Oxazolidine derivatives and pharmaceutically acceptable salts thereof

This is a 371 of PCT/JP93/00559 filed Apr. 28, 1993.
TECHNICAL FIELD
The present invention relates to novel oxazolidine derivatives and pharmaceutically acceptable salts thereof which have an activity to decrease triglyceride and cholesterol in the blood and which is useful as an anti-hyperlipidemic agent.
BACKGROUND ART
According to epidemiological investigation in Helsinki, it is considered that triglyceride and cholesterol in the blood are closely associated with the onset of hyperlipidemia (Circulation, 1992; vol. 85: 37-45). Therefore, for more effective and proper suppression of hyperlipidemia, it is desired to inhibit both the synthesis of triglyceride and cholesterol in the blood. Now there is a strong demand for the development of drugs capable of potently inhibiting their syntheses in the blood. However, while the phenylcarboxylic acid derivatives and the like disclosed in Japanese Unexamined Patent Publications Nos. 56452/1990 corresponding to U.S. Pat. No. 4,999,378, and 275666/1991 corresponding to U.S. Pat. No. 5,145,865 are known as compounds capable of lowering blood triglyceride and cholesterol, a compound which can satisfactorily produce the effect of lowering both of them has not yet been developed.
DISCLOSURE OF THE INVENTION
The present inventors conducted extensive research in view of the problems in the prior art and found that novel oxazolidine derivatives represented by the following formula (I) and pharmaceutically acceptable salts thereof have an excellent activity to inhibit the synthesis of triglyceride and activity to inhibit the synthesis of cholesterol and are useful as a medicament. The present invention has been accomplished based on this finding.
The present invention provides an oxazolidine derivative represented by the formula (I) ##STR2## wherein R.sup.1, R.sup.2 and R.sup.3 are the same or different, and each represents a hydrogen atom, a lower alkyl group optionally having one or more halogen atoms, a lower alkoxy group optionally having one or more halogen atoms, a hydroxyl group, a halogen atom, a nitro group, an amino group optionally having one or more acetyl or lower alkyl groups, a carboxyl group, a lower alkoxycarbonyl group, a cyano group, a lower alkanoyl group or a 2-oxazolyl group, or R.sup.1 and R.sup.2 may be combined with each other to represent an alkylene chain --(CH.sub.2).sub.p -- or an alkylenedioxy chain --O(CH.sub.2).sub.q O-- wherein p is 3, 4 or 5, q is 1, 2 or 3, thus forming a cyclic structure, m and n are each 0 or 1, R.sup.4 and R.sup.5 are the same or different and each represents a hydrogen atom or a lower alkyl group, X is a carbon atom or a nitrogen atom, Y is a hydroxymethyl group, an aldehyde group or a group represented by COOR.sup.6 (R.sup.6 is a lower alkyl group, a benzyl group or a hydrogen atom), A is a lower alkylene group, a carbonyl group or a sulfonyl group, B is a lower alkylene group, E is a lower alkylene group which may be substituted with a halogen atom or is a lower alkenylene group, Z is an oxygen atom or a sulfur atom, with the proviso that when n is 0, a compound wherein m is 1 and Y is a hydroxymethyl group is excluded and that when n is 0, a compound wherein Y is a group represented by COOR.sup.6 (R.sup.6 is a lower alkyl group) is excluded; or a pharmaceutically acceptable salt thereof.
With the oxazolidine derivative of the formula (I), optical isomers and geometrical isomers exist. The present invention includes these isomers and mixtures thereof.
The compounds of the formula (I) and pharmaceutically acceptable salts thereof according to the present invention have an activity to decrease blood triglyceride and cholesterol. These compounds have the features of being highly absorbable in the living body, having a long-sustained efficacy, and being excellent in the safety, the absorption and the excretion and less toxic. Thus the compounds are useful as drugs such as an anti-hyperlipidemic agent, an agent for preventing and treating arteriosclerosis, an anti-obesity agent and the like.
Thus the present invention provides an anti-hyperlipidemic composition, a composition for treating arteriosclerosis and a composition for treating obesity, each containing an effective amount of the compound of the formula (I) and a pharmaceutically acceptable carrier.
The present invention also provides a method of treating hyperlipidemia, arteriosclerosis or obesity, characterized by administering an effective amount of the compound of the formula (I) to a patient.
The invention further provides a process for preparing the compound of the formula (I).
Given below are specific examples of the groups as defined by R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5 and R.sup.6, A, B, E and Y in the formula (I) and the groups described herein.
Examples of the lower alkyl group optionally having one or more halogen atoms are a lower alkyl group and a lower alkyl group having one or more halogen atoms.
Examples of the lower alkyl group are straight- or or branched-chain alkyl groups having 1 to 6 carbon atoms such as methyl, ethyl, n-propyl, isopropyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, pentyl, iso-pentyl, hexyl and the like.
Examples of the lower alkyl group having one or more halogen atoms are straight- or branched-chain alkyl groups containing 1 to 6 carbon atoms and having 1 to 3 halogen atoms such as chloromethyl, bromomethyl, iodomethyl, fluoromethyl, dichloromethyl, dibromomethyl, difluoromethyl, trichloromethyl, tribromomethyl, trifluoromethyl, 2-chloroethyl, 2-bromoethyl, 2-fluoroethyl, 1,2-dichloroethyl, 2,2-difluoroethyl, 1-chloro-2-fluoroethyl, 2,2,2-trifluoroethyl, 2,2,2-trichloroethyl, 3-fluoropropyl, 3,3,3-trichloropropyl, 4-chlorobutyl, 5-chloroheptyl, 6-chlorohexyl, 3-chloro-2-methylpropyl, etc.
Examples of the lower alkoxy group optionally having one or more halogen atoms are lower alkoxy groups or lower alkoxy groups having one or more halogen atoms.
Examples of the lower alkoxy group are straight- or branched-chain alkoxy groups having 1 to 6 carbon atoms such as methoxy, ethoxy, n-propoxy, iso-propoxy, n-butoxy, iso-butoxy, sec-butoxy, tert-butoxy, n-pentyloxy, iso-pentyloxy, n-hexyloxy, etc.
Examples of the lower alkoxy group having one or more halogen atoms are straight- or branched-chain lower alkoxy groups containing 1 to 6 carbon atoms and having 1 to 3 halogen atoms such as chloromethoxy, bromomethoxy, iodomethoxy, fluoromethoxy, dichloromethoxy, dibromomethoxy, difluoromethoxy, trichloromethoxy, tribromomethoxy, trifluoromethoxy, 2-chloroethoxy, 2-bromoethoxy, 2-fluoroethoxy, 1,2-dichloroethoxy, 2,2-difluoroethoxy, 1-chloro-2-fluoroethoxy, 2,2,2-trifluoroethoxy, 2,2,2-trichloroethoxy, 3-fluoropropoxy, 3,3,3-trichloropropoxy, 4-chlorobutoxy, 5-chlorohexoxy, 6-chlorohexyloxy, 3-chloro-2-methylpropyloxy, etc.
Examples of halogen atoms are fluorine, chlorine, bromine and iodine atoms.
Examples of the amino group optionally having one or more acetyl or lower alkyl groups are amino group, acetylamino group or an amino group having one or more lower alkyl groups.
The amino group having one or more lower alkyl groups is an amino group wherein one of the hydrogen atoms thereof is mono-substituted with any of the lower alkyl groups exemplified above or the two hydrogen atoms thereof are di-substituted with the same or different lower alkyl groups exemplified above, and includes, for example, an amino group having one or more straight- or branched-chain alkyl groups containing 1 to 6 carbon atoms, such as methylamino, ethylamino, n-propylamino, iso-propylamino, n-butylamino, tert-butylamino, pentylamino, hexylamino, dimethylamino, diethylamino, di-n-propylamino, di-isopropylamino, di-n-butylamino, di-tert-butylamino, dipentylamino, dihexylamino, methylethylamino, methyl n-propylamino, ethyl n-propylamino, ethyl n-butylamino, ethyl iso-butylamino, etc.
The lower alkoxycarbonyl group is an ester group of a carboxyl group with one of the alkyl groups as exemplified above, and includes, for example, a lower alkoxycarbonyl group containing a straight- or branched-chain alkoxy group having 1 to 6 carbon atoms, such as methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl, iso-propoxycarbonyl, n-butoxycarbonyl, iso-butoxycarbonyl, sec-butoxycarbonyl, tert-butoxycarbonyl, n-pentyloxycarbonyl, iso-pentyloxycarbonyl, n-hexyloxycarbonyl, etc.
Examples of the lower alkanoyl group are straight- or branched-chain alkanoyl groups having 1 to 6 carbon atoms such as formyl, acetyl, propionyl, butyryl, isobutyryl, pentanoyl, hexanoyl, etc.
Examples of the alkylene chain --(CH.sub.2).sub.p -- wherein p is 3, 4 or 5 are alkylene chains having 3 to 5 carbon atoms such as propylene, butylene, pentylene, etc.
Examples of the alkylenedioxy chain --O(CH.sub.2).sub.q O-- wherein q is 1, 2 or 3 are alkylenedioxy chains having 1 to 3 carbon atoms such as methylenedioxy, ethylenedioxy, propylenedioxy, etc.
Examples of the lower alkylene group are straight- or branched-chain alkylene groups having 1 to 4 carbon atoms such as methylene, ethylene, trimethylene, tetramethylene, methylmethylene, 2-methyltrimethylene, etc.
Examples of the lower alkylene group which may be substituted with a halogen atom are lower alkylene groups or lower alkylene groups which are substituted with a halogen atom.
Examples of the lower alkylene group which is substituted with a halogen atom are straight- or branched-chain alkylene groups having 1 to 4 carbon atoms such as fluoromethylene, chloromethylene, bromomethylene, 1-chloroethylene, 2-chloroethylene, 1-bromoethylene, 2-bromoethylene, 2-chlorotrimethylene, 2-chlorotetramethylene, chloromethylmethylene, 2-chloromethyltrimethylene, etc.
Examples of the lower alkenylene group are straight- or branched-chain cis- or trans-alkenylene groups having 2 to 4 carbon atoms such as vinylene, 2-methylvinylene, propenylene, butenylene, etc.
The salt of the compound of the formula (I) include an acid addition salt or a basic salt prepared by causing a pharmaceutically acceptable acid or basic compound to act on the compound of the formula (I). Examples of the acid addition salt are salts of the compounds of the formula (I) having a basic group, especially an amino group, or a mono- or di-lower alkylamino group with an acid, such as an inorganic acid including hydrochloric acid, sulfuric acid, phosphoric acid, hydrobromic acid or the like, or an organic acid including oxalic acid, maleic acid, fumaric acid, malic acid, tartaric acid, citric acid, benzoic acid, acetic acid, p-toluenesulfonic acid, ethanesulfonic acid or the like. Examples of the basic salt include salts of the compounds of the formula (I) having an acidic group, especially carboxyl group with a base, e.g., salts of alkali metals such as sodium, potassium or the like or salts of alkaline earth metals such as magnesium, calcium or the like, and further include organic salts of the compounds of the formula (I) with amines such as ammonia, methylamine, dimethylamine, piperidine, cyclohexylamine, triethylamine or the like.
In the compound of the formula (I),
m is 0 or 1, preferably m is 0;
n is 0 or 1, preferably n is 0;
B is bonded to the 4- or 5-position of the oxazolidine ring, preferably is bonded to the 5-position thereof;
Y is preferably a carboxyl group;
R.sup.4 is preferably a hydrogen atom;
R.sup.5 is preferably a hydrogen atom; and
Z is preferably an oxygen atom.
Preferred compounds are those wherein m and n are 0 and B is bonded to the 5-position of the oxazolidine ring.
Preferably, m is 0, B is attached to the 5-position of the oxazolidine ring, R.sup.4 and R.sup.5 represent a hydrogen atom, and Z is an oxygen atom. Preferably, m and n are 0, B is attached to the 5-position of the oxazolidine ring, R.sup.4 and R.sup.5 represent a hydrogen atom, and Z is an oxygen atom.
The oxazolidine derivatives of the formula (I) according to the present invention can be prepared from a variety of starting compounds, for example, by Processes A to F described below.
In the following processes, the compound wherein Y in its formula is a hydroxymethyl group or a carboxyl group can also be subjected to the reaction after protecting said group with a suitable protective group. Useful protective groups are not specifically limited insofar as the protective group does not produce adverse effect when the said protective group is removed by a deprotection reaction. For protecting a hydroxymethyl group, useful protective groups include methyl, ethyl and like lower alkyl groups, methoxymethyl, methoxyethyl and like lower alkoxyalkyl groups, tetrahydropyranyl, benzyl, trimethylsilyl, benzoyl and like acyl groups, and for protecting a carboxyl group, methyl, ethyl and like lower alkyl groups, benzyl and the like can be used.
When R.sup.1, R.sup.2 and R.sup.3 represent a hydroxyl or carboxyl group in the formula of the compound, the compound can also be subjected to the reaction after protecting said group with a suitable protective group. Useful protective groups are not specifically limited insofar as the said protective group does not produce adverse effect when the protective group is removed by a deprotection reaction. For protecting a hydroxyl group, useful protective groups include methyl, ethyl and like lower alkyl groups, methoxymethyl, methoxyethyl and like lower alkoxyalkyl groups, tetrahydropyranyl, benzyl, trimethylsilyl, benzoyl and like acyl groups. For protecting a carboxyl group, methyl, ethyl and like lower alkyl groups, benzyl and the like can be used.
When R.sup.1, R.sup.2 and R.sup.3 are a primary or secondary amino group which may have one or more lower alkyl groups, the compound in question may be subjected to the reaction after protecting said group with a suitable protective group. Useful protective groups are not specifically limited insofar as the said protective group does not produce adverse effect when the protective group is removed by a deprotection reaction. Usable as such protective groups are acetyl, benzoyl and like acyl groups, benzyl, Boc, Cbz and like urethane-type protective groups.
These protective groups can be deprotected by conventional methods. ##STR3##
In the above formulas, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, A, B, E, X, Y, Z, m and n are as defined above, W is a halogen atom, an optionally substituted lower alkanesulfonyloxy group or an optionally substituted arylsulfonyloxy group.
In the compound of the formula (III), halogen atoms represented by W include the same atoms as exemplified above; and optionally substituted lower alkanesulfonyloxy groups are those having 1 to 6 carbon atoms which may be halogen-substituted, such as methanesulfonyloxy, ethanesulfonyloxy, propanesulfonyloxy, trifluoromethanesulfonyloxy and the like; optionally substituted arylsulfonyloxy groups include those which may be substituted with an alkyl group having 1 to 6 carbon atoms, a halogen atom or a nitro group, such as benzenesulfonyloxy, toluenesulfonyloxy, p-chlorobenzenesulfonyloxy, m-nitrobenzenesulfonyloxy and the like.
The steps in the above reaction scheme are carried out as described below in more detail.
(Step 1)
The compounds of the formula (IV), which in part include novel compounds, can be prepared by reacting the known compound of the formula (II) with the known compound of the formula (III) in a suitable solvent in the presence of a basic compound according to, for example, the process disclosed in Journal of Synthesis Organic Chemistry, Japan, 24, 60 (1966).
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of such solvents are diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, pyridine, piperidine, triethylamine and like amines, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, methanol, ethanol, propanol and like alcohols, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, hexamethylphosphoramide and like aprotic polar solvents, etc.
Examples of the basic compounds are organic basic compounds such as triethylamine, pyridine and like tertiary amines, and inorganic basic compounds such as sodium carbonate, potassium carbonate and like alkali metal carbonates, sodium hydrogencarbonate, potassium hydrogencarbonate and like alkali metal hydrogencarbonates, sodium hydroxide, potassium hydroxide and like alkali metal hydroxides, sodium, potassium and like alkali metals, and sodium hydride and like alkali metal hydrides.
As to the proportions of the reactants, it is preferable that 1 to 2 mole equivalents of the compound of the formula (III), and 1 to 10 mole equivalents, preferably 1 to 3 mole equivalents, of the basic compound are used per mole of the compound of the formula (II). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 0.degree. to 80.degree. C. The reaction time is 0.5 to 48 hours, preferably 1 to 24 hours.
The compound of the formula (IV) prepared by the above reaction can be used in Step 2 after isolation or without isolation.
(Step 2)
The compounds of the formula (I-a) according to the invention can be prepared by reacting the compound of the formula (IV) with the known compound of the formula (V) in a suitable solvent in the presence of lithium bromide and tri-n-butylphosphine oxide.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are benzene, toluene, xylene and like aromatic hydrocarbons, diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide and like aprotic polar solvents, etc.
As to the proportions of the reactants, it is preferable that 1 to 1.5 mole equivalents of the compound of the formula (V), and 0.01 to 0.3 mole equivalent, preferably 0.03 to 0.05 mole equivalent, of each of lithium bromide and tri-n-butylphosphine oxide are used per mole of the compound of the formula (IV). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 70.degree. to 140.degree. C. The reaction time is 0.1 to 6 hours, preferably 0.5 to 2 hours. ##STR4##
In the above formulas, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, A, B, E, W, X, Y, Z, m and n are as defined above.
The steps in the above reaction scheme are carried out as described below in more detail.
(Step 1)
The compound of the formula (VI) can be prepared by reacting the known compound of the formula (V) with the known compound of the formula (III) in a suitable solvent in the presence of lithium bromide and tri-n-butylphosphine oxide.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of solvents are benzene, toluene, xylene and like aromatic hydrocarbons, diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide and like aprotic polar solvents, etc.
As to the proportions of the reactants, it is preferable that 1 to 1.5 mole equivalents of the compound of the formula (III), and 0.01 to 0.3 mole equivalent, preferably 0.03 to 0.05 mole equivalent, of each of lithium bromide and tri-n-butylphosphine oxide are used per mole of the compound of the formula (V). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 70.degree. to 140.degree. C. The reaction time is 0.1 to 6 hours, preferably 0.5 to 3 hours.
The compound of the formula (VI) prepared by the above reaction can be used in Step 2 after isolation or without isolation.
(Step 2)
The compound of the formula (I-a) according to the invention can be prepared by reacting the compound of the formula (VI) with the compound of the formula (II) in a suitable solvent in the presence of a basic compound.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are benzene, toluene, xylene and like aromatic hydrocarbons, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide and like aprotic polar solvents, diethyl ether, tetrahydrofuran, dioxane and like ethers, methanol, ethanol, propanol and like alcohols, dichloromethane, chloroform and like halogenated hydrocarbons, pyridine, piperidine, triethylamine and like amines, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, etc.
Examples of the basic compounds are organic basic compounds such as triethylamine, pyridine and like tertiary amines, and inorganic basic compounds such as sodium carbonate, potassium carbonate and like alkali metal carbonates, sodium hydrogencarbonate, potassium hydrogencarbonate and like alkali metal hydrogencarbonates, sodium hydroxide, potassium hydroxide and like alkali metal hydroxides, sodium, potassium and like alkali metals, sodium hydride and like alkali metal hydrides and so on.
As to the proportions of the reactants, it is preferable that 1 to 1.5 mole equivalents of the compound of the formula (VI), and 1 to 10 mole equivalents, preferably 1 to 3 mole equivalents, of the basic compound are used per mole of the compound of the formula (II). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 0.degree. to 80.degree. C. The reaction time is 0.5 to 48 hours, preferably 2 to 12 hours.
The compound of the formula (I-a) obtained by (Process A) or (Process B) wherein Y is COOR.sup.6 (R.sup.6 is a lower alkyl group or a benzyl group) is subjected to hydrolysis or to catalytic reduction by a known conventional method, giving the compound of the present invention wherein R.sup.6 is a hydrogen atom.
For example, the hydrolysis reaction is conducted in a suitable inert solvent by causing the acidic compound or basic compound to act on the compound of the formula (I-a).
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are dimethyl ether, diethyl ether, tetrahydrofuran, dioxane, anisole and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, benzene, toluene, xylene and like aromatic hydrocarbons, pyridine, piperidine, triethylamine and like amines, hexane, heptane, octane and like aliphatic hydrocabons, methanol, ethanol, propanol and like alcohols, methyl acetate, ethyl acetate, and like acetic acid esters, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, hexamethylphosphoramide and like aprotic polar solvents, carbon disulfide, acetic acid, water, mixtures of water and these organic solvents and so on.
Examples of acidic compounds are anhydrous aluminum chloride, stannic chloride, titanium tetrachloride, boron trichloride, boron trifluoride-ethyl ether complex, zinc chloride and like Lewis acids, hydrochloric acid, nitric acid, sulfuric acid and like inorganic acids, trichloroacetic acid, trifluoroacetic acid, methanesulfonic acid, acetic acid and like organic acids, acid-type ion-exchange resins and so on. Examples of basic compounds are organic basic compounds such as triethylamine, tributylamine and like trialkylamines, pyridine, picoline, 1,5-diazabicyclo[4,3,0]nonene-5 (DBN), 1,8-diazabicyclo[5,4,0]undecene-7 (DBU), 7,4-diazabicyclo[2,2,2]octane (DABCO) and the like, and inorganic basic compounds such as sodium carbonate, potassium carbonate and like alkali metal carbonates, sodium hydrogencarbonate, potassium hydrogencarbonate and like alkali metal hydrogencarbonates, sodium hydroxide, potassium hydroxide and like alkali metal hydroxides, sodium, potassium and like alkali metals, sodium hydride and like alkali metal hydrides and the like. It is recommended that the above acidic compound or basic compound is used in an amount of about 1 to about 100 mole equivalents, preferably about 1 to about 20 mole equivalents, per mole of the compound of the formula (I-a). Said reaction is carried out at about -20.degree. to about 150.degree. C., preferably -10.degree. to 120.degree. C. for about 0.5 to about 48 hours, preferably 1 to 24 hours.
The catalytic reduction is performed in an inert solvent in the presence of a catalyst. Useful solvents are not specifically limited insofar as they do not participate in the reaction. For example, ethyl acetate, methanol, tetrahydrofuran, dimethylformamide, acetic acid and the like can be used alone or in combination. Useful catalysts include, for example, palladium carbon, platinum, and so on. For the reaction, it is desired that 0.01 to 2 g, preferably 0.1 to 0.5 g, of the catalyst is used per gram of the compound of the formula (I-a). The hydrogen pressure ranges from atmospheric pressure to 3 atms., preferably atmospheric pressure to 2 atms. The reaction temperature is 0.degree. to about 100.degree. C., preferably room temperature to 70.degree. C. The reaction time is 0.5 to 12 hours, preferably 1 to 4 hours.
The compound of the formula (I-a) obtained by (Process A) or (Process B) wherein Y is COOR.sup.6 (R.sup.6 is a hydrogen atom, a lower alkyl group or a benzyl group) is subjected to reduction by a known conventional method, giving the compound of the present invention wherein Y is a hydroxymethyl group. Stated more specifically, the compound is obtained by reduction in an inert solvent in the presence of lithium aluminum hydride or the like.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are tetrahydrofuran, dioxane, diethyl ether and so on. These solvents can be used alone or in combination. As to the proportions of the reactants, it is preferred that 0.5 to 3 mole equivalents of lithium aluminum hydride is used per mole of the compound of the formula (I-a). The reaction temperature is 0.degree. to 100.degree. C., preferably 0.degree. to 50.degree. C. The reaction time is 0.1 to 24 hours, preferably 0.5 to 6 hours.
Using an optically active compound of the formula (III) in Process A and Process B, an optically active oxazolidine derivative of the formula (I-a) according to the invention can be prepared. An optically active compound can be produced from a racemate in a conventional manner. ##STR5##
In the above formulas R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, A, B, E, W, X, Y, Z, m and n are as defined above.
The steps in the above reaction scheme are carried out as described below in more detail.
(Step 1)
The compounds of the formula (VIII), which in part include novel compounds, can be prepared by reacting the known compounds of the formulas (V) and (VII) in an inert solvent in the presence of triethylamine according to, for example, the process disclosed in Chemistry Letter, 1991, 1245.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are benzene, toluene, xylene and like aromatic hydrocarbons, diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide and like aprotic polar solvents, etc.
As to the proportions of the reactants, it is preferred that 1 to 1.5 mole equivalents of the compound of the formula (VII), and 0.5 to 10 mole equivalents, preferably 1 to 3 mole equivalents, of triethylamine are used per mole of the compound of the formula (V). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 0.degree. to 80.degree. C. The reaction time is 0.5 to 48 hours, preferably 2 to 24 hours.
The compound of the formula (VIII) prepared by the above reaction can be used in Step 2 after isolation or without isolation.
(Step 2)
The compound of the formula (IX) can be prepared by reacting the compound of the formula (VIII) with a halogenating agent, an alkanesulfonyl chloride having 1 to 6 carbon atoms which may be halogen-substituted or an optionally substituted arylsulfonyl chloride in an inert solvent in the presence or absence of an organic basic compound.
The reaction is carried out in a suitable solvent. Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are benzene, toluene, xylene and like aromatic hydrocarbons, triethyl amine, pyridine and like tertiary amines, diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide and like aprotic polar solvents, etc.
Examples of the organic basic compounds are triethylamine, pyridine and like tertiary amines. Useful halogenating agents include, for example, thionyl chloride, phosphorus oxychloride, phosphorus pentachloride, phosphorus tribromide, etc. Examples of the alkanesulfonyl chloride having 1 to 6 carbon atoms which may be halogen-substituted or optionally substituted arylsulfonyl chloride are methanesulfonyloxy chloride, ethanesulfonyloxy chloride, propanesulfonyloxy cloride, trifluoromethanesulfonyloxy chloride, benzene sulfonyloxy chloride, toluenesulfonyloxy chloride, p-chlorobenzenesulfonyloxy chloride, m-nitrobenzenesulfonyloxy chloride, etc.
As to the proportions of the reactants, it is preferred that 1 to 3 mole equivalents of the organic basic compound, and 1 to 2 mole equivalents of the halogenating agent, alkanesulfonyl chloride having 1 to 6 carbon atoms which may be halogen-substituted or optionally substituted arylsulfonyl chloride are used per mole of the compound of the formula (VIII). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 0.degree. to 100.degree. C. The reaction time is 0.1 to 24 hours, preferably 0.5 to 3 hours.
The compound of the formula (IX) prepared by the above reaction can be used in Step 3 after isolation or without isolation.
(Step 3)
The compound of the formula (I-b) according to the invention can be prepared by reacting the compound of the formula (IX) with the known compound of the formula (II) in a suitable solvent in the presence of a basic compound.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of solvents are diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, pyridine, piperidine, triethylamine and like amines, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, methanol, ethanol, propanol and like alcohols, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, hexamethylphosphoramide and like aprotic polar solvents, etc.
Examples of the basic compounds are organic basic compounds such as triethylamine, pyridine and like tertiary amines, and inorganic basic compounds such as sodium carbonate, potassium carbonate and like alkali metal carbonates, sodium hydrogencarbonate, potassium hydrogencarbonate and like alkali metal hydrogencarbonates, sodium hydroxide, potassium hydroxide and like alkali metal hydroxides, sodium, potassium and like alkali metals, sodium hydride and like alkali metal hydrides and so on.
As to the proportions of the reactants, it is desirable that 1 to 2 mole equivalents of the compound of the formula (II), and 1 to 5 mole equivalents, preferably 1 to 2 mole equivalents, of the basic compound are used per mole of the compound of the formula (IX). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 0.degree. to 80.degree. C. The reaction time is 0.5 to 48 hours, preferably 1 to 8 hours.
The compound of the formula (I-b) obtained by (Process C) wherein Y is COOR.sup.6 (R.sup.6 is a lower alkyl group or a benzyl group) is subjected to hydrolysis or to catalytic reduction by a known conventional method, giving the compound of the present invention wherein Y is a hydrogen atom. Additionally the compound of the invention wherein Y is a hydroxymethyl group can be prepared by reducing the compound of the formula (I-b) wherein Y is COOR.sup.6 (R.sup.6 is a hydrogen atom, a lower alkyl group or a benzyl group) by a known conventional method. For example, the compound can be prepared by the same method as used for preparing the compound of the formula (I-a).
Using an optically active compound of the formula (VII) in this process, an optically active oxazolidine derivative of the formula (I-b) according to the invention can be prepared. An optically active compound can be produced from a racemate in a conventional manner.
Some of the compounds according to the invention can be prepared by other processes given below, i.e. Processes D to F. ##STR6##
In the above formulas, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, A, B, X, Z and m are as defined above, and R.sup.7 is an optionally substituted lower alkyl group or an optionally substituted aryl group.
Examples of optionally substituted lower alkyl groups are alkyl groups having 1 to 6 carbon atoms which may be halogen-substituted, such as methyl, ethyl, propyl, trifluoromethyl and the like. Examples of optionally substituted aryl groups are aryl groups which may be substituted with an alkyl group having 1 to 6 carbon atoms, a halogen atom or a nitro group, such as phenyl, tolyl, p-chlorophenyl, p-nitrophenyl and the like.
The steps in the above reaction scheme are carried out as described below in more detail.
(Step 1)
The compound of the formula (XI) can be prepared by reacting the known compound of the formula (V) with the known compound of the formula (X) in a suitable solvent in the presence of lithium bromide and tri-n-butylphosphine oxide.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are benzene, toluene, xylene and like aromatic hydrocarbons, diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide and like aprotic polar solvents, etc.
As to the proportions of the reactants, it is desirable that 1 to 1.5 mole equivalents of the compound of the formula (V), and 0.01 to 0.3 mole equivalent, preferably 0.03 to 0.05 mole equivalent, of each of lithium bromide and tri-n-butylphosphine oxide are used per mole of the compound of the formula (X). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 70.degree. to 140.degree. C. The reaction time is 0.1 to 6 hours, preferably 0.5 to 2 hours.
The compound of the formula (XI) prepared by the above reaction can be used in Step 2 after isolation or without isolation.
(Step 2)
The compound of the formula (XII) can be prepared by a conventional hydrolysis by causing an acidic compound or a basic compound to act on the compound of the formula (XI) in a suitable inert solvent.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are diethyl ether, tetrahydrofuran, dioxane, anisole and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, benzene, toluene, xylene and like aromatic hydrocarbons, pyridine, piperidine, triethylamine and like amines, hexane, heptane, octane and like aliphatic hydrocarbons, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, methanol, ethanol, propanol and like alcohols, methyl acetate, ethyl acetate and like acetic acid esters, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, hexamethylphosphoric acid triamide and like aprotic polar solvents, carbon disulfide, acetic acid, water, mixtures of water and these organic solvents and so on.
Examples of the acidic compound are anhydrous aluminum chloride, stannic chloride, titanium tetrachloride, boron trichloride, boron trifluoride-ethyl ether complex, zinc chloride and like Lewis acids, hydrochloric acid, nitric acid, sulfuric acid and like inorganic acids, trichloroacetic acid, trifluoroacetic acid, methanesulfonic acid, acetic acid and like organic acids, acid-type ion-exchange resins and so on.
Examples of the basic compound are organic basic compounds such as triethylamine, pyridine and like tertiary amines, and inorganic basic compounds such as sodium carbonate, potassium carbonate and like alkali metal carbonates, sodium hydrogencarbonate, potassium hydrogencarbonate and like alkali metal hydrogencarbonates, sodium hydroxide, potassium hydroxide and like alkali metal hydroxides, sodium, potassium and like alkali metals, sodium hydride and like alkali metal hydrides and so on.
As to the proportions of the reactants, it is desirable that 1 to 100 mole equivalents, preferably 1 to 20 mole equivalents, of the acidic compound or basic compound, is used per mole of the compound of the formula (XI). The reaction temperature is -20.degree. C. to the boiling point of the solvent, preferably -10.degree. to 120.degree. C. The reaction time is 0.5 to 48 hours, preferably 1 to 24 hours.
The compound of the formula (XII) prepared by the above reaction can be used in Step 3 after isolation or without isolation.
(Step 3)
The compound of the formula (XIV) can be prepared by reacting the compound of the formula (XII) with p-fluorobenzonitrile of the formula (XIII) in a suitable solvent in the presence of a basic compound.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are diethyl ether, tetrahydrofuran, dioxane and like ethers, dichloromethane, chloroform and like halogenated hydrocarbons, pyridine, piperidine, triethylamine and like amines, acetone, methyl ethyl ketone, methyl. isobutyl ketone and like alkyl ketones, methanol, ethanol, propanol and like alcohols, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, hexamethylphosphoramide and like aprotic polar solvents, etc.
Examples of the basic compound are organic basic compounds such as triethylamine, pyridine and like tertiary amines, and inorganic basic compounds such as sodium carbonate, potassium carbonate and like alkali metal carbonates, sodium hydrogencarbonate, potassium hydrogencarbonate and like alkali metal hydrogencarbonates, sodium hydroxide, potassium hydroxide and like alkali metal hydroxides, sodium, potassium and like alkali metals, sodium hydride and like alkali metal hydrides and so on.
As to the proportions of the reactants, it is desirable that 1 to 2 mole equivalents of p-fluorobenzonitrile of the formula (XIII), and 1 to 5 mole equivalents, preferably 1 to 2 mole equivalents, of the basic compound are used per mole of the compound of the formula (XII). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 0.degree. to 80.degree. C. The reaction time is 0.5 to 48 hours, preferably 1 to 8 hours.
The compound of the formula (XIV) prepared by the above reaction can be used in Step 4 after isolation or without isolation.
(Step 4)
The compound of the formula (I-c) can be prepared by causing a Raney nickel to act on the compound of the formula (XIV) in a suitable inert solvent.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of solvents are formic acid, acetic acid, water, mixtures of water and these organic solvents, etc.
As to the proportions of the reactants, it is desirable that 0.5 to 10 g, preferably 1 to 3 g, of the Raney nickel is used per gram of the compound of the formula (XIV). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 50.degree. to 100.degree. C. The reaction time is 0.5 to 12 hours, preferably 1 to 3 hours.
The compound of the formula (I-c) prepared by the above reaction, which per se has an activity to reduce the lipid content in the blood, can be used in Step 5 as an intermediate after isolation or without isolation.
(Step 5)
The compound of the formula (I-d) according to the invention can be prepared by reducing the compound of the formula (I-c) in an inert solvent in the presence of sodium boron hydride or the like.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of solvents are tetrahydrofuran, dioxane, diethyl ether and like ethers, methanol, ethanol, propanol and like alcohols, etc. These solvents can be used alone or in combination. As to the proportions of the reactants, it is desirable that 0.5 to 3 mole equivalents of sodium boron hydride is used per mole of the compound of the formula (I-c). The reaction temperature is 0.degree. to 100.degree. C., preferably 0.degree. to 50.degree. C. The reaction time is 0.1 to 24 hours, preferably 0.5 to 6 hours.
Using an optically active compound of the formula (X) in this process, an optically active oxazolidine derivatives of the formulas (I-c) and (I-d) according to the invention can be prepared. An optically active compound can be produced from a racemate in a conventional manner. ##STR7##
In the above formulas, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, A, B, X, Z and m are as defined above, R.sup.1', R.sup.2' or R.sup.3' are the same as R.sup.1, R.sup.2, R.sup.3 except that they are other than a nitro group or a nitrile group, and R.sup.8 is a lower alkyl group.
The steps in the above reaction scheme are carried out as described below in more detail.
(Step 1)
The compound of the formula (I-f) according to the invention can be prepared by reacting the compound of the formula (I-e) (identical with the compound of the formula (I-c)) with a malonic acid of the formula (XV) in a suitable solvent in the presence of the basic compound and subsequently esterifying the obtained carboxylic acid compound by the Fischer esterification method as described, for example, in Org. Synth. Coll., vol. 2, 414 (1943).
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of solvents are benzene, toluene, xylene and like aromatic hydrocarbons, triethylamine, pyridine and like tertiary amines, diethyl ether, tetrahydrofuran, dioxane, dimethoxyethane and like ethers, methanol, ethanol, propanol, 2-propanol, butanol and like alcohols, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, hexamethylphosphoric acid triamide and like aprotic polar solvents, etc.
Examples of the basic compound are organic basic compounds such as sodium acetate, potassium acetate and like alkali metal fatty acid salts, triethylamine, pyridine and like tertiary amines, piperidine and the like, and inorganic basic compounds such as sodium carbonate, potassium carbonate and like alkali metal carbonates, sodium hydrogencarbonate, potassium hydrogencarbonate and like alkali metal hydrogencarbonates, sodium, potassium and like alkali metals, sodium hydride and like alkali metal hydrides and the like.
As to the proportions of the reactants, it is desirable that 1 to 3 mole equivalents of the malonic acid of the formula (XV), and 0.05 to 50 mole equivalents, preferably 0.1 to 10 mole equivalents, of the basic compound are used per mole of the compound of the formula (I-e). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 80.degree. to 120.degree. C. The reaction time is 0.5 to 48 hours, preferably 1 to 12 hours.
Further, the carboxylic acid compound thus obtained (compound of the invention) is esterified in a suitable solvent in the presence of an acid catalyst to thereby obtain an ester compound. The solvent is suitably selected depending on the desired ester and includes, for example, methanol, ethanol, propanol and like alcohols. Useful acid catalysts include, for example, hydrochloric acid, sulfuric acid and like inorganic acids, etc. As to the proportions of the reactants, it is desirable that 0.01 to 1 ml, preferably 0.1 to 0.5 ml, of the acid catalyst is used per gram of the carboxylic acid compound. The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 20.degree. to 100.degree. C. The reaction time is 0.5 to 48 hours, preferably 2 to 24 hours.
The compound of the formula (I-f) per se has an activity to reduce the lipid content in the blood and can be used in Step 2 as an intermediate after isolation or without isolation.
(Step 2)
The compound of the formula (I-g) according to the invention is produced by subjecting the compound of the formula (I-f) to catalytic reduction in an inert solvent in the presence of a catalyst.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are ethyl acetate, methanol, tetrahydrofuran, dioxane, N,N-dimethylformamide, acetic acid, etc. These solvents can be used alone or in combination. Useful catalysts include palladium carbon, platinum, etc. As to the proportions of the reactants, it is desirable that 0.01 to 2 g, preferably 0.1 to 0.5 g, of the catalyst is used per gram of the compound of the formula (I-f). The hydrogen pressure is in the range of atmospheric pressure to 20 atms. The reaction temperature is approximately 0.degree. to 100.degree. C., preferably room temperature to 50.degree. C. The reaction time is 0.5 to 24 hours, preferably 1 to 8 hours.
The compound of the formula (I-g) prepared by the above reaction per se has an activity to reduce the lipid content in the blood and can be used in Step 3 as an intermediate after isolation or without isolation.
(Step 3)
The compound of the formula (I-h) according to the invention can be prepared by subjecting the compound of the formula (I-g) to reduction in an inert solvent in the presence of lithium aluminum hydride or the like.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are tetrahydrofuran, dioxane, diethyl ether and so on. These solvents can be used alone or in combination. As to the proportions of the reactants, it is desirable that 0.5 to 3 mole equivalents of lithium aluminum hydride is used per mole of the compound of the formula (I-h). The reaction temperature is 0.degree. to 100.degree. C., preferably 0.degree. to 50.degree. C. The reaction time is 0.1 to 24 hours, preferably 0.5 to 6 hours.
Using an optically active compound of the formula (I-e) in this process, an optically active oxazolidine derivatives of the formulas (I-f) to (I-h) according to the invention can be prepared. An optically active compound can be produced from a racemate in a conventional manner. ##STR8##
In the above reaction scheme, R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5, R.sup.8, A, B, X, Z and m are as defined above (except for a compound wherein R.sup.1, R.sup.2 or R.sup.3 is a nitro group), and T is a halogen atom.
The steps in the above reaction scheme are carried out as described below in more detail.
(Step 1)
The compound of the formula (XVII) can be prepared by subjecting the known compound of the formula (XVI) to catalyst reduction in an anert solvent in the presence of a catalyst. The compound of the formula (XVI) can be prepared by reacting N-aryl urethane with p-nitrophenyl glycidyl ether as disclosed, for example, in Journal of Synthesis Organic Chemistry, Japan, 24, 60 (1966).
Useful solvents are not specifically limited insofar as they do not participate in the reaction. For example, ethyl actate, methanol, tetrahydrofuran, dioxane, N,N-dimethylformamide, acetic acid and the like can be used alone or in combination. Useful catalysts include, for example, palladium carbon, platinum, etc.
As to the proportions of the reactants, it is desirable that 0.01 to 2 g, preferably 0.1 to 0.5 g, of the catalyst is used per gram of the compound of the formula (XVI). The hydrogen pressure ranges from atmospheric pressure to 100 atms., preferably atmospheric pressure to 20 atms. The reaction temperature is 0.degree. to 100.degree. C., preferably room temperature to 60.degree. C. The reaction time is 0.5 to 48 hours, preferably 2 to 24 hours.
The compound of the formula (XVII) prepared by the above reaction can be used in Step 2 after isolation or without isolation.
(Step 2)
The compound of the formula (I-i) can be prepared by diazotizing the compound of the formula (XVII) in a suitable solvent in the presence of a hydrogen halide (HT) using sodium nitrite and then reacting the obtained compound with acrylic acid ester of the formula (XVIII) in the presence of cuprous oxide.
Useful solvents are not specifically limited insofar as they do not participate in the reaction. Examples of the solvent are diethyl ether, tetrahydrofuran, dioxane and like ethers, acetone, methyl ethyl ketone, methyl isobutyl ketone and like alkyl ketones, methanol, ethanol, propanol and like alcohols, N,N-dimethylformamide, N,N-dimethylacetamide, acetonitrile, dimethylsulfoxide, hexamethylphosphoric acid triamide and like aprotic polar solvents, water, acetic acid, etc. These solvents can be used alone or in combination.
As to the proportions of the reactants, it is desirable that 1 to 50 mole equivalents of the hydrogen halide (HT), 1 to 2 mole equivalents of sodium nitrite, 1 to 10 mole equivalents of the acrylic acid ester of the formula (XVIII), and 0.05 to 0.5 mole equivalent of the cuprous oxide are used per mole of the compound of the formula (XVII). The reaction temperature is approximately 0.degree. C. to the boiling point of the solvent, preferably 0.degree. to 50.degree. C. The reaction time is 0.1 to 24 hours, preferably 0.5 to 3 hours.
Using an optically active compound of the formula (XV) in this process, an optically active oxazolidine derivative of the formula (I-i) according to the invention can be prepared. An optically active compound can be produced from a racemate in a conventional manner.
The compounds of the formula (I) according to the present invention prepared by any of Processes A to F can be isolated from the reaction product by a conventional separation technique such as column chromatography, recrystallization, distillation under reduced pressure, etc.
The salts of the compounds of the formulas (I-a), (I-b), (I-c), (I-d), (I-e), (I-f), (I-g), (I-h) and (I-i) can be easily produced by reacting each free compound with any of the above-exemplified acids or basic compounds by a conventional method.
For use as medicaments, the compounds of the present invention can be made into various pharmaceutical dosage forms according to a preventive or therapeutic purpose. Examples of pharmaceutical dosage forms are oral preparations, injections, suppositories, ointments, plasters and so on. Such preparations can be formulated in a manner already known and conventional to those skilled in the art.
For the formulation of solid preparations for oral administration, an excipient and, when required, a binder, disintegrator, lubricant, coloring agent, corrigent, flavor, etc. are added to the compound of the invention, and then a preparation is formulated in a conventional way as tablets, coated tablets, granules, powders, capsules or the like. Such additives are those already known in the art, and useful examples are excipients such as lactose, sucrose, sodium chloride, glucose, starch, calcium carbonate, kaolin, microcrystalline cellulose and silicic acid; binders such as water, ethanol, propanol, simple syrup, glucose solution, starch solution, gelatin solution, carboxymethyl cellulose, hydroxypropyl cellulose, hydroxypropyl starch, methyl cellulose, ethyl cellulose, shellac, calcium phosphate and polyvinyl pyrrolidone; disintegrators such as dried starch, sodium alginate, agar powder, sodium hydrogencarbonate, calcium carbonate, sodium lauryl sulfate, stearic acid monoglyceride and lactose; lubricants such as purified talc, stearic acid salt, borax and polyethylene glycol; corrigents such as sucrose, bitter orange peel, citric acid and tartaric acid, etc.
For the formulation of liquid preparations for oral administration, a corrigent, buffer, stabilizer, flavor, etc. are added to the compound of the present invention, and the mixture can be formulated in a conventional way into an oral liquid preparation, syrup, elixir or the like. Examples of useful corrigents are those exemplified above. Examples of buffers are sodium citrate, etc. Examples of stabilizers are tragacanth, gum arabic, gelatin, etc.
Injections can be prepared as a subcutaneous, intramuscular or intravenous injection in a conventional way by adding to the compound of the invention a pH adjusting agent, buffer, stabilizer, isotonic agent, local anesthetic, etc. Examples of pH adjusting agents and buffers are sodium citrate, sodium acetate, sodium phosphate, etc. Examples of stabilizers are sodium pyrosulfite, EDTA, thioglycolic acid, thiolactic acid, etc. Examples of local anesthetics are procaine hydrochloride, lidocaine hydrochloride, etc. Examples of isotonic agents are sodium chloride, glucose, etc.
Suppositories can be prepared in a usual manner by adding to the compound of the invention a pharmaceutically acceptable carrier already known in the art, such as polyethylene glycols, lanolin, cacao fat and oil, fatty acid triglycerides and, if desired, a surfactant such as Tween (registered trademark).
For the preparation of ointments, a base, a stabilizer, a humectant, a preservative and the like commonly used in the art are used as required. These additives together with the compound of the present invention are formulated into ointments by conventional methods. Useful examples of the base include, for example, liquid paraffin, white petrolatum, bleached beeswax, octyl dodecyl alcohol, paraffin, etc. As preservatives, there can be mentioned methyl para-hydroxybenzoate, ethyl para-hydroxybenzoate, para-hydroxy propyl benzoate, etc.
For the preparation of plasters, said ointment, cream, gel or paste of the drug is applied to a substrate commonly employed in the art in a conventional manner. Suitable examples of substrates are woven or non-woven fabrics of cotton, rayon, chemical fibers or the like and films or foamed sheets of soft vinyl chloride, polyethylene, polyurethane or the like.
The amount of the compound of the present invention to be incorporated into each of the unit dosage forms varies with the symptoms of the patient or with the type of the preparations. The preferable amount per dosage unit is about 1 to about 1,000 mg for oral preparations, about 0.1 to about 500 mg for injections, or about 5 to about 1,000 mg for suppositories. The dosage per day of the drug in the above dosage forms is variable with the symptoms, body weight, age, sex and other factors of the patient, but usually ranges from about 0.1 to about 5,000 mg, preferably from about 1 to about 1,000 mg for human adult per day. The preparation is preferably administered in a single dose or in two to four divided doses.

EXAMPLES
Reference Examples and Examples are given below to illustrate the present invention in further detail.
Reference Example 1
Synthesis of (R)-(-)-4-(oxiranylmethoxy)-benzaldehyde
In 800 ml of anhydrous methyl ethyl ketone was dissolved 23.54 g of 4-hydroxybenzaldehyde and 50 g of (R)-(-)-glycidyl m-nitrobenzenesulfonate. To the solution was added 34.6 g of anhydrous potassium carbonate, and the mixture was refluxed with heating for 2.5 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. The obtained residue was extracted with ethyl acetate. The extract was washed with water, dried with magnesium sulfate and filtered, and the filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified with chloroform to give 30.6 g of the title compound (yield 89%).
Melting point: 32.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =-5.83.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.2.79 (1H, dd, J=7.4, 5.0 Hz), 2.94(1H, dd, J=5.0, 4.3 Hz), 3.39(1H, m), 4.02(1H, dd, J=11.2, 5.9 Hz), 4.35(1H, dd, J=11.2, 2.9 Hz), 7.03(2H, d, J=8.9 Hz), 7.85 (2H, d, J=8.9 Hz), 9.93(1H, s) MASS spectrum (EI) m/z 178 (M.sup.+)
Reference Example 2
Synthesis of (S)-(+)-4-(oxiranylmethoxy)-benzaldehyde
The same procedure of Reference Example 1 was repeated except that (S)-(+)-glycidyl m-nitrobenzenesulfonate was used in lieu of (R)-(-)-glycidyl m-nitrobenzenesulfonate to give the title compound (yield 91%).
Melting point: 32.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =+6.65.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.2.79 (1H, dd, J=7.4, 5.0 Hz), 2.94(1H, dd, J=5.0, 4.3 Hz), 3.39(1H, m), 4.02(1H, dd, J=11.2, 5.9 Hz), 4.35(1H, dd, J=11.2, 2.9 Hz), 7.03(2H, d, J=8.9 Hz), 7.85 (2H, d, J=8.9 Hz), 9.93(1H, s) MASS spectrum (EI) m/z 178 (M.sup.+)
Reference Example 3
Synthesis of 4-(oxiranylethoxy)-benzaldehyde
The procedure of Reference Example 1 was repeated except that oxiranylethyl methanesulfonate was used in lieu of (R)-(-)-glycidyl m-nitrobenzenesulfonate to give the title compound as an oil (yield 78%).
NMR spectrum (CDCl.sub.3) .delta.1.95 (1H, m), 2.20(1H, m), 2.60(1H, dd, J=5.0, 2.6 Hz), 2.85(1H, dd, J=5.0, 4.0 Hz), 3.16(1H, m), 4.20(2H, m), 7.01 (2H, d, J=8.9 Hz), 7.84(2H, d, J=8.9 Hz), 9.89(1H, s) MASS spectrum (FAB) 193 (M.sup.+ +1)
Reference Example 4
Synthesis of benzyl 4-(oxiranylmethoxy)-benzoate
In 120 ml of anhydrous N,N-dimethylformamide was dissolved 25.9 g of benzyl 4-hydroxybenzoate and 12.7 ml of epibromohydrin. To the solution was added 23.6 g of anhydrous potassium carbonate, and the mixture was stirred at 70.degree. C. for 16 hours. The reaction mixture was concentrated under reduced pressure, and the obtained residue was extracted with ethyl acetate. The extract was washed with water, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by hexane-ethyl acetate gradient elution to give 24.5 g of the title compound as an oil (yield 76%).
NMR spectrum (CDCl.sub.3) .delta.2.77 (1H, dd, J=5.0, 2.6 Hz), 2.92(1H, dd, J=5.0, 4.3 Hz), 3.37(1H, dddd, J=5.8, 5.0, 4.3, 3.0, 2.6 Hz), 3.97(1H, dd, J=11.2, 5.8 Hz), 4.29(1H, dd, J=11.2, 3.0 Hz), 5.34 (2H, s), 6.93(2H, d, J=9.2 Hz), 7.3-7.5(5H, m), 8.03 (2H, d, J=9.2 Hz) MASS spectrum (EI) m/z 284(M.sup.+)
Reference Example 5
Synthesis of methyl (R)-(-)-4-(oxiranylmethoxy)-benzoate
The same procedure of Reference Example 4 was repeated except that methyl 4-hydroxybenzoate was used in lieu of benzyl 4-hydroxybenzoate, and (R)-(-)-glycidyl toluenesulfonate was used in lieu of epibromohydrin to give the title compound (yield 90%).
Melting point: 34.degree.-36.degree. C. Specific rotation: [.alpha.].sub.D.sup.23 =-7.7.degree. (c=1.0, CH.sub.2 Cl.sub.2) NMR spectrum (CDCl.sub.3) .delta.2.79 (1H, dd, J=5.0, 2.6 Hz), 2.93(1H, dd, J=5.0, 4.3 Hz), 3.38(1H, dddd, J=5.8, 5.0, 4.3, 3.0, 2.6 Hz), 3.89(3 H, s), 3.99(1H, dd, J=11.2, 5.8 Hz), 4.30 (1H, dd, J=11.2, 3.0 Hz), 6.94(2H, d, J=8.9 Hz), 7.99(2H, d, J=8.9 Hz)
______________________________________Elementary analysis: (for C.sub.11 H.sub.12 O.sub.4) C H______________________________________Calculated 63.45 5.81Found 63.47 5.76______________________________________
Reference Example 6
Synthesis of methyl (S)-(+)-4-(oxiranylmethoxy)-benzoate
The same procedure of Reference Example 4 was repeated except that methyl 4-hydroxybenzoate was used in lieu of benzyl 4-hydroxybenzoate, and (S)-(+)-glycidyl toluenesulfonate was used in lieu of epibromohydrin to give the title compound (yield 90%).
Melting point: 34.degree.-36.degree. C. Specific rotation: [.alpha.].sub.D.sup.23 =+7.9.degree. (c=1.0, CH.sub.2 Cl.sub.2) NMR spectrum (CDCl.sub.3) .delta. 2.79 (1H, dd, J=5.0, 2.6 Hz), 2.93(1H, dd, J=5.0, 4.3 Hz), 3.38(1H, dddd, J=5.8, 5.0, 4.3, 3.0, 2.6 Hz), 3.89(3 H, s), 3.99(1H, dd, J=11.2, 5.8 Hz), 4.30 (1H, dd, J=11.2, 3.0 Hz), 6.94(2H, d, J=8.9 Hz), 7.99(2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.11 H.sub.12 O.sub.4) C H______________________________________Calculated 63.45 5.81Found 63.20 5.79______________________________________
Reference Example 7
Synthesis of 5-(chloromethyl)-3-(4-chlorophenyl)-2-oxooxazolidine
A toluene (10 ml) solution of 5.9 g of 4-chlorophenyl isocyanate and 3.3 ml of epichlorohydrin was added dropwise to a toluene (1 ml) solution of 0.2 g of lithium bromide and 0.42 g of tri-n-butylphosphine oxide at 100.degree. C. The mixture was stirred at the same temperature for 3 hours. The reaction mixture was concentrated under reduced pressure. Ethanol was added to the obtained residue to collect the crystals by filtration. Thus, 8.9 g of the title compound was obtained (yield 93%).
Melting point: 119.degree.-120.degree. C. NMR spectrum (CDCl.sub.3) .delta.3.75 (1H, dd, J=11.8, 6.5 Hz), 3.81(1H, dd, J=11.8, 4.1 Hz), 3.94(1H, dd, J=9.0, 5.8 Hz), 4.15(1H, dd, J=9.0, 8.9 Hz), 4.88(1H, m), 7.34 (2H, d, J=9.2 Hz), 7.50(2H, d, J=9.2 Hz)
______________________________________Elementary analysis (for C.sub.10 H.sub.9 NO.sub.2 Cl.sub.2) C H N______________________________________Calculated 48.81 3.69 5.69Found 48.56 3.71 5.53______________________________________
Reference Example 8
Synthesis of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate
A xylene (6 ml) solution of 1.13 ml of 4-methoxyphenyl isocyanate and 2.06 g of (2S, 3S)-(-)-3-methylglycidyl p-nitrobenzoate was added dropwise to a xylene (1 ml) solution of 55 mg of lithium bromide and 110 mg of tri-n-butylphosphine oxide at 140.degree. C. The mixture was stirred at the same temperature for 2 hours. The reaction mixture was concentrated under reduced pressure, and ethanol was added to the obtained residue to collect the crystals by filtration. Thus, 2.53 g of the title compound was obtained (yield 75%).
Melting point: 138.degree.-140.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =-55.39.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.38 (3 H, d, J=6.2 Hz), 3.81(3 H, s), 4.23(1H, m), 4.4-4.75(3 H, m), 6.92 (2H, d, J=11.2 Hz), 7.27 (2H, d, J=11.2 HZ), 8.19 (2H, d, J=8.9 HZ), 8.28 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.18 N.sub.2 O.sub.7) C H N______________________________________Calculated 59.07 4.70 7.25Found 59.38 4.73 7.42______________________________________
Reference Example 9
Synthesis of (R)-(-)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate
The same procedure of Reference Example 8 was repeated except that (R)-(-)-2-methylglycidyl p-nitrobenzoate was used in lieu of (2S, 3S)-(-)-3-methylglycidyl p-nitrobenzoate to give the title compound (yield 92%).
Melting point:155.degree.-157.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =7.28.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.60 (3 H, s), 3.74(3 H, s), 3.94(1H, d, J=9.4 Hz), 4.10(1H, d, J=9.4 Hz), 4.49 (1H, d, J=11.8 Hz), 4.54 (1H, d, J=11.8 Hz), 6.97 (2H, d, J=9.2 Hz), 7.46 (2H, d, J=9.2 Hz), 8.12 (2H, d, J=8.9 Hz), 8.30 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.18 N.sub.2 O.sub.7) C H N______________________________________Calculated 59.07 4.70 7.25Found 59.20 4.78 7.16______________________________________
Reference Example 10
Synthesis of (S)-(+)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate
The same procedure of Reference Example 8 was repeated except that (S)-(+)-2-methylglycidyl p-nitrobenzoate was used in lieu of (2S, 3S)-(-)-3-methylglycidyl p-nitrobenzoate to give the title compound (yield 96% ).
Melting point: 156.degree.-158.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =+71.79.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.60 (3H, s), 3.74(3H, s), 3.94(1H, d, J=9.4 Hz), 4.10(1H, d, J=9.4 Hz), 4.49 (1H, d, J=11.8 Hz), 4.54 (1H, d, J=11.8 Hz), 6.97 (2H, d, J=9.2 Hz), 7.46 (2H, d. J=9.2 Hz), 8.12 (2H, d, J=8.9 Hz), 8.30 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.18 N.sub.2 O.sub.7) C H N______________________________________Calculated 59.07 4.70 7.25Found 59.28 4.69 7.22______________________________________
Reference Example 11
Synthesis of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl alcohol
A 3.8 ml quantity of 8% sodium hydroxide aqueous solution was added to a methanol (20 ml) solution of 2.43 g of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate obtained in Reference Example 8. The mixture was stirred at 50.degree. C. for 20 minutes. The reaction mixture was concentrated under reduced pressure, and the obtained residue was extracted with ethyl acetate. The extract was washed with water, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the residue was subjected to silica gel column chromatography and purified by hexane-ethyl acetate gradient elution to give 1.04 g of the title compound (yield 70%).
Melting point: 99.degree.-101.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =-21.19.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.29 (3 H, d, J=5.9 Hz), 2.13 (1H, dd, J=7.3, 6.3 Hz), 3.75 (1H, ddd, J=12.5, 4.0, 3.6 Hz), 3.81 (3H, s), 3.98 (1H, ddd, J=12.5, 6.0, 3.0 Hz), 4.2-4.34 (2H, m), 6.92 (2H, d, J=9.2 Hz), 7.26 (2H, d, J=9.2 Hz)
Reference Example 12
Synthesis of (R)-(-)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl alcohol
The same procedure of Reference Example 11 was repeated except that (R)-(-)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate obtained in Reference Example 9 was used in lieu of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate to give the title compound (yield 90% ).
Melting point: 133.degree.-134.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =-24.89.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.50 (3H, s), 2.39 (1H, dd, J=8.3, 5.6 Hz), 3.58 (1H, dd, J=12.2, 8.3 Hz), 3.63 (1H, d, J=8.6 Hz), 3.78 (1H, dd, J=12.2, 5.6 Hz), 3.80 (3H, s), 4.08 (1H, d, J=8.6 Hz), 6.89 (2H, d, J=8.9 Hz), 7.43 (2H, d, J=8.9 Hz)
Reference Example 13
Synthesis of (S)-(+)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl alcohol
The same procedure of Reference Example 11 was repeated except that (S)-(+)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate obtained in Reference Example 10 was used in lieu of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl p-nitrobenzoate to give the title compound (yield 95%).
Melting point: 131.degree.-132.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =+21.39.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.50 (3H, s), 2.39 (1H, dd, J=8.3, 5.6 Hz), 3.58 (1H, dd, J=12.2, 8.3 Hz), 3.63 (1H, d, J=8.6 Hz), 3.78 (1H, dd, J=12.2, 5.6 Hz), 3.80 (3H, s), 4.08 (1H, d, J=8.6 Hz), 6.89 (2H, d, J=8.9 Hz), 7.43 (2H, d, J=8.9 Hz)
Reference Example 14
Synthesis of 4-[(4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile
To a suspension of 200 mg of 60% sodium hydride in anhydrous N,N-dimethylformamide (1 ml) was added dropwise an N,N-dimethylformamide (7 ml) solution of 0.98 g of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl alcohol obtained in Reference Example 11 at room temperature in a stream of nitrogen, and the mixture was stirred at 50.degree. C. for 25 minutes. A solution of 500 mg of p-fluorobenzonitrile in anhydrous N,N-dimethylformamide (2 ml) was added thereto at the same temperature and the mixture was stirred for 30 minutes. The reaction mixture was concentrated under reduced pressure and the obtained residue was extracted with ethyl acetate. The extract was washed with water, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by hexane-ethyl acetate gradient elution to give 0.98 g of the title compound (yield 70%).
Melting point: 127.degree.-128.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =-74.70.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.39 (3H, d, J=6.3 Hz), 3.82 (3H, s), 4.28 (2H, d, J=4.6 Hz), 4.35 (1H, dq, J=4.9, 6.3 Hz), 3.51 (1H, dt, J=4.9, 4.6 Hz), 6.94 (2H, d, J=8.9 Hz), 6.99 (2H, d, J=8.9 Hz), 7.30 (2H, d, J=8.9 Hz), 7.62 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.18 N.sub.2 O.sub.4) C H N______________________________________Calculated 67.45 5.36 8.28Found 67.39 5.41 8.27______________________________________
Reference Example 15
Synthesis of 4-[(R)-(-)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile
The same procedure of Reference Example 14 was repeated except that (R)-(-)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl alcohol obtained in Reference Example 12 was used in lieu of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl alcohol to give the title compound (yield 76%).
Melting point: 147.degree.-149.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =-83.56.degree. (c=1.0, CHCl.sub.3)
NMR spectrum (CDCl.sub.3) .delta.1.68 (3H, s), 3.79 (1H, d, J=8.9 Hz), 3.80 (3H, s), 4.03 (1H, d, J=9.6 Hz), 4.12 (1H, d, J=8.9 Hz), 4.17 (1H, d, J=9.6 Hz), 6.92 (2H, d, J=9.2 Hz), 6.96 (2H, d, J=9.2 Hz), 7.45 (2H, d, J=9.2 Hz), 7.60 (2H, d, J=9.2 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.18 N.sub.2 O.sub.4) C H N______________________________________Calculated 67.45 5.36 8.28Found 67.62 5.38 8.30______________________________________
Reference Example 16
Synthesis of 4-[(S)-(+)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile
The same procedure of Reference Example 14 was repeated except that (S)-(+)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-ylmethyl alcohol obtained in Reference Example 13 was used in lieu of (4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-ylmethyl alcohol to give the title compound (yield 76%).
Melting point: 146.degree.-147.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =+73.86.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.68 (3H, s), 3.79 (1H, d, J=8.9 Hz), 3.80 (3H, s), 4.03 (1H, d, J=9.6 Hz), 4.12 (1H, d, J=8.9 Hz), 4.17 (1 H, d, J=9.6 Hz), 6.92 (2H, d, J=9.2 Hz), 6.96 (2H, d, J=9.2 Hz), 7.45 (2H, d, J=9.2 Hz), 7.60 (2H, d, J=9.2 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.18 N.sub.2 O.sub.4) C H N______________________________________Calculated 67.45 5.36 8.28Found 67.63 5.40 8.27______________________________________
Reference Example 17
Synthesis of 3-(4-chlorophenyl)-2-oxooxazolidin-4-ylmethyl alcohol
A 8.5 ml quantity of triethylamine was added dropwise to a dichloromethane (25 ml) solution of 2.5 g of 4-chlorophenyl isocyanate and 2.5 g of glycidol at 40.degree. C., and the mixture was stirred at the same temperature for 20 hours. The reaction mixture was washed with 5% hydrochloric acid, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by dichloromethane-ethanol gradient elution to give 5.30 g of the title compound as an oil (yield 69%).
NMR spectrum (CDCl.sub.3) .delta.2.50 (1H, t), 3.60-3.80 (2H, m), 4.40-4.60 (3H, m), 7.30-7.50 (4 H, m)
Reference Example 18
Synthesis of 3-phenyl-2-oxooxazolidin-4-ylmethyl alcohol
The same procedure of Reference Example 17 was repeated except that phenyl isocyanate was used in lieu of 4-chlorophenyl isocyanate to give the title compound as an oil (yield 31%).
NMR spectrum (CDCl.sub.3) .delta.2.15 (1H, t), 3.65-3.85 (2H, m), 4.45-4.65 (3H, m), 7.20-7.55 (5H, m)
Reference Example 19
Synthesis of 3-(4-chlorophenyl)-2-oxooxazolidin-4-ylmethyl methanesulfonate
Methanesulfonyl chloride (3.0 g) was added dropwise to a dichloromethane (50 ml) solution of 5.30 g of 3-(4-chlorophenyl)-2-oxooxazolidin-4-ylmethyl alcohol obtained in Reference Example 17 and 8.5 ml of triethylamine with ice-cooling, and the mixture was stirred at the same temperature for 2 hours. The reaction mixture was washed with water, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by chloroform-ethanol gradient elution to give 6.50 g of the title compound (yield 91%).
Melting point 124.degree.-126.degree. C.
______________________________________Elementary analysis (for C.sub.11 H.sub.12 NO.sub.5 ClS) C H N______________________________________Calculated 43.21 3.96 4.58Found 43.04 4.16 4.61______________________________________
Reference Example 20
Synthesis of 3-phenyl-2-oxooxazolidin-4-ylmethyl methanesulfonate
The same procedure of Reference Example 19 was repeated except that 3-phenyl-2-oxooxazolidin-4-ylmethyl alcohol obtained in Reference Example 18 was used in lieu of 3-(4-chlorophenyl-2-oxooxazolidin-4-ylmethyl alcohol to give the title compound as an oil (yield 89%).
NMR spectrum (CDCl.sub.3) .delta.3.88 (3H, s), 4.2-4.45 (3H, m), 4.55-4.80 (2H, m), 7.20-7.50 (5H, m)
Reference Example 21
Synthesis of 4-[3-(2-pyridyl)-2-oxooxazolidin-5-yl]methoxyaniline
A 0.47 g quantity of 10% palladium carbon was added to a solution of 4.64 g of 4-[3-(2-pyridyl)-2-oxooxazolidin-5-yl]methoxynitrobenzene in 50 ml of 1,4-dioxane and 150 ml of N,N-dimethylformamide. The mixture was stirred at room temperature for 2.5 hours in a stream of hydrogen under 5 atmospheric pressure. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure. Methanol was added to the obtained residue to collect the crystals by filtration. Thus, 3.41 g of the title compound was obtained (yield 81%).
Melting point: 141.degree.-143.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.4.02 (1H, dd, J=10.2, 6.6 Hz), 4.08 (1H, dd, J=11.2, 5.3 Hz), 4.15 (1H, dd, J=11.2, 3.3 Hz), 4.29 (1H, dd, J=10.2, 9.2 Hz), 4.66 (2H, s), 5.00 (1H, m), 6.50 (2H, d, J=8.9 Hz), 6.67 (2H, d, J=8.9 Hz), 7.14 (1H, dd, J=7.3, 5.0 Hz), 7.85 (1H, ddd, J=8.6, 7.3, 1.0 Hz), 8.10 (1H, d, J=8.6 Hz), 8.37 (1H, dd, J=5.0, 1.0 Hz)
______________________________________Elementary analysis (for C.sub.15 H.sub.15 N.sub.3 O.sub.3) C H N______________________________________Calculated 63.15 5.30 14.73Found 63.05 5.35 14.65______________________________________
Reference Example 22
Synthesis of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxyaniline and 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyaniline
The same procedure of Reference Example 21 was repeated except that 3.65 g of a mixture of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxynitrobenzene and 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxynitrobenzene was used in lieu of 4-[3-(2-pyridyl)-2-oxooxazolidin-5-yl]methoxynitrobenzene to give 2.89 g of a mixture the title compounds.
Example 1
Synthesis of 4-[3-(4-methoxyphenyl)-2-oxooxazolidin-5-yl]methoxybenzaldehyde
The same procedure of Reference Example 8 was repeated except that 4-(oxiranylmethoxy)-benzaldehyde obtained in Reference Example 3 was used in lieu of (2S, 3S)-(-)-3-methylglycidyl p-nitrobenzoate to give the title compound (compound 1) in a yield of 91%.
Melting point: 135.degree.-137.degree. C. NMR spectrum (CDCl.sub.3) .delta.3.81 (3H, s), 4.03 (1H, dd, J=8.9, 5.9 Hz), 4.21 (1H, t, J=8.9 Hz), 4.29 (1H, dd, J=10.2, 4.3 Hz), 4.33 (1H, dd, J=10.2, 4.6 Hz), 5.01 (1H, m), 6.93 (2H, d, J=9.2 Hz), 7.03 (2H, d, J=8.8 Hz), 7.46 (2H, d, J=9.2 Hz), 7.86 (2H, d, J=8.8 Hz), 9.91 (1H, s)
______________________________________Elementary analysis (for C.sub.18 H.sub.17 NO.sub.5) C H N______________________________________Calculated 66.05 5.23 4.28Found 66.23 5.36 4.40______________________________________
Example 2
Using proper starting materials, compounds 2 to 34 shown in Table 1, compounds 35 to 39 shown in Table 2, compounds 40 to 43 shown in Table 3 and compounds 45 to 48 shown in Table 4 were synthesized in the same manner as in Example 1.
Example 3
Synthesis of methyl 4-[3-(4-nitrophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate
A xylene (15 ml) solution of 5.4 g of 4-nitrophenyl isocyanate and 6.9 g of methyl 4-(oxiranylmethoxy)-benzoate was added dropwise to a xylene (2 ml) solution of 170 mg of lithium bromide and 360 mg of tri-n-butylphosphine oxide at 140.degree. C. and the mixture was stirred at the same temperature for 2 hours, and the reaction mixture was concentrated under reduced pressure. Ethanol was added to the obtained residue to collect the crystals by filtration. Thus, 11.0 g of the title compound (compound 50) was obtained in a yield of 90%.
Melting point: 200.degree.-201.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.3.82 (3H, s), 4.05 (1H, dd, J=9.2, 6.1 Hz), 4.34 (1H, dd, J=9.2, 9.2 Hz), 4.38 (1H, dd, J=11.2, 6.6 Hz), 4.44 (1H, dd, J=11.2, 3.3 Hz), 5.17 (1H, m), 7.07 (2H, d, J=8.9 Hz), 7.85 (2H, d, J=9.3 Hz), 7.92 (2H, d, J=8.9 Hz), 8.31 (2H, d, J=9.3 Hz)
______________________________________Elementary analysis (for C.sub.18 H.sub.15 N.sub.2 O.sub.7) C H N______________________________________Calculated 58.07 4.33 7.52Found 58.03 4.30 7.38______________________________________
Example 4
Synthesis of methyl 4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate
A 1.52 g quantity of methyl 4-hydroxy-benzoate was added to a suspension of 0.42 g of 60% sodium hydride in anhydrous N,N-dimethylformamide (15 ml) with ice-cooling in a stream of nitrogen. To the mixture was added dropwise an anhydrous N,N-dimethylformamide (15 ml) solution of 2.46 g of 5-(chloromethyl)-3-(4-chlorophenyl)-2-oxooxazolidine obtained in Reference Example 7 at the same temperature, and the mixture was stirred at 40.degree. C. for 48 hours. The reaction mixture was concentrated under reduced pressure, and the obtained residue was extracted with ethyl acetate. The extract was washed with water, dried with magnesium sulfate and filtered. The filtrate was then concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by hexane-ethyl acetate gradient elution to give 1.75 g of the title compound (compound 51) in a yield of 48%.
Melting point: 146.degree.-148.degree. C. NMR spectrum (CDCl.sub.3) .delta.3.89 (3H, s), 4.05 (1H, dd, J=8.9, 5.9 Hz), 4.20 (1H, dd, J=8.9, 8.9 Hz), 4.28 (1H, dd, J=10.2, 4.3 Hz), 4.31 (1H, dd, J=10.2, 4.6 Hz), 5.02 (1H, dddd, J=8.9, 5.9, 4.6, 4.3 Hz), 6.92 (2H, d, J=8.9 Hz), 7.36 (2H, d, J=8.9 Hz), 7.53 (2H, d, J=8.9 Hz), 8.01 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.18 H.sub.16 NO.sub.5 Cl) C H N______________________________________Calculated 59.76 4.46 3.87Found 59.88 4.39 3.88______________________________________
Example 5
Using proper starting materials, compounds 52 to 80 and 116 shown in Table 5, compound 117 shown in Table 6, compounds 119 to 128 shown in Table 7, compounds 136 to 143 shown in Table 8, compounds 153 to 160 shown in Table 9 and compounds 169 and 170 shown in Table 10 were synthesized in the same manner as in Example 3.
Example 6
Synthesis of methyl (R)-(-)-4-[3-(4-acetylphenyl)-2-oxooxazolidin-5-yl]methoxybenzoate
The same procedure of Example 4 was repeated except that (R)-(-)-4-[3-(4-acetylphenyl)-2-oxooxazolidin-5-yl]methyl methanesulfonate was used in lieu of 5-(chloromethyl)-3-(4-chlorophenyl)-2-oxooxazolidine to give the title compound (compound 144) in a yield of 82%.
Melting point: 130.degree.-132.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 32 -107.6.degree. (c=1.0, CH.sub.2 Cl.sub.2) NMR spectrum (CDCl.sub.3) .delta.2.60 (3H, s), 3.89 (3H, s), 4.13 (1H, dd, J=8.9, 5.9 Hz), 4.25-4.37 (3H, m), 5.05 (1H, m), 6.92 (2H, d, J=8.9 Hz), 7.69 (2H, d, J=8.9 Hz), 8.00 (2H, d, J=8.9 Hz), 8.01 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.20 H.sub.19 NO.sub.6) C H N______________________________________Calculated 65.03 5.18 3.79Found 65.00 5.24 3.79______________________________________
Example 7
Synthesis of 4-[3-(4-nitrophenyl)-2-oxooxazolidin-5-yl]methoxybenzoic acid
A solution of 2.0 g of methyl 4-[3-(4-nitrophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate (compound 50) obtained in Example 3 in 18 ml of acetic acid and 6 ml of concentrated hydrochloric acid was refluxed with heating for 12 hours. After ice-cooling the reaction solution, ether was added thereto and the crystals formed were collected by filtration. Thus, 1.64 g of the title compound (compound 81) was obtained (yield 85%).
Melting point: 236.degree.-238.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.4.04 (1H, dd, J=9.2, 6.0 Hz), 4.34 (1H, dd, J=9.2, 9.2 Hz), 4.38 (1H, dd, J=11.2, 6.6 Hz), 4.44 (1H, dd, J=11.2, 3.3 Hz), 5.17 (1H, m), 7.04 (2H, d, J=8.9 Hz), 7.85 (2H, d, J=9.3 Hz), 7.92 (2H, d, J=8.9 Hz), 8.31 (2H, d, J=9.3 Hz), 12.68 (1H, s)
______________________________________Elementary analysis (C.sub.17 H.sub.14 N.sub.2 O.sub.7) C H N______________________________________Calculated 56.99 3.94 7.82Found 57.13 4.16 7.82______________________________________
Example 8
Using proper starting materials, compounds 82 to 111 shown in Table 5, compound 118 shown in Table 6, compounds 129 to 133 shown in Table 7, compounds 145 to 152 shown in Table 8 and compounds 161 to 168 shown in Table 9 were synthesized in the same manner as in Example 7.
Example 9
Synthesis of methyl 4-[3-(4-aminophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate
A 6.0 g quantity of zinc powder was added to an acetic acid (60 ml) solution of 3.0 g of methyl 4-[3-(4-nitrophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate (compound 50) obtained in Example 3 at 60.degree. C., and the mixture was stirred at the same temperature for 3 hours. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Ethanol was added to the obtained residue to collect the crystals by filtration. Thus, 3.0 g of the title compound (compound 112) was obtained in a quantitative yield.
Melting point: 139.degree.-142.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.3.81 (1H, dd, J=8.9, 6.3 Hz), 3.82 (3H, s), 4.12 (1H, dd, J=9.2, 8.9 Hz), 4.30 (1H, dd, J=11.2, 5.3 Hz), 5.0 (1H, m), 6.58 (2H, d, J=8.6 Hz), 7.09 (2H, d, J=8.9 Hz), 7.18 (2H, d, J=8.6 Hz), 7.93 (2H, d, J=8.9 Hz) MASS spectrum (EI) m/z 342 (M.sup.+)
Example 10
Synthesis of methyl 4-[3-(4-acetamidophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate
A 1.2 ml quantity of anhydrous acetic acid was added dropwise to an acetic acid (60 ml) solution of 3.0 g of methyl 4-[3-(4-aminophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate obtained in Example 9 at room temperature, and the mixture was stirred at the same temperature for 1 hour. The crystals were collected by filtration and washed with ethanol to give 3.05 g of the title compound (compound 113) in a yield of 99%.
Melting point: 188.degree.-190.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.2.03 (3H, s), 3.82 (3H, s), 3.91 (1H, dd, J=8.9, 6.3 Hz), 4.21 (1H, dd, J=9.1, 8.9 Hz), 4.33 (1H, dd, J=11.0, 5.3 Hz), 4.39 (1H, dd, J=11.0, 3.3 Hz), 5.07 (1H, m), 7.08 (2H, d, J=8.9 Hz), 7.50 (2H, d, J=9.2 Hz) 7.60 (2H, d, J=9.2 Hz), 7.93 (2H, d, J=8.9 Hz), 9.95 (1H, s)
______________________________________Elementary analysis (for C.sub.20 H.sub.20 N.sub.2 O.sub.6.1/4H.sub.2 O) C H N______________________________________Calculated 61.77 5.31 7.20Found 61.55 5.20 7.07______________________________________
Example 11
Synthesis of 4-[3-(4-aminophenyl)-2-oxooxazolidin-5-yl]methoxybenzoic acid hydrochloride
The same procedure of Example 7 was repeated except that methyl 4-[3-(4-aminophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate (compound 112) obtained in Example 9 was used in lieu of methyl 4-[3-(4-nitrophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate to give the title compound (compound 114) in a yield of 64%.
Melting point: 248.degree.-252.degree. C. (decomposition) NMR spectrum (DMSO-d.sub.6) .delta.3.91 (1H, dd, J=8.9, 6.3 Hz), 4.21 (1H, dd, J=9.2, 8.9 Hz), 4.33 (1H, dd, J=10.9, 5.3 Hz), 4.38 (1H, dd, J=10.9, 3.3 Hz), 5.10 (1H, m), 7.05 (2H, d, J=8.9 Hz), 7.50 (2H, d, J=8.9 Hz), 7.69 (2H, d, J=8.9 Hz), 7.90 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.17 H.sub.16 N.sub.2 O.sub.5.HCl) C H N______________________________________Calculated 55.96 4.70 7.68Found 55.65 4.64 7.69______________________________________
Example 12
Synthesis of 4-[3-(4-acetamidophenyl)-2-oxooxazolidin-5-yl]methoxybenzoic acid
The same procedure of Example 10 was repeated except that 4-[3-(4-aminophenyl)-2-oxooxazolidin-5-yl]methoxy benzoic acid (compound 114) obtained Example 11 was used in lieu of methyl 4-[3-(4-aminophenyl)-2-oxooxazolidin-5-yl]methoxybenzoate to give the title compound (compound 115) in a yield of 88%.
Melting point: 288.degree.-291.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.3.91 (1H, dd, J=8.9, 6.3 Hz), 4.21 (1H, dd, J=9.2, 8.9 Hz), 4.33 (1H, dd, J=10.9, 5.3 Hz), 4.38 (1H, dd, J=10.9, 3.3 Hz), 5.07 (1H, m), 7.04 (2H, d, J=8.9 Hz), 7.51 (2H, d, J=8.9 Hz), 7.60 (2H, d, J=8.9 Hz), 7.90 (2H, d, J=8.9 Hz), 9.94 (1H, s), 12.64 (1H, s)
______________________________________Elementary analysis (for C.sub.19 H.sub.18 N.sub.2 O.sub.6) C H N______________________________________Calculated 61.62 4.90 7.56Found 61.30 4.93 7.54______________________________________
Example 13
Synthesis of 4-(3-benzoyl-2-oxooxazolidin-5-yl)methoxybenzoic acid.
A 1.0 g quantity of 10% palladium carbon was added to a solution of 3.8 g of benzyl 4-(3-benzoyl-2-oxooxazolidin-5-yl)methoxybenzoate (compound 120) obtained in Example 5 in 50 ml of acetic acid and 25 ml of N,N-dimethylformamide. The mixture was stirred at 60.degree. C. for 5 hours in a stream of hydrogen. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Ethanol was added to the obtained residue to collect the crystals by filtration. Thus, 235 mg of the title compound (compound 134) was obtained (yield 8%).
Melting point: 219.degree.-221.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.3.96 (1H, dd, J=10.6, 5.9 Hz), 4.24 (1H, dd, J=10.6, 8.9 Hz), 4.42 (2H, m), 5.12 (1H, m), 7.08 (2H, d, J=8.9 Hz), 7.4-7.7 (4 H, m), 7.85-7.95 (3H, m)
______________________________________Elementary analysis (for C.sub.18 H.sub.15 NO.sub.6) C H N______________________________________Calculated 63.34 4.43 4.10Found 63.24 4.37 4.07______________________________________
Example 14
Synthesis of 4-[3-(4-methylbenzenesulfonyl)-2-oxooxazolidin-5-yl]methoxybenzoic acid
The same procedure of Example 13 was repeated except that benzyl 4-[3-(4-methylbenzenesulfonyl)-2-oxooxazolidin-5-yl]methoxybenzoate (compound 123) obtained in Example 5 was used in lieu of benzyl 4-(3-benzoyl-2-oxooxazolidin-5-yl)methoxybenzoate to give the title compound (compound 135) in a yield of 62%.
Melting point: 252.degree.-254.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.2.46 (3H, s), 3.99 (1H, dd, J=9.2, 5.6 Hz), 4.21-4.33 (3H, m), 5.07 (1H, m), 6.80 (2H, d, J=8.9 Hz), 7.52 (2H, d, J=8.2 Hz), 7.86 (2H, d, J=8.9 Hz), 7.90 (2H, d, J=8.2 Hz)
______________________________________Elementary analysis (for C.sub.18 H.sub.17 NO.sub.7 S) C H N______________________________________Calculated 55.24 4.38 3.58Found 55.26 4.36 3.60______________________________________
Example 15
Synthesis of 4-(3-phenyl-2-oxazolidinethion-5-yl)methoxybenzoic acid
A 8.7 ml quantity of aqueous solution of 0.5N potassium hydroxide was added to 75% ethanol (80 ml) solution of 750 mg of methyl 4-(3-phenyl-2-thiooxooxazolidin-5-yl)methoxybenzoate (compound 169) obtained in Example 5, and the mixture was stirred at room temperature for 5 days. The reaction mixture was concentrated under reduced pressure, and a dilute hydrochloric acid was added to the obtained residue and the crystals were collected by filtration. Thus, 235 mg of the title compound (compound 171) was obtained (yield 33%).
Melting point: 214.degree.-215.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.3.45 (1H, dd, J=11.2, 8.6 Hz), 3.66 (1H, dd, J=11.2, 6.6 Hz), 4.36 (1H, dd, J=10.9, 5.9 Hz), 4.44 (1H, dd, J=10.9, 3.4 Hz), 5.08 (1H, m), 6.88 (2H, d, J=7.3 Hz), 6.95-7.4 (5H, m), 7.93 (2H, d, J=8.9 Hz), 12.69 (1H, s)
______________________________________Elementary analysis (for C.sub.17 H.sub.15 NO.sub.4 S) C H N______________________________________Calculated 61.99 4.59 4.25Found 61.99 4.60 4.09______________________________________
Example 16
Synthesis of 4-[(4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-yl]methoxybenzaldehyde
A 1.8 g quantity of Raney nickel was added to a solution of 0.88 g of 4-[(4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile obtained in Reference Example 14 in 25 ml of an 80% aqueous solution of formic acid. The mixture was refluxed with heating for 1.5 hours. The reaction mixture was concentrated under reduced pressure, and the obtained residue was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium bicarbonate, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by hexane-ethyl acetate gradient elution to give 0.71 g of the title compound (compound 172) in a yield of 80%.
Melting point: 115.degree.-116.degree. C. Specific rotation: [.alpha.].sub.D.sup.25 =-68.99.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.39 (3H, d, J=6.0 Hz), 3.82 (3H, s), 4.31 (2H, d, J=4.6 Hz), 4.37 (1H, dq, J=4.9, 6.3 Hz), 3.52 (1H, dt, J=4.9, 4.6 Hz), 6.94 (2H, d, J=8.9 Hz), 7.04 (2H, d, J=8.9 Hz), 7.31 (2H, d, J=8.9 Hz), 7.87 (2H, d, J=8.9 Hz), 9.92 (1H, s)
______________________________________Elementary analysis (for C.sub.19 H.sub.19 NO.sub.5) C H N______________________________________Calculated 66.85 5.61 4.10Found 67.02 5.82 4.30______________________________________
Example 17
Synthesis of 4-[(R)-(-)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-yl]methoxybenzaldehyde
The same procedure of Example 16 was repeated except that 4-[(R)-(-)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile obtained in Reference Example 15 was used in lieu of 4-[(4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile to give the title compound (compound 44) as an oil (yield 85%).
Specific rotation: [.alpha.].sub.D.sup.25 =-75.79.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDC1.sub.3) .delta.1.69 (3H, s), 3.80 (1H, d, J=8.9 Hz), 3.81 (3H, s), 4.07 (1H, d, J=9.6 Hz), 4.13 (1H, d, J=8.9 Hz), 4.21 (1H, d, J=9.6 Hz), 6.92 (2H, d, J=9.2 Hz), 7.01 (2H, d, J=8.9 Hz), 7.46 (2H, d, J=9.2 Hz), 7.85 (2H, d, J=8.9 Hz), 9.90 (1H, s)
______________________________________Elementary analysis (for C.sub.19 H.sub.19 N.sub.2 O.sub.5.1/5 H.sub.2O) C H N______________________________________Calculated 66.16 5.67 4.06Found 66.32 5.66 4.09______________________________________
Example 18
Synthesis of 4-[(S)-(+)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-yl]methoxybenzaldehyde
The same procedure of Example 16 was repeated except that 4-[(S)-(+)-3-(4-methoxyphenyl)-5-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile obtained in Reference Example 16 was used in lieu of 4-[(4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile to give the title compound (compound 49) as an oil (yield 85%).
Specific rotation: [.alpha.].sub.D.sup.25 =+72.39.degree. (c=1.0, CHCl.sub.3) NMR spectrum (CDCl.sub.3) .delta.1.69 (3H, s), 3.80 (1H, d, J=8.9 Hz), 3.81 (3H, s), 4.07 (1H, d, J=9.6 Hz), 4.13 (1H, d, J=8.9 Hz), 4.21 (1H, d, J=9.6 Hz), 6.92 (2H, d, J=9.2 Hz), 7.01 (2H, d, J=8.9 Hz), 7.46 (2H, d, J=9.2 Hz), 7.85 (2H, d, J=8.9 Hz), 9.90 (1H, s)
______________________________________Elementary analysis (for C.sub.19 H.sub.19 N.sub.2 O.sub.5.1/5H.sub.2 O) C H N______________________________________Calculated 66.16 5.67 4.06Found 66.34 5.77 4.04______________________________________
Example 19
Synthesis of 4-[3-(4-formylphenyl)-2-oxooxazolidin-5-yl]methoxybenzaldehyde
The same procedure of Example 16 was repeated except that 4-[3-(4-cyanophenyl)-2-oxooxazolidin-5-yl]methoxybenzaldehyde (compound 34) obtained in Example 2 was used in lieu of 4-[(4S, 5S)-(-)-3-(4-methoxyphenyl)-4-methyl-2-oxooxazolidin-5-yl]methoxybenzonitrile to give the title compound (compound 173) in a yield of 89%.
Melting point: 130.degree.-132.degree. C. NMR spectrum (CDCl.sub.3 ) .delta.4.15 (1H, dd, J=11.9, 5.9 Hz), 4.27-4.41 (3H, m), 5.04-5.14 (1H, m), 7.02 (2H, d, J=8.9 Hz), 7.78 (2H, d, J=8.9 Hz), 7.86 (2H, d, J=8.9 Hz), 7.93 (2H, d, J=8.9 Hz), 9.91 (1H, s), 9.97 (1H, s)
______________________________________Elementary analysis (for C.sub.18 H.sub.15 NO.sub.5) C H N______________________________________Calculated 66.46 4.65 4.31Found 66.39 4.70 4.60______________________________________
Example 20
Synthesis of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxybenzyl alcohol
A 114 mg quantity of sodium borohydride was added to a methanol (30 ml) solution of 1.00 g of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]-methoxybenzaldehyde (compound 7) obtained in Example 2, and the mixture was stirred at 60.degree. C. for 5 minutes. The reaction mixture was concentrated under reduced pressure. To the obtained residue was added a 5% hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The obtained residue was recrystallized from ethanol to give 862 mg of the title compound (compound 174) in a yield of 86%.
Melting point: 149.degree.-150.degree. C. NMR spectrum (CDCl.sub.3) .delta.4.05 (1H, dd, J=8.9, 5.9 Hz), 4.18 (1H, t, J=8.9 Hz), 4.23 (2H, d, J=4.6 Hz), 4.63 (2H, s), 4.95-5.03 (1H, m), 6.89 (2H, d, J=8.9 Hz), 7.30 (2H, d, J=8.9 Hz), 7.35 (2H, d, J=9.2 Hz), 7.53 (2H, d, J=9.2 Hz)
______________________________________Elementary analysis (for C.sub.17 H.sub.16 NO.sub.4 Cl) C H N______________________________________Calculated 61.18 4.83 4.20Found 61.40 4.74 4.27______________________________________
Example 21
Synthesis of 4-[3-(4-tolyl)-2-oxooxazolidin-5-yl]methoxybenzyl alcohol
The same procedure of Example 20 was repeated except that 4-[3-(4-tolyl)-2-oxooxazolidin-5-yl]methoxybenzaldehyde (compound 20) obtained in Example 2 was used in lieu of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxybenzaldehyde to give the title compound (compound 175) in a yield of 63%.
Melting point: 163.degree.-165.degree. C. NMR spectrum (CDC1.sub.3) .delta.2.34 (3H, s), 4.04 (1H, dd, J=8.9, 5.9 Hz), 4.18 (1H, dd, J=8.9, 8.6 Hz), 4.22 (2H, d, J=4.6 Hz), 4.63 (2H, s), 4.92-5.04 (1H, m), 6.89 (2H, d, J=8.6 Hz), 7.19 (2H, d, J=8.6 Hz), 7.30 (2H, d, J=8.6 Hz), 7.44 (2H, d, J=8.6 Hz )
______________________________________Elementary analysis (for C.sub.18 H.sub.19 NO.sub.4) C H N______________________________________Calculated 69.00 6.11 4.47Found 69.06 6.24 4.40______________________________________
Example 22
Synthesis of methyl 4-[3-(4-chlorophenyl)-2-oxooxazolidin-4-yl]methoxybenzoate
In 20 ml of N,N-dimethylformamide was dissolved 1.50 g of 3-(4-chlorophenyl)-2-oxooxazolidin-4-ylmethyl methanesulfonate and 0.80 g of methyl 4-hydroxybenzoate. To the solution was added 0.80 g of anhydrous potassium carbonate, and the mixture was stirred at 60.degree. C. for 12 hours. The reaction mixture was concentrated under reduced pressure and water was added thereto. The obtained residue was recrystallized from methanol to give 1.60 g of the title compound (compound 176) in a yield of 90%.
Melting point: 135.degree.-136.degree. C.
______________________________________Elementary analysis (for C.sub.18 H.sub.16 NO.sub.5 Cl) C H N______________________________________Calculated 59.76 4.46 3.87Found 59.67 4.56 3.96______________________________________
Example 23
Synthesis of methyl 4-(3-phenyl-2-oxooxazolidin-4-yl)methoxybenzoate
The same procedure of Example 22 was repeated except that 3-phenyl-2-oxooxazolidin-4-ylmethyl methanesulfonate obtained in Reference Example 20 was used in lieu of 3-(4-chlorophenyl)-2-oxooxazolidin-4-ylmethyl methanesulfonate to give the title compound (compound 177) in a yield of 60%.
Melting point: 158.degree.-159.degree. C.
______________________________________Elementary analysis (for C.sub.18 H.sub.17 NO.sub.5) C H N______________________________________Calculated 66.05 5.23 4.28Found 66.09 5.21 4.34______________________________________
Example 24
Synthesis of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-4-yl]methoxybenzaldehyde
The same procedure of Example 22 was repeated except that 4-hydroxybenzaldehyde was used in lieu of methyl 4-hydroxybenzoate to give the title compound (compound 178) in a yield of 92%.
Melting point: 120.degree.-122.degree. C.
______________________________________Elementary analysis (for C.sub.17 H.sub.14 NO.sub.4 Cl) C H N______________________________________Calculated 61.55 4.25 4.22Found 61.48 4.70 4.22______________________________________
Example 25
Synthesis of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-4-yl]methoxybenzoic acid
A solution of 1.30 g of methyl 4-[3-(4-chlorophenyl)-2-oxooxazolidin-4-yl]methoxybenzoate (compound 176) obtained in Example 22 in 18 ml of acetic acid and 10 ml of concentrated hydrochloric acid was refluxed with heating for 24 hours. The reaction mixture was concentrated under reduced pressure and the obtained residue was recrystallized from acetic acid-water to give 0.80 g of the title compound (compound 179) in a yield of 64%.
Melting point: 219.degree.-221.degree. C.
______________________________________Elementary analysis (for C.sub.17 H.sub.14 NO.sub.5 Cl) C H N______________________________________Calculated 66.05 5.23 4.28Found 66.09 5.21 4.34______________________________________
Example 26
Synthesis of 4-(3-phenyl-2-oxooxazolidin-4-yl)methoxybenzoic acid
The same procedure of Example 25 was repeated except that methyl 4-(3-phenyl-2-oxooxazolidin-4-yl)methoxybenzoate (compound 177) obtained in Example 23 was used in lieu of methyl 4-[3-(4-chlorophenyl)-2-oxooxazolidin-4-yl]methoxybenzoate to give the title compound (compound 180) in a yield of 61%.
Melting point: 255.degree.-257.degree. C.
______________________________________Elementary analysis (for C.sub.17 H.sub.15 NO.sub.5.1/5 H.sub.2 O C H N______________________________________Calculated 64.43 4.90 4.42Found 64.57 4.81 4.39______________________________________
Example 27
Synthesis of 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxycinnamic acid
In 1 ml of pyridine was dissolved 250 mg of 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxybenzaldehyde (compound 19) obtained in Example 2 and 131 mg of malonic acid. Piperidine (0.05 ml) was added to the solution, and the mixture was stirred at 100.degree. C. for 3 hours. To the mixture was added 10% sulfic acid, and the obtained residue was washed with methanol to give 240 mg of the title compound (compound 181) in a yield of 84%.
Melting point: 239.degree.-240.degree. C. NMR spectrum (DMSO-d.sub.6) .delta.3.93 (1H, dd, J=9.2, 6.3 Hz), 4.26 (1H, dd, J=9.2, 8.9 Hz), 4.30 (1H, dd, J=11.2, 5.6 Hz), 4.36 (1H, dd, J=11.2, 3.6 Hz), 5.03-5.12 (1H, m), 6.39 (1H, d, J=15.8 Hz), 7.00 (2H, d, J=8.9 Hz), 7.14 (1H, t, J=7.3 Hz), 7.41 (2H, dd, J=8.2, 7.3 Hz), 7.52-7.67 (5H, m)
______________________________________Elementary analysis (for C.sub.19 H.sub.17 NO.sub.5) C H N______________________________________Calculated 67.25 5.05 4.13Found 67.59 4.95 4.28______________________________________
Example 28
Using proper starting materials, compounds 182 to 184 shown in Table 14 were synthesized in the same manner as in Example 27.
Example 29
Synthesis of methyl 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxycinnamate
In 20 ml of methanol was dissolved 200 mg of 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxycinnamic acid (compound 181) obtained in Example 27. Concentrated sulfic acid (0.05 ml) was added to the solution, and the mixture was refluxed with heating for 16 hours. The reaction mixture was concentrated under reduced pressure and the obtained residue was washed with water and methanol to give 195 mg of the title compound (compound 185) in a yield of 94%.
Melting point: 179.degree.-181.degree. C. NMR spectrum (CDCl.sub.3 ) .delta.3.79 (3H, s), 4.06 (1H, dd, J=8.9, 5.9 Hz), 4.22 (1H, dd, J=8.9, 7.6 Hz), 4.25 (2H, d, J=4.6 Hz), 4.95-5.04 (1 H, m), 6.32 (1H, d, J=15.8 Hz), 6.91 (2H, d, J=8.9 Hz), 7.16 (1H, dd, J=8.2, 7.3 Hz), 7.36-7.67 (7H, m)
______________________________________Elementary analysis (for C.sub.20 H.sub.19 NO.sub.5) C H N______________________________________Calculated 67.98 5.42 3.96Found 67.51 5.66 3.97______________________________________
Example 30
Using proper starting materials, compounds 186 to 188 shown in Table 14 were synthesized in the same manner as in Example 29.
Example 31
Synthesis of methyl 3-[4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyphenyl]propionate
A 200 mg quantity of 10% palladium carbon was added to a tetrahydrofuran (50 ml) solution of 1.75 g of methyl 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxycinnamate (compound 185) obtained in Example 29. The mixture was stirred at room temperature for 2.5 hours in a stream of hydrogen at 3 atmospheric pressure. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure and washed with methanol to give 1.59 g of the title compound (compound 189) in a yield of 88%.
Melting point: 138.degree.-139.degree. C. NMR spectrum (CDCl.sub.3) .delta.2.59 (2H, t, J=7.6 Hz), 2.90 (2H, t, J=7.6 Hz), 3.66 (3H, s), 4.06 (1H, dd, J=8.9, 5.9 Hz), 4.15-4.24 (3H, m), 4.93-5.02 (1H, m), 6.83 (2H, d, J=8.6 Hz), 7.12 (2H, d, J=8.6 Hz), 7.16 (1H, t, J=6.6 Hz), 7.39 (2H, dd, J=8.6, 6.6 Hz), 7.57 (2H, d, J=8.6 Hz)
______________________________________Elementary analysis (for C.sub.20 H.sub.21 NO.sub.5) C H N______________________________________Calculated 67.59 5.96 3.94Found 67.67 5.96 3.93______________________________________
Example 32
Using proper starting materials, compounds 190 and 191 shown in Table 14 were synthesized in the same manner as in Example 31.
Example 33
Using proper starting materials, compounds 192 and 193 shown in Table 14 were synthesized in the same manner as in Example 25.
Example 34
Synthesis of 3-{4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxyphenyl}propyl alcohol
Lithium aluminum hydride (59 mg) was added to a tetrahydrofuran (15 ml) solution of 750 mg of methyl 3-{4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxy-phenyl}propionate (compound 191) obtained in Example 32. The mixture was stirred with ice-cooling for 40 minutes in a stream of nitrogen. To the reaction mixture was added 5% hydrochloric acid, and the mixture was extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by hexane-ethyl acetate gradient elution to give 498 mg of the title compound (compound 194) in a yield of 71%.
Melting point: 119.degree.-120.degree. C. NMR spectrum (CDCl.sub.3) .delta.1.27 (1H, br-s), 1.80-1.91 (2H, m), 2.66 (2H, t, J=7.6 Hz), 3.67 (2H, t, J=6.3 Hz), 4.04 (1H, dd, J=8.9, 5.9 Hz), 4.17 (1H, t, J=8.9 Hz), 4.20 (2H, d, J=4.6 Hz), 4.89-5.02 (1H, m), 6.83 (2H, d, J=8.6 Hz), 7.12 (2H, d, J=8.6 Hz), 7.34 (2H, d, J=8.9 Hz), 7.52 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.20 NO.sub.4 Cl) C H N______________________________________Calculated 63.07 5.57 3.87Found 62.77 5.56 3.87______________________________________
Example 35
Synthesis of 3-[4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyphenyl]propyl alcohol
The same procedure of Example 34 was repeated except that methyl 3-[4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyphenyl]propionate (compound 189) obtained in Example 31 was used in lieu of methyl 3-{4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxyphenyl}propionate to give the title compound (compound 195) in a yield of 48%.
Melting point: 123.degree.-124.degree. C. NMR spectrum (CDCl.sub.3) .delta.1.27 (1H, br-s), 1.81-1.91 (2H, m), 2.66 (2H, t, J=7.6 Hz), 3.66 (2H, t, J=6.4 Hz), 4.06 (1H, dd, J=8.9, 5.9 Hz), 4.14-4.25 (3H, m), 4.93-5.02 (1H, m), 6.83 (2H, d, J=8.6 Hz), 7.12 (2H, d, J=8.6 Hz), 7.14 (1H, t, J=6.6 Hz), 7.39 (2H, dd, J=8.6, 6.6 Hz), 7.56 (2H, d, J=8.6 Hz)
______________________________________Elementary analysis (for C.sub.19 H.sub.21 NO.sub.4) C H N______________________________________Calculated 69.71 6.47 4.28Found 69.81 6.61 4.34______________________________________
Example 36
Synthesis of methyl 3-{4-[3-(2-pyridyl)-2-oxooxazolidin-5-yl]methoxyphenyl}-2-bromopropionate
A 0.90 g quantity of sodium nitrite was added to a solution of 3.30 g of 4-[3-(2-pyridyl)-2-oxooxazolidin-5-yl]methoxyaniline obtained in Reference Example 21 in 40 ml of methanol, 10 ml of acetone and 8.0 g of 47% hydrobromic acid. The mixture was stirred with ice-cooling for 0.5 hour. To the mixture was added 6.4 ml of methyl acrylate, and 256 mg of cuprous oxide was added thereto at 40.degree. C. and the mixture was stirred at the same temperature for 20 minutes. The reaction mixture was concentrated under reduced pressure and the obtained residue was extracted with ethyl acetate. The extract was washed successively with aqueous ammonia and an aqueous solution of sodium chlorides, dried with magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure. The residue was subjected to silica gel column chromatography and purified by hexane-ethyl acetate gradient elution to give 2.7 g of the title compound (compound 196) as an oil (yield 53%).
NMR spectrum (CDCl.sub.3) .delta.3.18 (1H, dd, J=14.2, 7.9 Hz), 3.40 (1H, dd, J=14.2, 8.6 Hz), 3.72 (3H, s), 4.2-4.45 (4H, m), 5.02 (1H, m), 6.79 (2H, d, J=8.9 Hz), 7.05 (1H, dd, J=5.0, 4.0 Hz), 7.39 (2H, d, J=8.9 Hz), 7.73 (1H, ddd, J=8.6, 5.0, 1.0 Hz), 8.24 (1H, d, J=8.6 Hz), 8.34 (1H, dd, J=4.0, 1.0 Hz)
Example 37
Synthesis of methyl 3-[4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyphenyl]-2-chloropropionate and methyl 3-{4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxyphenyl}-2-chloropropionate
The same procedure of Example 36 was repeated except that 2.89 g of a mixture of 4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxyaniline and 4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyaniline obtained in Reference Example 22 was used in lieu of 4-[3-(2-pyridyl)-2-oxooxazolidin-5-yl]methoxyaniline, and concentrated hydrochloric acid was used in lieu of 47% hydrobromic acid. The residue was subjected to silica gel chromatography and purified by hexane-ethyl acetate gradient elution to give 210 mg of methyl 3-[4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyphenyl]-2-chloropropionate (compound 197) and 180 mg of methyl 3-{4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxyphenyl}-2-chloropropionate (compound 198). Methyl 3-[4-(3-phenyl-2-oxooxazolidin-5-yl)methoxyphenyl]-2-chloropropionate
Melting point 83.degree.-84.degree. C. NMR spectrum (CDCl.sub.3) .delta.3.12 (1H, dd, J=14.2, 7.6 Hz), 3.31 (1H, dd, J=14.2, 7.1 Hz), 3.74 (3H, s), 4.06 (1H, dd, J=8.8, 6.1 Hz), 4.17-4-24 (3H, m), 4.40 (1H, dd, J=7.6, 7.3 Hz), 4.97 (1H, m), 6.85 (2H, d, J=8.6 Hz), 7.10-7.20 (3H, m), 7.40 (2H, dd, J=8.2, 7.6 Hz), 7.57 (2H, d, J=7.6 Hz)
______________________________________Elementary analysis (for C.sub.20 H.sub.20 NO.sub.5 Cl) C H N______________________________________Calculated 61.62 5.17 3.59Found 61.71 5.07 3.63______________________________________
Methyl 3-{4-[3-(4-chlorophenyl)-2-oxooxazolidin-5-yl]methoxyphenyl}-2-chloropropionate
Melting point 94.degree.-95.degree. C. NMR spectrum (CDCl.sub.3) .delta.3.10 (1H, dd, J=14.2, 7.2 Hz), 3.29 (1H, dd, J=14.2, 7.2 Hz), 3.73 (3H, s), 4.00 (1H, dd, J=8.9, 5.9 Hz), 4.11-4.23 (3H, m), 4.40 (1H, dd, J=7.6, 7.3 Hz), 4.95 (1H, m), 6.83 (2H, d, J=8.6 Hz), 7.13 (2H, d J=8.6 Hz), 7.32 (2H, d, J=8.9 Hz), 7.50 (2H, d, J=8.9 Hz)
______________________________________Elementary analysis (for C.sub.20 H.sub.19 NO.sub.5 Cl.sub.2) C H N______________________________________Calculated 56.62 4.51 3.30Found 56.70 4.44 3.30______________________________________
The structures and properties of the compounds synthesized in Examples of the present invention are shown below.
TABLE 1__________________________________________________________________________ ##STR9## Elementary analysis (%) Calculated (Found) orCompound Melting H-NMR (DMSO-d.sub.6)No. R.sup.1 R.sup.2 R.sup.3 point (.degree.C.) Yield (%) C H N__________________________________________________________________________ 1 4-OMe H H 135-137 91 66.05 5.23 4.28 (66.23 5.36 4.40) 2 3-OMe H H 177-179 86 66.05 5.23 4.27 (66.24 5.03 4.32) 3 2-OMe H H 93-95 42 66.05 5.23 4.27 (65.90 4.94 4.33) 4 2-OMe 4-OMe H 137-139 85 63.86 5.36 3.92 (63.48 5.48 3.81) 5 4-OEt H H 132-134 85 66.85 5.61 4.10 (66.94 5.75 4.12) 6 2-OEt H H Oil 92 60.78 4.88 6.16 (60.66 4.89 6.04) 7 4-Cl H H 113-115 69 61.55 4.25 4.22 (61.52 4.25 4.26) 8 2-F 4-Br H 130-133 87 51.80 3.32 3.55 (51.78 3.34 3.61) 9 4-F H H 161-164 75 64.76 4.48 4.44 (64.72 4.44 4.41)10 2-F 4-F H 129-131 79 61.26 3.93 4.20 (61.29 4.07 4.20)11 2-F 4-F 6-F 115-116 53 58.13 3.44 3.99 (58.10 3.46 3.93)12 3-F 4-F H 141-143 67 61.26 3.93 4.20 (61.31 3.97 4.15)13 2-Cl 4-Cl H 111-113 37 55.76 3.58 3.82 (55.74 3.51 3.86)14 3-Cl 4-Cl H 136-139 83 55.76 3.58 3.82 (55.81 3.69 3.84)15 3-F H H 159-161 86 64.76 4.48 4.44 (64.90 4.48 4.41)16 2-Cl H H 92-93 46 61.55 4.25 4.22 (61.58 4.17 4.22)17 2-F 4-Cl H 129-131 70 58.38 3.75 4.00 (58.38 3.71 4.09)18 4-COOEt H H 151-152 79 65.03 5.18 3.79 (65.12 5.22 3.81)19 H H H 168-169 81 68.68 5.09 4.71 (68.69 5.13 4.63)20 4-Me H H 158-160 86 69.44 5.50 4.50 (69.66 5.73 4.59)21 4-Et H H 120-122 78 70.14 5.88 4.31 (70.40 5.91 4.37)22 4-iso-Pr H H 131-134 84 70.78 6.24 4.13 (70.73 6.20 4.11)23 ##STR10## H 140-142 94 71.20 (71.18 5.68 5.71 4.15 4.18)24 4-NMe.sub.2 H H 183-185 70 67.05 5.92 8.23 (67.18 6.00 8.24)25 ##STR11## H H 122-124 78 67.60 (67.75 5.95 6.01 3.94 4.01)26 4-OCF.sub.3 H H 96-98 33 56.70 3.70 3.67 (56.97 3.72 3.69)27 4-CF.sub.3 H H 129-130 85 59.18 3.86 3.83 (59.03 3.93 3.81)28 3-CF.sub.3 H H 119-120 58 59.18 3.86 3.83 (59.35 3.93 3.77)29 2-CF.sub.3 H H 64-66 64 58.23 3.98 3.77 (.1/3 H.sub.2 O) (58.23 3.86 3.79)30 ##STR12## H 160-162 88 63.34 (63.39 4.43 4.50 4.10 4.11)31 ##STR13## H 196-197 88 64.22 (64.32 4.82 4.87 3.94 3.96)32 ##STR14## H H 230-232 49 65.93 (65.80 4.43 4.46 7.69 7.61)33 4-NO.sub.2 H H 167-169 99 59.65 4.12 8.18 (59.34 4.05 8.26)34 4-CN H H 180-182 66 4.12(1H, dd), 4.30(1H, dd), 4.34(1H, dd), 4.42(1H, dd), 5.12(1H, m), 7.04(2H, d), 7.70(2H, d), 7.75(2H, d), 7.85(2H, d), 9.90(1H,__________________________________________________________________________ s)
TABLE 2__________________________________________________________________________ ##STR15## Elementary analysis (%) Calculated (Found) orCompound Melting H-NMR (DMSO-d.sub.6)No. R B point (.degree.C.) Yield (%) C H N__________________________________________________________________________35 ##STR16## CH.sub.2 67-69 82 62.38 (62.57 5.14 5.11 3.83 3.86)36 ##STR17## CH.sub.2 CH.sub.2 116-117 57 66.85 (66.78 5.61 5.70 4.10 4.27)37 ##STR18## CH.sub.2 CH.sub.2 129-131 53 60.16 (59.97 4.25 4.23 3.69 3.70)38 ##STR19## CH.sub.2 135-137 27 ##STR20##39 ##STR21## CH.sub.2 153-155 58 ##STR22##__________________________________________________________________________
TABLE 3__________________________________________________________________________ ##STR23## Specific rotation [.alpha.].sub.D.sup.25 Elementary analysis (%)Compound (concentration, Melting Calculated (Found)No. R.sup.1 R.sup.2 R.sup.5 solvent) point (.degree.C.) Yield (%) C H N__________________________________________________________________________40 4-CF.sub.3 H H -74.45.degree. 132-133 68 59.18 3.86 3.83 (1.0, CHCl.sub.3) (59.30 3.81 3.78)41 4-OMe H H -78.68.degree. 105-107 64 66.05 5.23 4.28 (1.0, CHCl.sub.3) (65.76 5.53 4.49)42 4-Cl 2-F H -88.62.degree. 103-105 59 58.38 3.75 4.00 (1.0, CHCl.sub.3) (58.43 3.58 4.05)43 4-F 3-F H -69.19.degree. 108-110 60 61.26 3.93 4.20 (1.0, CHCl.sub.3) (61.22 3.89 4.18)44 4-OMe H Me -75.79.degree. Oil 85 66.16 5.67 4.06 (1.0, CHCl.sub.3) (.1/5 H.sub.2 O) (66.32 5.66 4.09)__________________________________________________________________________
TABLE 4__________________________________________________________________________ ##STR24## Specific rotation [.alpha.].sub.D.sup.25 Elementary analysis (%)Compound (concentration, Melting Calculated (Found)No. R.sup.1 R.sup.2 R.sup.5 solvent) point (.degree.C.) Yield (%) C H N__________________________________________________________________________45 4-CF.sub.3 H H +76.27.degree. 132-133 75 59.18 3.89 3.83 (1.0, CHCl.sub.3) (59.23 3.82 3.80)46 4-OMe H H +77.04.degree. 103-105 79 66.05 5.23 4.28 (1.0, CHCl.sub.3) (65.99 5.38 4.65)47 4-Cl 2-F H +87.59.degree. 105-107 64 58.38 3.75 4.00 (1.0, CHCl.sub.3) (58.36 3.59 4.01)48 4-F 3-F H +63.39.degree. 108-109 50 61.26 3.93 4.20 (1.0, CHCl.sub.3) (61.32 3.92 4.19)49 4-OMe H Me +72.39.degree. Oil 85 66.16 5.67 4.06 (1.0, CHCl.sub.3) (.1/5 H.sub.2 O) (66.34 5.77 4.04)__________________________________________________________________________
TABLE 5__________________________________________________________________________ ##STR25## Elementary analysis (%) Calculated (Found) orCompound Melting H-NMR (DMSO-d.sub.6)No. R.sup.1 R.sup.2 R.sup.6 point (.degree.C.) Yield (%) C H N__________________________________________________________________________50 4-NO2 H Me 200-201 90 58.07 4.33 7.52 (58.03 4.30 7.38)51 4-Cl H Me 146-148 89 59.76 4.46 3.87 (59.88 4.39 3.88)52 4-Me H Me 140-142 92 66.85 5.61 4.10 (66.85 5.54 4.06)53 4-Et H Me 139-141 96 67.59 5.96 3.94 (67.50 5.83 3.93)54 4-iso-Pr H Me 145-147 94 68.28 6.28 3.79 (68.26 6.30 3.95)55 4-t-Bu H Me 175-177 95 68.91 6.57 3.65 (68.97 6.69 3.69)56 4-n-Bu H Me 126-127 93 68.91 6.57 3.65 (68.88 6.62 3.65)57 4-iso-Bu H Me 144-146 89 68.91 6.57 3.65 (68.91 6.60 3.63)58 ##STR26## Me 152-153 92 68.65 (68.67 5.76 5.71 3.81 3.79)59 ##STR27## Et 137-138 72 63.15 (63.25 5.30 5.30 3.15 3.49)60 3-Cl H Me 127-128 86 59.76 4.46 3.87 (59.86 4.42 3.86)61 4-Br H Me 150-151 90 53.22 3.97 3.45 (53.19 3.85 3.40)62 2-F H Me 116-118 83 62.61 4.67 4.06 (62.66 4.71 4.04)63 3-F H Me 145-146 90 62.61 4.67 4.06 (62.81 4.64 4.13)64 4-F H Me 126-127 91 62.61 4.67 4.06 (62.74 4.59 4.06)65 3-Cl 4-Cl Me 142-143 83 54.56 3.82 3.54 (54.60 3.72 3.59)66 2-Cl 4-Cl Me 135-138 93 54.56 3.82 3.54 (54.41 3.76 3.53)67 2-F 4-F Me 104-106 88 59.51 4.16 3.86 (59.51 4.16 3.87)68 2-F 4-Br Me 154-155 79 50.96 3.56 3.30 (51.03 3.56 3.13)69 4-CF.sub.3 H Me 152-154 93 57.73 4.08 3.54 (57.73 3.99 3.60)70 3-OMe H Me 124-126 95 63.86 5.36 3.92 (63.85 5.29 3.94)71 4-OMe H Me 133-134 93 63.86 5.36 3.92 (63.83 5.37 3.97)72 4-OEt H Me Oil 83 -- -- --73 4-O-iso-Pr H Me 152-153 92 65.44 6.01 3.63 (65.40 6.20 3.85)74 2-OMe 4-OMe Me 137-138 83 62.01 5.46 3.62 (62.06 5.47 3.61)75 4-OCF.sub.3 H Me 142-143 93 55.48 3.92 3.41 (55.47 3.87 3.41)76 4-Ac H Me 168-169 94 65.03 5.18 3.79 (65.02 5.14 3.77)77 4-COOEt H Me 139-140 97 63.15 5.30 3.51 (63.01 5.23 3.50)78 4-CN H Me 155-156 91 64.77 4.58 7.95 (65.05 4.45 7.98)79 H H Et 93-94 53 66.85 5.61 4.10 (66.86 5.61 4.08)80 3-NO.sub.2 H Me 154-155 80 58.07 4.33 7.52 (57.94 4.13 7.73)81 4-NO.sub.2 H H 236-238 85 56.99 3.94 7.82 (57.13 4.16 7.82)82 H H H 248-249 93 65.17 4.83 4.47 (65.34 4.87 4.45)83 4-Me H H 252-253 93 66.05 5.23 4.28 (66.16 5.24 4.26)84 4-Et H H 233-234 93 66.85 5.61 4.10 (66.88 5.63 4.20)85 4-iso-Pr H H 254-255 95 67.59 5.96 3.94 (67.81 5.91 4.00)86 4-t-Bu H H 270-271 85 68.28 6.28 3.79 (68.10 6.27 3.73)87 4-n-Bu H H 213-214 92 68.28 6.28 3.79 (68.28 6.24 3.81)88 4-iso-Bu H H 220-221 83 68.28 6.28 3.79 (68.61 6.18 3.86)89 ##STR28## H 257-260 96 67.98 (68.17 5.42 5.28 3.96 4.13)90 ##STR29## H 239-240 83 61.45 (61.59 4.61 4.55 3.77 3.77)91 3-Cl H H 220-222 87 58.72 4.06 4.03 (58.97 4.01 3.90)92 4-Cl H H 240-242 89 58.72 4.06 4.03 (58.69 4.00 3.96)93 4-Br H H 260-261 97 52.06 3.60 3.57 (52.02 3.50 3.56)94 2-F H H 164-166 81 61.63 4.26 4.23 (61.89 4.24 4.22)95 3-F H H 229-230 85 61.63 4.26 4.23 (61.83 4.22 4.22)96 4-F H H 229-231 82 61.63 4.26 4.23 (61.79 4.28 4.25)97 3-Cl 4-Cl H 250-252 95 53.42 3.43 3.66 (53.31 3.41 3.70)98 2-Cl 4-Cl H 218-220 61 53.42 3.43 3.66 (53.32 3.41 3.70)99 2-F 4-F H 200-202 67 58.46 3.75 4.01 (58.54 3.76 4.01)100 2-F 4-Br H 204-205 89 49.78 3.19 3.41 (49.63 3.18 3.35)101 4-CF.sub.3 H H 236-238 79 56.70 3.70 3.67 (56.82 3.73 3.74)102 4-OH H H 271-272 76 62.00 4.59 4.25 (61.78 4.76 4.14)103 3-OMe H H 209-211 87 61.12 5.13 3.75 (61.12 5.53 3.83)104 4-OMe H H 211-213 84 62.97 4.99 4.08 (63.14 5.02 4.16)105 2-OMe 4-OMe H 218-220 89 62.97 4.99 4.08 (63.13 4.86 4.02)106 4-OEt H H 166-167 84 63.86 5.36 3.92 (63.62 5.29 3.93)107 4-O-iso-Pr H H 231-232 89 64.68 5.70 3.77 (64.79 5.78 3.85)108 4-OCF.sub.3 H H 208-209 91 54.42 3.55 3.53 (54.33 3.53 3.51)109 4-Ac H H 253-254 94 64.22 4.82 3.94 (64.23 4.81 3.95)110 4-COOH H H >300 95 60.51 4.23 3.92 (60.10 4.12 3.85)111 3-NO.sub.2 H H 266-268 91 56.99 3.94 7.82 (56.61 3.83 8.11)112 4-NH.sub.2 H Me 139-142 100 3.81(1H, dd), 3.82(3H, s), 4.12(1H, dd), 4.30(1H, dd), 4.36(1H, dd), 5.01(1H, m), 6.58(2H, d), 7.09(2H, d), 7.18(2H, d), 7.93(2H, d)113 4-NHAc H Me 188-190 99 61.77 5.31 7.20 (61.55 5.20 7.07)114 4-NH.sub.2 H H 248-252 64 55.96 4.70 7.68 .HCl (decomp.) (55.65 4.64 7.69)115 4-NHAc H H 288-291 88 61.62 4.90 7.56 (61.30 4.93 7.54)116 4-NMe.sub.2 H Me 170-172 86 64.85 5.99 7.56 (64.95 6.03 7.60)__________________________________________________________________________
TABLE 6__________________________________________________________________________ ##STR30## Elementary analysis (%)Compound Melting Calculated (Found)No. R.sup.1 R.sup.2 R.sup.3 R.sup.6 point (.degree.C.) Yield (%) C H N__________________________________________________________________________117 2-F 4-F 6-F Et 67-69 71 57.73 4.08 3.54 (57.66 4.02 3.48)118 2-F 4-F 6-F H 223-224 55 55.59 3.29 3.81 (55.64 3.17 3.79)__________________________________________________________________________
TABLE 7__________________________________________________________________________ ##STR31## Elementary analysis (%)Compound Melting Calculated (Found)No. R.sup.1 A R.sup.6 point (.degree.C.) Yield (%) C H N__________________________________________________________________________119 Me CO Me 150-151 90 65.04 5.18 3.79 (65.40 5.20 3.78)120 H CO CH.sub.2 C.sub.6 H.sub.5 126-128 96 69.60 4.91 3.25 (69.78 4.90 3.21)121 H CO Me 138-139 86 68.91 6.57 3.65 (68.88 6.62 3.65)122 H SO.sub.2 Me 129-131 95 55.24 4.38 3.58 (55.34 4.29 3.55)123 Me SO.sub.2 CH.sub. 2 C.sub.6 H.sub.5 146-147 93 62.36 4.81 2.91 (62.47 4.77 2.91)124 H CH.sub.2 Me 85-86 52 66.85 5.61 4.10 (66.85 5.63 4.08)125 Me CH.sub.2 Me 112-113 63 67.70 5.96 3.94 (67.66 5.98 4.03)126 Cl CH.sub.2 Me 67-70 61 60.72 4.83 3.73 (60.81 4.77 3.74)127 H CH.sub.2 CH.sub.2 Me 112-113 83 67.59 5.96 3.94 (67.72 5.95 3.94)128 Me CH.sub.2 CH.sub.2 Me 143-144 84 68.28 6.28 3.79 (68.35 6.24 3.77)129 H CH.sub.2 H 172-174 91 66.05 5.23 4.28 (66.09 5.53 4.33)130 Me CH.sub.2 H 188-189 62 66.85 5.61 4.10 (67.06 5.63 4.32)131 Cl CH.sub.2 H 197-199 75 59.76 4.46 3.87 (59.68 4.49 3.92)132 H CH.sub.2 CH.sub.2 H 194-196 73 66.85 5.61 4.10 (66.85 5.62 4.09)133 Me CH.sub.2 CH.sub.2 H 172-174 39 67.59 5.96 3.94 (67.69 6.00 4.07)134 H CO H 219-221 8 63.34 4.43 4.10 (63.24 4.37 4.07)135 Me SO.sub.2 H 252-254 62 55.24 4.38 3.58 (55.26 4.36 3.60)__________________________________________________________________________
TABLE 8__________________________________________________________________________ ##STR32## Specific rotation [.alpha.].sub.D.sup.25 Elementary analysis (%)Compound (concentration, Melting Calculated (Found)No. R.sup.1 R.sup.2 R.sup.6 solvent) point (.degree.C.) Yield (%) C H N__________________________________________________________________________136 H H Me -75.5.degree. 114-115 85 66.05 5.23 4.28 (1.0, CH.sub.2 Cl.sub.2) (65.90 5.12 4.26)137 4-t-Bu H Me -75.8.degree. 163-165 87 68.91 6.57 3.65 (1.0, CH.sub.2 Cl.sub.2) (68.99 6.68 3.74)138 4-CF.sub.3 H Me -67.5.degree. 131-132 65 57.73 4.08 3.54 (1.0, CH.sub.2 Cl.sub.2) (57.68 3.93 3.61)139 4-OMe H Me -69.9.degree. 119-120 87 63.86 5.36 3.92 (1.0, CH.sub.2 Cl.sub.2) (63.76 5.32 3.93)140 4-Cl H Me -84.8.degree. 162-163 90 59.76 4.46 3.87 (1.0, CH.sub.2 Cl.sub.2) (59.68 4.37 3.85)141 3-Cl 4-Cl Me -79.8.degree. 167-168 88 54.56 3.82 3.54 (1.0, CH.sub.2 Cl.sub.2) (54.63 3.75 3.51)142 2-F 4-Br Me -76.8.degree. 136-137 80 50.96 3.56 3.30 (1.0, CH.sub.2 Cl.sub.2) (50.89 3.53 3.29)143 4-OCF.sub.3 H Me -63.1.degree. 124-125 86 55.48 3.92 3.41 (1.0, CH.sub.2 Cl.sub.2) (55.66 3.79 3.42)144 4-Ac H Me -107.6.degree. 130-132 82 65.03 5.18 3.79 (1.0, CH.sub.2 Cl.sub.2) (65.00 5.24 3.79)145 H H H -99.3.degree. 218-219 92 65.17 4.83 4.47 (0.3, MeOH) (65.03 4.82 4.44)146 4-t-Bu H H -96.0.degree. 265-267 90 68.28 6.28 3.79 (1.0, DMF) (68.02 6.25 3.78)147 4-CF.sub.3 H H -92.3.degree. 206-208 98 56.70 3.70 3.67 (0.5, MeOH) (56.86 3.64 3.70)148 4-OMe H H -91.3.degree. 204-205 80 62.97 4.99 4.08 (0.3, MeOH) (62.75 4.89 4.01)149 4-Cl H H -106.2.degree. 200-202 92 58.72 4.06 4.03 (0.5, MeOH) (58.50 4.03 3.93)150 3-Cl 4-Cl H -115.0.degree. 229-231 80 53.42 3.43 3.66 (1.0, DMF) (53.29 3.38 3.58)151 2-F 4-Br H -102.0.degree. 193-195 93 49.78 3.19 3.41 (0.5, MeOH) (49.69 3.12 3.35)152 4-OCF.sub.3 H H -81.4.degree. 208-210 99 54.42 3.55 3.53 (1.0, DMF) (54.59 3.50 3.58)__________________________________________________________________________
TABLE 9__________________________________________________________________________ ##STR33## Specific rotation [.alpha.].sub.D.sup.25 Elementary analysis (%)Compound (concentration, Melting Calculated (Found)No. R.sup.1 R.sup.2 R.sup.6 solvent) point (.degree.C.) Yield (%) C H N__________________________________________________________________________153 H H Me +73.5.degree. 110-113 75 66.05 5.23 4.28 (1.0, CH.sub.2 Cl.sub.2) (66.04 5.16 4.23)154 4-t-Bu H Me +73.0.degree. 163-164 83 68.91 6.57 3.65 (1.0, CH.sub.2 Cl.sub.2) (69.07 6.66 3.69)155 4-CF.sub.3 H Me +64.6.degree. 125-127 37 57.73 4.08 3.54 (1.0, CH.sub.2 Cl.sub.2) (57.75 3.94 3.52)156 4-OMe H Me +65.6.degree. 127-129 84 63.86 5.36 3.92 (1.0, CH.sub.2 Cl.sub.2) (63.79 5.29 3.92)157 4-Cl H Me +88.5.degree. 162-163 93 59.76 4.46 3.87 (1.0, CH.sub.2 Cl.sub.2) (59.96 4.41 3.89)158 3-Cl 4-Cl Me +86.0.degree. 165-166 84 54.56 3.82 3.54 (1.0, CH.sub.2 Cl.sub.2) (54.67 3.77 3.49)159 2-F 4-Br Me +82.8.degree. 133-135 69 50.96 3.56 3.30 (1.0, CH.sub.2 Cl.sub.2) (50.84 3.49 3.21)160 4-OCF.sub.3 H Me +65.7.degree. 123-124 84 55.48 3.92 3.41 (1.0, CH.sub.2 Cl.sub.2) (55.58 3.79 3.38)161 H H H +84.8.degree. 217-220 86 65.17 4.83 4.47 (0.3, MeOH) (65.11 4.72 4.49)162 4-t-Bu H H +89.2.degree. 265-267 90 68.28 6.28 3.79 (1.0, DMF) (68.01 6.18 3.83)163 4-CF.sub.3 H H +83.4.degree. 194-197 73 56.70 3.70 3.67 (0.5, MeOH) (56.59 3.52 3.70)164 4-OMe H H +87.2.degree. 193-195 88 62.97 4.99 4.08 (0.3, MeOH) (62.77 4.91 4.02)165 4-Cl H H +114.4.degree. 199-201 86 58.72 4.06 4.03 (0.5, MeOH) (58.74 4.04 4.02)166 3-Cl 4-Cl H +99.2.degree. 225-227 85 53.42 3.43 3.66 (1.0, DMF) (53.29 3.26 3.67)167 2-F 4-Br H +93.6.degree. 186-188 91 49.78 3.19 3.41 (0.5, MeOH) (49.61 3.09 3.39)168 4-OCF.sub.3 H H +86.4.degree. 209-211 98 54.42 3.55 3.53 (1.0, DMF) (54.43 3.53 3.54)__________________________________________________________________________
TABLE 10______________________________________ ##STR34##Com- Melting Elementary analysis (%)pound point Yield Calculated (Found)No. R.sup.1 R.sup.6 (.degree.C.) (%) C H N______________________________________169 H Me 144-145 50 62.96 4.99 4.08 (62.92 5.09 4.01)170 Me Me 148-149 49 63.85 5.36 3.92 (63.95 5.26 3.93)171 H H 214-215 33 61.99 4.59 4.25 (61.99 4.60 4.09)______________________________________
TABLE 11__________________________________________________________________________ ##STR35## Elementary analysis (%)Compound Melting Yield Calculated (Found)No. R.sup.1 R.sup.4 Y point (.degree.C.) (%) C H N__________________________________________________________________________172 OMe Me CHO 115-116 80 66.85 5.61 4.10 (67.02 5.82 4.30)__________________________________________________________________________
TABLE 12__________________________________________________________________________ ##STR36## Elementary analysis (%)Compound Melting Calculated (Found)No. R.sup.1 Y point (.degree.C.) Yield (%) C H N__________________________________________________________________________173 CHO CHO 130-132 89 66.46 4.65 4.31 (66.39 4.70 4.60)174 Cl CH.sub.2 OH 149-150 86 61.18 4.83 4.20 (61.40 4.74 4.27)175 Me CH.sub.2 OH 163-165 63 69.00 6.11 4.47 (69.04 6.24 4.40)__________________________________________________________________________
TABLE 13__________________________________________________________________________ ##STR37## Elementary analysis (%)Compound Melting Calculated (Found)No. R.sup.1 Y point (.degree.C.) Yield (%) C H N__________________________________________________________________________176 Cl COOMe 135-136 90 59.76 4.46 3.87 (59.67 4.56 3.96)177 H COOMe 158-159 60 66.05 5.23 4.28 (66.09 5.21 4.34)178 Cl CHO 120-122 92 61.55 4.25 4.22 (61.48 4.70 4.22)179 Cl COOH 219-221 64 66.05 5.23 4.28 (66.09 5.21 4.34)180 H COOH 255-257 61 64.43 4.90 4.42 (64.57 4.81 4.39)__________________________________________________________________________
TABLE 14__________________________________________________________________________ ##STR38## Elementary analysis (%)Compound Melting Calculated (Found)No. R.sup.1 (E).sub.n Y point (.degree.C.) Yield (%) C H N__________________________________________________________________________181 H ##STR39## 239-240 84 ##STR40## ##STR41## ##STR42##182 CF.sub.3 ##STR43## 234-236 97 ##STR44## ##STR45## ##STR46##183 Cl ##STR47## 223-224 84 ##STR48## ##STR49## ##STR50##184 Me ##STR51## 241-243 93 ##STR52## ##STR53## ##STR54##185 H ##STR55## 179-181 94 ##STR56## ##STR57## ##STR58##186 CF.sub.3 ##STR59## 187-188 92 ##STR60## ##STR61## ##STR62##187 Cl ##STR63## 170-172 84 ##STR64## ##STR65## ##STR66##188 Me ##STR67## 183-185 97 ##STR68## ##STR69## ##STR70##189 H ##STR71## 138-139 88 ##STR72## ##STR73## ##STR74##190 CF.sub.3 ##STR75## 136-137 88 ##STR76## ##STR77## ##STR78##191 Cl ##STR79## 133-134 85 ##STR80## ##STR81## ##STR82##192 H ##STR83## 185-187 79 ##STR84## ##STR85## ##STR86##193 Cl ##STR87## 162-163 79 ##STR88## ##STR89## ##STR90##194 Cl ##STR91## 119-120 71 ##STR92## ##STR93## ##STR94##195 H ##STR95## 123-124 48 ##STR96## ##STR97## ##STR98##__________________________________________________________________________
TABLE 15__________________________________________________________________________ ##STR99## Elementary analysis (%) Calculated (Found) orCompound Melting H-NMR (DMSO-d.sub.6)No. R.sup.1 X (E).sub.n Y point (.degree.C.) Yield (%) C H N__________________________________________________________________________196 H N ##STR100## Oil 53 ##STR101##197 H C ##STR102## 83-84 -- ##STR103## ##STR104## ##STR105##198 4-Cl C ##STR106## 94-95 -- ##STR107## ##STR108## ##STR109##__________________________________________________________________________
Preparation Examples
Given below are preparation examples wherein the compounds of the present invention are used. Preparation Example 1 Tablets
Tablets were prepared in a conventional manner using the following components in the proportions indicated below.
______________________________________Compound 8 100 mgLactose 47 mgCorn starch 50 mgCrystalline cellulose 50 mgHydroxypropyl cellulose 15 mgTalc 2 mgMagnesium stearate 2 mgEthyl cellulose 30 mgUnsaturated fatty acid glyceride 2 mgTitanium dioxide 2 mgPer tablet 300 mg______________________________________
Preparation Example 2 Granules
Granules were prepared in a conventional manner using the following components in the proportions indicated below.
______________________________________Compound 81 200 mgMannitol 540 mgCorn starch 100 mgCrystalline cellulose 100 mgHydroxypropyl cellulose 50 mgTalc 10 mgPer wrapper 1000 mg______________________________________
Preparation Example 3 Fine granules
Fine granules were prepared in a conventional manner using the following components in the proportions indicated below.
______________________________________Compound 83 200 mgMannitol 520 mgCorn starch 100 mgCrystalline cellulose 100 mgHydroxypropyl cellulose 70 mgTalc 10 mgPer wrapper 1000 mg______________________________________
Preparation Example 4 Capsules
Capsules are prepared in a conventional manner using the following components in the proportions indicated below.
______________________________________Compound 93 100 mgLactose 50 mgCorn starch 47 mgCrystalline cellulose 50 mgTalc 2 mgMagnesium stearate 1 mgPer capsule 300 mg______________________________________
Preparation Example 5 Syrups
Syrup was prepared in a conventional manner using the following components in the quantities indicated below.
______________________________________Compound 98 1 gPurified sucrose 60 gEthyl parahydroxybenzoate 5 mgButyl parahydroxybenzoate 5 mgFlavor suitable amountColoring agent suitable amountPurified water q.s.Total 100 ml______________________________________
Preparation Example 6 Injections
Injection was prepared in a conventional manner using the following components in the quantities indicated below.
______________________________________Compound 130 100 mgDistilled water for injection q.s.Per ampule 2 ml______________________________________
Preparation Example 7 Suppositories
Suppositories were prepared in a conventional manner using the following components in the proportions indicated below.
______________________________________Compound 147 100 mgWitepsol W-35 1400 mg(Trademark of Dynamite Nobel,a mixture of mono-, di- andtri-glycerides of saturatedfatty acid from lauric acid tostearic acid)Per suppository 1500 mg______________________________________
Pharmacological Test Example 1
Effects on sterol and fatty acid biosynthesis systems obtained from a rat liver slices
Pharmacological tests were carried out according to the procedure mentioned below, referring to the following document: Endo, A., Tsujita, Y., Kuroda, M. and Tanzawa, K., Eur. J. Biochem., 77, 31-36 (1977).
The liver was extirpated from a male Wistar rat (body weight: about 200 g) immediately after sacrifice by decapitation, and sufficiently perfused with ice-cold Krebs-Ringer bicarbonate buffer solution. The liver slices (100 mg) were added to 1 ml of Krebs-Ringer bicarbonate buffer solution containing [1-.sup.14 C] acetic acid (2 .mu.ci/.mu.mol) and one of test compounds adjusted to various concentrations, and the reaction was carried out at 37.degree. C. for 2 hours in 95% O.sub.2 -5% CO.sub.2 gas mixture. After cooling the reaction mixture, 2 ml of petroleum ether was added thereto to extract the sterol fraction with shaking. The extract was concentrated and 1 ml of 1% digitonin solution was added thereto. After standing, the mixture was centrifuged. The sterol fraction obtained as the sediment was washed several times with an organic solvent and dissolved in 1 ml of acetic acid. Subsequently, radioactivity of the sterol fraction was measured. Then the concentration of the test compound (IC.sub.50) was determined at which the radioactivity was inhibited by 50% compared with the radioactivity observed in the control group wherein the test compounds were not used.
In a similar manner, the radioactivity of fatty acid fraction was determined which was obtained by treating, with hydrochloric acid, the lower layer of the petroleum ether mentioned in the above procedure.
The results are shown in Table 16.
TABLE 16______________________________________Compound IC.sub.50 (.mu.M)No. Sterol Fatty acid______________________________________ 1 10.2 5.6 8 6.4 2.9 81 3.79 1.30 83 5.74 2.89 93 3.23 1.55101 4.80 3.17130 29.52 14.80147 8.08 4.78149 3.36 1.99164 0.84 1.23165 1.15 1.09171 34.50 9.81175 4.8 2.7180 7.1 33.7183 17.4 5.7193 16.4 3.8194 4.8 4.0195 23.2 7.3______________________________________
Pharmacological Test Example 2
Male Sprague-Dawley rats (body weight: about 130 g) were preliminarily bred for one week, and divided into groups, each group consisting of five rats. Each of the test compounds was suspended in a 0.5% hydroxy-propylmethylcellulose (HPMC) aqueous solution, and the suspensions were orally administered to the rats at a dose of 300 mg/kg at 9:00 a.m. everyday for 14 days. Twenty-four hours after the last administration, the rats were subjected to celiotomy under etherization and blood was drawn from the inferior vena cava. The blood was allowed to stand and centrifuged to obtain serum. Lipid (triglyceride and cholesterol) in the obtained serum was measured by the enzymic method using an autoanalyzer.
Pharmacological activities of the test compounds were determined as the rate of decrease (%) in serum lipid compared with the control group to which only 0.5% aqueous HPMC solution was administered.
The results are shown in Table 17.
TABLE 17______________________________________ Rate of decrease in Rate of decrease inCompound total cholesterol triglyceride inNo. in serum (%) serum (%)______________________________________ 98 26.8 65.5100 32.4 62.9108 50.4 83.0______________________________________

Number	Name	Date
3020262	Speranza	Feb 1962
4602093	Baldwin	Jul 1986
4999378	Fujii et al.	Mar 1991
5145865	Fujii et al.	Sep 1992

Number	Date	Country
0086403	Feb 1983	EPX
3-275666	Dec 1991	JPX
93-22298	Nov 1993	WOX

Oxazolidine derivatives and pharmaceutically acceptable salts thereof

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Entry
Iwakura et al Chem. Abst. vol. 67, Entry 108577 (1966).
Ulrich et al. Jour. Org. Chem. vol. 34 No. 10 pp. 3200-3201 (1969).
Iwakura et al Yuki Gosei Kagaku Kyokaishi vol. 24, No. 1 pp. 60-65 (1966).
Breslow et al. Jour Am. Chem. Soc. vol. 72 pp. 4244-4246 (1950).
Iwakura et al. Chemical Abstracts, vol. 64, No. 6, 14 Mar. 1966, Entry 8163a.