EP2358681A1 - Substituierte 4-(1,2,3,4-tetrahydroisochinolin-2-yl)-4-oxo-buttersäureamide als kcnq2/3 modulatoren - Google Patents
Substituierte 4-(1,2,3,4-tetrahydroisochinolin-2-yl)-4-oxo-buttersäureamide als kcnq2/3 modulatorenInfo
- Publication number
- EP2358681A1 EP2358681A1 EP09795712A EP09795712A EP2358681A1 EP 2358681 A1 EP2358681 A1 EP 2358681A1 EP 09795712 A EP09795712 A EP 09795712A EP 09795712 A EP09795712 A EP 09795712A EP 2358681 A1 EP2358681 A1 EP 2358681A1
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- Prior art keywords
- phenyl
- unsubstituted
- polysubstituted
- alkyl
- oxo
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- C07D217/06—Heterocyclic compounds containing isoquinoline or hydrogenated isoquinoline ring systems with only hydrogen atoms or radicals containing only carbon and hydrogen atoms, directly attached to carbon atoms of the nitrogen-containing ring; Alkylene-bis-isoquinolines with the ring nitrogen atom acylated by carboxylic or carbonic acids, or with sulfur or nitrogen analogues thereof, e.g. carbamates
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- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
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- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Definitions
- the invention relates to substituted Tetrahydroisochinolinyl ⁇ -oxo-butterklaamide, process for their preparation, medicaments containing these compounds and the use of these compounds for the preparation of medicaments.
- K + channels of the molecular subtype KCNQ2 / 3 (Kv7.2 / 7.3) are expressed in neurons of different regions of the central (hippocampus, amygdala) and peripheral (dorsal root ganglia) nervous system and regulate their excitability. Activation of KCNQ2 / 3 K + channels leads to hyperpolarization of the cell membrane and concomitant decrease in the electrical excitability of these neurons.
- KCNQ2 / 3-expressing neurons of the dorsal root ganglia are involved in the transmission of nociceptive excitations from the periphery to the spinal cord (Passmore et al., J Neurosci., 2003; 23 (18): 7227-36).
- the KCNQ2 / 3 agonist retigabine has demonstrated analgesic efficacy in preclinical neuropathy and inflammatory pain models (Blackburn-Munro and Jensen, Eur J Pharmacol., 2003; 3): 109-16; Dost et al., Naunyn Schmiedeberg's Arch Pharmacol 2004; 369 (4): 382-390).
- the KCNQ2 / 3 K + channel thus provides a suitable starting point for the treatment of pain; in particular pain selected from the group consisting of chronic pain, neuropathic pain, inflammatory pain and muscular pain (Nielsen et al., Eur J Pharmacol. 2004; 487 (1-3): 93-103), especially neuropathic and inflammatory pain represents.
- the KCNQ2 / 3 K + channel is a suitable target for the therapy of a variety of other diseases such as migraine (US2002 / 0128277), cognitive disorders (Gribkoff, Expert Opin Ther Targets 2003; 7 (6): 737-748), Anxiety states (Korsgaard et al., J Pharmacol Exp Ther.
- PK / PD Pharmacokinetic / Pharmacodynamic
- a weak or non-existent interaction with transporter molecules involved in the uptake and excretion of drugs should also be considered as an indication of improved bioavailability and, if necessary, low drug interactions.
- the interactions with the degradation and excretion of carbohydrates should also be considered Enzymes involved enzymes should be as low as possible, since such test results also indicate that at best little or no drug interactions are to be expected
- the compounds show a high selectivity towards other receptors of the KCNQ family (specificity), for example with respect to KCNQ1, KCNQ3 / 5 or KCNQ4.
- High selectivity may have a favorable effect on the side effect profile.
- Compounds which (also) bind to KCNQ1 bring with them a high risk of cardiac side effects, so high selectivity to KCNQ1 may be desirable.
- High selectivity may, however, also be advantageous over other receptors.
- Low affinity for hERG ion channel or L Calcium ion channel may be advantageous because these receptors are associated with the onset of cardiac side effects.
- improved selectivity for binding to other endogenous proteins ie, B receptors or enzymes for improvement the side effect profile, and thus lead to an improved compatibility
- An object of the invention was therefore to provide novel compounds which have advantages over the compounds of the prior art.
- the compounds should be suitable in particular as pharmacologically active substances in medicaments, preferably in medicaments for the treatment of disorders or diseases which are at least partially through KCNQ2 / 3 K + channels
- substituted Tetrahydro ⁇ soch ⁇ nol ⁇ nyl-4-oxo-buttersaureamide the following general formula (1) are suitable for the treatment of pain
- substituted Tetrahydro ⁇ soch ⁇ nol ⁇ nyl-4-oxo-buttersauream ⁇ de the general formula given below (1 ) also have an excellent affinity for the KCNQ2 / 3K + channel and are therefore suitable for the treatment of disorders or diseases that are mediated at least in part by KCNQ2 / 3K + channels.
- the substituted tetrahydro-isoquinolinyl-4-oxo-butyric acid amides act as Modulators, ie agonists or antagonists, of the KCNQ2 / 3K + channel
- An object of the invention are substituted Tetrahydro ⁇ soch ⁇ nol ⁇ nyl-4-oxobuttersaureamide of the general formula (1)
- R 0 is C 1-10 -alkyl or C 2-10 -heteroalkyl, in each case saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted, C 3 -C 5 -cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted, aryl or heteroaryl, each unsubstituted or substituted one or more times, over Ci s-alkyl verbrucktes C 3 7 cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or mono- or polysubstituted, wherein the alkyl chain branched or unbranched, in each case saturated or unsaturated, may be unsubstituted, mono- or poly-substituted, or C 1 8 may be alkyl verbrucktes aryl or heteroaryl, in
- R 2 is H, F, Cl, Br, or C 10 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted,
- R 1 and R 2 together with the linking carbon atom as ring member is a C 3 7 -cycloalkyl, preferably C 3 6 cycloalkyl, or form heterocyclyl, in each case saturated or unsaturated, unsubstituted or substituted one or more times, each optionally with (hetero- ) aryl condensed, unsubstituted or monosubstituted or polysubstituted,
- R 7, R 8, R 9, R 10 are each independently H, F, Cl, Br, Ci 10 alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted, are provided,
- R 11 is H, F, Cl, Br, CN, R 0 ,
- R 12 is H, F, Cl, Br, CN, or C 10 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted,
- R 13 is H, F, Cl, Br, CN, Ci. 10 -alkyl or C 2 i 0 heteroalkyl, in each case saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted, C 3 7 -cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or mono- or polysubstituted, aryl or heteroaryl each unsubstituted or substituted one or more times via C 8 alkyl verbrucktes C 3 7 cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or mono- or polysubstituted, wherein the alkyl chain branched or unbranched, in each case saturated or unsaturated, unsubstituted or mono- may be mono- or polysubstituted, or C 8 alkyl-verbrucktes aryl or heteroaryl, in each case unsubstitute
- R 14 is H, F, Cl, Br, CN, or C 10 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted,
- R 11 and R 13 together with the carbon atoms connecting them as R mg member a C 3 . 7 -cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted, optionally with (hetero) aryl condensed, unsubstituted or monosubstituted or polysubstituted, or R 11 and R 12 ; or R 13 and R 14 together with the linking carbon atoms as ring members, a C 3 _ 7 cycloalkyl or heterocyclyl form, in each case saturated or unsaturated, unsubstituted or mono- or polysubstituted, in each case optionally aryl fused with (hetero) unsubstituted or monosubstituted or polysubstituted;
- R 15 is R 0 ;
- aryl substituted and “heteroaryl substituted” mean the substitution of one or more hydrogen atoms each independently of one another by F; Cl; Br; I; NO 2 ; CF 3 ; CN; R 0 ; C (O) H; C (O) R 0 ; CO 2 H; C (O) OR 0 ; CONH 2 ; C (O) NHR 0 ; C (O) N (R 0 J 2 ; OH; OR 0 ; O-fd- ⁇ -Alky O-O; 0-C (O) -R 0 ; 0-C (O) -OR 0 ; 0- (CO ) -NH-R 0 ; 0-C (O) -N (R °) 2 ; 0-S (O) 2 -R 0 ; 0-S (O) 2 OH; 0-S (O) 2 OR 0 ; 0-S (O) 2 NH 2 ; O-S (O) 2 NHR 0
- Ci 2 alkyl "C 1-4 -alkyl", “Ci 6 alkyl.”, “Ci -8 alkyl”, “C ⁇ -alkyl”, “C 2 4 -.
- Alkyl "and” C 2 - 8 alkyl "for the purposes of this invention acyclic saturated or unsaturated hydrocarbon radicals, which may be branched or unbranched and unsubstituted or mono- or polysubstituted, with 1 to 2 or 1 to 4 or 1 to 8 or 1 to 10 or 2 to 4 or 2 to 8 C atoms, ie Ci. 2- alkanyle and ci- 2- alkeny! Ci- 4 alkenyls and C 2 .
- Ci -8 - Alkanyle 4- alkenyls or Ci -8 - Alkanyle, Ci-s-alkenyls and C ⁇ - ⁇ -alkynyls or Ci- 10 -Alkanyle, Ci_io-alkenyls and C 2 . 10 alkynyls or C 2 ⁇ -Alkanyle, C 2-4 alkenyls and C 2 ⁇ -Alkinyle or C 2 . 8 alkynyls, C 2-8 alkenyls and C 2-8 alkynyls.
- Alkenyls have at least one CC double bond and alkynyls at least one CC triple bond.
- one, two or three carbon atoms of a C 2 -io-heteroalkyl are represented by a heteroatom or a heteroatom group, respectively
- each heteroatom or each heteroatom group must have at least two carbon atoms as a binding partner.
- C 2 10 -Heteroalkenyls have at least one CC bond or one CN double bond and C 2 -C 10 -heteroalkyls at least one CC triple bond to C 2 10 heteroalkyl is preferably selected from the group consisting of -CH 2 -O-CH 3 , -CH 2 -CH 2 -O-CH 3 , -CH 2 -CH 2 -O-CH 2 - CH 3 , -CH 2 - CH 2 -O-CH 2 -CH 2 -O-CH 3 , -CH 2 -NH-CH 3 , -CH 2 -CH 2 -NH-CH 2 -CH 3 , -CH 2 -CH 2 -NH-CH 2 --CH 2 -NH-CH 3 , -CH 2 -N (CH 3 ) -CH 3 , -CH 2 -CH 2 -N (CH 3 ) -CH 2 -CH 3 , -CH 2 -CH 2 -N (
- cycloalkyl means cychsche hydrocarbons having 3 5, 6 or 7 carbon atoms, optionally wherein said hydrocarbons are saturated or unsaturated ( but not aromatic), unsubstituted or monosubstituted or polysubstituted.
- the cycloalkyl can be attached to the general structure above any and possible ring member of the cycloalkyl radical.
- the cycloalkyl radicals can also be saturated with further, (partially) unsaturated heterocychschen be fused aromatic or heteroaromatic ring systems that may be in turn unsubstituted or mono- or polysubstituted the cycloalkyl radicals may be bridged such as in the case of adamantyl or dicyclopentadienyl
- C 3 7 further one or more times - cycloalkyl selected from the group selected from cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohep tyl, cyclopentenyl, cyclohexenyl and cycloheptenyl
- heterocyclyl includes saturated or unsaturated (but not aromatic) cycloalkyls of three to seven ring-ghedes in which one, two or three carbon atoms are replaced by a heteroatom, each independently selected from the group S, N or O, said ringgheder
- the heterocyclyl can be attached to the general structure above any and possible ring member of the heterocyclyl radical.
- the heterocyclyl radicals can also be condensed with further saturated, (partially) unsaturated or aromatic or heteroaromatic ring systems which in turn is unsubstituted or simple or can be substituted several times.
- heterocyclyl radicals from the group azetidinyl, aziridinyl, azepanyl, quinolinyl, dioxanyl, dioxolanyl, furanyl, imidazolidinyl, isoxazolidinyl, isoquinolinyl, indolinyl, morpholinyl, pyranyl, pyrrolyl, pyridinyl, pyrrolyl, pyrrolidinyl, piperazinyl, piperidinyl, pyrazolidinyl, pyrazolinonyl or thiomorpholinyl.
- aryl in the context of this invention means aromatic hydrocarbons having up to 14 ring members, i.a. Phenyle and naphthyls.
- Each aryl radical can be unsubstituted or monosubstituted or polysubstituted, where the aryl substituents can be the same or different and in any desired and possible position of the aryl.
- the attachment of the aryl to the general structure above can take place via any and possible ring member of the aryl radical.
- the aryl radicals can also be condensed with further saturated, (partially) unsaturated, heterocyclic, aromatic or heteroaromatic ring systems, which in turn may be unsubstituted or monosubstituted or polysubstituted.
- Aryl is preferably selected from the group comprising phenyl, 1-naphthyl and 2-naphthyl, which may each be unsubstituted or monosubstituted or polysubstituted.
- a particularly preferred aryl is phenyl, unsubstituted or monosubstituted or polysubstituted.
- heteroaryl represents a 5-, 6- or 7-membered cyclic aromatic radical containing at least 1, optionally also 2, 3, 4 or 5 heteroatoms, wherein the heteroatoms are each independently selected from the group S, N or O and the heteroaryl radical may be unsubstituted or mono- or polysubstituted; in the case of heteroaryl substitution, the substituents may be the same or different and may be in any and possible position of the heteroaryl.
- Preferred heteroatoms are S, N and O. Particularly preferred are S and N.
- the bond to the general structure above can take place via any and possible ring member of the heteroaryl radical.
- the heteroaryl may also be part of a bi- or polycyclic system having up to 14 ring members, wherein the ring system may be formed with further saturated, (partially) unsaturated, heterocyclic or aromatic or heteroaromatic rings, which in turn may be unsubstituted or mono- or polysubstituted ,
- the heteroaryl radical is selected from the group the benzofuranyl, benzoimidazolyl, benzothiazinyl, benzothiadiazolyl, benzothiazolyl, benzotiazolyl, benzodioxolanyl, benzodioxanyl, quinazolinyl, carbazolyl, quinolinyl, furyl (furanyl), imidazolyl, indazolyl, indolizinyl, indolyl, isoquinolmyl, isoxazoyl, isothiazolyl, indolyl, oxadiazolyl, phthaloyl,
- Ci- ⁇ alkyl or C 2 ⁇ -alkyl verbrucktes aryl, heteroaryl, heterocyclyl or cycloalkyl
- Ci 2 alkyl or CI_ 4 alkyl or ds-alkyl or C 2 means in the context of the invention, that Ci 2 alkyl or CI_ 4 alkyl or ds-alkyl or C 2 .
- aryl or heteroaryl or heterocyclyl or cycloalkyl have the meanings defined above and the aryl or heteroaryl or heterocyclyl or cycloalkyl radical via a Ci 2 alkyl or a C ⁇ alkyl or a Ci ⁇ -alkyl or the alkyl chain can in any case be saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted
- radical “N (R 0 or H) 2 " may be "NH 2 ", "NHR 0" and “N (R 0 J 2" are, if R 0 as in the case of "N (R 1 V 'occurs more than once within a radical, then R 0 are each identical or different meanings in the present example of" N (R °) 2 ", R 0 may, for example, be aryl twice, giving rise to the functional group” N (aryl) 2 ", or R 0 may be aryl once and C 10 -alkyl once, giving rise to the functional group” N (aryl) (C 10 -alkyl) "
- the functional group aryl-NHCi 10 -alkyl C 10 -alkyl can then be substituted again, for example with Cl (
- the substituents of the 2 generation can not be substituted again, ie there are then already no substituents of the 3 generation.
- the functional groups for R 0 to R 23 may each be optionally substituted, the respective substituents can then not be substituted again in turn
- the compounds of the invention are defined by substituents which, together with the carbon or heteroatom (s) joining them as a ring member or as ring members form a ring, for example a C3. 7 -cycloalkyl or a heterocyclyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted.
- These ring systems thus formed may optionally be condensed with (hetero) aryl, ie with an aryl such as phenyl or a heteroaryl such as pyridyl, where the (hetero) aryl radical may be unsubstituted or monosubstituted or polysubstituted.
- the ring systems thus formed are condensed with an aryl, more preferably with phenyl.
- this cyclohexyl ring may be fused with phenyl to form tetrahydronaphthyl.
- the term salt formed with a physiologically acceptable acid means salts of the respective active ingredient with inorganic or organic acids which are physiologically compatible, in particular when used in humans and / or mammals.
- Particularly preferred is the hydrochloride.
- physiologically acceptable acids are: hydrochloric acid, hydrobromic acid, sulfuric acid, methanesulfonic acid, formic acid, acetic acid, oxalic acid, succinic acid, tartaric acid, mandelic acid, fumaric acid, maleic acid, lactic acid, citric acid, glutamic acid, saccharic acid, monomethyl sebacic acid, 5-oxoproline, hexane 1-sulfonic acid, nicotinic acid, 2-, 3- or 4-aminobenzoic acid, 2,4,6-thmethyl-benzoic acid, ⁇ -lipoic acid, acetylglycine, hippuric acid, phosphoric acid and / or aspartic acid.
- citric acid and hydrochloride examples of physiologically
- Physiologically acceptable salts with cations or bases are salts of the respective compound - as an anion with at least one, preferably inorganic, cation, which are physiologically compatible - especially when used in humans and / or mammals.
- Particularly preferred are the salts of the alkali and alkaline earth metals but also ammonium salts, but especially (mono-) or (di) sodium, (mono-) or (di) potassium, magnesium or calcium salts
- the substituent R 1 is selected from the group consisting of Ci 10 alkyl, preferably Ci 6 alkyl, or C 2 10 heteroalkyl, in each case saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted, C 3 7 -cycloalkyl, preferably C 3 6 cycloalkyl, in each case saturated or unsaturated, unsubstituted or mono- or polysubstituted aryl or heteroaryl, in each case unsubstituted or mono- or polysubstituted on C 8 alkyl verbrucktes 3 C 7 -cycloalkyl, preferably C 3 6-Cycloalkyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted, where the alkyl chain can be branched or unbranched, saturated or unsaturated, unsubstituted, monosubstituted or polysubstituted, where the al
- R 2 is selected from the group consisting of H or C 10 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted
- the substituent R 1 is selected from the group consisting of C 10 alkyl, saturated or unsaturated, branched or unbranched, unsubstituted, C 3 7 -cycloalkyl, saturated or unsaturated, unsubstituted or mono- or polysubstituted by phenyl, Thienyl or Py ⁇ dyl, each unsubstituted or mono- or polysubstituted, via Ci.
- R 2 is selected from the group consisting of H or Ci.io-alkyl, saturated or unsaturated, branched or unbranched, unsubstituted.
- the substituent R 1 is selected from the group consisting of
- Ci.io-alkyl saturated, branched or unbranched, unsubstituted
- R 16a and / or R 16b monosubstituted or disubstituted by R 16a and / or R 16b ;
- R 16c and / or R 16d monosubstituted or disubstituted by R 16c and / or R 16d ;
- h is 0, 1, 2, 3 or 4, preferably 0;
- e is 0, 1, 2, 3 or 4, preferably 0;
- R 16a , R 16b , R 16c , R 16d , R 16e and R 16f are each independently selected from the group consisting of H, F, Cl, Br, CN, NH 2 , OCF 3 , SCF 3 , CF 3 , C 1-8 -AlkVl or O-Ci- 8 alkyl, in each case saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted; Aryl, heteroaryl, in each case unsubstituted or monosubstituted or polysubstituted;
- R 17a and R 17b are independently selected from the group consisting of H, F, Cl, Br, CN, NH 2 , OCF 3 , SCF 3 , CF 3 , C 1-8 alkyl or OC ⁇ alkyl, each saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; Aryl, heteroaryl, in each case unsubstituted or monosubstituted or polysubstituted.
- R 16a and R 16b are independently selected from the group consisting of H, F, Cl, CH 3 , OCH 3 and CF 3 , more preferably R 16a and R 16b are each H.
- R 16c and R 16d are independently selected from the group consisting of H, F, Cl, CH 3 , OCH 3 and CF 3 , more preferably R 16c and R 16d are each H.
- R 16e and R 16f are independently selected from the group consisting of H, F, Cl, CH 3 , OCH 3 and CF 3 , more preferably R 16e and R 16f are each H.
- H is preferably 2 or 3, more preferably 3.
- R 17a and R 17b are independently selected from the group consisting of H, F, Cl, Br, CH 3 , OCH 3 and CF 3 , more preferably R 17a and R 17b are each H.
- the substituent R 1 is selected from the group consisting of C ⁇ alkyl or C3 - ⁇ cycloalkyl, each being saturated, branched or unbranched, unsubstituted.
- the substituents R 3 , R 4 , R 5 and R 6 are each independently selected from the group consisting of H, F, Cl 1 Br, CN, CF 3 , NH 2 , OCF 3 , SCF 3 , C 1 - B -alkyl, 0-C 1 8 alkyl, NH (C 1 ⁇ -alkyl), N (C 1 8 alkyl) 2, OH, and SH
- the substituents R 3 , R 4 , R 5 and R 6 are each independently selected from the group consisting of H, F, Cl, OCH 3 , CH 3 , CF 3 and OCF 3
- R 3 and R 5 are each H and R 4 and R 6 are each independently selected from the group consisting of H, F, OCH 3 , CH 3 and CF 3
- the substituents R 7 , R 8 , R 9 and R 10 are each independently selected from the group consisting of H, C 1 10 alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted
- the substituents R 7 , R 8 , R 9 and R 10 are each independently selected from the group consisting of H or C 1 10 alkyl, saturated, unbranched, unsubstituted
- the substituents R 7 , R 8 , R 9 and R 10 are each independently selected from the group consisting of H or CH 3
- the substituent R 11 is selected from the group consisting of H, F, Cl, Br, CN, C 1 -oalkyl, saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted, phenyl or heteroaryl , in each case unsubstituted or monosubstituted or polysubstituted, phenyl or heteroaryl bridged via C 1 -C 4 -alkyl, in each case unsubstituted or monosubstituted or polysubstituted, the alkyl chain in each case being branched or unbranched, saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted,
- R 13 is selected from the group consisting of H, F, Cl, Br, CN, Ci 10 alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted, phenyl or heteroaryl, in each case unsubstituted or mono- or polysubstituted substituted, phenyl or heteroaryl bridged via C 2 4 -alkyl, in each case unsubstituted or monosubstituted or polysubstituted, where the alkyl chain in each case may be branched or unbranched, saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted,
- R 11 and R 13 together with the carbon atoms connecting them as Ringghedern a C 3 7 -cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or mono- or polysubstituted, optionally with phenyl, unsubstituted or mono- or polysubstituted
- R 11 is selected from the group consisting of H, C- M o-alkyl, saturated or unsaturated, branched or unbranched, unsubstituted, phenyl, unsubstituted or mono- or polysubstituted, phenyl over C 4 alkyl-substituted, unsubstituted or mono- or polysubstituted, where the alkyl chain can be branched or unbranched, saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted,
- R 13 is selected from the group consisting of H, C 1-10 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted, phenyl, unsubstituted or monosubstituted or polysubstituted, phenyl bridged via C 2 , -alkyl, unsubstituted or mono- or polysubstituted, where the alkyl chain may each be branched or unbranched, saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted
- R 11 is particularly preferably selected from the group consisting of H, C 1-4 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted, phenyl or benzyl, in each case unsubstituted or monosubstituted or polysubstituted, and the radical R 13 is selected from the group consisting of H; C 1-4 alkyl, saturated or unsaturated, branched or unbranched, unsubstituted; Phenyl, u ⁇ substituiert or monosubstituted or polysubstituted.
- radicals R 11 and R 13 are each independently selected from the group consisting of H and CH 3 , in particular R 11 and R 13 are each H.
- R 12 and R 14 are each independently selected from the group consisting of H; C- M o-alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted.
- R 12 and R 14 are each independently selected from the group consisting of H; C- ⁇ - 4 alkyl, saturated or unsaturated, branched or unbranched, unsubstituted.
- radicals R 12 and R 14 are each independently selected from the group consisting of H and CH 3 , in particular R 12 and R 14 are each H.
- the substituent R 15 is selected from the group consisting of C 3 .i 0 -alkyl or C 2 -io-heteroalkyl, in each case saturated or unsaturated; branched or unbranched, unsubstituted or monosubstituted or polysubstituted; C 3 . 7 -cycloalkyl, saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted; Aryl or heteroaryl, unsubstituted or monosubstituted or polysubstituted; C 3 bridged via C 1 - ⁇ -alkyl.
- alkyl chain may each be branched or unbranched, saturated or unsaturated, unsubstituted, monosubstituted or polysubstituted;
- the substituent R 15 is selected from the group consisting of C3.10 alkyl or C 2 -io-heteroalkyl, each saturated or unsaturated; branched or unbranched, unsubstituted or monosubstituted or polysubstituted; C 3-7 -cycloalkyl, saturated or unsaturated, unsubstituted or mono- or polysubstituted; Aryl or heteroaryl, unsubstituted or monosubstituted or polysubstituted; C 3 bridged via C 1 .8 alkyl.
- the radical R 15 is C 3 .io-alkyl, saturated or unsaturated; branched or unbranched, unsubstituted or monosubstituted or polysubstituted; or is selected from the following substructures A, B or C,
- n 0, 1, 2, 3, 4, 5, 6, 7 or 8; particularly preferably represents 0, 1, 2 or 3, in particular 1;
- the ring X may contain one or two N atoms as Rnggl ⁇ ed (er),
- the ring Y contains at least 1 heteroatom selected from N, O or S and may contain up to 3 heteroatoms independently selected from N, O or S, and / or may contain one or two double bonds,
- R 18 and R 19 together with the carbon or nitrogen atoms connecting them as ring-glands, denote an aryl or heteroaryl fused to the phenyl or heteroaryl ring, in each case unsubstituted or monosubstituted or polysubstituted, or one fused to the phenyl or heteroaryl ring C 3 7 cycloalkyl or hetero- cyclyl, respectively saturated or unsaturated, unsubstituted or mono- or polysubstituted form,
- R 20 and R 21 are independently H or Ci 10 alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted, are C 3 7 cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or mono- or polysubstituted,
- R 20 and R 21 together with the carbon or hetero atoms connecting them as ring members form an aryl or heteroaryl fused to the ring Y, in each case unsubstituted or monosubstituted or polysubstituted,
- R 22 and R 23 independently of one another are H, or C 10 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted
- R 15 has the meaning of substructure A.
- the radical R 15 is selected from the following substructures Aa, Ba or Ca,
- n 0, 1, 2 or 3, particularly preferably 1;
- n 0, 1, 2 or 3;
- the ring X may contain an N atom as a ring member
- the ring Y contains a heteroatom selected from N, O or S and / or contains one or two double bonds;
- R 18 and R 19 are independently H; F; Cl; Br; I; NO 2 ; CN; NH 2 ; C ⁇ 10 -AlkVl, saturated or unsaturated; branched or unbranched, unsubstituted; benzyl; CF 3 ; NH (C 1 - I0 -alkyl); N (C 1 ⁇ 0 -AlkVl) 2 ; OH; Od-io alkyl; OCF 3 ; 0- (C L10 -AlkVl) -O; O-benzyl; SH; SC 1-10 alkyl; SCF 3 ; S-benzyl; Phenyl, unsubstituted or monosubstituted or polysubstituted; mean;
- R 18 and R 19 together with their connecting carbon or nitrogen atoms as ring members a phenyl or heteroaryl fused to the phenyl or heteroaryl ring, in each case unsubstituted or mono- or polysubstituted; form;
- R 20 and R 21 together with their connecting carbon or hetero atoms as ring members a phenyl fused to the ring Y, in each case unsubstituted or monosubstituted or polysubstituted; form;
- R 20 and R 21 together with their connecting carbon or hetero atoms as ring members an aryl or heteroaryl fused to the ring Y, in each case unsubstituted or monosubstituted or polysubstituted; form.
- R 22 and R 23 independently of one another are H or CH 3 , in particular R 22 and R 23 are each H;
- n 0, 1, 2 or 3, in particular 1; means;
- the ring X contains no N atom as ring member
- R 18 and R 19 are independently H; F; Cl; Br; CN; NH 2 ; C 1-4 alkyl; CF 3 ; OH; O-Ci 4 alkyl; OCF 3 ; or SCF 3 ; in particular R 18 and R 19 independently of one another H; F; Cl, CH 3 , OCH 3 or CF 3 ;
- R 18 and R 19 together with the phenyl ring X an indazolyl, unsubstituted or mono- or polysubstituted; or together with their connecting carbon atoms of the phenyl ring X as ring members 0-CH 2 -O; or 0-CH 2 -CH 2 -O; form.
- a further preferred embodiment of the compounds of the general formula (1) according to the invention has the general formula (2)
- R 1 is Ci-io-alkyl, preferably Ci- 6 alkyl, or C 2 -io-heteroalkyl, in each case saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted; C 3 _ 7 cycloalkyl, preferably C. 3 6 -cycloalkyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted; Phenyl, thienyl or pyridyl, each unsubstituted or monosubstituted or polysubstituted; about C
- R 7 , R 8 , R 9 , R 10 are each independently H; or C 4 -alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or mono- or polysubstituted; stand;
- R 11 and R 13 are each independently H; Ci.io-alkyl, saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; stand; or R 11 and R 13 together with their connecting carbon atoms as ring members a C 3 . 7 -cycloalkyl or heterocyclyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted;
- R 15 is C 3 .io-alkyl, saturated or unsaturated; branched or unbranched, unsubstituted or monosubstituted or polysubstituted; C 3 . 7 -cycloalkyl, saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted; Aryl or heteroaryl, unsubstituted or monosubstituted or polysubstituted; C 3 bridged via C 1-8 -alkyl.
- R 1 is selected from Ci_io-alkyl, Ci- preferably 6 alkyl, C 3rd 7- cycloalkyl, preferably C 3 . 6 -cycloalkyl, in each case branched or unbranched, saturated, unsubstituted; Phenyl, unsubstituted or monosubstituted or disubstituted with substituents independently selected from the group consisting of F, Cl, CH 3 , OCH 3 and CF 3 ; Thienyl, unsubstituted or monosubstituted or disubstituted with F, Cl, CH 3 , OCH 3 or CF 3 ; Pyridyl, unsubstituted or mono- or di-substituted with F, Cl, CH 3 , OCH 3 or CF 3 ; phenyl bridged via C 1 -C 3 -alkyl, unsubstituted, where the alkyl chain is unbranched, saturated and unsubstituted;
- R 2 is selected from H or CH 3 , but preferably H is;
- R 3 , R 4 , R 5 and R 6 are each independently H; F; Cl; CH 3 ; OCH 3 or CF 3 ;
- R 7 , R B , R 9 and R 10 are each independently H or CH 3 ;
- R 11 , R 12 , R 13 and R 14 are each independently H or CH 3 ;
- R 15 is Ci.io-alkyl, saturated or unsaturated, branched or unbranched; Phenyl, unsubstituted or monosubstituted or disubstituted with substituents independently selected from the group consisting of F, Cl, CH 3 , OCH 3 and CF 3 ; phenyl bridged via C 1 -C 4 -alkyl, unsubstituted or monosubstituted or disubstituted with substituents independently of one another selected from the group consisting of F, Cl, CH 3 , OCH 3 , CF 3 , -O-CH 2 -O-; naphthyl, thienyl, furanyl, indolyl or pyridyl bridged via C 1-4 -alkyl, in each case unsubstituted; Indazolyl, unsubstituted or monosubstituted with CH 3 ; stands.
- R 1 is selected from methyl, prop-2-yl, 2-methyl-prop-2-yl and cyclohexyl; Phenyl, unsubstituted; Thienyl, unsubstituted; Pyridyl, unsubstituted;
- R 2 is H
- R 3 and R 5 are each H
- R 4 and R 6 are each independently H; F; CF 3 ; CH 3 ; or OCH 3 ;
- R 7 , R 8 , R 9 and R 10 are each independently H or CH 3 ;
- R 11 , R 12 , R 13 and R 14 are H;
- R 15 is Ci- 4 alkyl, saturated and unbranched; Phenyl, unsubstituted or monosubstituted or disubstituted with substituents independently selected from the group consisting of F, Cl, and OCH 3 ; Benzyl, unsubstituted or monosubstituted or disubstituted with substituents independently selected from the group consisting of F; Cl; CH 3 ; OCH 3 ; CF 3 ; -O-CH 2 -O-; phenyl bridged via C 2 _ 4 -alkyl, unsubstituted; Naphthyl bridged by CH 2 , thienyl, furanyl or pyridyl, each unsubstituted; indolyl bridged via C 2 H 4 , unsubstituted; Indazolyl, monosubstituted with CH 3 .
- substituted tetrahydroisoquinolinyl-4-oxo-butyric acid amides according to the invention and in each case the corresponding acids, bases, salts and solvates are suitable as pharmaceutical active ingredients in medicaments.
- Another object of the invention is therefore a medicament containing at least one inventive substituted tetrahydroisoquinolinyl-4-oxobutterklamid the general formula (1), wherein the radicals R 1 -R 15, the above as well as, if necessary, one or more pharmaceutically acceptable excipients
- the medicaments according to the invention optionally contain suitable additives and / or adjuvants, such as carriers, fillers, solvents, diluents, dyes and / or binders and can be used as liquid dosage forms in the form of injection solutions, drops or juices
- suitable additives and / or adjuvants such as carriers, fillers, solvents, diluents, dyes and / or binders and can be used as liquid dosage forms in the form of injection solutions, drops or juices
- Semi-solid dosage forms in the form of granules, tablets, pellets, patches, capsules, patches / aerosols or aerosols The choice of excipients etc and the quantities to be used depend on whether the drug is oral, peroral, parenteral, intravenous, intraperitoneal, intradermal , intramuscular, intranasal, buccal, rectal or local, for example, to the skin, the mucous membranes or the eyes, to be applied
- medicaments according to the invention are suitable for influencing KCNQ2 / 3 channels and exert an agonistic or antagonistic, in particular an agonistic action
- the medicaments according to the invention are preferably suitable for the treatment of disorders or diseases which are mediated at least in part by KCNQ2 / 3 channels
- the medicaments according to the invention are preferably suitable for the treatment of one or more diseases selected from the group consisting of pain, preferably pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, muscular pain and inflammatory pain, epilepsy, urinary incontinence, states of anxiety , Dependence, mania, bipolar disorder, migraine, cognitive disorders, dystonia-associated dyskinesia and / or urinary incontinence
- the medicaments according to the invention are particularly preferably suitable for the treatment of pain, very particularly preferably of chronic pain, neuropathic pain, inflammatory pain and muscular pain
- the medicaments according to the invention are particularly preferably suitable for the treatment of epilepsy
- Another object of the invention is the use of at least one inventive substituted Tetrahydro ⁇ soch ⁇ nol ⁇ nyl-4-oxo-buttersauream ⁇ ds and optionally one or more pharmaceutically acceptable excipients for the manufacture of a medicament for the treatment of disorders or diseases that are mediated at least partially by KCNQ2 / 3 channels
- At least one inventive substituted Tetrahydro ⁇ soch ⁇ nol ⁇ nyl-4-oxo-buttersauream ⁇ des and optionally one or more pharmaceutically acceptable excipients for the manufacture of a medicament for the treatment of pain, most preferably chronic pain, neuropathic pain, inflammatory pain and muscular pain.
- At least one substituted tetrahydroisoquinolinyl-4-oxo-butyric acid amide according to the invention and optionally one or more pharmaceutically acceptable excipients for the manufacture of a medicament for the treatment of epilepsy.
- Another object of the invention is at least one inventive substituted tetrahydroisoquinolinyl-4-oxo-butyric acid amide and optionally one or more pharmaceutically acceptable excipients for the treatment of disorders or diseases that are mediated at least partially by KCNQ2 / 3 channels.
- Another object of the invention is at least one substituted tetrahydroisoquinolinyl-4-oxo-butyric acid amide according to the invention and optionally one or more pharmaceutically acceptable excipients for the treatment of pain, preferably pain selected from the group consisting of acute pain, chronic pain, neuropathic pain, muscular Pain and inflammatory pain; Epilepsy, urinary incontinence, anxiety, dependence, mania, bipolar disorder, migraine, cognitive disorders, dystonia-associated dyskinesias and / or urinary incontinence.
- Another object of the invention is the use of at least one substituted tetrahydroisoquinolinyl-4-oxo-butterklamids invention and optionally one or more pharmaceutically acceptable adjuvants for the treatment of disorders or diseases mediated, at least in part, by KCNQ2 / 3 channels
- Efficacy against pain can be demonstrated, for example, in the Bennett or Chung model (Bennett, GJ and Xie, YK, Apeppheral mononeuropathy in rat that produces the disorders of pam sensation hke those lakes in man, Pain 1988, 33 (1), 87 -107, Kim, SH and Chung, JM, An exemplary model for penelopheral neuropathy produced by segmental spinal nerve ligation in the rat, Pain 1992, 50 (3), 355-363).
- the efficacy against epilepsy can be found, for example, in the DBA / 2 mouse Model (De Sarro et al., Naunyn-Schmiedeberg's Arch Pharmacol 2001, 363, 330-336)
- the substituted Tetrahydro ⁇ soch ⁇ ol ⁇ nyl-4-oxo-buttersaureamide according to the invention an EC 50 -WeIi of at most 11 uM or at most 5 uM, more preferably at most 3 uM or at most 2 uM, more preferably at most 1, 5 uM or at most 1 uM, most preferably not more than 0.8 ⁇ M or not more than 0.6 ⁇ M and in particular not more than 0.4 ⁇ M or not more than 0.2 ⁇ M methods for determining the ECso value are known in the art.
- the determination of the EC 50 value is carried out by a fluorometric method, particularly preferably as described below "Pharmacological experiments" described
- Another object of the invention are methods for preparing the inventive substituted Tetrahydro ⁇ soch ⁇ nol ⁇ nyl-4-oxo-buttersauream ⁇ de
- the chemicals and reaction components used in the reactions described below are commercially available or can each be prepared by conventional methods known to those skilled in the art.
- step 1 nurse of the general formula II with Succinanhyd ⁇ den of the general formula IM, in a reaction medium, preferably selected from the group consisting of acetone, acetonitrile, chloroform, dioxane, dichloromethane, ethanol, ethyl acetate, nitrobenzene, methanol and tetrahydrofuran, if necessary in the presence of an inorganic base, preferably potassium carbonate or an organic base, preferably selected from the group consisting of T ⁇ ethylamin, Pyridm, Dimethylaminopy ⁇ din and Dnsopropylethylamin preferably at Temperatures of -20 0 C to 160 ° C to Carbo ⁇ sauren the general formula V implemented
- step 2 carboxylic acids of the general formula IV wherein PG is a Ci ⁇ - alkyl group, preferably methyl, ethyl, iso-propyl or tert-butyl, with amines of the general formula II by the method described in step 4 to give compounds of the general formula VI implemented
- step 2 compounds of the general Formal IV wherein PG is a C 6 - alkyl group, preferably methyl, ethyl, iso-propyl or tert-butyl is initially activated on the acid function, for example by conversion to the corresponding acid halide, preferably Saurechlond, or in reactive esters, preferably pentafluorophenol esters, and then with amines of the general formula II in a reaction medium, preferably selected from the group consisting of diethyl ether, tetrahydrofuran, acetonitrile, methanol, ethanol, dimethylformamide and dichloromethane, with or without the addition of at least one organic or inorganic Base, for example T ⁇ ethylamin, Dimethylaminopy ⁇ din, Py ⁇ din or Dnsopropylamin, if appropriate in the presence of at least one organic base, preferably selected from the group consisting of T ⁇ ethylamin, Dimethyl- aminopy
- carboxylic acids of the general formula V are
- step 5 amines of the general formula VII are reacted with succinic anhydrides of the general formula III, according to the process described under step 1 to give carboxylic acids of the general formula XVI
- step 6 amines of general formula VII are reacted with carboxylic acids of general formula VIII, according to the method described in step 2 to give compounds of general formula IX
- step 7 carboxylic acid esters of the general formula IX in which PG is a Ci 6 - alkyl group, preferably methyl, ethyl, iso-propyl or tert-butyl, are cleaved by the method described in step 3 to give carboxylic acids of the general formula XVI
- step 8 amines of the general formula II are reacted with carboxylic acids of the general formula XVI according to the process described under step 4 to give compounds of the general formula I.
- Scheme 3 (Pictet-Spengler Synthesis):
- a reaction medium preferably selected from the group consisting of acetonitrile, chloroform, dichloromethane, diethyl ether, ethanol, methanol, tetrahydrofuran, toluene and X
- step 10 the general formula XII are optionally in a reaction medium, preferably selected from the group consisting of benzene, ethanol, methanol, toluene, water and XyIoI, with the addition of an acid, preferably selected from the group consisting of hydrochloric acid, T ⁇ fluoressigsaure or T ⁇ fluormethansulfonsaure , preferably cyclized at temperatures of 0 ° C to 160 0 C to give compounds of general formula II Scheme 4 (Bischler-Napieralski synthesis):
- step 11 amines of the general formula X are reacted with carboxylic acids of the general formula XIII according to the process described in step 4 to give amides of the general formula XIV.
- step 12 amides of the general formula XIV in a reaction medium, preferably selected from the group consisting of benzene, chloroform, toluene or xylene in the presence of a suitable Zyklmaschinesreagens, preferably Phopsphoryltrichlorid or phosphorus pentachloride, optionally with the addition of phosphorus pentoxide, preferably at temperatures of Cyclized at 20 ° C to 150 ° C to give compounds of general formula XV.
- a suitable Zyklmaschinesreagens preferably Phopsphoryltrichlorid or phosphorus pentachloride, optionally with the addition of phosphorus pentoxide, preferably at temperatures of Cyclized at 20 ° C to 150 ° C to give compounds of general formula XV.
- a suitable reducing agent preferably selected from the group consisting of sodium borohydride, sodium cyanoborohydride, lithium aluminum hydride or hydrogen , possibly. with addition of a catalyst, preferably selected from the group consisting of
- the stationary phase used for the column chromatography was silica gel 60 (0 040-0 063 mm)
- the mixture was diluted with DCM and washed successively with a 10% strength aq hydrochloric acid, a saturated Na 2 CO 3 solution, a saturated NH 4 Cl solution and brine organic phase was dried over Na 2 SO 4 , filtered and concentrated in vacuo.
- Human KONQ2 / 3-cell-expanding CHO-K1 cells are incubated in cell culture flasks (eg 80 cm 2 TC flasks, Nunc) with DMEM-high glucose (Sigma Ald ⁇ ch, OlUl) including 10% FCS (PAN Biotech, eg B 3302- P270521) or alternatively MEM Alpha medium (1x, LIQUID, Invitrogen, # 22571), 10% Fetal CAIF serum (FCS) (Invitrogen, # 10270-106, heat inactivated) and the necessary selection antibiotics at 37 0 C, 5% CO 2 and 95% humidity adharently cultivated
- FCS Fetal CAIF serum
- the cells are washed with a 1 x DPBS buffer without Ca 2 VMg 2+ (eg Invitrogen, # 14190-094) and removed from the bottom of the culture vessel using Accutase (PAA Laboratories, # L1 1-007) (incubation with Accutase for 15 min at 37 0 C) the determination of the cell count then present is with a CASY TM cell counter (model TCC, Scharfe system) carried out subsequently, depending on the density optimization for the individual cell line 20000-30000 cells / Apply well / 100 ⁇ l of the described nutrient medium to the 96 well Corning TM CellBIND TM (Fiat Clear Bottom Black Polystyrene Microplates, # 3340) plates.
- Accutase PAA Laboratories, # L1 1-007
- CASY TM cell counter model TCC, Scharfe system
- the voltage-sensitive fluorescent dye from the Membrane Potential Assay Kit (Red TM BuIk format part R8123 for FLIPR, MDS Analytical Technologies TM) is prepared by adding the contents of one vessel of Membrane Potential Assay Kit Red Component A to 200 ml of Extracellular Buffer (ES buffer, 120 1 mM KCl, 10 mM HEPES, 2 mM CaCl 2 , 2 mM MgCl 2 , 10 mM glucose, pH 7.4). After the nutrient medium has been taken off, the cells are washed with 200 ⁇ l of ES buffer, then with 100 ml of NaCl Overlaid ⁇ l of the above-prepared dye solution and incubated for 45 min at room temperature under light
- the fluorescence measurements are performed with a BMG Labtech FLUOstar TM, BMG Labtech NOVOstar TM or BMG Labtech POLARstar TM instrument (525 nm Exation, 560 nm Emission, Bottom Read mode).
- 15 ⁇ l of a 100 mM KCl solution final concentration 92 mM
- the change in fluorescence is then measured until all relevant readings are obtained (primarily 5-30 min) at a fixed time
- KCl-apphcation a fluorescence value F 2 is determined, in this case for Time of fluorescence peak
- the fluorescence intensity F 2 is compared with the fluorescence intensity Fi and from this the agonistic activity of the target compound on the potassium channel is determined.
- F 2 and Fi are calculated as follows
- a substance has an agonistic activity on the potassium channel when - greater than - is
- patch-clamp measurements (Hamill OP, Marty A, Neher E, Sakmann B, Sigworth FJ Improved patch-clamp techniques for high-resolution current recording from cells and cell-free Membrane patches, Pflugers Arch 1981 Aug, 391 (2) 85-100) were performed in voltage-clamp mode on a stably transfected hKCNQ2 / 3 CHO-K1 cell line.
- the cells were first clamped to a holding potential of -60 mV Subsequently, depolarizing voltage jumps were applied up to a potential of +20 mV (increment 20 mV, duration 1 second) to confirm the functional expression of KCNQ2 / 3 typical currents Substance testing was performed at a potential of -40 mV the retigabine (10 ⁇ M) induced increase in power at -40 mV was recorded as a positive control The test substance (10 ⁇ M) was applied to wash out the retigabine effect (duration 80 s). The increase in current induced by the test substance was normalized to the retigab effect and indicated as relative efficacy (see below).
- the formalin test (Dubuisson, D and Dennis, SG, 1977, Pam, 4, 161-174) represents a model for both acute and chronic pain.
- the chronic pain component (II phase of the formal tooth test, time interval 21 - 27m ⁇ n after Formalinapphkation) evaluated By a one-off Formahn-injection into the dorsal side of a hind paw in bisexual experimental animals a biphasische nociceptive reaction is induced, which is detected by observation of three clearly distinguishable behavioral patterns
- Formalin is administered subcutaneously in the dorsal side of the right hind paw of each animal with the volume of 50 ⁇ l and a concentration of 5%.
- the vehicle and the substances to be tested are administered intravenously 5 mm, or orally 30 min, prior to the Formahn injection
- the specific behavioral changes such as raising and debris of the paw, weight shifts of the animal as well as biting and leaking reactions are continuously observed and registered until 60 minutes after formalinapphaging.
- the behavioral changes are weighted differently (Score 0-3) and a Pam rate (PR) is calculated following formula
- T 0 Ti T 2 T 3 correspond in each case to the time in seconds in which the animal dies
- Rats of the strain Sprague Dawley (Janvier, Belgium) are used as animal strain.
- the substituted Tetrahydro ⁇ soch ⁇ nol ⁇ nyl-4-oxo-buttersaure- amides according to the invention are characterized in comparison to substituted tetrahydropyrrolopyrazines, which are known from WO 2008/046582, by an improved activity in vitro or in vivo, as the following comparative experiments illustrate
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Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP09795712A EP2358681A1 (de) | 2008-12-17 | 2009-12-16 | Substituierte 4-(1,2,3,4-tetrahydroisochinolin-2-yl)-4-oxo-buttersäureamide als kcnq2/3 modulatoren |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP08021880 | 2008-12-17 | ||
EP09795712A EP2358681A1 (de) | 2008-12-17 | 2009-12-16 | Substituierte 4-(1,2,3,4-tetrahydroisochinolin-2-yl)-4-oxo-buttersäureamide als kcnq2/3 modulatoren |
PCT/EP2009/009040 WO2010075973A1 (de) | 2008-12-17 | 2009-12-16 | Substituierte 4-(1,2,3,4-tetrahydroisochinolin-2-yl)-4-oxo-buttersäureamide als kcnq2/3 modulatoren |
Publications (1)
Publication Number | Publication Date |
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EP2358681A1 true EP2358681A1 (de) | 2011-08-24 |
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Application Number | Title | Priority Date | Filing Date |
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EP09795712A Withdrawn EP2358681A1 (de) | 2008-12-17 | 2009-12-16 | Substituierte 4-(1,2,3,4-tetrahydroisochinolin-2-yl)-4-oxo-buttersäureamide als kcnq2/3 modulatoren |
Country Status (17)
Country | Link |
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US (1) | US8367700B2 (ja) |
EP (1) | EP2358681A1 (ja) |
JP (1) | JP2012512214A (ja) |
KR (1) | KR20110100651A (ja) |
CN (1) | CN102256947A (ja) |
AU (1) | AU2009335340A1 (ja) |
BR (1) | BRPI0922489A2 (ja) |
CA (1) | CA2747094A1 (ja) |
CL (1) | CL2011001428A1 (ja) |
CO (1) | CO6440542A2 (ja) |
EC (1) | ECSP11011095A (ja) |
IL (1) | IL213565A0 (ja) |
MX (1) | MX2011006384A (ja) |
NZ (1) | NZ593994A (ja) |
PE (1) | PE20120076A1 (ja) |
WO (1) | WO2010075973A1 (ja) |
ZA (1) | ZA201105262B (ja) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8367700B2 (en) | 2008-12-17 | 2013-02-05 | Gruenenthal Gmbh | Substituted 4-(1.2,3,4-tetrahydroisoquinolin-2-yl)-4-oxobutyric acid amide as KCNQ2/3 modulators |
Families Citing this family (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI475020B (zh) | 2009-03-12 | 2015-03-01 | The substituted nicotine amide as a KCNQ2 / 3 modifier | |
AR082733A1 (es) | 2010-08-27 | 2012-12-26 | Gruenenthal Gmbh | 2-amino-quinolina-3-carboxamidas sustituidas como moduladores de kcnq2/3 |
PT2609083E (pt) | 2010-08-27 | 2015-07-01 | Gruenenthal Gmbh | 2-oxi-quinolina-3-carboxamidas substituídas como moduladores de kcnq2/3 |
PE20140214A1 (es) | 2010-08-27 | 2014-02-19 | Gruenenthal Chemie | 2-oxo- y 2-tioxo-dihidroquinolina-3-carboxamidas sustituidos como moduladores kcnq2/3 |
AU2011297937B2 (en) * | 2010-09-01 | 2015-10-01 | Grunenthal Gmbh | Substituted 1-oxo-dihydroisoquinoline-3-carboxamides as KCNQ2/3 modulators |
CN105461626B (zh) * | 2015-12-17 | 2018-05-08 | 浙江工业大学 | 芳环或稠杂环联3,4-二氢异喹啉类共轭结构化合物及其应用 |
US10370355B2 (en) * | 2016-04-13 | 2019-08-06 | Ucb Biopharma Sprl | Tetrahydroisoquinoline derivatives |
AU2018336171B2 (en) | 2017-09-22 | 2023-01-05 | Jubilant Epipad LLC | Heterocyclic compounds as PAD inhibitors |
CA3076476A1 (en) | 2017-10-18 | 2019-04-25 | Jubilant Epipad LLC | Imidazo-pyridine compounds as pad inhibitors |
WO2019087214A1 (en) | 2017-11-06 | 2019-05-09 | Jubilant Biosys Limited | Pyrimidine derivatives as inhibitors of pd1/pd-l1 activation |
KR20200092346A (ko) | 2017-11-24 | 2020-08-03 | 주빌런트 에피스크라이브 엘엘씨 | Prmt5 억제제로서의 헤테로사이클릭 화합물 |
JP7279063B6 (ja) | 2018-03-13 | 2024-02-15 | ジュビラント プローデル エルエルシー | Pd1/pd-l1相互作用/活性化の阻害剤としての二環式化合物 |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
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GB8916395D0 (en) * | 1989-07-18 | 1989-09-06 | Zambeletti Spa L | Pharmaceuticals |
US6855829B2 (en) | 2001-02-20 | 2005-02-15 | Bristol-Myers Squibb Company | 3-fluoro-2-oxindole modulators of KCNQ potassium channels and use thereof in treating migraine and mechanistically related disease |
DE102006049452A1 (de) | 2006-10-17 | 2008-05-08 | Grünenthal GmbH | Substituierte Tetrahydropyrolopiperazin-Verbindungen und deren Verwendung in Arzneimitteln |
US8367700B2 (en) | 2008-12-17 | 2013-02-05 | Gruenenthal Gmbh | Substituted 4-(1.2,3,4-tetrahydroisoquinolin-2-yl)-4-oxobutyric acid amide as KCNQ2/3 modulators |
-
2009
- 2009-12-11 US US12/635,800 patent/US8367700B2/en not_active Expired - Fee Related
- 2009-12-16 MX MX2011006384A patent/MX2011006384A/es active IP Right Grant
- 2009-12-16 NZ NZ593994A patent/NZ593994A/xx not_active IP Right Cessation
- 2009-12-16 EP EP09795712A patent/EP2358681A1/de not_active Withdrawn
- 2009-12-16 CN CN200980150661XA patent/CN102256947A/zh active Pending
- 2009-12-16 WO PCT/EP2009/009040 patent/WO2010075973A1/de active Application Filing
- 2009-12-16 PE PE2011001141A patent/PE20120076A1/es not_active Application Discontinuation
- 2009-12-16 AU AU2009335340A patent/AU2009335340A1/en not_active Abandoned
- 2009-12-16 KR KR1020117016288A patent/KR20110100651A/ko not_active Application Discontinuation
- 2009-12-16 JP JP2011541202A patent/JP2012512214A/ja not_active Withdrawn
- 2009-12-16 CA CA2747094A patent/CA2747094A1/en not_active Abandoned
- 2009-12-16 BR BRPI0922489A patent/BRPI0922489A2/pt not_active IP Right Cessation
-
2011
- 2011-06-02 EC EC2011011095A patent/ECSP11011095A/es unknown
- 2011-06-03 CO CO11069300A patent/CO6440542A2/es not_active Application Discontinuation
- 2011-06-10 CL CL2011001428A patent/CL2011001428A1/es unknown
- 2011-06-15 IL IL213565A patent/IL213565A0/en unknown
- 2011-07-15 ZA ZA2011/05262A patent/ZA201105262B/en unknown
Non-Patent Citations (1)
Title |
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See references of WO2010075973A1 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8367700B2 (en) | 2008-12-17 | 2013-02-05 | Gruenenthal Gmbh | Substituted 4-(1.2,3,4-tetrahydroisoquinolin-2-yl)-4-oxobutyric acid amide as KCNQ2/3 modulators |
Also Published As
Publication number | Publication date |
---|---|
WO2010075973A1 (de) | 2010-07-08 |
KR20110100651A (ko) | 2011-09-14 |
ZA201105262B (en) | 2012-03-28 |
PE20120076A1 (es) | 2012-02-06 |
MX2011006384A (es) | 2011-07-13 |
JP2012512214A (ja) | 2012-05-31 |
ECSP11011095A (es) | 2011-07-29 |
CN102256947A (zh) | 2011-11-23 |
CL2011001428A1 (es) | 2011-11-18 |
CO6440542A2 (es) | 2012-05-15 |
CA2747094A1 (en) | 2010-07-08 |
US20100152234A1 (en) | 2010-06-17 |
IL213565A0 (en) | 2011-07-31 |
BRPI0922489A2 (pt) | 2015-12-15 |
US8367700B2 (en) | 2013-02-05 |
AU2009335340A1 (en) | 2011-08-04 |
NZ593994A (en) | 2012-08-31 |
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