GB2075983A

GB2075983A - Pyridoxine derivatives, process for preparing them and use in therapeutics

Info

Publication number: GB2075983A
Application number: GB8114275A
Authority: GB
Original assignee: Labaz NV
Current assignee: Labaz NV
Priority date: 1980-05-19
Filing date: 1981-05-11
Publication date: 1981-11-25
Also published as: GB2075983B

Abstract

Disclosed are pyridoxine derivatives represented by the general formula: <IMAGE> in which: R represents a radical <IMAGE> in which n represents 0 or 1, X and X1, which are different, represent hydrogen or methyl, Y represents hydrogen or methyl and R2 represents a phenyl group non-substituted or bearing one or two substituents selected from the group consisting of fluorine, chlorine and bromine and of the radicals methyl, ethyl, n-propyl, isopropyl and methoxy, and R1 represents hydrogen or a radical of formula <IMAGE> in which R3 represents a straight-chain alkyl radical having from 1 to 4 carbon atoms and pharmaceutically acceptable acid addition salts thereof. In addition to possessing ???- antiadrenergic properties, some of these compounds also exhibit ???- antiadrenergic, antihypertensive and central depressant effects.

Description

SPECIFICATION Pyridoxine derivatives, process for preparing them and use in therapeutics This invention relates to novel pyridine derivatives and is concerned with novel pyridoxine derivatives and with a method of preparing the said derivatives.

The pyridoxine derivatives with which the present invention is concerned are the compounds represented by the general formula:

in which: R represents a radical

in which n represents 0 or 1, X and X1, which are different, represent hydrogen or methyl, Y represents hydrogen or methyl and R2 represents a phenyl group non-substituted or bearing one or two substituents selected from the group consisting of fluorine, chlorine and bromine and of the radicals methyl, ethyl, n-propyl, isopropyl and methoxy, and R1 represents hydrogen or a radical of formula

in which R3 represents a straight-chain alkyl radical having from 1 to 4 carbon atoms.The invention also relates to the pharmaoeutically acceptable acid addition salts of the compounds of formula I, for instance those obtained from hydrochloric acid, oxalic acid, fumaric acid, maleic acid and pamoic acid.

One class of compounds falling within the scope of general formula i are those wherein X, X, Y and n have the same meaning as given therein, R2 represents a phenyl group non-substituted or substituted by one or two methyl radicals, or by a 2-ethyl, 2-n-propyl-, 2-isopropyl or 2-methoxy-phenyl, a 3,4-dimethoxy-phenyl, a 2-isopropyl-5-methyl-phenyl or a 4-chloro-phenyl group and R, represents hydrogen or a N-methylcarbamoyl radical as well as the pharmaceutically acceptable acid addition salts thereof.

Examples of compounds falling within the scope of the present invention are listed hereunder: 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-phenyl-1-methyl-ethylamino)-propoxy]-2-methyl-pyridine 4,5-Di hydroxymethyl-3-(2-hydroxy-3-phenoxyethylam ino-propoxy)-2-methylpyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-[(3-phenyl-1-methyl-1-propyl)-amino]-propoxy]-2-mothyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(3-methyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[3-(2-ethyl-phenoxyethylamino)-2-hydroxy-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[3-(2,6-dimethyl-phenoxyethylamino)-2-hydroxypropoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(3,5-dimethyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methoxy-phenoxyethylamino))-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-phenoxy-2-methyl-ethylamino)-propoxy]-2-methy-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3(1-methyl-2-phenoxy-ethylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-isospropyl-5-methyl-phenoxyethylamino)-propoxy]-2-methylpyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(4-methyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-n-propyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-isopropyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(3,4-dimethyl-phenoxypropylamino)-propoxy]-2-methyl-pyridine 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(4-chloro-phenoxyethylamino)-propoxy]-2-methyl-pyridine 4,5-Di-(N-methylca rba moyloxymethyl )-3-L2-hydroxy-3-(2-methyí-phenoxyethylamino)-propoxyi-2- methyl-pyridine 4,5-Di-(N-methylcarba moyloxymethyl)-3-(2-hydroxy-3-phenoxyethylamino-propoxy)-2-methyl-pyridine as well as the pharmaceutically acceptable acid addition salts of these compounds for instance those obtained from hydrochloric acid, oxalic acid, fumaric acid, maleic acid and pamoic acid.

The compounds of formula I hereabove possess in the chain in the 3-position one or more isomeric centres and thus can be produced as optical isomers, positions isomers or mixtures of these isomers. The mixture of these isomers can be resolved, if desired, at appropriate stages during their process of preparation by methods known to those skilled in the art to provide the respective individual isomers.

The invention also relates to the individual isomers in question and to racemic mixtures of these isomers.

The pyridoxine derivatives of the invention have been found to possess valuable pharmacological properties capable of rendering them useful in the treatment of arterial hypertension, angina pectoris or in the treatment of circulatory deficiencies in the brain or in the myocardium.

Another object of the invention is concerned with pharmaceutical or veterinary compositions comprising as active ingredient at least one pyridoxine derivative of formula I or a pharmaceutically acceptable acid addition salt of this derivative, in association with a suitable pharmaceutical carrier or excipient.

Another object of the invention is to provide a process for preparing pharmaceutical or veterinary compositions whereby at least one pyridoxine derivative of formula I or a pharmaceutically acceptable acid addition salt thereof, is associated with a suitable pharmaceutical carrier or excipient.

Yet another object of the present invention is to provide a method of treating arterial hypertension, angina pectoris and circulatory deficiencies in the brain or in the myocardium in a subject needing such treatment, which method comprises administering to said subject an effective dose of at least one pyridoxine derivative of formula I or a pharmaceutically acceptable acid addition salt thereof.

The compounds of formula I can be prepared starting from z -isopropylidenepyridoxol of formula:

or a salt of this compound, for instance the hydrochloride.

The compound of formula ll above is a known compound which has been described by W.

KORYTNYK in J. Org. Chem. 1962, 27, 3724.

A. Preparation of the compounds of formula I in which R, represents hydrogen The dimethylketal derivative of formula ll is first condensed with allyl chloride under reflux and in an appropriate solvent such as a lower alcohol having from 1 to 3 carbon atoms, for instance ethanol or methanol, and in the presence of sodium to give 3-O-allyl-Qa-isoprnpylidenepyridoxol of formula:

which is further reacted, at room-temperature, with N-bromosuccinimide in the presence of water and in an appropriate solvent, for instance benzene, diethyl ether or diisopropyl ether, to obtain a mixture of two bromhydrines which, after treatment with sodium hydroxide, provides 3-0-(2,3-epoxypropyl)-,- isopropylidenepyridoxol of formula::

The epoxide of formula IV is then condensed under reflux and in an appropriate solvent such as a lower alcohol having from 1 to 3 carbon atoms, for instance methanol, with a primary amine of general formula: H2N-P V in which R has the same meaning as given above.

The intermediate ketal so obtained is subsequently hydrolysed in a strong acid medium, for instance hydrochloric acid, and at a temperature between 25 and 80"C, to obtain the required compounds in free base form.

B. Preparation of the compounds of formula I in which R1 is different from hydrogen The ketal function of the compound of formula Ill is hydrolysed by means of, for example, hydrochloric acid and the two free hydroxymethyl functions so obtained are then condensed with an appropriate isocyanate of general formula: P3-N=C=O VI in which R3 has the same meaning as given above, to provide the compounds of general formula:

in which R, represents a

radical as defined above.

The compounds of general formula VII are then converted to bromhydrines of general formula:

in which R, represents a

radical as defined above, through the action of N-bromosuccinimide in the presence of water and in a mixture of appropriate solvents, such as an ethyl ether/methylene chloride mixture, to obtain the desired bromhydridines which are then condensed under reflux and in a solvent such as an alcohol from 1 to 3 carbon atoms for instance methanol with an appropriate primary amine of general formula V above, to provide the required compounds of formula I in free base form.

In accordance with another procedure, compounds of general formula I in which R, is different from hydrogen can also be obtained by reacting an appropriate alkali metal hydroxide, for example sodium hydroxide, with a bromhydrine of general formula VIII to provide an epoxide of general formula:

in which R, represents a

radical as defined above and subsequently condensing this epoxide with an appropriate primary amine of general formula V to obtain the desired compounds in free base form.

The pharmaceutically acceptable acid addition salts of the invention, can be obtained, through a classical procedure, by reacting the corresponding pyridoxine derivative of formula I with an appropriate inorganic acid such as, for example, hydrochloric acid or an organic acid such as, for example, oxalic acid, fumaric acid, maleic acid or pamoic acid. Pyridine derivatives are described in U.S. Patent No 4,115,575 and a blocking action of adrenergic ,B-receptors is attributed to them. Likewise, pyridine derivatives are disclosed in Belgian Patent No 864,917 as possessing antiarrhythmic and/or local anaesthetic properties.

An enormous number of final prodoucts are included within the scope of these patents which cover several pyridoxine derivatives of the present invention through the combination of the various substituents on the pyridine ring which are cited therein.

However, no derivatives having the typical structure of pyridoxine and, in consequence, no derivative of the present invention is specifically cited or described in these references.

Amongst the pyridine derivatives of the aforesaid prior art specific mention is made of derivatives containing a 2-hydroxy3N-substituted-amino-propoxy radical. Numerous values are attributed to the substituent on the nitrogen atom of this radical and it is surprising to observe that only alkyl radicals are exemplified namely the t-butyl radical and, in the vast majority of cases, the isopropyl radical.

In the course of the development of the present invention, trials were undertaken using pyridoxine derivatives having, in the 3-position, a 2-hydroxy-3-amino-propoxy radical substituted on the nitrogen atom by one alkyl radical i.e. a n-propyl, isopropyl, 1 -methyl-propyl, isobutyl or t-butyl radical or again by a phenoxyalkyl radical i.e. a (2-methoxy-phenoxy)-ethyl or (2-methyl-phenoxy)-ethyl radical.

The purpose of such trials was to verify the pharmacological properties attributed to the compounds described in the above-cited patents. However, the N-alkyl derivatives in question did not show the predicted p-blocking properties or even any antiadrenergic properties of the a- or ,B-type.

With respect to the phenoxyethyl derivatives, no antiarrhythmic or local anaesthetic properties were observed to any significant degree.

It has now been surprisingly discovered that pyridine derivatives not described in the two abovecited patents and formed from a 4,5-dihydroxymethyl-2-methyl-3-pyridinyl moiety, which is not described in either of the said references, and furthermore having a 2-hydroxy-3-N-substituted-aminopropoxy radical which is also not exemplified in the patents in question, present pharmacological properties quite impossible to predict from the teaching of the prior art.

Thus, it has been found that the replacement of the substituents most frequently exemplified in the prior art i.e. the N-isopropyl or N-t-butyl radicals, by a N-phenoxyalkyl or N-phenylalkyl radical of which the phenyl moiety may be substituted or not, provides pyridoxine derivatives having, as a common feature, powerful antiadrenergic properties with respect to the a-receptors, most these compounds presenting, in addition, valuable antiadrenergic properties with respect to the p-receptors as well.

Furthermore, some compounds of the invention have been found to present a marked hypotensive effect in the anaesthetized animal with normal blood-pressure and an antihypertensive effect in the conscious animal presenting high blood-pressure.

This effect is probably due to an a-antiadrenergic action which provokes a decrease in the peripheral resistances and probably in part to a reserpine-like effect as well.

Stimulation of the adrenergic receptors by the endogenous catecholamines causes an increase in the work done by the heart and a still greater increase in the cardiac consumption of energy. It is thus recognized that a compound possessing antiadrenergic properties can exert an antianginal action by protecting the myocardium against the hypermetabolizing effect of the catecholamines.

The compounds of the invention which are endowed with a- and p-antiadrenergic activity will, therefore, be indicated in the treatment of angina pectoris also. They will be particularly valuable in this indication because they reduce the work of the myocardium since they cause a decrease in arterial pressure and consequently lower resistance to cardiac ejection.

It is a well-known fact that compounds presenting an a-antiadrenergic action, such as the semisynthetic ergot of rye derivatives, for example nicergoline, are valuable in the treatment of a certain number of cerebral deficiencies of vascular origin, particularly cerebral circulatory insufficiency and migraine.

This effect is particularly valuable in the case of the compounds of the invention since it is linked to a weak central depressant effect which should be accompanied by a decrease on the cerebral metabolism.

For the treatment of cerebral insufficiency, the most valuable compounds of the invention are those which exert the most powerful antiadrenergic effects together with the least potent hyoptensive action.

Finally, it has been found quite surprisingly that the compounds of the present invention have a very low degree of toxicity, whether by intravenous or oral route. This imparts to the compounds of the invention a very favourable toxico-pharmacological index which is far superior notably to that of therapeutic compounds presently used in the same indications.

Amongst the compounds of the invention which have show the most valuable spectrum of pharmacological activity, the following may be cited: 4,5-Di hydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy]-2-methyl-pyridi ne and 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methoxy-phenoxyethyla mino)-propoxy]-2-methyl-pyridine, these compounds being in the form of the free base or of a pharmaceutically acceptable acid addition salt such as, for example, the oxalate, fumarate or dihydrochloride.

Pharmacological tests carried out with 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2 methylphenoxyethylamino)-propoxy]-2-methyl-pyridine in the form of its sesquioxalate (referred to as Compound A hereunder) have show that this compound possesses a-antiadrenergic properties at a dose as low as 2 mg/kg and an antihypertensive effect from 0.1 to 0.2 mg/kg, both actions being determined by intravenous route in the dog.

Similarly 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2-methoxy-phenoxyethyla mino)-propoxy]-2methyl-pyridine in the form of its dihydrochloride (referred to as Compound U hereunder) showed prolonged a-antiadrenergic activity at a dose as low as 0.5 mg/kg by intravenous route in the dog.

The results of pharmacological tests carried out with the compounds of the invention in order to determine their cardiovascular and central depressant effects are given hereunder.

A. Antiadrenergic properties The purpose of this test was to determine the capacity of the compounds under study to reduce epinephrine-increased blood-pressure (anti-a- effect) and epinephrine-accelerated heart-rate (anti-p effect) in the dog previously anaeththetized with pentobarbital (30 mg/kg) and atropinized (1 mg/kg).

-Anti-a effect For each dog, the dose of epinephrine was first determined which provoked a reproducible increase in arterial pressure of about 100 mm.Hg (between 5 and 10 g/kg).

After that, the dose of epinephrine so determined was administered followed by a dose, by intravenous route, of the compound to be studied.

The percentage of reduction of hypertension produced by the compound under study in comparison with the hypertension previously obtained (about 100 mm.Hg) was then registered.

--Anti-P effect During the same test as that described above, the epinephrine provoked a reproducible increase in the heart-rate of about 70 beats/min. The percentage of reduction of the epinephririe-induced acceleration of heart-rate obtained by means of the compounds under study in comparison with the tachycardia previously measured (about 70 beats) was then registered.

In both cases, the results were expressed as follows: + for a < 50%-reduction of the increase in pressure or cardiac frequency ++ for a > 50%-reduction of the increase in pressure or cardiac frequency for for the almost complete suppression of the increase in pressure or cardiac frequency.

The following results were registered with compounds of formula I used in the form of a salt with oxalic acid.

R R, R (mglkg) douse | ANTI- | ANTI- , POUND EFFECT P I I I 22 t | H | 10 | +++ | + | A 22 OCH I I I I 2)2 -o ) H j 3.5 | +++ j +++ | B I I I I yH3 -(CH ) - H 10 fff t C CH3 I I I I I I -CH2-CH-O < H 10 +++ ++ D I CH, -CH CH2-Oe H 7.5 +|+ + E I I I I -CH-CH2 < ] H ! 10 1 +++ | 1 F CH3 I I I I I -(CH2)2-O H 2 +++ +

-CH-CH2-CH2 < H 10 1 ++ ss ++ I H CH3 1 I I I -(CH )-Oe H H I 10 I ++ I + I I I I I -(CH2)2-O | 10 1 +++ j + S ,C, I I I I I 2 2 X | H | Ao | ++ ] ++ j K CH3 I I I I -OCH2)2-04 H 1 | 10 | +++ | I L CH(CH3)2 I JL -(CH2)2-OCH3 ill H | 10 10 ill ++ I ill M n -C3H7 I I III -(CH2)2- t III H | 7 1 +++ I ++ | N illi I

CH(CH3)2 ! ! ss -(CH2)2-O < | H +++ 2 | 2 1 1 l I I I I I -(CH2)2-O e | conch3| 10 +++ 0 U (CH2)2-O I CONHCH31 10 j ++ | O | R I I I I CH(CH3)2 -(CH2)2-O H 10 H | 10 | +++ | ++ | S (*) 'I I I I I -(CH2)3-O 5CH3 | H | 10 ++ ++ | ++ T I I I I OCH I I I I I -(CH2 )2O ) H | 10 | +++ | ++ | U ( II I -o H I 10 ++ I + I Cl | I | 10 | ++ | I | I I I 1 1

(*) used in base form (**) used in dihydrochloride form B. Antihypertensive properties a) Hypotension in the anaesthetized dog The hypotensive effect was determined for at least one hour after the intravenous injection of a dose of the compound under study in the dog previously anaesthetized with pentobarbital (30 mg/kg) and atropinized (1 mg/kg).

Arterial pression was registered on a femoral artery.

The results were expressed as follows: ++ for a lasting reduction of about 30% in arterial pressure + for a short-lived reduction of about 20% in arterial pressure.

Trials were undertaken with Compounds A to W above as well as with the compound hereunder in its dioxalate form:

R R1 | COMPOUND OCH3 (C 2)2 CH3 ! H | X The following results were registered:

Dose Decrease in arterial -Compound (mg/ kg) pressure A 2 ++ B 3.5 + E 10 + G 2 ++ F 10 + x j 10 . + b) Hypotension in the Okamoto rat In this trial, the rats used belonged to a race specifically bred to produce animals having high blood-pressure.The arterial pressure of these rats was determined (about 1 80 mm.Hg) at the beginning of the test and a dose of the compound to be studied was then administered.

The decrease in arterial pressure was registered every hour for 6 hours after the administration of the compound in question.

By oral route, the compound of the invention which was found to be the most active in acute treatment was Compound A above. This compound provoked hypotension at a dose as low as 25 mg/kg inducing a maximum decrease of 21 mm.Hg.

In chronic treatment, involving one single administration, Compound A was found to be active at a dose as low as 50 mg/kg.

C. Reserpine-like properties These properties were demonstrated after the administration to the anaesthetized dog of successive intravenous injections of 1,2 and 4 mg/kg of the compound to be tested and the following parameters were determined.

- the increase in cardiac frequency -the increase of dP dt at its maximum, i.e. the increase of the maximum of the derivative of the left ventricular pressure in relation to time.

This derivative thus represented an index of contractility.

Trials were undertaken with Compounds A to X above as weli as with the compound hereunder in its oxalate form :

R R P1 Compound / 43 H Z -(CH2)2 The results showed that Compounds A, C, E, J, L, M, P and Z provoked a 10 to 30%-increase in cardiac frequency and in the contractility of the myocardium at a dose of 1 mg/kg.

At higher doses, the effects idicated hereabove are not increased and can even be reversed.

These effects are suppressed in the dog having previously received reserpine. This was demonstrated notably with Compound A.

Therefore, these effects are induced by the liberation of the intragranular reserve of catecholamines as occurs with the reserpine derivatives thus leading to an antihypertensive effect.

D. Central depressant properties.

Thirty minutes after the intragastric administration of a dose of the compound to be studied, batches of mice were placed in a container through which a ray of light was projected. By means of a photoelectric cell, a record was made of the number of animals passing through the light ray over a period of 1 5 minutes. The same test was performed with control animals.

The ADso was then calculated i.e. the dose of the compound under study which provoked a depressant action in 50% of the animals.

The results hereunder were registered:

Compound - ADsn in mg/kg A 50 1 33 J 47 K 44 L 40 N 42 P 42 Z 33 E. Acute toxicity Acute toxicity tests were also undertaken in rats and mice with compounds of the invention.

The following results were registered with the compounds hereunder: I)

R | R1 CH -ICH2)2-0 t H a) In sesquioxalate form: 1) In mice By intragastric route: LDso = 700 mg/kg By intraperitoneal route: LD50= 290 mg/kg By intravenous route: LD50= 11 8 mg/kg 2) In rats By intragastric route: LD50 = 2200 mg/kg By intraperitoneal route: LD50= 320 mg/kg By intravenous route: LD50= 170 mg/kg b) In fumarate form 1) In rats By intragastric route: LD, > 2500 mg/kg By intravenous route:LD= 200 mg/kg (II)

R R, OCH -(CH2)2-O ! H 1 In dihydrochloride form 1) In mice By intragastric route: LD50 > 5000 mg/kg 2) In rats By intravenous route: LD50 = 245 mg/kg It will be appreciated that for therapeutic use the compounds of the invention will normally be administered in the form of a pharmaceutical or veterinary composition, which may be in a dosage unit form appropriate to the desired mode of administration.

Thus the pharmaceutical or veterinary composition may be in a dosage unit form suitable for oral administration for example a coated or uncoated tablet, a hard- or soft-gelatin capsule, a package powder or syrup.

The composition may alternatively take the form of a suppository for rectal administration, or of a solution or suspension for parenteral administration.

Irrespective of the form which the composition takes, the pharmaceutical or veterinary composition of the invention will normally be prepared by associating at least one of the compounds of formula I or a pharmaceutically acceptable acid addition salt thereof with an appropriate pharmaceutical carrier or excipient therefor, for example one or more of the following substances: milk sugar, starches, talc, magnesium stearate, polyvinylpyrolidone, alginic acid, colloidal silica, distilled water, benzyl alcohol or flavouring agents.

The following non-limitative Examples illustrate the preparation of the compounds of the invention together with a therapeutic composition: EXAMPLE 1 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxye thylamin o)-propoxy]-2-methyl-pyridine and salts thereof 3-0-A llyl-a, a-isoprop yliden ep yridoxol Into a 1-I flask fitted with a condenser and a stirrer, were poured 400 ml of absolute ethanol to which 9.2 g (0.4 at-g) of sodium were added by fractions.

When the reaction was terminated and after cooling, 49,1 5 g (0.2 mol) of a,a- isopropylidenepyridoxol were added followed by 15.31 g (0.2 mol) of allyl chloride. While stirring, the solution so obtained was refluxed for 4 days. The major part of the ethanol was evaporated off under vacuum and the residue was taken up in water. The medium was extracted with ether and the ethereal extract was washed several times with an aqueous solution of sodium hydroxide (about 2.5 N) and then with water. After drying, the ether was evaporated off and the residue was used as such.

In this manner, 30 g of 3-0-allyl-a,c-isopropylidenepyridoxol were obtained.

Yield: 60% M.P. after recrystallization of the oxalate from ethyl acetate: 97-980C.

b) 3-O-(2,3-Ep oxy-prop yl)-a, a4soprop ylldenep yridoxol Into a 1-l flask fitted with a stirrer, were poured 200 ml of ethyl ether, 49.8 g (0.2 mol) of 3-0-allyl a,a-isopropylidenepyridoxol, 36.6 g (0.2 mol of N-bromosuccinimide and 200 ml of water.

The mixture so obtained was stirred for five days at 200 C.

After neutralization with sodium bicarbonate, the insoluble matter was filtered out and washed with water and ethyl ether. An initial quantity of bromhydrine was thus obtained. A second amount was obtained starting from the ether solution which was washed, dried and evaporated to dryness under vacuum. The residue was taken up in diisopropyl ether or in ethyl ether, thoroughly mixed and then filtered out. The two fractions were collected to provide a mixture of 52 to 55 g which melted at about 1 300C and presented two spots in thin layer chromatography.

This mixture was suspended in 1 60 ml of ethyl ether and stirred for 4 hours at 200C in the presenceof 160 ml of a normal aqueous solution of sodium hydroxide. After decantation, washing and drying, the ethyl ether phase was evaporated to dryness under vacuum (Yield: from 90 to 100%).

The residue was optionally recrystallized from diisopropyl ether.

In this manner, 3-0-(2,3-epoxy-propyl)-a,a-isopropylidenepyridoxol was obtained after recrystallization in a yield of about 90%.

M.P.: 760C.

C) 4, 5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy]2-,nethyl-p yridine For 4 hours, a solution was refluxed of 795 g (3 mols) of 3-0-(2,3-epoxy-propyl)-a,- isopropylidenepyridoxol and 453 g (3 mols) of O-methyl-phenoxy-ethylamine in 250 ml of methanol.

After that, the reaction medium was evaporated to dryness under vacuum.

The residue was hydrolysed by stirring first for 12 hours at 200C in the presence of a solution of 700 ml of hydrochloric acid in 2500 ml of water and then for 30 minutes at 800C. After cooling, the medium was made alkaline by adding 700 g of potassium carbonate and then extracted first with a 2000 ml/400 ml chloroform/n-butanol mixture and then with 500 ml of chloroform. The organic phases were collected, washed 3 times with water and dried on sodium sulphate. After filtration, 2000 ml of methanol were added.

In this manner, 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy]- 2-methyl-pyridine was obtained in free base form.

M'.P.:about1000C.

d) 4, 5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy]-2-methyl-p yridine sesquioxalate To the free base obtained above were added 540 g of anhydrous oxalic acid in 1000 ml of methanol. The oxalate which precipitated was filtered out and washed with methanol.

After three crystallizations from methanol, 380 g of 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2- methyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine sesquioxalate were obtained.

M.P.: 150-1510C.

e) 4,5-Dihydroxymethyl-3-f2-hydroxy-3-(2-methyl-phen oxyethylamino)-prop oxy]-2-me thyl-p yridine monofumarate Into a flask, 37.6 g (0.1 mol) of the free base obtained in para.c above dissolved in isopropanol were introduced. After that, 23.2 g (0.2 mol) of fumaric acid in isopropanol were added. The medium were refluxed and then concentrated. After this operation ethyl acetate was added and the medium was again concentrated. On cooling, a mass formed which was taken up in ethyl acetate. After filtration, the medium was crystallized from an ethyl acetate/methanol mixture.

In this manner, 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethyl-a m ino)-propoxy]-2methyl-pyridine monofumarate was obtained.

M.P.: 119-1 200C (decomposition) f) 4, 5-Dihydroxymeth yI-3-[2-hydroxy-3-(2-methyl-phen ox ye th ylamin o)-prop oxy]-2 -methyl-p yridine dihydrochloride.

Into a flask, 37.6 g (0.1 mol) of the free base obtained in para.c. above, dissolved in a methanol/ethyl ether mixture were introduced. After that dry hydrochloric acid was bubbled through and ethyl ether was added. The precipitate so formed was then twice recrystallized from an ethyl acetate/methanol mixture.

In this manner, 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy]-2- methyl-pyridine dihydrochloride was obtained.

M.P.: 151-1 520C (decomposition) g) 4,5-Dihydroxymeth yl-3-[2-h ydroxy-3-(2-meth yl-phenoxye th ylamino)-propoxy]-2-me thyl-p yridine dimaleate In a flask, 37.6 g of the free base obtained in para.c above, dissolved in methanol was refluxed in the presence of 23.2 g (0.2 mol) of maleic acid. The mixture was brought to dryness under vacuum and washed twice with dry ethyl ether. After that the medium was crystallized from an acetone/ethyl acetate mixture and then recrystallized from an isopropanol-methanol mixture.

In this manner, 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy]-2- methyl-pyridine pamoate was obtained.

M.P.: 113-1160C h) 4,5-Dihydroxymethyl-3-[2-h ydroxy-3-(2-methyl-phenoxye thylamino)-propoxy]-2-me th yl-p yridine pamoate In a flask, 37.6 g (0.1 mol) of the free base obtained in para.c above dissolved in methanol was refluxed in the presence of 38.8 g (0.1 mol) of pamoic acid. The mixture was brought to dryness under vacuum and the residue was washed with dry ethyl ether. After that the medium was crystallized from isopropanol and then recrystailized from a methanol/isopropanol mixture.

In this manner 4,5-dihydroxymethyl-3-[2-hydroxy-3-(2-methyl-phenoxyethyla mino)-propoxy] 2-methyl-pyridine pamoate was obtained.

M.P.: 177-1790C.

Using the same method as that described above, the following compounds were prepared: Compound M.P. C 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-phenyl- 1 - methyl-ethylam ino)-propoxy]-2-methyl-pyridine 98-99 dioxalate (isopropanol) 4,5-Dihydroxymethyl-3-(2-hydroxy-3-phenoxyethyl- 110--115 amino-propoxy)-2-methyl-pyridine dioxalate (methanol) 4,5-Dihydroxymethyl-3-j2-hydroxy-3-[3-phenyl- 1-methyl-I -propyl)-a m i no]-propoxy-2-methyI- 152-1 54 pyridine dioxalate (isopropanol/methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(3-methyl- phenoxyethylamino)-propoxy]-2-methyl-pyridine 1 68-169 sesquioxalate (methanol) Compound M.P. C 4,5-Dihdyroxymethyl-3-[3-(2-ethyl-phenoxyethylamino)-2-hydroxy-propoxy]-2-methyl-pyridine 149-151 sesquioxalate (methanol) 4,5-Dihydroxymethyl-3-[3-(2,6-di methyl-phenoxy- ethylam ino)-2-hydroxy-propoxy]-2-methyl 133-135 pyridine sesquioxalate (methanol) 4,5-Dihyd roxymethyl-3-[2-hydroxy-3-(3,5-di methylphenoxyethylamino)-propoxy]-2-methyl-pyridine 178-179 sesquioxalate (methanol) 4,5-Dihydroxymethyl-3-(2-hydroxy-3-phenylethyl- 160-161 amino-propoxy)-2-methyl-pyridine oxalate (methanol) 4,5-Dihydroxymethyl-3-[3-(3,4-dimethoxyphenethylamino)-2-hydroxy-propoxy]-2-methyl- 116-118 pyridine dioxalate (methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methoxy- phenoxyethylamino)-propoxy]-2-methyl-pyridine 132-133 sesquioxalate (methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-phenoxy- 2-methyl-ethylamino)-propoxy]-2-methyl-pyridine 111-115 sesquioxalate (methanol) 4,5-Dihdyroxymethyl-3-[2-hydroxy-3-(1-methyl2-phenoxy-ethylamino)-propoxy]-2-methyl-pyridine 180-181 oxalate (isopropanol/methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-isopropyí- 5-methylphenoxyethylamino)-propoxy]-2-methyl 164-165 pyridine dioxalate (methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(4-methyl phenoxyethylamino)-propoxy]-2-methyl-pyridine 133-135 sesquioxalate (methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-n-propyl- phenoxyethylamino)-propoxy]-2-methyl-pyridine 143-145 dioxalate (methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-isopropylphenoxyethylamino-propoxy]-2-methyl-pyridine 165-166 dioxalate (methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3(3,4-dimethylphenoxyethylamino)-propoxy]-2-methyl-pyridine 184-185 sesquioxalate (methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-isopropyl- 102-103 phenoxyethylamino)-propoxy]2-methyl-pyridine (diisopropyl ether/ methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(3,4- dimethyl-phenoxy-propylamino)-propoxy]-2 147-150 methyl-pyridine sesquioxalate (diisopropyl ether/ methanol) 4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2- methoxy-phenoxyethylamino)-propoxy]-2- 107-110 methyl-pyridine di hydrochloride (ethyl acetate/methanol) Compound M.P. C 4,5-Dihydroxymethyl-3-[2-hydroxy-3 (4-chloro-phenoxyethylamino)-propoxy]- 112-115 2-methyl-pyridine sesquioxalate (methanol) EXAMPLE 2 Preparation of 4,5-di-(N-methylcarbamoyloxymethyl)-3-[2-hydroxy-3-(2-methyl-phenoxye th ylam)'n o)- prop oxyj-2-me thylpyddine oxalate a) 3-A llyloxy-4,5-dih ydroxym ethyl-2 -methyl-p yridin e For about 8 hours, 83 g of 3-0-allyl-a,a-isopropylidenepyridoxol were treated, at roomtemperature with a solution of 747 ml of water and 83 ml of concentrated hydrochloric acid. The solution so obtained was brought to 500C by means of a water-bath and potassium carbonate in excess was added.The solution was extracted with three fractions of chloroform and washed with an aqueous solution of soldium chloride.

This solution was brought to dryness under reduced pressure. The residue was taken up in diisopropyl ether and filtered.

In this manner 64 to 65 g of 3-allyloxy-4,5-dihydroxymethyl-2-methyl-pyridine were obtained.

Yield: 9092% M.P.:+1250C b) 3-Allyloxy-4,5-di-(N-methylcarbamoyloxymethyl)-2-methyl-pyridine In a flask, 33.7 g (0.16 mol) of 3-allyloxy-4,5-dihydroxymethyl-2-methyl-pyridine in 150 ml of anhydrous tetrahydrofuran were treated with 80 ml of methyl isocyanate. The mixture was allowed to stand at room-temperature for about 8 hours and then refluxed for 24 hours. The progress of the reaction was controlled by thin layer chromatography (eluent: 45/45/10 mixture of chloroform/hexane/methanol) in the presence of ammonia vapors and the duration of heating was modified as required. The solution was heated to dryness under vacuum using a water bath of 35 to 400 C. The residue was taken up in diisopropyl ether, filtered and washed.

In this manner about 49 g of 3-aliyloxy-4,5-di-(N-methylcarbamoyloxymethyl)-2-methyl-pyridine were obtained.

Yield:"' 94% M.P. + 100--1020C.

When recrystallized from ethyl acetate, a sample of the desired product melted at 1 09--1 1 OOC.

c) 3-63-Bromo-2-hydroxy-propoxy)-4,5-di-KN-methylcarbamoyloxymethyl-2-methyl-pyridine In an ethyl ether/methylene chloride mixture were dissolved 43.4 g (0.134 mol) of 3-allyloxy-4,5di-(N-methyl-carbamoyloxymethyl)-2-methylpyridine. To this solution, 1 30 ml of water were added.

While stirring 23.85 g of N-bromosuccinimide were slowly added.

The mixture was then stirred at room-temperature for 3 days. After filtration, the medium was washed with water and ethyl ether to give 40 g of the desired product melting at about 1 350C (yield: 71%).

The organic phase was decanted, washed, dried and brought to dryness under vacuum. The residue was taken up in ethyl acetate mixed with a small fraction of ethyl ether.

A second fraction of 6 g of desired product was thus obtained melting at 1 26.80C (yield: about 10%) In this manner, 3-(3-bromo-2-hydroxy-propoxy)-4,5-di-(N-methylcarbamoyloxymethyl)2-methylpyridine was obtained.

d) 4,5-Di-(N-methylcarbamoyloxymethyl)-3-[2-hydroxy-3-(2-methyl-phenoxyethylamino)-propoxy] 2-methyl-p yridine oxalate While stirring a mixture was refluxed for 24 hours of 5 g (0.012 mol) of 3-(3-bromo-2-hydroxy propoxy)-4,5-di-(N-methyl-carbamoyloxymethyl)-2-methylpyridine and 1.81 g (0.012 mol) of 0tolyloxyethylamine in 100 ml of methanol containing 5 g of sodium bicarbonate. This mixture was brought to dryness under reduced pressure and the residue was taken up in a water/chloroform mixture or in methylene chloride. The organic phase was washed with a little water, dried on sodium sulphate and heated to dryness under vacuum.

The residue was washed with isopropyl ether and dissolved in isopropanol.

After that, a solution of oxalic acid in isopropanol was added and the medium was filtered and crystallized three times from methanol.

In this manner 4,5-di-(Nmethylcarbamoyloxymethyl)-3-[2-hydroxy-3-(2 -methyl-phenoxyethylamino)-propoxy]-2-methyl-pyridine oxalate was obtained.

M.P.: 192-1 930C (methanol) Using the same procedure as that described above but starting from the appropriate products the compound hereunder was prepared: Compound M.P. OC 4,5-Di-(N-methylcarbamoyloxymethyl)-3- (2-hydroxy-3-phenoxyethylamino-propoxy)-2- 172-174 methyl-pyridine oxalate (methanol) EXAMPLE 3 Preparation of 4,5-di-(N-methylcarbamoyloxymethyl)-3-[2-hydroxy-3-(2-methylphenoxye thylamino)- propoxy]-2-methyl-pyridine.

a) 4,5-di-(N-methylcarbamoyloxymethyl)-3-(2,3-epoxy-propoxy)-2-methyl-pyridine.

Into a flask 33.9 g (0.1 mol) of 3-(3-bromo-2-hydroxy-propoxy)4,5-di-(N-methylcarbamoyloxy- methyl)-2-methyl-pyridine in ethyl ether were introduced. There were then added 8 g (0.2 mol) of sodium hydroxide in water at room-temperature and the medium was maintained at this temperature for 4 hours. After that, the mixture was decanted, washed with water, dried and heated to dryness under vacuum. The residue was then crystallized from diisopropyl ether optionally containing a small amount of methanol.

In this manner, 4,5-di-d(N-methylcarbamoyloxymethyl)-3-(2,3-epoxy-propoxy)-2-methyl-pyridine was obtained.

M.P.: + 1350C.

b) 4,5-di-(N-m e thylcarbam oyloxyme thylj-3-[2 -h ydroxy-3-(2 -me th yl-phenoxye th ylamin o)-prop oxy]- 2-methylpyridine This compound was prepared from the epoxide previously obtained and O-tolyloxyethylamine in accordance with the process described in Example 2 para. d.

EXAMPLE4 A unit for oral administration was prepared by introducing 300 mg of 4,5-dihydroxymethyl-3-[2 hydroxy-3-(2-methyl-phenoxyethyla mino)-propoxy-2-methyl-pyridine sesquioxalate into a soft-gelatin capsule.

Claims

1. Pyridoxine derivatives represented by the general formula:

in which: R represents a radical

in which n represents 0 or 1, X and X1, which are different, represent hydrogen or methyl, Y represents hydrogen or methyl and R2 represents a phenyl group non-substituted or bearing one dr two substituents selected from the group consisting of fluorine, chlorine and bromine and of the radicals methyl, ethyl, npropyl, isopropyl and methoxy, and R, represents hydrogen our a radical of formula

in which R3 represents a straight-chain alkyl radical having from 1 to 4 carbon atoms, as well as the pharmaceutically acceptable acid addition salts thereof.

2. Pyridoxine derivatives according to Claim 1 in which X, X,, Y and n have the same meaning as given therein, R2 represents a phenyl group non-substituted or bearing one or two methyl radicals, a 2 ethyl-, 2-n-propyl-, 2-isopropyl- or 2-methoxy-phenyl, a 3,4-dimethoxy-phenyl, a 2-isopropyl-5-methylphenyl or a 4-chloro-phenyl group and R1 represents hydrogen or a N-methylcarbamoyl radical as well as the pharmaceutically acceptable acid addition salts thereof.

3. 4,5-Dihydrnxymethyl-3-[2-hydrnxy-3-(2-methyl- phenoxyethylamino)-propoxy]-2-methylpyridine and pharmaceutically acceptable acid addition salts thereof.

4.4,5-Dihydroxymethyl-3-[2-hydroxy-3-(2-methoxy-phenoxyethylamino)-propoxy]-2-methyl- pyridine and pharmaceutically acceptable acid addition salts thereof.

5. Pyridoxine derivatives according to any of Claims 1 to 4 in the form of a pharmaceutically acceptable acid addition salt obtained from hydrochloric acid, oxalic acid, fumaric acid, maleic acid or pamoic acid.

6. Process for preparing pyridoxine derivatives according to Claim 1, wherein a primary amine of general formula: H2N-P in which R has the same meaning as in Claim 1 is condensed under reflux and is an appropriate solvent: either with 3-0-(2,3-epoxy-propyl-a,a-isopropylidenepyridoxol of formula:

to obtain a ketal which is subsequently hydrolysed in a strong acid medium and at a temperature between 25 and 800C to provide the required pyridoxine derivative, in which R, represents hydrogen, in the form of a free base or with a bromhydrine of general formula:

in which P1 represents a

radical as defined in Claim 1, the said bromhydrine being reacted as such or after conversion to an epoxide of general formula::

in which R, represent a

radical as defined in Claim 1, by means of an alkali metal hydroxide, so as to obtain the required pyridoxine derivative, in which R, is different from hydrogen, in the form of a free base, the free base obtained in both cases being further reacted, if desired, with an appropriate organic or inorganic acid to form a pharmaceutically acceptable acid addition salt.

7. Process according to Claim 6, wherein the solvent is methanol, the strong medium is hydrochloric acid and the alkali metal hydroxide is sodium hydroxide.

8. Process according to Claim 6, wherein the free base is reacted with hydrochloric acid, oxalic acid, fumaric acid, maleic acid or pamoic acid to form a pharmaceutically acceptable acid addition salt.

9. A pharmaceutical or veterinary composition comprising as active ingredient at least one pyridoxine derivative according to any of Claims 1 to 5 in association with a pharmaceutical carrier or excipient therefor.

10. A method of treating arterial hypertension, angina pectoris and circulatory deficiencies in the brain or in the myocardium in a subject needing such treatment which method comprises administering to said subject an effective dose of at least one pyridoxine derivative according to any of Claims 1 to 5.

11. Process for preparing a pyridoxine derivative or pharmaceutically acceptable acid addition salt thereof, substantially as described in the foregoing Example 1, 2 or 3.

1 2. A pharmaceutical composition substantially as described in the foregoing Example 4.