Dihydropyridine derivatives

Abstract

The instant invention relates to compounds of the general formula: ##STR1## wherein R.sub.1 represents an alkyl, alkenyl, phenylalkyl radical, R.sub.2 represents a straight-chain alkyl, a straight- or branched-chain alkenyl or alkynyl radical, a .omega.-halogenoethyl radical, an optionally substituted benzyl radical, or a radical of the formula R.sub.4 --O--(CH.sub.2).sub.n --wherein n is 2, 3 or 4 and R.sub.4 represents a substituted alkyl radical.The compounds of the foregoing formula have been found to be useful as stabilizers for vinyl resins.

Description

This invention relates to new additives for plastic materials and, more particularly, to new stabilizers for vinyl resins such as, for instance, polyvinyl chloride.

The stabilizers with which the invention is concerned are the substances represented by the general formula: ##STR2## wherein R.sub.1 represents a branched- or straight-chain alkyl group containing from 1 to 16 carbon atoms, a branched- or straight-chain alkenyl group containing from 4 to 12 carbon atoms, a phenyl-alkyl radical in which the alkyl radical is a straight-chain alkyl group containing from 1 to 6 carbon atoms, R.sub.2 represents a straight-chain alkyl group containing from 1 to 18 carbon atoms, a branched- or straight-chain alkenyl or alkynyl group containing from 3 to 11 carbon atoms, an .omega.-halogenoethyl group, a benzyl radical substituted on the ortho- or para-position by a halogen atom or by a methyl or methoxy, radical of the formula R.sub.4 --O--(CH.sub.2).sub.n --, wherein n is 2, 3 or 4 and R.sub.4 represents a branched- or straight-chain alkyl group containing from 1 to 4 carbon atoms, substituted in the .omega.-position by a halogen atom or a methoxy radical, with the proviso that when R.sub.1 represents a methyl radical, R.sub.2 does not represent an alkyl radical.

The substances of formula I which are listed hereunder are new and certain of them are claimed herein:

2,6-Dimethyl-3,5-dicarboallyloxy-1,4-dihydropyridine (1) 2,6-Dimethyl-3,5-dicarbopropargyloxy-1,4-dihydropyridine (2) 2,6-Dimethyl-3,5-di-(2'-carbochloro-ethoxy)-1,4-dihydropyridine (3) 2,6-Dimethyl-3,5-di-(4'-carbomethoxy-benzyloxy)-1,4-dihydropyridine (4) 2,6-Dimethyl-3,5-di-(2'-carbochloro-benzyloxy)-1,4-dihydropyridine (5) 2,6-Dimethyl-3,5-di-(2'-carbomethyl-benzyloxy)-1,4-dihydropyridine (6) 2,6-Dimethyl-3,5-di-(4'-carbochloro-benzyloxy)-1,4-dihydropyridine (7) 2,6-Dimethyl-3,5-dicarbomethoxy-4-hexyl-1,4-dihydropyridine (8) 2,6-Dimethyl-3,5-dicarbomethoxy-4-propyl-1,4-dihydropyridine (9) 2,4,6-Trimethyl-3,5-dicarbophenoxy-1,4-dihydropyridine (10) 2,4,6-Trimethyl-3,5-di-(4'carbomethylphenoxy)-1,4-dihydropyridine (11) 2,4,6-Trimethyl-3,5-dicarbobenzyloxy-1,4-dihydropyridine (12) 2,4,6-Trimethyl-3,5-dicarboallyloxy-1,4-dihydropyridine (13) 2,4,6-Trimethyl-3,5-di-(4'carbochloro-benzyloxy)-1,4-dihydropyridine (14) 2,6-Dimethyl-3,5-dicarbomethoxy-4-(1-propenyl)-1,4-dihydropyridine (15) 2,6-Dibenzyl-3,5-dicarbethoxy-1,4-dihydropyridine (16) 2,6-Di-(3-butenyl)-3,5-dicarbomethoxy-1,4-dihydropyridine (17) 2,6-Diphenyl-3,5-dicarbomethoxy-1,4-dihydropyridine (18) 2,6-Dimethyl-3,5-di-(2"-carbochloro-2'ethoxy-ethoxy)-1,4-dihydropyridine (19) 2,6-Ditridecyl-3,5-dicarbomethoxy-1,4-dihydropyridine (20)

As against this, the substances listed hereunder are already known but are considered as new stabilizers of polyvinyl chloride:

2,6-Dimethyl-3,5-dicarbobenzyloxy-1,4-dihydropyridine (21) 2,6-Dimethyl-3,5-dicarbocinnamyloxy-1,4-dihydropyridine (22) 2,6-Dimethyl-3,5-dicarbomethoxy-4-phenyl-1,4-dihydropyridine (23) 2,6-Diphenyl-3,5-dicarboethoxy-1,4-dihydropyridine (24) 2,6-Dimethyl-3,5-di-(2'-carbomethoxy-ethoxy)-1,4-dihydropyridine (25) 2,6-Dimethyl-3,5-di-(2'-carboethoxy-ethoxy)-1,4-dihydropyridine (26) 2,6-Dimethyl-3,5-di-(2'-carbobutoxy-ethoxy)-1,4-dihydropyridine (27) 2,6-Dimethyl-3,5-di-(2'-carbophenoxy-ethoxy)-1,4-dihydropyridine (28) 2,4,6-Trimethyl-3,5-dicarbomethoxy-1,4-dihydropyridine (29)

The invention also relates to the process of preparation of the compounds of formula I.

The compounds of the invention may be prepared according to the HANTZSCH synthesis, described in Chemical Reviews 72, I, 1972, by reacting a compound of the general formula: ##STR3## wherein R.sub.1 and R.sub.2 have the same meanings as in formula I, with an aldehyde of the general formula: ##STR4## wherein R.sub.3 has the same meanings as in formula I and with ammonia.

The compounds of formula II, wherein R.sub.1 represents a methyl radical, can be prepared by one or the other of the following methods:

(1) By reacting a compound of the formula ##STR5## with an alcohol of the general formula:

R.sub.2 OM IV wherein R.sub.2 has the same meanings as in formula I, as described in Journal of Chemical Society, 854-60, 1954 and in Organic Synthesis 42, 28, 1962;

(2) By transesterifying in a known manner methyl acetoacetate of the formula ##STR6## by means of an alcohol of the above formula IV.

The compounds of general formula II, wherein R.sub.1 represents an alkyl chain containing from 2 to 16 carbon atoms may be prepared by reacting a halogenated derivative of the general formula:

R.sub.5 X V wherein R.sub.5 has the same meanings as R.sub.1 as defined above but having one carbon atom less, with a compound of formula II wherein R.sub.1 represents a methyl group, as described in Journal of American Chemical Society 4, 6702-6704, 1970 and in Bulletin de la Societe Chimique de France, 945-51, 1964.

Vinyl resins are known to deteriorate under the influence of heat and it is necessary to add a stabilizing agent to these masses of synthetic materials in order to retard thermodegradation and thus delay coloration of the resin.

Vinyl resins are also known to deteriorate under the influence of sunlight and a change in the original coloration may result therefrom. This problem is particularly important where containers for food and drink are concerned: it is readily appreciated that food and drink could not be packed in containers of which the coloration may change in course of time.

That is why stabilizers which are both thermostabilizers and photostabilizers are specially recommanded for vinyl resins.

Amongst the organic stabilizers are known 1,4-dihydropyridine derivatives, such as the compounds described in British Pat. No. 1,443,613.

2-Phenyl-indole, however, is specially valuable due both to its good stabilizing power and to its low toxicity. It is, moreover, widely used in the plastic industry to stabilize vinyl polymers and co-polymers, especially those which are to be used for containing food and drink.

The compounds of the invention have many advantages over the 1,4-dihydropyridines hereabove mentioned and also over 2-phenyl-indole.

For instance, the compounds of the invention already show a good stabilizing power when they are introduced into a vinyl resin in the proportion of 0.01% to 0.2%, whereas the dihydropyridines of British Pat. No. 1,443,613 are to be used in a proportion of 0.2% to 1.5% and 2-phenyl-indole in a minimum proportion of 0.2%.

This possibility of using lower proportions of stabilizers is a definite asset as far as plastic containers for food and drink are concerned. Besides the lower cost-price obtained, it should be remembered that when the concentration in stabilizer is lower, the amount of stabilizer extracted by the food or drink will also be lower.

Moreover, the compounds of the invention present a photostabilizing power which is far from negligible resulting in a better resistance of the resin to sunlight, i.e. in a reduced tendency to darken.

In addition, in resins requiring the use of a dye, which is very frequent in bottles for mineral water, the dihydropyridines according to the invention improve the basic colour and markedly increase the stability of the coloration.

Finally, the dihydropyridines of the invention possess valuable antioxidant properties, which are superior to those of the phenols, which are the most widely used antioxidants in vinyl resins (for instance, 2,6-diterbutyl-4-methyl-phenol).

When compared more particularly, to 2-phenyl-indole, the dihydropyridines according to the invention also present the following advantages:

Better transparency of the resin;

The colorations which are obtained do not affect the transparency of the resin and are perfectly stable;

Absence of yellowish tinges which are very common in vinyl resins. This enables the use of blue-tinting agents to be avoided;

When the dihydropyridines of the invention are used as secondary stabilizers in resins containing as primary stabilizers calcium and calcium-zinc salts, they enable, when compared to 2-phenyl-indole used in the same conditions, the content of zinc in the resin to be diminished without affecting the thermostability of the latter. This is important since it is known that too much zinc causes defects in resin;

When the compounds of the invention are used as secondary stabilizers in a plastified resin, i.e. a resin containing as primary stabilizers barium-cadmium and calcium-zinc salts, they enable the content in cadmium, a very expensive and very toxic product, to be diminished while improving appreciably the basic colour and increasing thermostability.

Amongst the compounds of the invention, the stabilizers listed hereunder have been found to be particularly valuable:

2,6-Dimethyl-3,5-dicarboallyloxy-1,4-dihydropyridine (1) 2,6-Dimethyl-3,5-dicarbopropargyloxy-1,4-dihydropyridine (2) 2,6-Dimethyl-3,5-dicarbobenzyloxy-1,4-dihydropyridine (21) 2,4,6-Trimethyl-3,5-dicarbomethoxy-1,4-dihydropyridine (29)

The toxicity of the stabilizers of the invention was studied first and the satisfactory results obtained were such as to justify continuation of the investigation.

A. Acute toxicity

The acute toxicity of the stabilizers of the invention was measured by determining the dose of substance which provoked the death of 50% of the treated animals (LD.sub.50).

A LD.sub.50 superior to 2 g/kg was found in both mice and rats, no toxic symptoms being observed after 15 days.

B. Study of thermostabilizing power

The study of the thermostabilizing power of the compounds of the invention was extremely thorough.

It covers several phases, each of which is important from the point of view of the use of these stabilizers.

(1) Static thermostability

This study was carried out according to the GARDNER method, described in British Pat. No. 1,489,685.

The reference substance was 2-phenyl-indole, a well-known and widely used stabilizer.

The stabilizer (dihydropyridine or 2-phenyl-indole) and the other usual ingredients were mixed with powdered vinyl resins and the mixtures were calendered at a temperature of 160.degree. C. to give rigid sheets.

The sheets were then heated in a thermostated oven (185.degree. C. or 210.degree. C.) for different intervals of time until incipient carbonization.

The coloration of the samples was compared to a standard scale of coloration, known as the GARDNER scale and was expressed in terms of the reference figures of the GARDNER scale.

This study was carried out with the following resin:

______________________________________Ingredients Parts by weight______________________________________Polyvinyl chloride resin 100Anti-shock resin 9Epoxide soja bean oil 2Calcium-12-Hydroxy-stearate 0.2SL 2016 0.1Stabilizer 0.3 or 1.55.10.sup.-3 mol______________________________________

SL 2016 is a solution of zinc-2-ethyl-hexanoate in a mixture of hydrocarbons boiling between 158.degree. C. and 184.degree. C.

The first trial was carried out at 210.degree. C. with a resin containing 0.3 part by weight of stabilizer, the sheets being removed from the oven every three minutes over a period of 21 minutes.

The following results were obtained:

______________________________________Time in minutesStabilizer 0 3 6 9 12 15 18 21______________________________________1 1 1 2 4 7 Burnt21 1 1 2 3 5.5 14 Burnt2-Phenyl- 1 2 2 10 11 16 Burntindole4 1 1 2 4 6 11 Burnt23 1 2 3 13 14 15 Burnt29 1 2 3 6 7 10 10.5 Burnt8 1 2 3 6 8 10.5 11 Burnt2-Phenyl- 1 2 3.5 10.5 13 14 Burntindole6 1 1 1.5 3 4 7 Burnt2-Phenyl- 1 1 3 8 13 13 Burntindole5 1 1 2 3 6 10.5 Burnt2-Phenyl- 1 3 3 4 11 13 Burntindole22 1 1 2 4 11 Burnt2-Phenyl- 1 2 2 9 11 Burntindole3 1 1 3 4 5 10.5 Burnt2-Phenyl- 1 1 3 5 10.5 11 Burntindole2 1 1 1 4 8 12 Burnt2-Phenyl- 1 2 3 11 14 18 Burntindole7 1 1 2 4 10.5 14 Burnt2-Phenyl- 1 1 2 6 14 14 Burntindole17 1 1 2 8 9 Burnt2-Phenyl- 1 1 2 11 13 16 Burntindole16 1 1 3 4 11 18 Burnt2-Phenyl- 1 1 3 9 14 18 Burntindole25 1 1 1 1 1 4 11 172-Phenyl- 1 2 2.5 2.5 10 13 16 Burntindole26 1 1 1 1 1.5 3 11 Burnt18 1 1 2 2 2 3 6 Burnt20 1 1 1.5 2 2 2.5 4 72-Phenyl- 1 1 1 2 2 4 10.5 11indole19 1 1 1 2 3 10 13 Burnt2-Phenyl- 1 1 1 2 4 11 13 Burntindole27 1 1 1 2 5 14 Burnt2-Phenyl- 1 1 2 3 5 14 17 Burntindole28 1 1 1 3 4 5 10 Burnt2-Phenyl- 1 1 1 3 6 11 13 Burntindole______________________________________

The above results show a marked superiority of the thermostabilizing power of the dihydropyridines over 2-phenyl-indole, at least up to 12 minutes.

The coloration of the resins stabilized with compounds 1, 2, 4, 5 and 21 is considerably less over the period from 0 to 3 minutes.

Compounds 1, 2, 3, 16 and 17 have proved to be greatly superior to 2-phenyl-indole.

A second trial was performed at a temperature of 185.degree. C., with a resin containing 0.3 part of stabilizer, the samples being removed from the oven every 6 minutes over a period of 24 minutes, then every 3 minutes until the 42nd minute (or until carbonization).

The results given hereunder were obtained:

__________________________________________________________________________Time in minutesStabilizer 0 6 12 18 24 27 30 33 36 39 42__________________________________________________________________________21 1 1 2 10 12 12 13 14 Burnt4 1 1 2 8 13 14 17 18 Burnt5 1 1 2 9 11 11 13 14 14 Burnt6 1 1 2 9 11 11 13 14 Burnt2-Phenyl- 1 1 3 5 13 14 15 15 16 16 Burntindole1 1 1 3 3 5 7 10 10.5 11 16 Burnt2 1 1 2 4 6 7 8.5 9 10.5 12 182-Phenyl- 1 1 4 9 13 14 14 14 14 15 15indole3 1 1 5 8 10 10.5 13 14 18 18 Burnt2-Phenyl- 1 1 5 10.5 11 13 14 14 15 16 18indole__________________________________________________________________________

The above results taken as a whole show the superiority of the dihydropyridines over 2-phenyl indole during 30 minutes.

Finally, a trial was performed at 185.degree. C., with resins containing equimolecular quantities of the dihydropyridines or of 2-phenyl-indole, namely 1.55.times.10.sup.-3 mol. In this case too, the samples were removed from the oven every 6 minutes over a period of 24 minutes and then every 3 minutes until the 42nd minute (or until carbonization).

The following results were obtained:

______________________________________Time in minutesStabilizer 0 6 12 18 24 27 30 33 36 39 42______________________________________21 1 1 1 4 6 8 11 15 burnt4 1 1 1 4 6 8 11 15 burnt5 1 1 1 5 10 11 13 14 15 burnt6 1 1 2 4 10 13 B.2-Phenyl- 1 2 3 10 13 14 14 14 16 16 burntindole______________________________________

The dihydropyridines, when used in an equimolecular quantity to 2-phenyl-indole, show up to the 30th minutes a thermostabilizing power superior to that of this latter compound.

(2) Study of the duration of thermostabilization

This study was carried out with vinyl resins which are used for manufacturing bottles for mineral water, namely resins containing calcium and zinc stearates, epoxy soja bean oil and either 2-phenyl-indole or a dihydropyridine of the invention (compound 1).

The following trials were carried out with various resins:

(1) The resin was mixed in a cylinder-mixer and the following parameters were measured:

The stability of the colour, i.e. the time which elapsed between the start of the mixing and the first visible change in the colour of the resin.

The thermostability, i.e. the time which elapsed between the start of the mixing and the carbonization of the resin.

With a resin containing 0.2% of stabilizer, it was found, after mixing at 220.degree. C., that the resin containing 2-phenyl-indole as stabilizer changed colour after 3 minutes and carbonized after 13 minutes, whereas the resin containing 2,6-dimethyl-3,5-dicarboallyloxy-1,4-dihydropyridine (compound 1) changed colour after five minutes and carbonized after 13.3 minutes.

(2) Examination of the colour of the resin after each passage (3 in all) in a blower-extruder, the mould being a 250 ml cylindrical flask.

Four resins were tested, the first containing 0.2% of 2-phenyl-indole and the others 0.2%, 0.03% and 0.015% of compound 1 respectively.

After the first passage, the flask presented with all four resins, a brilliant sky-blue colour.

After the second passage, the flask made with the resin containing 2-phenyl-indole presented a blue colour tending towards green, whereas the three others flasks had kept the same colour.

After the third passage, the flask corresponding to the resin stabilized with 2-phenyl-indole had become greenish-blue, whereas the three other flasks still had the same brilliant sky-blue colour.

Two conclusions may be drawn from the above findings:

In equal concentrations, compound 1 provides vinyl resin with a stability of colour which is markedly superior to that obtained with 2-phenyl-indole.

At a concentration of 0.015%, compound 1 is at all times superior to 2-phenyl-indole used at a concentration of 0.2%.

Trials were also carried out with resins containing a larger quantity of zinc stearate.

The various proportions of calcium and zinc stearate and of the stabilizers are given in the following table:

__________________________________________________________________________Additive Quantity of stabilizerN of the resin 1 2 3 4 5 6 7 8 9__________________________________________________________________________Calcium stearate 0.29 0.29 0.29 0.29 0.29 0.29 0.29 0.29 0.15Zinc stearate 0.32 0.32 0.32 0.32 0.32 0.32 0.15 -- 0.322-Phenyl-indole 0.15 -- -- -- -- -- -- -- --Compound 1 -- 0.15 0.075 0.05 0.03 0.015 0.15 0.15 0.075__________________________________________________________________________

The same trials as hereabove were carried out and the following results were obtained (mixing at 220.degree. C.)

______________________________________ ResinTrial 1 2 3 4 5 6 7 8 9______________________________________Stability of thecolour in min. 2 to 3 5 4 4 3 3 3 <1 3Thermostabilityin min. 9 8.5 8 8 8 8 15 <7 5______________________________________

The results show that the improvement of the stability of the colour with compound 1 is very good, this latter compound being 10 to 15 times more effective than 2-phenyl-indole.

Compound 1 does not directly influence thermostability but it enables, by preserving the colour, the amount of zinc stearate to be reduced and also thermostability to be increased.

Examination of the colour of the resin after each passage through the blower-extruder, clearly showed the excellent behaviour of the resins containing compound 1.

(3) Study of the stabilization of plastified vinyl resins

This study was carried out by pressing plates from sheets which had been mixed for 5 minutes at 180.degree. C., the pressing also lasting 5 minutes but at 170.degree. C.

The same parameters as hereabove were studied, namely the duration of the stability of the colour, the duration of the thermostability and the colour of the pressed plate.

The following resins were used:

__________________________________________________________________________Ingredients Parts by weightN of the resin 1 2 3 4 5 6 7 8 9__________________________________________________________________________Polyvinyl chlorideresin 100 100 100 100 100 100 100 100 100Wax E 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3 0.3Dioctylic Phthalate 50 50 50 50 50 50 50 50 50Barium stearate -- 0.375 -- 0.375 0.375 0.375 0.375 0.375 0.375Cadmium stearate -- -- 0.375 0.375 0.375 0.15 0.15 0.05 0.05Compound 1 -- -- -- -- 0.1 -- 0.05 -- 0.05__________________________________________________________________________

The following results were obtained:

______________________________________ N of the resinTrial 1 2 3 4 5 6 7 8 9______________________________________Stability of thecolour in min. <5 <5 25 35 50 30 45 20 35Thermostability inmin. <5 5 25 35 50 30 55 25 50______________________________________

It can be noted that compound 1 has a favourable influence on the stability of the plate in plastified resin since it:

increases the time elapsing between the start of the treatment and the first visible change of colour; increases the time elapsing between the start of the treatment and the carbonization of the resin.

Examination of the colour of the various resins shows that the addition of compound 1 has a favourable influence on the basic colour, this latter approaching the colourless.

C. Study of photostabilizing power

The photostabilizing power of the compounds of the invention was studied by exposing to the sun polyvinyl chloride plates which had been stabilized either by a dihydropyridine of the invention or by 2-phenylindole, or again by 2-(3'methoxy-4'-hydroxy)-indole. This last product is an extremely valuable thermostabilizer for thermoplastic resins and is described in British Pat. No. 1,489,685.

The resin given hereunder was prepared by mixing on cylinders at 160.degree. C.

______________________________________Ingredients Parts by weight______________________________________Polyvinyl chloride resin 100Anti-shock resin 8Epoxide soja bean oil 4Acrylic resin 0.5Trinonylphenyl phosphate 0.3SL 2016 0.25Calcium behenate 0.4Hydrogenated castor oil 0.2Glyceryl trimontanate 0.4Stabilizer 0.3______________________________________

The plates of stabilized polyvinyl chloride, together with a plate which had not been stabilized, were stood in the sun under the same conditions and at the same time. Their colour was measured after 6 hours and 12 hours of exposure.

The coloration of the plates was determined according to two methods:

On the plates themselves, in comparison to the GARDNER scale, as in the section on thermostability, On a solution of these plates in tetrahydrofuran, the coloration of the solution being measured according to the French Pharmacopeia (IXth edition, II-338).

The following results were obtained:

______________________________________ Coloration Coloration of the plates of the plates GARDNER FRENCH PHARMACOPEIA Time of Time of exposure to sun exposure to sunStabilizer 0 6h 12h 0 6h 12h______________________________________Standard 3+ 3+ 3+ J5 J5 J52-(3'-Methoxy-4'-hydroxy-phe- 1 4 8 B5 B4 to JB4 B3 to JB3nyl)-indole2-Phenyl-indole 2- 3 5+ J6 J5 J4Compound 1 1 1 1.5 J6 J5 J5Compound 2 1 1 1.5 JV6 JV6 JV5Compound 21 1 1 1.5 JV6 JV6 JV5Compound 29 2- 3 5 JV6 JV5 JV4______________________________________

The sign + means that the coloration lies between the lower unit and the upper half-unit. Thus, 3+ means that the coloration lies between 3 and 3.5. Similarly, the sign - means that the coloration lies between the lower half-unit and the upper unit.

It may be concluded from the above results that the dihydropyridines according to the invention have a photostabilizing power markedly superior to that of 2-phenyl-indole and of its derivative.

D. Study of antioxidant power

The value of the antioxidant power of the 1,4-dihydropyridines of the invention was demonstrated by two differents methods:

By a polarographic study of their oxidation potential, compared to well-known antioxidants such as 2,6-diterbutyl-4-methyl-phenol, 2-terbutyl-4-methoxy-phenol, 4-methoxy-phenol and hydroquinone. By direct comparison, on a polyvinyl chloride resin, of the antioxidant power of compound 1 of the invention and that of an antioxidant known as one of the most valuable and frequently used in polyvinyl chloride, namely 2,6-diterbutyl-4-methyl-phenol.

(1) Polarographic study of the oxidation potential

(a) Operating conditions

Electrodes

Reference electrode: Calomel electrode containing a saturated solution of anhydrous lithium perchlorate as bridge liquid. Working electrode: Vitrous carbon rotating electrode (2,500 r.p.m.) Counter-electrode: Platinium electrode

Chemical products

Acetonitrile containing less than 0.1% of water and presenting no polarographic waves between -2.5 V and +2.5 V. Anhydrous lithium perchlorate containing less than 1% of water.

Reactant

A 0.1 M solution of lithium perchlorate in acetonitrile, treated and preserved on a 4 A molecular sieve.

Polarographic conditions

Tension: 10 m V Initial potential: 0 V Amplitude of exploration: 0 to 2 V Speed of exploration: 10 m V/second Sensitivity: 1.25 .mu.A to 50 .mu.A Mean concentration: about 0.3.times.10.sup.-3 mol/liter

Precautions

Between each measurement, the vitrous carbon electrode and the platinium electrode are carefully cleaned with Joseph paper.

Results

______________________________________Substance Oxidation potential in volts______________________________________ 1 0.75 .+-. 0.01 21 0.73 .+-. 0.01 2 0.80 .+-. 0.012,6-Diterbutyl-4-methyl-phenol 1.11 .+-. 0.022-Terbutyl-4-methoxy-phenol 0.81 .+-. 0.01Hydroquinone 0.83 .+-. 0.014-Methoxy-phenol 0.89 .+-. 0.01______________________________________

The above results show that the dihydropyridines are more reducing than the substances usually used as antioxidants.

(2) Trial on a polyvinyl chloride resin

The antioxidant power of compound 1 was compared to that of 2,6-diterbutyl-4-methyl-phenol (compound 2) by using the following resin:

______________________________________Ingredients Parts by weight______________________________________Polyvinyl chloride resin 100Anti-shock agent 10Acrylic resin 0.5Epoxide soja bean oil 3SL 2016 0.1Zinc and calcium stearates 0.2Hydrogenated castor oil 1.5Polyethylene wax 0.3Antioxidant from 0.05 to 1______________________________________

The study was carried out according to the GARDNER method, the samples being removed from an oven at 185.degree. C. every 10 minutes over a period of 80 minutes.

The following results were obtained:

__________________________________________________________________________Concentra-tion partper 100 Time in minutesparts Antioxidant 0 10 20 30 40 50 60 70 80__________________________________________________________________________0.05 Compound Z >1 1+ 2- 5+ >6 7 7 8 Burnt Compound 1 1 1 1+ 3+ 4- 6+ 7 8 B0.1 Compound Z >1 1+ 2- >5 >6 7 7 8 B Compound 1 1 1 1+ <2 3+ 5+ 7 7 B0.2 Compound Z >1 1+ 2+ 5- >6 7 7 8 B Compound 1 1 1 1 1+ 2 3 5 >6 B0.3 Compound Z <1+ 1+ >2 6 7 8 8 8+ B Compound 1 1 1 1 1 2 >2 8 8 B0.4 Compound Z <1+ >1+ 3 >6 8- 9 9 9 B Compound 1 1 1 1 1 1+ >2+ 4 8 B0.5 Compound Z <1+ >1+ 3 >6 >7 8- 8 8 B Compound 1 1 1 1 >1 1+ >2+ 4- 8 B1.0 Compound Z 1+ 2- >3 8 8 8 9 9 B Compound 1 1 1 1 1 1+ 4 8 B__________________________________________________________________________

The signs + and - have the same meanings as in the previous table and >2 means that the coloration lies between 2 and 2+.

The following conclusions be drawn from the above table: up to 50 minutes in the oven at 185.degree. C., compound 1 proved to be superior to compound Z at every concentration.

Moreover, no concentration in compound Z gives the best results obtained with compound 1.

The same trials were carried out in a Metrastat oven at 210.degree. C.

The following results were obtained:

______________________________________Concen-tration Time in minutespart per 0 to 10 to 20 to 25 to 30 to 35 to100 parts Antioxidant 10 20 25 30 35 40______________________________________ Compound Z 2- 2 3- 4+ 10 >100.05 B/38' Compound 1 1 1 1 1 5- >10 B/40' Compound Z 2- 2 3- 4+ 11 >110.1 B/39' Compound 1 1 1 1 1 5- >10 B/38' Compound Z 2- 2 3- 4+ 11 >110.2 B/39' Compound 1 1 1 1 1 5- <9 B/39' Compound Z <1 2- 3- 3 9 <100.3 B/39' Compound 1 1 1 1 1 3+ <9 B/39' Compound Z 2- 2 3 3+ 10 >100.4 B/38' Compound 1 1 1 1 1 4- 6- B/38' Compound Z 2- 2 3 3+ 10+ >10+0.5 B/38' Compound 1 1 1 1 1 3+ 6- B/38'______________________________________

As in the previous trial, Compound 1 has been found to be markedly superior to Compound Z. Moreover, all the samples containing Compound Z gave from the time zero pink-coloured sheets, which is another disadvantage as compared to the dihydropyridine of the invention.

The following Examples provide a non-limitative illustration of the process of preparation of the compounds of the invention.

EXAMPLE 1

Preparation of 2,6-dimethyl-3,5-dicarboallyloxy-1,4-dihydropyridine

Into a reactor cooled in an ice-bath were introduced 28.4 g (0.2 mol) of allyl acetoacetate and 0.2 g of diethylamine.

The solution was cooled to 0.degree. C. and 7.5 g (0.1 mol) of a 40% aqueous solution of formic aldehyde was introduced drop-by-drop in 90 minutes, care being taken to maintain the temperature below or equal to 10.degree. C.

The reaction medium was maintained at 0.degree. C. for 6 hours, and then at room-temperature for 40 hours.

The solution was decanted and the aqueous phase was extracted with ether. The ethereal phase was added to the oily phase and was dried over anhydrous sodium sulphate.

The solution was filtered, the ether eliminated and the oily residue diluted with one part of methanol.

Ammonia was bubbled through the solution obtained, the temperature being maintained at 0.degree. C., and the solution saturated with ammonia was allowed to stand at room-temperature for 12 hours.

The solution was filtered on a Buchner funnel and the solid residue so obtained was recrystallized from acetone to give 2,6-dimethyl-3,5-dicarboallyloxy-1,4-dihydropyridine.

Yield: 75% Melting point: 167.degree. C.

By the method described above but using the appropriate starting-products, the following compounds were prepared:

______________________________________ YieldCompound % Melting point .degree.C.______________________________________2,6-Dimethyl-3,5-dicarbopropar-gyloxy-1,4-dihydropyridine 60 202-203 (acetone)2,6-Dimethyl-3,5-di-(2'-carbochloro-ethoxy)-1,4-dihydropyridine 31 158 (acetone)2,6-Dimethyl-3,5-di-(4'-carbomethoxy-benzyloxy)-1,4-dihydropyridine 18 143 (benzene 55.degree. C.)2,6-Dimethyl-3,5-dicarbobenzyloxy-1,4-dihydropyridine 57 122 (benzene)2,6-Dimethyl-3,5-dicarbocinnamyloxy-1,4-dihydropyridine 37 156 (benzene then acetone)2,6-Dimethyl-3,5-di-(2'-carbochloro-benzyloxy)-1,4-dihydropyridine 44 190 (acetone)2,6-Dimethyl-3,5-di-(2'-carbomethyl-benzyloxy)-1,4-dihydropyririne 47 149 (acetone)______________________________________

EXAMPLE 2

Preparation of 2,6-dimethyl-3,5-dicarbopropargyloxy-1,4-dihydropyridine

Into a reactor were introduced 14 g (0.1 mol) of propargyl acetoacetate, 10.5 g (0.075 mol) of tetramine hexamethylene, 2.9 g (0.038 mol) of ammonium acetate, 36 g of methanol and 5 g of water.

Under a light flow of nitrogen, the reaction medium was refluxed for one hour and was allowed to cool to room-temperature and was then poured into a mixture of water and ice.

The precipitate which formed was filtered off and was washed with hot acetone in order to eliminate the excess of tetramine hexamethylene.

The precipitate was dried to constant weight and washed with hot acetone to give 2,6-dimethyl-3,5-dicarbopropargyloxy-1,4-dihydropyridine.

Yield: 75% Melting point: 206.degree. C.

By the above procedure but using the appropriate starting-product, the following compounds were prepared:

______________________________________ Yield MeltingCompound % Point .degree.C.______________________________________2,6-Dimethyl-3,5-dicarboallyloxy-1,4-dihydropyridine 86 168 (washing with hot acetone)2,6-Dimethyl-3,5-di-(4'-carbochloro-benzyloxy)-1,4-dihydropyridine 82 171 (acetone)2,6-Dimethyl-3,5-dicarbobenzyloxy-1,4-dihydropyridine 75 120 (methanol)2,6-Dimethyl-3,5-di-(2'-carbobutoxy-ethoxy)-1,4-dihydropyridine 40 95 (methanol)2,6-Dimethyl-3,5-di-(2'-carbomethoxy-ethoxy)-1,4-dihydropyridine 70 107 (methanol)2,6-Dimethyl-3,5-di-(2'-carboethoxy-ethoxy)-1,4-dihydropyridine 65 109 (methanol then acetone)2,6-Dimethyl-3,5-di-(2'-carbophenoxy-ethoxy)-1,4-dihydropyridine 55 132 (acetone)2,6-Diphenyl-3,5-dicarbethoxy-1,4-dihydropyridine 10 142 (ethylic ether)2,6-Dibenzyl-3,5-dicarbethoxy-1,4-dihydropyridine 51 118 (methanol)2,6-Di-3-butenyl-3,5-dicarbomethoxy-1,4-dihydropyridine 46 79 (benzene/ pentane 10/30)2,6-Dimethyl-3,5-di-(2"-carbochloro-2'-ethoxy-ethoxy)-1,4-dihydropyridine 79 110 (methanol)2,6-Diphenylethyl-3,5-dicarbomethoxy-1,4-dihydropyridine 59 156 (methanol acetone 80/20)2,6-Ditridecyl-3,5-dicarbomethoxy-1,4-dihydropyridine 73 61 (acetone)______________________________________

Claims

1. A compound of the general formula: ##STR7## wherein R.sub.1 represents a branched- or straight-chain alkyl group containing from 1 to 16 carbon atoms, a branched- or straight-chain alkenyl group containing from 4 to 12 carbon atoms, a straight-chain phenylalkyl radical in which the alkyl chain contains from 1 to 6 carbon atoms, R.sub.2 represents a straight-chain alkyl group containing from 1 to 18 carbon atoms, a branched- or straight-chain alkenyl or alkynyl group containing from 3 to 11 carbon atoms, an .omega.-halogenoethyl radical, a benzyl radical substituted on the para- or ortho-position by a halogen atom or a methyl or methoxy radical, or a radical of the formula R.sub.4 --O--(CH.sub.2).sub.n --, wherein n is 2, 3 or 4 and R.sub.4 represents a branched- or straight-chain alkyl group containing from 1 to 4 carbon atoms, substituted on the .omega.-position by a halogen atom or by a methoxy radical, with the proviso that when R.sub.1 represents a methyl radical, R.sub.2 does not represent an alkyl radical.

2. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is allyl.

3. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is propargyl.

4. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is chloroethyl.

5. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is 4-methoxybenzyl.

6. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is 2-chlorobenzyl.

7. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is 2-methylbenzyl.

8. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is 4-chlorobenzyl.

9. A compound according to claim 1 wherein R.sub.1 is benzyl and R.sub.2 is ethyl.

10. A compound according to claim 1 wherein R.sub.1 is 3-butenyl and R.sub.2 is methyl.

11. A compound according to claim 1 wherein R.sub.1 is tridecyl and R.sub.2 is methyl.

12. A compound according to claim 1 wherein R.sub.1 is methyl and R.sub.2 is 2-(2-chloroethoxy)ethyl.