IE63838B1 - Diphenyl-methane derivative pharmaceutical composition and use - Google Patents

Description

Diphenyl-Methane Derivative, Pharmaceutical Composition and Use The invention relates to a diphenyl-methane derivative, a process for preparing the sane and the pharmaceutical use thereof. In particular, it relates to a diphenylethylene derivative and a benzophenone oxime ether derivative.

The most serious diseases for mankind at present include acute vascular diseases such as myocardial infarction, cerebral apoplexy, cerebral thrombosis, cerebral infarction# pulmonary embolus, deep phlebothrombosis and peripheral arteriothrombosis.

Recently antiplatelet agents have attracted public attention and been clinically employed for treating these diseases. However their application has been only lately realized. Thus it is expected to develop better drugs in future.

The invention provides diphenyl-methane derivatives having the formula (I) and pharmacologically acceptable salts thereof: in which Rl and R2 each are hydrogen, hydroxyl or a alkoxy, W is -CH2-CO-CH2-COOR1'^, R3^ being hydrogen or a C, to Cc alkyl, -CH,-C(-NOR14)-CH,-COOR15, 6 2 2 14 R being hydrogen or a Cj^ to Cg alkyl, R being a C, to Cc alkyl, -CH(CN)-(CH,) -COOR16, 1 6 2 q R being hydrogen or a to Cg alkyl, q being an integer of 1 to 3, or -(CH2)p-Z, Z being -SH, -SCN or 1-pyrrolyl, l-(l,2,3,4-tetrazolyl), 1-pyrrolidinyl, 1,3-dithianyl and 3-allylmercapto-l,2,4-triazolyl groups, p being 1 or 2.

In addition, the invention provides a plurality of processes for preparing the above defined diphenylmethane derivative. Each process is explained below in detail.

Moreover the invention provides a pharmaceutical composition which comprises a a pharmacologically effective amount of the diphenyl-methane derivative as defined above or a pharmacologically acceptable salt thereof and a pharmacologically acceptable carrier.

In the definition of formula I the Cx to C6 alkyl group as mentioned with regard to R^3, R^z includes straicht-chain or branched alkyl groups carrying one to six carbon atoms, e.g., methyl, ethyl, n-propyl, n-butyl, isopropyl, isobutyl, 1-methylpropy1, tert-butyl, npentyl, 1-ethylpropyl, isoamyl and n-hexyl groups. An alkoxy group as mentioned with regard to R" and R includes any lower alkoxy group derived from the lower alkyl groups as cited above; Among these groups, methyl and ethyl groups are the most desirable lower alkyl groups while a methoxy group is the most desirable lower alkoxy group.

A pharmaceutically acceptable salt of the aimed compound of the formula (I) in which R^3, and/or r^6 are hydrogen atoms includes metal salts such as Na, K, Ca and Mg salts.

Further some of the aimed compounds can be converted into acid addition salts by reacting the same with a pharmaceutically acceptable inorganic or organic acid. Examples of such inorganic acids are hydrochloric, hydrobromic, hyaroiodic and sulfuric acids. Examples of such organic acids are maleic, fumaric, succinic, acetic, malonic, citric, benzoic, oxalic and methanesulfonic acids.

Process for Preparation There may be various processes for preparing the compounds ( I) of the invention. Typical examples thereof are as follows.

Preparation process 1 [Step 1] (Step 2] (XII) (XIII) (XIV) (XI) wherein R t R end W are as defined above; and Hal represents a halogen atom.

Namely, a benzophenone compound of the formula (XII) is reacted with a hydroxylamine to give a benzophenone oxime of the formula (XIII) (Step 1) . Then the compound (XIII) is condensed with a halide of the formula (XIV) to give the aimed compound (XV) (Step 2) . The obtained product may be converted into a pharmaceutically acceptable salt in a conventional manner, if required.

Step 1 may ba usually'carried out at a temperature of approximately 0 to 200eC, preferably at room temperature to 100*C with the use of a solvent such as msthanol, ethanol, propanol, benzene, toluene or water.

Step 2 may be usually carried out at a temperature of approximately 0 to 100°C with the use of a solvent such as dimethylformamide (DMF), dimethyl sulfoxide (DMSO), methanol, ethanol, propanol, benzene or toluene. The reaction may be carried out in the presence of a base such as sodium hydride (NaH) , triethylamine, dimethylaniline, potassium hydroxide, methoxysodium (NaOMe), ethoxysodium (NaOSt) or tert-buthoxypotasslum to give a preferable -result. Preparation process 2 For preparing compounds where R1^, r15 and R16 are 14 hydrogen, R is C. to C, alkyl and q is an * 0 13 integer of 1 to 3 compounds of formula (I) where R , R1S and R16 are to Cg alkyl and q and R14 are as defined above, are hydrolyzed Ί • in a conventional manner, for example, with an alkali such as caustic soda to civ the aimed compound.

Preparation process 3 Tor preparing a compound of the general formula (I), wherein R1 and R2 are as defined in Claim 1, where W represents a group of the formula -CH2-C-CH2-COOR15 N-OR where R represents a C. to Cc alkyl group; and 15 lb R represents a hydrogen atom or a Cj^ to Cg alkyl group, or a pharmaceutically aceptable salt thereof a compound of formula (XVI): — O —- CH» (XVI) C— CHX—COOR5 fl where R15 is as a compound of formula defined above is reacted with (XVII): H2N-OR14 (XVII) where R14 is as defined above and if necessary converted into a pharmaceutically acceptable salt. ferablv carried out 20 to 200'C in a rooanol, benzene, This reaction may be pre at a temperature of approximately solvent such as methanol, ethanol, p toluene or water.

In order to further illustrate the present invention, and not by way of limitation, typical examples of the compound of the present invention will be given. Each compound will be shown in free form. 4,4’-dimethoxybenzophenone 0- (3-methoxycarbonyl-2oxopropyl)oxime, 4,4’ -dimethoxybenzophenone 0- {3-ethoxycarbonyl-2oxopropyl)oxime, 4,4’-dimethoxybenzophenone 0- (3-methoxycarbonyl-2methoxyiminopropyl) oxime, 4,4 * -dimethoxybenzophenone 0- (3-sthoxycarbonyl-2methoxyiminopropyl) oxime, 4,4’-dimethoxybenzophenone 0- (3-carboxy-2-methoxyiminopropyl)oxime, 4,4 ’-dimethoxybenzophenone 0- (l-cyano-3-methoxycarbonylpropyl)oxime, 4,4' -dimethoxy benzophenone 0- (1-cyano-3-ethoxycarbony Ipropyl)oxime, 4,4’-dimethoxybenzophenone 0-(l-cyano-3-carboxyprocyl)oxime, 4,4’-dimethoxybenzophenone 0- (l-cyano-4-methcxycarbonylbutyl)oxime, 4,4'-dimethoxybenzophenone 0- (1-cyano-4-carbcxybutyl)oxime, 4,4' -dimethoxybenzophenone 0-(2-(3-allylmercapto1,2,4-triazolyl) ] ethyljoxime, 4,4’-dimethoxybenzophenone 0-(2-(1-(1,2,3,4tetrazolyl, JethylJoxime, 4,4' -dimethoxybenzophenone 0-(2- (2- (1,3-dithianyl, J ethyl}oxime, 4,4'-dimethoxybenzophenone 0-(2- (1-pyrrolicinyl) ethyl]oxime, 4,4 ’-dimethoxybenzophenone 0- (2-thiccyanatoethyl, oxime, 4,4’-dimethoxybenzophenone 0- (2-mercaptoethyl)oxime, 4,4’-dimethoxybenzophenone 0- [2- (1-pyrrolyl) ethyl] oxime, 4,4’-diethoxybenzophenone 0- (3-ethoxycarbonyl-2oxopropyl,oxime, 4,4’ ciethcxybenzophencne 0— (3—etnoxycamony 1—z— methoxy iminopropyl, oxime, 4,4'-diethoxybenzophenone O- (3-carboxy-2-methoxyiminopropyl,oxime, 4,4 * -diethoxybenzophenone 0- (l-cyano-3-ethoxycarbonylpropyl, oxime, 4,4'-diethoxybenzophenone C-(l-cyano-3-carboxypropyl,oxime, 4-methoxybenzophenone 0- (3-ethoxycarbonyl-2oxopropyl)oxime, 4-methoxybenzophenone 0- (3-ethoxycarbonyl-2methoxyimi.nopropyl) oxime, 4-methoxybenzophenone Ο-(3-carboxy-2-methoxyiminopropyl) oxime, 4-methoxybenzophenone O- (l-cyano-3-ethoxycarbonylpropyl) oxime, and 4-methoxybenzophenone 0- (l-cyano-3-carboxypropyl) oxime.

Benzophenone oxime ether derivatives exhibit an excellent effect in the pharmacological point of view. They effectively inhibit the agglutination of platelets and eventually are useful as antiplatelet and antithrombotic agents. In particular they are useful for treating and/or preventing cerebrovascular diseases such as transient ischemic attack (TIA), cerebral infarction (thrombus and embolus) and cerebral arteriosclerosis; postoperative thrombus, embolus and blood stream disorders accompanying vascular operation and extracorporeal circulation; chronic arterial obstructions such as 3uerger's disease, obstructive arteriosclerosis, peripheral arteriosclerosis, SLS and Raynaud’s disease; and ischemic cardial diseases such as stenocardia and myocardial infarction. They are further useful for preventing recurrence of these diseases and for improving prognosis thereof.

When the compound of the present invention is used as an antiplatelet and antithrombotic agent, it may be orally or parenterally, for example, intramuscularly, subcutaneously or intravenously administered. The dose thereof may vary depending on, for example, the disease, the condition and the age of each patient. Unless particularly limited, it may be administered in a cose of 0.1 to 300 mg, preferably 0.1 to 60 mg, particularly preferably 0.3 to 30 mg, further particularly preferably 0.6 to 10 mg to'an adult per cay.

The compound of the present invention may be formulated into, for example, tablets, granules, povcers, capsules, injections or suppositories in conventional manners known in the art.

When it is to be formulated into solid preparations for oral administration, excipients and, if required, other additives such as binders, disintegrants, lubricants, colorants and corrigents are added to the base and the obtained mixture is then formulated into, for example, tablets, coated tablets, granules, powders or capsules in conventional manners.

Examples of the excipients are lactose, corn starch, white sugar, glucose, sorbitol and crystalline cellulose. Examples of the binders are polyvinyl alcohol, polyvinyl ether, ethylcellulose, methylcellulose, gum arabic, tragacanth, gelatin, shellac, hydroxypropylcellulose, hydroxypropylstarch and polyvinylpyrrolidone. Examples of the disintegrants are starch, agar, powdery gelatin, crystalline cellulose, calcium carbonate, calcium hydrogencarbonate, calcium citrate, dextrin and pectin. Examples of the lubricants are magnesium stearate, talc, polyethylene glycol, silica and hardened vegetable oils. Examples of the colorants are those approved as additives for drugs. Examples of the corrigents are cocoa powder, methol, aromatic acids, peppermint oil, Borneo camphor and cinnamon powder. These tablets and granules may be, as a matter of course, coated with, for example, sugar or gelatin if required.

When an injection is to be prepared, various additives such as pH adjustors, buffers, stabilizers and preservatives are added to the base and the obtained mixture is formulated into an injection for subcutaneous, intramuscular or intravenous administration.

To further illustrate the present invention, and not by way of limitation, the following Examples will be given.’ Example 1: 4,4’ -dimethoxybenzophenone-O- (3-ethoxycarbonyl-2-oxopropyl) oxime (1) Synthesis of 4,4'-dimethoxybenzophenone oxime 242 g (1 mole) of .4,4’-dimethoxybenzophenone was suspended in 2,000 ml ox ethanol and 210 g (3 mole) of hydroxylamine hydrochloride and 300 ml (3 mole) of a 10 N aqueous solution of NaOH were added thereto. Then the obtained mixture was heated under reflux. After two or three hours, the ethanol was distilled off in vacuo and then a saline solution was added thereto followed by extracting with chloroform. The chloroform phase was washed with water and dried over magnesium sulfate.

After distilling the chloroform off, the residue was recrystallized from ethanol. Thus 240 g of the title compound was obtained in the form of colorless needles, m.p.: 131 to 132’C.

NMR (CDClj)o: 9.60 (b-s, IH), 7.50 (a, 8H), 3.83 (s, 3H) 3.80 (s, 3H) . (2) Synthesis of 4,4’-dimethoxybenzophenone O-(2-ethoxycarbonyl-2-oxopropyl)oxime 2.57 g (0.01 mol) ox the 4,4’-dimethoxyben2ochenone oxime as obtained in (1) was dissolved in 5 ml of dimethylformamide and 1.2 g of potassium tert-butoxide was added thereto under ice cooling. The resulting mixture was stirred for ten minutes. Then 1.8 g of ethyl 4-chloroacetoacetate was added thereto and the . 5 obtained mixture was stirred at room temperature. After two hours, the reaction mixture was poured into diluted hydrochloric acid and extracted with ethanol. The crude product thus obtained was purified by silica gel chromatography to give 3.1 g of the title compound. .10 o NMR (CDClj) d : 6.7-7.4 (8H), 4.6 (2H) 3.9-4.2 (2H) • 3.8 (6H) 3.5 (2H), 1.2 (3H) Example 2: 4,4 ’-Dimethoxybenzophenone 0-(3-ethoxycarbonyl-2-me thoxy iminopropyl) oxime 3.85 g of the 4,4*-dimethoxybenzophenone 0-(3ethoxycarbonyl-2-oxopropyl) oxime as obtained in Example 1 was dissolved in 5 ml of pyridine and 1 g of methoxylamine hydrochloride was added thereto. Then the obtained mixture ' was stirred at room temperature. After two hours, the reaction mixture was poured into ethyl acetate, washed with diluted hydrochloric acid and then with a saturated saline solution and purified by silica gel chromatography. Thus 4 g of the title compound was obtained in the form of a colorless oily product. Ο NMR (CDCIS) δ : 6.7-74 (8H), 54), 4.7 (2H), 33-4.2 (2H) 33 (9K) 33, 34 <2Κ) 143—1.2 (3Η) Example 3: 4,4'-Dimethoxybenzophenone O- (3-carboxy-2methoxyiminopropyl)oxime 4.14 g of the 4,4’-dimethoxybenzophenone 0-(3ethoxycarbonyl-2-methoxyiminopropyl) oxime as obtained in Example 2 was dissolved in 20 ml of methanol and 3 ml of a 5 N acueous solution of caustic soda was added thereto. The obtained mixture was stirred at room temperature for five hours. After the completion of the reaction, the reaction mixture was acidified with diluted hydrochloric acid and extracted with ethyl acetate. Thus 3.8 g of the title compound was obtained in the form of a colorless oily product.

O NMH(CDCU) δ : 9.50 (IE), 6.8— 7.5(815), .0, 6.8 (2E), 3.8—3.9 (9H), 3.5, 3.3 (2H) Example 4: 4,4'-Dimethoxybenzophenone 0-(l-cyano-3ethoxycarbonylpropyl)oxime The procedure of Example 1 vas followed except that the ethyl 4-chloroacetoacetate was replaced by 2.2 g of ethyl 4-bromo-4-cyanobutyrate. Thus 3.6 g of the title compound having the following properties was obtained. o NMR (CDC13) δ : 63—73 <8H), SO (IH), 33 (6H), 1.2 (3H) 43—43 (2H), 2.2—23 (4H), Example 5: 4,4'-Dimethoxybenzophenone 0-(l-cyano-3carboxypropyl)oxime 3.96 g of the 4,4’-dimethoxybenzophenone 0-(l-cyano3-ethoxycarbonylpropyl)oxime was dissolved in 20 ml of dioxane and 3 ml of a 5 N acueous solution of caustic soca was added thereto. Then the mixture was allowed to react at 60°C for five hours. After the completion of the reaction, the reaction mixture was acidified and extracted with ethyl acetate. Thus 3.6 g of the title compound was obtained in the form of a colorless oily product. o NMR (CDCl,) δ : 6.7-7-5 (8H), 5.0 (IE) 35 (6H) 2.1—2.7 (4H) Example 6; 4,4'-Dimethoxybenzophenone 0- (l-cyano-4me thoxycarbonylbutyl, oxime The procedure of Example 1 was followed except that the ethyl 4-chloroacetoacetate was replaced by 2.2 g of methyl 5-bromo-5-cyanopentanoate. Thus 3.7 g of the title compound of the following properties was obtained.

O NMS(CDC1,) 3 : 6-3—7.S (8H). 4.9 (IH), (SH), 3.S (3H), 2.4 (2E>, 10 1.6-2.2 (4K) Example.7: 4,4'-Dimethoxybenzophenone 0-(l-cyano-4carboxybutyl,oxime According to the procedure of Example 5, the title compound of the following properties was obtained. oNMH(CDClj)4 : 6.7-7.5 (8H), 4.9 (lH), 3-3 (6H), 2.4 (2H), 1.5-2.2 (4H)

Claims (16)

1. -pyrrolidinyl, 1,3-dithianyl and 3-allylmercapto1,2,4-thiazolyl groups; and p is an integer of 1 or 1 2 1 2 forth in Claim 1, wherein both*of R and R are C^ to Cg alkoxy groups and W is a group of the formula 1,3-dithianyl and 3-allylmercapto-l,2,4-triazolyl groups, p being 1 or 2. 1 2

1. A diphenyl-methane derivative having the formula (I) c N-O-U/ and a pharmacologically* acceptable salt thereof, 2. ) , and a pharmaceutically acceptable salt thereof.

2. A substituted benzophenone oxime ether derivative as set l 2 forth in Claim 1, wherein both of R and R are to Cg alkoxy groups and W is a group of the formula -CH_-C-CH_-COOR^ 3 (wherein R^ represents a

3. A substituted benzophenone oxime ether derivative as set

4. A substituted benzophenone oxime ether derivative as set 5. Salt thereof.

5. A substituted benzophenone oxime ether derivative as set . . 1 2 forth m Claim 1, wherein both of R and R are C^ to Cg alkoxy groups and W is a group of the formula -(CH 2 )p-Z (wherein Z represents a group of the 25 formula -SCN or 1-pyrrolyl, l-(l,2,3,4-tetrazolyl), 5 hydrogen atom or a C 1 to Cg alkyl group), and a pharmaceutically acceptable salt thereof. 5 in which R and R each are hydrogen, hydroxyl or a C 1 t0 C 6 alkoxy ' W is -CH 2 -CO-CH 2 -COOR 13 , R 13 being hydrogen or a C. to C c alkyl, -CH.-C<-NOR 14 )-CH,-COOR 15 ,

6. A substituted benzophenone oxime ether derivative as set . 1 2 forth in Claim 1, wherein both of R and R are methoxy groups and W is a group of the formula -CH^-C-CH^-COOR 15 (wherein R 15 represents a -- n-och 3 hydrogen atom or a lower alkyl group), and a pharmaceutically acceptable salt thereof.

7. A substituted benzophenone oxime ether derivative as set 1 2 forth m Claim 1, wherein both of R and R are • methoxy groups and W is a group of the formula -CH 2 -C-CH 2 -COOH, and a pharmaceutically acceptable n-och 3

8. A substituted benzophenone oxime ether derivative as set . l 2 forth m Claim 1, wherein both of R and R are methoxy groups and W is a group of the formula -CH-(CH 2 ) q -COOR 16 (wherein R 1 ® represents a 20 hydrogen atom or a C^ to C g alkyl group; and q is an integer of 1 to 3), and a pharmaceutically acceptable salt thereof.

9. A substituted benzophenone oxime ether derivative as set 1 2 forth in Claim 1, wherein both of R and R are methoxy groups and W is a group of the formula -CH-(CH 2 ) 2 -COOC 2 H 5 , and a pharmaceutically CN acceptable salt thereof. 10. Pharmacologically acceptable carrier.

10. A substituted benzophenone oxime ether derivative as set . 1 2 forth in Claim 1, wherein both of R and R are methoxy groups and W is a group of the formula -CH-(CH 2 ) 2 »COOH, and a pharmaceutically acceptable CN · . 10 -CH2-C-CH2-COOR 15 (wherein R 15 represents a N-OR 14 14 hydrogen atom or a C^ to Cg alkyl group; and R x represents a to Cg alkyl group), and a pharmaceutically acceptable salt thereof. 10 being a C. to C- alkyl, -CH(CN)-(CH.) -COOR 16 , 1 6 l 6 z q R being hydrogen or a to C g alkyl, q being an integer of 1 to 3, or -(CH 2 )p-Z, Z being -SH, -SCN or 1-pyrrolyl, l-(l,2,3,4-tetrazolyl), 1-pyrrolidinyl,

11. A pharmaceutical composition which comprises a pharmacologically effective amount of the diphenylmethane derivative as defined in Claim 1 or a pharmacologically acceptable salt thereof and a

12. Use of the compounds of any of Claims 1 to 10 in the preparation of a medicament for the treatment of diseases caused by blood stream disorders.

13. A compound according to Claim 1, substantially as

14. A process for preparing a compound according to Claim 1, substantially as hereinbefore described and exemplified.

15. A compound according to Claim 1, whenever prepared 20 by a process claimed in Claim 14. 15 hereinbefore described and exemplified. 15 salt thereof. 15 forth in Claim 1, wherein both of R and R are C^ to Cg alkoxy groups and W is a group of the formula -CH-(CH-) -COOR^ (wherein R 1 ® represents a 1 2 9 CN hydrogen atom or a C^ to Cg alkyl group; and g is an integer of 1 to 3), and a pharmaceutically acceptable 20 salt thereof. 15 6 2 2 14 R being hydrogen or a C^ to C g alkyl, R

16. A pharmaceutical composition according to Claim 11, substantially as hereinbefore described.