AU2010200453A8 - The application of 2,5-dihyroxymethyl-3,6-dimethyl pyrazine and its derivates in pharmacy - Google Patents

Abstract

Abstract The application of 2, 5 -dihydroxymethyl -3, 6 - dimethyl pyrazine and its derivates in the preparation of drugs for the treatment and prevention of heart failure and the structural formula of the said compound is as follows: CH 3 CH 2OR' R"OCH 2 N CH 3 N - 15 -

Description

The application of 2,5 -dihydroxymethyl -3,6 - dimethyl pyrazine and its derivates in pharmacy I. Field of the invention 5 This invention refers to the applications of 2,5 -dihydroxymethyl-3,6-dimethyl pyrazine (Liguzinediol) and its derivates, and particularly relates to their usage in medical fields. II. Background of the invention Positive inotropic drugs have been widely used in the treatment on congestive 10 heart failure, and particularly it is a kind of very important method for the improvement in the myocardial systolic functions by using positive inotropic drugs during the aggravation stage of diseases. Currently, the conventional positive inotropic drugs mainly include: (I) cAMP-dependent positive inotropic drugs include: 15 1. p-receptor agonist: such drugs include dopamine, dobutamine and noradrenaline, which are used to improve the hemodynamic parameters of heart failure patients that suffer from myocardial function impairment in acute aggravation stage. Due to the signal dysfunction in early or late congestive heart failure (down-regulation of p-receptor and signal uncoupling), the application of 20 p receptor agonists in the treatment of this kind of congestive heart failure only show relatively poor therapeutic effects. In addition, denopamine is also a kind of newly developed P31 receptor partial agonist for oral administration. 2. Phosphodiesterase (PDE) III inhibitor: cAMP can directly regulate the contractility and diastole of normal myocardium and produce positive inotropic 25 effect and positive lusitropic effect. This kind of drugs can increase cAMP by inhibiting PDE III and reducing cAMP degradation, such as amrinone, milrinone, olprinone, vesnarinone and others. 3. Adenylate cyclase agonist: such drugs include forskolin, colforsin -1daropate hydrochloride (i.e. Adehl or NKH-477) and others. (II) cAMP-independent positive inotropic drugs mainly include: 1. Na+/K+-ATPase inhibitors: they can increase the influx of Ca2+ by inhibiting Na+/K+-ATPase, such as digitalis cardiac glycoside including 5 digoxin, digitoxin and lanatoside C. 2. Calcium sensitizer: such as pimobendam, sulmazole, thiadizinone and others, they take effects on the coupled excitation-contraction process of myocardium and induce a transient Ca2+ increase, thus increase the sensitivity of muscular fibers or the responsibility to Ca2+. 10 Great advancements have been achieved in the investigations on positive inotropic drugs during the past several decades, but currently available drugs have shown adverse effects in different degrees, particularly in cardiac arrhythmias and others, and the therapeutic effect is not satisfactory and thus it still needs further improvement. 15 Tetramethylpyrazine is one of the active ingredients of ligusticum chuanxiong hort, which has significant therapeutic effects on cardiovascular and cerebrovascular diseases and little side effects. Liguzinediol is the derivate of tetramethylpyrazine. The Chinese patent application 200710092853.2 disclosed that 2, 5-di-(choline phosphate) methyl-3, 6-dimethyl pyrazine, which is obtained 20 by using liguzinediol as precursor, can inhibit the activity of C-reactive protein. However, the positive inotropic activity of tetramethylpyrazine derivate has not been reported now. III. Contents of the invention Technical problem: the present invention provides a kind of application of 2,5 25 dihydroxymethyl -3,6 - dimethyl pyrazine (Liguzinediol) and its derivates in the preparation of drugs for the treatment and prevention of heart failure. Technical solution: the technical solution of this invention is the application of Liguzinediol and its derivates in the preparation of drugs for the treatment and prevention of heart failure, and the structural formula of the said compound is as 30 follows: -2- N

CH

3 - CH 2 OR'

R"OCH

2 N CH 3 N In the formula, R' and R" are selected from the following substituent groups: Hydrogen; Acyl and substituted acyl with 1-26 carbon atoms; 5 Alkyl and substituted alkyl with 1-26 carbon atoms; Dioic acid monoacyl with 2-10 carbon atoms; Phosphate monoacyl and its ester; Sulphuric monoacyl and its ester; Nitryl; 10 Cross combinations of the above-mentioned groups. R' and R" of the said liguzinediol derivate are hydrogen, acyl with 1-6 carbon atom, alkyl with 1-6 carbon atom or dioic acid monoacyl with 2-6 carbon atoms. R' and R" of the said liguzinediol derivate are inorganic acid esters and their salts. 15 The application of Liguzinediol in the preparation of drugs for the treatment and prevention of heart failure and the structural formula of the said compound is as follows: N

CH

3

-CH

2 OH

HOCH

2 -CH 3 N 20 The application of 2, 5-diacetoxymethyl-3, 6-dimethyl pyrazine in the preparation of drugs for the treatment and prevention of heart failure and the -3structural formula of the said compound is as follows: N

CH

3 - CH 2 OAc AcOCH 2 a:: CHr 3 The terminology N alkyl" refers to 5 linear chain, branched chain or circular groups and their combinations, such as methyl, ethyl, propyl, isopropyl, butyl, s- and t-butyl, pentyl, hexyl, cyclohexyl, phenyl, benzyl and others. The terminology "acyl" refers to acyl containing marked number of carbon atoms and linear chain, branched chain or circular structures, such as formyl, acetyl, 10 propionyl, butyryl, isobutyryl, cyclohexyl-carbonyl, benzoyl and others. The compounds mentioned in the present invention refer to effective ingredients with positive inotropic effects. The present invention includes positive inotropic pharmaceutical compositions and drugs for the treatment on heart failure. These diseases include congestive heart failure, particularly acute heart failure and 15 serious terminal stage of chronic heart failure when the diseases are in the aggravation stage. The compounds mentioned in the present invention may be also effective in the treatment on heart failures that are induced by other reasons. The compound in this invention can be used solely or combined with other drugs in the treatments on the above-mentioned diseases. 20 The pharmaceutical composition of the compound in this invention should comprise at least a kind of compound in formula I or a kind of its pharmaceutically acceptable salt, and it may also comprise a kind of excipient, medium or carrier for medical use; the terminology "pharmaceutically acceptable salt" refers to the salt that is produced with pharmaceutically acceptable non 25 toxic acid or alkali. The mentioned compounds of the invention includes the salt unless otherwise mentioned; the terminology "salt" refers to the salt that is produced with inorganic and/or organic acid and alkali; furthermore, the salt may include zwitter ions (internal salts), for example, a compound in formula I that not only includes the basic part such as pyrazine but also includes the acidic part 30 such as carboxylic acid. The pharmaceutically acceptable salt (non-toxic, physiologically acceptable) do not lead to significant toxicity and biological -4activities, such as metal salts and amine salts having cations. However, other salts may be also useful. Therefore, other salts are also involved in the research scope of this invention. The separation and purification procedures that may be employed during the preparation process can be used to prepare the salts for the 5 compound of formula I, for example, by using ion exchange chromatography or employing the free base group of the compound of formula I to react with a stoichiometric amount or excessive amount of organic or inorganic acids in proper solvents. The pharmaceutically acceptable non-toxic salts include those which originate from inorganic acid such as hydrochloric acid, hydrobromic acid, 10 sulfuric acid, phosphoric acid, nitric acid, boric acid, thiocyanic acid and others. The salts that are produced by using organic acids include acetates (such as acetic acid or trihaloacetic acids, e.g. trifluoroacetic acid), propionates, butyrates, pivalates, caproates, heptylates, undecylates, cyclopentane propionates, benzoates, 3-phenpropionates, oxalates, succinates, maleates, adipates, alginate, 15 ascorbates, aspartates, lactates, tartrates, citrates, camphorates, glucarates, fumarates, gluceptates, pectate, salicylates, picrates, nicotinate, glycerophosphates, sulfonates (for example, methanesulfonates, esylates, 2 hydroxyl esylates, benzenesulphonates, tosylates, 2-napsylates, camphorsulfonates and others), laurilsulfates and others. 20 Similarly, the salts of acidic compounds are produced by their reactions with proper inorganic or organic alkali. The typical salt groups include ammonium salts and alkaline- metal salts such as sodium, lithium and potassium salts; alkaline earth such as calcium and magnesium, barium, zinc and aluminium salts; the salts that are formed with organic alkali (such as organic amines) 25 include trialkylamine, such as triethylamine, procaine, dibensylamine, N-benzyl p-phenethylamine, 1-ephedra amine, N, N' -dibenzylidene diamine, dehydroabietylamine, N-ethyl piperidine, benzylamine, dicyclohexylamine, or similar pharmaceutically acceptable amines and the salts that are formed with amino acids such as arginine, lysine and others. Alkali groups containing 30 nitrogen may react with elementary halogenated hydrocarbons (such as methyl, ethyl, propyl and butyl chlorides, bromides and iodides), dialkyl sulphate (such as dimethyl, dihexyl, dibutyl and dipentyl sulphates), long chain halogenated hydrocarbons (such as decyl, lauryl, tetradecyl, octadecyl chlorides, bromides and iodides), halogenated aromatic hydrocarbons (such as benzyl and phenethyl 35 bromides) and others to conduct quaternization. -5- The suitable salts include hydrochlorides, bisulfates, methanesulfonates or nitrates. The present invention also refers to the precursor and solvents of the compounds. The terminology "pharmaceutical precursor" refers to the compound that can be 5 transformed into formula (1) and/or a salt and/or a solvent. The examples for these precursor derivates are shown in: (a) Design of Prodrugs, edited by H. Bundgaard, (Elsevier, 1985) and Methods in Enzymology, Vol.42, p. 309-396, edited by K. Widder, et al. (Acamedic Press, 1985); 10 (b) A Textbook of Drug Design and Development, edited by Krosgaard Larsen and H. Bundgaard, Chapter 5, "Design and Application of Prodrugs," by H. Bundgaard, p. 113-191 (1991); (c) H. Bundgaard, Advanced Drug Delivery Reviews, 8, 1-38 (1992) Since the compound containing hydroxyl and carboxyl can form biodegradable 15 ester, it can be hydrolyzed in vivo and produce the compound of formula I as a pharmaceutical precursor. Many hydrolytic cases take place due to the effects from digestive enzyme, and thus this kind of pharmaceutical precursor can be oral administered. If the ester itself is bioactive or it can be hydrolyzed in blood, parenteral administration can be carried out. The biodegradable ester of the 20 compound of formula (I) include C1-6 alkyl benzyl, 4-methoxybenzyl, 2,3 indanyl (C9H9-), phthaloyl, methoxymethyl, C1-6 alkylacyloxy-C1 -6 alkyl, such as acetoxymethyl, pivaloyl oxymethyl or propionyloxymethyl, C1-6 alcoxylformyloxy -C1-6 alkyl, such as methoxyformyloxymethyl, or ethoxyformyloxymethyl, glyacyloxymethyl, phenylglyacyloxymethyl, (5-methyl 25 2-oxo-1,3--dioxolane-4-)-methyl and other adopted physiologically hydrolyzed esters, such as penicillin and cephalosporin. The compounds of the present invention may be in free form or hydrate form. The compounds of the present invention can be made into prescriptions with drug media or blend diluents for oral, local and parenteral administration, such as 30 intramuscular, intravenous or hypodermal injection, or blend diluents for inhalant spraying. The pharmaceutical formulations can be blended with solid or -6liquid media, dilutions and proper additaments by using conventional methods. The compounds can be produced into tablets, capsules, granules, powder, lozenges, aqueous or oily suspensions and others for oral administration. The compositions of the oral prescriptions can be prepared according to currently 5 available methods for drug prescriptions, and the prescription may include one or more ingredients that are selected from sweeteners, toners and preservatives. For example, the tablets should include at least a compound of formula I that is defined as above or its pharmaceutically acceptable salts, which can be mixed with excipients, such as lactose, starch, magnesium stearate, cellulose 10 derivatives. The tablets may be not coated or be coated in order to postpone disintegration and absorption and thus retain the pharmacodynamic action for long term. The drug prescription for oral administration in the present invention can be produced into hard capsules, in which the active ingredients are mixed with 15 neutral solid diluents such as calcium carbonate and calcium phosphate; or it can be produced into soft capsules, in which the active ingredients are mixed with water, miscible solvents such as propenyl glycol, polyethylene glycol and ethanol, or oily solvents such as peanut oil and liquid paraffin. The content of the compounds in the prescription ranges from 0.01% to 100%, depending on the 20 preparation process, dosage, administration route, indications, different diseases and other factors. The dosage of the compounds of present invention ranges from 0.1mg to 500mg by parenteral administration in the form of injectable preparation, and it can also be orally administered in the form of tablets or capsules with the dosage ranging 25 from 1mg to 1000mg. Adults with an average body weight of 60-70 kilograms can be administered once or more times a day. The unit dose composition of this drug prescription includes the active ingredient ranges from 1mg to 500mg, and the typical dosages are 1mg, 5mg, 10mg, 25mg, 50mg, 100mg, 200mg, 300mg, 400mg and 500mg. 30 The prescriptions and dosages containing the compounds of present invention that are used in the treatments on specific patients depend on many factors, including body mass, age, gender, medical conditions, serious degree of disease, administration route and frequency. -7- Beneficial effects: the present invention provides the application of 2,5 dihydroxymethyl -3,6 - dimethyl pyrazine (Liguzinediol) and its derivates in the preparation of drugs for the treatment and prevention of heart failure. IV. Brief description of drawings 5 Figure 1 shows the effects of compound 2 (Liguzinediol) on the left ventricular pressure of rats. In Figure 1, a indicates the left ventricular pressure of rats before before administration; b indicates the left ventricular pressure of rats after administration. V. Embodiments 10 Further detailed descriptions of this invention are carried out by following embodiments, and the embodiments are shown here to better illustrate this invention and can not be be interpreted as the limitations to the scope of the invention. Embodiment 1: The efficacy on isolated heart of rats 15 Procedure 1: Preparation of 2,5- dihydroxymethyl -3,6-dimethyl pyrazine (compound 1) N

CH

3 -C CH 2 OAc AcOCH 2 N CH 3 N 20 Anhydrous tetramethylpyrazine (6.80g, 50mmol), acetic acid (1OmL) and 30% hydrogen peroxide (mass concentration, 11 mL, 300mmol) are mixed and heated at 98L] for 12 h, and the mixture is cooled down to room temperature and then subjected to concentration in vacuo at 0.03Mpa till it is 8mL, subsequently 20% sodium hydroxide (mass concentration) is added to adjust the pH value to 9.0. 25 The separated solid is then filtered and subjected to recrystallization with acetic ether, and white needle crystal of tetramethylpyrazine dinitrogenoxide is obtained (5.80 g, the yield is 68.7%). IR(KBr)cm-1: 1523, 1504 (C=N), 1335 (C=C), 1306 (CH3). EI-MSm/z (%): 168.1(100), 152.1(37.96), 151.1(19.28), 135.1(18.99), 134.1(38.35), 93.1(15.71), 53.0(37.20). -8- Tetramethylpyrazine dinitrogenoxide (1.68g, 10mmol) is transferred to a round bottom flask and 12mL acetic acid is then added. The mixture is heated at 100 for 4 h and excessive acetic anhydride is removed by evaporation in vacuo at 0.01MPa. The residue is purified by silica gel column chromatography and 0.81g 5 light yellow liquid is thus obtained with a yield of 32.1%. IR(KBr)cm-1: 1743(C=O), 1458(C=C), 1376(C=N), 1236(CH3), 1059(C-O). EI-MSm/z (%): 252.1(0.94), 210.1(21.32), 209.1(17.15), 150.1(95.39), 149.1(100), 43.0(20.14). Procedure 2: Preparation of Liguzinediol (compound 2) 10 N

CH

3 - -CH 2 OH HOCH2 N -CH 3 N 2,5- dihydroxymethyl -3,6-dimethyl pyrazine (compound 1) (2.52g,10mmol) is fully mixed with a solution of 20% (mass concentration) sodium hydroxide (10 15 mL) and kept still for lh, then acetic acid is added to adjust the pH value to 7. The mixture is subjected to evaporation in vacuo at 0.03MPa, and the residue is separated by silica gel column chromatography, thus white needle crystal is finally obtained (1.10 g, the yield is 65.5%). mp116-117 L. UV(MeOH)kmaxnm: 223, 278.5; IR(KBr)cm-1: 3243(-OH), 2858 (CH3), 2922 20 (CH2), 1425, 1365(C=C), 1316, 1250(C=N); 1H-NMR(DMSO-D6, 500MHz) 6: 4.56(4H, d), 5.15(2H, t), 2.51(6H, s); 13C-NMR (DMSO-D6, 500MHz) 6: 151.15, 148.12, 62.85(CH2), 20.13(CH3); EI-MS m/z(%): 168.1(76.38), 167.1(28.90), 151.1(11.95), 150.1(18.66), 139.1(100), 138.1(26.9), 122.1(13.41), 121.1(61.54), 110.1(15.87). 25 Procedure 3: Effects on the cardiac contractility of isolated hearts of rats Intraperitoneal injection of 1.2g/kg urethane is carried out on rats and the hearts are collected. After the hearts are rinsed and cut in 100% oxygen saturated physiological saline at 0] ,they are connected to modified Langendorff heart perfusion equipments to couduct retrogressive perfusion via the aorta. The 30 perfusate (in mmol/L) is NaCl 117, KC1 5.7, CaCI2 1.8, NaHCO3 4.4, NaH2PO4 -9- 1.5, MgCl2 1.7, HEPES 20, Glucose 11, Creatine 10, Taurine 20, and NaOH is used to adjust the pH value to 7.3. The probe of the pressure receptor is inserted into the left ventricle via the left auricle, and BioAmp amplifier is used to record the left ventricular pressure, and the electrocardiogram is measured at the same 5 time. The results are shown in Table 1. The results show that compound I and 2 (0.1mmol/L) can significantly increase the cardiac contractility of isolated hearts of rats, and the differences of left ventricular systolic pressure (LVSP), left ventricular diastolic pressure (LVEDP), maximum value of left ventricular pressure increase (+dp/dtmax) and maximum value of left ventricular pressure 10 decrease (-dp/dtmax) were statistically significant, and no statistically significant difference is found in the change in heart rate (see the figure), and no heart dysrhythmia is found. Table 1 The effects of compound I and 2 on the cardiac contractility of isolated hearts of rats Compound 1 Compound 2 (Liguzinediol) Indexes Before After Before After administration administration administration administration LVSP 18.8±9.8 26.1±12.5* 11.9±2.6 26.9±5.9** LVEDP -10.6±5.8 -14.4±7.2* -6.0±1.2 -13.0 2.3** +dp/dtmax 669.6±259.1 831.9±268.2** 415.3±117.0 790.3+251.6* -dp/dtmax -665.8±273.0 -884.9±347.0* -441.7+128.5 -763.5±188.0** Heart rate 202.6:44.1 191.6±58.0' 145.0±19.1 154.4±28.8' 15 Comparison to those before administration, *p < 0.05, **p < 0.01, p > 0.5 Figure 1 shows the effects of compound 2 (Liguzinediol) on the left ventricular pressure of rats. Figure la shows the results before administration and Figure lb shows the results after administration. Example 2: Effects on the changes in heart functions and hemodynamics of rats -10 - After the rats are paralysed with 20% ethyl urethane (urethane) (1 g/kg) and fixed on a thermostatical operation table on their backs, needle-electrodes for electrocardiogram are subcutaneously inserted from their extremities and the lead II echocardiogram (ECG) and the heart rate (HR) are measured by inputting into the multiplying channel 5 device. The right common carotid artery is isolated from the inner side of sternocleidomastoid muscle after the echocardiogram and temperature (370) become stable, and the right common carotid artery is ligated at its head end and left ventricular cannulation is carried out. It is connected with the polygraph via a pressure transducer to measure the heart function indexes of left ventricle, in the meantime, the right femoral 10 vein is isolated and venous cannulation is carried out for the intravenous administration, and the non-inserted end is connected to a syringe that is filled with 40IU/mL heparin physiological saline, the multi-channel physiological signal acquisition and processing system is used to record the data. After the measured indexes become stable, the data at one minute before the drug administration are recorded as the blank control, and 15 Liguzinediol is dissolved in physiological saline and then use 5, 10 and 20 mg/kg respectively as the low, mediate and high dosage groups, and the results within one minute after the intravenous administration are shown in Table 2. The heart rate aberration that is induced by Liguzinediol is not found in the three dosage groups after administration. The results show that 5,10 and 20 mg-kg-l liguzinediol can significantly 20 increase LVSP, +dp/dtmax, -dp/dtmax and other heart function indexes and decrease LVEDP, indicating that liguzinediol can significantly increase the left ventricular contraction and improve the diastolic function of rat heart. 25 30 - 11 - Table 2 Effects of Liguzinediol on the heart functions of normal rats X ±s, n=1 0 5mg/kg 10mg/kg 20mg/kg Indexes Before After Before After Before After administration administration administration administration administration administration LVSP 122.8+13.2 132.7±9. 1* 1225±13.8 135.7L10.9** 121.2±10.2 1 39.7±4.6** LVEDP 9. 1±6.7 7.9+6.3 10.1±5.2 6.9+6.,1** 12.1+4.1 6.3±4.8* +dp/dtmax 10272±1496 12027±1388** 9831+1409 11484±1410** 9716+980 12347±1030** -dp/dtmax -9156±1284 -8138±808 -9667+670** -8138±1161 -9964±1045** 10238± 1247** Comparison to those before administration, *P < 0.05 and **P < 0.01 Toxicity test For the acute toxicity test with one single administration, Liguzinediol is produced into 5 aqueous solution and intravenous injection administration is carried out via tail vein. The mice all survive when intravenous injection administration via tail vein is carried out in 1.5g/kg, indicating that this compound has excellent safety. - 12 -

Claims (5)

1. The application of 2, 5 -dihydroxymethyl -3, 6 -dimethyl pyrazine and its derivates in the preparation of drugs for the treatment and prevention of heart failure and the 5 structural formula of the said compound is as follows: N CH 3 -; CH 2 OR' R"OCH 2 N CH 3 N in the formula, R and R are selected from the substituent groups as below: (a) Hydrogen; (b) Acyl and substituted acyl with 1-26 carbon atoms; 10 (c) Alkyl and substituted alkyl with 1-26 carbon atoms; (d) Dioic acid monoacyl with 2-10 carbon atoms; (e) Phosphate monoacyl and its ester; (f) Sulphuric monoacyl and its ester; (g) Nitro; 1s (h) Cross combinations of the above-mentioned groups.

2. According to the said application of Liguzinediol and its derivate in the preparation of drugs for the treatment and prevention of heart failure diseases, their characteristic is that R and R in the above-mentioned Liguzinediol and its derivates 20 are hydrogen, acyl with 1-6 carbon atoms, alkyl with 1-6 carbon atoms or dioic acid monoacyl with 2-6 carbon atoms.

3. According to the said application of Liguzinediol and its derivate in the preparation of drugs for the treatment and prevention of heart failure diseases, their characteristic is that R and R in the above-mentioned Liguzinediol and its derivates 25 are esters and salts of inorganic acids.

4. According to the said application of Liguzinediol in the preparation of drugs for the treatment and prevention of heart failure diseases, the structural formula of the said compound is as follows: - 13 - N CH 3 N CH 2 OH HOCH 2 N CH 3

5. According to the said application of 2, 5- -dihydroxymethyl -3, 6-dimethyl pyrazine in the preparation of drugs for the treatment and prevention of heart failure diseases, the 5 structural formula of the said compound is as follows: N CH 3 CH 2 OAc AcOCH 2 N CH3 N - 14 -