Patent Application
20060211731
The present invention relates to new substituted pyridine or piperidine compounds and to their use as facilitators of memory and cognition and as antalgic agents.
Ageing of the population due to increased life expectancy has brought with it a major increase in cognitive disorders associated with normal cerebral ageing and with pathological cerebral ageing occurring in the course of neurodegenerative diseases such as, for example, Alzheimer's disease.
The majority of substances used today in treating cognitive disorders associated with ageing act by facilitating the central cholinergic systems—either directly, as in the case of acetylcholinesterase inhibitors (tacrine, donepezil) and cholinergic agonists (nefiracetam), or indirectly, as in the case of nootropic agents (piracetam, pramiracetam) and cerebral vasodilators (vinpocetine).
Besides their cognitive properties, substances acting directly on the central cholinergic systems often have antalgic properties but also have hypothermic properties, which can be undesirable.
It has been therefore been especially valuable to synthesise new compounds that are capable of opposing the cognitive disorders associated with ageing and/or of improving cognitive processes and that can possess antalgic properties without having hypothermic activity.
The literature discloses substituted piperidine compounds which are described as products of synthesis and/or of alkaloids (J. Chem. Soc., Perkin Trans. 1, 1991, (3), pp. 611-616; Heterocycles, 1985, 23 (4), pp. 831-834; Can. J. Chem., 1996, 74 (12), pp. 2444-2453).
Substituted pyridine compounds have also been described with reference to their synthesis (J. Chem. Soc., Dalton Trans., 1998, (6), pp. 917-922) or their interactions in metal complexes (J. Chem. Soc., Chem. Commun., 1987, (19), pp. 1457-1459; J. Am. Chem.
Soc., 1985, 107 (4), pp. 917-925).
The compounds of the present invention are new and have properties that, from a pharmacological point of view, are especially valuable.
More specifically, the present invention relates to compounds of formula (I):
wherein:
Among the pharmaceutically acceptable acids there may be mentioned, without implying any limitation, hydrochloric acid, hydrobromic acid, sulphuric acid, phosphonic acid, acetic acid, trifluoroacetic acid, lactic acid, pyruvic acid, malonic acid, succinic acid, glutaric acid, fumaric acid, tartaric acid, maleic acid, citric acid, ascorbic acid, methanesulphonic acid, camphoric acid, oxalic acid etc.
Among the pharmaceutically acceptable bases there may be mentioned, without implying any limitation, sodium hydroxide, potassium hydroxide, triethylamine, tert-butylamine etc.
Preferred compounds of the invention are compounds of formula (I) wherein the group
represents a pyridinyl group, an N-methylpyridinium group, a piperidinyl group or an N-methylpiperidinyl group.
Preferred substituents R4 are a phenyl group or substituted phenyl group, especially substituted by a halogen atom, preferably a bromine atom.
Advantageously, the invention relates to compounds of formula (I) wherein R5 represents a hydrogen atom or a group of formula (II).
Preferred groups R2 and R3 are those wherein R2 and R3 together form an oxo group or R2 represents a hydrogen atom and R3 represents a hydroxy group.
Even more advantageously, the invention relates to the compounds of formula (I) which are:
The enantiomers and diastereoisomers, as well as the addition salts with a pharmaceutically acceptable acid or base, of the preferred compounds of the invention form an integral part of the invention.
The invention relates also to a process for the preparation of compounds of formula (I), which process is characterised in that there is used as starting material the compound of formula (III):
wherein X represents a hydrogen or fluorine atom, which is alkylated by means of an agent such as, for example, alkyl para-toluenesulphonate or alkyl trifluoromethanesulphonate to yield the compound of formula (IV):
wherein X is as defined hereinbefore, R′6 represents a linear or branched (C1-C6)alkyl group and Y− represents a para-toluenesulphonate or trifluoromethanesulphonate group for example,
which is reacted with one or two compounds, which may be the same or different, of formula (V):
wherein Ra and Rb, together with the nitrogen atom carrying them, form a 5- or 6-membered heterocycle which may contain, in addition to the nitrogen atom, another hetero atom selected from sulphur, oxygen and nitrogen, and Rc represents a hydrogen atom or a group of formula (VI):
wherein R4 and R1 are as defined hereinbefore,
it being understood that at least one of the compounds of formula (V) contains a group of formula (VI),
to yield the compound of formula (I/a), a particular case of the compounds of formula (I):
wherein R1, R4, Ra, Rb, R′6 and Y− are as defined hereinbefore and X′ represents a hydrogen atom, a group —NR′aR′b (wherein R′a and R′b may have any of the meanings of Ra and Rb, respectively) or a group of formula (VII):
wherein R′a, R′b, R′1 and R′4 may have any of the meanings of Ra, Rb, R1 and R4, respectively,
which compound of formula (I/a) may be subjected to halohydric acid such as HCl, HBr or HI, or to the action of ammonium salts such as NH4+PF6− to yield a compound of formula (I/a′):
wherein R1, R4, Ra, Rb, R′6 and X′ are as defined hereinbefore and Y′− represents a halogen anion or a PF6− group,
which compound of formula (I/a′) may be hydrolysed using a concentrated hydrochloric acid solution to yield the compound of formula (I/b), a particular case of the compounds of formula (I):
wherein R1, R4, R′6 and Y′− are as defined hereinbefore and X″ represents a hydrogen atom, a group —NR′aR′b as defined hereinbefore or a group of formula (VIII):
wherein R′1 and R′4 may have any of the meaningys of R1 and R4, respectively,
the compounds of formula (I/a), (I/a′) and (I/b) constituting the compound of formula (I/c), a particular case of the compounds of formula (I):
wherein R′1, R4 and R′6− are as defined hereinbefore, Y″− represents a group Y− or Y′− as defined hereinbefore, R2a and R3a together form an oxo group, or R2a and R1 form an additional bond and, in that case, R3a represents a group NR′aR′b as defined hereinbefore, and X′″ represents a hydrogen atom, a group NR′aR′b or a group of formula (IX):
wherein R′1, R′2a, R′3a and R′4 may have any of the meanings of R1, R2a, R3a and R4, respectively,
which is converted into a corresponding iodinated salt by the action of NaI to yield the compound of formula (I/d), a particular case of the compounds of formula (I):
wherein R1, R2a, R3a, R4, R′6 and X′″ are as defined hereinbefore,
which is
The invention relates also to pharmaceutical compositions comprising as active ingredient at least one compound of formula (I) together with one or more appropriate, inert, non-toxic excipients. Among the pharmaceutical compositions according to the invention there may be mentioned more especially those that are suitable for oral, parenteral (intravenous or subcutaneous) and nasal administration, tablets or dragees, sublingual tablets, gelatin capsules, lozenges, suppositories, creams, ointments, dermal gels, injectable preparations, drinkable suspensions etc.
The dosage used can be adapted to the nature and the severity of the disorder, the administration route and the age and weight of the patient. The dosage varies from 0.01 mg to 1 g per day in one or more administrations.
The following Examples illustrate the invention but do not limit it in any way.
The following Preparations yield compounds of the invention or synthesis intermediates that are useful in the preparation of compounds of the invention.
10 mmol of 2-fluoropyridine and 10 mmol of methyl 4-methylbenzenesulphonate are mixed in a 50 ml round-bottomed flask and stirred for 6 hours at 70° C. under a nitrogen atmosphere. The salt obtained in the form of a white solid is used without additional purification in the following step.
100 g of molecular sieve are heated at 500° C. for 8 hours and then added to a mixture of 20 mmol of acetophenone and 22 mmol of pyrrolidine in 200 ml of anhydrous ether. The reaction mixture is stirred at ambient temperature until, in the infra-red, no more free ketone (C═O 1689 cm−1) is detected in the supernatant and the absorption for the enamine (C═C—N 1600 cm−1) is at a maximum. The mixture is then filtered and the molecular sieve is washed with ether. The solvent is evaporated off under reduced pressure and the crude residue is purified by distillation under reduced pressure.
Boiling point: 110° C./2 mm Hg
Preparations 3 to 11 are obtained by proceeding as in Preparation 2.
Boiling point: 125° C./2 mm Hg
Boiling point: 135° C./10 mm Hg
Boiling point: 160° C./0.4 mm Hg
Boiling point: 125° C./10 mm Hg
Boiling point: 160° C./0.3 mm Hg
Boiling point: 140° C./0.3 mm Hg
Boiling point: 130° C./0.3 mm Hg
Boiling point: 165° C./0.3 mm Hg
1 g of para-toluenesulphonic acid is added to a mixture of 20 mmol of cyclohexanone and 22 mmol of pyrrolidine in 200 ml of dry benzene. The reaction mixture is stirred at reflux until, in the infra-red, the ketone has disappeared, with the enamine concomitantly appearing. The solvent is then evaporated off and the crude residue is purified by distillation in vacuo.
Boiling point: 110° C./15 mm Hg
The procedure is as in Preparation 11, the benzene being replaced by toluene and the pyrrolidine by morpholine.
Boiling point: 140° C./15 mm Hg
10 mmol of 2,6-difluoropyridine and 10 mmol of trifluoromethanesulphonic acid are mixed in a 50 ml round-bottomed flask and the mixture is stirred for 1 hour at ambient temperature under a nitrogen atmosphere. The white solid obtained is used directly in the following reaction without further purification.
The procedure is as in Preparation 2.
The procedure is as in Preparation 2.
The procedure is as in Preparation 2.
The procedure is as in Preparation 2.
Title product is obtained using the same procedure than in Preparation 1 replacing methyl-4-methylbenzenesulfonate by ethyl-4-methylbenzenesulfonate.
20 mmol of the compound obtained in Preparation 1 are dissolved in 15 ml of anhydrous acetonitrile under a nitrogen atmosphere, and 22 mmol of the compound obtained in Preparation 4, in 10 ml of acetonitrile, are added dropwise at ambient temperature. The reaction mixture is stirred at 80° C. for 2 hours and the solution becomes red. The solvent is evaporated off in vacuo and the viscous red residue is taken up in 30 ml of concentrated hydrochloric acid and heated at reflux for 3 hours. The dark brown solution obtained is cooled to ambient temperature and then 22 mmol of ammonium hexafluorophosphate are added. The precipitate obtained is filtered off, washed with cold water and with ethyl acetate, and then recrystallised from ethanol.
Melting point: 163-165° C.
Elementary microanalysis:
10 mmol of the compound obtained in Example 1 are dissolved in 35 ml of acetone, and 15 mmol of NaI are added in portions of 100 mg. A white precipitate is obtained immediately and the mixture is stirred for 14 hours in a sealed tube at ambient temperature. The white solid obtained is filtered off and washed with acetone.
Melting point: 191-193° C.
Elementary microanalysis:
The procedure in Examples 3 to 14 is as in Examples 1 and 2.
Starting compounds: Preparations 1 and 5
Melting point: 168-170° C.
Elementary microanalysis:
Starting compound: Example 3
Melting point: 214-216° C.
Elementary microanalysis:
Starting compounds: Preparations 1 and 6
Melting point: 152-154° C.
Elementary microanalysis:
Starting compound: Example 5
Melting point: 212-214° C.
Elementary microanalysis:
Starting compounds: Preparations 1 and 7
Melting point: 185-187° C.
Elementary microanalysis:
Starting compound: Example 7
Melting point: 222-224° C.
Elementary microanalysis:
Starting compounds: Preparations 1 and 11 or 12
Elementary microanalysis:
Starting compound: Example 9
Melting point: 151-153° C.
Elementary microanalysis:
Starting compounds: Preparations 1 and 10
Starting compound: Example 11
Melting point: 217-218° C.
Elementary microanalysis:
Starting compounds: Preparations 1 and 9
Starting compound: Example 13
Melting point: 204-205° C.
Elementary microanalysis:
The procedure is as in Examples 1 and 2, starting from the compound obtained in Preparation 15.
3 mmol of the compound obtained in Example 15a are dissolved in 150 ml of ethanol, and 50 mg of platinum oxide are added all at once. Hydrogenation is carried out at an initial pressure of 5 atm at 24° C. When the calculated theoretical volume of hydrogen has been absorbed (after approximately 3 hours), the catalyst is filtered off and washed with ethanol. The solvent is evaporated off and the residue obtained is recrystallised.
Melting point: 118-119° C.
Examples 16 to 21 are obtained by proceeding as in Example 15b.
Starting compound: Example 4
Melting point: 201-203° C.
Elementary microanalysis:
Starting compound: Example 6
Melting point: 158-160° C.
Elementary microanalysis:
Starting compound: Example 8
Melting point: 182-184° C.
Elementary microanalysis:
A solution of oxalyl chloride (5 mmol) in dry CH2Cl2 (10 ml) was placed in an oven-dried 25 ml flask, which was degassed and filled with nitrogen. DMSO (10 mmol) was added dropwise through a syringe at −50 to −60° C. The reaction mixture was stirred for minutes. A solution of compound of Example 60 (2) 0,5 mmol) in CH2Cl2 (5 ml) was then added dropwise within 5 minutes and stirring was continued for another 30 minutes. Triethylamine (30 mmol) was added and the solution was stirred for 10 minutes and then allowed to warm to room temperature. Water was then added to the reaction mixture and the aqueous solution was extracted with CH2Cl2. The combined organic phases was dried (MgSO4) and concentrated. The residue was purified by flash column chromatography (silica gel, AcOEt-MeOH-NH4OH) affording an unstable light yellow oil which was immediately dissolved in an HCl-ether solution forming a white solid. Recrystallisation of this solid from MeOH-ether produced pure title product.
Melting point: 191-194° C.
[a]=+10 (c=0.1; MeOH)
The title product is obtained using the same procedure than in Example 18a starting from compound of Example 60 (1).
Melting point: 192-194° C.
[a]=−9 (c=0.1; MeOH)
Starting compound: Example 10
Melting point: 160-162° C.
Starting compound: Example 12
Melting point: 134-136° C.
Elementary microanaysis:
Starting compound: Example 14
Melting point: 163.5-164° C.
Elementary microanalysis:
20 mmol of the compound obtained in Preparation 1 are dissolved in 15 ml of dry acetonitrile under a nitrogen atmosphere. A solution of 22 mmol of the compound obtained in Preparation 2 in 10 ml of acetonitrile is added dropwise, with stirring, at ambient temperature. The reaction mixture is stirred for 14 hours at ambient temperature and then for 2 hours at 80° C. The solution becomes red. The solvent is evaporated off under reduced pressure, and 30 ml of cold water and then 22 mmol of ammonium hexafluorophosphate in 20 ml of ethyl acetate/ether (1/1) are added to the viscous red residue obtained. After filtration and washing with water and then with AcOEt/Et2O (1/1), the pure title product is obtained.
Melting point: 143-145° C.
Elementary microanalysis:
The same procedure is used as in Example 2.
Melting point: 200-202° C.
The same procedure is used as in Example 22.
Starting compounds: Preparations 1 and 3
Melting point: 168-170° C.
Elementary microanalysis:
The procedure is as in Example 2.
20 mmol of the compound obtained in Preparation 13 are dissolved in 15 ml of dry acetonitrile under a nitrogen atmosphere. 22 mmol of morpholine and 22 mmol of the compound obtained in Preparation 3 are added and the mixture is stirred for 14 hours at ambient temperature and then for 2 hours at 80° C. The procedure is then as in Example 22.
The procedure is as in Example 2.
Melting point: 214-216° C.
20 mmol of the compound obtained in Preparation 13 are dissolved in 15 ml of dry acetonitrile. A solution, in 15 ml of acetonitrile, of 44 mmol of the compound obtained in Preparation 2 is added dropwise at 0° C., with stirring, under a nitrogen atmosphere. The reaction mixture is then stirred for 14 hours at ambient temperature. The solution becomes red; the solvent is then evaporated off and the viscous red residue obtained is taken up in 50 ml of concentrated hydrochloric acid and heated at reflux for 3 hours. After cooling to ambient temperature, the title compound crystallises out in the form of white needles, which are filtered off and then washed with cold water and with ethyl acetate.
Melting point: 175° C.
Elementary microanalysis:
The procedure is as in Example 2.
Melting point: 197-199° C.
Elementary microanalysis:
The procedure is as in Example 28.
Starting compounds: Preparations 13 and 7
The procedure is as in Example 2.
20 mmol of the compound obtained in Preparation 13 are dissolved in 15 ml of acetonitrile, and 44 mmol of the compound obtained in Preparation 11, dissolved in 15 ml of acetone, are added at 0° C. under a nitrogen atmosphere. The reaction mixture is returned to ambient temperature and stirred for 3 hours at 80° C. The solution becomes red and, after the solvent has been evaporated off under reduced pressure, the residue is taken up in 50 ml of concentrated hydrochloric acid and heated at reflux for 3 hours. After cooling, the solution lo is filtered to remove any solid impurities and 22 mmol of NH4PF6 are added. After extraction with ethyl acetate and drying over MgSO4, the solvent is evaporated off under reduced pressure and the solid obtained is recrystallised from an ethanol/ethyl acetate mixture.
Elementary microanalysis:
The procedure is as in Example 2.
20 mmol of the compound obtained in Preparation 13 are dissolved in 15 ml of dry acetonitrile, and then 22 mmol of the compound obtained in Preparation 2, in 10 ml of acetonitrile, are added dropwise at 0° C. under a nitrogen atmosphere. The reaction mixture is then returned to ambient temperature and stirred for 3 hours at that temperature. 22 mmol of the compound obtained in Preparation 4, in 10 ml of acetonitrile, are then added and the reaction mixture is stirred for a further 14 hours. The solvent is then evaporated off and the viscous red residue obtained is taken up in 50 ml of concentrated hydrochloric acid and heated at reflux for 3 hours. After cooling, the title compound crystallises out in the form of white needles, which are filtered off and washed in succession with water and ethyl acetate.
Melting point: 188-190° C.
Elementary microanalysis:
The procedure is as in Example 2.
Melting point: 205-206° C.
Elementary microanalysis:
Examples 36 to 49 are obtained by proceeding as in Examples 34 and 35.
Starting compounds: Preparations 13, 2 and 6
Melting point: 199-201° C.
Starting compound: Example 36
Melting point: 213-215° C.
Starting compounds: Preparations 13, 2 and 8
Starting compound: Example 38
Melting point: 220-222° C.
Starting compounds: Preparations 13, 2 and 7
Starting compound: Example 40
Melting point: 218-220° C.
Starting compounds: Preparations 13, 6 and 7
Melting point: 226-228° C.
Starting compound: Example 42
Melting point: 226-227° C.
Starting compounds: Preparations 13, 2 and 5
Melting point: 193-195° C.
Starting compound: Example 44
Melting point: 203-205° C.
Starting compounds: Preparations 13, 5 and 8
Melting point: 208-210° C.
Starting compound: Example 46
Melting point: 219-220° C.
Starting compounds: Preparations 13, 4 and 5
Starting compound: Example 48
3 mmol of the compound obtained in Example 49 are dissolved in 150 ml of ethanol and then 70 mg of platinum oxide are added all at once. Hydrogenation is carried out using an initial pressure of 3 atmospheres at 24° C. When the theoretical volume of hydrogen has been absorbed (after approximately 3 hours), the catalyst is filtered off and washed with ethanol. The solvent is then evaporated off and the title product is obtained in the form of a white solid.
Examples 51 to 56 are obtained by proceeding as in Example 50.
Starting compound: Example 35
Melting point: 192-193° C.
Starting compound: Example 37
Melting point: 152-154° C.
Starting compound: Example 39
Meting point: 152-154° C.
Starting compound: Example 43
Melting point: 200-202° C.
Starting compound: Example 41
Starting compound: Example 31
The procedure is as in Examples 1 and 2, starting from the compound obtained in Preparation 14.
8 mmol of the compound obtained in Example 57a are added to 15 g of boiling pyridine hydrochloride and the dark solution obtained is heated at reflux for 10 minutes. The hot reaction mixture is poured onto 30 g of ice and 20 ml of ammonium hydroxide 37%. After cooling in an ice bath for approximately 2 hours, the title compound crystallises out and the crystals are filtered off and washed with cold water.
Step A: 1-(4-Bromophenyl)-2-(2-pyridinyl)-1-ethanone
8 mmol of the compound obtained in Example 8 are added to 15 g of boiling pyridine hydrochloride and the dark solution obtained is heated at reflux for 10 minutes. The hot reaction mixture is poured onto 30 g of ice and 20 ml of ammonium hydroxide 37%. After cooling in an ice bath for approximately 2 hours, the title compound crystallises out in the form of yellow-green crystals, which are filtered off and washed with cold water.
Step B: 1-(4-Bromophenyl)-2-(2-pyridinyl)-1-ethanol
1 mmol of the compound obtained in Step A is dissolved in 15 ml of ethanol, and 1.5 mmol of NaBH4 are added in two portions. The reaction mixture is stirred for 3 hours; the reaction is then quenched using 0.5 ml of acetic acid; the mixture is rendered basic with 10% NaOH, and extracted with dichloromethane (3×15 ml). The organic phase is dried over MgSO4, evaporated and the solid obtained is recrystallised from ethanol.
A solution of NaBH4 (1,51 g, 40 mmol) modified with ethanol (2.34 ml) and tetrahydrofurfuryl alcohol (20 ml) in CHCl3 (40 ml) was added dropwise to a solution of the compound obtained in step A of Example 58 (8.28 g, 30 mmol) and (R,R)-(−)-Jacobsen's MnCl catalyst (420 mg) in CHCl3 (30 ml) at −20° C. under a nitrogen atmosphere. The reaction was monitored by TLC and quenched by addition of sat. NH4Cl solution (15 ml) on completion. The aqueous solution was extracted with CH2Cl2 and the extract dried and evaporated. The residue was purified by column chromatography (silica gel, ethyl acetate-petroleum ether) to afford title product.
Melting point: 161-162° C.
[a]=−34 (c=1, CHCl3)
Elmentary microanalysis:
Title product is obtained using the same process than in Example 58a with (S,S)-(+)-Jacobsen's MnCl catalyst.
Melting point: 161-162.5° C.
[a]=+34 (c=1, CHCl3)
Elementary microanalysis:
1 mmol of the compound obtained in Example 58 is dissolved in 20 ml of acetic acid, and 8 mg of platinum oxide are added. The hydrogenation is carried out starting from an initial pressure of 3 atmospheres at 24° C. After reacting for 3 hours, the catalyst is filtered off and washed with dichloromethane. The solvents are evaporated off and the residue obtained is dissolved in 10% sodium hydroxide solution and extracted with dichloro-methane. The organic phase is washed with water, dried over MgSO4 and then evaporated off to yield the title compound in the form of a white solid.
The procedure is as in Step B of Example 58, starting from the compound obtained in Example 18.
To compound obtained in Example 58a (1 mmol) in acetic acid (20 ml) was added platinum oxide (20 mg) and the solution hydrogenated at 5 atm. and 20° C. Removal of the catalyst and then the solvent, followed by addition of dichloromethane and aqueous sodium carbonate, washing and drying of the organic layer, followed by evaporation, gave a mixture of two diastereoisomers of (S,S)-(−)4′-bromo-norsedamine and (R,S)-(−)-4′-bromo-norallosedamine. Recrystallisation from ethyl acetate/petroleum ether (1:1) gave the pure S,S-isomer of 1-(4-bromophenyl)-2-(2-piperidinyl)ethanol which was dissolved in acetonitrile (25 ml) and aqueous formaldehyde (37%, 25 ml). Then sodium cyano-borohydride (0.312 g, 5 mmol) was added. The mixture was stirred at ambient for 1 hour and acetic acid added. After 20 minutes the solution was neutralised with aqueous sodium hydroxide, extracted with dichloromethane, the extract dried and evaporated and the residue purified by silica gel chromatography to give the title product (recrystallised from ethyl acetate-petroleum ether 1:1).
Melting point: 102-104° C.
[a]=−28 (c=1, EtOH)
Elementary microanalysis:
Title product is obtained using the same procedure than in Example 60 (1) starting from compound obtained in Example 58b.
Melting point: 102-104° C.
[a]=+28 (c=1, EtOH)
Elementary microanalysis:
The procedure is as in Examples 1 and 2, starting from the compound obtained in Preparation 16.
The procedure is as in Example 57b, starting from the compound obtained in Example 61a.
Melting point: 118-119.5° C.
The procedure is as in Step B of Example 58, starting from the compound obtained in Example 6.
Melting point: 172-173.5° C.
The procedure is as in Step B of Example 58, starting from the compound obtained in Example 61a.
Melting point: 145-148° C.
The procedure is as in Step B of Example 58, starting from the compound obtained in Example 57a.
The procedure is as in Step B of Example 58, starting from the compound obtained in Example 61b.
The procedure is as in Examples 1 and 2, starting from the compound obtained in Preparation 17.
Step A: 2-(2-Pyridinyl)-1-[4-(trifluoromethyl)phenyl]ethanone
The procedure is as in Example 57b, starting from the compound obtained in Example 66a.
Step B: 2-(2-Pyridinyl)-1-[4-(trifluoromethyl)phenyl]ethanol
Starting from the compound obtained in Step A, the procedure is as in Step B of Example 58.
Melting point: 156-158° C.
The procedure is as in Example 66b, starting from the compound obtained in Example 15a.
Melting point: 71-73° C.
The procedure is as in Example 66b, starting from the compound obtained in Example 12.
Melting point: 82-84° C.
The procedure is as in Example 66b, starting from the compound obtained in Example 14. Oil.
The procedure is as in Example 59, starting from the compound obtained in Example 66b.
Melting point: 95-98° C.
The procedure is as in Step B of Example 58, starting from the compound obtained in Example 17.
Melting point: 84-87° C.
The procedure is as in Step B of Example 58, starting from the compound obtained in Step A of Example 66b.
Title product is obtained using the same procedure than in Example 1 starting from Preparations 1 and 7 without addition of ammonium hexafluorophosphate.
Melting point: 112-114° C.
Title product is obtained using the same procedure than in step B of Example 58 starting from the compound of Example 8.
Melting point: 64-65° C.
The acute toxicity was evaluated after oral administration to groups each comprising 8 mice (26±2 grams). The animals were observed at regular intervals during the course of the first day, and daily for the two weeks following treatment. The LD50 (dose that causes the death of 50% of the animals) was evaluated and demonstrated the low toxicity of the compounds of the invention.
Intraperitoneal administration of an alcoholic solution of PBQ causes abdominal cramps in the mouse (SIEGMUND et al., Proc. Soc. Exp. Biol., 1957, 95, 729-731). The cramps are characterised by repeated contractions of the abdominal musculature, accompanied by extension of the hind limbs. Most analgesics antagonise these abdominal cramps (COLLIER et al., Brit. J. Pharmacol. Chem., 1968, 32, 295-310). At t=0 min., the animals are weighed and the compound being studied is administered by the IP route. A group of control animals is given the solvent used for the compound. At t=30 min., an alcoholic solution of PBQ (0.2%) is administered by the IP route in a volume of 0.25 ml/mouse. Immediately after administration of the PBQ, the animals are placed in cylinders of plexiglass (L=19.5 cm; I.D.=5 cm). From t=35 min. to t=45 min., the animals' reaction is observed and the experimenter notes the total number of abdominal cramps per animal. The results are expressed as the percentage inhibition of the number of abdominal cramps measured in the control animals, at the active dose of the compound studied.
The results obtained show a percentage inhibition ranging from 30 to 90% for low active doses. which attests the antalgic properties of the compounds of the invention.
Initially described in 1982 by THOR and HOLLOWAY, (J. Comp. Physiol., 1982, 96, 1000-1006), the social recognition test has subsequently been proposed by various authors (DANTZER et al., Psychopharmacology, 1987, 91, 363-368; PERIO et al., Psychopharmacology, 1989, 97, 262-268) for studying the mnemocognitive effects of new compounds. The test is based on the natural expression of the olfactory memory of the rat and its natural tendency to forget and allows evaluation of memorisation, by recognition of a young congeneric animal, by an adult rat. A young rat (21 days), taken at random, is placed for 5 minutes in the cage housing an adult rat. With the aid of a video device, the experimenter observes the social recognition behaviour of the adult rat and measures its overall duration. The young rat is then removed from the adult rat's cage and is placed in its own cage until the second introduction. The adult rat is given the compound under test and, after 2 hours, is again brought into the presence (5 minutes) of the young rat. The social recognition behaviour is then observed again and its duration measured. The assessment criterion is the difference (T2-T1), expressed in seconds, between the “recognition” times of the 2 encounters.
The results obtained show a difference (T2-T1) ranging from −20 s to −45 s for doses ranging from 0.3 to 3 mg/kg, which shows that the compounds of the invention very greatly enhance memorisation, even at a low dose.
The object recognition test in the Wistar rat was initially developed by ENNACEUR and DELACOUR (Behav. Brain Res., 1988, 31, 47-59). The test is based on the spontaneous exploratory activity of the animal and has the characteristics of episodic memory in humans. This memory test is sensitive to ageing (SCALI et al., Eur. J. Pharmacol., 1997, 325, 173-180) and to cholinergic dysfunctions (BARTOLINI et al., Pharm. Biochem. Behav. 1996, 53(2), 277-283) and is based on the differences in the exploration of 2 objects of fairly similar shape—one familiar, the other new. Prior to the test, the animals are habituated to the environment (an enclosure without an object). In the course of a first session, the rats are placed (3 minutes) in the enclosure, in which there are 2 identical objects. The duration of exploration is measured for each object. In the course of the second session (3 minutes), 24 hours later, 1 of the 2 objects is replaced by a new object. The duration of exploration is measured for each object. The assessment criterion is the difference, Delta, expressed in seconds, between the exploration times for the new object and for the familiar object in the course of the second session. The control animals, previously treated with the carrier by the IP route 30 minutes before each session, explore the familiar object and the new object in an identical manner, which indicates that the object introduced earlier has been forgotten. Animals treated with a compound that facilitates mnemocognition preferentially explore the new object, which indicates that the object introduced earlier has been remembered.
The results obtained show a difference, Delta, ranging from 5 s to 10 s, for doses ranging from 0.03 to 3 mg/kg, which shows that the compounds of the invention greatly enhance memorisation, even at a very low dose.
Formulation for the preparation of 1000 tablets each comprising 10 mg of active ingredient:
| Number | Date | Country | Kind |
|---|---|---|---|
| 99.05690 | May 1999 | FR | national |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 09564527 | May 2000 | US |
| Child | 10377843 | Mar 2003 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10844956 | May 2004 | US |
| Child | 11438169 | May 2006 | US |
| Parent | 10377843 | Mar 2003 | US |
| Child | 10844956 | May 2004 | US |
