Furo (2,3d) pyrimidines

Abstract

Compounds of the formula ##STR1## wherein R is alkyl of 1-4 carbon atoms, phenyl, or phenyl substituted by one or more halogen or trifluoromethyl, and Z is ##STR2## wherein R.sub.1 is hydrogen, alkyl of 1-4C, 2,2-dimethyldioxolan-4-yl methyl, or 2,3-dihydroxy prop-1-yl, R.sub.2 is ##STR3## wherein ##STR4## is morpholino, pyrrolidino, piperidino or hexamethyleneimino, and n is an integer from 4 to 7.The compounds are prepared by reacting R-substituted 4-chloro-2-methyl furo (2,3d) pyrimidine with HZ. The compounds possess antiulcerous, antibronchoconstrictive and anticholinergic, analgesic, antihistamine, diuretic, cardiovascular analeptic, antiinflammatory and hypertensive properties.

Description

The present invention relates to novel furo (2,3d) pyrimidines, their process of preparation and their therapeutic application.

The compounds according to the invention correspond to the general formula: ##STR5## in which: R represents an alkyl radical containing up to 4 carbon atoms or a phenyl ring optionally substituted by one or more halogen atoms, or by a trifluoromethyl radical; and

Z represents one of the following: ##STR6## in which: R.sub.1 represents a hydrogen atom, an alkyl radical containing up to 4 carbon atoms, a 2,2-dimethyl dioxolan-4-yl methyl radical or a 2,3-dihydroxy prop-1-yl radical, R.sub.2 represents: a .beta.-amino ethoxy group of formula ##STR7## a carboxamide group of formula ##STR8## or a group of formula ##STR9## the symbol ##STR10## representing a morpholino, pyrrolidino, piperidino or a hexamethyleneimino radical, and n is an integer of between 4 and 7.

The process according to the invention consists in condensing a 4-chloro-2-methyl furo (2,3d) pyrimidine of formula: ##STR11## in which R represents an alkyl radical containing up to 4 carbon atoms or a phenyl ring optionally substituted by one or more halogen atoms, or by a trifluoromethyl radical, with an amine derivative of formula III

hz' (iii) in which Z' represents one of the following: ##STR12## in which: R.sub.1 ' represents a hydrogen atom, an alkyl radical containing up to 4 carbon atoms, R.sub.2 represents a .beta.-amino ethoxy group of formula ##STR13## a carboxamide group of formula ##STR14## or a group of formula ##STR15## the symbol ##STR16## representing a morpholino, pyrrolidino, piperidino or a hexamethyleneimino radical, and n is an integer of between 4 and 7. to produce a derivative corresponding to the formula: ##STR17## and, optionally subjecting a derivative of the formula I' in which Z' represents a 2-methoxycarbonyl anilino radical, to a transesterification in the presence of sodium with 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane, to give the derivate of formula: ##STR18## which may be then transformed into a derivative of formula: ##STR19## by opening of the dioxolane cycle with hydrochloric acid.

It is to be noted that the condensation of the 4-chloro-2-methyl furo (2,3d) pyrimidines of formula (II) with the amine derivatives of formula (III) is conducted:

in benzene under reflux when Z' represents a ##STR20## radical, in which n is an integer of between 4 and 7, and in acetic acid, in the presence of catalytic quantities of concentrated hydrochloric acid, when Z' represents a radical ##STR21##

The following preparations are given, by way of example, to illustrate the invention.

EXAMPLE 1

2-methyl-4-pyrrolidino-6-(metatrifluoromethyl phenyl) furo (2,3d) pyrimidine (Code No. 72497)

14.2g (0.2 mol) of pyrrolidine was added, drop by drop, to a solution of 31.3g (0.1 mol) of 2-methyl-4-chloro-6-(metatrifluoromethyl phenyl) furo (2,3d) pyrimidine in 350 c.c. of benzene heated at 60.degree. C, and the mixture was then refluxed for 6 hours. The mixture is filtered whilst warm, the filtrate is evaporated under vacuum, and the residue is recrystallised from methylethyl ketone.

Melting point = 203.degree. C Yield = 58% Empirical formula = C.sub.18 H.sub.16 F.sub.3 N.sub.3 O ______________________________________Elementary analysis: C H N______________________________________Calculated (%) 62.24 4.64 12.10Found (%) 62.13 4.69 12.03______________________________________

EXAMPLE 2

N-(2,6-dimethyl furo (2,3d) pyrimidin-4-yl) methyl anthranilate (Code No. 7280)

A suspension of 4.55 g. (0.03 mol) of methyl anthranilate, 5.45 g. (0.03 mol) of 2,6-dimethyl-4-chloro furo (2,3d) pyrimidino and 0.1 c.c. of concentrated hydrochloric acid in 30 c.c. of acetic acid were heated at 80.degree. to 90.degree. C for 30 minutes. The precipitate formed is filtered, placed in suspension with 50 c.c. of ethanol, alkalinised with concentrated ammonia, diluted with 200 c.c. of water, filtered, washed with water, recrystallised from ethanol and then from acetone.

Melting point = 186.degree. C Yield = 34% Empirical formula = C.sub.16 H.sub.15 N.sub.3 O.sub.3 ______________________________________Elementary analysis: C H N______________________________________Calculated (%) 64.63 5.09 14.14Found (%) 64.75 5.26 14.14______________________________________

EXAMPLE 3

N-(2,6-dimethyl furo (2,3d) pyrimidin-4-yl)-4'-methyl-2',2'-dimethyl-1',3'-dioxolane anthranilate (Code No. 730 367)

0.3 g of sodium is dissolved, with warming, in 260 c.c. of 2,2-dimethyl-4-hydroxymethyl-1,3-dioxolane. After cooling, 65.5 g (0.22 mol) of N-(2,6-dimethyl furo (2,3d) pyrimidin-4-yl) methyl anthranilate of code No. 7280 obtained as indicated in the preceding example, is added thereto and the resultant mixture is heated for 5 hours at 140.degree.-150.degree. C, the methanol formed being distilled off under nitrogen. The mixture is diluted with 2l of water, filtered, washed with water and recrystallied from ethanol.

Melting point = 160.degree. C Yield = 50% Empirical formula = C.sub.21 H.sub.23 N.sub.3 O.sub.5 ______________________________________Elementary analysis: C H N______________________________________Calculated (%) 63.46 5.93 10.57Found (%) 63.42 5.95 10.37______________________________________

EXAMPLE 4

4-(.beta.,.gamma.-2'-dihydroxypropoxycarbonyl-phen-1'yl amino)-2,6-dimethyl furo (2,3d) pyrimidine (Code No. 730 387)

A suspension of 58g (0.147 mol) or N-(2,6-dimethyl furo (2,3d) pyrimidin-4-yl)-4'-methyl-2',2'-dimethyl-1',3'-dioxolane anthranilate of Code No. 730 367 obtained as indicated in example 3, in 500 c.c. of 2N hydrochloric acid is heated for 45 minutes under reflux. The mixture is filtered whilst warm, neutralised with 100 c.c. of triethylamine, the precipitate formed is filtered, washed with water and recrystallised from ethanol.

Melting point = 179.degree. C Yield = 30% Empirical formula = C.sub.18 H.sub.19 N.sub.3 O.sub.5 ______________________________________Elementary analysis: C H N______________________________________Calculated (%) 60.49 5.36 11.70Found (%) 60.62 5.36 11.71______________________________________

The compounds listed in the following Table I have been prepared according to the same mode of operation.

TABLE I__________________________________________________________________________ ##STR22## MeltingCode Empirical Molecular Point Yield Elementary Analysis.No. R Z Formula Weight (.degree. C) % C H N__________________________________________________________________________72 498 ##STR23## ##STR24## C.sub.19 H.sub.18 F.sub.3 N.sub.3 O 361.36 129 29 Calculated (%) Found 63.15 63.00 5.02 5.06 11.63 11.5572 557 ##STR25## ##STR26## C.sub.18 H.sub.16 F.sub.3 N.sub.3 O.sub.2 363.33 178 42 Calculated (%) Found 59.50 59.36 4.44 4.49 11.57 11.6772 535 ##STR27## ##STR28## C.sub.20 H.sub.20 F.sub.3 N.sub.3 0 375.38 126 53 Calculated (%) Found 63.99 63.77 5.37 5.45 11.19 11.0272 561 ##STR29## ##STR30## C.sub.21 H.sub.22 F.sub.3 N.sub.3 O 389.41 145 45 Calculated (%) Found 64.77 64.74 5.69 5.77 10.79 10.3571 334 ##STR31## ##STR32## C.sub.17 H.sub.16 ClN.sub.3 O 313.78 186 43 Calculated (%) Found 65.07 64.89 5.14 5.15 13.39 13.2272 544 ##STR33## ##STR34## C.sub.18 H.sub.18 Cl N.sub.3 O 327.81 187 39 Calculated (%) Found 65.95 65.74 5.53 5.45 12.82 12.6072 545 ##STR35## ##STR36## C.sub.17 H.sub.16 ClN.sub.3 O.sub.2 329.78 226 29 Calculated (%) Found 61.91 62.01 4.89 4.87 12.74 12.3672 700 ##STR37## ##STR38## C.sub.19 H.sub.20 Cl N.sub.3 O 341.83 147 32 Calculated (%) Found 66.76 66.59 5.90 5.76 12.29 12.1472 682 ##STR39## ##STR40## C.sub.20 H.sub.22 Cl N.sub.3 O 355.86 126 24 Calculated (%) Found 67.50 67.48 6.23 6.26 11.81 11.96730372 CH.sub.3 ##STR41## C.sub.15 H.sub.13 N.sub.3 O.sub.3 283.28 260 39 Calculated (%) Found 63.59 63.50 4.63 4.82 14.83 15.03740119 CH.sub.3 ##STR42## C.sub.21 H.sub.24 N.sub.4 O.sub.4 396.43 152 55 Calculated (%) Found 63.62 63.83 6.10 6.30 14.13 14.16730 525 CH.sub.3 ##STR43## C.sub.19 H.sub.20 N.sub.4 O.sub.2 + 1/2 H.sub.2 O 345.39 225 20 Calculated (%) Found 66.07 66.29 6.29 6.25 16.22 16.04730508 CH.sub.3 ##STR44## C.sub.19 H.sub.20 N.sub.4 O.sub.3 352.38 200 44 Calculated (%) Found 63.04 64.94 5.72 5.75 15.90 15.80730693 CH.sub.3 ##STR45## C.sub.20 H.sub.24 N.sub.4 O.sub.3 368.42 134 62 Calculated (%) Found 65.20 65.15 6.57 6.76 15.21 15.25__________________________________________________________________________

The compounds of formula I have been tested on animals in the laboratory and have been shown to possess antiulcerous, antibronchoconstrictive and anticholinergic, analgesic, antihistaminic, diuretic, cardiovascular analoptic, antiinflammatory and hypertensive properties.

1. Antiulcerous properties analgesic,

The compounds of formula I, administered by oral means, reduce the extent of gastric ulcers provoked in a rat by tying of the pylorus (Shay ulcers).

Thus, the compound of Code No. 72 498, administered in a dose of 50 mg/Kg/i.d., permits a reduction of 35% of the Shay ulcers in a rat.

2. Antibronchoconstrictive and anticholinergic properties

Injected by intraduodonal means, the compounds of formula I are capable of opposing the bronchoconstriction provoked in the guinea-pig by the intraveinous injection of acetylcholine and evaluated by the Kenzett method.

By way of example, the administration of 100 mg/Kg/i.d. of the compound of Code No. 72 544, permits an inhibition of 50% of the bronchoconstriction provoked in the guinea-pig by the intraveinous injection of acetylcholine.

3. Analgesic properties

The compounds of formula I, administered to the mouse or rat by oral means, are capable of reducing the number of painful stretchings caused by the intraperitoneal injection of acetic acid or phenylbenzoquinone and they protect the rat against crying or jumping in the Randall and Selitto test.

By way of example:

Table II lists the DE50 of different compounds according to the invention, and Table III indicates the results obtained by the administration of 100 mg/Kg/po of other compounds of formula I. Table II______________________________________ Code No. ofNature of compound DE 50test effected tested Animal (mg/Kg/po)______________________________________Test with 730 387 mouse 80phenylbenzo- rat 43quinone 730 372 mouse 20 rat 52 730 367 mouse 72 rat 95Randall & 730 387 rat 42Selittotest 730 372 rat 40______________________________________ Table III______________________________________ Percentage diminution ofNature of test Code No. of number of painfuleffected compound tested stretchings (%)______________________________________Test with 730 693 70acetic acid 72 545 70Test withphenylbenzo- 730 508 60quinono______________________________________

4. Antihistaminic properties

The compounds of formula I, introduced in the conserving medium, are capable of opposing the contractural action of histamine on the isolated ileon of the guinea-pig. This activity is evaluated taking promothazine as standard.

Thus, the compound of Code No. 72561 provides an anti-histaminic activity equivalent to 1/15th that of promethazine.

5. Diuretic properties

The compounds of formula I, administered by oral means to the mouse, simultaneously with a volume of 1 ml. of an isotonic solution of sodium chloride per 25g of the corporeal weight of the mouse, are capable of provoking an augmentation of the volume of urine emitted by reference to control animals, the volume being measured for 6 hours following administration.

Thus, the administration of 25 mg/Kg/po of the compounds of Code Nos. 730 508 and 730387 produced an augmentation of the urinary elimination by 70% and 55%, respectively.

6. Cardiovascular analeptic properties

These properties are shown by an augmentation of the force of contractions (positive inotrope action) in the isolated heart of the guinea-pig maintained in a conserving medium and under appropriate experimental conditions.

By way of example, the compounds of Code Nos. 730 387 and 730 372 respectively provoke an augmentation of 75% and of 50% in the force of contractions in a concentration of 0.5 .mu.g/ml.

7. Antiinflammatory properties

The compounds of formula I administered to the rat by oral means, provoke a diminution of the local oedema caused by the sub-plantar injection of carraghenine or Kaolin and oppose the inflammation caused by the Freund adjuvant. Administered by oral means to the guinea-pig, they reduce the erytheme caused by ultra-violet irradiation:

The results are listed in the following table V

__________________________________________________________________________ Reduction of Protection against Protection against oedema with erythema by arthitis by carraghenine ultra-violet Freund adjuvantCode No. or Kaolin Dose Doseof compound DE 50 administered Protection administered Protectiontested (mg/Kg/po) (mg/Kg/po) (%) (mg/Kg/po) (%)__________________________________________________________________________730 387 38(carraghenine) 100 60 -- -- 27(carraghenine)730 372 27(carraghenine) 200 55 6(Kaolin) -- --730 367 47(carraghonine) 100 50 -- --__________________________________________________________________________

Also, the administration of the compound of Code No. 730 367 in a dose of 100 mg/Kg/po permits a diminution by 75% of the local oedema caused by the injection of Kaolin.

8. Hypertonsive properties

Administered by intraveinous means, the compounds of formula I provoke an increase in the arterial pressure of an anaesthetised rat.

By way of example, the administration of the compound of Code No. 730 693 in a dose of 2 mg/Kg/i.v., provokes an increase an the arterial pressure of an anaesthetised rat by 25% for a period of the order of 30 minutes.

As a result of a comparison between the pharmacologically active doses mentioned above and the lethal doses listed in the following Table V, the difference between said doses is sufficiently great to permit the utilisation of the compounds of formula I in therapeutics.

______________________________________Code No. ofcompound Dose administered Percentage mortalitytested (mg/Kg/po) %______________________________________72 498 2000 072 544 2000 072 561 2000 072 545 2000 0730 387 2000 0730 372 1500 ##STR46##730 367 2000 0730 508 2000 0730 693 2000 ##STR47##______________________________________

The compounds of formula I are useful in the treatment of gastro-duodenal ulcers, visceral spasms, asthma, diverse originating pains and painful inflammations, allergies, oedemas and hypotension.

They may be administered by oral means in the form of tablets, dragees and gelules, containing 50 to 500 mg. of active ingredient (one to six times a day), by parenteral means in the form of injectable ampoules containing 10 to 250 mg of active ingredient (one to three times a day) by rectal means in the form of suppositories containing 25 to 400 mg of active ingredient (one to three times a day) and in the form of suspensions containing 0.5 to 5% of active ingredient (20 to 60 drops, one to three times a day).

Accordingly, the present invention also relates to a therapeutic composition comprising a compound of the general formula I, together with a therapeutically acceptable carrier.

Claims

1. A compound having the formula ##STR48## in which R is alkyl having one to 4 carbon atoms, phenyl, or phenyl substituted with at least one halogen or by a trifluoromethyl, and

Z is ##STR49## in which R.sub.2 is ##STR50## wherein ##STR51## is morpholino, pyrrolidino, piperidino or hexamethyleneimino.

2. A compound as claimed in claim 1 in which R is CH.sub.3 and Z is ##STR52##

3. A compound as claimed in claim 1 in which R is CH.sub.3 and Z is ##STR53##