Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
  • C07D295/027—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring
  • C07D295/033—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements containing only one hetero ring with the ring nitrogen atoms directly attached to carbocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
  • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/22—Anxiolytics
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/24—Antidepressants
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P25/00—Drugs for disorders of the nervous system
  • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P9/00—Drugs for disorders of the cardiovascular system
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/02—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms containing only hydrogen and carbon atoms in addition to the ring hetero elements
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
  • C07D295/096—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings

Definitions

• X represents a hydrogen atom, a hydroxy group, a C ⁇ _ C 3 alkoxy group or a cyclopropylmethoxy group
• Y represents a hydrogen atom, a hydroxy group or a methoxy group.
• the compounds according to the invention can exist in the form of bases or of addition salts.
• the compounds of general formula (I) can be prepared by methods illustrated by schemes 1 to 3 which follow.
• an LH-indene-3-acetic acid derivative of general formula (II) is treated, in which Y 'represents a hydrogen atom or a methoxy group, with a reducing agent, simple or complex, such as an alkaline or metallic hydride, for example lithium hydride and Diagram 1
• This alcohol is then treated with 4-methylbenzenesulfonic acid chloride, in the presence of an organic base such as triethylamine or pyridine, and optionally in the presence of an inert solvent, at a temperature of 0 to 40 °. C, to obtain the derivative of general formula (IV).
• the latter is then reacted with a piperazine derivative of general formula (V), in which X is as defined above, at a temperature of 100 to 150 ° C, preferably at 130 ° C, optionally in a solvent with a high boiling point, such as toluene, xylene, N, N-dimethylformamide or 1-methylpyrrolidin-2-one, to obtain the derivative of general formula (VI).
• a compound of general formula (VI), in which Y 'represents a methoxy group is subjected to demethylation by means of boron tribro ⁇ , in an inert aprotic solvent, for example dichloromethane, at a temperature of -70 ° C to -5 ° C.
• a 2,3-dihydro-1H-indene-1-ethanol derivative of general formula (VII), in which Y is as defined above, is reacted with 4- acid chloride methylbenzenesulfonic, in the presence of an organic base, for example triethylamine or pyridine, optionally in an inert solvent, at a temperature of 0 to 40 ° C, to obtain a derivative of general formula (VIII).
• an organic base for example triethylamine or pyridine
• an inert solvent optionally in an inert solvent
• a derivative of 2,3-dihydro-1H-indene-1-acetic acid, racemic or optically pure, of general formula (IX) is treated, in which Y is as defined above, with N, N '-carbonyldiimidazole, in an inert solvent, for example a chlorinated or ethereal solvent such as dichloromethane or tetrahydrofuran, at a temperature of 20 to 50 ° C, to obtain the corresponding imidazolide, then this is treated last with a piperazine derivative of general formula (V), in which X is as defined above, to obtain an amide of general formula (X), and finally Diagram 3
• a simple or complex reducing agent such as an alkali metal hydride, for example lithium aluminum hydride
• an aromatic or ethereal inert solvent for example toluene, tetrahydrofuran or dioxane
• a simple or complex reducing agent such as an alkali metal hydride, for example lithium aluminum hydride
• an aromatic or ethereal inert solvent for example toluene, tetrahydrofuran or dioxane
• the compounds of general formula (I) in which X and Y each represent a hydroxy group can be obtained by conventional methods, for example by treatment of the corresponding compounds in which X and Y each represent a methoxy group with an agent such as tribromide boron, in an inert solvent such as dichloromethane, at a temperature of -20 to + 40 ° C.
• the racemic acids of general formula (IX) can be obtained by catalytic hydrogenation of the mixture of esters mentioned above with respect to the starting acids of general formula (II), according to the method described in J. Am. Chem. Soc. (1952) 74 2274, followed by hydrolysis, or by catalytic hydroge ⁇ nation of these acids themselves.
• the starting acids of general formula (IX) optically pure can be obtained from the corresponding racemates, by splitting by means of an optically pure chiral amine, for example (+) - or (-) - ⁇ -phenylethylamine, according to J. Am. Chem. Soc. (1992) 114 2181. They can also be obtained from the corresponding racemic esters by enantioselective hydrolysis by means of enzymes such as lipases, for example pseudomonas or acetone powder from pig liver.
• the mixture is allowed to cool, it is hydrolyzed with 1.6 ml of 10% aqueous potassium and sodium double tartrate solution, it is heated to boiling for 1 h, it is filtered, rinsing the residue with tetrahydrofuran, and the filtrate is evaporated under reduced pressure.
• the brain is removed and the hippocampus is excised.
• the tissue is ground in an Ultra-Turrax Polytron apparatus for 30 seconds at half the maximum speed in 10 volumes of 50 mM Tris buffer, pH adjusted to 7.4, with hydrochloric acid (i.e. 100 mg of fresh tissue per ml).
• the homogenized tissues are washed three times at 4 ° C, centrifuging them each time for 10 min at 48000 ⁇ g and resuspending the pellet in fresh cooled buffer. Finally, the last pellet is suspended in the buffer to arrive at a concentration of 100 mg of starting tissue per ml of 50 mM buffer. Then allowed to incubate at 37 ° C for 10 min.
• the binding with [ 3 H] -8-OH-DPAT (1 nM) is determined by incubation of 100 ⁇ l of suspension of membranes in a final volume of 1 ml of buffer containing 10 ⁇ M of pargyline and 3 ⁇ M of paroxetine.
• the membranes are recovered by filtration on Whatman GF / B TM filters which are washed three times with aliquots of 5 ml of ice-cold buffer.
• the filters are extracted from the scintillation liquid and the radioactivity is measured by liquid scintigraphy.
• the specific binding of [ 3 H] -8-OH-DPAT is defined as the radioactive amount retained on the filters and which can be inhibited by co-incubation in 5-hydroxy tryptamine at 10 ⁇ M.
• the specific binding represents 90% of the total radioactivity recovered on the filter.
• the concentration IC 50 a concentration which inhibits 50% of the binding.
• the IC 50 are between 1 and 300 nM.
• the compounds of the invention have also been the subject of an in vitro study as to their affinity for the 5HT 1D serotoninergic receptors present in the caudate nucleus of cattle, demonstrated by the displacement of a specific brand ligand, t H] -5-hydroxytryptamine, essentially as described by Heuring and Peroutka in J. Neurosci. , (1987), 7, 804-903.
• the caudate bovine nucleus (Collectorgane, Paris) is stored at -80 ° C until use.
• the tissue is ground in an Ultra-Turrax PolytronTM apparatus for 30 s at half the maximum speed in 10 volumes of 50 mM Tris buffer, the pH of which is adjusted to 7.4 with hydrochloric acid (i.e. 100 mg of fresh tissue per ml).
• the homogenized tissues are washed twice at 4 ° C. and centrifuged for 10 min at 40,000 ⁇ g, the pellet being resuspended each time in ice-cold buffer.
• the last pellet is suspended in the buffer to arrive at a concentration of 100 mg of starting tissue per ml of 50 mM buffer, and left to incubate at 37 ° C for 15 min.
• the membranary suspension is then centrifuged for 10 min at 40,000 ⁇ g and the pellet is resuspended in 8 volumes of incubation medium containing Tris (50 mM), ascorbic acid (0.1%), chloride of calcium (4mM), pargylline (10 ⁇ M), mesulergin (100nM) and 8-hydroxy-dipropylamino-tetralin (100nM), and whose pH is adjusted to 7.4 with hydrochloric acid .
• the bond with [ ⁇ H] -5-hydroxytryptamine (2nM) is determined by incubation of 100 ⁇ l of suspension of membranes in a final volume of 1 ml of incubation medium. After an incubation of 30 min at 37 ° C followed by an incubation of 5 min between 0 and 4 ° C, the membranes are recovered by filtration through Whatman GF / B TM filters which are washed twice with aliquots of 1 ml of ice-cold 50mM Tris buffer, and the pH of which is adjusted to 7.4 with hydrochloric acid. The filters are extracted into the scintillation liquid and the radioactivity is measured by liquid scintigraphy.
• the specific binding of [ 3 H] -5-hydroxytryptamine is defined as the amount of radioactivity retained on the filters and which can be inhibited by co-incubation with 5-hydroxytryptamine at 0.1 ⁇ M. At a concentration of 2nM of [ 3 H] -5-hydroxytryptamine the specific binding represents 70% of the total radioactivity recovered on the filter. For each concentration of compound studied, the percentage of inhibition of the binding with [ 3 H] -5-hydroxyxyptptamine is determined, then the concentration IC 50 , a concentration which inhibits 50% of the binding.
• the most active compounds of the invention in this test, have an IC 50 of less than 40 nM.
• the compounds of the invention have also been the subject of an in vi tro test for displacement of the spiperone bond on the serotonergic receptors (5-HT 2 ) of the rat cerebral cortex.
• 5-HT 2 serotonergic receptors
• the homogeneous mixture is centrifuged at 40000 ⁇ g for 10 min then, twice, the pellet is recovered, it is washed by suspending it in the same buffer mixture, it is homogenized again and it is centrifuged. Finally, the final pellet is diluted in the same buffer mixture at the rate of 100 mg of wet tissue for 1 ml of buffer. The tissue is then subjected to a prior incubation of
• the IC 50 concentrations of the compounds of the invention are between 50 and 1500 nM.
• the compounds of the invention were the subject of an in vitro study as to their affinity for the 5HT 1C serotoninergic receptors present in the pig choroid plexus, demonstrated by the displacement of the ligand binding.
• specific labeled [H] mesulergin essentially as described by Pazos et al. in Eur. J. Pharmacol. , (1984), 106, 539-546, and by Yagalof and Hartig in Mol. Pharmacol. , (1986), 26, 120-125.
• the choroid plexus (Collectorgane, Paris) is stored at -80 ° C until use.
• the tissue is homogenized in a Potter TM homogenizer by 10 a-. 15 movements (800 rpm) in 10 volumes of sucrose (0.32M) at a temperature of 0 to 4 ° C.
• the membrane suspension is centrifuged for 10 min at lOOOxg (4 ° C) and the supernatant is centrifuged for 20 min at 30,000xg (4 ° C).
• the pellet is suspended in 10 volumes of 50 mM Tris buffer, pH adjusted to 7.4 with hydrochloric acid, and is then incubated at 37 ° C for 15 min.
• the binding with [ 3 H] mesulergin (lnM) is determined by incubation of 100 ⁇ l of suspension of membranes in a final volume of 500 ⁇ l of incubation medium. After an incubation of 30 min at 37 ° C followed by an incubation of 5 min between 0 and 4 ° C, the membranes are recovered by filtration on Whatman GF / B TM filters, previously treated for 30 min with polyethyleneimine at 0.05%, and washed with twice 1 ml of ice-cold 50 mM Tris buffer, the pH of which is adjusted to 7.4 with hydrochloric acid. The filters are extracted into the scintillation liquid and the radioactivity is measured by liquid scintigraphy.
• the specific binding of [ 3 H] mesulergin is defined as the amount of radioactivity retained on the filters and which can be inhibited by co-incubation with 5-hydroxy-tryptamine at 10 ⁇ M. At a lnM concentration of [ 3 H] mes ⁇ sulergin the specific binding represents 90% of the total radioactivity recovered on the filter.
• the percentage of inhibition of the binding with [ 3 H] mesuler ⁇ gine is determined, then the concentration IC 50 , a concentration which inhibits 50% of the binding.
• the compounds of the invention have, in this test, IC 50 values of 5 to 500 nM.
• the results of the tests show that the compounds of the invention have a strong affinity for serotonergic receptors of the 5HT 1A , 5HT 1D and 5HT 1C types, as well as a moderate affinity for the 5HT 2 receptors.
• the compounds can be used for the treatment of all conditions linked to dysfunctions of the serotonergic receptors of the 5HT 1A , 5HT 1D , 5HT 1C and / or 5HT 2 type , in particular for the treatment of anxiety states, depression, including psychotic depression, sleep disorders, phobias, panic states, obsessive compulsive disorder, alcohol or drug abuse or withdrawal disorders, productive or schizophrenia deficient, neuroleptic-induced acute or chronic extrapyramidal syndromes, disorders of sexual behavior, for the regulation of food, and also for the treatment of vascular or cardiovascular disorders such as migraine and hypertension.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• Engineering & Computer Science (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Veterinary Medicine (AREA)
• Public Health (AREA)
• General Health & Medical Sciences (AREA)
• Medicinal Chemistry (AREA)
• Animal Behavior & Ethology (AREA)
• Pharmacology & Pharmacy (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Biomedical Technology (AREA)
• Neurosurgery (AREA)
• Neurology (AREA)
• Psychiatry (AREA)
• Cardiology (AREA)
• Addiction (AREA)
• Heart & Thoracic Surgery (AREA)
• Pain & Pain Management (AREA)
• Epidemiology (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
• Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Applications Claiming Priority (3)

Publications (1)

Family

ID=9481836

Family Applications (1)

Country Status (20)

Families Citing this family (2)

Family Cites Families (6)

• 1995
  • 1995-08-09 FR FR9509684A patent/FR2737724B1/fr not_active Expired - Fee Related
• 1996
  • 1996-08-01 NZ NZ315363A patent/NZ315363A/xx unknown
  • 1996-08-01 PL PL96324966A patent/PL324966A1/xx unknown
  • 1996-08-01 WO PCT/FR1996/001216 patent/WO1997006155A1/fr not_active Application Discontinuation
  • 1996-08-01 JP JP9508161A patent/JP2000501699A/ja active Pending
  • 1996-08-01 IL IL12318796A patent/IL123187A0/xx unknown
  • 1996-08-01 SK SK167-98A patent/SK16798A3/sk unknown
  • 1996-08-01 CN CN96197512A patent/CN1199398A/zh active Pending
  • 1996-08-01 BR BR9609977A patent/BR9609977A/pt not_active Application Discontinuation
  • 1996-08-01 CA CA002228843A patent/CA2228843A1/en not_active Abandoned
  • 1996-08-01 CZ CZ98368A patent/CZ36898A3/cs unknown
  • 1996-08-01 AU AU67053/96A patent/AU707372B2/en not_active Ceased
  • 1996-08-01 EP EP96927120A patent/EP0843670A1/fr not_active Withdrawn
  • 1996-08-01 KR KR1019980700615A patent/KR19990035954A/ko not_active Application Discontinuation
  • 1996-08-01 HU HU9802546A patent/HUP9802546A3/hu unknown
  • 1996-08-01 US US09/011,807 patent/US5929078A/en not_active Expired - Fee Related
  • 1996-08-06 CO CO96041580A patent/CO4750833A1/es unknown
  • 1996-08-08 ZA ZA9606772A patent/ZA966772B/xx unknown
  • 1996-08-08 AR ARP960103928A patent/AR003222A1/es unknown
• 1998
  • 1998-02-06 NO NO980529A patent/NO980529L/no not_active Application Discontinuation

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events