Patent Application
20090156806
The present invention relates to a process for the preparation of antibacterial oxazolidinone derivatives, particularly [(S)—N-[[3-(3-fluoro-4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide], and to the intermediates useful for the synthesis thereof.
Antibacterial oxazolidinone derivatives are known from WO 95/07271, which specifically describes the synthesis of linezolid, namely [(S)—N-[[3-(3-fluoro-4-morpholinyl)phenyl]-2-oxo-5-oxazolidinyl]methyl]acetamide], according to the following scheme:
Other synthetic routes for the preparation of linezolid are reported for example in U.S. Pat. No. 6,107,519 and in Tetrahedron Letters, Vol 37, No 44, pages 7937-7940, wherein the chiral compound shown below is used instead of glycidyl butyrate as a synthon containing the molecule stereocenter.
It should be appreciated that all of the known approaches to the preparation of linezolid make use of chiral synthons for the construction of the stereocenter. These are small molecules characterized by a high cost, therefore they are not suitable for the production of the compound on an industrial scale.
There is therefore the need for an alternative synthesis which provides oxazolidinone derivatives, linezolid included, from inexpensive starting materials, and which does not require a chiral synthon for the construction of the molecule, so that it can be used for the industrial preparation of such derivatives.
The 1H-NMR spectra were recorded with the Varian Mercury 300/Bruker 400 spectrometer, using DMSO-d6 or deuterated chloroform as the solvent.
The particles size was determined with the known laser light scattering technique using a Malvern Mastersizer MS1 instrumentation under the following operative conditions:
An object of the invention is a process for the preparation of a compound of formula (I), or a salt thereof, both as the single (S) or (R) enantiomer, and as a mixture thereof,
wherein R and R1, which can be the same or different, are hydrogen, CH3, CN, COOH or COOC1-C4 alkyl;
R2 and R3, which can be the same or different, are hydrogen, F or Cl; and
R4 is C1-C4 alkyl;
which process comprises:
a) the activation of the hydroxyl group in a compound of formula (II), or a salt thereof, as the single (S) or (R) enantiomer or as a mixture thereof, by means of a derivatization reagent to form a leaving group, and subsequent cyclization reaction in the presence of a catalyst or an azide compound; or
b) the cyclization reaction of a compound of formula (II), or a salt thereof, as the single (S) or (R) enantiomer or as a mixture thereof, in presence of a strong base;
wherein R5 is optionally substituted C1-C4 alkyl, aryl-C1-C4 alkyl or aryl; and R-R4 are as defined above; and
if desired, the resolution of a mixture of the enantiomers of formula (I) to obtain the single enantiomer (S) or (R); and/or, if desired, the conversion of a compound of formula (I) to a salt thereof, or vice versa.
A C1-C4 alkyl group or residue, which can be straight or branched, is preferably methyl, ethyl, propyl, isopropyl, n-butyl or isobutyl or t-butyl; in particular methyl or ethyl or t-butyl.
An aryl-C1-C4 alkyl group is, for example, phenyl-C1-C4 alkyl or naphthyl-C1-C4 alkyl; in particular phenyl-C1-C2 alkyl, preferably benzyl.
An aryl group is, for example, phenyl or naphthyl; in particular phenyl.
An alkyl group or residue, when substituted, is substituted with 1 to 5 substituents, preferably 1 or 2, independently selected from hydroxy, C1-C6 dialkyl-amino, nitro, cyano and halogen.
An aryl group, when substituted, is substituted with 1 to 5 substituents, preferably 1 or 2, independently selected from hydroxy, C1-C6 alkyl, C1-C6 dialkyl-amino, nitro, cyano and halogen.
Preferably, in a compound of formula (I), in particular as the single (S) enantiomer, R, R1 and R3 are hydrogen; R2 is fluorine; and R4 is methyl. Preferably, in a compound of formula (II), R5 is benzyl, t-butyl, isopropyl, isobutyl, methyl or ethyl; more preferably t-butyl when using alternative a) of the process of the invention, or ethyl when using alternative b).
A derivatizing agent can be for example a sulfonyl chloride of formula R5SO2Cl, wherein R5 is as defined above, e.g. methanesulfonyl chloride or toluenesulfonyl chloride; or an alkyl or aryl phosphine, e.g. triphenylphosphine, and an azadicarboxylate, e.g. diethylazadicarboxylate; or a carbonyl diimidazole. Preferably methanesulfonyl chloride; or triphenylphosphine and diethyl-azadicarboxylate (Mitsunobu system).
A leaving group thus obtained is an easily displaceable hydroxyl-derived group, preferably a mesylate group.
A catalyst can be a Lewis acid, for example BF3, AlCl3, ZnCl2, trifluoromethanesulfonic acid, trifluoroacetic acid, acetic acid, trimethylsilyl triflate, tert-butyldimethylsilyl triflate. Alternatively, an azide compound can be used, e.g. sodium azide but in stoichiometric amount
A strong base can be a strong organic or inorganic base, in particular a alkali C1-C6 alkoxide, e.g. sodium or potassium methoxide, ethoxide or t-butoxide; a tertiary amine, e.g. 1,4-diazabicyclo[2.2.2]octane or 1,8-diazabicyclo[5.4.0]-undec-7-ene, or diisopropylethylamine; a carbanion, e.g. butyl lithium or hexyl lithium; an azanion, e.g. lithium diisopropylamide or lithium tetramethylpiperidide; sodium hydride; sodium or potassium hexamethyldisilazide. Preferably sodium hydride or potassium t-butoxide.
According to alternative a) of the process of the invention, when the compound of formula (II) is the (S) enantiomer, the resulting product of formula (I) has (R) configuration. When the compound of formula (II) is the (R) enantiomer, the resulting product of formula (I) has (S) configuration. When the compound of formula (II) is a mixture of the two enantiomers, the resulting product of formula (II) is a mixture of the two enantiomers.
According to alternative b), when the compound of formula (II) is the (S) enantiomer, the resulting product of formula (I) has (S) configuration. When the compound of formula (II) is the (R) enantiomer, the resulting product of formula (I) has (R) configuration. When the compound of formula (II) is a mixture of the two enantiomers, the resulting product of formula (I) is a mixture of the two enantiomers.
According to alternative a), the compound of formula (II) preferably has (R) configuration, whereas according to alternative b), the compound of formula (II) preferably has (S) configuration.
The cyclization reaction of a compound of formula (II), according to alternatives a) and b), can be carried out in the presence of an organic solvent, selected from e.g. a dipolar aprotic solvent, typically dimethylformamide, dimethylacetamide, acetonitrile, dimethylsulfoxide; an ether, typically diethyl ether, methyl-tert-butyl ether, tetrahydrofuran or dioxane; a chlorinated solvent, typically dichloromethane, chloroform or chlorobenzene; an apolar solvent, typically an aliphatic hydrocarbon, e.g. hexane or cyclohexane, or an aromatic hydrocarbon, typically benzene or toluene; a carboxylic acid, typically acetic acid or trifluoroacetic acid, or an alkanol, typically methanol, ethanol, isopropanol or n-butanol. The reaction is preferably carried out in tetrahydrofuran or dioxane, in particular when the base is sodium hydride; or in an alcohol, preferably ethanol, when the base is an alkoxide.
The reaction can be carried out at a temperature approx. ranging from −15° C. to the reflux temperature of the solvent, preferably at room temperature.
The separation of a mixture of enantiomers of the compound of formula (I) into the single (S) and (R) enantiomers can be carried out according to known methods, for example by crystallization of a diastereomeric salt of addition with a strong acid such as camphorsulfonic acid, mandelic acid, tartaric acid, dibenzoyltartaric acid.
A compound of formula (I), or a salt thereof, in particular linezolid, obtained according to the process of the invention, has purity equal to or higher than 95%; preferably equal to or higher than 99%; more preferably equal to or higher than 99.7%.
A salt of a compound of formula (I) is for example a pharmaceutically acceptable salt, in particular a pharmaceutically acceptable acid addition salt.
A compound of formula (I) can be converted to a salt, and vice versa, according to known methods.
The purity of the resulting product can be increased by crystallization of a salt of addition with a mineral acid, such as hydrochloric acid or sulfuric acid. If desired, said salts can be cleaved by treatment with a basic agent, for example sodium hydroxide, to obtain the product as the free base, in particular linezolid.
The crystallization of a linezolid salt and its subsequent cleavage is a useful method for the purification of linezolid. This method is novel and is a further object of the present invention.
The resulting Linezolid, or a salt thereof, has particle mean size D50 ranging from about 10 to 250 micrometres; said size can be further reduced by a fine grinding process according to known techniques.
The compounds of formula (II), both as the single (S) or (R) enantiomers, and as mixtures thereof, as well as the salts thereof, are novel, and are a further object of the invention.
Preferred examples of compounds of formula (II) are:
A compound of formula (II), or a salt thereof, both as the single (S) or (R) enantiomer, and as a mixture thereof, can be obtained by a process comprising the reduction respectively of the (R) or (S) enantiomer, or of the mixture thereof, of a compound of formula (III), or a salt thereof,
wherein R-R5 are as defined above; to obtain a compound of formula (IV), or a salt thereof, both as the single (S) or (R) enantiomer, and as a mixture thereof,
wherein R-R5 are as defined above; the acylation thereof; and, if the case, the conversion to a salt thereof, or vice versa.
The reduction reaction of a compound of formula (III), or a salt thereof, can be carried out for example by catalytic hydrogenation in the presence of a homogeneous or heterogeneous metal catalyst, e.g. based on Pd, Pt, Ni, Rh or Ru; preferably based on Pd;
When the metal catalyst is heterogeneous, it is preferably deposited on an inert support, such as charcoal, barium hydroxide, alumina, calcium carbonate; preferably charcoal.
The concentration of the metal on the support can approximately range from 1 to 30%, preferably from about 5 to 10%.
The hydrogen pressure used can approximately range from 1 atm to 10 atm; the reaction is preferably carried out at atmospheric pressure.
The molar amount of catalyst used, based on the compound of formula (II), or a salt thereof, approximately ranges from 0.1 to 10%, preferably approximately from 0.5 to 5%.
The reaction can be carried out in the presence of an organic solvent, selected e.g. from a dipolar aprotic solvent, typically dimethylformamide, dimethylacetamide, acetonitrile, dimethylsulfoxide; an ether, typically tetrahydrofuran, dioxane or methyl-tert-butyl ether; an apolar solvent, e.g. an aliphatic hydrocarbon, typically hexane or cyclohexane, or an aromatic hydrocarbon, typically benzene or toluene; an alkanol, e.g. a C1-C4 alkanol, typically methanol, ethanol, isopropanol or butanol; an ester, typically ethyl acetate, isopropyl acetate, butyl acetate; a ketone, typically acetone, methyl ethyl ketone, methyl isobutyl ketone; a carboxylic acid, typically acetic acid or propionic acid; or mixtures of two or more, preferably two or three, of said solvents. Alternatively, the reaction can be carried out in water or an aqueous solution of a mineral acid, e.g. hydrochloric acid or sulfuric acid, or mixtures thereof with one, two or three of the organic solvents mentioned above. The reaction is preferably carried out in a C1-C4 alkanol, in particular methanol.
Alternatively, the reduction reaction of a compound of formula (III), or a salt thereof, can be carried out by hydrogen transfer reaction, using a homogeneous or heterogeneous metal catalyst, for example as reported above, substantially in the same molar amounts; and a hydrogen donor, optionally in the presence of a solvent.
A hydrogen donor can be selected e.g. from the group comprising cyclohexene, cyclohexadiene, methylcyclohexene, limonene, dipentene, mentene, hydrazine, phosphinic acid or derivatives thereof, e.g. sodium hypophosphite, indoline, ascorbic acid, formic acid or the sodium or ammonium salts thereof, and secondary alcohols, e.g. isopropanol. Cyclohexene or ammonium formate are preferred.
The molar ratio of the hydrogen donor to the compound of formula (III), or a salt thereof, can approximately range from 3 to 50, preferably from 3 to 10.
A solvent can be an organic solvent, selected from e.g. the solvents mentioned above for the reduction of the same compound of formula (III), or mixtures of two or three of said solvents or with water.
The acylation reaction of a compound of formula (IV), or a salt thereof, to give a compound of formula (II) can be carried out according to known methods, using e.g. a C1-C4 acyl chloride or an anhydride as the acylating agent.
The stoichiometric ratio of the acylating agent to the compound of formula (IV) can approximately range from 0.8 to 1.2.
If desired, the reduction and the acylation can be carried out at the same time or in succession without isolating the compound of formula (IV).
The compounds of formula (III) and (IV), both as the single (R) or (S) enantiomers, and as a mixture thereof, and the salts thereof, are novel and are a further object of the present invention.
Preferred examples of compounds of formula (III) are:
both as the single (R) or (S) enantiomers, and as mixtures thereof.
Preferred examples of compounds of formula (IV) are:
both as the single (R) or (S) enantiomers, and as mixtures thereof.
A compound of formula (III), or a salt thereof, can be obtained starting from an achiral compound of formula (V), or a salt thereof,
wherein R, R1, R2, R3 and R5 have the meanings reported above. In particular:
A base can be an organic base, for example tetrabutylammonium fluoride or diazabicycloundecene.
An optically pure chiral catalyst can be for example a complex of Cu(II) with a bisoxazolidine, in particular (3aR,3a′R,8aS,8a′S)-2,2′-(propane-2,2-diyl)bis8(8,8a-dihydro-3 aH-indeno[1,2-d]oxazole) (1R,2S)-Inda-Box, prepared according to the procedure reported in Tetrahedron Letters, 45 (2004), pages 145-148.
A solvent can be, for example, an organic solvent selected from those reported above; preferably a C1-C4 alkanol; more preferably ethanol.
The molar ratio of nitromethane to a compound of formula (V), or a salt thereof, can range from 1 to 20, preferably about 10.
The molar ratio of the base to a compound of formula (V), or a salt thereof, can range from 0.01 to 1, preferably about 0.5.
The molar ratio of the chiral catalyst and to a compound of formula (V), or a salt thereof, can approximately range from 0.005 to 0.2; preferably approximately from 0.01 to 0.1.
A compound of formula (II) or (III), or a salt thereof, as the single (R) or (S) enantiomer, obtained according to the processes herein reported, has enantiomeric purity equal to or higher than 90%; said purity can be further increased by techniques known to those skilled in the art. Linezolid obtained starting from a compound of formula (II), or a salt thereof, with said enantiomeric purity characteristics, can have similar enantiomeric purity characteristics, namely equal to or higher than 90%, particularly equal to or higher than 99.5%.
The compounds of formula (V), and the salts thereof, are novel and are an object of the present invention.
Examples of compounds of formula (V) are:
A compound of formula (V), or a salt thereof, can be prepared for example starting from a compound of formula (VI), or a salt thereof, by the process reported in Scheme A,
wherein R6 is a straight or branched C1-C4 alkyl group, preferably methyl, and R, R1, R2, R3 and R5 have the meanings reported above, comprising:
The reactions represented in Scheme A are known and can be carried out according to known methods.
Alternatively, a compound of formula (V), or a salt thereof, can be prepared starting from a compound of formula (VI), or a salt thereof, by a process, reported in Scheme B,
wherein each R7 is independently C1-C6 alkyl, which can be straight or branched, preferably a C1-C4 alkyl group; more preferably methyl or ethyl, or the two R7 groups taken together form a 5- or 6-membered ring, and R, R1, R2, R3 and R5 have the meanings reported above, which process comprises:
A dialkoxyacetaldehyde of formula CHOCH(OR7)2 is preferably dimethoxyacetaldehyde.
A chloroacetaldehyde dialkylacetal of formula ClCH2CH(OR7)2, can be, for example, chloroacetaldehyde dimethylacetal or chloroacetaldehyde diethylacetal; preferably chloroacetaldehyde diethylacetal.
The reactions represented in Scheme B are known, and can be carried out according to known methods.
A salt of a compound of formula (II), (III), (IV), (V), (VI), (VII), (VIII), (IX) or (X) is for example a pharmaceutically acceptable salt, in particular a pharmaceutically acceptable acid addition salt.
The compounds of formula (VII), (VIII), (IX), (X) and the salts thereof are novel and are an object of the present invention.
Preferred examples of compounds of formula (VII), (VIII), (IX) and (X) are:
A compound of formula (VI) is known and can be prepared according to the procedure reported in WO 95/07271.
The following examples illustrate the invention.
A solution of a 3-fluoro-4-morpholinoaniline (200 mg, 1.019 mmol), of formula (VI), in CH3CN (5 ml) is added with K2CO3 (282 mg, 2.03 mmol), methyl bromoacetate (100 μl, 1.22 mmol) and a catalytic amount of tetrabutylammonium iodide. The mixture is microwave heated in a closed vessel, at about 150° C. for approximately 20 minutes. Afterwards, acetonitrile is evaporated off, the solid is taken up with water and the mixture is extracted 3 times with ethyl acetate. The combined organic phases are dried over Na2SO4 and evaporated under reduced pressure. The product is then purified by flash chromatography (hexane:acetate 6:4), to obtain a white solid.
1H NMR (400 MHz, CDCl3) ppm 6.87 (t, J=8.9 Hz, 1H), 6.42-6.33 (m, 2H), 4.21 (bs, 1H), 3.90-3.85 (m, 6H), 3.81 (s, 3H), 3.02-2.96 (m, 4H).
A solution of methyl 2-(3-fluoro-4-morpholinophenylamino)acetate (100 mg, 0.372 mmol), of formula (VII), in 1,2-dichloroethane (3.72 ml) is added with a catalytic amount of dimethylaminopyridine, triethylamine (50 μl, 0.372 mmol) and isobutyl chloroformate (100 μl, 0.744 mmol). The mixture is microwave heated in a closed vessel, at about 150° C. for approximately 30 minutes, then a further 2 equivalents of isobutyl chloroformate are added, heating at the same temperature and under the same conditions for about 30 minutes. Afterwards, the mixture is diluted with CH2Cl2 and the organic phase is washed with a NaHCO3 aqueous solution. The organic phases are dried over Na2SO4 and evaporated under reduced pressure. The product is purified by flash chromatography (hexane:acetate 7:3) to obtain a white solid in 80% yield.
1H NMR (400 MHz, CDCl3) ppm 7.16-7.00 (bm, 2H), 6.95-6.85 (m, 1H), 4.31 (s, 2H), 3.99-3.85 (m, 6H), 3.78 (s, 3H), 3.13-3.06 (m, 4H), 2.02-1.78 (bm, 1H), 1.01-0.78 (bm, 6H).
According to a similar procedure, the following compounds are obtained:
A solution of methyl 2-(3-fluoro-4-morpholinophenylamino)acetate (400 mg, 1.49 mmol), of formula (VII), in DMF (14 ml) is added with a catalytic amount of dimethylaminopyridine, and di-t-butylcarbonate (2.928 g, 13.41 mmol). The mixture is heated at 120° C. for about 30 minutes. Afterwards, the mixture is diluted with diethyl ether and the organic phase is washed with water. The organic phases are dried over Na2SO4 and evaporated under reduced pressure. The product is purified by flash chromatography to obtain 404 mg of product in 67% yield.
1H NMR (400 MHz, CDCl3) ppm 7.17-6.95 (bs, 2H), 6.89 (t, J=8, 5 Hz, 1H), 4.26 (s, 2H), 3.94-3.84 (m, 4H), 3.78 (s, 3H), 3.16-3.02 (m, 4H), 1.46 (s, 9H).
According to a similar procedure, the following compounds are obtained:
A solution of 2-((3-fluoro-4-morpholinophenyl)(t-butoxycarbonyl)amino) methyl acetate (404 mg, 1.09 mmol) of formula (VIII), in toluene (5.5 ml), cooled at about −78° C. and under N2 atmosphere, is dropwise added with a 1.0 M solution of Dibal-H in CH2Cl2 (1.65 ml, 1.65 mmol). Afterwards, the mixture is reacted 1 hour, then 893 μl of methanol are dropped therein, keeping a temperature of about −78° C. The reaction mixture is then left to warm at room temperature and added with a NH4Cl saturated solution. The aqueous phase is extracted three times with ethyl acetate (the formed Al3+ salts should be removed from the resulting mixture by filtration through Celite). The combined organic phases are separated, dried over Na2SO4 and evaporated under reduced pressure. The product is recovered by flash chromatography to obtain 315.3 mg of product, in 86% yield.
1H NMR (400 MHz, CDCl3) ppm 9.70 (s, 1H), 7.14-6.81 (m, 3H), 4.32 (s, 2H), 3.93-3.85 (m, 4H), 3.13-3.05 (m, 4H), 1.46 (s, 9H)
According to a similar procedure, the following compounds are obtained:
A solution of methyl 2-(3-fluoro-4-morpholinophenylamino)acetate (200 mg, 1.019 mmol), of formula (VI), in CH3CN (1 ml) is added with diisopropylethylamine (266 μl, 1.528 mmol), chloroacetaldehyde diethylacetal (611 μl, 4.077 mmol) and a catalytic amount of tetrabutylammonium iodide. The solution is microwave heated in a closed vessel, at 170° C. for about 30 minutes. After that, acetonitrile is evaporated off under reduced pressure, the residue is taken up with water and extracted 3 times with ethyl acetate. The combined organic phases are dried over Na2SO4 and evaporated under reduced pressure. The product is purified by flash chromatography (hexane:acetate 7:3) to a 22% final yield.
1H NMR (400 MHz, CDCl3) ppm 6.85 (b, 1H), 6.49-6.3 (m, 2H), 4.67 (t, J=5.4 Hz, 1H), 3.87 (m, 4H), 3.74 (qd, J=9.42, 7.08 Hz, 2H), 3.58 (qd, J=9.37, 7.02 Hz, 2H), 3.21 (m, 2H), 2.99 (m, 4H), 1.25 (t, J=7.07 Hz, 6H).
A solution of methyl 2-(3-fluoro-4-morpholinophenylamino)acetate (3 g, 15.289 mmol), of formula (VI), in EtOH (61 ml), under N2 atmosphere, is added with a dimethoxyacetaldehyde aqueous solution 60% weight/weight (3.068 ml, 20.33 mmol) and the mixture is left under stirring for about 2 hours. After that, 300 mg of Pd/C are added and the mixture is kept under H2 atmosphere at atmospheric pressure. After approximately 12 hours the reaction is completed, the catalyst is filtered through Celite, the residue is washed with ethanol and ethyl acetate, the solvent mixture is evaporated off under reduced pressure, the crude is taken up with ethyl acetate and the organic phase is washed 3 times with H2O. The combined organic phases are dried over Na2SO4 and evaporated under reduced pressure. The resulting product is recrystallized from hexane in a yield higher than 90%.
1H NMR (400 MHz, CDCl3) ppm 7.04-6.76 (bm, 1H), 6.46-6.34 (m, 2H), 4.56 (t, J=5.5 Hz, 1H), 3.98-3.79 (m, 5H), 3.43 (s, 6H), 3.21 (d, J=5.5 Hz, 2H), 3.07-2.95 (bm, 4H).
A solution of N-(2,2-diethoxyethyl)-3-fluoro-4-morpholinoaniline (500 mg, 1.758 mmol), of formula (IX), in CH3CN (17.58 ml) is added with diisopropylethylamine (306 μl, 1.758 mmol), ethyl chloroformate (336 μl, 3.517 mmol) and a catalytic amount of dimethylaminopyridine. The mixture is microwave heated in a closed vessel at about 170° C. for approximately 30 minutes. After that, a further equivalent of ethyl chloroformate is added and the mixture is heated for a further 30 minutes under the same conditions at about 170° C. Afterwards, acetonitrile is evaporated off under reduced pressure, then the resulting solid is taken up with H2O (pH should be basic) and the aqueous phase is extracted 3 times with ethyl acetate. The organic phases are dried over Na2SO4 and evaporated under reduced pressure. The product is crystallized from MeOH and H2O in 80% yield.
1H NMR (400 MHz, CDCl3) ppm 7.16-6.95 (m, 2H), 6.85 (t, J=9.17 Hz, 1H), 4.56 (m, 1H), 4.20-4.01 (m, 2H), 3.80-3.75 (m, 4H), 3.67 (d, 2H), 3.31 (s, 6H), 1.34-1.14 (m, 9H).
According to a similar procedure, the following compounds are obtained:
A solution of N-(2,2-dimethoxyethyl)-3-fluoro-4-morpholinoaniline (25.0 g, 87.9 mmol), of formula (IX), in toluene (250 ml) is added with 12.8 g of N,N-diisopropyl ethylamine (99.0 mmol) and heated to 50° C. A solution of 14.3 g of ethyl chloroformate (132 mmol) in 30 ml of toluene is then dropped therein in about 30 minutes. After completion of the addition, the mixture is reacted at 50° C. for about 20 minutes, then left to cool, and added with 220 ml of a solution prepared from 9.5 g of 37% HCl and purified water. The phases are separated, the aqueous phase is extracted again with toluene and the combined organic phases are washed with water. The combined organic phases are dried over Na2SO4 and evaporated under reduced pressure.
1H NMR (400 MHz, CDCl3) ppm 7.16-6.95 (m, 2H), 6.85 (t, J=9.17 Hz, 1H), 4.56 (m, 1H), 4.20-4.01 (m, 2H), 3.90-3.85 (m, 4H), 3.67 (d, 2H), 3.31 (s, 6H), 3.08-3.03 (m, 4H), 1.24-1.14 (m, 3H).
According to a similar procedure, the following compounds are obtained:
A solution of ethyl 2,2-dimethoxyethyl(3-fluoro-4-morpholino-phenyl)carbamate (500 mg, 1.6 mmol), of formula (X), in CH3CN (16 ml) is added with a 3 N HCl aqueous solution (about 500 μl). The solution is then microwave heated in a closed vessel at about 170° C. for approximately 30 minutes. After that, the solvent is evaporated off under reduced pressure and the product is purified by flash chromatography (hexane:acetate 6:4) to provide an oil in 60% yield.
1H NMR (400 MHz, CDCl3) ppm 9.70 (s, 1H), 7.06-6.95 (m, 2H), 6.93-6.86 (m, 1H), 4.38 (s, 2H), 4.20 (q, J=7.1 Hz, 2H), 3.90-3.86 (m, 4H), 3.12-3.07 (m, 4H), 1.25 (t, J=7.0 Hz, 3H).
According to a similar procedure, the following compounds are obtained:
A solution of ethyl 2,2-dimethoxyethyl-(3-fluoro-4-morpholino-phenyl)carbamate (28.5 g, 80 mmol), of formula (X), in 9:1 CH3CN:H2O (300 ml) is added with 136 g (1.2 mol) of CF3COOH in about 1.5 h keeping the inner temperature below 30° C. The mixture is reacted for 18 h. After completion of the reaction, the solvent is evaporated off under reduced pressure, repeatedly removing water with toluene. The residue is then taken up with ethyl acetate and water and the aqueous phase is basified with K2CO3. The phases are separated, the aqueous phase is extracted again with ethyl acetate and the combined organic phases are washed with water. The combined organic phases are dried over Na2SO4 and evaporated under reduced pressure. 24.3 g of a light color solid is obtained.
1H NMR (400 MHz, CDCl3) ppm 9.70 (s, 1H), 7.06-6.95 (m, 2H), 6.93-6.86 (m, 1H), 4.38 (s, 2H), 4.20 (q, J=7.1 Hz, 2H), 3.90-3.86 (m, 4H), 3.12-3.07 (m, 4H), 1.25 (t, J=7.0 Hz, 3H).
According to a similar procedure, the following compounds are obtained:
66 μl of tetrabutylammonium fluoride, 1 M solution in tetrahydrofuran, equivalent to 0.9 eq, is diluted in tetrahydrofuran (1.5 ml) under nitrogen stream and magnetic stirring. The solution is cooled to about 0° C. and the resulting mixture is added with a solution of 2.4 eq of CH3NO2 (9.6 μl) in tetrahydrofuran (290 μl). The reaction mixture is left under stirring at about 0° C. and a solution of ethyl 3-fluoro-4-morpholinophenyl(2-oxoethyl) carbamate (25 mg, 1 eq), of formula (V), in 0.6 ml of tetrahydrofuran is dropped therein under nitrogen stream. After about 20 minutes at 0° C. the reaction is completed. The reaction mixture is poured in an ammonium chloride aqueous saturated solution. The aqueous phase is extracted 3 times with ethyl acetate and the combined organic phases are washed with water and subsequently dried over dry Na2SO4. The solvent is evaporated off under reduced pressure, then the product is purified by flash chromatography (eluent hexane/acetate 1:1) to obtain an ivory white solid in 75% yield.
1H NMR (400 MHz, CDCl3) ppm 7.07-6.87 (m, 3H), 4.59-4.49 (m, 1H), 4.49-4.41 (m, 2H), 4.18 (q, J=7.1 Hz, 2H), 3.92-3.81 (m, 5H), 3.76 (dd, J=14.6, 4.6 Hz, 1H), 3.73-3.53 (b, 1H), 3.15-3.07 (m, 4H), 1.23 (t, J=7.0 Hz, 3H).
According to a similar procedure, the following compounds are obtained:
A solution of (3aR,3a′R,8aS,8a′S)-2,2′-(propane-2,2-diyl)bis(8,8a-dihydro-3aH-indeno[1,2-d]oxazole) (Indabox; 6 mg, 0.11 eq) and copper acetate hydrate (3 mg, 0.1 eq) in ethanol (240 μl) is prepared, and kept under stirring for 60 minutes; then ethyl 3-fluoro-4-morpholinophenyl(2-oxoethyl)carbamate (50 mg, 1 eq), of formula (V), and nitromethane (86.6 μl, 10 eq) are added. After about 6 days, the solvent is evaporated off under reduced pressure and the product is purified by flash chromatography (eluent: CH2Cl2/Et2O 8:2), to obtain an ivory white solid in 66% yield. Chiral HPLC analysis shows that the two enantiomers (S) and (R) are present in a 93.6 to 6.4 ratio.
1H NMR (400 MHz, CDCl3) ppm 7.07-6.87 (m, 3H), 4.59-4.49 (m, 1H), 4.49-4.41 (m, 2H), 4.18 (q, J=7.1 Hz, 2H), 3.92-3.81 (m, 5H), 3.76 (dd, J=14.6, 4.6 Hz, 1H), 3.73-3.53 (b, 1H), 3.15-3.07 (m, 4H), 1.23 (t, J=7.0 Hz, 3H).
A solution of (3aR,3a′R,8aS,8a′S)-2,2′-(propane-2,2-diyl)bis(8,8a-dihydro-3aH-indeno[1,2-d]oxazole) (Indabox; 125 mg, 0.11 eq) and copper acetate hydrate (66 mg, 0.1 eq) in ethanol (5.2 ml) is prepared, and kept under stirring for 60 minutes; then ethyl 3-fluoro-4-morpholinophenyl(2-oxoethyl)carbamate (1.0 g, 3.2 mmol), of formula (V), and nitromethane (1.7 ml, 10 eq) are added. After about 7 days, the reaction mixture is concentrated under reduced pressure and the crude diluted in ethyl acetate and washed with a diluted aqueous solution of ammonia. After separation, the organic phase is washed with water, dried over sodium sulfate, filtered and concentrated under reduced pressure to a residue. The crude is purified by crystallization from toluene to give a white solid in 80% yield. Chiral HPLC analysis shows that the two enantiomers (S) and (R) are present in a 94.4 to 5.6 ratio.
1H NMR (400 MHz, CDCl3) ppm 7.07-6.87 (m, 3H), 4.59-4.49 (m, 1H), 4.49-4.41 (m, 2H), 4.18 (q, J=7.1 Hz, 2H), 3.92-3.81 (m, 5H), 3.76 (dd, J=14.6, 4.6 Hz, 1H), 3.73-3.53 (b, 1H), 3.15-3.07 (m, 4H), 1.23 (t, J=7.0 Hz, 3H).
According to a similar procedure, the following compounds are obtained:
The resulting compounds of formula (III) have enantiomeric purity of approximately 99.7%.
Following a similar procedure to that of Example 12, using a solution of (3aS,3a′ S,8aR,8a′R)-2,2′-(propane-2,2-diyl)bis(8,8a-dihydro-3aH-indeno[1,2-d]oxazole), the three compounds of Example 12 are obtained, as (R) enantiomers.
A methanol solution of racemic ethyl 3-fluoro-4-morpholinophenyl(2-hydroxy-3-nitropropyl) carbamate (500 mg, 1 eq), of formula (III), is added with 100 mg of 10% Pd/C. The reaction mixture is kept under H2 atmosphere for about 4 hours. Afterwards, the reaction mixture is filtered through Celite. The celite pad is repeatedly washed with ethyl acetate. The solvent is evaporated off under reduced pressure and the product is purified by flash chromatography (eluent: CH2Cl2/MeOH 9:1 1% TEA). The yield is 54%.
1H NMR (400 MHz, CDCl3) ppm 7.06-6.85 (m, 3H), 4.99-4.50 (b, 3H)(exchange with D2O), 4.24-4.08 (m, 3H), 3.93-3.85 (m, 4H), 3.82 (dd, J=14.4, 8.0 Hz, 1H), 3.65 (dd, J=14.4, 4.1 Hz, 1H), 3.17-3.04 (m, 5H), 3.04-2.90 (m, 1H), 1.21 (t, J=6.9 Hz, 3H).
According to a similar procedure, the following compounds are obtained:
According to a similar procedure, starting from the (R) or (S) enantiomers of the respective compounds of formula (III), the (S) or (R) enantiomers of the compounds of formula (IV) are respectively obtained.
A solution of racemic ethyl 3-amino-2-hydroxypropyl(3-fluoro-4-morpholinophenyl) carbamate (50 mg, 1 eq), of formula (IV), in 1.5 ml of CH2Cl2, under nitrogen atmosphere, is added with 13.2 μl, 1 eq of acetic anhydride and 19.48 μl, 1 eq of triethylamine. After 2 hours the reaction mixture is poured in water and the aqueous phase is extracted 3 times with CH2Cl2; the combined organic phases are dried over dry Na2SO4. The solvent is evaporated off under reduced pressure and the product is recovered by flash chromatography (eluent: acetate). The yield is 25%.
1H NMR (400 MHz, CDCl3) ppm 7.07-6.84 (m, 3H), 4.25-4.09 (m, 2H), 4.08-3.96 (m, 1H), 3.94-3.84 (m, 4H), 3.79 (dd, J=14.6, 7.7 Hz, 1H), 3.69 (dd, J=14.6, 4.0 Hz, 1H), 3.18-3.04 (m, 5H), 2.96 (dd, J=13.3, 8.1 Hz, 1H), 2.09 (s, 3H), 1.23 (t, J=7.0 Hz, 3H).
According to a similar procedure, the following compounds are obtained:
According to a similar procedure, starting from the (R) or (S) enantiomers of the respective compounds of formula (IV), the (R) or (S) enantiomers of the compounds of formula (II) are obtained respectively.
A solution of 10 mg of racemic ethyl 3-acetamido-2-hydroxypropyl(3-fluoro-4-morpholinophenyl) carbamate, of formula (II), in tetrahydrofuran, under nitrogen stream at room temperature, is dropped into a round-bottom flask containing 1 mg of NaH. After about 90 minutes the reaction is completed. An ammonium chloride aqueous saturated solution is added and the aqueous phase is extracted 3 times with ethyl acetate. The combined organic phases are dried over dry Na2SO4 and the solvent is evaporated off under reduced pressure. The product is recovered by flash chromatography (eluent acetate/MeOH 9:1) in 30% yield.
1H NMR (400 MHz, CDCl3) ppm 7.47 (dd, J=14.4, 2.6 Hz, 1H), 7.13-7.07 (m, 1H), 6.98 (t, J=9.1 Hz, 1H), 6.13 (t, J=5.9 Hz, 1H), 4.83-4.75 (m, 1H), 4.04 (t, J=9.0 Hz, 1H), 3.93-3.87 (m, 4H), 3.80-3.68 (m, 2H), 3.68-3.58 (m, 1H), 3.12-3.05 (m, 4H), 2.04 (s, 3H).
A solution of 4.8 g (12.5 mmol) of racemic ethyl 3-acetamido-2-hydroxypropyl(3-fluoro-4-morpholinophenyl) carbamate, of formula (II), in ethanol (35 ml) is added with potassium t-butoxide (1.5 g, 12.7 mmol) and the mixture is reacted at room temperature. After about 20 minutes, a solid precipitates which is filtered and washed with ethanol, to obtain 2.1 g of product (50% yield).
1H NMR (400 MHz, CDCl3) ppm 7.47 (dd, J=14.4, 2.6 Hz, 1H), 7.13-7.07 (m, 1H), 6.98 (t, J=9.1 Hz, 1H), 6.13 (t, J=5.9 Hz, 1H), 4.83-4.75 (m, 1H), 4.04 (t, J=9.0 Hz, 1H), 3.93-3.87 (m, 4H), 3.80-3.68 (m, 2H), 3.68-3.58 (m, 1H), 3.12-3.05 (m, 4H), 2.04 (s, 3H).
According to a similar procedure, the following compounds are obtained:
starting from the (R) or (S) enantiomer of an alkyl carbamate of formula (II), obtained in example 15, the title compound is obtained as the single (R) or (S) enantiomer.
The resulting compounds of formula (I), have enantiomeric purity approximately equal to 99.7% and mean particle size D50 of about 50 micrometres.
| Number | Date | Country | Kind |
|---|---|---|---|
| MI 2007 A 002359 | Dec 2007 | IT | national |
