Arylic Derivatives of Piperazine, the Method of Preparing Same and Their Application in Therapeutics

The present invention relates to new arylic derivatives of piperazine, their salts and the method or preparing same as well as the application in therapeutics of these derivatives and of these salts.

The new derivatives of the invention correspond more precisely to the general formula: ##STR4## in which X represents: either the chain of trans configuration ##STR5## or the chain ##STR6## connected to Ar by their carbon atom 3, in which case A represents: a carbohydroxamic (--CONHOH) or hydroxymethyl (--CH.sub.2 OH) group, Ar then representing the (3,4,5-trimethoxy)phenyl nucleus,

an ethoxycarbonyl (COOEt) group, Ar then representing the para-fluorophenyl, (3,4-dichloro)phenyl, (2,3,4-trimethoxy)phenyl or (2,4,6-trimethoxy)phenyl nucleus,

a carboxyl group (COOH), Ar then representing the parachlorophenyl, para-hydroxyphenyl, (3,4-methylenedioxy)phenyl or (3,5-dimethoxy, 4-hydroxy)phenyl nucleus, or

an amido group of structure CO--NR.sub.2 R.sub.3 in which the pair (R.sub.2,R.sub.3) takes on one of the following meanings: (H,H), (H, C.sub.1 -C.sub.4 alkyl) (C.sub.1 -C.sub.4 alkyl, C.sub.1 -C.sub.4 alkyl), (H, C.sub.3 -C.sub.6 cycloalkyl), (H, C.sub.3 -C.sub.6 cycloalkylmethyl), (H, phenyl), (H, phenyl substituted by one or more halogen atoms), (H, phenyl substituted by one or more methyl or methoxy groups), (H, benzyl), (H, benzyl substituted by one or more halogen atoms), (H, benzyl substituted by one or more methyl or methoxy groups), (CH.sub.3, benzyl), (CH.sub.3, benzyl substituted by one or more halogen atoms), (CH.sub.3, benzyl substituted by one or more methyl or methoxy groups), (H, allyl), (H, propargyl), R.sub.2, R.sub.3 being also able to form jointly with the nitrogen atom to which they are linked, a pyrrolidino, piperidino, tropanic ##STR7## or morpholino radical; Ar then representing a phenyl nucleus, a phenyl nucleus substituted by one or more halogen atoms, by one or more methoxy groups, by a methyl group, by a trifluoromethyl group or by one or two hydroxyl radicals, a 1,3-benzodioxolyl group ##STR8## a 1,4-benzodioxannyl group ##STR9## a (5-methoxy) 1,4-benzodioxannyl group ##STR10## a naphthyl group, the (3-methoxy 4-hydroxy)phenyl group, the (3-hydroxy 4-methoxy)phenyl group, the (3,5-dimethoxy 4-hydroxy)phenyl group or a (4-C.sub.2 -C.sub.4 alkoxy 3,5-dimethoxy)phenyl group;

A not however being able to assume the following values: CONHCH.sub.3, CONHC.sub.2 H.sub.5, CONHC.sub.3 H.sub.7 n, CONHC.sub.3 H.sub.7 iso, CON(CH.sub.3).sub.2, CON(C.sub.2 H.sub.5).sub.2, CON(C.sub.3 H.sub.7 n).sub.2, CON(C.sub.3 H.sub.7 iso).sub.2, ##STR11## when Ar represents the (3,4,5-trimethoxy)phenyl or (3,5-dimethoxy 4-hydroxy)phenyl group;

or the chain of trans configuration ##STR12## linked to Ar by its carbon atom 1 or the chain --CH.sub.2 --CH.sub.2 --CH.sub.2 --, in which case A represents a carboxamido, N-isopropylcarboxamido, pyrrolidinocarbonyl or piperidinocarbonyl group, Ar then representing a (3,4,5-trimethoxy)phenyl or (3,4-methylenedioxy)phenyl group.

Among the derivatives of formula (I), there may be mentioned as particularly interesting the compounds in which X represents the trans chain ##STR13## and A represents a COOH group or a group of formula CONR.sub.2 R.sub.3 and more especially the group ##STR14##

The present invention relates also to the mineral or organic acid (for example hydrochloric acid and maleic or oxalic acid) addition salts of the derivatives of formula (I), as well as the hydrates of said derivatives and salts.

The process of the invention for preparing the compounds of formual (I) in which X represents the chain of trans configuration ##STR15## or the chain (--CH.sub.2 --CH.sub.2 --CO--) and Ar has the same meanings as in formula (I), except the values p-hydroxyphenyl, (4-hydroxy 3-methoxy)phenyl, (4-hydroxy 3,5-dimethoxy)phenyl, (3,4-dihydroxy)phenyl and (3-hydroxy 4-methoxy)phenyl consists:

(A) in the case where A represents an ethoxycarbonyl or amido group of structure ##STR16## where R.sub.2 and R.sub.3 have the same meanings as in formula (I):

in forming the chloride of the acids or formula:

or

in which Ar.sub.1 has the same meanings as Ar in formula (I), except for the values p-hydroxyphenyl, (4-hydroxy 3-methoxy)phenyl, (4-hydroxy 3,5-dimethoxy)phenyl, (3-hydroxy 4-methoxy)phenyl and (3,4-dihydroxy)phenyl, preferably by action of thionyl chloride, in solution in toluene, benzene, chloroform, methylene chloride or T.H.F. on these acids, then in condensing the intermediate acid chlorides thus obtained, with the appropriate compounds of formula: ##STR17## in which A.sub.1 represents an ethoxycarbonyl or amido group of structure ##STR18## where R.sub.2 and R.sub.3 have the same meanings as in formula (I),

in condensing the acids of formula (II) or (IIa) and the appropriate compounds of formula (III) according to the so-called "BOISSONNAS" reaction, or

in treating the acids of formula (II) or (IIa) with the triphenylphosphine-carbon tetrachloride complex, preferably in solution in dioxanne, then condensing the amines of formula (III) on the intermediates obtained;

(B) in the case where A represents an ethoxycarbonyl, carboxyl or amido group of structure CONR.sub.2 R.sub.3 where R.sub.2 and R.sub.3 have the same meanings as in formula (I), in condensing the compounds of formula: ##STR19## or ##STR20## in which Ar.sub.1 has the same meanings as in formula (II) with the appropriate compounds of formula:

in which A.sub.2 represents a carboxyl, ethoxycarbonyl or amido group of structure ##STR21## where R.sub.2 and R.sub.3 have the same meanings as in formula (I), this condensation being preferably carried out in an aprotic medium (acetonitrile, acetone, THF, DMF or toluene for example) and in the presence of potassium carbonate. As for the compounds of formula (IV) and formula (IVa), they are respectively obtained by condensing, in an acetic acid medium, the acid chlorides of formula (II) and formula (IIa) with the piperazine hydrochloride of formula: ##STR22## (C) in the case where A represents an amido group of structure ##STR23## where R.sub.2 and R.sub.3 have the same meanings as in formula (I):

either in condensing, by the "BOISSONNAS" method, the acids of formula: ##STR24## or ##STR25## in which Ar.sub.1 has the same meanings as in formula (II) with the appropriate amines of formula: ##STR26## in which R.sub.2 and R.sub.3 have the same meanings as in formula (I), the compounds of formula (VII) and (VIIa) being obtained according to the method described in preceding point B,

or in condensing the compounds of formula: ##STR27## or ##STR28## in which Ar.sub.1 has the same meanings as in formula (II), with the appropriate compounds of formula (VIII), in the presence of ammonium chloride, the compounds of formula (IX) or (IXa) being prepared according to the methods described in the preceding points (A) and (B).

The process of the invention for preparing compounds of formula (I) in which X represents the trans ##STR29## chain or the ##STR30## chain, A represents an ethoxycarbonyl or amido group of structure CONR.sub.2 R.sub.3 where R.sub.2 or R.sub.3 have the same meanings as in formula (I) and Ar represents a para-hydroxyphenyl, (4-hydroxy 3-methoxy)phenyl, (4-hydroxy 3,5-dimethoxy)phenyl, (3-hydroxy 4-methoxy)phenyl or (3,4-dihydroxy)phenyl nucleus consists in condensing, in the presence of dicyclohexylcarbodiimide (DCCI) and preferably in solution in chloroform, the acids of formula:

or

in which Ar.sub.2 represents a 4-hydroxy phenyl, (4-hydroxy 3-methoxy)phenyl, (4-hydroxy 3,5-dimethoxy)phenyl, (3-hydroxy 4-methoxy)phenyl or (3,4-dihydroxy)phenyl nucleus, with the compounds of formula (III).

The process of the invention for preparing the compounds of formula (I) in which X represents the trans ##STR31## chain or the ##STR32## chain, A represents the carboxyl group and Ar represents a 4-hydroxy phenyl or (4-hydroxy 3,5-dimethoxy)phenyl nucleus consists in hydrolyzing, preferably with aqueous NaOH the compounds of formula (I) having the particular structure: ##STR33## or ##STR34## in which Ar.sub.3 represents a parahydroxyphenyl or (4-hydroxy 3,5-dimethoxy)phenyl group.

The compounds of formulae (Ia) and (Ib) are prepared according to the above-described process from the compounds of formula (IIb) or (IIc) and the compounds of formula (III).

The process of the invention for preparing the compounds of formula (I) in which A represents the hydroxymethyl chain consists in condensing the compounds of formula (IV) or (IVa), in which Ar.sub.1 represents (3,4,5-trimethoxy)phenyl nucleus, with ethylene oxide, preferably in solution in ethanol.

The process of the invention for preparing the compounds of formula (I) in which A represents the carbohydroxamic group (--CONHOH) consists in condensing hydroxylamine, preferably in hydrochloride form and in the presence of sodium methylate, on the compounds of formula (I) having the particular structure: ##STR35## or ##STR36##

The process of the invention for preparing the compounds of formula (I) in which X represents the trans ##STR37## chain consists: either in condensing the aldehydes of formula:

in which Ar.sub.4 represents a (3,4,5-trimethoxy)phenyl or (3,4-methylenedioxy)phenyl group with the compounds of formula (III) in which Ar.sub.1 represents a carboxamido, N-isopropylcarboxamido, pyrrolidinocarbonyl or piperidinocarbonyl group, then in reducing the intermediate compounds thus obtained preferably with sodium borohydride in solution in methanol, the compounds (X) being known or prepared according to the technique described in Indian J. Chem. Vol. 13 pages 10-15 (1975);

or in condensing the halogenated derivatives of formula:

in which Ar.sub.4 has the same meanings as in formula (X) and hal designates a halogen atom, with the compounds of formula (III) in which A.sub.1 represents a carboxamido, N-isopropylcarboxamido, pyrrolidinocarbonyl or piperidinocarbonyl group, preferably in toluene and in the presence of a base such as triethylamine, the compound of formula (XI) being known or prepared in accordance with the technique described in German patent No. 2 252 080.

The process of the invention for preparing the compounds of formula (I) in which X represents the propylene chain (--CH.sub.2 --CH.sub.2 --CH.sub.2 --) consists in halogenating the compounds of formula:

in which Ar.sub.4 has the same meanings as in formula (X), preferably with phosphorous tribromide, then in causing to react on the intermediate halogenated derivative obtained, the compounds of formula (III) in which A.sub.1 represents a carboxamido, N-isopropylcarboxamido, pyrrolidincarbonyl or piperidinocarbonyl group.

The compounds of formula (XII) are known or prepared by reduction with AlLiH.sub.4 in THF of the corresponding ethyl cinnamoates, themselves known or prepared according to the technique described in Indian J. Chem. Vol 13, pages 10-15 (1975).

The compounds of formula (I) in which X represents the ##STR38## chain, A represents an ethoxycarbonyl group or a group of structure CONR.sub.2 R.sub.3, where R.sub.2 and R.sub.3 have the same meanings as in formula (I) and Ar has the same meanings as Ar.sub.1 in formula (II), may also be obtained by catalytic reduction, prefarably in the presence of 10% palladium on charcoal and in alcohol medium, of the compounds of formula (I) having the particular structure: ##STR39## in which Ar.sub.1 has the same meanings as in formula (IV) and A.sub.1 hs the same meanings as in formula (III).

The derivatives of formula (I) may be salified by the usual methods. Salification may for example be obtained by action on these derivatives of a mineral acid such as hydrochloric acid or an organic acid such as oxalic or maleic acid, this operation being preferably carried out in a solvent or a mixture of solvents such as acetone, ethanol or water.

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

To a solution of 38.5 g of cinnamoyl chloride (trans) in 200 ml of toluene are slowly added, at room temperature, 22.1 g of 4-pyrrolidinocarbonylmethyl piperazine (III). Then it is left under agitation at room temperature for 4 hours, the precipitate is filtered and recrystallized in alcohol. 15 g of the expected compound were thus isolated (Yield .perspectiveto.42%).

By the same process, but from the corresponding reagents, the compounds of formula (I) were obtained, shown under code numbers 3 to 6, 10 to 16, 18 to 24, 27 to 34, 37 to 57 and 78 to 89 in table I below.

To a solution cooled to 5.degree. C. of 19.2 g trans(3,4-methylenedioxy)cinnamic acid (II) in 200 ml of dimethylformamide, are added 14 ml of triethylamine, then 9.6 ml of ethyl chloroformiate. It is left at 5.degree. C. for 30 minutes, then 39.4 g of 4-pyrrolidinocarbonylmethyl piperazine (III) are slowly added. Then it is left for 12 hours at room temperature. Thus, 13 g (Yield .perspectiveto.36%) of the expected product were obtained.

By the same process, but from the corresponding reagents, the compounds of formula (I) were obtained, shown under code numbers 3 to 6, 10 to 16, 18 to 24, 27 to 34, 36 and 38 to 57, in table I.

Similarly, by this process, but from the compounds of formula (VII) or (VIIa) and the amines of formula (VIII), the compounds of formula (I) were obtained; shown under code numbers 10 to 16, 18 to 24, 27 to 34, 36 to 57 and 78 to 89.

A solution of 26 g of triphenylphosphine in 100 ml of carbon tetrachloride and 300 ml of dioxane is maintained for an hour at 70.degree. C. Then it is cooled to 5.degree.-10.degree. C., 14.9 g of trans(2,4,6-trimethoxy)cinnamic acid are added, it is left for 30 minutes at 5.degree.-10.degree. C., then 55.5 g of 4-N-isopropylaminocarbonylmethyl piperazine (III) are added and the solution is heated at about 70.degree. C. for two hours. Then it is filtered, the filtrate evaporated, the residue is taken up in chloroform, then extracted with a dilute oxalic acid solution, the aqueous phase is washed with ether, neutralized with sodium bicarbonate, the precipitate formed (base-melting point 93.degree. C.) is filtered, dissolved in acetone, an acetonic solution of oxalic acid is added, the precipitate formed filtered and recrystallized in n-butanone. Thus 9 g (Yield .perspectiveto.36%) of the expected compound are obtained.

By the same process, but from the corresponding reagents, the compounds of formula (I) are obtained shown under code numbers 3 to 6, 10 to 15, 18 to 24, 27 to 34, 36 to 57 and 78 to 89 in table I.

A suspension of 15.3 g of trans(3,4,5-trimethoxy)cinnamoylpiperazine (IV), 9.3 g of chloroacetamide and 20.7 g of potassium carbonate in 200 ml of acetonitrile is heated to reflux for 3 hours. Then it is filtered, the filtrate evaporated and the residue recrystallized in ethanol. Thus, 13 g (Yield .perspectiveto.72%) of the expected compound are obtained.

By the same process, but from the corresponding reagents, the compounds of formula (I) are obtained which are shown in table I under code numbers 3 to 10, 12 to 16, 18 to 24, 27 to 34, 36 to 57 and 78 to 89.

A mixture of 19.6 g of 1-(3,4,5-trimethoxy)cinnamoyl 4-ethoxycarbonylmethyl piperazine trans (IX), 42 g of cyclopentylamine (VIII) and 2 g of ammonium chloride is heated to 90.degree.-100.degree. C. for 7 hours. Then the excess amine is evaporated in a vacuum and the residue is taken up in water, extracted with chloroform, washed with water, dried on sodium sulfate, filtered and the filtrate evaporated. The product obtained in crystallized in ether and recrystallized in ethyl acetate, then in isopropylic alcohol. Thus, 2.6 g of the expected compound are obtained (Yield .perspectiveto.12%).

By the same process, but from the corresponding reagents, the compounds of formula (I) are obtained which are shown in table I under code number 10 to 16, 18 to 24, 27 to 34, 36 to 57 and 78 to 89.

To a solution, cooled to 0.degree. C., of 9.7 g of trans(4-hydroxy 3-methoxy)cinnamic acid (IIb) and 9.2 g of N-isopropylaminocarbonylmethyl piperazine (III) in 250 ml of dioxanne are added 10.3 g of DCCI. Then it is left at room temperature for 70 hours, filtered, the filtrate is evaporated and the residue chromatographed on a silica column. By eluting with the methylene chloride (95%)--methanol (5%) mixture, 6 g (Yield .perspectiveto.33%) of the expected product are obtained which is recrystallized in isopropylic ether.

By the same process, but from the corresponding reagents, the compounds of formula (I) shown in table I under code numbers 25 and 74 to 77 are obtained, as well as the compound of formula (Ia): trans-1-para-hydroxycinnamoyl 4-ethoxycarbonylmethyl piperazine, hydrochloride whose characteristics are the following:

Melting point: 248.degree. C.

Empirical formula: C.sub.17 H.sub.23 ClN.sub.2 O.sub.4

Molecular weight: 354.83

Elementary analysis:

A solution of 3.5 g of 1-parahydroxycinnamoyl 4-ethoxycarbonylmethyl piperazine (Ia) in 30 ml of 1N aqueous NaOH is heated at 60.degree. C. for 90 minutes, then it is acidified to pH 6-5 with 1N aqueous hydrochloric acid, the precipitate obtained is filtered and washed on the filter with ethanol. Thus, 1.6 g (Yield .perspectiveto.55%) of the expected product is obtained.

A solution of 15 g of trans-(3,4,5-trimethoxy)cinnamoyl piperazine (IV) and 2 ml of piperidine in 40 ml of alcohol is heated to 60.degree. C. Then an ethylene oxide gas stream is passed therethrough (until 0.05 mole has been absorbed) and it is left at 60.degree. C. for 1 hour, then at room temperature for 12 hours. Then it is evaporated and the residue chromatographed on a silica column. It is eluted with a methylene chloride (95%)--methanol (5%) mixture and the pure product obtained is dissolved in acetone. An acetonic solution of maleic acid is added and the formed precipitate is filtered. Thus, the expected product was isolated with a yield of 76%.

To a solution, cooled to 5.degree. C., of 13.8 g of sodium in 300 ml of methanol is added a solution of 20.8 g of hydroxylamine hydrochloride in 200 ml of methanol. It is filtered and to the filtrate, at room temperature, are added 68.8 g of ethylic ester of [4-(3,4,5-trimethoxy cinnamoyl)piperazine-1-yl]acetic acid (trans). After 20 hours of reaction, the solvent is evaporated, the residue is taken up in water, washed with ether, then a solution of 18 g of acetic acid in 30 ml of water is added. The precipitate obtained is filtered, washed with water, dried in a vacuum and recrystallized in 280 ml of acetone at 70%. 37 g of the expected product are isolated (Yield .perspectiveto.47%).

A mixture of 8.8 g of trans(3,4,5-trimethoxy)cinnamaldehyde (X) and 7.4 g of 4-N-isopropylaminocarbonylmethyl piperazine (III) in 300 ml of methanol is heated at 40.degree. C. for 1 hour, then 6 g of sodium borohydride are slowly added. After an hour, the solvent is evaporated, the residue is taken up in chloroform, washed with water, dried on sodium sulfate, filtered and the filtrate evaporated. The product obtained is recrystallized in isopropylic ether then in ethyl acetate. Thus, 2 g (Yield .perspectiveto.16%) of the expected product are obtained.

To a solution of 2.6 g of 4-pyrrolidinocarbonylmethyl piperazine (III) in 16 ml of toluene and 0.9 ml of triethylamine is slowly added at room temperature, 1.6 g of trans-3-(3,4-methylenedioxy)phenyl 1-bromo prop-2-ene (XI). Then it is left at room temperature for 12 hours, filtered, the filtrate is evaporated and the residue crystallized in ether. 1.5 g (Yield .about.65%) of a product is obtained which corresponds to the expected product in base form (melting point 110.degree. C.). This product is then dissolved in ethanol, a solution of hydrochloric acid .perspectiveto.6.5N in ethanol is added and the precipitate obtained is filtered which corresponds to the expected product.

To a solution of 24 g of 3-(3,4,5-trimethoxy)phenyl propan-1-ol (XII) in 200 ml of chloroform are slowly added 57.2 g of phosphorous tribromide (PBr.sub.3). Then it is left under agitation at room temperature for 1 hour, it is diluted with water, the organic phase is decanted, it is washed with a saturated solution of sodium bicarbonate, dried on sodium sulfate, filtered and the filtrate evaporated. The residue is crystallized in petroleum ether and dissolved in 150 ml of acetonitrile. 13.8 g of potassium carbonate and 6.8 g of 4-N-isopropylaminocarbonylmethyl piperazine (III) are added and the mixture is heated at reflux for 7 hours. Then the insoluble matter is filtered, the filtrate is evaporated, the residue is dissolved in chloroform, washed with water, dried on sodium sulfate, filtered, the filtrate is evaporated, the residue is dissolved in ethanol, an ethanol solution of oxalic acid is added, the precipitate obtained is filtered and recrystallized in absolute alcohol. Thus, 4 g (Yield .about.20%) of the expected product is isolated.

The compound of formula (I) shown under code number 63 in table I may also be prepared by using the same process, but from the corresponding reagents.

A suspension of 6 g of compound (I) of code number 29 and 1 g of 10% palladium on charcoal in 500 ml of ethanol is heated for 5 hours 30 minutes at 50.degree. C. under a hydrogen pressure. Then it is filtered and the filtrate is evaporated. The residue is chromatographed on a silica column. By eluting with a methylene chloride (90%)--methanol (10%) mixture, 5.4 g of the expected product are isolated (Yield .perspectiveto.90%). ##STR40## (I) Melting Code Molecular point ELEMENTARY ANALYSIS Number Ar X A Form Empirical Formula weight (.degree.C.) % C H N 1 ##STR41## CHCHCO(trans) CONHOH Base C.sub.18 H.sub.25 N.sub.3 O.sub.6 379.40 134 Cal.Obt. ---- ---- ---- 2 " CHCHCO CH.sub.2 OH Maleate C.sub.22 H.sub.30 N.sub.2 O.sub.9 466.48 159 Cal. 56.64 6.48 6.01 (trans) Obt. 56.35 6.43 6.16 3 ##STR42## CHCHCO(trans) COOEt HCl C.sub.17 H.sub.22 ClFN.sub.2 O.sub.3 356.82 205 C al.Obt. 57.2257.19 6.216.23 7.857.93 4 ##STR43## CHCHCO(trans) " Base C.sub.17 H.sub.20 Cl.sub.2 N.sub.2 O.sub.3 371.26 92 Cal.Obt. 54.9954.79 5.435.41 7.557.69 5 ##STR44## CHCHCO(trans) " Maleate C.sub.24 H.sub.32 N.sub.2 O.sub.10 508.51 127 Cal.Obt. 56.6856.59 6.346.40 5.515.53 6 ##STR45## CHCHCO (trans) " Oxalate C.sub.22 H.sub.30 N.sub.2 O.sub.10 482.48 177 Cal.Obt. 54.7654.36 6.276.30 5.815.75 7 ##STR46## CHCHCO(trans) COOH Base + 1.8H.sub.2 O C.sub.15 H.sub.17 ClN.sub.2 O.sub.3 +1.8 H.sub.2 O 314.42 176 Cal.Obt. 57.3056.88 5.656.34 8.918.85 8 ##STR47## CHCHCO(trans) " Base +5.4% H.sub.2 O C.sub.15 H.sub.18 N.sub.2 O.sub.4 5 +.4% H.sub.2 O 306.91 >260 Cal.Obt. 58.6959.04 6.516.62 9.139.07 9 ##STR48## CHCHCO(trans) " Base +1.4% H.sub.2 O C.sub.16 H.sub.18 N.sub.2 O.sub.5 1 +.4% H.sub.2 O 322.84 186 Cal.Obt. 59.5259.41 5.786.06 8.688.59 10 ##STR49## CHCHCO(trans) CONH.sub.2 HCl C.sub.15 H.sub.19 Cl.sub.2 N.sub.3 O.sub.2 344.24 253 Cal.Obt. 52.33 52.08 5.565.54 12.2112.22 11 ##STR50## CHCHCO(trans) " Base C.sub.18 H.sub.25 N.sub.3 O.sub.5 363.40 202 Cal.Obt. 59.4959.35 6.926.82 11.5611.70 12 ##STR51## CHCHCO(trans) " HCl +3.7% H.sub.2 O C.sub.16 H.sub.20 ClN.sub.3 O.sub.4 +3.7% H.sub. 2 O 367.39 195 Cal.Obt. 52.3052.48 5.906.03 11.4411.76 13 " CHCHCO(trans) ##STR52## HCl C.sub.18 H.sub.24 ClN.sub.3 O.sub.4 381.85 254 Cal.Obt. 56.6156.41 6.346.54 11.0110.94 14 ##STR53## CHCHCO(trans) ##STR54## Base C.sub.22 H.sub.27 N.sub.3 O.sub.2 365.46 140 Cal.Obt. 72.3072.36 7.457.33 11.5011.71 15 ##STR55## CHCHCO(trans) " Oxalate C.sub.23 H.sub.33 N.sub.3 O.sub.9 495.51 170 Cal.Obt. 55.7555.76 6.716.90 8.488.63 16 ##STR56## CHCHCO(trans) " " " " 191 Cal.Obt. 55.7555.46 6.716.40 8.488.55 18 ##STR57## CHCHCO(trans) ##STR58## HCl C.sub.18 H.sub.26 ClN.sub.3 O.sub.2 351.87 >260 Cal.Obt. 61.4461.43 7 .457.37 11.9411.92 19 ##STR59## CHCHCO(trans) " Oxalate +3/5 H.sub.2 O C.sub.21 H.sub.27 N.sub.3 O.sub.8 +3/5 H.sub.2 O 460.26 188 Cal.Obt. 54.8055.24 6.186.54 9.138.89 20 ##STR60## CHCHCO(trans) ##STR61## Base C.sub.22 H.sub.33 N.sub.3 O.sub.5 419.51 188 Cal.Obt. 62.9863.17 7.937.88 10.0210.25 21 " CHCHCO(trans) CONHC.sub.4 H.sub.9n " C.sub.22 H.sub.33 N.sub.3 O.sub.5 419.51 148 Cal.Obt. 62.9862.94 7.938.16 10.0210.10 22 " CHCHCO(trans) ##STR62## " C.sub.22 H.sub.33 N.sub.3 O.sub.5 " 156 Cal.Obt. 62.9863.20 7.938.01 10.02 9.76 23 " CHCHCO(trans) ##STR63## " C.sub.23 H.sub.33 N.sub.3 O.sub.5 431.52 163 Cal.Obt. 64.0164.10 7.717.82 9.749.79 24 " CHCHCO(trans) ##STR64## " C.sub.24 H.sub.35 N.sub.3 O.sub.5 445.54 138 Cal.Obt. 64.6964.41 7.927.85 9.439.16 25 ##STR65## CHCHCO(trans) ##STR66## HCl +1.4% H.sub.2 O C.sub.18 H.sub.26 ClN.sub.3 O.sub.3 +1.4% H.sub.2 O 372.94 244 Cal.Obt. 57.9758.18 7.177.54 11.2611.19 26 ##STR67## CHCHCO(trans) " Base C.sub.19 H.sub.27 N.sub.3 O.sub.4 361.43 159 Cal.Obt. 63.1462.94 7.537.84 11.6311.93 27 ##STR68## CHCHCO(trans) ##STR69## " C.sub.21 H.sub.29 N.sub.3 O.sub.5 403.47 155 Cal.Obt. 62.5162.27 7.257.20 10.4210.42 28 " CHCHCO(trans) ##STR70## " C.sub.21 H.sub.27 N.sub.3 O.sub.5 401.45 161 Cal.Obt. 62.8262.45 6.786.37 10.4710.42 29 " CHCHCO(trans) ##STR71## " C.sub.28 H.sub.37 N.sub.3 O.sub.8 543.60 174 Cal.Obt. 61.8661.73 6.867.04 7.737.75 30 " CHCHCO(trans) ##STR72## " C.sub.26 H.sub.33 N.sub.3 O.sub.5 467.55 200 Cal.Obt. 66.7966.58 7.117.04 8.098.84 31 " CHCHCO(trans) ##STR73## " C.sub.26 H.sub.29 Cl.sub.2 N.sub.3 O.sub.5 598.43 >250 Cal.Obt. 52.1752.09 4.884.92 7.027.13 32 ##STR74## CHCHCO(trans) ##STR75## Maleate C.sub.25 H.sub.35 N.sub.3 O.sub.9 533.56 109 Cal.Obt. 58.5258.40 6.616.74 7.887.99 33 ##STR76## CHCHCO(trans) " 1.5 Oxalate C.sub.25 H.sub.34 N.sub.3 O.sub.11 552.55 200 Cal.Obt. 54.3454.25 6.206.25 7.607.63 34 " CHCHCO(trans) ##STR77## " C.sub.26 H.sub.36 N.sub.3 O.sub.11 566.57 218 Cal.Obt. 55.1155.22 6 6.63.40 7.347.42 36 ##STR78## CHCHCO(trans) ##STR79## HCl C.sub.19 H.sub.26 ClN.sub.3 O.sub.2 363.88 >260 Cal.Obt. 62.7162.57 7 .207.59 11.5511.53 37 ##STR80## CHCHCO(trans) " " C.sub.20 H.sub.26 ClN.sub.3 O.sub.4 407.86 >260 Cal.Obt. 58.8958.63 6.436.16 10.3010.50 38 ##STR81## CHCHCO(trans) " Oxalate C.sub.21 H.sub.26 FN.sub.3 O.sub.6 435.44 156 Cal.Obt. 57.9257.52 6.026.00 9.659.52 39 ##STR82## CHCHCO(trans) " Base +1/4 H.sub.2 O C.sub.21 H.sub.29 N.sub.3 O.sub.4 +1/4 H.sub.2 O 391.97 176 Cal.Obt. 64.3464.60 7.597.64 10.7210.84 40 ##STR83## CHCHCO(trans) " HCl C.sub.19 H.sub.24 Cl.sub.3 N.sub.3 O.sub.2 432.78 >260 Cal.Obt. 52.7352.46 5.595.47 9.719.44 41 ##STR84## CHCHCO(trans) " " C.sub.20 H.sub.25 ClF.sub.3 N.sub.3 O.sub.2 431.88 >260 Cal.Obt. 55.6255.41 5.835.88 9.739.64 42 ##STR85## CHCHCO(trans) " HCl +1/3 H.sub.2 O C.sub.21 H.sub.28 ClN.sub.3 O.sub.4 +1/3 H.sub.2 O 427.92 236 Cal.Obt. 58.9459.16 6.756.66 9.829.82 43 ##STR86## CHCHCO(trans) " 1.5 Oxalated +1/5 H.sub.2 O C.sub.24 H.sub.32 N.sub.3 O.sub.10 +1/5 H.sub.2 O 526.12 188 Cal.Obt. 54.7954.79 6.216.00 7.997.70 44 ##STR87## CHCH CO(trans) " Oxalate +2/5 H.sub.2 O C.sub.23 H.sub.31 N.sub.3 O.sub.8 +2/5 H.sub.2 O 484.71 193 Cal.Obt. 56.9956.78 6.616.53 8.678.52 45 ##STR88## CHCHCO(trans) " 5/4 Oxalate +1/5 H.sub.2 O C.sub.20 H.sub.27 N.sub.3 O.sub.2 +5/4 C.sub.2 H.sub.2 O.sub.4 +1/5 H.sub.2 O 457.49 202 Cal.Obt. 59.0558.94 6.597.05 9.188.65 46 ##STR89## CHCHCO(trans) " HCl C.sub.20 H.sub.28 ClN.sub.3 O.sub.2 377.90 >260 O Cal.bt. 63.5663.61 7.477.71 11.1211.24 47 ##STR90## CHCHCO(trans) " " C.sub.19 H.sub.25 Cl.sub.2 N.sub.3 O.sub.2 398.33 >260 Cal.Obt. 57.2957.37 6.336.47 10.5510.35 48 ##STR91## CHCHCO(trans) " Oxalate +2/5 H.sub.2 O C.sub.22 H.sub.29 N.sub.3 O.sub.7 +2/5 H.sub.2 O 454.68 193 Cal.Obt. 58.1158.13 6.616.58 9.248.62 49 ##STR92## CHCHCO(trans) " HCl +1/4 H.sub.2 O C.sub.21 H.sub.30 ClN.sub.3 O.sub.4 +1/4 H.sub.2 O 428.43 240 Cal.Obt. 58.8158.85 7.187.03 9.819.85 50 ##STR93## CHCHCO(trans) " Oxalate +1/4 H.sub.2 O C.sub.21 H.sub. 26 ClN.sub.3 O.sub.6 +1/4 H.sub.2 O 456.40 120 Cal.Obt. 55.2655.23 5.856.15 9.219.04 51 ##STR94## CHCHCO(trans) " HCl +1/6 H.sub.2 O C.sub.23 H.sub.34 ClN.sub.3 O.sub.5 1 +/6 H.sub.2 O 496.81 230 Cal.Obt. 55.6055.95 7.557.20 8.468.75 52 ##STR95## CHCHCO(trans) " HCl +1/5 H.sub.2 O C.sub.20 H.sub.28 ClN.sub.3 O.sub.3 1 +/5 H.sub.2 O 397.51 249 Cal.Obt. 60.4360.18 7.207.16 10.5710.59 53 ##STR96## CHCHCO(trans) " Oxalate +3/4 H.sub.2 O C.sub.24 H.sub.31 N.sub.3 O.sub.9 +3/4 H.sub.2 O 519.02 245 Cal.Obt. 55.5455.78 6.316.01 8.108.03 54 ##STR97## CHCHCO(trans) " 1.4 HCl +4/10 H.sub.2 O C.sub.24 H.sub.35 N.sub.3 O.sub.5 +1.4 HCl +4/10 H.sub.2 O 503.80 218 Cal.Obt. 57.2156.94 7.447.48 8.348.65 55 ##STR98## CHCHCO(trans) ##STR99## HCl C.sub.21 H.sub.28 ClN.sub.3 O.sub.4 421.91 250 Cal.Obt. 59.7859.36 6 .697.03 9.969.97 56 ##STR100## CHCHCO(trans) " " C.sub.20 H.sub.27 Cl.sub.2 N.sub.3 O.sub.2 412.35 254 C al.Obt. 58.2558.04 6.606.75 10.1910.23 57 ##STR101## CH.sub.2 CH.sub.2CO ##STR102## Base C.sub.28 H.sub.39 N.sub.3 O.sub.8 545.62 159 Cal.Obt. 61.6361.40 7.217.31 7.707.39 58 " CHCHCH.sub.2(trans) ##STR103## " C.sub.21 H.sub.33 N.sub.3 O.sub.4 391.49 130 Cal.Obt. 64.6264.18 8.508.69 10.7310.54 59 " CHCHCH.sub.2(trans) ##STR104## dioxalate C.sub.24 H.sub.35 N.sub.3 O.sub.8 583.58 240 Cal.Obt. 53.5153.26 6.396.46 7.207.11 60 " CHCHCH.sub.2(trans) ##STR105## 2.2oxalate C.sub.23 H.sub.35 N.sub.3 O.sub.4 +2.2 (C.sub.2 H.sub.2 O.sub.4) 615.61 188 Cal.Obt. 53.4553.42 6.456.83 6.836.78 61 ##STR106## CHCHCH.sub.2(trans) ##STR107## 1.35 HCl +2.7% H.sub.2 O C.sub.20 H.sub.27 N.sub.3 O.sub.3 +1.35 HCl +2.7% H.sub.2 O 417.80 207 Cal.Obt. 57.4957.38 7.147.00 10.0610.13 62 ##STR108## (CH.sub.2).sub.3 ##STR109## dioxalate +1/2 H.sub.2 O C.sub.25 H.sub.39 N.sub.3 O.sub.12 +1/2 H.sub.2 O 582.59 188 Cal.Obt. 51.5451.34 6.926.76 7.217.04 63 " " ##STR110## dioxalate C.sub.26 H.sub.39 N.sub.3 O.sub.12 585.59 260 Cal.Obt. 53.3252.95 6.716.68 7.187.17 74 ##STR111## CHCHCO(trans) ##STR112## Oxalate C.sub.21 H.sub.27 N.sub.3 O.sub.7 433.45 .perspectiveto.200(decompo-sition) Cal.Obt. 58.1958.19 6.286.45 9.709.71 75 ##STR113## CHCHCO(trans) " " C.sub.21 H.sub.27 N.sub.3 O.sub.8 449.45 .perspectiveto.200(decompo-sition) Cal.Obt. 56.1255.86 6.066.28 9.359.28 76 ##STR114## CHCHCO(trans) ##STR115## " C.sub.22 H.sub.29 N.sub.3 O.sub.7 447.48 227 Cal.Obt. 59.0559.11 6.536.75 9.399.50 77 ##STR116## CHCHCO(trans) " " C.sub.22 H.sub.29 N.sub.3 O.sub.8 463.48 195 Cal.Obt. 5 7.0157.20 6.316.59 9.079.13 78 ##STR117## CHCHCO(trans) " Base C.sub.22 H.sub.29 N.sub.3 O.sub.3 371.47 127 Cal.Obt. 67.9067.92 7.877.95 11.3111.43 79 ##STR118## CHCHCO(trans) " HCl +4.3% H.sub.2 O C.sub.21 H.sub.30 ClN.sub.3 O.sub.3 +4.3% H.sub.2 O 426.30 220 Cal.Obt. 59.1759.21 7.577.31 9.869.84 80 ##STR119## CHCHCO(trans) " HCl C.sub.21 H.sub.30 ClN.sub.3 O.sub.3 407.93 210 Cal.Obt. 61.8361.65 7.417.47 10.3010.30 81 ##STR120## CHCHCO(trans) " Base C.sub.22 H.sub.31 N.sub.3 O.sub.4 401.49 106 Cal.Obt. 65.8165.68 7.787.63 10.4710.34 82 ##STR121## CHCHCO(trans) " " C.sub.22 H.sub.31 N.sub.3 O.sub.4 401.49 119 Cal.Obt. 6 5.81 65.57 7.787.51 10.4710.58 83 ##STR122## CHCHCO(trans) " 1.5 Oxalate C.sub.22 H.sub.31 N.sub.3 O.sub.4 (base) +1.5 oxalate(C.sub.25 H.sub.34 N.sub.3 O.sub.10) 536.55 240 Cal.Obt. 55.9655.84 6.396.36 7.837.66 84 ##STR123## CHCHCO(trans) " HCl C.sub.23 H.sub.34 ClN.sub.3 O.sub.5 467.98 190 Cal.Obt. 59.0359.22 7.327.51 8.989.01 85 ##STR124## CHCHCO(trans) " " C.sub.22 H.sub.30 ClN.sub.3 O.sub.4 435.94 .perspectiveto.200(decompo-sition) Cal.Obt. 60.61 60.60 6.947.10 9.649.49 86 ##STR125## CHCHCO(trans) " " C.sub.21 H.sub.30 ClN.sub.3 O.sub.2 391.93 220 Cal.Obt. 64.3564.33 7.727.73 10.7210.99 87 ##STR126## CHCHCO(trans) " " C.sub.21 H.sub.27 ClF.sub.3 N.sub.3 O.sub.2 445.91 >200(decompo-sition) Cal.Obt. 56.5656.76 6.105.86 9.429.50 88 ##STR127## CHCHCO(trans) " Base C.sub.20 H.sub.25 Cl.sub.2 N.sub.3 O.sub.2 410.34 153 Cal.Obt. 58.5458.40 6.146.05 10.2410.01 89 ##STR128## CHCHCO(trans) ##STR129## " C.sub.25 H.sub.35 N.sub.3 O.sub.5 457.55 175 NMR spectrum (CDCl.sub.3) .delta.ppm; 6.68 and 7.5, d(J=15Hz): C.sub.--HC.sub.--H trans; 6.65,s: 2 aro-matic Hs; 4,4,m: 2 tropanicprotons in positions 1 and 5; 3.82,s: 3C.sub.--H.sub.3 O; 3.65,m: 4 piperazinic Hs; ##STR130##

The derivatives of formula (I) and the salts and hydrates thereof were tested on laboratory animals and revealed pharmacological activities and especially activities stimulating, protecting and/or correcting cerebral functions.

These activities were shown, more particularly by the mnesic retention test of exploratory activity effected according to the following method:

In an APELAB ACTIMETER [BOISSIER and SIMON, Arch. Inter. Pharmacodyn. 158, 212, (1965)], the exploratory activity during 5 mn of male SWISS-WEBSTER mice is measured, then the animals receive an intraperitoneal (or an oral injection dose), of the compounds of formula (I) or the salts thereof or of physiological serum. After a week, the exploratory activity of the treated animals is again measured by an habituation, that is by a statistically significant decrease (t of STUDENT by mated groups) of the exploratory activity.

To illustrate the invention, we give in Table II below, the results obtained with some compounds of the invention.

The approximate acute toxicity is determined according to the method described by MILLER and TAINTER in Proc. Soc. Exp. Biol. Med. 57, 261 (1944).

The results obtained with some compounds of the invention are also given, by way of examples in this table II.

As the above results show, the compounds of the invention present marked pharmacological activities and low toxicity. These compounds find then an application in therapeutics. Thus, they will be more particularly used for stimulating intellectual efficiency in normal subjects, for preserving the cerebral functions in aged subjects and for treating trouble of vigilance and/or memorization consequent on different pathologies, particularly brain traumatisms, cerebral disturbances or acute or sub-acute cerebro-vascular accidents.

The present invention further extend to pharmaceutical compositions containing as active ingredient, one at least of the derivatives of formula (I) or by the salts or hydrates thereof, these compositions being able to be formulated more especially with a view to their oral or parenteral administration. Thus, they may be administered orally in the form of pills, capsules or tablets, or in the form of drinkable solutions, in an amount up to 2.5 g/day, to be taken in several doses per day (up to six doses) or parenterally in the form of injectable ampoules containing up to 1 g of active ingredient (1 to 3 injections per day).

In the case of the oral administration in the form of pills, capsules or tablets, the latter advantageously comprise a vehicle (such as cellulosic derivatives, vinylic polymers or gums for example) allowing modulation of drug release. The drinkable solutions are preferably aqueous solutions or suspensions (vehicle=water) or partially aqueous solutions or suspensions (vehicle=water+alcohol, water+glycerine or water+propylene glycol). In the case of the parenteral administration, the active ingredient may be injected in the form of suspensions or solutions of freeze drying products containing said active ingredient.