EP0000322B1 - Compounds having an anti-depressive or tranquilizing activity, pharmaceutical compositions containing them, and processes and intermediates for their preparation - Google Patents
Compounds having an anti-depressive or tranquilizing activity, pharmaceutical compositions containing them, and processes and intermediates for their preparation Download PDFInfo
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- EP0000322B1 EP0000322B1 EP78850006A EP78850006A EP0000322B1 EP 0000322 B1 EP0000322 B1 EP 0000322B1 EP 78850006 A EP78850006 A EP 78850006A EP 78850006 A EP78850006 A EP 78850006A EP 0000322 B1 EP0000322 B1 EP 0000322B1
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- 0 CC(CCC1)CCC1(*)C1(C)CCCCC1 Chemical compound CC(CCC1)CCC1(*)C1(C)CCCCC1 0.000 description 4
- QABPHCOJPSYIIS-MOSHPQCFSA-N CC(/C=C(\C1C(C2CC=CCC2)C=CNC1)/c(cc1)ccc1Br)N Chemical compound CC(/C=C(\C1C(C2CC=CCC2)C=CNC1)/c(cc1)ccc1Br)N QABPHCOJPSYIIS-MOSHPQCFSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
- C07C17/14—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms in the side-chain of aromatic compounds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/2635—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions involving a phosphorus compound, e.g. Wittig synthesis
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/54—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
- C07C217/56—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms
- C07C217/62—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups bound to carbon atoms of at least one six-membered aromatic ring and amino groups bound to acyclic carbon atoms or to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by carbon chains not further substituted by singly-bound oxygen atoms linked by carbon chains having at least three carbon atoms between the amino groups and the six-membered aromatic ring or the condensed ring system containing that ring
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/69—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to carbon-to-carbon double or triple bonds
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C07C45/74—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with dehydration
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/20—Unsaturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/213—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing six-membered aromatic rings
- C07C49/217—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing six-membered aromatic rings having unsaturation outside the aromatic rings
- C07C49/223—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing six-membered aromatic rings having unsaturation outside the aromatic rings polycyclic
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/20—Unsaturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/227—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing halogen
- C07C49/233—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings
- C07C49/235—Unsaturated compounds containing keto groups bound to acyclic carbon atoms containing halogen containing six-membered aromatic rings having unsaturation outside the aromatic rings
Definitions
- the present invention is related to new compounds of the diarylalkylamine type having thereapeutic activity, to methods for preparing such compounds, to pharmaceutical preparations comprising such compounds and to methods of treatment employing such compounds.
- the object of the invention is to obtain compounds having a therapeutical activity in the central nervous system, especially an anti-depressive or a tranquilizing activity.
- British Patent 1,429,068 discloses compounds corresponding to the general formula: having anti-depressive activity.
- Belgian Patent 835,802 discloses compounds of the general formula: having anti-depressive activity.
- South African Patent 62/4154 discloses i.a. a compound having the formula claimed to have a therapeutic utility especially as an antitussive.
- Chemical Abstract vol. 82 (1975) 170339c discloses the compound of the formula as a chemical intermediate.
- Ar represents the group wherein Y is bound in the 2-, 3-, or 4-position and represents a lower alkyl group, a lower alkoxy group, a halogen, a trifluoromethyl group, or an amino or a mono- or di-lower alkyl amino group, or Ar represents a pyridyl group bound in the 2-, 3- or 4-position,
- X represents hydrogen, a lower alkyl group, a lower alkoxy group, a halogen, a trifluoromethyl group, an amino group or a mono- or di-lower alkyl amino group
- R is a lower alkyl group and R 1 is hydrogen or a lower alkyl group.
- lower alkyl and alkoxy groups are meant groups comprising up to 3 carbon atoms.
- Halogen may be any of the elements F, Cl, Br or I.
- Therapeutically acceptable salts of the compounds of the invention as well as differently hydrated or anhydrous forms of such compounds or salts are within the scope of the invention.
- the compounds of formula la above wherein Ar is identical to the group contain one asymmetric carbon atom.
- the remaining compounds of formula la contain two asymmetric carbon atoms and can therefore exist in two diastereomeric forms which can be separated by methods known in the art.
- the compounds of formula la above may be resolved into their optical enantiomers by using optically active acids such as i.a. tartaric acid, mandelic acid, dibenzoyl tartaric acid as known in the art.
- the compounds of the invention may be used as mixtures of diastereomeric forms or as racemic mixtures of the pure diastereomers or as the pure enantiomers mentioned above.
- the therapeutic properties may reside to a greater or lesser extent in one of the enantiomers or mixtures mentioned above.
- the compound of formula Ib in which the group Ar is not identical with the group may exist in different stereoisomeric forms, that is in cis-trans isomers or, according to the IUPAC nomenclature (J. Org. Chem. 35, 2849-2867, Sept. 1970), in an E-form and a Z-form.
- the compound may be used therapeutically as a mixture of geometrical isomers or in pure E or Z form.
- the pure geometrical isomers may be prepared from an isomer mixture, from an isomer-pure starting material or directly by a stereoselective synthesis.
- All the compounds of formula Ib further contain one asymmetric carbon atom.
- the compounds of formula Ib may be resolved into their optical enantiomers by using optically active acids such as i.a. tartaric acid, mandelic acid, dibenzoyl tartaric acid as known in the art.
- optically active acids such as i.a. tartaric acid, mandelic acid, dibenzoyl tartaric acid as known in the art.
- the compounds of formula Ib may be used as mixtures especially racemic mixtures, or as the pure enantiomers of the geometrical isomers mentioned above.
- the therapeutic properties may reside to a greater or lesser extent in one of the enantiomers or mixtures mentioned above.
- the invention relates in one aspect to pharmaceutical compositions comprising as active ingredient a therapeutically effective amount of a compound of the formula I.
- the invention relates also to compounds of the formula I for use in the treatment of depressions and for use in the treatment of anxiety.
- the invention also relates to such compounds per se of the formula I wherein X is hydrogen.
- the compounds of the invention show an activity in the central nervous system which makes them useful as neuropharmacological agents for treatment of various diseases in animals including man.
- the compounds are expected to be especially useful as anti-depressive, anxiolytic or tranquilizing agents in man.
- R 1 represents hydrogen and R represents a methyl group.
- the compounds of the formula I may be prepared by
- the intermediates of formula II may be prepared by reacting the ketone of the formula IV above a hydroxylamine derivative of formula NH 2 0R I , wherein R 1 has the meaning defined above.
- the intermediate of formula III may be prepared by hydride reduction of the compound of formula IV which, in turn, may be obtained by
- the compounds of formula la are preferably prepared by method a).
- the reaction according to method a) is preferably performed in diethyl ether with a slight excess of lithium aluminium hydride under inert atmosphere.
- the new compounds of formula la may be used therapeutically as the racemic mixtures of (+)-and (-)-forms, which in the usual case are obtained at the synthesis. Isomer mixtures obtained may be resolved by methods known per se into corresponding optically active modifications. If desired, the optically active modifications may be prepared by way of direct synthesis, e.g. via an optically active compound as described above.
- the compounds of the formula I in the invention may be prepared by:
- the dehydration of the starting material may be done by means of treatment with hydrochloric acid HCI and heating of the reaction mixture.
- the dehydration of the starting material may also be done by means of other types of acid-catalysis, such as by means of sulfuric acid H 2 SO 4 , phosphoric acid H 3 P0 4 , potassium hydrogen sulphate KHS0 4 , or oxalic acid (COOH) 2 .
- Other methods for the dehydration of the starting material to the formation of a compound of the formula I are dehydration using phosphoroxichloride POCI 3 in pyridine, and dehydration with thionylchloride, SOCI 2 , in pyridine.
- a catalytic dehydration of the starting material may be used. The dehydration is in this case carried out at a temperature of about 300 to 500°C using a catalyst such as kaolin, alumina or aluminium oxide.
- This reaction is also useful for preparation of the compounds of formula la by employing as a starting material a saturated compound corresponding to the compound of formula VIII.
- the intermediate formula VIII may be isolated (cf. Example 15) and subsequently dehydrated or alternatively the crude product in the preparation of formula VII may be dehydrated directly (cf. Example 17).
- Z 1 Br
- Z 1 OH
- the latter compound may be transformed to a reactive derivative III by treatment with an agent such as SOCl; 2 , SOBr 2 or PBr 3 or with ClSO 2 R 1 .
- the compounds of the formula I will normally be administered orally, rectally or by injection, in the form of pharmaceutical preparations comprising the active ingredient either as a free base or as a pharmaceutically acceptable non-toxic, acid addition salt, e.g. the hydrochloride, hydrobromide, lactate, acetate, phosphate, sulphate, sulphamate, citrate, tartrate, oxalate and the like in association with a pharmaceutically acceptable carrier.
- a pharmaceutically acceptable non-toxic, acid addition salt e.g. the hydrochloride, hydrobromide, lactate, acetate, phosphate, sulphate, sulphamate, citrate, tartrate, oxalate and the like in association with a pharmaceutically acceptable carrier.
- the carrier may be a solid, semisolid or liquid diluent or capsule.
- These pharmaceutical preparations constitute a further aspect of this invention.
- the active substance will constitute from 0.1 to 99% by weight of the preparation, more specifically between 0.5 and 20% by weight for preparations intended for injection and between 2 and 50% by weight for preparations suitable for oral administration.
- the selected compound may be mixed with a solid pulverulent carrier, e.g. lactose, saccharose, sorbitol, mannitol, starches such as potato starch, corn starch or amylopectin, cellulose derivatives, a binder such as gelatine or polyvinyl-pyrrolidone, and a lubricant such as magnesium stearate, calcium stearate, polyethylene glycol waxes, and the like, and then compressed to form tablets.
- a solid pulverulent carrier e.g. lactose, saccharose, sorbitol, mannitol, starches such as potato starch, corn starch or amylopectin, cellulose derivatives, a binder such as gelatine or polyvinyl-pyrrolidone, and a lubricant such as magnesium stearate, calcium stearate, polyethylene glycol waxes, and the like, and then compressed to form tablets.
- the tablet can be coated with a lacquer in a readily volatile organic solvent or mixture of organic solvents.
- Dyestuff may be added to these coatings in order to readily distinguish between tablets containing different active substances or different amounts of the active compounds.
- soft gelatine capsules pearl shaped closed capsules consisting of gelatine and for example, glycerol or similar closed capsules
- the active substance may be admixed with a vegetable oil.
- Hard gelatine capsules may contain granulates of the active substance in combination with solid, pulverulent carriers such as lactose, saccharose, sorbitol, mannitol, starches (e.g. potato starch, corn starch or amylopectin), cellulose derivatives or gelatine.
- Dosage units for rectal application can be prepared in the form of suppositories comprising the active substance in admixture with a neutral fatty base, or gelatine rectal capsules comprising the active substance in admixture with vegetable oil or paraffin oil.
- Liquid preparations for oral application may be in the form of syrups or suspensions, for example, solutions containing from about 0.2% to about 20% by weight of the active substance herein described, the balance being sugar and a mixture of ethanol, water, glycerol, and propyleneglycol.
- Such liquid preparations may contain colouring agents, flavouring agents, saccarine and carboxymethylcellulose as a thickening agent.
- Solutions for parenteral applications by injection can be prepared in an aqueous solution of a water-soluble pharmaceutically acceptable salt of the active substance preferably in a concentration of from about 0.5% to about 10% by weight.
- These solutions may also contain stabilizing agents and/or buffering agents and may conveniently be provided in various dosage unit ampoules.
- Suitable daily doses of the compounds of the formula I in therapeutic treatment is 25 to 250 mg for peroral administration, preferably 50 to 150 mg, and 5 to 50 mg for parenteral administration preferably 10 to 30 mg.
- a preparation in dosage unit form for oral administration may contain 10 to 50 mg, preferably 10 to 25 mg of active substance per dosage unit.
- the solvents of the first mother liquors of the diamine oxalate prepared according to example 2 were evaporated and the residue was extracted with ether from an alkaline solution. There was obtained 1.2 g of free amine.
- the fumarate was prepared in ethyl acetate from half an equivalent of fumaric acid and recrystallized twice from acetonitrile-isopropylalcohol affording 0.28 g of the pure beta isomer as the diamine fumarate, mp 184-186°C.
- the oxalate had mp 106-111°C from acetone.
- the maleate was prepared by addition of a hot ethanolic solution of 4.9 g of maleic acid into a warm solution of the amine in 100 ml of ethyl acetate. Recrystallization from EtOH-EtOAc gave 8.4 g of the maleate, mp 158-161 °C.
- 3,3-di-(4-fluorophenyl)-1-methylallylamine (0.9 g, 0.003 mol) was dissolved in 100 ml of ethanol and transferred to a Parr hydrogenation flask. 1.0 ml of concentrated hydrochloric acid was added followed by 0.2 g of 5% palladium on charcoal. The hydrogenation was effected at a pressure of 3.9 atm for 5.5 hours. The reaction mixture was filtered to remove the catalyst and the solvent of the filtrate was evaporated. Crystallization from EtOAc-i-Pr 2 0 gave 0.75 g of the desired product, mp 225-229°C.
- the mixture was stirred and then made alkaline and filtered. After separation of the ether phase the aqueous phase was extracted with ether. The combined ethereal layers were extracted twice with 2 M hydrogen chloride. The aqueous phase was made alkaline and extracted with ether and dried over sodium sulphate. After evaporation of the solvent 10.1 g of yellow oil was obtained, which was dissolved in 75 ml of acetic acid and 15 ml of conc. aqueous hydrogen chloride.
- the amine was converted to the fumarate, which was recrystallized twice from ethanol/ethyl acetate/hexane to give 6.2 g (17% yield) of the fumaric acid salt in the form C 18 H 21 NO 2 ⁇ 3/4C 4 H 4 O 4 . M.p. 167167.5°C.
- the product was extracted with 3 x 50 ml of 0.5 M HCI, the combined aqueous layer was made alkaline with 10 M NaOH and extracted with 2 x 50 ml of ether. Drying and evaporation of the solvent gave 0.23 g of the title compound as an oil.
- the maleate had m.p. 174-176°C from ethanol.
- the UV spectrum in ethanol had ⁇ max 237 nm.
- NMR of a sample in CDCI 3 showed a double quartet at 5.0 ppm from TMS and a doublet at 6.6 ppm.
- TLC on silica in diisopropylether showed a spot with Rf 0.28, identical with the Rf-value of the material prepared according to Example 22.
- 500 g of active substance were mixed with 500 g of corn oil, whereupon the mixture was filled in soft gelatin capsules, each capsule containing 100 mg of the mxiture (i.e. 50 mg of active substance).
- depressions are considered to be connected with changes in the biochemical processes of the brain which processes control the mood.
- the nature of these biochemical processes are largely unknown but in depressive states there is evidence for a decreased activity of monoaminergic brain neurons.
- the monoamines, noradrenaline (NA), dopamine (DA) and 5-hydroxytryptamine (5-HT), are of great interest in this respect.
- NA, DA and 5-HT is localised in three different types on neurons and may function as transmittors in the central nervous system.
- the monoamines are stored in special structures, granules, situated in enlargements of the nerve endings, varicosities.
- the varicosity is separated from the effector neuron by a space, the synaptic cleft or Simonm.
- the transmittor is released from the granule into the synaptic cleft and reaches the receptor of the effector neuron and generates a nerve impulse.
- the amines After impulse generation the amines are inactivated by mainly two mechanisms: a re-uptake mechanism at the cell membrane and enzymatic conversion by catechol-0-methyltransferase to form methylated metabolites. There is also an inactivating enzyme within the varicosities, monoamine oxidase (MAO), that is stored in the mitochondria and inactivates the amines intracellularly.
- MAO monoamine oxidase
- An antidepressant effect should thus be obtained with compounds which are able to inhibit the re-uptake of one or both NA and 5-HT.
- test method described in Europ. J. Pharmacol. 17, 107, 1972. This method involves the measurement of the decrease in the uptake of 14C-5-hydroxytryptamine ( 14 C-5-HT) and 3 H-noradrenaline ( 3 H-NA) in brain slices from mice after in vivo and in vitro administration of the test substance.
- 14 C-5-HT 14C-5-hydroxytryptamine
- 3 H-NA 3 H-noradrenaline
- test substances were administered intraperitoneally half an hour before the animals were killed.
- the midbrain was taken out, sliced and incubated in a mixture consisting of 0.2 nmole of 14 C-5-HT, 0.2 nmole of 3 H-NA and 11 ⁇ mole of glucose in 2 ml of Krebs Henseleit-buffer, pH 7.4 per 100 mg of brain slices.
- the incubation time was 5 minutes with 5 minutes of preincubation before the labelled amines were added.
- the slices were dissolved in Soluene (Trade Mark) and the amounts of radioactive amines taken up were determined by liquid scintillation.
- the doses producing 50 percent decrease of the active uptake (ED 50 ) of 14 C-5-HT and 3 H-NA were determined graphically from dose response curves. Active uptake is defined as that part of the radioactive uptake which is inhibited by a high concentration of cocaine.
- the pharmacological tests show that the compounds are able to inhibit the uptake of noradrenaline and 5-hydroxytryptamine.
- a pronounced non-selective activity is shown for the compounds having codes CPK 170, CPK 171, CPK 180 and CPK 184.
- a pronounced selective activity on uptake of noradrenaline is seen in compounds CPK 185, CPK 215 and CPK 217 while a pronounced selective activity on uptake of 5-hydroxytryptamine is seen in compounds FLA 611, FLA 615, CPK 198 and CPK 204.
- a strong non-selective activity is considered to be especially advantageous, as compounds having such activity may be employed in the treatment of depressions in which the neurotransmittor deficiency is unknown as well as in those cases wherein it is established that the deficiency pertains to both noradrenaline and 5-hydroxytryptamine.
Description
- The present invention is related to new compounds of the diarylalkylamine type having thereapeutic activity, to methods for preparing such compounds, to pharmaceutical preparations comprising such compounds and to methods of treatment employing such compounds.
- The object of the invention is to obtain compounds having a therapeutical activity in the central nervous system, especially an anti-depressive or a tranquilizing activity.
-
- Compounds following within the general formula
-
-
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- Certain intermediates disclosed in the present specification are claimed in a European divisional patent application having no. 80105028.7.
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- In the compounds of formula I Ar represents the group
- The compounds of formula la above wherein Ar is identical to the group
- Due to the lack of free rotation in the double bond the compound of formula Ib in which the group Ar is not identical with the group
- It should be noted that in the IUPAC nomenclature compounds of formula Ib in the form of pure geometrical isomers which are similar in structure may be named the E-form for one subgroup of compounds and the Z-form for another subgroup. The two structural formulas below illustrate this fact.
- All the compounds of formula Ib further contain one asymmetric carbon atom. The compounds of formula Ib may be resolved into their optical enantiomers by using optically active acids such as i.a. tartaric acid, mandelic acid, dibenzoyl tartaric acid as known in the art. The compounds of formula Ib may be used as mixtures especially racemic mixtures, or as the pure enantiomers of the geometrical isomers mentioned above. The therapeutic properties may reside to a greater or lesser extent in one of the enantiomers or mixtures mentioned above.
- The invention relates in one aspect to pharmaceutical compositions comprising as active ingredient a therapeutically effective amount of a compound of the formula I.
- The invention relates also to compounds of the formula I for use in the treatment of depressions and for use in the treatment of anxiety.
- The invention also relates to such compounds per se of the formula I wherein X is hydrogen.
- The compounds of the invention show an activity in the central nervous system which makes them useful as neuropharmacological agents for treatment of various diseases in animals including man. The compounds are expected to be especially useful as anti-depressive, anxiolytic or tranquilizing agents in man.
-
- As preferred individual compounds should be mentioned:
- (β)-3-(4-fluorophenyl)-1-methyl-3-phenylpropylamine,
- (β)-3-(4-bromophenyl)-1-methyl-3-phenylpropylamine,
- (a)-3-(4-methoxyphenyl)-1-methyl-3-phenylpropylamine, and
- (/3)-3-(3-bromophenyl)-1-methyl-3-phenylpropylamine being non-selective inhibitors of neuronal noradrenaline and 5-hydroxytryptamine uptake;
- (a)-3-(2-bromophenyl)-1-methyl-3-phenylpropylamine,
- (E)-3-amino-1-(3-bromophenyl)-1-phenylbutene, and
- (Z)-3-amino-1-(3-bromophenyl)-1-phenylbutene being selective inhibitors of neuronal noradrenaline uptake; and
- 3-amino-1,1-di-(4-methoxyphenyl)-1-butene,
- 3,3-di-(4-fluorophenyl)-1 -methylpropylamine,
- (β)-3-(4-methoxyphenyl)-1-methyl-3-phenylpropylamine, and
- (E)-3-amino-1-(4-bromophenyl)-1-phenylbutene,
- Generally preferred in all classes of the compounds of the invention are those wherein R1 represents hydrogen and R represents a methyl group.
- The compounds of the formula I may be prepared by
- a) reducing a compound of the formula
- b) preparing a reactive ester of an alcohol of the formula
- c) reducing a compound of the formula
- d) reacting a ketone of the formula
- The intermediates of formulae II, III, and IV above are novel.
- The intermediates of formula II may be prepared by reacting the ketone of the formula IV above a hydroxylamine derivative of formula NH20RI, wherein R1 has the meaning defined above.
- The intermediate of formula III may be prepared by hydride reduction of the compound of formula IV which, in turn, may be obtained by
- 1) reacting an alpha, beta-unsaturated ketone of the formula
- 2) reacting a diarylcarbinol of the formula
- The compounds of formula la are preferably prepared by method a). The reaction according to method a) is preferably performed in diethyl ether with a slight excess of lithium aluminium hydride under inert atmosphere.
- The new compounds of formula la may be used therapeutically as the racemic mixtures of (+)-and (-)-forms, which in the usual case are obtained at the synthesis. Isomer mixtures obtained may be resolved by methods known per se into corresponding optically active modifications. If desired, the optically active modifications may be prepared by way of direct synthesis, e.g. via an optically active compound as described above.
- The compounds of the formula I in the invention may be prepared by:
- e) Dehydration of a carbinol of the formula
- The dehydration of the starting material may be done by means of treatment with hydrochloric acid HCI and heating of the reaction mixture. The dehydration of the starting material may also be done by means of other types of acid-catalysis, such as by means of sulfuric acid H2SO4, phosphoric acid H3P04, potassium hydrogen sulphate KHS04, or oxalic acid (COOH)2. Other methods for the dehydration of the starting material to the formation of a compound of the formula I are dehydration using phosphoroxichloride POCI3 in pyridine, and dehydration with thionylchloride, SOCI2, in pyridine. Also a catalytic dehydration of the starting material may be used. The dehydration is in this case carried out at a temperature of about 300 to 500°C using a catalyst such as kaolin, alumina or aluminium oxide.
- f) Reaction of a compound of the formula
- This reaction is also useful for preparation of the compounds of formula la by employing as a starting material a saturated compound corresponding to the compound of formula VIII.
- g) Oxidation (halogenation) of the benzylic carbon atom of a compound of formula IX
- The intermediates of formulae VII, VIII, IX and X above are novel.
-
- The intermediate formula VIII may be isolated (cf. Example 15) and subsequently dehydrated or alternatively the crude product in the preparation of formula VII may be dehydrated directly (cf. Example 17).
- The intermediate of formula VIII may be obtained from a compound of formula
- In clinical practice the compounds of the formula I will normally be administered orally, rectally or by injection, in the form of pharmaceutical preparations comprising the active ingredient either as a free base or as a pharmaceutically acceptable non-toxic, acid addition salt, e.g. the hydrochloride, hydrobromide, lactate, acetate, phosphate, sulphate, sulphamate, citrate, tartrate, oxalate and the like in association with a pharmaceutically acceptable carrier. Accordingly, terms relating to the compounds of the formula I whether generically or specifically are intended to include both the free amine base and the acid addition salts of the free base, unless the context in which such terms are used, e.g. in the specific examples would be inconsistent with the broad concept. The carrier may be a solid, semisolid or liquid diluent or capsule. These pharmaceutical preparations constitute a further aspect of this invention. Usually the active substance will constitute from 0.1 to 99% by weight of the preparation, more specifically between 0.5 and 20% by weight for preparations intended for injection and between 2 and 50% by weight for preparations suitable for oral administration.
- To produce pharmaceutical preparations containing a compound of the formula I in the form of dosage units for oral application the selected compound may be mixed with a solid pulverulent carrier, e.g. lactose, saccharose, sorbitol, mannitol, starches such as potato starch, corn starch or amylopectin, cellulose derivatives, a binder such as gelatine or polyvinyl-pyrrolidone, and a lubricant such as magnesium stearate, calcium stearate, polyethylene glycol waxes, and the like, and then compressed to form tablets. If coated tablets are required, the cores, prepared as described above, may be coated with a concentrated sugar solution which may contain, e.g. gum arabic, gelatine, talcum, titanium dioxide, and the like. Alternatively, the tablet can be coated with a lacquer in a readily volatile organic solvent or mixture of organic solvents. Dyestuff may be added to these coatings in order to readily distinguish between tablets containing different active substances or different amounts of the active compounds.
- For the preparation of soft gelatine capsules (pearl shaped closed capsules) consisting of gelatine and for example, glycerol or similar closed capsules, the active substance may be admixed with a vegetable oil. Hard gelatine capsules may contain granulates of the active substance in combination with solid, pulverulent carriers such as lactose, saccharose, sorbitol, mannitol, starches (e.g. potato starch, corn starch or amylopectin), cellulose derivatives or gelatine.
- Dosage units for rectal application can be prepared in the form of suppositories comprising the active substance in admixture with a neutral fatty base, or gelatine rectal capsules comprising the active substance in admixture with vegetable oil or paraffin oil.
- Liquid preparations for oral application may be in the form of syrups or suspensions, for example, solutions containing from about 0.2% to about 20% by weight of the active substance herein described, the balance being sugar and a mixture of ethanol, water, glycerol, and propyleneglycol. Optionally such liquid preparations may contain colouring agents, flavouring agents, saccarine and carboxymethylcellulose as a thickening agent.
- Solutions for parenteral applications by injection can be prepared in an aqueous solution of a water-soluble pharmaceutically acceptable salt of the active substance preferably in a concentration of from about 0.5% to about 10% by weight. These solutions may also contain stabilizing agents and/or buffering agents and may conveniently be provided in various dosage unit ampoules.
- Suitable daily doses of the compounds of the formula I in therapeutic treatment is 25 to 250 mg for peroral administration, preferably 50 to 150 mg, and 5 to 50 mg for parenteral administration preferably 10 to 30 mg. A preparation in dosage unit form for oral administration may contain 10 to 50 mg, preferably 10 to 25 mg of active substance per dosage unit.
- To 2.4 g (0.10 mol) of magnesium turnings, covered with 20 ml of anhydrous diethyl ether and treated with some crystals of iodine under nitrogen atomosphere, 23.5 g (0.10 mol) of 1,3-dibromobenzene in 80 ml of ether was added. The rate of addition was adjusted, to maintainn a gentle reflux of the solvent. When the Mg turnings had disappeared (30 min) 0.75 g (0.005 mol) of cuprous bromide was added and the mixture was stirred for 10 min at room temperature. A solution of 13.6 g (0.09 mol) of benzalacetone in 100 ml of ether was added dropwise at +10°C. Then the reaction mixture was allowed to reach room temperature for 2 hours. The mixture was poured into 400 ml of 10% aqueous solution of ammonium chloride, the aqueous layer was separated and the product was extracted with 2 x 200 ml of ether. The ethereal layer was washed with water, dried with Na2SO4 and the solvent was evaporated. The crude 4-(3-bromophenyl)-4-phenylbutan-2-one obtained (26.5 g, 0.086 mol) was added to a solution of 20 g (0.28 mol) of hydroxylamine hydrochloride in 300 ml of ethanol and 100 ml of anhydrous pyridine. The mixture was heated under reflux for 4 hours. After cooling the solvent was evaporated in vacuo and the ketoxime was extracted with ether from an aqueous solution. Washing of the extract with water and drying followed by evaporation of the solvent gave 27.5 g of 4-(3-bromophenyl)-4-phenylbutan-2-one oxime.
- To the oxime obtained according to Example 1 (27.5 g) 100 ml of carbon tetrachloride was added and evaporated twice in order to remove traces of water. The residue was dissolved in a mixture of 300 ml of anhydrous ether and 150 ml of anhydrous tetrahydrofuran. To the stirred mixture 3.5 g (0.0086 mol) of lithium aluminium hydride was added in portions under nitrogen atmosphere at room temperature. The reaction mixture was stirred for 8 hours. Then 25 ml of 2M NaOH was dropwise added and the precipitated inorganic salts were removed by filtration. The filtrate was shaken with 3 x 300 ml of 1 M HCI and the combined aqueous layers were made alkaline by addition of 35 ml of 30% NaOH. Extraction with 3 x 200 ml of methylene chloride, washing, drying and evaporation of the solvent gave 8.9 of the primary amine as an oil. To a hot solution of 7.9 g (0.026 mol) of the amine in 100 ml of isopropylalcohol 1.1 g (0.014 mol) of oxalic acid in 10 ml of ethanol was added. 6.2 g of the diamine oxalate was collected. Recrystallization from 160 ml of a mixture of ethanol and isopropylalcohol (1:1) yielded 4.43 g, mp 134-138°C.
- Analysis: C calcd 58.5%, found 58.7%; H calcd 5.48%, found 5.80%; N calcd 4.01%, found 4.07%.
- The free amine (2.9 g, 0.009 mol) obtained from 3.8 g of the oxalate prepared according to Example 2, was dissolved in 40 ml of ethyl acetate. A hot solution of 1.1 g (0.009 mol) of maleic acid in 20 ml of ethanol was added. There was obtained 1.3 g of the maleate. Recrystallization from 18 ml of isopropylalcohol gave 0.65 g of the pure alpha isomer, mp 163-165°C. The high field part of the NMR spectrum (COCI,) displayed a triplet at 4.1 ppm (J=7.8 Hz), a quartet at 2.8 ppm (J=6.2 Hz), a double dublet at 2.0 ppm (two protons) and a doublet at 1.5 ppm (J=6.1 Hz) (three protons).
- Analysis: C calcd 57.15%, found 57.45%; H calcd 5.28%, found 5.35%; Br calcd 19.1%, found 19.05%; N calcd 3.33%, found 3.20%; 0 calcd 15.23%, found 15.00%.
- The solvents of the first mother liquors of the diamine oxalate prepared according to example 2 were evaporated and the residue was extracted with ether from an alkaline solution. There was obtained 1.2 g of free amine. The fumarate was prepared in ethyl acetate from half an equivalent of fumaric acid and recrystallized twice from acetonitrile-isopropylalcohol affording 0.28 g of the pure beta isomer as the diamine fumarate, mp 184-186°C.
- Analysis: C calcd 59.7%, found 60.3%; H calcd 5.6%, found 5.7%; N calcd 3.9%, found 3.7%.
- (a1-3-(4-fluorophenyl)-1-methyl-3-phenylpropylamine oxalate, mp 186-188°C (EtOH-EtOAc, 1:1) and (f3)-3-(4-fluorophenyl)-1-methyl-3-phenylpropylamine hydrochloride, mp 171-172°C (EtOAc) were prepared from 4-(3-fluorophenyl)-4-phenylbutan-2-one oxime in accordance with Examples 2 and 3.
- (a)-3-(4-bromophenyl)-1-methyl-3-phenylpropylamine maleate, mp 168-170°C (EtOH-EtOAc, 1:1) and (β)-3-(4-bromophenyl)-1-methyl-3-phenylpropylamine maleate, mp 161-162°C (i-PrPH-EtOAc, 3:1) were prepared from 4-(4-bromophenyl)-4-phenylbutan-2-one oxime in accordance with Examples 2 and 3.
- (a)-3-(4-methoxyphenyll-1-methyl-3-phenylpropylamine maleate, mp 146-148°C (i-PrOH) and (f3)-3-(4-methoxyphenyl)-1-methyl-3-phenylpropylamine maleate, mp 124-133°C (EtOAc) were prepared from 4-4-methoxyphenyl)-4-phenylbutan-2-one oxime in accordance with Examples 2 and 3.
- (a)-1-methyl-3-(4-trifluoromethylphenyl)-3-phenylpropylamine maleate, mp 165-166°C and (β)-1-methyl-3-(4-trifluoromethylphenyl)-3-phenylpropylamine maleate, mp 165-167°C were prepared from 4-(4-trifluoromethylphenyl)-4-phenylbutan-2-one oxime in accordance with Examples 2 and 3.
- To a solution of 24.3 g (0.13 mol) of 2-bromobenzaldehyde in 80 ml of acetone, 1.0 ml of 10 M NaOH was slowly added at 0°C. The reaction mixture was allowed to reach room temperature and stirred for another 2 hours. Then it was poured into 400 ml of water, to which 10 ml of 2 M HCI had been added. Extraction with ether, drying and evaporation of the solvent gave 18.9 g of 2-bromo- benzalacetone as an oil. This was dissolved in 150 ml of ether and added to a Grignard reagent prepared from 1.1 g (0.045 mol) of magnesium turnings 6.6 g (0.042 mol) of bromobenzene and 0.2 g of CuBr in 150 ml of ether. The mixture was stirred under nitrogen atmosphere for 2 hours. It was poured into 450 ml of ice-water to which 18 g of ammonium chloride had been added. Extraction with ether gave 11.0 g of the desired ketone as an oil.
- (α)-3-12-bromophenyl)-1-methyl-3-phenylpropylamine maleate, mp 145-146°C (i-PrOH) and (f3)-3-(2-bromophenyl)-1-methyl-3-phenyl-propylamine maleate, mp 135-137°C (EtOH-EtOAc, 1:4) were prepared from 4-(2-bromophenyl)-4-phenylbutan-2-one oxime in accordance with Examples 2 and 3.
- The free base of 3-(4-bromophenyl)-1-methyl-3-phenylpropylamine (0.07 g, 0.0023 mol) was dissolved in 50 ml of chloroform. 1.2 ml (0.0024 mol) of 2 M NaOH and 0.25 g (0.0024 mol) of ethyl chloroformate were added separately and dropwise with vigorous stirring at 15°C. Stirring was continued for 2 hours at room temperature.
- Then 25 ml of water was added and the organic layer was separated, dried, and the solvent was evaporated to give 1.0 g of N-ethoxycarbonyl-3-(4-bromophenyl)-1-methyl-3-phenylpropylamine as a colourless oil.
- Treatment of the carbamate with 0.25 g (0.006 mol) of LiAIH4 in 60 ml of ether for 14 hours gave 0.20 g of the secondary amine after extraction with ether/hydrochloride and NaOH/ether. The hydrochloride was prepared and recrystallized from 18 ml of acetone to give 0.12 g, mp 146-148°C.
- The oxalate had mp 106-111°C from acetone.
- A mixture of 22.1 g (0.073 mol) of 4-(3-bromophenyl)-4-phenylbutan-2-one and 230 ml of formamide was heated for 8 hours at 180°C. After cooling water was added and the product was taken up in ether. Drying and evaporation of the solvent gave 30.5 g of a residue.
- To this residue 85 ml of conc. hydrochloric acid was added and the mixture was heated under refluxing conditions for 3 hours. Water was added and the non basic materials were removed by shaking the reaction mixture with 100 ml of ether. The aqueous layer was separated and made alkaline by addition of 120 ml of 10 M NaOH. Extraction with 3 x 200 ml of ether, drying (Na2S04) and evaporation of the solvent gave 12.9 g of the desired amine.
- The maleate was prepared by addition of a hot ethanolic solution of 4.9 g of maleic acid into a warm solution of the amine in 100 ml of ethyl acetate. Recrystallization from EtOH-EtOAc gave 8.4 g of the maleate, mp 158-161 °C.
- Analysis: C calcd 57.2%, found 57.5%; H calcd 5.28%,found 5.35%; Br calcd 19.0%, found 19.1%; N calcd 3.33%, found 3.20%; O calcd 15.2%, found 15.0%.
- 3,3-di-(4-fluorophenyl)-1-methylallylamine (0.9 g, 0.003 mol) was dissolved in 100 ml of ethanol and transferred to a Parr hydrogenation flask. 1.0 ml of concentrated hydrochloric acid was added followed by 0.2 g of 5% palladium on charcoal. The hydrogenation was effected at a pressure of 3.9 atm for 5.5 hours. The reaction mixture was filtered to remove the catalyst and the solvent of the filtrate was evaporated. Crystallization from EtOAc-i-Pr20 gave 0.75 g of the desired product, mp 225-229°C.
- Analysis: C calcd 64.5%, found 64.5%; H calcd 6.09%, found 6.11%; CI calcd 11.9%, found 11.8%; F calcd 12.8%, found 12.7%; N calcd 4.70%, found 4.55%.
- By the same method there were prepared from the appropriate allylamines:
- By the method of Example 12 3,3-di-(4-methoxyphenyl)-1-methyl-propylamine fumarate, mp 153-157°C, (EtOH-i-PrzO) was prepared from the corresponding allylamine.
- By the method of Example 12 1,3',3"-trimethyl-3,3-diphenyl-propylamine oxalate, mp 214-215°C, (EtOH-EtOAc) was prepared from the corresponding allylamine.
- A solution of 81.5 g (0.35 mol) 1,4-dibromobenzene in 500 ml of diethyl ether was added to a stirred mixture of 8.3 g (0.35 mol) magnesium turnings in 25 ml diethyl ether at such a rate that reflux was maintained. After an additional stirring for 1.5 hours at room temperature the mixture was cooled in an ice-bath and a solution of 11.3 g (0.11 mol) of ethyl 3-amino-butyrate in 25 ml of diethyl ether was added during 15 min.
- The mixture was stirred for 1.25 hours at ice-cooling and then for 2.5 hours at reflux. A cold aqueous solution of 25 g ammonium chloride was slowly added, and after stirring the mixture was extracted twice with ether. The ethereal layer was dried over sodium sulphate and the amine was precipitated (10.9 g, 20% yield) with oxalic acid dissolved in ether. M.p. 191-194°C.
- Elemental analysis: C18H19Br2NO5: Found: C 44.5, H 4.0, N 2.7, and O 16.8%. Calculated: C 44.20, H 3.91, N 2.86 and 0 16.35%.
- A solution of 3.8 g 4,4-di(4-bromophenyl)-4-hydroxy-2-butylamine oxalate, 25 ml acetic acid and 5 ml conc. aqueous hydrogen chloride was heated under reflux for 30 min. The solvent was evaporated and the residue was made alkaline with sodium hydroxide and extracted twice with ether. The ethereal layer was dried over sodium sulphate and the solvent was evaporated. Acetronitrile and hydrogen chloride in ether were added and the hydrochloride of the title compound (1.7 g) was obtained after recrystallization from acetonitrile/ether. M.p. 216-220°C.
- Elemental analysis: C16H16Br2CIN; Found: C 46.7, H 3.9, CI 8.8 and N 3.1 %. Calculated: C 46.02, H, 3.86, CI 8.49 and N 3.35%.
- A solution of 58.0 g (0.31 mol) of 4-bromoanisole in 300 ml diethyl ether was added dropwise to a stirred mixture of 7.78 g (0.32 mol) magnesium turnings in 250 ml of diethyl ether during 2 hours. The mixture was stirred at room temperature for another 1.5 hours and then heated under reflux for 1.5 hours. The mixture was cooled in an ice-bath and a solution of 10.3 g (0.10 mol) ethyl 3-aminobutyrate in 25 ml diethyl ether was added during 20 min. After stirring over night at room temperature an aqueous solution of 16.6 g (0.31 mol) ammonium chloride was slowly added. The mixture was stirred and then made alkaline and filtered. After separation of the ether phase the aqueous phase was extracted with ether. The combined ethereal layers were extracted twice with 2 M hydrogen chloride. The aqueous phase was made alkaline and extracted with ether and dried over sodium sulphate. After evaporation of the solvent 10.1 g of yellow oil was obtained, which was dissolved in 75 ml of acetic acid and 15 ml of conc. aqueous hydrogen chloride.
- The solution was heated under reflux for 30 min and then the solvent was evaporated. The residue was made alkaline and extracted with ether. The ethereal layer was washed with water and extracted with 0.5 M hydrogen chloride. The aqueous phase was washed with ether, made alkaline and extracted with ether. After drying over sodium sulphate the ether was evaporated to give 5.9 g of the title compound as an oil in 21% yield.
- The amine was converted to the fumarate, which was recrystallized twice from ethanol/ethyl acetate/hexane to give 6.2 g (17% yield) of the fumaric acid salt in the form C18H21NO2·3/4C4H4O4. M.p. 167167.5°C.
- Elemental analysis: C21H24NO5: Found: C 67.8, H 6.52, N 3.89 and 0 21.5%.Calculated: C 68.09, H 6.53, N 3.78 and 0 21.60%.
- 3-amino-1,1-di-(4-fluorophenyl)-l-butene fumarate was prepared according to Example 17. M.p. 225-231 °C.
- 3-amino-1,1-di-(3-methylphenyl)-1-butene hydrochloride was prepared according to Example 17. M.p. 216-217.5°C.
- Sodium dimethylsulfoxide in DMSO, prepared by heating 3.8 g (0.08 mol) sodium hydride (50% in oil) in 100 ml dimethylsolfoxide at 80°C for 40 min, was mixed with 27.0 g (0.07 mol) propyltriphenylphosphonium bromide, prepared by heating propylbromide and triphenylphosphine in toluene at reflux temperature for 14 hours. The mixture was stirred under nitrogen atmosphere at room temperature for 1.5 hours. THen a solution of 13.1 g (0.05 mol) of 4-bromobenzophenone, in a mixture of 100 ml dimethylsulfoxide and 100 ml of anhydrous tetrahydrofuran was added at room temperature. The reaction mixture was stirred for 2 hours, then it was poured into 1,000 ml of ice-water. The product was extracted with 3 x 300 ml of ether, the combined ethereal layer was washed with 100 ml of water. Drying (Na2SO4) and evaporation of the solvent gave 18 g of oily residue. After trituration with 100 ml of diisopropylether crystal of triphenylphosphine oxide was separated by filtration. Distillation of the filtrate at 4 Pa gave 12.2 of 1-(4-bromophenyl)-1-phenyl-butene, b.p. 120-130°C. Yield 85%.
- To a solution of 22.6 g (0.0787 mol) of 1-(4-bromophenyl)-1-phenylbutene in 800 ml of carbon tetrachloride 14.0 g (0.0787 mol) of N-bromosuccinimide was added. The mixture was heated to reflux temperature after the addition of 0.7 g of alpha, alpha-azobisbutyronitrile. After 3.5 hours all NBS had been consumed and the reaction mixture was cooled and filtered. 7.8 g of succinimide was separated and the volume of the filtrate was reduced to 50 ml by evaporation at 35°C. TLC of a sample on silica in diisopropyletherhexane (1:1) showed a new spot at Rf 0.62 (the starting olefin had Rf 0.55). The material was being used without further isolation or purification due to its high reactivity with nucleophilic agents.
- A solution of crude 3-(4-bromophenyl)-3-phenyl-1-methylallylbromide (29 g, 0.08 mol) in 50 ml carbon tetrachloride was mixed with 15.0 g (0.08 mol) of N-potassiumpthalimide and 120 ml of anhydrous dimethylformamide. The mixture was stirred at 50°C for 14 hours.
- Dilution with water (excess) and extraction of the product with diethylether gave 18 g of an oil after drying and evaporation of the solvent. Column chromatography on silica with diisopropylether as the eluent afforded the geometrical isomers: 2.6 g of the (Z)-form, Rf = 0.30, and 3.7 g of the (E)-form, Rf = 0.26 in diisopropylether-hexane (1:1).
- To a stirred solution of 0.43 g (0.001 mol) of (Z)-3-phtalimido-1-(4-bromophenyl)-1-phenyl- butene in 30 ml of methanol 0.25 g (0.005 mol) of hydrazine hydrate was added at room temperature. In order to dissolve all the phtalimide 10 ml of carbon tetrachloride was added.The mxiture was stirred and heated at 60°C for 2 hours. After cooling the solvent was removed in vacuo and the residue was taken up in ether. The product was extracted with 3 x 50 ml of 0.5 M HCI, the combined aqueous layer was made alkaline with 10 M NaOH and extracted with 2 x 50 ml of ether. Drying and evaporation of the solvent gave 0.23 g of the title compound as an oil. The maleate had m.p. 174-176°C from ethanol. The UV spectrum in ethanol had λ max 237 nm.
- Elemental analysis: C20H20BrNO4; Found: C 57.1, H 4.80, Br 20.3, N 3.10 and 0 15.2%. Calculated: C 57.43, H 4.82, Br 19.10, N 3.35 and 0 15.30%.
- (E)-3-amino-1-(4-bromophenyl)-1-phenylbutene oxalate was prepared from the corresponding phthalimide according to Example 23. M.p. 145-1480C.
- To a stirred solution of 0.43 g (0.001 mol) of (Z)-3-phtalimido-1-(3-bromophenyl)-1-phenyl- butene in 40 ml of methanol 0.35 g (0.007 mol) of hydrazine hydrate was added at room temperature. The mixure was heated under reflux for 2.5 hours. The solvent was evaporated and the residue was taken up in ether. Extraction with 3 x 25 ml of 0.5 M HCI followed by alkalization of the combined aqueous layer with 10 M NaOH and extraction with 2 x 50 ml of ether gave 0.19 g of residue after drying and evaporation of the solvent. The maleate was prepared from 15 ml ethylacetate - ethanol (2:1) to give 0.12 g (28%). M.p. 198-200°C.
- Elemental analysis: C2oH2oBrN04: Found: C 56.3, H 4.7 and N 3.2%. Calculated C 57.43, H 4.82 and N 3.35%.
- (E)-3-amino-1-(3-bromophenyl)-1-phenylbutene hydrochloride was prepared from the corresponding phthalimide according to Example 25. M.p. 118-123°C.
- (Z)-3-amino-1-(4-bromophenyl)-1-(3-pyridyl)-butene oxalate was prepared from the corresponding phthalimide according to Example 25. M.p.
- 3-(4-bromophenyl)-1-methyl-3-phenylpropylamine as the free base (41.2 g, 0.136 mol) was dissolved in 350 ml of acetic acid. Phthalic anhydride (20.0 g, 0.136 mol) was added and the mixture was heated with stirring under reflux (bath temperature 120°C) for 2 hours. After cooling the solvent was evaporated in vacuo. The residue was shaken with a mixture of 800 ml of ether and 500 ml of 2 M NaOH. The ethereal layer was separated and washed with 100 ml I M hydrochloric acid. Drying and evaporation gave 49.5 g of a tan oil. Thin layer chromatography on silica in diisopropylether showed one spot of Rf 0.42. NMR showed a four proton multiplet at 7.7 ppm from TMS, characteristic of phthalimides. The material was used without further purification. Yield: 83%.
- To a stirred solution of 24.6 g (0.057 mol) 3-(N-phthaiimido)-1-(4-bromophenyi)-1-phenyi- butane in 400 ml of carbon tetrachloride 10.0 g (0.057 mol) of N-bromosuccinimide was added. The mixture was stirred and 0.5 g of alpha, alpha-azoisobutyronitrile was added as radical initiator. Stirring was continued under reflux temperature for 2.5 hours. The reaction mixture was cooled and filtered. Upon evaporation of the solvent 32.4 g of a residue was obtained. NMR of a sample in CDCI3 showed a double quartet at 5.0 ppm from TMS and a doublet at 6.6 ppm. TLC on silica in diisopropylether showed a spot with Rf 0.28, identical with the Rf-value of the material prepared according to Example 22.
- The following examples illustrate how the compound of the present invention may be included in pharmaceutical preparations.
- 500 g of active substance were mixed with 500 g of corn oil, whereupon the mixture was filled in soft gelatin capsules, each capsule containing 100 mg of the mxiture (i.e. 50 mg of active substance).
- 500 g of active substance were mixed with 750 g of peanut oil, whereupon the mixture was filled in soft gelatin capsules, each capsule containing 125 mg of the mixture (i.e. 50 mg of active substance).
- 50 kg of active substance were mixed with 20 kg of silicic acid of the trade mark Aerosil. 45 kg of potato starch and 50 kg of lactose were mixed therewith and the mixture was moistened with a starch paste prepared from 5 kg of potato starch and distilled water, whereupon the mixture was granulated through a sieve. The granulate was dried and sieved, whereupon 2 kg of magnesium stearate was mixed into it. Finally the mixture was pressed into tablets each weighing 172 mg.
- 100 g of active substance were dissolved in 2500 g of peanut oil. From the solution thus obtained, 90 g of gum arabic, aroma and colouring agents (q.s.) and 2500 g of water an emulsion was prepared.
- 100 g of active substance were dissolved in 300 g of 95% ethanol, whereupon 300 g of glycerol, aroma and colouring agents (q.s.) and 1000 ml of water were mixed therein. A syrup was obtained.
- 100 g of active substance were dissolved in 2000 g of polyoxyethylene sorbitane monooleate, whereupon flavouring agents and colouring agents (q.s.) and water to 5000 ml was mixed therein. A dropping solution was obtained.
- 100 g of active substance, 140 g of finely divided citric acid, 100 g of finely divided sodium hydrogen carbonate, 3.5 g of magnesium stearate and flavouring agents (q.s.) were mixed and the mixture was pressed into tablets each containing 100 mg of active substance.
- 100 g of active substance were mixed with 300 g of ethanol, whereupon 300 g of glycerol, water to 1000 ml, aroma and flavouring agents (q.s.) and 0.1 N sodium hydroxide solution (to pH 4.5 to 5.5) was added while stirring. A dropping solution was obtained.
- 200 g of active substance were melted together with 50 g of stearic acid and 50 g of carnauba wax. The mixture thus obtained was cooled and ground to a particle size of at most 1 mm in diameter. The mixture thus obtained was mixed with 5 g of magnesium stearate and pressed into tablets each weighing 305 mg. Each tablet thus contains 200 mg of active substance.
- Depressions are considered to be connected with changes in the biochemical processes of the brain which processes control the mood. The nature of these biochemical processes are largely unknown but in depressive states there is evidence for a decreased activity of monoaminergic brain neurons. The monoamines, noradrenaline (NA), dopamine (DA) and 5-hydroxytryptamine (5-HT), are of great interest in this respect.
- It has been demonstrated that NA, DA and 5-HT is localised in three different types on neurons and may function as transmittors in the central nervous system. The monoamines are stored in special structures, granules, situated in enlargements of the nerve endings, varicosities. The varicosity is separated from the effector neuron by a space, the synaptic cleft or spatium. As a result of a nerve stimulation the transmittor is released from the granule into the synaptic cleft and reaches the receptor of the effector neuron and generates a nerve impulse. After impulse generation the amines are inactivated by mainly two mechanisms: a re-uptake mechanism at the cell membrane and enzymatic conversion by catechol-0-methyltransferase to form methylated metabolites. There is also an inactivating enzyme within the varicosities, monoamine oxidase (MAO), that is stored in the mitochondria and inactivates the amines intracellularly.
- When MAO-inhibitors are administered, an increased amount of transmittor substance becomes available for release at the nerve ending.
- Another way of increasing the amine levels at the receptor is exerted by the tricyclic antidepressants. It has been shown that this type of compounds inhibits the re-uptake mechanism of NA and 5-HT, and the antidepressive action is assumed to be related to the uptake inhibition of NA and 5-HT.
- It has been proposed, that some depressions are caused by deficiency in either one of the neuro- transmittors and some of deficiency in both.
- An antidepressant effect should thus be obtained with compounds which are able to inhibit the re-uptake of one or both NA and 5-HT.
- The test method described in Europ. J. Pharmacol. 17, 107, 1972. This method involves the measurement of the decrease in the uptake of 14C-5-hydroxytryptamine (14C-5-HT) and 3H-noradrenaline (3H-NA) in brain slices from mice after in vivo and in vitro administration of the test substance.
- The test substances were administered intraperitoneally half an hour before the animals were killed. The midbrain was taken out, sliced and incubated in a mixture consisting of 0.2 nmole of 14C-5-HT, 0.2 nmole of 3H-NA and 11 µmole of glucose in 2 ml of Krebs Henseleit-buffer, pH 7.4 per 100 mg of brain slices. The incubation time was 5 minutes with 5 minutes of preincubation before the labelled amines were added. The slices were dissolved in Soluene (Trade Mark) and the amounts of radioactive amines taken up were determined by liquid scintillation. The doses producing 50 percent decrease of the active uptake (ED50) of 14C-5-HT and 3H-NA were determined graphically from dose response curves. Active uptake is defined as that part of the radioactive uptake which is inhibited by a high concentration of cocaine.
- In the vitro administration method slices of mouse midbrain were preincubated for 5 minutes with solution of the compound to be tested and then incubated as described above. The concentration producing 50 per cent inhibition of the active uptake IC50 of 14C-5-HT and 3-H-NA was determined graphically from dose response curves.
-
- The pharmacological tests show that the compounds are able to inhibit the uptake of noradrenaline and 5-hydroxytryptamine. A pronounced non-selective activity is shown for the compounds having codes CPK 170, CPK 171, CPK 180 and CPK 184. A pronounced selective activity on uptake of noradrenaline is seen in compounds CPK 185, CPK 215 and CPK 217 while a pronounced selective activity on uptake of 5-hydroxytryptamine is seen in compounds FLA 611, FLA 615, CPK 198 and CPK 204.
- A strong non-selective activity is considered to be especially advantageous, as compounds having such activity may be employed in the treatment of depressions in which the neurotransmittor deficiency is unknown as well as in those cases wherein it is established that the deficiency pertains to both noradrenaline and 5-hydroxytryptamine.
being selective inhibitors of neuronal 5-hydroxytryptamine uptake; as well as salts and precursors of said compounds. The neuronal uptake mechanism are discussed further in the chapter "Pharmacological evaluation" below.
Claims (24)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB27992/77A GB1602290A (en) | 1977-07-04 | 1977-07-04 | Substituted aralkyl amines and amino-aryl alkenes having therapeutic activity |
GB2124978 | 1978-05-22 | ||
GB2124978 | 1978-05-22 | ||
GB2799277 | 1978-05-31 |
Related Child Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP80105028A Division EP0028682A3 (en) | 1977-07-04 | 1978-07-03 | Intermediates useful at the preparation of compounds having anti-depressive or tranquilizing activity |
EP80105028.7 Division-Into | 1978-07-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
EP0000322A1 EP0000322A1 (en) | 1979-01-10 |
EP0000322B1 true EP0000322B1 (en) | 1982-05-05 |
Family
ID=26255230
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP80105028A Withdrawn EP0028682A3 (en) | 1977-07-04 | 1978-07-03 | Intermediates useful at the preparation of compounds having anti-depressive or tranquilizing activity |
EP78850006A Expired EP0000322B1 (en) | 1977-07-04 | 1978-07-03 | Compounds having an anti-depressive or tranquilizing activity, pharmaceutical compositions containing them, and processes and intermediates for their preparation |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP80105028A Withdrawn EP0028682A3 (en) | 1977-07-04 | 1978-07-03 | Intermediates useful at the preparation of compounds having anti-depressive or tranquilizing activity |
Country Status (3)
Country | Link |
---|---|
EP (2) | EP0028682A3 (en) |
JP (1) | JPS5511563A (en) |
IE (1) | IE47628B1 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SE7909514L (en) * | 1979-11-16 | 1981-05-17 | Astra Laekemedel Ab | NEW HALOPHENYL-PYRIDYL-ALLYLAMINE DERIVATIVES |
DE9409012U1 (en) * | 1994-06-03 | 1995-10-05 | Kemper Gmbh Maschf | Machine for mowing and chopping corn and the like stem-like crop |
JP2944431B2 (en) * | 1994-10-18 | 1999-09-06 | 富士車輌株式会社 | Garbage truck |
IT1277597B1 (en) * | 1995-09-15 | 1997-11-11 | Smithkline Beecham Spa | DIARYLALKENYLAMINE DERIVATIVES |
WO2000002551A2 (en) * | 1998-07-13 | 2000-01-20 | Nps Pharmaceuticals, Inc. | Methods and compounds for treating depression |
GB0016271D0 (en) | 2000-07-04 | 2000-08-23 | Meritor Automotive Inc | Vehicle braking systems |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB624117A (en) * | 1946-12-07 | 1949-05-27 | Wellcome Found | Improvements in and relating to the preparation of substituted allylamines and propylamines |
FR1226401A (en) * | 1948-11-09 | 1960-07-11 | Basic compounds and their preparation | |
FR1021301A (en) * | 1949-04-07 | 1953-02-17 | Lundbeck Corp | Unsaturated amines and their preparation |
NL90373C (en) * | 1953-03-19 | |||
BE520042A (en) * | 1953-05-18 | |||
FR1578702A (en) * | 1961-10-10 | 1969-08-22 |
-
1978
- 1978-07-03 EP EP80105028A patent/EP0028682A3/en not_active Withdrawn
- 1978-07-03 IE IE1333/78A patent/IE47628B1/en unknown
- 1978-07-03 EP EP78850006A patent/EP0000322B1/en not_active Expired
-
1979
- 1979-04-18 JP JP4677479A patent/JPS5511563A/en active Pending
Also Published As
Publication number | Publication date |
---|---|
IE47628B1 (en) | 1984-05-16 |
IE781333L (en) | 1979-01-04 |
JPS5511563A (en) | 1980-01-26 |
EP0000322A1 (en) | 1979-01-10 |
EP0028682A3 (en) | 1981-08-05 |
EP0028682A2 (en) | 1981-05-20 |
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