reagent, such as dimethyl carbonate, dimethyl sulfate, trimethoxymethane, alkyl halide and the like.
The above reaction in the invention can be carried out under the action of the organic solvent. The organic solvent may be the solvent commonly used in substitution, alkylation and cyanation reaction. The organic solvent include DMF, DMSO, NMP, 1,4-dioxane, methanol, ethanol, ethyl acetate, THF, MTBE, and acetonitrile et al.
The intermediate compound of this invention is used for preparing loxoprofen. It is best that the compound of formula III-3 can be hydrolyzed to produce related product, the reaction is shown as follows:
The definition of R1 and R3 are the same as above, when R1 is methyl, the structure is loxoprofen.
The hydrolytic reagent uses for the hydrolysis reaction is an acid commonly used in this field, which can be an organic or inorganic acid, such as sulfuric acid, hydrochloric acid or trifluoroacetic acid.
The invention uses 1,4-bis(halomethyl)benzene compound as the starting material, and through substitution reaction, cyanation reaction and alkylation reaction in any order to produce the intermediate of formula III,
Wherein R1 is H or short chain alkyl groups, R2 is halogen or cyano group, R3 is low-substituted alkyl groups.
When R1 is methyl, R2 is cyano group, R3 is short chain alkyl groups, the compound of formula III-3 can be hydrolyzed to produce loxoprofen.
The invention discloses a preparation method for loxoprofen-like compounds, including a step for conversion of a cyclopentanone group in the form of a precursor to cyclopentanone. For example, the commonly used cyclization reaction in this field is used. The precursor compound of loxoprofen is used to prepare loxoprofen compounds.
On the other hand, the invention also provides a preparation method of loxoprofen compounds prepared by substitution reaction, decarboxylation reaction, cyanation reaction and alkylation reaction of 1,4-bis(halomethyl)benzene, the reaction is shown as follows:
Wherein X is halogen, the definition of R1 and R3 are the same as above.
The preparation method provided by the invention has the following beneficial effects. Firstly, it provides an alternative method for preparing derivatives of substituted phenylacetic acid. Secondly, the preparation method of the invention is not reported by any prior arts. It is completely different from the compound used in the U.S. Pat. No. 5,681,979. Thirdly, in the reaction process, using 1,4-bis(halomethyl)benzene as starting material is cheap and convenient. At last, the preparation method provided by the invention is suitable for industrial scale production and has certain economic benefits.
1,4-bis(chloromethyl)benzene (30 g, 0.17 mol), DMF (150 g, 4.74 vol) and sodium carbonate (19.8 g, 0.19 mol) were added to a 250 mL round bottom flask. The reaction mixture was stirred and heated to 60° C. Then methyl 2-oxocyclopentanecarboxylate (22.1 g, 0.16 mol) was added to the reaction mixture dropwise in one hour, afterwards maintain the reaction temperature for 30 minutes. Then the reaction mixture was cooled to 25° C., filtrated and mixed the mother liquor with water. The solid is separated. The mother liquor was extracted with EtOAc. Concentrate the organic phase to give the compound of Formula III-1 (47.0 g) with a yield of 83.3% (HPLC purity of 83.3%) (wherein R1 is H, R2 is Cl, R3 is methyl).
The compound of Formula III-1 (wherein R1 is H, R2 is Cl, R3 is methyl) (10 g, 0.036 mol), acetonitrile (50 g, 5 vol), NaCN (1.9 g, 0.039 mol) were added to a 100 mL round bottom flask. The reaction mixture was refluxed. When starting material disappeared, the reaction mixture was cooled to 25° C. After filtration and evaporation, adding EtOAc and water while stirring. The organic layer was separated and evaporated to give the compound of Formula III-2 (9.8 g) with the yield of 94.7% (HPLC purity of 93.7%) (wherein R1 is H, R2 is CN, R3 is methyl).
The compound of Formula III-2 (wherein R1 is H, R2 is CN, R3 is methyl) (30 g, 0.11 mol), dimethyl carbonate (24.8 g, 0.28 mol), K2CO3 (1.5 g, 0.011 mol), and tetrabutylammonium bromide (1.8 g, 0.006 mol) were added to an autoclave. The reaction mixture was stirred under 130-140° C. for 10 h. The pressure of the autoclave is approximately 0.3 Mpa. Then the reaction mixture was cooled to 28° C., quenched by adding small amount of benzaldehyde. Filtration and the filter cake was washed by EtOAc, 1 N HCl and water. The organic layer was separated and evaporated to give the compound of Formula III-3 (32.6 g) with the yield of 80.5% (HPLC purity of 78.1%) (wherein R1 is methyl, R2 is CN, R3 is methyl).
The compound of Formula III-3 (wherein R1 is methyl, R2 is CN, R3 is methyl) (18.5 g, 0.065 mol) and H2SO4 (80 wt. % solution in water, 16 g, 0.13 mol) were added to a 100 mL round bottom flask. The reaction mixture was stirred under 80-90° C. for 5 h. When the starting material disappeared, the reaction mixture was cooled to 25° C., adding EtOAc to extract. The organic layer was washed by water and evaporated to give loxoprofen with a yield of 96.2% (HPLC purity of 93.7%).
The compound of Formula III-1 (wherein X is Cl, R3 is methyl) (21 g, 0.075 mol), AcOH (37 mL, 2 vol) and HCl (35 wt. % solution in water, 63 mL, 3 vol) were added to a 100 mL round bottom flask. The reaction mixture was stirred under 90-95° C. for 2.5-3.5 h. When starting material disappeared, the reaction mixture was cooled to 15-25° C. afterwards added water and EtOAc. The organic layer was washed with 5% NaHCO3 solution, saturated NaCl solution and water. The organic layer was separated and evaporated to give the compound of Formula IV (19.7 g) with the yield of 96.1% (HPLC purity of 81.4%) (wherein X is Cl).
The compound of Formula IV (wherein X is Cl) (10 g, 0.045 mol), acetonitrile (50 g, 5 vol), NaCN (2.4 g, 0.049 mol) were added to a 100 mL round bottom flask. The reaction mixture was refluxed. When starting material disappeared, the reaction mixture was cooled to 25° C. After filtration and evaporation, adding EtOAc and water to stir. The organic layer was washed by saturated NaCl solution and water; Then the organic layer was separated and evaporated to give the compound of Formula V (9.68 g) with the yield of 94.7% (HPLC purity of 93.7%).
The compound of Formula V (30 g, 0.14 mol), dimethyl carbonate (31.5 g, 0.35 mol), K2CO3 (1.5 g, 0.011 mol), and tetrabutylammonium bromide (1.8 g, 0.006 mol) were added to a 100 mL autoclave. The reaction mixture was stirred under 130-140° C. for 10 h. The pressure of autoclave is approximately 0.3 Mpa. Then the reaction mixture was cooled to 28° C., and quenched by adding small amount of benzaldehyde. Filtration and the filter cake was washed by EtOAc, 1 N HCl and water. The organic layer was separated and evaporated to give the compound of Formula VI (31.7 g) with a yield of 80.4% (HPLC purity of 81.1%) (wherein R1 is H).
The compound of Formula VI (wherein R1H) (18.5 g, 0.081 mol) and AcOH (37 mL, 2 vol) and HCl (35 wt. % solution in water, 55.5 mL, 3 vol) were added to a 100 mL round bottom flask. The reaction mixture was stirred under 90-95° C. for 2.5-3.5 h. When starting material was disappeared, the reaction mixture was cooled to 15-25° C. and was added water and EtOAc. The organic layer was washed with saturated NaCl solution and water; The organic layer was separated and evaporated to give loxoprofen (20.5 g) with the yield of 96.2% (HPLC purity of 93.7%).
| Number | Date | Country | Kind |
|---|---|---|---|
| 201710800788.8 | Sep 2017 | CN | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/CN2018/099121 | 8/7/2018 | WO | 00 |
