Patent Application
20080306270
The present invention relates to a process for the preparation of Montelukast, as well as to some new intermediates useful in such preparation process.
Montelukast, is the International Non-proprietary Name (INN) of 1-[[[(1R)-1-[3-[(1E)-2-(7-chloro-2-quinolinyl)ethenyl]phenyl]-3-[2-(1-hydroxy-1-methylethyl)phenyl]propyl]sulfanyl]methyl]cyclopropaneacetic acid, and CAS No. 158966-92-8. Montelukast monosodium salt (CAS No 151767-02-1) is currently used in treatment of asthma, inflammation, angina, cerebral spasm, glomerular nephritis, hepatitis, endotoxemia, uveitis and allograft rejection.
The structure of Montelukast monosodium salt corresponds to formula (I):
Different synthetic strategies for the preparation of Montelukast and its salts are known. EP 480.717 discloses certain substituted quinolone compounds including Montelukast sodium salt, methods for their preparation, and pharmaceutical compositions using these compounds. Several preparation processes of Montelukast sodium are reported in this document. Example 161 relates to the preparation of Montelukast sodium salt. According to this Example, preparation of Montelukast sodium salt proceeds through its corresponding methyl ester, whose preparation comprises sodium hydride or cesium carbonate assisted coupling of methyl-1-(mercaptomethyl)-cyclopropaneacetate with the protected mesylate (2-(2-(2-(3(S)-(3-(2-(7-chloro-2-quinolinyl)-ethenyl)phenyl)-3-(methanesulfonyloxy)propyl)phenyl)-2-propoxy)tetrahydropyran, generated in situ. The methyl ester thus obtained is hydrolyzed to the Montelukast free acid which is then converted directly to the sodium salt. This process is not particularly suitable for large scale production because it requires tedious chromatographic purification of the methyl ester intermediate and/or the final product, and yields of intermediates and final product are low. Another process for the preparation of Montelukast sodium salt comprises the reaction of the thioacetate with the following formula:
with hydrazine or an alkoxide, followed by reaction with an appropriate 1-substituted cyclopropyl acetate, followed by deprotection of the tertiary alcohol to afford Montelukast.
EP 737.186 relates to a process for the preparation of Montelukast or its salts thereof, which comprises reacting the dilithium dianion of 1-(mercaptomethyl)cyclopropaneacetic acid with the corresponding mesylate alcohol ((2-(2-(2-(3(S)-(3-(2-(7-chloro-2-quinolinyl)-ethenyl)phenyl)-3-(methanesulfonyloxy)propyl)phenyl)-2-propanol), to obtain Montelukast, which is further converted to the corresponding sodium salt via dicyclohexyl amine salt.
CN 1.420.113 A relates to a process for the preparation of Montelukast or its sodium salt thereof, which comprises the reaction of the thioacetic acid ester with the following formula:
and methyl magnesium iodide to afford the thiol alcohol with the following formula:
Montelukast is synthesized by reaction between the mentioned above thiol alcohol intermediate and appropriate 1-halo substituted cyclopropyl acetate, followed by hydrolysis of the ester group.
US 2005107612 describes a process for the preparation of Montelukast or a salt thereof, which comprises reacting a late intermediate compound which is 2-[1-[1-R-3-[2-(7 chloro quinolin-2-yl) vinyl [phenyl]-3-[2-methoxy carbonyl phenyl]propyl sulfonyl methyl]cyclopropyl]acetic acid or a salt thereof with methyl magnesium chloride or methyl magnesium bromide.
Finally, US 2005/0234241 describes a process for the preparation of Montelukast based on the reaction of 2-(2-(3(S)-3-(2-(7-chloro-2-quinolinyl)ethenyl)phenyl)-3-sulfonyl oxy propyl)phenyl)-2-propanol with a salt of 1-(mercaptomethyl)cyclopropane acetonitrile or of 1-(mercaptomethyl)cyclopropane acetamide, followed by an hydrolysis reaction with a base.
Although certain processes for the preparation of Montelukast are known, there continue being a need for new processes for the preparation of Montelukast and its salts.
Inventors have found a new efficient preparation process of Montelukast from new intermediate compounds, which proceeds with high yields and without the need of chromatographic purifications.
Thus, according to one aspect of the present invention, it is provided a preparation process of Montelukast (I), or a pharmaceutically acceptable salt, or a solvate thereof, including a hydrate,
which comprises the steps of: (a) reacting a compound of formula (IV) wherein R1 is a radical selected from (C1-C4)-alkyl, phenyl, and phenyl mono- or disubstituted by a (C1-C4)-alkyl radical, with an alkaline metal cyanide, to give a compound of formula (III) and isolating said compound (III) as free base or as a salt thereof;
(b) Optionally, hydrolysing the compound of formula (III) obtained in step (a) in reaction conditions that lead to a compound of formula (II) and isolating said compound (II) from the reaction medium;
(c) submitting the compound obtained in step (a) or in step (b) to an hydrolysis reaction in reaction conditions that lead to Montelukast (I); and (d) optionally treating Montelukast (I) with a pharmaceutically acceptable base to form the corresponding salt.
Previously, in a further step of the preparation process, the alcohol of formula (V) is reacted with a sulphonyl chloride of formula C1—SO2—R1, wherein R1 has the same meaning mentioned above, to give the compound of formula (IV).
In another further step, the compound of formula (VI) is reacted with a Grignard reagent selected from methyl lithium and methyl magnesium halide, optionally in the presence of cerium chloride, to give the compound of formula (V) that can be isolated as free base or as a salt thereof.
In another further step, the compound of formula (VII) where R2 is a radical selected from (C1-C4)-alkyl, phenyl, and phenyl mono- or disubstituted by (C1-C4)-alkyl radicals, is reacted with a compound of formula (VIII), in the presence of a base selected from cesium carbonate, sodium hydroxide, and lithium bis(trimethylsilyl)amide, to give the compound of formula (VI) that can be isolated as free base or as a salt thereof.
The above defined compounds of formula (IV), (V) or its salts, and (VI) or its salts are new and are also part of the invention. Thus, another aspect of the present invention is to provide new intermediate compounds for the preparation of Montelukast, in particular those of formula (IV), (V) and (VI). It also forms part of the invention the salts of compound (V), in particular the citrate salt, the salts of compound (VI), in particular the oxalate salt, and the salts formed by the compound of formula (III) with oxalic acid, L(−)-malic acid, L-(+)-tartaric acid, maleic acid, fumaric acid, succinic acid, benzoic acid, 4-hydroxymandelic acid, citric acid, benzensulfonic acid and mandelic acid.
The process of the present invention is particularly advantageous in its practical industrial realization because is cost effective and suited for scale up. Unlike other known processes for the preparation of Montelukast, this process avoids intramolecular cyclizations of the intermediate compounds. Thus, all intermediates are formed cleanly, and therefore chromatographic separations were not required. Furthermore, the final product is obtained in high chemical and optical purity and with high yields.
As it is described above, the cyano compound of formula (III) as free base or as a salt thereof is obtained from the sulfonate of formula (IV). Preferably, the compound of formula (III) is obtained as free base from the compound of formula (IV). The conversion is carried out by reaction of the compound (IV) with an alkaline metal cyanide such as sodium or potassium cyanide, in an appropriate solvent such as dimethylformamide, dimethylsulfoxide, ethyl acetate or acetonitrile, and at a temperature comprised between 0° C. and reflux temperature. Preferably, the reaction is carried out at about 60° C. The reaction can be carried out in the presence of a phase transfer catalyst. Example of suitable phase transfer catalysts are tri-C8-10-alkylmethylammonium chlorides, tetrabutylammonium bromide, hexadeciltrimethylammonium chloride, methyltrioctilammonium chloride, tetrabutylammonium chloride or tetrabutylammonium hydrogen sulfate. In a preferred embodiment the tetrabutylammonium hydrogen sulfate is used as phase transfer catalyst.
In the present invention, preferred sulfonate compounds of formula (IV) are those where the sulfonate (IV) is a mesylate (R1=methyl), a besylate (R1=phenyl) or a tosylate (R1=4-methylphenyl). The most preferred sulfonate (IV) is the mesylate.
The compound of formula (III) can be converted into its salts, and its salts can be converted into the free compound by methods known in the art.
The amide compound of formula (II) can be prepared from the cyano compound of formula (III) as free base or as a salt by hydrolysis. Preferably, the compound of formula (II) is obtained from the compound of formula (III) as free base. For instance, hydrolysis can be achieved using mild conditions and/or by shortening the reaction time. The conditions to carry out the hydrolysis may be easily determined by the person skilled in the art by routine tests. For example, the hydrolysis can be carried out using the same reacting conditions for carrying out the hydrolysis of the cyano compound to Montelukast but reducing the reaction time, as it illustrated in Example 9, followed by the isolation of the amide compound (II).
The last step of the process is a hydrolysis reaction. The compound of formula (II) can be hydrolyzed to afford Montelukast. The hydrolysis reaction can also be directly performed from the cyano compound (III) as free base or as a salt to afford Montelukast. Preferably, the hydrolysis of the compound of formula (II) or of the compound of formula (III) as free base or as a salt is carried out with a base. Preferably the base is an alkaline metal hydroxide or an alkaline earth metal hydroxide. More preferably, the base is sodium hydroxide, potassium hydroxide or lithium hydroxide. The most preferred one is sodium hydroxide. The reaction can be carried out in different solvent systems. Preferably the solvent system is a solvent mixture comprising C1-C4 alcohol and water. Preferably the C1-C4 alcohol is ethanol or isopropanol. The most preferred one is ethanol. Typically, the hydrolysis of the cyano compound (III) to montelukast (I) is carried out at reflux temperature and it is essentially complete within 24 hours.
Other suitable solvent system can be a two-phase solvent mixture comprising water and a suitable organic solvent non-miscible in water or sparingly miscible in water, optionally in the presence of a phase transfer catalyst. Preferably the organic solvent is a (C6-C8)-aromatic hydrocarbon. The most preferred one is toluene. Suitable phase transfer catalyst include for instance, an ammonium quaternarium salt such as tetrabutylammonium bromide, tri-C8-C10-alkylmethylammonium chlorides, methyltrioctilammonium chloride or hexadeciltrimethylammonium chloride. The hydrolysis can be carried out at a temperature comprised between room temperature and reflux temperature. Typically, in these reaction conditions the hydrolysis of the cyano compound (III) to montelukast (I) is carried out at 120° C. and it is essentially complete within about seven days.
The isolation of crude Montelukast can be accomplished by diluting the crude with toluene and washing the solution with aqueous acetic acid and subsequently with water at room temperature, followed by evaporation of the solvent. The obtained Montelukast can be purified by several methods, for instance, by aqueous acid-base extractions or by recrystallization.
Montelukast free acid obtained by the process of the present invention may be converted into pharmaceutically acceptable salts, and salts may be converted into free acid compounds, by known methods described in the art. It is also possible to isolate a salt of Montelukast from the hydrolysis reaction, i.e. without isolating the montelukast free acid.
The sulfonate compounds of formula (IV) are prepared from the alcohol of formula (V) by reaction with the corresponding sulfonyl chloride. This reaction is carried out in an appropriate solvent and in the presence of a tertiary amine, at a temperature comprised between −20° C. and room temperature. Preferably, the reaction is carried out at low temperatures. Common solvents for the reaction include chlorine-containing solvents such as methylene chloride or 1,2-dichloroethylene, aromatic hydrocarbons such as toluene or xylene, and dimethylformamide. Examples of suitable tertiary amines are diisopropylethylamine and triethylamine.
The preparation of the alcohol of formula (V) as free base or as a salt from the compound of formula (VI) is carried out by reaction with a methyl magnesium halide such as methyl magnesium chloride or methyl magnesium bromide, optionally in the presence of cerium chloride, or by reaction with methyl lithium, in the presence of a suitable solvent. Examples of suitable solvents include an ether such as tetrahydrofurane, or an aromatic hydrocarbon such as toluene or xylene, or mixtures of them. Preferably the reaction is carried out at a temperature comprised between −78° C. and 20° C., more preferably, at −20° C.
The alcohol of formula (V) can be converted into its salts, and its salts can be converted into the free compound by methods known in the art. For instance, the citrate salt is prepared by reaction of the compound of formula (V) as free base with citric acid in the presence of a suitable solvent.
The compound of formula (VI) as free base or as a salt can be prepared from the known compound of formula (VII), which is reacted with the compound of formula (VIII) in a suitable solvent such as dimethylformamide, dimethylsulfoxide, dichloromethane, toluene or tetrahydrofurane, and in the presence of a base such as cesium carbonate, sodium hydroxide and lithium bis(trimethylsilyl)amide. Preferably, the reaction is carried out at a temperature comprised between −10° C. and 60° C., more preferably, at a 0-5° C.
The compound of formula (VI) can be converted into its salts, and its salts can be converted into the free compound by methods known in the art. For instance, the oxalate salt is prepared by reaction of the compound of formula (VI) as free base with oxalic acid in the presence of a suitable solvent.
The compound of formula (VII) may be prepared according to a known process described in US 2005107612. The process described in this document comprises the reaction of the methyl-2-((S)-3-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-hydroxypropyl)benzoate of formula (IX) with methane sulfonyl chloride or toluene sulfonyl chloride to form the methyl-2-((S)-3-(3-(E)-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-[(methylsulfonyl)oxy]propyl)benzoate or the corresponding tosylate. Analogously, the besylate of formula (VII) can be obtained from the corresponding benzene sulfonyl chloride.
The compound of formula (VIII) can be prepared from 5,7-dioxa-6-thiaspiro[2.5]octane 6-oxide according to the process summarized in Scheme 1.
The preparation process of the compound of formula (VIII) involves the reaction of the compound of formula (XI) with potassium ethanethioate to give the compound of formula (X). Typically, such reaction is carried out with an excess of potassium ethanethiolate in an appropriate solvent. Examples of suitable solvents include dimethylsulfoxide, dimethylformamide, ethyl acetate, acetonitrile or mixtures thereof. Preferably the reaction is carried out at a temperature comprised between room temperature and 70° C. After the isolation of the compound of formula (X), it can be hydrolyzed using an acid or a basic catalyst to give the compound of formula (VIII). Examples of suitable acids are hydrochloric acid, sulfuric acid, acetic acid and formic acid. Examples of suitable bases are hydroxides, carbonates and alcoxide of an alkaline or an earth alkaline metal. Example of suitable solvents are (C1-C6)-alcohols, (C6-C8)-aromatic hydrocarbons, dimethylformamide, dimethylsulfoxide, or mixtures of them.
The best conditions to carry out the process of the present invention vary according to the parameters considered by a person skilled in the art, such as the starting materials, molar ratio, temperature, and similar. Such reaction conditions may be easily determined by a person skilled in the art by routine tests, and with the teaching of the examples included in this document.
Throughout the description and claims the word “comprise” and variations of the word, are not intended to exclude other technical features, additives, components, or steps. The abstract of this application is incorporated herein as reference. Additional objects, advantages and features of the invention will become apparent to those skilled in the art upon examination of the description or may be learned by practice of the invention. The following examples are provided by way of illustration, and they are not intended to be limiting of the present invention.
200 g of 5,7-dioxa-6-thiaspiro[2.5]octane 6-oxide were dissolved in 1.2 l of dimethyl sulfoxide and 308 g of potassium ethanethioate were poured to the solution. Then, the suspension was heated at 40° C. for 5. Once the reaction was completed, a combination of 3.6 l of ethyl acetate and 3.61 of water was added. The organic phase was separated, washed with water and concentrated to dryness. 200 g of S-(1-(hydroxymethyl)cyclopropyl)methyl ethanethioate were recovered. Yield: 78% corrected by GC. 1H NMR (400 MHz, CDCl3): 3.45 (2H, d, J: 6.4 Hz); 3.01 (2H, s); 2.53 (OH, broad triplet, J: 6.4 Hz); 2.39 (3H, s); 0.54 (4H, m).
200 g of S-(1-(hydroxymethyl)cyclopropyl)methyl ethanethioate were dissolved in 2 l of methanol. Then, 111 ml of concentrated HCl were added under a nitrogen blanket and the solution was stirred at room temperature for 10. The solvent was distilled off and the residue was re-dissolved in 1.5 l of dimethylformamide to be used in the preparation of methyl 2-((R)-3-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(((1-(hydroxymethyl)cyclopropyl)methyl)sulfanyl)propyl)benzoate. Yield: 100%. 1H NMR (400 MHz, CDCl3): 3.57 (2H, s); 2.63 (2H, d, J: 8.0 Hz); 2.45 (OH, broad signal,); 1.43 (5H, t, J: 8.0 Hz); 0.52 (4H, m).
12.1 ml de diisopropylethylamine were poured to a stirred solution of 24.5 g of methyl 2-((S)-3-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-hydroxypropyl)benzoate in 120 ml of dichloromethane. The mixture is cooled to −20° C. and 5 ml of mesyl chloride were added slowly. Once the reaction was completed, the crude solution was successively washed with 120 ml of an aqueous 10% NaHCO3 solution and 120 ml of water. Finally, the solvent was distilled off to obtain 29 g of the title compound. The product was re-dissolved in 290 ml of dimethylformamide to be used as a solution in the next step. Yield: 100%.
A solution of 19 g of (1-(mercaptomethyl)cyclopropyl)methanol in 190 ml of dimethylformamide was cooled to 0° C. Then, 52 g of Cs2CO3 were added in one portion. After 10 min, the outcome solution from the previous example was added and the suspension was maintained at the same temperature for 18 hours. Finally, a mix of 380 ml of ethyl acetate and 380 ml of water was poured to the solution crude. The organic phase was washed with 380 ml of water and concentrated to dryness. 30 g of brown oil were recovered. Yield: 86%, corrected after HPLC analysis. 1H NMR (400 MHz, DMSO-d6): 8.38 (1H, d, J: 8.4 Hz); 8.00-7.26 (14H, m); 4.50 (OH, t, J: 5.4 Hz); 3.92 (1H, t, 7.2 Hz); 3.76 (3H, s); 3.33 (1H, dd, J: 11.0 Hz, 5.4 Hz); 3.25 (1H, dd, J: 11.0 Hz, 5.4 Hz); 2.98-2.88 (1H, m); 2.83-2.74 (1H, m); 2.52 (1H, d, J: 12.7 Hz); 2.39 (1H, d, J: 12.7 Hz); 2.10 (2H, m); 0.46-0.18 (4H, m).
The product obtained in the previous example was dissolved in 300 ml of tetrahydrofuran. The mixture was cooled to 0° C. and 307 ml of 1.4M solution of methylmagnesium bromide were added under a nitrogen blanket. The reaction was maintained at 0° C. for 18 hours. Then, 400 ml of 2M aqueous solution of acetic acid were added slowly, followed of 400 ml of ethyl acetate. The organic phase was successively washed with 400 ml of an aqueous 10% NaHCO3 solution and 400 ml of water. Finally, the solvent was distilled off to yield 30 g of crude. Yield: 81% corrected after HPLC analysis. 1H NMR (400 MHz, DMSO-d6): 8.39 (1H, d, J: 8.6 Hz); 8.00-7.06 (14H, m); 4.91 (OH, s); 4.51 (OH, t, J: 5.5 Hz); 3.99 (1H, t, 7.3 Hz); 3.34 (1H, dd, J: 11.0 Hz, 5.5 Hz); 3.26 (1H, dd, J: 11.0 Hz, 5.5 Hz); 3.05 (1H, m); 2.74 (1H, m); 2.54 (1H, d, J: 12.7 Hz); 2.41 (1H, d, J: 12.7 Hz); 2.15 (2H, m); 1.44 (6H, s); 0.45-0.36 (2H, m); 0.33-0.22 (2H, m).
1.3 g of anhydrous cerium chloride were stirred in 10 ml of dry tetrahydrofuran for 18 hours at room temperature. Then, the suspension was cooled to −20° C. and 1.5 ml of a 3M solution of methylmagnesium chloride were added under a nitrogen blanket. After a period of time, a 2.5 ml tetrahydrofuran solution of 0.5 g of the product obtained in example 4 was added. The mixture was stirred for 18 hours at the same temperature and 10 ml of 2M aqueous solution of acetic acid were added slowly, followed of 10 ml of ethyl acetate. The organic phase was successively washed with 10 ml of an aqueous 10% NaHCO3 solution and 10 ml of water. Finally, the solvent was distilled off to yield 0.5 g of crude. Yield: 80% corrected after HPLC analysis.
6.5 ml de diisopropylethylamine were poured to a stirred solution of 16 g of 2-(2-((R)-3-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(((1-(hydroxymethyl)cyclopropyl)methyl)sulfanyl)propyl)phenyl)propan-2-ol in 160 ml of dichloromethane. The mixture was cooled to −20° C. and 2.7 ml of mesyl chloride were added slowly. The mixture was stirred at the same temperature for one hour and then, it was washed twice with 300 ml of water. The solvent was distilled off and 18 g of crude were recovered. Yield: 100%. 1H NMR (400 MHz, DMSO-d6): 8.41 (1H, d, J: 9.6 Hz); 8.02-7.03 (14H, m); 4.91 (OH, s); 4.12 (2H, m); 4.02 (1H, t, J: 7.1 Hz); 3.12 (3H, s); 3.09-3.02 (1H, m); 2.78-2.71 (1H, m); 2.54 (1H, d, J: 13.2 Hz); 2.46 (1H, d, J: 13.2 Hz); 2.15 (2H, m); 1.43 (3H, s); 1.42 (3H, s); 0.68-0.45 (4H, m).
The crude obtained in the previous example was dissolved in 180 ml of dimethylformamide and 2.1 g of sodium cyanide were added in one portion to the solution. After 18 hours of stirring at 60° C., 270 ml of ethyl acetate was poured into the mixture previously warmed to room temperature. Then, two washes with 270 ml of water were carried out and the solvent was distilled off to afford 14 g of crude. Yield: 75% corrected after HPLC analysis. 1H NMR (400 MHz, DMSO-d6): 8.39 (1H, d, J: 8.6 Hz); 8.00-7.05 (14H, m); 4.90 (OH, s); 4.04 (1H, t, J: 7.2 Hz); 3.06 (1H, m); 2.76 (1H, m); 2.67 (1H, m); 2.33 (1H, m); 2.30 (2H, s); 2.13 (2H, m); 1.43 (6H, s); 0.59-0.43 (4H, m).
1.8 g of crude obtained in example 8 were dissolved in 3.6 ml of toluene. Then, 3.6 ml of water was added followed of 14.7 g of sodium hydroxide and 0.44 g of tetrabutylammonium bromide. The mixture was stirred at 120° C. for 30 hours. After this period of time, 10 ml of toluene and 10 ml of water were added to the reaction solution previously cooled to room temperature. The organic phase was separated and washed with 10 ml of water. Finally, the solvent was distilled off and the crude was purified by standard methods in order to recover 77 mg of the title compound. Yield: 6%. 1H NMR (400 MHz, DMSO-d6): 8.41 (1H, d, J: 8.6 Hz); 8.03-7.07 (15H, m); 6.74 (1H, s); 4.91 (OH, s); 4.02 (1H, t, J: 7.3 Hz); 3.04 (1H, m); 2.75 (1H, m); 2.57 (1H, d, J: 13.3 Hz); 2.45 (1H, d, J: 13.3 Hz); 2.16 (4H, m); 1.43 (6H, s); 0.50-0.27 (4H, m).
5.2 g of crude obtained in example 8 were dissolved in 10 ml of toluene. Then, 10 ml of water was added followed of 14.7 g of sodium hydroxide and 0.44 g of tetrabutylammonium bromide. The mixture was stirred at 120° C. for 7 days. After this period of time, 10 ml of toluene and 10 ml of water were added to the reaction solution previously cooled to room temperature. The organic phase was separated and successively washed with 10 ml of acetic acid and 10 ml of water. Finally, the solvent was distilled off to recover 4.6 g of product, that can be purified by standard methods if it is necessary. Yield: 83%. 1H NMR (400 MHz, DMSO-d6): 12.02 (1H, s); 8.39 (1H, d, J: 8.6 Hz); 8.01-7.04 (14H, m); 4.90 (OH, s); 4.00 (1H, t, J: 7.3 Hz); 3.05 (1H, m); 2.76 (1H, m); 2.56 (1H, d, J: 12.9 Hz); 2.47 (1H, d, J: 12.9 Hz); 2.32 (2H, s); 2.16 (2H, m); 1.44 (6H, s); 0.52-0.33 (4H, m). IR (KBr)=3573.1, 3436.9, 2919.2, 1716.9, 1608.9, 1499.9, 1408.8, 1315.7, 1223.9, 1201.6, 1173.0, 1148.0, 1134.9, 1074.8, 965.9, 950.8, 933.2, 863.6, 842.7, 766.0 cm−1.
1.05 g of sodium hydroxide were poured to a solution of 1 g of (R,E)-2-(1-((1-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(2-hydroxypropan-2-yl)phenyl)propyl)sulfanyl)methyl)cyclopropyl)acetonitrile in 5 ml of a mixture of ethanol:water (96:4, v/v). The outcome suspension was stirred at reflux temperature for 15 hours. After this period of time, the reaction mixture was cooled down to room temperature and diluted with 10 ml of toluene. Then, 20 ml of a 2M aqueous solution of acetic acid were added slowly and the organic layer was separated and washed twice with 10 ml of water. Finally, the solvent was distilled off to recover 0.9 g of product that can be purified by standard methods if it is necessary. Yield: 91%.
2.6 g of Montelukast free acid were dissolved in 26 ml of toluene and 8.9 ml of 0.5M NaOH solution in methanol were added slowly at room temperature. The mixture was stirred for 1 hour and the solvent was removed under vacuum to obtain a residue. Then, heptane (24 ml) was added over 30 min to a well stirred solution of the residue in 4 ml of ethyl acetate at room temperature. Two hours after the addition, an off white solid was filtered off under a nitrogen atmosphere and washed with 5 ml of heptane. The wet product was dried under vacuum at 70-80° C. for 2 days to yield 2.7 g of amorphous solid form of Montelukast sodium. Yield: 100%. 1H NMR (400 MHz, DMSO-d6): 8.38 (1H, d, J: 8.6 Hz); 8.02-7.04 (14H, m); 5.19 (OH, s); 4.01 (1H, t, J: 7.2 Hz); 3.08 (1H, m); 2.72 (1H, m); 2.69 (1H, d, J: 12.4 Hz); 2.54 (1H, d, J: 12.4 Hz); 2.22 (1H, m); 2.10 (1H, d, J: 14.2 Hz); 2.10 (1H, m); 1.96 (1H, d, J: 14.2 Hz); 1.45 (3H, s); 1.44 (3H, s); 0.46-0.32 (2H, m); 0.28-0.15 (2H, m).
To a solution of 338 g (0.61 mol) of methyl 2-((R)-3-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(((1-(hydroxymethyl)cyclopropyl)methyl)sulfanyl)propyl)benzoate in 2.0 l of toluene a solution of 75 g (0.60 mol) of oxalic acid dihydrate in 1.0 l of acetonitrile was slowly added at room temperature. The outcome suspension was stirred at room temperature during ten hours. The solid was filtered off and washed several times with toluene/acetonitrile 2/1 (v/v) mixture. The wet solid was dried under vacuum at 25° C. 304 g of a yellow solid were obtained. Yield 78%. DSC: 121.6° C. (peak). 1H NMR (400 MHz, DMSO-d6): 8.42 (1H, d, J: 8.6 Hz); 8.00-7.28 (14H, m); 3.92 (1H, t, 7.3 Hz); 3.76 (3H, s); 3.31 (1H, d, J: 11.0 Hz); 3.25 (1H, d, J: 11.0 Hz); 2.98-2.90 (1H, m); 2.82-2.75 (1H, m); 2.52 (1H, d, J: 12.7 Hz); 2.39 (1H, d, J: 12.7 Hz); 2.14-2.08 (2H, m); 0.43-0.19 (4H, m). DSC measurement was carried out in a perforated pan at a scan rate of 5° C./minute from 25.0° C. to 150.0° C. with a DSC Mettler Toledo DSC822.
283 g of the oxalate salt prepared in Example 13 were suspended in 1.7 l of toluene and 1.7 l of water. 35% of aqueous hydrochloric acid solution was slowly added to the previous mixture until pH 6.5 was obtained. The organic phase was separated and washed with water. Finally the solvent was distilled off under vacuum. 243 g of an oil was obtained. Yield 100%.
A solution of 92.5 g of 2-(2-((R)-3-(3-((E)-2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(((1-(hydroxymethyl)cyclopropyl)methyl)sulfanyl)propyl)phenyl)propan-2-ol (HPLC: 78 area %) in 910 ml of toluene was heated to 55° C. Then, 34.8 g of citric acid monohydrate were added in one portion. After 1 hour of stirring at the same temperature, the mixture was gradually cooled to 20° C. in 2 hours and stirred at this temperature for 2 hours more. Finally, the suspension was filtered under vacuum and the cake was washed twice with 100 ml of toluene. The product was used as a wet solid in the next step. (HPLC: 97 area %). 1H NMR (400 MHz, DMSO-d6): 12.38 (2H, s); 8.39 (1H, d, J: 8.6 Hz); 8.02-7.11 (14H, m); 4.90 (OH, s); 4.51 (OH, s); 3.99 (1H, t, J: 7.3 Hz); 3.34 (1H, d, J: 11.0 Hz); 3.27 (1H, d, J: 11.0 Hz); 3.06 (1H, td, J: 12.3 Hz; J: 4.9 Hz); 2.77 (2H, d, J: 15.4 Hz); 2.73 (1H, m); 2.66 (2H, d, J: 15.4 Hz); 2.54 (1H, d, J: 12.7 Hz); 2.41 (1H, d, J: 12.7 Hz); 2.17 (2H, m); 1.44 (6H, s); 0.44-0.36 (2H, m); 0.32-0.22 (2H, m). IR (KBr)=3411, 3052, 2970, 2922, 2593, 1727, 1632, 1599, 1488, 1437, 1409, 1376, 1318, 1223, 1208, 1153, 1080, 1026, 961, 927, 861, 840, 760, 729, 694, 598, 471 cm−1.
The wet solid obtained in Example 15 was partitioned with 800 ml of toluene and 800 ml of an aqueous solution of NaHCO3 5%. The organic layer was separated, washed with 800 ml of water and concentrated to dryness by rotary evaporation under vacuum at 30° C. 29.7 g of a pale yellow solid were recovered. Overall yield for the 2 steps: 39% (HPLC: 96 area %).
5 ml of water were added to a 96 g of a toluene solution containing 10 g of (R,E)-(1-((1-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(2-hydroxypropan-2-yl)phenyl)propylthio)methyl)cyclopropyl)methyl methanesulfonate; followed of 0.5 g of tetrabutylammonium hydrogen sulfate and 0.85 g of sodium cyanide. The mixture was stirred at 60° C. for 20 hours. Then, it was cooled to room temperature and the organic layer was washed three times with 100 ml of water. Finally, the outcome toluene solution was concentrated to dryness by rotary evaporation under vacuum at 30° C. 9.5 g were obtained.
To a solution of 0.5 g (8.82 mmol) of (R,E)-2-(1-((1-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(2-hydroxypropan-2-yl)phenyl)propyl)sulfanyl)methyl)cyclopropyl)acetonitrile in 3.5 ml of toluene a solution of 8.82 mmol of the acid in acetonitrile or tetrahydrofurane was slowly added at room temperature. The solvent was distilled off and the theoretical amount of the salt was obtained as a yellow solid.
The general example has been repeated using the corresponding acids indicated in the following examples:
Preparation of Oxalate Salt of the Compound (III) Using Oxalic acid. Yield: 100%; IR (KBr) (cm−1): 3420, 2970, 2925, 1719, 1626, 1600, 1486, 1408, 1205, 1157, 1.080, 762, 695; 1H RMN(400 MHz, DMSO-d6): 8.41 (1H, d, J: 8.7 Hz); 8.0-7.1 (14H, m); 4.04 (1H, t, 7.3 Hz); 3.1 (1H, m); 2.8 (1H, m); 2.63 (2H, s); 2.51 (2H, under semideuterated DMSO); 2.2 (2H, m); 1.44 (3H, s); 1.43 (3H, s); 0.60-0.40 (4H, m).
Preparation of malate salt of the compound (III) using L-(−)-malic acid; Yield: 100%; IR (KBr) (cm−1): 3436, 2976, 2930, 1721, 1628, 1607, 1498, 1409, 1161, 1078, 761, 696; 1H RMN(400 MHz, DMSO-d6): 12.41 (1H, broad); 8.40 (1H, d, J=8.69 Hz); 8.0-7.1 (14H, m); 4.91 (1H, s); 4.26 (1H, dd, J 7.83 Hz, J=4.78 Hz); 4.04 (1H, t, 7.35 Hz); 3.11-3.01 (1H, m); 2.80-2.70 (1H, m); 2.61 (1H, dd, J=15.66 Hz, J=4.80 Hz); 2.51 (2H, under semideuterated DMSO), 2.44 (1H, dd, J=15.66 Hz, J=7.84 Hz); 2.26-2.10 (2H, m); 1.44 (3H, s); 1.43 (3H, s); 0.60-0.40 (4H, m).
Preparation of tartrate salt of the compound (III) using L-(+)-Tartaric acid; Yield: 100%; IR (KBr) (cm−1): 3401, 2970, 2927, 1726, 1626, 1605, 1487, 1408, 1205, 1130, 1080, 762, 696; 1H RMN(400 MHz, DMSO-d6):12.68 (1H, broad); 8.41 (1H, d, J: 8.64 Hz); 8.04-7.04 (14H, m); 4.91 (1H, s); 4.31 (2H, s); 4.04 (1H, t, J=7.34 Hz); 3.12-3.00 (1H, m); 2.81-2.70 (1H, m); 2.64 (2H, s); 2.51 (2H, under semideuterated DMSO); 2.26-2.07 (2H, m); 1.44 (3H, s); 1.43 (3H, s); 0.60-0.40 (4H, m).
The following salts of the compound (III) were also prepared using the process of the general example from the corresponding acids: maleate, fumarate, succinate, benzoate, 4-hydroxymandelate, citrate and mandelate.
To a solution of 3.14 g (5.53 mmol) of (R,E)-2-(1-((1-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(2-hydroxypropan-2-yl)phenyl)propyl)sulfanyl)methyl)-cyclopropyl)acetonitrile in 21.5 ml of toluene a solution of 0.68 g (5.42 mmol) of oxalic acid dihydrate in 10 ml acetonitrile was added at room temperature. The solution was concentrated under vacuum to half the initial volume and stirred at room temperature overnight. The outcome solid was filtered off and dried under vacuum. 2.71 g (71% yield) of a yellow solid were obtained. 1H NMR (400 MHz, DMSO-d6): 8.41 (1H, d, J: 8.7 Hz); 8.0-7.1 (14H, m); 4.04 (1H, t, 7.3 Hz); 3.1 (1H, m); 2.8 (1H, m); 2.63 (2H, s); 2.51 (2H, under semideuterated DMSO); 2.2 (2H, m); 1.44 (3H, s); 1.43 (3H, s); 0.60-0.40 (4H, m). IR (KBr)=3420, 2970, 2925, 1719, 1626, 1600, 1486, 1408, 1205, 1157, 1.080, 762, 695 cm−1.
To a solution of 1.0 g (1.76 mmol) of (R,E)-2-(1-((1-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-(2-(2-hydroxypropan-2-yl)phenyl)propyl)sulfanyl)methyl)-cyclopropyl)acetonitrile in 6 ml of toluene a solution of 0.303 g (1.73 mmol) of benzensulfonic acid 90% in 0.6 ml acetonitrile was added at room temperature. The solution was stirred at room temperature overnight. The outcome solid was filtered off and dried under vacuum. 0.96 g (75% yield) of a yellow solid were obtained. 1H NMR (400 MHz, DMSO-d6): 8.74 (1H, d, J: 8.7 Hz); 8.27-7.04 (19H, m); 4.07 (1H, t, 7.3 Hz); 3.1 (1H, m); 2.8 (1H, m); 2.63 (2H, s); 2.51 (2H, under semideuterated DMSO); 2.2 (2H, m); 1.44 (3H, s); 1.43 (3H, s); 0.61-0.41 (4H, m). IR (KBr)=3430, 3050, 2910, 1625, 1600, 1480, 1230, 1150, 1125, 1020, 990, 690, 610 cm−1
| Number | Date | Country | Kind |
|---|---|---|---|
| EP 05110348.9 | Nov 2005 | ES | national |
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/EP2006/068052 | 11/3/2006 | WO | 00 | 5/2/2008 |
| Number | Date | Country | |
|---|---|---|---|
| 60733553 | Nov 2005 | US |
