EP0724577A1 - Amines heterocycliques pour le traitement des acces ischemiques - Google Patents

Amines heterocycliques pour le traitement des acces ischemiques

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Publication number
EP0724577A1
EP0724577A1 EP94929558A EP94929558A EP0724577A1 EP 0724577 A1 EP0724577 A1 EP 0724577A1 EP 94929558 A EP94929558 A EP 94929558A EP 94929558 A EP94929558 A EP 94929558A EP 0724577 A1 EP0724577 A1 EP 0724577A1
Authority
EP
European Patent Office
Prior art keywords
formula
compound
alk
heptyl
group
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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Application number
EP94929558A
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German (de)
English (en)
Inventor
David Gwyn Cooper
Ronald Joseph King
Thomas Henry Brown
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SmithKline Beecham Ltd
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SmithKline Beecham Ltd
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Publication date
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Publication of EP0724577A1 publication Critical patent/EP0724577A1/fr
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    • 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
    • C07D295/084—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 attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/088—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 attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • 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
    • A61K31/13—Amines
    • A61K31/135—Amines having aromatic rings, e.g. ketamine, nortriptyline
    • 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
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445—Non condensed piperidines, e.g. piperocaine
    • 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
    • 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
    • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • 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
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • 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
    • A61P25/06—Antimigraine agents
    • 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
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • 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
    • A61P9/08—Vasodilators for multiple indications
    • 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
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • 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
    • C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
    • C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C217/06—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted
    • C07C217/14—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring
    • C07C217/18—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted
    • C07C217/20—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having only one etherified hydroxy group and one amino group bound to the carbon skeleton, which is not further substituted the oxygen atom of the etherified hydroxy group being further bound to a carbon atom of a six-membered aromatic ring the six-membered aromatic ring or condensed ring system containing that ring being further substituted by halogen atoms, by trihalomethyl, nitro or nitroso groups, or by singly-bound oxygen 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
    • C07D295/04—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
    • C07D295/10—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 doubly bound oxygen or sulphur atoms
    • C07D295/104—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 doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/108—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 doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/06—Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08—Systems containing only non-condensed rings with a five-membered ring the ring being saturated

Definitions

  • the present invention relates to amine derivatives, more particularly aryloxy-, arylthio- or aroyl-alkylamino compounds, to processes for their preparation, pharmaceutical compositions containing them and their use in therapy, in particular in the treatment of ischaemic stroke.
  • Stroke is reportedly the third most common cause of death in the developed world.
  • Current therapies for ischaemic stroke are limited and have a number of disadvantages, such as the risk of exacerbating haemorrhage. There is therefore a need for new and improved treatments for ischaemic stroke.
  • EP- A- 103252 discloses a broad class of aryloxyalkylamino derivatives. These compounds are said to have utility as herbicides.
  • French Patent Application No. 1601591 describes a class of nitrogen-containing heterocyclic compounds derived from phenoxyalkyl alcohols, which are said to be cholesterol-lowering agents.
  • British Patent No. 924961 describes, as intermediates for the preparation of anti- nematodal agents, compounds of formula R.W.CH2.CH2.NXY, wherein R is phenyl optionally substituted by inter alia halogen, alkyl or alkoxy, X and Y are inter alia alkyl, or NXY represents a pyrrolidino, piperidino or morpholino group and W is a straight saturated chain containing up to 16 carbon atoms and 1 to 3 non-adjacent oxygen atoms.
  • the present invention therefore provides, in a first aspect, the use of a compound of formula (I):
  • n is preferably from 5 to 9, most preferably 7.
  • Alk 1 and Alk 2 preferably independently represent CH2 or when branched, C(H)(CH3) or C(CH3)2-
  • a is oxygen q is preferably zero and p is preferably zero or 1.
  • p + q is preferably 1 or 2.
  • p and q are preferably both zero.
  • tricyclic heteroaryl groups Ar include dibenzofuranyl, dibenzothienyl, carbazole, N-methylcarbazole, acridine and dibenzoxepine.
  • the tricyclic moiety can be linked to the remainder of formula (I) via any suitable ring atom.
  • Suitable substituents for Ph, and tricyclic heteroaryl groups include, for example, 1 to 3 substituents selected from halogen, trifluoro methyl, trifluoromethoxy, C ⁇ 4alkyl and C ⁇ 4alkoxy.
  • Ar is phenyl mono-substituted by a halogen atom or by a group selected from phenoxy, benzoyl, halobenzoyl or benzyl or benzyloxy in which the -CH2- moiety may optionally be substituted by one or two methyl groups; or Ar is phenyl disubstituted by a halogen atom; or Ar is 2-dibenzofuranyl.
  • Ar is phenyl substituted by benzyl, benzoyl, fluorobenzoyl, chlorobenzoyl or benzyloxy.
  • the substituent is preferably at the 3- or 4- position of the phenyl ring.
  • Alkyl groups present in the compounds of formula (I), alone or as part of another group, can be straight or branched.
  • a C ⁇ galkyl group may be for example methyl, ethyl, n-propyl, n-butyl, n-pentyl, n-hexyl or any branched isomer thereof such as isopropyl, t-butyl, or sec-pentyl.
  • a salt of a compound (I) should be pharmaceutically acceptable.
  • pharmaceutically acceptable salts include inorganic and organic acid addition salts such as hydrochloride, hydrobromide, sulphate, phosphate, acetate, fumarate, maleate, citrate, lactate, tartrate, methanesulphonate or similar pharmaceutically acceptable inorganic or organic acid addition salts.
  • Other non- pharmaceutically acceptable salts may be used for example in the isolation of a final product and are included within the scope of this invention.
  • the compounds of formula (I) may contain one or more asymmetric centres. Such compounds will exist as optical isomers (enantiomers). Both the pure enantiomers, racemic mixtures (50% of each enantiomer) and unequal mixtures of the two are included within the scope of the invention. Further, all diastereomeric forms possible (pure enantiomers and mixtures thereof) are within the scope of the invention. Certain compounds of formula (I) are believed to be novel. Thus, in a further aspect the invention provides novel compounds of formula (IA):
  • R 1 , R 2 , n and Ar are as defined for formula (I); and salts thereof.
  • the invention also provides a compound of formula (IB) : Formula (IB) and salts thereof, wherein R 1 , R 2 , and X are as defined for formula (I) and Ar 1 represents phenyl optionally substituted by a group Ph(Alk 1 )pA(Alk 2 )q- or a tricyclic heteroaryl group as defined for formula (I), provided that when X is O or S, and NR- ⁇ R 2 represents a heterocyclic ring which does not contain an optional further heteroatom then Ar 1 is phenyl substituted by a group Ph(Alk 1 )pC(O)(Alk 2 )q-.
  • Particular compounds of the invention which are believed to be novel compounds include: N-[7-(4-benzyloxyphenoxy)heptyl]-N-methylcyclohexylamine,
  • the compounds of the present invention can be prepared by processes analogous to those known in the art.
  • the present invention therefore provides in a further aspect, a process for the preparation of a novel compound of formula (I) which comprises: (a) to prepare a compound wherein X represents O or S reaction of a compound of formula (II):
  • reaction between a compound of formula (II) and a compound of formula (IH) can be carried out under standard conditions.
  • L 1 is hydroxy
  • the reaction is carried out in the presence of diethyl azodicarboxylate and triphenyl phosphine.
  • Such a reaction is known as the Mitsunobu reaction (as described in Synthesis 1981, 1).
  • This reaction may optionally be effected in the presence of a solvent such as tetrahydrofuran.
  • the leaving group L 1 may be for example a halogen atom or a sulphonyloxy group eg. methane-sulphonyloxy or p-toluene sulphonyloxy.
  • the reaction may be effected in the absence or presence of solvent such as dimethylformamide or methylethylketone in the presence of a base such as sodium hydride or potassium carbonate and at a temperature in the range 0 to 200°C.
  • the reaction of a compound of formula (IV) with a compound of formula (V) according to process (b) may be effected in conventional manner, for example using excess amine as solvent or alternatively using an organic solvent, e.g. an alcohol such as methanol or ethanol; dimethylformamide, or chloroform.
  • the leaving group L 2 may be for example a halide such as bromide or chloride, an acyloxy group such as acetoxy or chloroacetoxy or a sulphonyloxy group such as methanesulphonyloxy or p- toluenesulphonyloxy.
  • reaction may be carried out in the presence of a base such as potassium carbonate, sodium hydride or potassium t-butoxide or an excess of the amine (V) may be employed.
  • a base such as potassium carbonate, sodium hydride or potassium t-butoxide
  • reductive amination of an aldehyde (Vl ⁇ ) may be effected using a reducing agent such as sodium cyanoborohydride in the presence of a compound of formula (V), according to procedures well known in the art.
  • a reducing agent such as sodium cyanoborohydride
  • reaction of compounds (EX) and (X) may be effected in an analogous manner to process (a) described above.
  • Reduction of a pyridinium derivative (XI) according to process (f) may be effected for example by hydrogenation, using a noble metal catalyst such as palladium on charcoal, platinum or platinum oxide (Adam's catalyst), suitably in a solvent such as an alcohol e.g. ethanol.
  • a noble metal catalyst such as palladium on charcoal, platinum or platinum oxide (Adam's catalyst)
  • a solvent such as an alcohol e.g. ethanol.
  • reaction between a compound of formula (XII) and a compound F-Ar is preferably effected in the presence of a strong base such as sodium hydride, and in a polar organic solvent such as dimethylsulphoxide or dimethylformamide.
  • Interconversion reactions according to process (h) may be carried out using standard methods.
  • a compound of formula (II) can be prepared under standard alkylation conditions by reacting a compound of formula (XIII) :
  • L 1 and L 2 are preferably selected so that the compound of formula (V) reacts selectively with L 2 .
  • L 1 is suitably hydroxy and L 2 is suitably halo.
  • Compounds of formula (IV) can be prepared by reacting a compound of formula (HI) as hereinbefore defined with a compound of formula (XIII) as hereinbefore defined.
  • L and L 2 can be identical, for example halo.
  • the reaction is suitably carried out in the presence of a weak base such as potassium carbonate.
  • the reaction may be carried out under phase transfer conditions using a strong base such as potassium hydroxide.
  • a compound of formula (TV) may be prepared by Friedel-Craft acylation of a compound HAr with an acylating agent of the formula L 2 (CH2) n C(O)Hal, where Hal represents a halogen atom such as bromo or chloro.
  • the carbonyl group in the resulting compound of formula (IV) may if desired subsequently be reduced.
  • Compounds of formula (VII) may be prepared by acylation of a compound of formula (V) for example with an appropriate acid chloride or ester, which may itself be prepared from a compound of formula (IE) by reaction with an appropriate, commercially available bromoalkyl ester or acid, followed if necessary or desired by conversion to an acid chloride.
  • a compound (VII) may be prepared by a method analogous to process (a).
  • An aldehyde of formula (VI-O) may be prepared for example by reduction of the corresponding nitrile using a reducing agent such as diisobutyl aluminium hydride, in the presence of an inert solvent such as toluene.
  • reductive animation of the aldehyde is carried out in situ, i.e. the compound of formula (I) is obtained from the nitrile in a one-pot reaction without isolation of the intermediate aldehyde.
  • the nitrile may itself be prepared by reacting a compound of formula (IV) wherein L 2 is halo with potassium cyanide.
  • Compounds (VTfl) may also be prepared by other standard procedures such as reduction of an ester or oxidation of an alcohol.
  • Compounds of formula (IX) may be prepared by methods analogous to any of processes (a) - (d) described herein. Alternatively a compound (IX) may be obtained by catalytic hydrogenation of a corresponding compound of formula (I) wherein Ar represents a benzyloxyphenyl group. This therefore provides a further method of converting a compound of formula (I) to a different compound of formula (I).
  • Suitable protecting groups include aralkyl groups such as benzyl, diphenylmethyl or triphenylmethyl and acyl groups such as acetyl, trifluoroacetyl, benzoyl, methoxycarbonyl, ethoxycarbonyl, t- butoxycarbonyl or benzyloxycarbonyl.
  • An aralkyl group such as benzyl may be cleaved by hydrogenolysis, and an acyl group such as benzoyl may be cleaved by hydrolysis.
  • a compound of formula (I) When a compound of formula (I) is obtained as a mixture of enantiomers, these may be separated by conventional methods such as crystallisation in the presence of a resolving agent, or chromatography, for example using a chiral HPLC column.
  • the invention also encompasses any novel intermediates described herein, in particular those of formulae (II), (IV), (VI), (VII), (IX) and (XI).
  • Compounds of the invention have been found to exhibit high calcium influx blocking activity, for example in neurons.
  • the compounds are expected to be of use in therapy in treating conditions and diseases related to an accumulation of calcium in the brain cells of mammals, in particular humans.
  • the compounds are expected to be of use in the treatment of anoxia, ischaemia including for example stroke, migraine, visceral pain, epilepsy, traumatic head or spinal injury, AIDS-related dementia, neurodegenerative diseases such as Alzheimer's disease and age-related memory disorders, mood disorders and drug addiction withdrawal such as ethanol addiction withdrawal.
  • the invention also provides a method of treatment of conditions or diseases related to (e.g. caused or exacerbated by) the accumulation of calcium in the brain cells of mammals which comprises administering to a subject in need thereof an effective amount of a compound of formula (I) as hereinbefore defined or a pharmaceutically acceptable salt thereof.
  • the present invention provides a method of treatment of anoxia, ischaemia including for example stroke, migraine, visceral pain, epilepsy, traumatic head or spinal injury, AIDS-related dementia, neurodegenerative diseases such as Alzheimer's disease and age-related memory disorders, mood disorders and drug addiction withdrawal such as ethanol addiction withdrawal, which comprises administering to a subject in need thereof, an effective amount of a compound of formula (I) or a pharmaceutically acceptable salt thereof.
  • the compounds of the present invention are usually administered in a standard pharmaceutical composition.
  • the present invention therefore provides in a further aspect pharmaceutical compositions comprising a novel compound of formula (I) as hereinbefore defined or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable carrier or excipient
  • the compounds of the invention may be administered by any convenient method for example by oral, parenteral, buccal, rectal or transdermal administration and the pharmaceutical compositions adapted accordingly. Parenteral administration is generally preferred.
  • the compounds of formula (I) and their pharmaceutically acceptable salts which are active when given orally can be formulated as liquids or solids, for example syrups, suspensions or emulsions, tablets, capsules and lozenges.
  • a liquid formulation will generally consist of a suspension or solution of the compound or pharmaceutically acceptable salt in a suitable liquid ca ⁇ ier(s) for example, ethanol, glycerine, non-aqueous solvent, for example polyethylene glycol, oils, or water with a suspending agent, preservative, flavouring or colouring agent.
  • a suitable liquid ca ⁇ ier(s) for example, ethanol, glycerine, non-aqueous solvent, for example polyethylene glycol, oils, or water with a suspending agent, preservative, flavouring or colouring agent.
  • a composition in the form of a tablet can be prepared using any suitable pharmaceutical carrier(s) routinely used for preparing solid formulations.
  • suitable pharmaceutical carrier(s) routinely used for preparing solid formulations.
  • suitable pharmaceutical carrier(s) include magnesium stearate, starch, lactose, sucrose and cellulose.
  • a composition in the form of a capsule can be prepared using routine encapsulation procedures.
  • pellets containing the active ingredient can be prepared using standard carriers and then filled into a hard gelatin capsule; alternatively, a dispersion or suspension can be.
  • any suitable pharmaceutical carrier(s) for example aqueous gums, celluloses, silicates or oils and the dispersion or suspension then filled into a soft gelatin capsule.
  • Compounds of the invention may also be administered parenterally, by bolus injection or continuous infusion.
  • Typical parenteral compositions consist of a solution or suspension of the compound or pharmaceutically acceptable salt in a sterile aqueous carrier or parenterally acceptable oil, for example polyethylene glycol, polyvinyl pyrrolidone, lecithin, arachis oil or sesame oil.
  • the solution can be lyophilised and then reconstituted with a suitable solvent just prior to administration.
  • Both liquid and solid compositions may contain other excipients known in the pharmaceutical art, such as cyclodextrins.
  • composition is in unit dose form such as a tablet, capsule or ampoule.
  • Each dosage unit for oral administration contains preferably from 1 to 250 mg (and for parenteral administration contains preferably from 0.1 to 60 mg) of a compound of the formula (I) or a pharmaceutically acceptable salt thereof calculated as the free base.
  • the daily dosage regimen for an adult patient may be, for example, an oral dose of between 1 mg and 500 mg, preferably between 1 mg and 250 mg, eg. 5 to 200 mg or an intravenous, subcutaneous, or intramuscular dose of between 0.1 mg and 100 mg, preferably between 0.1 mg and 60 mg, eg. 1 to 40 mg of the compound of the formula (I) or a pharmaceutically acceptable salt thereof calculated as the free base, the compound being administered 1 to 4 times per day.
  • the compounds of the invention may be administered by continuous intravenous infusion, preferably at a dose of up to 400 mg per day.
  • the total daily dosage by oral administration could be in the range 1 to 2000 mg and the total daily dosage by parenteral administration could be in the range 0.1 to 400 mg.
  • the compounds may be administered for a period of continuous therapy, for example for a week or more.
  • a compound of formula (I) or a pharmaceutically acceptable salt thereof may be administered in combination or concurrently with one or more other therapeutic agents, for example a thrombolytic agent such as anistreplase, streptokinase or a tissue plasminogen activator; an excitatory amino acid antagonist such as an NMDA antagonists; a free radical inhibitor; or a calpain inhibitor.
  • a thrombolytic agent such as anistreplase, streptokinase or a tissue plasminogen activator
  • an excitatory amino acid antagonist such as an NMDA antagonists
  • a free radical inhibitor such as an NMDA antagonists
  • a calpain inhibitor a compound of formula (I) or a pharmaceutically acceptable salt thereof
  • the pipette (internal solution) contained in mM: CsCl, 130; HEPES, 10; EGTA, 10; MgCl2, 4; ATP, 2; buffered to pH 7.2 with CsOH.
  • Cells were bathed in a normal Tyrodes solution before establishment of whole cell recording when the bathing solution was changed to one allowing isolation of Ca 2+ currents.
  • the external solution for recording Ca + channel currents contained in mM: BaCl2, 10; TEA-C1, 130; glucose, 10; HEPES, 10; MgCl2, 1; buffered to pH 7.3 with TEA-OH. Barium was used as the charge carrier as this assists in current isolation and calcium dependent inactivation of current is avoided.
  • Ca-2 + currents Peak voltage gated Ca + channel cunrents of up to 10 nA from dorsal root ganglion neurons were recorded using 10 mM Ba 2+ as charge carrier. Currents were evoked from a holding potential of -80 mV to a test potential of 0 or +10 mV every 15 seconds. This test potential was at the peak of the current voltage relationship and assessing block at this point reduced any errors due to drifting holding potential. Some cells showed slow rundown of current as is commonly seen when recording Ca + currents. The rundown rate was measured in control conditions and extrapolated through the time of drug application to derive a rundown corrected control value. Dorsal Root Ganglion Cells
  • Buffer Suitable buffers include citrate, phosphate, sodium hydroxide/hydrochloric acid.
  • Solvent Typically water but may also include cyclodextrins (1-100 mg) and co-solvents such as propylene glycol, polyethylene glycol and alcohol.
  • Diluent e.g. Microcrystalline cellulose, lactose, starch Binder : e.g. Polyvinylpyrrolidone, hydroxypropymethylcellulose
  • Disintegrant e.g. Sodium starch glycollate, crospovidone Lubricant : e.g. Magnesium stearate, sodium stearyl fumarate. Oral Suspension
  • Suspending agent e.g. Xanthan gum, microcrystalline cellulose
  • Diluent e.g. sorbitol solution, typically water
  • Preservative e.g. sodium benzoate
  • Buffer e.g. citrate
  • Co-solvent e.g. alcohol, propylene glycol, polyethylene glycol, cyclodextrin
  • 1,7-Dibromoheptane (12.9g) was added dropwise to a stirred solution of 4- benzyloxyphenol (lOg), sodium hydroxide (2.5g), benzyltriethylammonium chloride (0.4g) and water (30ml). The mixture was stirred at 50°C for 18 hours, water (50ml) added and the solution extracted with dichloromethane (2 x 100ml). The combined dichloromethane extracts were dried over magnesium sulphate, solvent was removed and the residue was chromatographed on silica gel eluted with hexane/dichloromethane to give the title compound (4.25g) as a solid, m.p. 56 - 59°C.
  • Example 1 N-[7-(4-Benzyloxyphenoxy)heptyl]-N-methylcyclohexylamine hydrochloride A mixture of 7-(4-benzyloxyphenoxy)-l-bromoheptane (1.88g), 80% sodium hydride (0.17g) and dimethylformamide (10ml) was stirred under nitrogen for 5 minutes. N- methylcyclohexylamine (0.65ml) was added by syringe and the mixture was stirred at 60°C for 4 hours. The solvent was removed and the residue treated with water and extracted with ether.
  • N-[7-(4-Benzyloxyphenoxy)heptyl]dimethylamine hydrochloride The title compound was prepared in a similar manner to Example 2 starting from 7-(4- benzyloxyphenoxyH-bromoheptane (1.25g), 33% dimethylamine in ethanol (10ml) and chloroform (50ml). Treatment with ethereal hydrogen chloride and recrystallisation from acetonitrile gave the title compound as a white solid, (0.638g), m.p. 152 - 153°C.
  • the title compound was prepared in a similar manner to Example 1 starting from 7-(4- benzyloxyphenoxyH-bromoheptane (1.88g), 80% sodium hydride (0.17g), N- methylpiperazine (0.55ml) and dimethylformamide (10ml). Treatment with ethereal hydrogen chloride and recrystallisation from ethanol gave the title compound as a white solid, (0.93g), m.p. 238 - 241 °C.
  • Example 13 l- ⁇ 7-[4-(4-Chlorobenzoyl)phenoxy]heptyl ⁇ piperidine hydrochloride
  • a solution of 7-piperidinoheptanol (l.Og), 4-chloro-4'-hydroxybenzophenone (1.16g), triphenylphosphine (1.31g) in tetrahydrofuran (20ml) was treated with diethyl azodicarboxylate (0.87g).
  • the resulting solution was stirred at room temperature for 18 hours, the solvent removed and the residue chromatographed on silica gel eluted with 10% methanol in chloroform.
  • the resulting oil was dissolved in ethyl acetate and treated with ethereal hydrogen chloride.
  • (+)-l- ⁇ 7-[4-(l-Phenylethyloxy]phenoxy]heptyl ⁇ piperidine hydrochloride A solution of 7-(4-hydroxyphenoxy)-l-piperidinoheptane (WO93/22302; 0.75g), ( ⁇ )-l- phenylethanol (0.3 lg), triphenylphosphine (0.61g) in tetrahydrofuran (20ml) was treated with diethyl azodicarboxylate (0.44g). The resulting solution was sti ⁇ ed at room temperature for 18 hours, the solvent removed and the residue chromatographed on silica gel eluted with 10% methanol in chloroform.
  • the title compound was prepared in a similar manner to Example 15 starting from 1- bromo-8-[4-(4-fluorophenoxy)phenyl]-8-oxyoctane (2.0g) and using corresponding molar amounts of the other reagents. Treatment with ethereal hydrogen chloride and crystallisation under ether gave the tide compound as a white solid, (1.53g), m.p. 111 - 112°C.
  • the title compound was prepared in a similar manner to Example 15 starting from 1- bromo-6-(4-phenoxy)phenyl-6-oxyhexane (1.5g) and using corresponding molar amounts of the other reagents. Treatment with ethereal hydrogen chloride and crystallisation under ether gave the title compound as a white solid, (1.35g), m.p. 87 - 89°C.

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Abstract

Utilisation de composés répondant à la formule (I), dans laquelle R1 et R2 indépendamment l'un de l'autre, représentent hydrogène, alkyleC¿1-8?, cycloalkyleC3-8, cycloalkyleC3-8alkyleC1-4, arylalkyleC1-4, hydroxyalkyleC2-6 ou R?3R4¿NalkyleC¿2-6? (où R?3 et R4¿, indépendamment l'un de l'autre, représentent H ou alkyleC¿1-4?) ou NR?1R2¿ représente un hétérocycle saturé renfermant de 4 à 9 éléments de cycle, dont l'un est éventuellement un hétéroatome supplémentaire choisi parmi 0, S ou NR?5, (où R5¿ représente H, alkyleC¿1-4? ou arylalkyleC1-4), ce cycle étant éventuellement substitué par un ou deux substituants choisis parmi alkyleC1-6 et alcoxyC1-6; X représente O, S, ou C=O; n est compris entre 5 et 11; et Ar représente phényle éventuellement substitué par 1 à 3 substituants choisis parmi halo, alkyleC1-8, alcoxyC1-8, alkylènedioxyC1-2, par exemple méthylènedioxy, trifluorométhyle, trifluorométhyloxy, ou par un groupe Ph(Alk?1)¿pA(Alk2)q- où Ph représente phényle éventuellement substitué, A représente une liaison, O, S, -C=O ou CH=CH, Alk?1 et Alk2¿, indépendamment l'un de l'autre, représentent alkyleC¿1-4? linéaire ou ramifié, et p et q, indépendamment l'un de l'autre, sont 0 ou 1, à condition que la longueur de -(Alk?1)¿pA(Alk2)q- ne dépasse pas 5 atomes, ou Ar représente un groupe hétéroaryle tricyclique éventuellement substitué (a), dans lequel Y1 représente Y2(CH2)r où r vaut 0 ou 1 et Y2 représente O, S ou NR6 où R6 représente hydrogène ou alkyleC¿1-4?, Z représente (CH2)s ou -CH=CH-, s vaut 0, 1 ou 2 ou Ar représente le système cyclique déshydro tricyclique correspondant; à condition que (i) si X représente O ou S, et si NR?1R2¿ représente un hétérocycle ne renfermant aucun hétéroatome supplémentaire, alors Ar représente phényle substitué par un groupe Ph(Alk1)pC(O)(Alk2)q-; (ii) si n vaut 5 et si l'un de R1 et R2 représente hydrogène, alkyleC¿1-4? ou arylalkyleC1-4, alors l'autre de R?1 et R2¿ ne représente pas R3R4Nalkyle¿2-6?; et leurs sels pharmaceutiquement acceptables; dans la fabrication d'un médicament destiné au traitement d'une pathologie où un antagoniste de calcium est nécessaire. On a également prévu certains nouveaux composés répondant à la formule (I), ainsi que leurs procédés de préparation.
EP94929558A 1993-10-22 1994-10-18 Amines heterocycliques pour le traitement des acces ischemiques Withdrawn EP0724577A1 (fr)

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PCT/EP1994/003425 WO1995011238A1 (fr) 1993-10-22 1994-10-18 Amines heterocycliques pour le traitement des acces ischemiques

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EP0755923B1 (fr) * 1995-01-23 2005-05-04 Daiichi Suntory Pharma Co., Ltd. Ameliorant ou remede contre des symptomes provoques par des maladies ischemiques et composes phenylpiperidiniques utiles a cet effet
GB9601651D0 (en) * 1996-01-26 1996-03-27 Ciba Geigy Ag Antiretroviral bases
US6251919B1 (en) 1998-02-27 2001-06-26 Warner-Lambert Heterocyclic substituted aniline calcium channel blockers
US6166052A (en) * 1998-03-11 2000-12-26 Warner-Lambert Company Heteroaryl alkyl alpha substituted peptidylamine calcium channel blockers
JP2000302737A (ja) * 1999-04-16 2000-10-31 Shiseido Co Ltd 二置換ベンゼン誘導体
WO2003018538A1 (fr) * 2001-08-31 2003-03-06 Ajinomoto Co., Inc. Nouveaux derives de diarylalcene et nouveaux derives de diarylalcane
US8425885B2 (en) 2009-11-09 2013-04-23 Conopco, Inc. Substituted 3-(phenoxymethyl) benzyl amines and personal care compositions
US8309064B2 (en) 2009-11-09 2012-11-13 Conopco, Inc. Skin care compositions comprising phenoxyalkyl amines

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BE588558A (fr) * 1959-03-13 1960-09-12
FR1601591A (en) * 1968-12-24 1970-08-31 Hypocholesterolaemic phenoxyalkylamines
GR78370B (fr) * 1981-12-24 1984-09-26 Delalande Sa
DE3233828A1 (de) * 1982-09-11 1984-03-15 Basf Ag, 6700 Ludwigshafen Aryloxyalkylamine, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
IL87181A (en) * 1987-08-07 1993-08-18 Sanofi Sa Aminoalkoxyphenyl derivatives, their preparation and pharmaceutical and veterinary compositions containing them
FR2642755B1 (fr) * 1989-02-07 1993-11-05 Sanofi
AU3959893A (en) * 1992-04-24 1993-11-29 Smithkline Beecham Plc N-aryloxy(thio)alkyl-azacycloalkanes useful as calcium channel antagonists

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See references of WO9511238A1 *

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WO1995011238A1 (fr) 1995-04-27
JPH09504016A (ja) 1997-04-22

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