Imino derivatives of 5-aminobenzodioxole-1,3 which are useful as medicaments

Abstract

New compounds of the general formula: ##STR1## wherein R.sub.1 is an unsaturated heterocyclic radical selected from the group consisting of: ##STR2## wherein R.sub.2 is H or one substituent selected from the group consisting of CH.sub.3, halogen, and nitro, are useful as anti-inflammatories and in the oral treatment of diabetes.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates to new imino derivatives of 5-aminobenzodioxole-1,3 which are useful as medicaments.

2. Description of the Prior Art

Some derivatives of 5-aminobenzodioxole-1,3 are already known. In particular, French Pat. No. 75 21,504, filed July 9, 1975, Publication No. 2,316,938, relates to N-substituted-3-amino-3H isobenzofuranones which contain the 5-aminobenzodioxole-1,3 group.

SUMMARY OF THE INVENTION

We now disclose some new derivatives having the general formula ##STR3## wherein R.sub.1 =an unsaturated heterocyclic radical such as ##STR4## and R.sub.2 =H or one or more substituents such as CH.sub.3, halogen, or nitro.

DETAILED DESCRIPTION OF THE INVENTION AND PREFERRED EMBODIMENTS

These compounds are useful in therapy by reason of their analgesic and anti-inflammatory activities and have the advantage of being practically devoid of ulcerogenic activity, in contrast to the classical anti-inflammatories.

The compounds of the invention are also useful in the oral treatment of diabetes. Such treatments employ medicaments belonging to two chemical classes, the sulfamides and biguanides. The hypoglycemic sulfamides act via the pancreas by stimulating the cells of the islands of Langerhans. The biguanides act through an extrapancreatic mechanism by increasing the utilization of glucose, by inhibiting the hepatic gluconeogenesis, and by decreasing the digestive absorption of glucose. Nevertheless, they have the drawback of being accompanied by rare, but often fatal, lactic acidosis. This has led to the abandonment of the commercial availability of phenformin in France, only metformin still being available.

The compounds of the present invention are prepared generally by the reaction between 5-aminobenzodioxole-1,3 and an aldehyde R.sub.1 CHO wherein R.sub.1 has the significance indicated above, in a suitable solvent such as benzene. The water produced in the course of the reaction is eliminated as it is formed.

The practice of the invention will be explained more precisely in the following examples.

EXAMPLE 1

Synthesis of N-thienylidene-5-aminobenzodioxole-1,3

A mixture of 10 g of 5-aminobenzodioxole-1,3,11 g of 2-thiophencarboxaldehyde and 70 cm.sup.3 of benzene is heated to 120.degree. C. with agitation. The water formed in the course of the reaction is eliminated using a Dean-Stark trap. The benzene is driven off by evaporation and the imine is distilled.

Properties:

Molecular weight: 231 Empirical formula: C.sub.12 H.sub.9 NO.sub.2 S Yellow solid; insoluble in water

M.P.=62.degree. C.

______________________________________NMR spectrum in CDCL.sub.3, TMS internal standard:______________________________________5.9 ppm singlet 2 protons OCH.sub.2O6.6-7.5 ppm broad complex 6 protons ##STR5##8.5 ppm singlet 1 proton CHN______________________________________

EXAMPLE 2

Synthesis of N-(5-methyl-2-thienylidene)-5-aminobenzodioxole-1,3

A mixture of 10 g of 5-aminobenzodioxole-1,3, 12 g of 5-methylthiophenecarboxaldehyde, and 70 cm.sup.3 of benzene is heated at 120.degree. C. with agitation. The water formed in the course of the reaction is eliminated using a Dean-Stark trap. The benzene is removed by evaporation and the imine is purified by distillation. Yield 90%.

______________________________________Properties:______________________________________Molecular weight: 245 Empirical formula: C.sub.13 H.sub.11 NO.sub.2 SYellow powder, insoluble in waterM.P. = 73.degree. C.______________________________________NMR spectrum in CDCl.sub.3, TMS internal standard:______________________________________2.5 ppm singlet 3 protons CH.sub.35.8 ppm singlet 2 protons OCH.sub.2O6.5-7.2 ppm broad complex 5 protons ##STR6##8.3 ppm singlet 1 proton CHN______________________________________

EXAMPLE 3

Synthesis of N-(3-pyridylidene)-5-aminobenzodioxole-1,3

This compound is synthesized by the same procedure as the two previous compounds, starting from a mixture of 10 g of 5-aminobenzodioxole-1,3, 10 g of pyridine-3-carboxaldehyde, and 70 cm.sup.3 of benzene.

______________________________________Properties:______________________________________Molecular weight: 226.2 Empirical formula: C.sub.13 H.sub.10 N.sub.2O.sub.2Yellow solid, insoluble in waterM.P. = 91.degree. C.______________________________________NMR spectrum in CDCl.sub.3, TMS internal standard:______________________________________5.9 ppm singlet 2 protons OCH.sub.2O6.7-9 ppm broad complex 8 protons ##STR7## ##STR8## (singlet at 8.4 ppm)______________________________________

EXAMPLE 4

Synthesis of N-(3-methyl-2-thienylidene)-5-aminobenzodioxole-1,3

This imine is synthesized as described in Example 2. After distillation it is dissolved in ethyl ether and petroleum ether is added thereto to induce crystallization. It is subsequently filtered and dried under vacuum at 50.degree. C. Yield 85%.

______________________________________Properties:______________________________________Molecular weight: 245 Empirical formula: C.sub.13 H.sub.11 NO.sub.2 SYellow powder, insoluble in waterM.P. = 69.degree. C.______________________________________NMR spectrum in CDCl.sub.3, TMS internal standard:______________________________________2.4 ppm singlet 3 protons CH.sub.35.9 ppm singlet 2 protons OCH.sub.2O6.6-7.4 ppm broad complex 5 protons ##STR9##8.5 ppm singlet 1 proton CHN______________________________________

Pharmacological results:

The percentages of mortality produced by the compounds of this invention when administered orally to Swiss mice are shown in Table 1. The animals, free from specific pathogenic organisms were housed in an air conditioned room for 24 to 48 hours before the start of the experiment. They were separated into groups of 5 males and 5 females. The materials were administered to animals which had been fasted for 24 hours by means of a gastric tube in suspension in a 6% thickened julep using a volume equivalent to 0.1 ml per 10 g of body weight. After administration, the animals were observed for one hour, and then at one hour intervals during the first day. They remained under observation for two weeks before being sacrificed and autopsied.

TABLE 1______________________________________TOXICITY IN THE MOUSE % mortality as a function of the doseCompound of expressed in mg/kgExample 500 750 1000 1250 1500 1750 2000 3000______________________________________1 0 20 60 702 10 20 0 603 0 10 1004 10 10 60 20 20______________________________________

The toxicities of the compounds of Examples 2 and 3 were determined in the Wistar rat. The protocol which was followed was the same as that described for the mice, except that the compounds were administered in a volume equivalent to 0.5 ml per 100 g of body weight of rat. The product of Example 2 showed no mortality at 3000 mg/kg. The product of Example 3 produced no mortality at 2000 mg/kg and 20% mortality at 3000 mg/kg.

The analgesic activity was determined in the male Swiss mouse using phenylbenzoquinone (PBQ) as the challenging agent (variation of the method of Siegmund et al, Proc. Soc. Exp. Biol. Med. 1975, 95, 729-31). Twenty five minutes after oral administration of the compounds to be tested in suspension in a 6% thickened julep, a solution of PBQ was injected, and the mice were observed at the end of five minutes and during the following 5 minutes. The results are shown in Table 2. The ED.sub.50 was determined by the method of Lichfield and Wilcoxon.

TABLE 2______________________________________Com-pound % analgesic activity as a function of theof dose expressed in mg/kgExample 50 75 100 125 150 200 250 300 ED.sub.50______________________________________1 34 43 69 73 130 (99- 171)2 19 49 51 403 23 44 65 92 110 (67- 179)4 21 40 37 62 67 170 (107- 270)______________________________________

Table 3 gives the percentage of inhibitory activity with respect to carageenan-induced edema. The inflammation is produced in the male Wistar rat by injection of 0.1 ml of a 0.5% suspension of carageenan in physiological serum, into the muscular fascia of the metatarsal region of the hind foot of the animal. The test substance is administered orally at the same time as the carageenan or 30 or 60 min before carageenan. The edema is measured by plethysmometry three hours after the adminstration of the carrageenan.

TABLE 3__________________________________________________________________________ Time of % inhibiting activity on carrageenen - induced edema Administration as a function of the dose expressed in mg/kgTreatment of the Compound 25 50 75 100 125 150 200 225 300 400 450__________________________________________________________________________Compound of T.sub.o 19 41 52 56 58Example 1Compound of T.sub.o 30 64 33 59Example 2 T.sub.o - 30 21 47 61 T.sub.o - 60 15 26 49 66Compound of T.sub.o 57 28 55Example 3 29 36 39 T.sub.o - 30 34 41 44 50 53 66 67 38 41 72 T.sub.o - 60 25 42 40 39 58 69Compound of T.sub.o 35 35 68Example 4Aspirin T.sub.o 40 46 68 64Niflumic T.sub.o 37 27 40 37Acid 59__________________________________________________________________________

Table 4 shows the percentage of inhibitory activity with respect to edema produced by serotonin. In the Wistar rat inflammation is induced by intrapedal injection of 0.1 ml of a 0.02% solution of serotonin in physiological serum. The test substance is administered orally 30 minutes before the serotonin and the edema is measured by plethysmometry one hour after its release.

TABLE 4______________________________________ % Inhibitory activity as a function of theCompound of dose expressed in mg/kgExample 100 200 400______________________________________2 39 29 373 27 21 26______________________________________

Table 5 shows the activity with respect to carrageenan-induced granulomas. Male Wistar rats weighing 130 to 150 grams were given a subcutaneous injection in the central part of the skin of the back of 0.5 ml of an aqueous suspension of carrageenan. Two doses of the test substance are administered, one 30 minutes before and the other 6 hours after carrageenan. At the end of 24 hours the rats were sacrificed and the granulomas were removed and weighed before and after drying for 24 hours at 50.degree. C. The difference in weight of the granulomas wet and dry represents the exudate

TABLE 5__________________________________________________________________________Dose Weight of wet Weight of dryin mg/kg granuloma granuloma ExudateCompound adminis- % ani- % ani- % ani-of tered % acti- mals 30% % acti- mals 30% % acti- mals 30%Example twice vity protected vity protected vity protected__________________________________________________________________________1 200 6 12.5 1 12.5 6 12.52 100 32 62 34 62 31 62 15 25 14 25 150 5 25 1 25 6 25 22 14 24 14 22 14 200 39 75 41 75 39 75 24 50 22 50 300 18 25 9 25 18 23 100 15 25 12 12 15 25 25 37 22 25 25 37 200 27 37 27 37 27 37 33 75 32 75 34 75 34 71 33 71 38 71 250 36 75 33 62 36 75 300 35 87 37 62 35 87 43 75 41 75 43 754 100 20.5 38 16 31 21 38 200 34 71 31 64 34.5 71 300 44.5 75 42.5 67 44.5 75Niflumic 25 42.5 100 41.5 87 42.5 100Acid__________________________________________________________________________

These results allowed calculation of the AD.sub.50 (doses which protect 50% of the animals to the extent of 30% with respect to the wet weight of the granuloma) for the compounds of Examples 2 and 3. These AD.sub.50 are respectively 175(142-215) and 175(150-205) mg/kg.

Table 6 shows the activities with respect to cotton pellet granulomas. Two cotton pellets weighing 70 mg were implanted under the back skin of male Sprague-Dawley rats anesthetized with ether. Starting the next day, the compound was administered orally daily for 10 days. The rats were sacrificed and the pellets were removed and weighed before and after drying at 50.degree. C. for 24 hours. The weights used were those obtained after deduction of the weight of the implants. The average of the quantities so calculated was determined for each group and compared to the averages of the control group.

TABLE 6______________________________________Compound of % inhibition with respect toExample Dose wet pellets dry pellets______________________________________2 150 12 5 300 17 233 150 0 54 150 13 10 300 14 19Niflumic Acid 50 3 12______________________________________

The ulcerogenic activity was determined in the female Wistar rat using a variation of the procedure described by J. M. Lwoff, J. Pharmacol. 1971, 3, 1, 81-3. The test substance was administered daily for 3 days to the animals maintained on a aqueous diet. The stomachs were removed after 1, 2, and 3 days of treatment and the ulcerations were classified from 0 to 4. The ulceration index is calculated for each group of animals as the product (average of the classes x the percentage of animals afflicted), while distinguishing acute ulcerations from ulcers which were in the process of healing. The results are presented in Table 7.

TABLE 7______________________________________ Dose Ulceration Index adminis- acute healing tered in Day Day Day Day Day DayTreatment mg/kg 1 2 3 1 2 3______________________________________Control 0 1 36 0 0 2Compound of 150 6 2 48 0 6 28Example 2Compound of 150 6 20 33 0 6 12Example 3Compound of 150 0 0 72 0 8 16Example 4Niflumic 100 330 1 119 0 400 378Acid______________________________________

The antidiabetic activity of the compounds of this invention was demonstrated in the following manner.

Female rats weighing 180-200 grams were given an intraperitoneal dose on day J0 of 100 mg/kg of streptozotocin in a 0.05 M citrate buffer at a pH of 4.5 calculated as 0.5 ml per 100 g of body weight. On day J2 hyperglycemic animals were selected by determining the blood sugar level by the orthotoludine method in a stream continuously removed from the retroorbital sinus. Only those animals were retained which had a blood sugar level equal to or greater than 2.5 g/l. On day J3, without previous fasting, the selected animals received the treatment. This consisted of oral administration of the test compound in a 6% aqueous suspension of gum arabic at a volume of 0.5 ml per 100 g of body weight.

The animals were sacrificed one, two, or four hours after the treatment and their blood sugar levels were determined. Each group of animals was compared to a control group of animals which received only the suspension of gum arabic. Metformin was the substance chosen as the control.

The results are given in Table 8 which indicates the percentage of decrease in the blood sugar level produced by the treatment. The symbol NS indicates that the difference between the blood sugar level in the treated animals and the control animals is not significant; the symbol S signifies that the difference is significant by Student's test at p.ltoreq.0.05.

TABLE 8__________________________________________________________________________ Percentage Decrease in the Blood Sugar as a Function of the Dose Administered Expressed in mg/kgPRODUCT 50 100 200 400__________________________________________________________________________N-(5-methyl-2-thienylidene)-5-aminobenzodioxole-1,3Treatment 1 h before sacrificing 13 S 22 S 24 S2 h before sacrificing 22 S 32 S 35 S4 h before sacrificing 12 S 27 S 31 SN-(3-pyridylidene)-5-aminobenzodi-oxole-1,3Treatment 1 h before sacrificing 16 S NS NS2 h before sacrificing NS 27 S 19 S4 h before sacrificing 23 S 29 S 28 SMetforminTreatment 1 h before sacrificing NS 14 S2 h before sacrificing NS NS4 h before sacrificing NS 15 S__________________________________________________________________________

By reason of their pharmacological properties, the compounds of this invention are useful in medicine for treating diseases involving pain and inflammation. For example, the compounds can be prescribed in treatment of rheumatic diseases (for example, inflammatory and degenerative rheumatism, affliction of the joints and other parts, and in acute crises of gout), in treatment of trauma (for example, sprains, fractures, dislocations, and tendonitis), in surgery (pre- and post-operative pain, physical therapy), in treatment of dermatophlebitis (phlebitis, periphlebitis, cutaneous ulcers) as well as in painful and inflammatory pathologies in the treatment of dental problems, cancer, visceral diseases, vascular diseases, neurological diseases and the like.

The compounds are also useful in therapy, in combination with diet, in the treatment of diabetes of the non-insulin-dependent type. They can be employed in certain types of insulin-dependent diabetes, in combination with hypoglycemic sulfamides or insulin therapy.

The compounds can be administered, in combination with the usual excipients, orally, rectally, percutaneously, or in numerous galenic preparations, such as compresses, suppositories, pomades, gels and the like.

The oral forms contain 100 to 500 mg of active ingredient in a unitary dose, the rectal forms contain 100 mg to 1 gram and the topical forms contain 2 to 10%. The average daily dose is from 200 mg to 2 g of active ingredient orally or rectally.

Claims

1. A compound of the general formula ##STR10## wherein R.sub.1 is an unsaturated heterocyclic radical selected from the group consisting of ##STR11## wherein R.sub.2 is H or one substituent selected from the group consisting of CH.sub.3, halogen, and nitro.

2. The compound of claim 1, having the formula ##STR12## wherein R.sub.1 is selected from the group consisting of ##STR13##

3. A pharmaceutical composition comprising an amount of a compound of claim 1 or claim 2 effective in treating inflammation and a pharmaceutically acceptable non-toxic excipient.

4. A pharmaceutical composition comprising an amount of a compound of claim 1 or claim 2 effective in treating non-insulin-dependent diabetes and a pharmaceutically acceptable non-toxic excipient.

5. An analgesic pharmaceutical composition for oral administration comprising 100 to 500 milligrams of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic excipient.

6. An analgesic pharmaceutical composition for rectal administration comprising 100 milligrams to 1 gram of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic excipient.

7. An analgesic pharmaceutical composition for topical administration comprising 2 to 10% by weight of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic excipient.

8. An anti-inflammatory pharmaceutical composition for oral administration comprising 100 to 500 milligrams of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic excipient.

9. An anti-inflammatory pharmaceutical composition for rectal administration comprising 100 milligrams to 1 gram of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic excipient.

10. An anti-inflammatory pharmaceutical composition for topical administration comprising 2 to 10% by weight of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic excipient.

11. An anti-diabetic pharmaceutical composition for oral administration comprising 100 to 500 milligrams of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic exceipient.

12. An anti-diabetic pharmaceutical composition for rectal administration comprising 100 milligrams to 1 gram of a compound of claim 1 or claim 2 and a pharmaceutically acceptable non-toxic excipient.