Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
  • C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
  • C07D241/04—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
• • 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
  • C07D295/16—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 acylated on ring nitrogen atoms
  • C07D295/18—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 acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
  • C07D295/182—Radicals derived from carboxylic acids
  • C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
• • 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
  • A61K31/495—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
  • A61K31/496—Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K51/00—Preparations containing radioactive substances for use in therapy or testing in vivo
  • A61K51/02—Preparations containing radioactive substances for use in therapy or testing in vivo characterised by the carrier, i.e. characterised by the agent or material covalently linked or complexing the radioactive nucleus
  • A61K51/04—Organic compounds
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P23/00—Anaesthetics
• • 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
  • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
  • C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
  • C07D215/12—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
  • C07D215/14—Radicals substituted by 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
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
  • C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
  • C07D295/08—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
  • C07D295/096—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
• • 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
  • C07D295/112—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 separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
• • 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
  • C07D295/12—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 or doubly bound nitrogen atoms
  • C07D295/135—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 or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
• • 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
  • C07D295/14—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 carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
  • C07D295/155—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 carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
• • 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
  • C07D295/16—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 acylated on ring nitrogen atoms
  • C07D295/20—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 acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
  • C07D295/205—Radicals derived from carbonic acid
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
  • C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
  • C07D307/78—Benzo [b] furans; Hydrogenated benzo [b] furans
  • C07D307/79—Benzo [b] furans; Hydrogenated benzo [b] furans with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to carbon atoms of the hetero ring
  • C07D307/81—Radicals substituted by nitrogen atoms not forming part of a nitro radical
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
  • C07C2601/00—Systems containing only non-condensed rings
  • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
  • C07C2601/14—The ring being saturated

Definitions

• the present invention is related to novel compounds, to a process for their preparation, their use and pharmaceutical compositions comprising the novel compounds.
• the novel compounds are used in therapy, and in particular for the treatment of pain.
• the ⁇ receptor has been identified as having a role in many bodily functions such as circulatory and pain systems. Ligands for the ⁇ receptor may therefore find potential use as analgesics, and/or as antihypertensive agents. Ligands for the ⁇ receptor have also been shown to posess immunomodulatory activities.
• the problem underlying the present invention was to find new analgesics having excellent analgesic effects, but also with an improved side-effect profile over current ⁇ agonists and potential oral efficacy.
• Analgesics that have been identified and are existing in the prior art have many disadvantages in that they suffer from poor pharmacokinetics and are not analgesic when administered by systemic routes. Also, it has been documented that preferred compounds, described within the prior art, show significant convulsive effects when administered systemically.
• novel compounds according to the present invention are defined by the formula (I)
• G is a carbon atom or a nitrogen atom; A is selected from
• each A substituent may be optionally and independently substituted by 1 or 2 substituents selected from hydrogen, CH3, (CH2) 0 CF3, halogen, CONR 7 R 8 , CO 2 R 7 , COR 7 , (CH 2 )oNR 7 R 8 , (CH 2 )oCH3(CH 2 )oSOR 7 , (CH 2 ) 0 SO 2 R 7 and
• R is selected from hydrogen; a branched or straight Ci-C ⁇ alkyl, C1-C6 alkenyl, -CO(C ⁇ -C6 alkyl); (Ci-C ⁇ alkyl)-B wherein B is as defined below; C3-C8 cycloalkyl, C4-C8 (alkyl-cycloalkyl) wherein alkyl is Cj -C2 alkyl and cycloalkyl is C3-C6 cycloalkyl; C6-C10 aryl; and heteroaryl having from 5 - 10 atoms selected from any of C, S, N and O; and whereby the C ⁇ -Cio aryl and the heteroaryl may optionally be substituted by 1 or 2
• R and R is each and independently as defined for R above;
• R is selected from hydrogen, CH3, OR , CO2R , and CH2CO2R wherein R is as defined above; R , R , R , R , R , R , R , R , and R , is each and independentiy as defined for R above;
• B is a substituted or unsubstituted aromatic; an optionally substituted C5-C10 hydroaromatic; a heteroaromatic or a heterohydroaromatic moiety, each having from 5 to 10 atoms selected from any of C, S, N and O, and each being optionally and independently substituted by 1 or 2 substituents independently selected from hydrogen, CH3, CF3, halogen, (CH 2 ) p CONR 7 R 8 , (CH 2 )pNR 7 R 8 , (CH 2 ) p COR 7 , (CH 2 )pCO 2 R 7 , OR 7 , (CH 2 ) p SOR 7 , (CH 2 ) p SO 2 R 7 , and (CH 2 ) p SO 2 NR 7 R 8 ;
• R , R , R and R is each and independently selected from R 7 , (CH 2 ) p CONR 7 R 8 , (CH 2 )pNR 7 R 8 , (CH 2 ) p CONR 7 R 8 , (CH 2 ) p CO 2 R 7 , (CH 2 )pPh,
• Z is hydroxy, and esters thereof; hydroxymethyl, and esters thereof; or amino, and carboxamides and sulfonamides.
• Preferred compounds according to the invention are compounds of the formula (I) wherein
• G is a carbon atom or a nitrogen atom; A is selected from
• each A substituent may be optionally and independently substituted by 1 or 2 substituents selected from hydrogen, CH3, (CH2) 0 CF3, halogen, CONR 7 R 8 , CO 2 R ? , COR 7 , (CH 2 )oNR 7 R 8 , (CH 2 )oCH 3 (CH2)oSOR 7 , (CH 2 ) 0 SO2R 7 and (CH2) 0 SO2NR 7 R 8 , wherein o is 0, 1, or 2, and R 7 and R 8 are as defined below; R , R and R is each and independently selected from hydrogen; a branched or straight
• R is hydrogen, methyl, or OR wherein R is as defined above;
• R , R , R , R , R , R , R , R , R , R , and R is each and independently as defined for R above;
• B is selected from phenyl, naphthyl, indolyl, benzofuranyl, dihydrobenzofuranyl, benzothiophenyl, pyrryl, furanyl, quinolinyl, isoquinolinyl, cyclohexyl, cyclohexenyl, cyclopentyl, cyclopentenyl, indanyl, indenyl, tetrahydronaphthyl, tetrahydroquinyl, tetrahydroisoquinolinyl, tetrahydrofuranyl, pyrrolidinyl, indazolinyl, and
• each B group being optionally substituted by 1-2 substituents independently selected from hydrogen, CH 3 , CF 3 , halogen, (CH 2 ) p CONR 7 R 8 , (CH 2 )pNR 7 R 8 , (CH 2 ) p COR 7 , (CH 2 ) p CO 2 R 7 , and OR 7 ;
• R , R , R and R is each and independently selected from hydrogen, CH3, CH(Me)2, CH 2 CH(Me) 2 .
• Z is hydroxy, and esters thereof; hydroxymethyl, and esters thereof; or amino, and carboxamides and sulfonamides.
• Especially preferred compounds according to the invention are compounds of the formula (I) wherein
• G is a nitrogen atom; A is selected from
• R ,R ,R ,R ,R ,R ,R ,R ,R , and R is each an ethyl group
• R is selected from hydrogen, methyl, ethyl, allyl, or CH2-cyclopropyl
• R is H, methyl, or OR , wherein Rl is as defined above;
• B is selected from phenyl, naphthyl, indolyl, benzofuranyl, dihydrobenzofuranyl, benzothiophenyl, furanyl, quinolinyl, isoquinolinyl, cyclohexyl, cyclohexenyl, cyclopentyl, cyclopentenyl, indanyl, indenyl, tetrahydronaphthyl, tetrahydroquinyl, tetrahydroisoquinolinyl, tetrahydrofuranyl, indazolinyl, and
• each B group being optionally substituted by 1-2 substituents independently selected from hydrogen, methyl, CF 3 , halogen, (CH 2 ) p CONR 7 R 8 , (CH 2 )pNR 7 R 8 , (CH 2 ) p COR 7 , (CH 2 ) p CO 2 R 7 , and OR 7 ,
• R , R , R and R is each and independently selected from H, CH3, CH(Me)2, CH 2 CH(Me) 2 , CH( e)CH 2 CH 3 (CH 2 ) p CONR ? R 8 , (CH 2 )pNR 7 R 8 , (CH 2 ) p CONR 7 R 8 , (CH 2 ) p CO 2 R 7 , (CH 2 )pPh, (CH 2 ) p (p-OH Ph), (CH 2 ) p -3-indolyl, (CH 2 ) p SR 7 , and (CH 2 ) p OR 7
• the substituents A and B respectively, may optionally be substituted at any position of the ring.
• halogen we mean chloro, fluoro, bromo and iodo.
• aryl we mean an aromatic ring having from 6 - 10 carbon atoms, such as phenyl and naphtyl.
• heteroaryl we mean an aromatic ring in which one or more of the 5 - 10 atoms in the ring are elements other than carbon, such as N, S and O.
• hydroaromatic we mean a partly or fully saturated aromatic ring structure having 5-10 carbon atoms in the ring.
• heterohydroaromatic we mean a partly or fully saturated aromatic ring structure in which one or more of the 5-10 atoms in the ring are elements other than carbon, such as N, S and O.
• isomers we mean compounds of the formula (I), which differ by the position of their functional group and/or orientation.
• orientation we mean stereoisomers, diastereoisomers, regioisomers and enantiomers.
• isoforms we mean compounds of the formula (I) which differ by their crystal lattice, such as crystalline compound and amorphous compounds.
• prodrug we mean pharmacologically acceptable derivatives, e.g. esters and amides, such the resulting biotransformation product of the derivative is the active drug.
• prodrug we mean pharmacologically acceptable derivatives, e.g. esters and amides, such the resulting biotransformation product of the derivative is the active drug.
• novel compounds of the present invention are useful in therapy, especially for the treatment of pain.
• the compounds are also useful for modulating the analgesic effects acting at the ⁇ opioid receptor subtype, the modulation of side effects seen with agents acting at the ⁇ opioid receptor subtype such as morphine, especially respiratory depression, gut motility and abuse liability.
• Compounds of the invention are also useful as immunomodulators, especially for autoimmune diseases, such as arthritis, for skin grafts, organ transplants and similar surgical needs, for collagen diseases, various allergies, for use as anti tumour agents and anti viral agents.
• Compounds of the invention arc useful in disease states where degeneration or dysfunction of opioid receptors is present or implicated in that paradigm. This may involve the use of isotopically labeled versions of the compounds of the invention in diagnostic techniques and imaging applications such as positron emission tomography (PET).
• PET positron emission tomography
• Compounds of the invention arc useful for the treatment of diarrhea, depression, urinary incontinence, various mental illnesses, cough, lung oedema, various gastro-intestinal disorders, spinal injury and drug addiction, including the treatment of alcohol, nicotine, opioid and other drug abuse and for disorders of the sympathetic nervous system for example hypertension.
• the best mode of performing the present invention known at present is to use the compounds according to Example 21 (compound 33), Example 22 (compound 34), Example 23 (compound 37), Example 24 (compound 38), Example 25 (compound 41), Example 26 (compound 42), Example 27 (compound 45), Example 29 (compound 51), Example 30 (compound 54), Example 35 (compound 64), Example 36 (compound 65), Example 50, and Example 51.
• the numbering of the compounds is in accordance with the Examples below, as well as in accordance with the numbering in the Schemes presented in the following. Methods of preparation
• An aldehyde or ketone is treated with a nucleophile such as a Grignard or organolithium species to produce the corresponding alcohol.
• This alcohol may then be converted into a suitable leaving group (X) such as an ester, sulphonate or halide which may in turn be displaced with a nucleophilic species such as a substituted or unsubstituted piperazine.
• X a suitable leaving group
• N- (4)-unsubstituted piperazine derivatives may then be suitably substituted with a variety of groups via their organo halide or equivalent species, or acylated with a number of different acylating compounds. This sequence of events will give rise to compounds according to general formula I.
• N-protected amino acid as its activated ester, may be reacted with a second amino acid ester.
• this species On treatment with an acid this species may then cyclize to form a piperazinedione.
• This dione may be reduced via a number of standard methods to the corresponding piperazine (e.g. a reducing agent such as lithium aluminium hydride, by conversion to the thioamide and subsequent desulphurization, hydrogenation in the presence of POCI3 etc.)
• This piperazine may then be alkylated or acylated on one or more of the nitrogens and/or may be used subsequently in generalized method A.
• the compound 7 was prepared by following the synthesis procedure as described for compound 2, but substituting compound 1 for compound 6.
• the compound 8 was prepared by following the synthesis procedure as described for compound 3, but substituting compound 2 for compound 7.
• Compound 10 (a mixture of two isomers) Its HCl salt: m.p. 160-162.5°C (Ether); Vj ⁇ ⁇ ( (KKBBrr)) ccmm ""11 33338800,, 11660000,, 11226611;; ⁇ nn ⁇ //..CCaallccdd..ffoorr CC; 27 H 32 N 2 O.2HCl. 0.50H 2 O: C, 67.21; H, 7.31; N, 5.81. Found: C, 67.13; H, 6.97; N, 5.47.
• the compound of this Example was prepared by following the synthesis procedure as described for Example 1.
• the compound 12 was prepared by following the synthesis procedure as described for compound 2, but substituting compound 1 for compound 11..
• the compound 13 was prepared by following the synthesis procedure as described for compound 3, but substituting compound 2 for compound 12.
• the compound 18 was prepared by following the synthesis procedure as described for compound 1, but substituting 1-naphtaldehyde for 6-quinolinecarboxaldehyde.
• the compound 19 was prepared by foUowing the synthesis procedure as described for compound 2, but substituting compound 1 for compound 18.
• Compound 21 (a mixture of two isomers, -25% compound 20): ba (400 MHz, CDCI3) 1.20 (m, 6H), 2.05 (m, IH), 2.73 (m, 2H), 2.87 (m, IH), 3.13 (m, 2H), 3.73 & 3.76 (s, 3H), 5.38 (s, IH), 6.38 (brs, NH), 6.70-8.15 (m, 9H), 8.84 (m, IH).
• the compound 26 was prepared by foUowing the synthesis procedure as described for compound 1, but substituting 1-naphtaldehyde for 4-quinolinecarboxaldehyde..
• the compound 27 was prepared by foUowing the synthesis procedure as described for compound 2, but substituting compound 1 for compound 26.
• the compound 32 was prepared by foUowing the synthesis procedure as described for compound 2, but substituting compound 1 for compound 31.
• the compound 35 was prepared by foUowing the synthesis procedure as described for compound 1, but substituting 3-bromoanisole for 2-b ⁇ omoanisole, and 1-naphtaldehyde for N,N-diethyl-4-carboxybenzamide.
• the compound 36 was prepared by foUowing the synthesis procedure as described for compound 2, but substituting compound 1 for compound 35.
• the compound of this Example was prepared by following the synthesis procedure as described for Example 1, but substituting compound 2 for compound 36.
• the compound 39 was prepared by foUowing the synthesis procedure as described for compound 31, but substituting 4-chlorophenylmagnesiumbromide for 4- toluylmagnesiumbromide.
• the compound 40 was prepared by following the synthesis procedure as described for compound 2.
• the compound of this Example was prepared by following the synthesis procedure as described for Examples 2 and 3.
• the compound 43 was prepared by foUowing the synthesis procedure as described for compound 31, but substituting 4-chlorophenylmagnesiumbromide for m-toluylmagnesiumbromide.
• Vmax (KBrVcm "1 3406, 2972, 1613, 1429, 1360, 1287, 1097, 1053, 789; u (400 MHz, CDC1 3 ) 1.10 (3H, br s), 1.22 (3H, br s), 2.34 (3H, s), 2.55 (IH, d, J 3.5), 3.25 (2H, br s), 3.52 (2H, br s), 5.80 (IH, d, J 3), 7.12-7.42 (8H, m);
• the compound 44 was prepared by foUowing the synthesis procedure as described for compound 2.
• the compound of this Example was prepared by foUowing the synthesis procedure as described for compound 3.
• the compound 46 was prepared by foUowing the synthesis procedure as described for compound 31. ⁇ H (400 MHz, CDC1 3 ) 0.85-2.0 (18H, m), 3.26 (2H, br s), 3.53 (2H, br s), 4.35-4.43 (IH, ), 7.28-7.36 (4H, m);
• the compound 47 was prepared by foUowing the synthesis procedure as described for compound 2.
• the compound of this Example was prepared by following the synthesis procedure as described for compound 3.
• the compound 49 was prepared by foUowing the synthesis procedure as described for compound 1. ⁇ H (400 MHz, CDCI3) 1.09 (3H, br s), 2.23 (6H, s), 2.85 (IH, d, J 3), 3.24 (2H, br s), 3.51 (2H, br s), 5.73 (IH, d, J 2), 7.03-7.12 (m, 3H), 7.26-7.39 ( , 4H);
• the compound 50 was prepared by foUowing the synthesis procedure as described for compound 2.
• the compound of this Example was prepared by following the synthesis procedure as described for compound 3.
• Vmax (KBrVcm "1 3304, 2939, 2810, 1626, 1429, 1286, 1096, 846; ⁇ H (400 MHz, CDCI3) 1.11 (3H, br s), 1.20 (3H, br s), 1.87 (IH, br s), 2.20 (3H, s), 2.22 (3H, s), 2.34 (4H, br s), 2.86-2.89 (4H, m), 3.25 (2H, br s), 3.51 (2H, br s), 4.15 (IH, s), 7.02-7.15 (3H, m), 7.26- 7.30 (2H, m), 7.42-7.46 (2H, m);
• the compound 52 was prepared by foUowing the synthesis procedure as described for compound 1. ⁇ H (400 MHz, CDC1 3 ) 1.06 (3H, br s), 1.20 (3H, br s), 3.01 (IH, d, J 4), 3.21 (2H, br s), 3.49 (2H, br s), 6.47 (IH, d, J 4), 7.24-7.48 (7H, m), 7.55-7.58 (IH, m), 7.78-7.87 (2H, m), 7.98-8.01 (IH, m);
• the compound 53 was prepared by foUowing the synthesis procedure as described for compound 2.
• the compound of this Example was prepared by following the synthesis procedure as described for compound 3.
• N-t-Butoxycarbonyl-2-aminoisobutyric acid (5.0g, 25mmol) and D,L-alanine methylester hydrochloride (3.5g, 25mmol) was dissolved in dry dichloromethane (50mL) and cooled to 0°C.
• Triethylamine (3.5mL, 25mmol) and then l-(3-dimethylaminopropyl)-3-ethyl- carbod ⁇ mide hydrochloride (4.8g, 25mmol) was added and the mixture was stirred at 0°C until lumps dissolved. The reaction mixture was then left in the freezer 4d at -20°C.
• IR (HCl salt, Kbr) (cm-1): 3400 (br, OH), 2500 (br, R 2 NH 2 +), 16200 (s) (C O or R 2 NH2+) > 1285, 1043 (C-O).
• l H NMR: (amine, CDC1 3 ): ⁇ 7.50-6.60 (m, 8H, Ar-H), 5.70 (m, IH, aUyl-H), 5.00 (m, 2H, aUyl-H), 4.70 (s, IH, CHAi 2 ), 3.70 (s, 3H, MeO), 3.5 +3.3 (2 br.
• the compound of this Example was prepared by foUowing the synthesis procedure as described for Example 3.
• the compound 62 was prepared by foUowing the synthesis procedure as described for compound 1.
• the compound 63 was prepared by foUowing the synthesis procedure as described for compound 2.
• the compound of this Example was prepared by foUowing the synthesis procedure as described for Examples 2 and 3.
• the compound 67 was prepared by foUowing the synthesis procedure as described for compound 55.
• the compound of this Example was prepared by foUowing the synthesis procedure as described for compound 3.
• the compound of this Example was prepared by following the synthesis procedure as described for compound 3.
• the compound of this Example was prepared by following the synthesis procedure as described for Examples 2 and 3.
• the compound 72 was prepared by foUowing the synthesis procedure as described for compound 1.
• the compound 73 was prepared by foUowing the synthesis procedure as described for compound 2.
• the compound of this Example was prepared by foUowing the synthesis procedure as described for compound 3.
• the compound of this Example was prepared by following the synthesis procedure as described for Example 3.
• the compound of this Example was prepared by foUowing the synthesis procedure as described for compound 82, but substituting ammonia for ethylamine.
• N,N-Diethy 1-4- [ (2,5, 5-trimethyl-l-piperazinyl)-3-methoxy benzyl] - benzamide N,N-Diethyl-4-(chloro-3-methoxybenzyl)-benzamide (1.6g, 4.8mmol) was reacted with piperazine (1.6g, 19mmol) in acetonitrile (20mL) for 4 h at 80 °C to give a total of 1.lg product (63%) which was converted into the dihydrochloride salt. Mp: 165-82 °C.
• IR amine. CDC1 3 in KBr ceU) (cm-1): 3688. 1611. 1458, 1436, 1285.
• IR (NaCl Film): v 2807, 1620, 1513, 1451, 1282, 1137cm 1 .
• novel compounds according to the present invention may be administered per oraUy, intramuscularly, subcutaneously, intraperitoneaUy, intrathoraciaUy, intravenously, intrathecaUy and intracerebroventricularly.
• the dosage will depend on the route of administration, the severity of the disease, age and weight of the patient and other factors normaUy considered by the attending physician, when determining the individual regimen and dosage level at the most appropriate for a particular patient
• inert, pharmaceuticaUy acceptable carriers can be either soHd or tiquid.
• SoUd form preparations include powders, tablets, dispersible granules, capsules, cachets, and suppositories.
• a sohd carrier can be one or more substances which may also act as dUuents, flavoring agents, solubilizers, lubricants, suspending agents, binders, or tablet disintegrating agents; it can also be an encapsulating material.
• the carrier is a finely divided solid which is in a mixture with the finely divided active component
• the active component is mixed with the carrier having the necessary binding properties in suitable proportions and compacted in the shape and size desired.
• a low-melting wax such as a mixture of fatty acid glycerides and cocoa butter is first melted and the active ingredient is dispersed therein by, for example, stirring. The molten homogeneous mixture is then poured into convenient sized molds and aUowed to cool and soUdify.
• Suitable carriers are magnesium carbonate, magnesium stearate, talc, lactose, sugar, pectin, dextrin, starch, tragacanth, methyl ceUulose, sodium carboxymethyl ceUulose, a low-melting wax, cocoa butter, and the like.
• PharmaceuticaUy acceptable salts are acetate, benzenesulfonate, benzoate, bicarbonate, bitartrate, bromide, calcium acetate, camsylate, carbonate, chloride, cetrate, dihydrochloride, edetate, edisylate, estolate, esylate, fumarate, glucaptate, gluconate.
• Preferred pharmaceuticaUy acceptable salts are the hydrochlorides and citrates.
• composition is intended to include the formulation of the active component with encapsulating material as a carrier providing a capsule in which the active component (with or without other carriers) is surrounded by a carrier which is thus in association with it Similarly, cachets are included. Tablets, powders, cachets, and capsules can be used as solid dosage forms suitable for oral administration.
• Liquid from compositions include solutions, suspensions, and emulsions.
• Sterile water or water-propylene glycol solutions of the active compounds may be mentioned as an example of liquid preparations suitable for parenteral administration.
• Liquid compositions can also be formulated in solution in aqueous polyethylene glycol solution.
• Aqueous solutions for oral administration can be prepared by dissolving the active component in water and adding suitable colorants, flavoring agents, stabilizers, and thickening agents as desired.
• Aqueous suspensions for oral use can be made by dispersing the finely divided active component in water together with a viscous material such as natural synthetic gums, resins, methyl ceUulose, sodium carboxymethyl ceUulose, and other suspending agents known to the pharmaceutical formulation art
• the pharmaceutical compositions is in unit dosage form.
• the composition is divided into unit doses containing appropriate quantities of the active component.
• the unit dosage form can be a packaged preparation, the package containing discrete quantities of the preparations, for example, packeted tablets, capsules, and powders in vials or ampoules.
• the unit dosage form can also be a capsule, cachet or tablet itself, or it can be the appropriate number of any of these packaged forms.
• Human 293S ceUs expressing cloned human ⁇ , ⁇ , and K receptors and neomycin resistance were grown in suspension at 37°C and 5% CO 2 in shaker flasks containing calcium-free DMEM 10% FBS, 5% BCS, 0.1% Pluronic F-68, and 600 ⁇ g/ml geneticin.
• CeUs were peUeted and resuspended in lysis buffer (50 mM Tris, pH 7.0, 2.5 mM EDTA, with PMSF added just prior to use to 0.1 mM from a 0.1 M stock in ethanol), incubated on ice for 15 min, then homogenized with a polytron for 30 sec. The suspension was spun at lOOOg (max) for 10 min at 4°C. The supernatant was saved on ice and the pellets resuspended and spun as before. The supernatants from both spins were combined and spun at 46,000 g(max) for 30 min. The pellets were resuspended in cold Tris buffer (50 mM Tris/ Cl, pH 7.0) and spun again.
• lysis buffer 50 mM Tris, pH 7.0, 2.5 mM EDTA, with PMSF added just prior to use to 0.1 mM from a 0.1 M stock in ethanol
• Membranes were thawed at 37°C, cooled on ice, passed 3 times through a 25-gauge needle, and diluted into binding buffer (50 mM Tris, 3 mM MgCl 2> 1 mg/ml BSA (Sigma A- 7888), pH 7.4, which was stored at 4°C after filtration through a 0.22 m filter, and to which had been freshly added 5 ⁇ g/ml aprotinin, 10 ⁇ M bestatin, 10 ⁇ M diprotin A, no DTT).
• binding buffer 50 mM Tris, 3 mM MgCl 2> 1 mg/ml BSA (Sigma A- 7888), pH 7.4, which was stored at 4°C after filtration through a 0.22 m filter, and to which had been freshly added 5 ⁇ g/ml aprotinin, 10 ⁇ M bestatin, 10 ⁇ M diprotin A, no DTT).
• the tubes were vortexed and incubated at 25°C for 60-75 min, after which time the contents are rapidly vacuum-filtered and washed with about 12 ml/tube iced wash buffer (50 mM Tris, pH 7.0, 3 mM MgCl ⁇ ) through GF/B filters (Whatman) presoaked for at least 2h in 0.1 % polyethyleneimine.
• the radioactivity (dpm) retained on the filters was measured with a beta counter after soaking the filters for at least 12h in minivials containing 6-7 ml scintillation fluid.
• the filtration is over 96-place PEI- soaked unifilters, which were washed with 3 x 1 ml wash buffer, and dried in an oven at 55°C for 2h.
• the filter plates were counted in a TopCount (Packard) after adding 50 ⁇ l MS-20 scintillation fluid/weU.
• the specific binding (SB) was calculated as TB-NS, and the SB in the presence of various test peptides was expressed as percentage of control SB.
• Values of IC50 -nd HiU coefficient (n ⁇ ) for ligands in displacing specificaUy bound radioligand were calculated from logit plots or curve fitting programs such as Ligand, GraphPad Prism, SigmaPlot, or ReceptorFit.
• Values of Kj were calculated from the Cheng-Prussoff equation. Mean ⁇ S.E.M. values of IC50, Kj and ⁇ H were reported for ligands tested in at least three displacement curves.
• RadioUgand K $ values were determined by performing the binding assays on ceU membranes with the appropriate radioUgands at concentrations ranging from 0.2 to 5 times the estimated Kg (up to 10 times if amounts of radioligand required are feasable). The specific radioligand binding was expressed as pmole/mg membrane protein. Values of Kg and BQ UX from individual experiments were obtained from nonlinear fits of specifically bound (B) vs. nM free (F) radioUgand from individual according to a one-site model. B) BIOLOGICAL MODEL (IN VIVO MODEL )
• mice Male Sprague-Dawley rats (Charles River, St-Constant, Canada) weighing 175-200g at the time of surgery were used. They were housed in groups of three in rooms thermostaticaUy maintained at 20° C with a 12: 12 hr Ught/dark cycle, and with free access to food and water. After arrival, the animals were aUowed to acclimatize for at least 2 days before surgery. The experiments were approved by the appropriate Medical Ethical Committee for animal studies.
• the rats were first anesthetized in a Halothane chamber after which lO ⁇ l of FCA was injected s.c. into the dorsal region of the left foot, between the second and third external digits. The animals were then aUowed to recover from anesthesia under observation in their home cage.
• Rats were anesthetized with a mixture of Ketamine / Xylazine i.p. (2ml/kg) and placed on their right side and an incision made over, and along the axis of, the lateral aspect of the left femur.
• the muscles of the upper quadriceps were teased apart to reveal the sciatic nerve on which a plastic cuff (PE-60 tubing, 2mm long) was placed around. The wound was then closed in two layers with 3-0 vicryl and silk sutures.
• Rats were placed in Plexiglas cages on top of a wire mesh bottom which aUowed access to the paw, and were left to habituate for 10-15 min. The area tested was the mid-plantar left hind paw, avoiding the less sensitive foot pads. The paw was touched with a series of 8 Von Frey hairs with logarithmicaUy incremental stiffness (0.41, 0.69, 1.20, 2.04, 3.63, 5.50, 8.51, and 15.14 grams; Stoelting, UI, USA).
• the von Frey hair was applied from underneath the mesh floor perpendicular to the plantar surface with sufficient force to cause a stight buckling against the paw, and held for approximately 6-8 seconds. A positive response was noted if the paw was sharply withdrawn. Flinching immediately upon removal of the hair was also considered a positive response. Ambulation was considered an ambiguous response, and in such cases the stimulus was repeated.
• TESTING PROTOCOL The animals were tested on postoperative day 1 for the FCA-treated group and on post ⁇ operative day 7 for the Sciatic Nerve Cuff group.
• the 50% withdrawal threshold was determined using the up-down method of Dixon (1980). Testing was started with the 2.04 g hair, in the middle of the series. Stimuli were always presented in a consecutive way, whether ascending or descending. In the absence of a paw withdrawal response to the initiaUy selected hair, a stronger stimulus was presented; in the event of paw withdrawal, the next weaker stimulus was chosen.
• Optimal threshold calculation by this method requires 6 responses in the immediate vicinity of the 50% threshold, and counting of these 6 responses began when the first change in response occurred, e.g. the threshold was first crossed.
• % MPE Drug treated threshold (g) - allodynia threshold (g) X 100 Control threshold (g) - allodynia threshold (g)
• Rats were injected (subcutaneously, intraperitoneaUy, or oraUy) with a test substance prior to von Frey testing, the time between administration of test compound and the von Frey test varied depending upon the nature of the test compound.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Health & Medical Sciences (AREA)
• Life Sciences & Earth Sciences (AREA)
• General Health & Medical Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Public Health (AREA)
• Veterinary Medicine (AREA)
• Medicinal Chemistry (AREA)
• Pharmacology & Pharmacy (AREA)
• Epidemiology (AREA)
• Chemical Kinetics & Catalysis (AREA)
• General Chemical & Material Sciences (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• Pain & Pain Management (AREA)
• Physics & Mathematics (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Neurosurgery (AREA)
• Proteomics, Peptides & Aminoacids (AREA)
• Rheumatology (AREA)
• Anesthesiology (AREA)
• Engineering & Computer Science (AREA)
• Neurology (AREA)
• Biomedical Technology (AREA)
• Optics & Photonics (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Plural Heterocyclic Compounds (AREA)
• Hydrogenated Pyridines (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Priority Applications (14)

Applications Claiming Priority (2)

Related Child Applications (2)

Publications (1)

Family

ID=20400739

Family Applications (1)

Country Status (27)

Cited By (47)

Families Citing this family (10)

Citations (9)

Family Cites Families (16)

• 1995
  • 1995-12-22 SE SE9504661A patent/SE9504661D0/xx unknown
• 1996
  • 1996-11-12 UA UA98074034A patent/UA71538C2/uk unknown
  • 1996-12-09 ZA ZA9610352A patent/ZA9610352B/xx unknown
  • 1996-12-11 KR KR10-1998-0704757A patent/KR100493832B1/ko not_active Expired - Fee Related
  • 1996-12-11 CA CA002239174A patent/CA2239174C/en not_active Expired - Fee Related
  • 1996-12-11 CN CN96180102A patent/CN1119336C/zh not_active Expired - Fee Related
  • 1996-12-11 EP EP96943426A patent/EP0915855A1/en not_active Withdrawn
  • 1996-12-11 JP JP09523557A patent/JP2000502679A/ja active Pending
  • 1996-12-11 IL IL124996A patent/IL124996A/en not_active IP Right Cessation
  • 1996-12-11 WO PCT/SE1996/001635 patent/WO1997023466A1/en not_active Ceased
  • 1996-12-11 EP EP20030028149 patent/EP1408037A1/en not_active Ceased
  • 1996-12-11 RU RU2002106503/04A patent/RU2307833C2/ru not_active IP Right Cessation
  • 1996-12-11 NZ NZ324887A patent/NZ324887A/xx not_active IP Right Cessation
  • 1996-12-11 HU HU9901304A patent/HUP9901304A3/hu unknown
  • 1996-12-11 SK SK822-98A patent/SK282743B6/sk not_active IP Right Cessation
  • 1996-12-11 RU RU98113786/04A patent/RU2194702C2/ru not_active IP Right Cessation
  • 1996-12-11 TR TR1998/01180T patent/TR199801180T2/xx unknown
  • 1996-12-11 EE EE9800194A patent/EE04640B1/xx not_active IP Right Cessation
  • 1996-12-11 US US08/836,830 patent/US6130222A/en not_active Expired - Fee Related
  • 1996-12-11 AU AU12162/97A patent/AU715547B2/en not_active Ceased
  • 1996-12-11 BR BR9612204A patent/BR9612204A/pt active IP Right Grant
  • 1996-12-11 KR KR1020057003491A patent/KR20050047534A/ko not_active Ceased
  • 1996-12-11 CZ CZ0176898A patent/CZ296159B6/cs not_active IP Right Cessation
  • 1996-12-11 PL PL327403A patent/PL193061B1/pl not_active IP Right Cessation
  • 1996-12-20 MY MYPI96005403A patent/MY115662A/en unknown
  • 1996-12-20 AR ARP960105834A patent/AR005420A1/es not_active Application Discontinuation
  • 1996-12-20 TW TW085115800A patent/TW458971B/zh not_active IP Right Cessation
  • 1996-12-21 EG EG19961162A patent/EG25688A/xx active
• 1998
  • 1998-06-11 IS IS4769A patent/IS1839B/is unknown
  • 1998-06-18 NO NO19982807A patent/NO310869B1/no not_active IP Right Cessation
• 2000
  • 2000-08-02 US US09/631,116 patent/US6680321B1/en not_active Expired - Fee Related
• 2001
  • 2001-02-05 AR ARP010100517A patent/AR034116A2/es active IP Right Grant
• 2003
  • 2003-11-17 US US10/714,447 patent/US20040138228A1/en not_active Abandoned

Patent Citations (9)

Also Published As

Similar Documents

Legal Events