EP2619178A1 - Substituierte benzamid-verbindungen - Google Patents

Substituierte benzamid-verbindungen

Info

Publication number
EP2619178A1
EP2619178A1 EP11761012.1A EP11761012A EP2619178A1 EP 2619178 A1 EP2619178 A1 EP 2619178A1 EP 11761012 A EP11761012 A EP 11761012A EP 2619178 A1 EP2619178 A1 EP 2619178A1
Authority
EP
European Patent Office
Prior art keywords
methyl
carboxylic acid
dihydro
acid amide
piperidin
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP11761012.1A
Other languages
German (de)
English (en)
French (fr)
Inventor
Melanie Reich
Stefan Schunk
Ruth Jostock
Jean De Vry
Christa Kneip
Tieno Germann
Michael Engels
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gruenenthal GmbH
Original Assignee
Gruenenthal GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Gruenenthal GmbH filed Critical Gruenenthal GmbH
Priority to EP11761012.1A priority Critical patent/EP2619178A1/de
Publication of EP2619178A1 publication Critical patent/EP2619178A1/de
Withdrawn legal-status Critical Current

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    • C07D401/02—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
    • 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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    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • 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
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    • C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44—Iso-indoles; Hydrogenated iso-indoles
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    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • 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
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    • 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
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    • C07D401/02—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
    • C07D401/06—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 carbon chain containing only aliphatic carbon atoms
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    • C07D401/14—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 three or more hetero rings
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    • C07D405/00—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
    • C07D405/14—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 three or more hetero rings
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    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
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    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
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Definitions

  • the present invention relates to substituted benzamide compounds, processes for their preparation, medicaments containing these compounds and the use of substituted benzamide compounds for the preparation of medicaments.
  • the bradykinin 1 receptor (B1R) is not or only weakly expressed in most tissues.
  • the expression of the B1R is inducible on different cells. For example, in the course of inflammatory reactions, a rapid and pronounced induction of B1R on neuronal cells but also on various peripheral cells such as fibroblasts, endothelial cells, granulocytes, macrophages and lymphocytes. Thus, in the course of inflammatory reactions, there is a switch from a B2R to a B1R dominance on the cells involved.
  • cytokines interleukin-1 (IL-1) and tumor necrosis factor alpha (TNFa) are of particular importance in this B1R up-regulation (Passos et al., J. Immunol., 2004, 172, 1839-1847).
  • B1 R-expressing cells may subsequently self-secrete pro-inflammatory cytokines such as IL-6 and IL-8 (Hayashi et al., Eur. Respir. J. 2000, 16, 452-458). This leads to the immigration of further inflammatory cells, e.g. neutrophilic granulocytes (Pesquero et al., PNAS 2000, 97, 8140-8145).
  • bradykinin B1R system can contribute to the chronicity of disease. This is confirmed by a large number of animal experiments (reviews in Leeb-Lundberg et al., Pharmacol Rev. 2005, 57, 27-77 and Pesquero et al., Biol. Chem. 2006, 387, 119-126). Human expression also shows enhanced expression of the B1 R, e.g. on enterocytes and macrophages in the affected tissue of patients with inflammatory bowel disease (Stadnicki et al., Am J. Physiol Gastrointest ..
  • Symptoms such as superficial infections of the skin to septic shock.
  • B1 R antagonists in acute and, in particular, chronic inflammatory diseases.
  • respiratory diseases bronchial asthma, allergies, COPD / chronic obstructive pulmonary disease, cystic fibrosis, etc.
  • inflammatory bowel disease ulcerative colitis, CD / Crohn's disease, etc.
  • neurological diseases multiple sclerosis, neurodegeneration, etc.
  • inflammation of the skin atopic dermatitis, psoriasis, bacterial infections, etc.
  • mucous membranes M. Behcet, pelvitis, prostatitis, etc.
  • bradykinin (receptor) system is also involved in the regulation of
  • Angiogenesis (potential as an angiogenesis inhibitor in cancer as well as macular degeneration in the eye) and B1 R knockout mice are protected from inducing obesity by a high fat diet (Pesquero et al., Biol. Chem. 2006, 387, 1 19-126). B1 R antagonists are therefore also suitable for the treatment of obesity.
  • B1 R antagonists are particularly suitable for the treatment of pain, in particular inflammatory pain and neuropathic pain (Calixto et al., Br. J. Pharmacol 2004, 1-16), here in particular diabetic neuropathy (Gabra et al., Biol. Chem. 2006, 387, 127-143). Furthermore, they are suitable for the treatment of migraine.
  • t 1, 2 or 3;
  • b 0, 1 or 2;
  • c and d are each independently 0, 1 or 2 with the proviso that the cycle has at most 7 ring members;
  • X is N (R 9a ) or C (R 9b ) (H);
  • D is one of the following radicals D1 or D2
  • D1 D2 q is 0 or 1;
  • s is 0 or 1;
  • r is 1, 2 or 3;
  • Qi and Q 2 independently of one another, are each C, CH or N;
  • R 1 is d 9-alkyl, aryl, heteroaryl, CH (aryl) 2 , C 3 . 8 cycloalkyl, heterocyclyl, or a bonded via a C ⁇ alkylene, C 2- 6 alkenylene group or C 2-6 alkynylene group aryl, heteroaryl, CH (aryl) 2, C 3-8 cycloalkyl or heterocyclyl;
  • R 2 is H, C 1 -e-alkyl, C 3 . 8 cycloalkyl, heterocyclyl, aryl, heteroaryl, or for a Ci -6 - bound alkylene C 3- 8 cycloalkyl, heterocyclyl, aryl or heteroaryl;
  • R 5 is 0, 1, 2, 3 or 4 substituents which are independently selected from the group consisting of F, Cl, CF 3l OCF 3, C -6 alkyl, and 0-d -6 alkyl and / or two adjacent substituents R 5 form a fused aryl, heteroaryl or de-cycloalkyl and / or two substituents R s attached to a carbon atom form a 3, 4 or 5 membered saturated carbocycle unsubstituted or attached to one or more of its carbon ring members one or more substituents independently selected from the group consisting of F, CF 3 and C 1-6 alkyl substituted;
  • R 6 is 0, 1, 2 or 3 substituents independently selected from the group consisting of F, Cl, Br, CF 3 , OCF 3 , OH, C 1-6 alkyl, C 3-8 cycloalkyl , 0-C 1-6 -alkyl, N0 2 , NH 2 , N (H) (C 1-6 -alkyl) and N (C 1-6 -alkyl) 2 and / or two adjacent substituents R 6, an annulated aryl , Heteroaryl or C 4 . 8 -cycloalkyl form;
  • R 7 is H, Ci-e-alkyl, C3-8 cycloalkyl, heterocyclyl, aryl or heteroaryl, or a C -6 alkylene group bonded via a C 3-8 cycloalkyl, heterocyclyl, aryl or heteroaryl,
  • R is H, de-alkyl, C 3-8 -cycloalkyl, aryl, heteroaryl, or C 3- e -cycloalkyl, aryl or heteroaryl bonded via a d -3 -alkylene group;
  • R 13 is C 1-6 alkyl, aryl, heteroaryl, CH (aryl) 2 , C 3 . 8 cycloalkyl, heterocyclyl, or a bonded via a C 1-6 alkylene group, C 2- 6 alkenylene group, or C 2- 6-alkynylene aryl, heteroaryl, C 3-8 cycloalkyl or heterocyclyl;
  • R 14 is H, C 1-6 alkyl, C 3-8 cycloalkyl, aryl, heteroaryl, or a via a C -3 - bound alkylene C 3-8 cycloalkyl, aryl or heteroaryl;
  • R 15 and R 16 are each H, C 1-4 -alkyl, C 3-8 -cycloalkyl, aryl or heteroaryl, or
  • R 17 and R 18 are each independently H, C 1-6 alkyl or C 3 . 8 -cycloalkyl, or
  • R 17 and R 18 together with the nitrogen atom connecting them form a heterocycle which is unsubstituted or at one or more, for example 1, 2 or 3, of its
  • Carbon ring members having one or more, for example 1, 2, 3 or 4,
  • R 23 are de-alkyl, C 3- 8 cycloalkyl, aryl, heteroaryl or a Ci -3 alkylene group bonded via a C 3-8 - cycloalkyl, aryl or heteroaryl;
  • R 19 is H, de-alkyl, C 3-8 -cycloalkyl, heterocyclyl, aryl, heteroaryl or C 2-6 -alkylene-NR 17 R 18 or a heterocyclyl bonded via a d-6-alkylene group, C 3-8 Cycloalkyl, aryl or heteroaryl;
  • R 20 and R 2 independently of one another, are each H, de-alkyl or C 3-8 -cycloalkyl, or
  • R 20 and R 21 together with the nitrogen atom connecting them form a heterocycle which is unsubstituted or at one or more, for example 1, 2 or 3, of its
  • Carbon ring members having one or more, for example 1, 2, 3 or 4
  • Heteroaryl in each case unsubstituted or singly or multiply with the same or
  • d-4-alkyl d -6 -alkyl, d -3 -alkylene, d. 6- alkylene, C 2-6 -alkylene, C 2-6 -alkenylene and C 2 . 6 alkynyls, each branched or unbranched; in the form of the free connection; the tautomers; the N-oxides; the racemate; of the
  • halogen preferably stands for the radicals F, Cl, Br and I, in particular for the radicals F and Cl.
  • C 1-9 -alkyl for the purposes of this invention comprises acyclic saturated hydrocarbon radicals having 1, 2, 3 , 4, 5, 6, 7, 8 or 9 C atoms or 1, 2, 3, 4, 5 or 6 C atoms or 1, 2, 3 or 4 C atoms or 1, 2 or 3 C atoms which may be branched or straight-chain (unbranched) and unsubstituted or mono- or polysubstituted, for example 2-, 3-, 4- or 5-fold, with the same or different radicals.
  • the alkyl radicals may be selected from the group consisting of methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, iso-pentyl, neo-pentyl and hexyl.
  • Particularly preferred alkyl radicals can be selected from the group consisting of methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl and tert-butyl.
  • C 3-8 -cycloalkyl For the purposes of this invention, the term "C 3-8 -cycloalkyl", “C 4 . 8 -cycloalkyl "or” C 3- 6 cycloalkyl "cyclic saturated hydrocarbons having 3, 4, 5, 6, 7 or 8, including 4, 5, 6, 7 or 8 or 3, 4, 5 or 6 Carbon atoms which may be unsubstituted or monosubstituted or polysubstituted, for example, by 2, 3, 4 or 5, identical or different radicals on one or more ring members and, if the cycloalkyl radicals have at least 4 carbon atoms, may also be substituted by further saturated, partially unsaturated or aromatic or heteroaromatic ring systems may be condensed, which in turn may be unsubstituted or monosubstituted or polysubstituted, for example, with 2, 3, 4 or 5, identical or different radicals ..
  • C 3 -e- cycloalkyl may be selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl
  • a cycloalkyl radical condensed with a phenyl radical tetrahydronaphthalene (tetrahydronaphthyl) called.
  • heterocyclyl includes saturated or unsaturated (but not aromatic)
  • Cycloalkyls having four to seven ring members in which one, two or three carbon atoms are replaced by a heteroatom each independently selected from the group S, N or O, wherein the ring members unsubstituted or mono- or polysubstituted could be.
  • the bonding of the heterocyclyl to the general structure above can take place via any and possible ring member of the heterocyclyl radical.
  • Heterocyclyl radicals can also be condensed with further saturated, (partially) unsaturated or aromatic or heteroaromatic ring systems, which in turn may be unsubstituted or monosubstituted or polysubstituted, for example 2, 3, 4 or 5 times.
  • heterocyclyl radicals from the group azetidinyl, oxetanyl, azepanyl, dioxanyl, dioxolanyl, morpholinyl, pyranyl, pyrrolidinyl, piperazinyl, piperidinyl, pyrazolidinyl, pyrazolinonyl, dihydroindenyl, tetrahydropyranyl, chromanyl or
  • Thiomorpholinyl Particularly preferred are heterocyclyl radicals from the group azetidinyl, oxetanyl, azepanyl, dioxanyl, dioxolanyl, morpholinyl, pyranyl, pyrrolidinyl, piperazinyl, piperidinyl, pyrazolidinyl, pyrazolinonyl or thiomorpholinyl.
  • aryl in the context of this invention means aromatic hydrocarbons, in particular phenyls and naphthyls.
  • the aryl radicals can also be condensed with further saturated, (partially) unsaturated or aromatic ring systems.
  • Each aryl radical can be unsubstituted or monosubstituted or polysubstituted, for example 2, 3, 4 or 5 times, substituted, where the aryl substituents can be identical or different and in any desired and possible position of the aryl.
  • aryl may be selected from the group consisting of phenyl, 1-naphthyl and 2-naphthyl, which may each be unsubstituted or mono- or polysubstituted, for example with 2, 3, 4 or 5 radicals.
  • heteroaryl in the context of the present invention is a 5-, 6- or 7-membered cyclic aromatic radical which has at least 1, optionally also 2, 3, 4 or 5
  • heteroatoms wherein the heteroatoms may be the same or different and the
  • Heteroaryl unsubstituted or mono- or polysubstituted may be substituted with identical or different radicals.
  • the substituents may be attached in any and possible position of the heteroaryl.
  • the heterocycle may also be part of a bicyclic or polycyclic, in particular a mono-, bi- or tricyclic system, which may then be more than 7-membered in total, preferably up to 14-membered.
  • Preferred heteroatoms are independently selected from the group consisting of N, O and S.
  • the heteroaryl radical can be selected from the group consisting of pyrrolyl, indolyl, furyl (furanyl), benzofuranyl,
  • Benzotriazolyl benzodioxolanyl, benzodioxanyl, benzooxazolyl, benzooxadiazolyl,
  • the heteroaryl radical can be selected from the group consisting of isooxazolyl, oxazolyl, pyridazinyl, pyrazinyl, thienyl, imidazoyl, thiazolyl, triazolyl, pyridinyl and pyrimidinyl.
  • d -3 -alkylene group for the purposes of the present invention comprises acyclic saturated hydrocarbon radicals having 1, 2 or 3 C atoms, 1, 2 , 3, 4, 5 or 6 C atoms or 2, 3, 4, 5 or 6 C atoms which are branched or straight-chain (unbranched) and unsubstituted or mono- or polysubstituted, for example 2-, 3-, 4 or 5-fold, may be substituted with the same or different radicals and linking a corresponding radical with the parent general structure.
  • the alkylene groups may be selected from the group consisting of -CH 2 -, -CH 2 -CH 2 -, -CH (CH 3 ) -, -CH 2 -CH 2 -CH 2 -, -CH (CH 3 ) -CH 2 -, -CH (CH 2 CH 3 ) -, -CH 2 - (CH 2 ) 2 -CH 2 -, -CH (CH 3 ) -CH 2 -CH 2 -, -CH 2 -CH ( CH 3 ) -CH 2 -, -CH (CH 3 ) - CH (CH 3 ) -, -CH (CH 2 CH 3 ) -CH 2 -, -C (CH 3 ) 2 -CH 2 -, -CH ( CH 2 CH 3 ) -, -C (CH 3 ) 2 -CH 2 -, -CH ( CH 2 CH 3 ) -, -C (CH 3 ) (CH 2 CH 3 ) -
  • the alkylene groups may be selected from the group consisting of -CH 2 -, -CH 2 -CH 2 - and -CH 2 -CH 2 -CH 2 -.
  • C 2-6 alkenylene group for the purposes of the present invention comprises acyclic, mono- or polyunsaturated, for example 2-, 3- or 4-membered, unsaturated
  • Hydrocarbon radicals having 2, 3, 4, 5 or 6 carbon atoms which are branched or straight-chained Hydrocarbon radicals having 2, 3, 4, 5 or 6 carbon atoms which are branched or straight-chained
  • C 2-6 -alkynylene group for the purposes of the invention comprises acyclic, mono- or poly-substituted, for example 2-, 3- or 4-membered, unsaturated hydrocarbon radicals having 2, 3, 4, 5 or 6 carbon atoms which are branched - or straight-chain (unbranched) and unsubstituted or one or more times, for example 2-, 3-, 4- or 5-fold, with the same or
  • the alkynylene groups may be substituted by different radicals and linking a corresponding radical with the parent general structure.
  • the alkynylene groups have at least one CsC triple bond.
  • Ci -3 alkylene group, a Ci -6 alkylene group C 2-6 alkylene "C. 2 6 alkenylene or C 2- 6-alkynylene group aryl or heteroaryl bonded" in the context of the present Invention that the Ci. 3- alkylene groups, C alkylene groups, C 2-6 alkylene groups, C 2-6 alkenylene groups, C 2 . 6 alkynylene groups and aryl or
  • Heteroaryl have the meanings defined above and the aryl or heteroaryl via a C 1-3 alkylene, C 1-6 alkylene, C 2-6 alkylene, C 2 . 6 alkenylene group or C 2 - $ - alkynylene group is bound to the parent general structure.
  • Examples include benzyl, phenethyl and phenylpropyl.
  • C 3-8 -cycloalkyl and heterocyclyl bonded via a C 1-3 -alkylene group, C 1-6 -alkylene group, C 2-6 -alkylene group, C 2-6 -alkenylene group or C 2-6 -alkynylene group means in the sense of the present invention, that the C 1-3 -alkylene group, C 1-6 -alkylene group, C 2-6 -alkylene group, C 2 .
  • 6 alkenylene, C 2-6 alkynylene, C 3-8 - cycloalkyl, and heterocyclyl are as defined above and C 3-8 cycloalkyl and heterocyclyl via a C -3 alkylene, Ci-e-alkylene group, C 2- 6 -alkylene group, C 2-6 -alkenylene group or C 2-6 -alkynylene group is bonded to the general structure above.
  • alkyl In the context of “alkyl”, “alkylene”, “alkenylene”, “alkynylene”, “cycloalkyl” and
  • Heterocyclyl is understood by the term “substituted” in the sense of this invention
  • the radicals which either on different or on the same atoms multiply, for example two or three times, for example, three times on the same carbon atom as in the case of CF 3 or CH 2 CF 3 or at different positions as in the
  • it is intended here to include the substitution of one or more hydrogen radicals by F, CN, CF 3 , NH 2 , N (CH 3 ) 2 , OH, phenyl, 0-CF 3 or 0-C 1-6 -alkyl.
  • NH-de-alkyl NH-Ci-6-alkylene-OH, N (Ci -6 alkyl) 2, N (C 1-6 alkylene-OH) 2, NH-aryl, N (aryl 1) 2, N (Ci-6-alkyl) aryl 1, pyrrolinyl, Pyrroldinyl, piperazinyl, N-methyl-piperazinyl, morpholinyl, azetidinyl, piperidinyl, thiazolinyl, azepanyl, diazepanyl, (C 1-3 alkylene) -azetidinyl, (C 1- 3 - alkylene) -Pyrrolinyl, (Ci -3 alkylene) piperidinyl, (C 3 alkylene) -morpholinyl, (C 1-3 alkylene) -.
  • alkyl, C3-6 cycloalkyl, 0-C 3 6 cycloalkyl, pyrrolidinyl, imidazolyl, benzyloxy, phenoxy, phenyl, naphthyl, pyridinyl, pyrimidinyl, -C 1-3 - alkylene-aryl 1, benzyl, thienyl, furyl or a Ci -6 alkylene group bonded OCF 3, OH, O-C 1-6 -alkyl, SH, SC 1-6 -alkyl, C 3-6 -cycloalkyl, O-C 3-6 -cycloalkyl, NR 20 R 21 , C ( O) - NR 20 R 21 , phenyl, pyridyl or pyrimidyl, wherein aryl 1 is phenyl, thiazolyl, thienyl or pyridinyl, on one or different atoms, wherein the abovementioned substituents
  • Substituents can be substituted.
  • the multiple substitution of aryl and heteroaryl can be made with the same or different substituents.
  • NH-de-alkyl NH-C 1-6 -alkylene-OH, N (d 6 -alkyl) 2 , N (C 1-6 -alkylene-OH) 2 , NH-aryl 1 , N (aryl 1 ) 2, N (Ci -6 alkyl) aryl 1, pyrrolinyl, Pyrroldinyl, piperazinyl, N-methyl-piperazinyl, morpholinyl, azetidinyl, piperidinyl, thiazolinyl, azepanyl, diazepanyl, (C 1-3 alkylene) -azetidinyl, (C 1-3 - alkylene) -Pyrrolinyl, (d 3 alkylene) piperidinyl, (Ci -3 alkylene) -morpholinyl, (C 1-3 alkylene) -.
  • 6- alkyl OCF 3 , CF 3 , -O-CH 2 -O-, -O-CH 2 - CH 2 -O-, -O-C (CH 3 ) 2 -CH 2 -, de-alkyl, C 3-6 -cycloalkyl, 0-C 3-6 -cycloalkyl, pyrrolidinyl,
  • Imidazolyl, benzyloxy, phenoxy, phenyl, naphthyl, pyridinyl, pyrimidinyl, -d. 3- alkylene-aryl- 1 , benzyl, thienyl, furyl or for a via a d -6- alkylene-bound OCF 3 , OH, 0-C 1-6 -alkyl, SH, Sd.6-alkyl, C 3-6 Cycloalkyl, O-C 3-6 -cycloalkyl, NR 20 R 21 , C ( O) -NR 20 R 21 , phenyl, pyridyl or pyrimidyl, wherein aryl 1 is phenyl, thiazolyl, thienyl or pyridinyl.
  • substituents for aryl and heteroaryl can be selected from the group consisting of -O-C 1-3 -alkyl, unsubstituted d -6- alkyl, F, Cl, CN, CF 3 , 0CF 3 , OH, NH 2 , NR 2 ° R 21 , phenyl, naphthyl, thiazolyl, thienyl and pyridinyl, in particular from the group consisting of tert-butyl, F, Cl, CN, CF 3 , CH 3 ; OCH 3 , OCF 3 , NH 2 and NR 20 R 21 .
  • Substitution pattern also the symbol " ⁇ " used, which group is not bound to a particular atom within the chemical structural formula, in contrast to the representation of a bond to a particular atom (R a is here exemplified by a substituent R with a by the variable "a "numbering shown).
  • the symbol used in formulas denotes a linkage of a corresponding remainder to the respective overall general structure.
  • groups such as or (C 1 - alkyl) 2, in which the two C1-4 alkyl groups may be identical or different, such as in N (CH 3) 2 or N (CH 3) (C 2 H 5).
  • physiologically tolerated salt preferably means salts of the compounds according to the invention with inorganic or organic acids which are physiologically compatible - in particular when used on humans and / or mammals, for example salts of hydrochloric acid (hydrochlorides).
  • this term also means compounds which are obtained by quaternization of a nitrogen atom present in the structure (for example pyridyl, N-methylpiperidinyl). Such compounds can be obtained for example by alkylation to generate the corresponding cation with counterions such as CI " and F " .
  • a is 0 or 1 and t is 1 or 2.
  • the partial structure (Ac) is one of the partial structures (Ac 1), (Ac 2), (Ac 5) or (Ac 6).
  • the partial structure D1 is selected from the group consisting of
  • the radical R 1 is preferably in the compounds of the invention for Ci. 9- alkyl, CH (phenyl) 2 , C 3 . 8 -cycloalkyl, heterocyclyl, phenyl, naphthyl, tetrahydronaphthyl,
  • 3 alkylene group bonded phenyl, C 3-6 cycloalkyl or C 4- 6-heterocyclyl very particularly preferably represents Ci -6 alkyl, CH (phenyl) 2, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, tetrahydropyranyl, oxetanyl, tetrahydrofuranyl, Piperidinyl, phenyl, naphthyl, tetrahydronaphthyl, pyridinyl, pyrimidinyl, pyrazolo [1, 5-a] pyrimidinyl, dihydroindenyl, chromanyl, isoquinolinyl, oxazolyl, isoxazolyl or phenyl bonded via a C 1 2 0 of the 3-alkylene group, cyclopropyl, cyclobutyl , Cyclopentyl, cyclohexy
  • the radical R 1 in the compounds according to the invention is dg-alkyl, CH (phenyl) 2 , C 3-8 -cycloalkyl, heterocyclyl, phenyl, naphthyl, tetrahydronaphthyl, chromanyl, indolyl, benzofuranyl, benzothiophenyl (benzothienyl) , Benzooxazolyl, benzooxadiazolyl, pyrrolyl, furanyl, thienyl, oxazolyl, isoxazolyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazolo [1, 5-a] pyrimidinyl, pyrazinyl, imidazothiazolyl, carbazolyl, dibenzofuranyl, dibenzothiophenyl (dibenzothienyl) or a via a C 1 -3
  • the radical R 1 may in particular denote d -6- alkyl, cyclopropyl, cyclobutyl, cyclopentyl,
  • Tetrahydrofuranyl piperidinyl, phenyl, naphthyl, tetrahydronaphthyl, pyridinyl, pyrimidinyl,
  • alkyl, alkylene, and cycloalkyl groups are each unsubstituted or monosubstituted or polysubstituted, for example 2-, 3-, 4- or 5-fold, identical or different, wherein the substituents are independently selected in particular from the group consisting of C 1 -C 3 -alkyl, F, Cl, CF 3 , OCF 3 , OH,
  • Thienyl and pyridinyl themselves are each unsubstituted or monosubstituted or polysubstituted, for example, 2-, 3-, 4- or 5-fold, same or different, wherein the
  • Substituents are independently selected in particular from the group consisting of C 1-4 alkyl, C 1 -C 3 alkyl, F, Cl, CF 3 , OCF 3 and OH.
  • the radical R 1 can be, in particular, d -6 -alkyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, tetrahydropyranyl, oxetanyl, tetrahydrofuranyl, piperidinyl, phenyl, naphthyl, tetrahydronaphthyl, pyridinyl, pyrimidinyl, pyrazolo [1, 5 a] pyrimidinyl, thienyl, oxazolyl, isoxazolyl or a bonded via a Ci, 2 0 of the 3-alkylene phenyl, cyclopropyl, cyclobutyl, cyclopentyl
  • radical R 1 can be selected from the group consisting of
  • R can in particular also for C -9 alkyl, C 3- 6 cycloalkyl or heterocyclyl or bonded via a C 1-6 alkylene C 3-6 - cycloalkyl, or Heterocyclyl, wherein Ci -6- alkyl unsubstituted or mono- or polysubstituted, for example, 2-, 3-, 4- or 5-fold, may be substituted, in particular with radicals selected from the group consisting of F, CF 3 , OCF 3 , OH and methoxy and wherein C 3-6 -cycloalkyl and heterocyclyl may be optionally fused with phenyl and
  • unsubstituted or mono- or polysubstituted for example 2-, 3-, 4- or 5-fold, may be substituted, in particular with radicals selected from the group consisting of F, CF 3 , OCF 3 , OH and methoxy.
  • the compounds according to the invention have the substructure D1-1, in which
  • R 1 is phenyl, pyridyl, preferably 3-pyridyl, oxazolyl or isoxazolyl, each of these radicals each being unsubstituted or monosubstituted or polysubstituted, for example 2-, 3-, 4- or 5-fold, identical or different, the substituents are independently selected in particular from the group consisting of 0-C 1-3 alkyl, d. e-alkyl, F, Cl, CN, CF 3 , 0CF 3 , and OH, preferably from the group consisting of O-CH 3 , CH 3 , F, Cl, and CF 3 , or
  • R is C 1-6 alkyl, C 3-6 cycloalkyl, C 4-6 heterocyclyl, or a bonded via a C 1-3 alkylene group or C 3-6 cycloalkyl C 4 -6-heterocyclyl, wherein the abovementioned alkyl, alkylene, cycloalkyl and heterocyclyl groups are each unsubstituted or monosubstituted or polysubstituted, for example, 2-, 3-, 4- or 5-fold, identical or different, wherein the substituents are independently selected particularly from the group consisting of 0-Ci -3 alkyl, C 1-4 alkyl, F, Cl, CF 3, OCF 3 and OH, or compounds of the invention have the partial structure D1-2 in which
  • R 1 is C 1 -e-alkyl, C 3-6 -cycloalkyl, C 4 - 6 -heterocyclyl, or a C 3 bonded via a C 1-3 -alkylene group. 6 -cycloalkyl or C 4-6 -heterocyclyl, wherein the abovementioned
  • Alkyl, alkylene, cycloalkyl and heterocyclyl groups are each unsubstituted or monosubstituted or polysubstituted, for example, 2-, 3-, 4- or 5-fold, identical or different, wherein the substituents are independently selected in particular from
  • a group consisting of 0-C 1-3 -alkyl, C-alkyl, F, Cl, CF 3 , OCF 3 , and OH or the compounds according to the invention have the substructure D2-1 in which R is 1 or 2 substituents which are selected independently of one another from the group consisting of F, Cl, CF 3l and CH 3 .
  • the radical R 2 in the compounds according to the invention is preferably H, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, CH 2 -CF 3 , cyclopropyl,
  • R 5 may be 0, 1, 2, 3 or 4 substituents which are independently selected from the group consisting of F, CF 3, OCF 3 and Ci -6 alkyl.
  • R 5 can be absent or stand for 1, 2, 3 or 4 methyl groups.
  • R 5 can be 0, 1, 2, 3 or 4 substituents which are selected independently of one another from the group consisting of F, CF 3 and OCF 3 , in particular fluorine.
  • R 5 may represent 0 substituents, ie be absent.
  • R 6 1 in likewise preferred embodiments of R 6 1 can be used for 0, are 2 or 3 substituents independently selected from the group consisting of F, Cl, CF 3, OCF 3, OH, Ci- 6 alkyl and Od-6- alkyl.
  • R 6 can be absent or stand for 1, 2 or 3 fluorine substituents.
  • R 6 may represent 0 substituents, ie be absent.
  • the radical R 10 in the compounds according to the invention is preferably H, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, CH 2 -CF 3 , cyclopropyl,
  • Further preferred embodiments of the compounds according to the invention are those in which the partial structure D2 is selected from the group consisting of
  • R 300 is 0, 1, 2, 3 or 4 substituents independently of one another selected from the group consisting of F, Cl, Br, I, CF 3 , O-CF 3 , C 1-4 -alkyl and O-4 alkyl;
  • R 310 is 0, 1, 2 or 3 substituents independently of one another selected from the group consisting of F, Cl, Br, I, CF 3 , 0-CF 3 , C 1-4 -alkyl and 0-C 1 4- alkyl;
  • R 320 is a substituent selected from the group consisting of H, F, Cl, Br, I, CF 3 , O-CF 3 and C 1-6 -alkyl;
  • R 330 is a substituent selected from the group consisting of H, C 1-6 alkyl, aryl, CH 2 -aryl and heteroaryl; r1 stands for 1 or 2 and
  • r2 stands for 1 or 2.
  • D 2 is a radical selected from the group consisting of
  • R 300 is a substituent selected from the group consisting of H, F, Cl, Br, I, CF 3 , -O-CF 3 , C 1-4 alkyl and 0-C 1-4 alkyl;
  • R 3 0 represents a substituent selected from the group consisting of H, F, Cl, Br, I, CF 3 , -O-CF 3 , C 1-4 alkyl and 0-C 1-4 alkyl ;
  • R 320 is a substituent selected from the group consisting of H, F, Cl, Br, I, CF 3 , -O-CF 3 and C 1-4 alkyl and
  • R 330 is a substituent selected from the group consisting of H, C 1-4 alkyl, aryl, CH 2 -aryl and heteroaryl.
  • D 2 is a radical selected from the group consisting of
  • radical D 2 in the compounds according to the invention may be the following radical:
  • the radical R 7 is preferably H, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec-butyl, tert-butyl, CH 2 -CF 3 , cyclopropyl,
  • Cyclobutyl, cyclopentyl or cyclohexyl particularly preferred for H, methyl, ethyl, iso-propyl, iso-butyl, tert-butyl or cyclopropyl.
  • the radical R 7 is H or methyl.
  • b 0.
  • b is 2.
  • b is 0 or 2, preferably 0.
  • X is N (R 9a ).
  • X is C (R 9b ) H.
  • the substructure (Cy) is selected from the list of the abovementioned radicals (Cy 1) to (Cy 22) and R 9a or R 9b are pyridinyl or pyrimidyl and where the pyridyl and Pyrimidyl are each unsubstituted or monosubstituted or polysubstituted, for example, 2-, 3-, or 4-fold, same or different, wherein the substituents are independently selected from the group consisting of azetidinyl, pyrrolidinyl, piperidinyl, morpholinyl, N-methylpiperazinyl , Pyridinyl, cyclopropyl, 0-Ci.
  • radicals which have an NR 9a grouping ie (Cy 1) to (Cy 8) and (Cy 19) to (Cy 22).
  • residues having an N-R moiety i. (Cy 1) to (Cy 8) and (Cy 19) to (Cy 22).
  • a group or a cyclopropyl or cyclobutyl radical which is unsubstituted or attached to one or more several of its carbon ring members with one or more substituents
  • R 9a is CHR 15 R 16 , aryl, heteroaryl or a via a Ci. 3- alkylene-bonded CHR 15 R 16 , aryl or heteroaryl,
  • R 20 and R 2 together with the nitrogen atom connecting them, form a heterocycle which is unsubstituted or independently selected from 1, 2, 3 or 4 substituents selected from the group consisting of F, Cl, Br, I, CF 3 , C 1-4 -alkyl , OC ⁇ alkyl, OH, OCF 3 , SH,
  • R 27 is d-4-alkyl, C 3-6 -cycloalkyl, aryl, heteroaryl or a bonded via a Ci -3 alkylene C. 3 6 - cycloalkyl, aryl or heteroaryl; in which
  • Aryl is phenyl or naphthyl
  • Heteroaryl in each case, pyridinyl, triazinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolinyl, isoquinolinyl, quinazolinyl, purinyl, thiazolyl, thiadiazolyl, imidazolyl, triazolyl, oxazolyl, isoxazolyl, thienyl, pyrrolyl, tetrazolyl, oxadiazolyl or oxathiazolyl, particularly preferably in each case for pyridinyl , Triazinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolinyl, isoquinolinyl, quinazolinyl, thiazolyl, thiadiazolyl, imidazolyl, triazolyl, oxazolyl, isoxazolyl, thien
  • methyl, isopropyl, tert-butyl, F, Cl, CF 3 , OCF 3 , methoxy, OH, S ( O) 2 -CH 3 , NH 2 , NH (CH 3 ), N ( CH 3 ) 2 , pyrrolidinyl, piperidinyl, cyclopropyl, CN,
  • R 17 and R 18 are each independently H, C 1-4 alkyl or C 3-6 cycloalkyl, or
  • Heteroaryl in each case represents pyridinyl, triazinyl, pyrimidinyl, pyrazinyl, pyridazinyl, quinolinyl, isoquinolinyl, quinazolinyl, thiazolyl, thiadiazolyl, imidazolyl, triazolyl, oxazolyl, isoxazolyl, thienyl, pyrrolyl, tetrazolyl, oxadiazolyl, oxathiazolyl, preferably for pyridinyl,
  • b is 0, 1 or 2;
  • 01 is O, 1, 2 or 3;
  • R 8 is 0, 1 or 2 methyl groups
  • R 101 is 0, 1, 2 or 3 substituents independently of one another selected from the group consisting of methyl, ethyl, isopropyl, tert-butyl, F, Cl, CF 3 , OCF 3 ,
  • R 102 is a substituent selected from the group consisting of H, methyl, ethyl, n -propyl, isopropyl, n -butyl, iso -butyl, sec -butyl, tert -butyl, CH 2 -CF 3 , Cyclopropyl and cyclobutyl.
  • R 9a is unsubstituted or mono- or polysubstituted heteroaryl
  • R is C 1-6 -alkyl, C 4 -C 6 -cycloalkyl or C -C 6 -heterocyclyl or a C 4 -C 6 -cycloalkyl or C 4 -C 6 bonded via a C 1 , 2 or 3-alkylene group Heterocyclyl and wherein R 2 is H, methyl, ethyl, n-propyl, isopropyl, isobutyl, tert-butyl or cyclopropyl,
  • R 1 is d -6- alkyl, C -C 6 -cycloalkyl or C 4 -C 6 -heterocyclyl or a C 4 -C 6 -cycloalkyl bound via a C 1 , 2 or 3-alkylene group or C 4 -C 6 -heterocyclyl and in which R 2 is H, methyl, ethyl, n-propyl, isopropyl, isobutyl, tert-butyl or cyclopropyl,
  • R 2 is H, methyl, ethyl, n-propyl, iso-propyl, iso-butyl, tert-butyl or cyclopropyl, and R 502 is 0, 1 or 2 substituents each independently selected from the group consisting of F, Cl, methyl, methoxy and CF 3 ;
  • R 2 is H, methyl, ethyl, n-propyl, iso-propyl, iso-butyl, tert-butyl or cyclopropyl
  • R 503 is 0, 1 or 2 substituents each independently selected from the group consisting of F, Cl, methyl, methoxy, and CF 3 ;
  • R 2 is H, methyl, ethyl, n-propyl, iso-propyl, iso-butyl, tert-butyl or cyclopropyl, and R 504 is 0, 1 or 2 substituents each independently selected are selected from the group consisting of F, Cl, methyl, methoxy and CF 3 ;
  • c and d are each independently 0, 1 or 2 with the proviso that the cycle has at most 7 ring members;
  • R 1 is de-alkyl, C3-8 cycloalkyl, heterocyclyl, phenyl, or a via a C -3 - bound alkylene C 3-8 cycloalkyl or heterocyclyl;
  • R 2 is H, methyl, ethyl, n -propyl, iso-propyl, iso -butyl, tert -butyl or cyclopropyl;
  • R 6 is H or F;
  • R 7 is H, methyl, ethyl, n-propyl, iso-propyl, iso-butyl, tert-butyl or cyclopropyl, preferably methyl;
  • R 8 is 1, 2, 3 or 4 substituents independently selected from the group consisting of H and methyl;
  • R 9a is pyridyl or pyrimidyl
  • R 10 is H, methyl, ethyl, n-propyl, iso-propyl, iso-butyl, tert-butyl or cyclopropyl, preferably methyl;
  • R 300 is 0, 1 or 2 substituents independently selected from the group consisting of F, Cl, CF 3 and methyl; wherein the abovementioned alkyl, alkylene, cycloalkyl and heterocyclyl groups are each unsubstituted or monosubstituted or polysubstituted, for example, 2-, 3-, 4- or 5-fold, identical or different, wherein the substituents are independently selected from the group consisting of C 1 -C 3 -alkyl, F, Cl, CF 3 , OCF 3 , OH, 0O, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, phenyl, phenoxy, naphthyl, thienyl and pyridinyl, preferably from the group consisting of C 1 -C 3 -alkyl, F, Cl, CF 3 , OCF 3 , OH, cyclopropyl, cyclobutyl, cycl
  • the compounds according to the invention can be selected from the group consisting of
  • H-1 1 (1 R) -1- (4-chloro-3-oxo-1,2-dihydro-isoindol-2-yl) -N-methyl-N- (1-pyridin-4-yl-piperidine 4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-12 (3R) -3- (4-Chloro-3-oxo-1,2-dihydroisoindol-2-yl) -N-methyl-N- (1-pyridin-4-yl-piperidine-4- yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-52 (1R) -1- (4-chloro-3-oxo-1,2-dihydro-isoindol-2-yl) -N-methyl-N - [[1- (2-methyl-pyridine-4 -yl) -piperidin-4-yl] -methyl] -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-53 (1R) -1- (4-chloro-3-oxo-1, 2-dihydro-isoindol-2-yl) -N-methyl-N- [1 - [(2-pyrrolidin-1-yl-pyridin-4-yl) -methyl] -piperidin-4-yl] -2,3 -dihydro-1H-indene-5-carboxylic acid amide
  • H-66 (3R) -3 - [(2-chloro-benzoyl) -amino] -N-methyl-N- [2- (1-pyridin-4-yl-piperidin-4-yl) -ethyl] -2, 3-dihydro-1H-indene-5-carboxylic acid amide
  • H-67 (3R) -3 - [(2-tert-butylbenzoyl) amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -
  • H-81 (4R) -4 - [(2-Chloro-benzoyl) -amino] -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl] -8-fluoro N-methyl-3,4-dihydro-2H-chromen-6-carboxylic acid amide
  • H-82 (3R) -3- (2,3-dihydro-1H-indene-1-carbonylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-103 (3R) -3 - [(2-Chlorobenzoyl) amino] -N-methyl-N - [(1S, 3R) -3- (4-methylpiperazin-1-yl) cyclohexyl] - 2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-104 (3R) -3 - [[(2-chlorophenyl) sulfonyl] amino] -N-methyl-N - [(1S, 3R) -3- (4-methylpiperazin-1-yl) cyclohexyl] 2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-120 (3R) -N- [1- (2-Dimethylamino-pyrimidin-4-yl) -piperidin-4-yl] -3- [isopropyl- (3-methyl-butanoyl) -amino] -N-methyl 2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-122 (3R) -3 - [(2-chloro-benzoyl) -amino] -N-methyl-N- [1 - (2-methyl-pyrimidine -4-yl) - piperidin-4-yl] -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-139 (3R) -3 - [(2-Chloro-benzoyl) amino] -N- [1- (2-isopropyl-6-methylpyrimidin-4-yl) -piperidin-4-yl] -N- Methyl 2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-140 (3R) -3 - [(2-Chloro-benzoyl) amino] -N-methyl-N- [1- (2-oxo 2-pyrrolidin-1-yl-ethyl) -piperidin-4-yl] -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-145 (3R) -3 - [(2-Chloro-benzoyl) -ethyl-amino] -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl] -N -methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-146 (3R) -3 - [(2-Chlorobenzoyl) amino] -N-methyl-N- (1-pyridin-4-ylazetidin-3-yl) -2,3-dihydro-1H -inde-5-carboxylic acid amide
  • H-151 (1 R) -1 - [(2-Chloro-benzoyl) amino] -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl] -6-fluoro N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-152 (1R) -1 - [(2-chloro-benzoyl) -amino] -6-fluoro-N-methyl-N - [1- (6-methyl-pyrimidin-4-yl) -piperidin-4-yl] -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-163 (3R) -3 - [(2-Chloro-6-fluoro-benzoyl) -amino] -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl] - N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-164 (3R) -3 - [(2-chloro-3-fluoro-benzoyl) amino] -N-methyl-N- ( 1-pyrimidin-4-yl-piperidine
  • H-165 (3R) -3 - [(2-Chloro-4-fluoro-benzoyl) -amino] -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl] - N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-166 (3R) -3 - [(2-chloro-benzoyl) -isopropyl-amino] -N- [1- (2- isopropyl-6-methyl-pyrimidin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-184 (3R) -3 - [(2-Chloro-benzoyl) -amino] -N- [4- (2-dimethylamino-pyridin-4-yl) -cyclohexyl] -N-methyl-2,3-dihydro- 1 H-indene-5-carboxylic acid amide
  • H-185 (3R) -3- (3-cyclopentyl-propanoyl-methyl-amino) -N- [1- (2-dimethylaminopyridin-4-yl) -piperidine-4 -yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-186 (3R) -3- (3-Cyclopentyl-propanoyl-methyl-amino) -N- [1- (2-dimethylamino-pyrimidin-4-yl) -piperidin-4-yl] -N-
  • H-230 (3R) -3- (cyclopentanecarbonyl-methyl-amino) -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl] -N-methyl-2,3 -dihydro-1H-indene-5-carboxylic acid amide
  • H-231 (3R) -3 - [(2-cyclopentyl-acetyl) -methyl-amino] -N- [1- (2,6-dimethyl-pyrimidine-4 - yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • H-232 (3R) -3- (3,4-dimethyl-pentanoyl-methyl) amino) -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl] -N-methyl-2,
  • H-236 (8R) -8 - [(2-chloro-benzoyl) -amino] -N- [1- (2-dimethylamino-pyrimidin-4-yl) -piperidin-4-yl] -N-methyl-5, 6,7,8-tetrahydro-naphthalene-2-carboxylic acid amide
  • H-237 (8R) -8 - [(2-chloro-benzoyl) -amino] -N- [1- (2-dimethylamino-6-methyl-pyrimidine 4-yl) piperidin-4-yl] -N-methyl-5,6,7,8-tetrahydronaphthalene-2-carboxylic acid amide
  • H-238 (3R) -3 - [(2-cyclopentyl-acetyl) -amino ] -N- [1- (2,6-dimethyl-pyrimidin-4-yl) -piperidin-4-yl]
  • CCJH-10 N- [7- [methyl- (1-pyridin-4-yl-piperidin-4-yl) -carbamoyl] -1,3,3,4-tetrahydronaphthalene-1-yl] -4- trifluoromethyl) -pyridine-3-carboxylic acid amide
  • CC_H-14 (cyclohexanecarbonylamino) -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -
  • CC_H-16 8 [[[2-Chloro-6- (trifluoromethyl) phenyl] sulfonyl] amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -5,6 , 7,8-tetrahydro-naphthalene-2-carboxylic acid amide
  • CC_H-17 3 [[2-chloro-6- (trifluoromethyl) benzoyl] amino] -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2, 3-dihydro-indene-5-carboxylic acid amide
  • CC_H-18 3- (3-cyclopentyl-propanoylamino) -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidine
  • CC_H-33 4 - [(2-Chloro-benzoyl) amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -3,4-dihydro-2H-chromen-6-ene carboxylic acid amide
  • CC_H-35 4 [(2,3-dichloro-benzoyl) amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -3,4-dihydro-2H-chromene 6-carboxylic acid amide
  • H-36 3 [(2-Chloro-5-fluoro-benzoyl) -amino] -N- [2- (1-pyridin-4-yl-piperidin-4-yl) -ethyl] -
  • CC_H-55 N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-3 - [[[2- (trifluoromethyl) -phenyl] -methylsulfonyl] -amino] -2,3-dihydro- 1 H-indene-5-carboxylic acid amide
  • CC_H-56 N-methyl-N- (1-pyridin-4-yl ⁇ iperidin-4-yl) -4 - [[[2- (trifluoromethyl) -phenyl] -methylsulfonyl] amino] -3,4-dihydro-2H-chromen-6-carboxylic acid amide
  • CC_H-58 1- (Cyclohexanecarbonylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-59 3- (3-Cyclopentyl-propanoylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -
  • CC_H-64 1 [(2-chloro-5-fluoro-benzoyl) -amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -
  • CC_H-65 1- (3-Cyclopentyl-propanoylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -
  • CC_H-69 3- (Cyclohexanecarbonyl-methyl-amino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-70 3- (3-Cyclopentyl-propanoyl-methyl-amino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene 5-carboxylic acid amide
  • CC_H-78 3- (3-Cyclopentyl-propanoylamino) -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-83 3 - [(2,3-dichloro-benzoyl) -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl 2,3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-84 3- (3-Cyclopentyl-propanoyl-methyl-amino) -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3 -dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-100 1 - [[2- (2-chlorophenyl) -2-methyl-propanoyl] amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3- di-ydro-1H-indene-5-carboxylic acid amide
  • CC_H-102 8 [[2- (2-chlorophenyl) -2-methyl-propanoyl] -amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -5,6, 7,8-tetrahydro-naphthalene-2-carboxylic acid amide
  • CC_H-103 3 [[2- (2-chlorophenyl) -2-methyl-propanoyl] amino] -N- [2- (1-pyridin-4-yl] piperidine
  • CC_H-104 3 [[(2-Chloro-phenyl) -methyl-carbamoyl] -amino] -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-2,3-dihydro-1H -inde-5-carboxylic acid amide
  • CC_H-1 13 N-Methyl-1- (3-methylbutanoylamino) -N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-123 3- (cyclohexanecarbonylamino) -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -
  • CC_H-132 3- (3-Methylbutanoylamino) -N- [2- (1-pyridin-4-yl-piperidin-4-yl) -ethyl] -2,3-dihydro-1H-indene-5 carboxylic acid amide
  • CC_H-134 3 [[[2-Chloro-6- (trifluoromethyl) -phenyl] sulfonyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidine-4 -yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-141 N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -3 - [[[2- (trifluoromethyl) -phenyl] -methylsulfonyl] -amino] -2,3-dihydro- 1 H-indene-5-carboxylic acid amide
  • CC_H-142 3 [[(2-Chloro-phenyl) -methyl-carbamoyl] -amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl- 2,3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-143 1 - [[[2-chloro-6- (trifluoromethyl) phenyl] sulfonyl] amino] -N-methyl-N- (1-pyridine -4-yl-piperidin
  • CC_H-205 3- (Cyclopropanecarbonylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-206 3- (3,3-Dimethylbutanoylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5 carboxylic acid amide,
  • CCJH-21 1 3- (Cyclohexanecarbonyl-methyl-amino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-212 3- (Cyclopropanecarbonyl-methyl-amino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide .
  • CC_H-213 3- (3,3-Dimethyl-butanoyl-methylamino) -N-methyl-N- (1-pyridin-4-yl-piperidine
  • CC_H-214 3 [(2-methoxy-acetyl) -metyl-amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -
  • CC_H-215 3- (acetylmethylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-
  • CC_H-217 3 [[(2-Chloro-phenyl) -carbamoyl] -methyl-amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-1 H-indene-5-carboxylic acid amide,
  • CC_H-220 3 [[(2,3-dichloro-phenyl) -carbamoyl] -methyl-amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3 -dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-221 3 [[(2,5-dichloro-phenyl) -carbamoyl] -methyl-amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3 -dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-226 3- (Cyclopropanecarbonylamino) -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-indene-5-carboxylic acid amide,
  • CC_H-227 3- (3,3-Dimethyl-butanoylamino) -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-indene-5 -carboxylic acid amide,
  • CC_H-228 3 [(2-methoxy-acetyl) -amino] -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -
  • CC_H-229 3-acetylamino-N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-indene-5-carboxylic acid amide,
  • CC_H-231 3 [[2-chloro-3- (trifluoromethyl) benzoyl] amino] -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2, 3-dihydro-indene-5-carboxylic acid amide,
  • CCJH-236 3 [[(2,5-dichloro-phenyl) -carbamoyl] -amino] -N, 1,1-tris-diethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2, 3-dihydro-indene-5-carboxylic acid amide,
  • CC_H-237 3 [[(3,5-dichloro-phenyl) -carbamoyl] -amino] -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2, 3-dihydro-indene-5-carboxylic acid amide,
  • CC_H-238 3 - [[(2,4-dichlorophenyl) -carbamoyl] amino] -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3- dihydro-indene-5-carboxylic acid amide,
  • CC_H-239 3 [[[2-Chloro-5- (trifluoromethyl) -phenyl] -carbamoyl] -amino] -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl ) -2,3-dihydro-indene-5-carboxylic acid amide, CC_H-240 3 - [[[4-chloro-2- (trifluoromethyl) -phenyl] -carbamoyl] -amino] -N, 1,1-trimethyl-N - (1-pyridin-4-yl-piperidin-4-yl) -2,3-dihydro-indene-5-carboxylic acid amide, CC_H-241 3 - [[(3-chloro-4-methyl-phenyl) -carbamoyl ] amino] -N, 1,1-trimethyl-N- (1-pyridin
  • CC_H-245 3 [[(2-Chlorophenyl) -metyl-carbamoyl] -amino] -N, 1,1-trimethyl-N- (1-pyridin-4-yl-piperidin-4-yl) -2,3 dihydro-indene-5-carboxylic acid amide,
  • CC_H-274 4- (Cyclopropanecarbonylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -3,4-dihydro-2H-chromen-6-carboxylic acid amide,
  • CC_H-275 4- (3,3-Dimethyl-butanoylamino) -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -3,4-dihydro-2H-chromen-6-carboxylic acid amide,
  • CC_H-277 4-Acetylamino-N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -3,4-dihydro-2H-chromen-6-carboxylic acid amide,
  • CC_H-283 4 - [[(2,5-dichloro-phenyl) -carbamoyl] -amino] -N-methyl-N- (1-pyridin-4-yl-piperidin-4-yl) -3,4-dihydro- 2H-chromene-6-carboxylic acid amide,
  • CC_H-294 3 [(2-chloro-5-fluoro-benzoyl) -amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl- 2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-302 N- [1- (2,6-Dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-3 - [[[2- (trifluoromethyl) -phenyl] -methylsulfonyl] -amino ] -2,3-dihydro-1H-indene-5-carboxylic acid amide, CC_H-303 3 - [[2-chloro-3- (trifluoromethyl) benzoyl] amino] -N- [1- (2,6- dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-304 3 [[(2-chlorophenyl) -carbamoyl] amino] -N- [1- (2,6-dimethylpyridin-4-yl) -piperidin-4-yl] -N-methyl-2, 3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-305 3 [[(3-chlorophenyl) carbamoyl] amino] - N - [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2, 3-dihydro-1H-indene-5-carboxylic acid amide
  • CC_H-306 3 [[(2,6-dichloro-phenyl) -carbamoyl] -amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N- methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-313 3 [[(3-Chloro-4-methyl-phenyl) -carbamoyl] -amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] - N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide, CC_H-314 3 - [[(3-chloro-4-fluoro-phenyl) -carbamoyl] -amino] -N- [1- ( 2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-317 3 [[(2,4-dichlorophenyl) -methyl-carbamoyl] -amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N- methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide, CC_H-318N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl- 3- (3-methylbutanoylamino) -2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-320 3- (3-Cyclopentyl-propanoylamino) -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1 H-indene-5-carboxylic acid amide,
  • CC_H-328 3 [(2,5-dichloro-benzoyl) -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl 2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-329 3- [t 2 -chloro-6- (trifluoromethyl) -benzoyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] - N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-330 3- (Cyclohexanecarbonyl-methyl-amino) -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3-di-dehydro 1 H-indene-5-carboxylic acid amide,
  • CC_H-331 3- (Cyclopropanecarbonyl-methyl-amino) -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1 H-indene-5-carboxylic acid amide,
  • CC_H-332 3- (3,3-Dimethyl-butanoyl-methylamino) -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2 , 3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-334 3- (Acetylmethylamino) -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1 H-indene-5-carboxylic acid amide,
  • CC_H-335 3 [[(2-Chloro-6-methyl-phenyl) -sulfonyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl ] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-336 3 [[(2-Chloro-phenyl) -carbamoyl] -methyl-amino] -N- [1- (2,6-dimethylpyridin-4-yl) -piperidin-4-yl] -N-methyl 2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-338 3 [[(2,6-dichloro-phenyl) -carbamoyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide, CC_H-339 3 - [[(2,3-dichloro-phenyl) -carbamoyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridine]
  • CC_H-344 3 - [[[4-chloro-2- (trifluoromethyl) -phenyl] -carbamoyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidine] 4-yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-345 3 - [[(3-Chloro-4-methyl-phenyl) -carbamoyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidine-4- yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-346 3 [[(3-Chloro-4-fluoro-phenyl) -carbamoyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidine-4- yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-348 3 [[(5-Chloro-2-methoxy-phenyl) -carbamoyl] -methyl-amino] -N- [1- (2,6-dimethyl-pyridin-4-yl) -piperidine-4- yl] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-354 3- (3-Cyclopentyl-propanoyl-methyl-amino) -N- [1- (2,6-dimethylpyridin-4-yl) -piperidin-4-yl] -N-methyl-2,3 -dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-358 3 - [(2-chloro-6-fluoro-3-methylbenzoyl) amino] -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-2,3- dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-362 3- (3,3-dimethylbutanoylamino) -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-
  • CC_H-374 3 [[(5-chloro-2-methoxy-phenyl) -carbamoyl] -amino] -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-2,3- dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-376 3 - [[(2,4-dichlorophenyl) -methyl-carbamoyl] -amino] -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-2,3-dihydro- 1H-indene-5-carboxylic acid amide,
  • CC_H-381 3- (3-Cyclopentyl-propanoylamino) -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide .
  • CC_H-382 3 - [(ethylsulfonyl) amino] -N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-383 N- (1-isoquinolin-6-yl-piperidin-4-yl) -N-methyl-3 - [[[3- (trifluoromethyl) -phenyl] -methylsulfonyl] -amino] -2,3-dihydro-1 H-indene-5-carboxylic acid amide, CC_H-384 3 - [[(2-fluorophenyl) methylsulfonyl] amino] -N- (1-isoquinolin-6-yl-piperidin-4-yl) -
  • CC_H-613 3- (3-cyclopentyl-propanoylamino) -N-methyl-N- [1- (2-methylsulfonyl-pyrimidine
  • CC_H-615 4- [4 - [[3- (3-cyclopentyl-propanoylamino) -2,3-dihydro-1H-indene-5-carbonyl] -methyl-amino] -piperidin-1-yl] -N, N-dimethyl-pyridine-2-carboxylic acid amide, CC_H-616 N- [1- (2-tert-butyl-pyrimidin-4-yl) -piperidin-4-yl] -3 - [(2-chloro-benzoyl) amino] -N-methyl-2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-620 3- (3-Cyclopentyl-propanoylamino) -N-methyl-N- [1- (2-pyrrolidin-1-yl-pyrimidine
  • CC_H-624 N- [1- (2-tert-Butyl-pyrimidin-4-yl) -piperidin-4-yl] -3- (3-cyclopentyl-propanoylamino) -N-methyl-2,3-dihydro-1H -inde-5-carboxylic acid amide, CC_H-626 3- (3-Cyclopentyl-propanoylamino) -N-methyl-N- [4- (5-methyl-3-oxo-1,2-dihydro-imidazo [5,1-e] -imidazol-2-yl ) -cyclohexyl] -2,3-dihydro-1H-indene-5-carboxylic acid amide,
  • CC_H-629 3- (3-Cyclopentyl-propanoylamino) -N- [1- (2-dimethylamino-pyrimidin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1H- indene-5-carboxylic acid amide,
  • CC_H-630 3- (3-Cyclopentyl-propanoylamino) -N- [1- (2-cyclopropyl-pyrimidin-4-yl) -piperidin-4-yl] -N-methyl-2,3-dihydro-1H- indene-5-carboxylic acid amide,
  • CC_H-632 3- (3-Cyclopentyl-propanoylamino) -N- [1- (5-fluoro-pyrimidin-4-yl) -piperidin-4-yl] -
  • CC_H-633 3 - [(2-Chlorobenzoyl) amino] -N-methyl-N- (1-pyridazin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5 -carboxylic acid amide and
  • CC_H-634 3- (3-Cyclopentyl-propanoylamino) -N-methyl-N- (1-pyridazin-4-yl-piperidin-4-yl) -2,3-dihydro-1H-indene-5-carboxylic acid amide , in the form of free compounds; the tautomers; the N-oxides; the racemate; of the
  • the compounds according to the invention have an antagonistic effect both on the human B1R receptor (hB1R) and on the B1R receptor of the rat (rB1R).
  • the compounds according to the invention have an inhibition of at least 15%, 25%, 50% in the FLIPR assay at a concentration of 10 ⁇ at the human B1R receptor and / or at the B1R receptor of the rat. 70%, 80% or 90% up.
  • the agonistic or antagonistic effect of substances can on the bradykinin receptor 1 (B1R) of the species human and rat using ectopically expressing cell lines (CHO K1 cells) and with the aid of a Ca 2+ -sensitive dye (Fluo-4) in the Fluorescent Imaging Plate Reader (FLIPR).
  • B1R bradykinin receptor 1
  • FLIPR Fluorescent Imaging Plate Reader
  • the indication in% activation is based on the Ca 2+ signal after addition of Lys-Des-Arg 9 -bradykinin (0.5 nM), or des-Arg 9 -bradykinin (100 nM).
  • Antagonists lead to a suppression of Ca 2+ influx after the addition of the agonist. Indicated are% inhibition compared to the maximum achievable inhibition.
  • the substances according to the invention act, for example, on the im
  • Another object of the invention are therefore medicaments containing at least one compound of the invention, and optionally suitable additives and / or auxiliaries and / or optionally other active ingredients.
  • the medicaments according to the invention optionally contain suitable additives and / or adjuvants, as well
  • Carrier materials, fillers, solvents, diluents, dyes and / or binders can be administered as liquid dosage forms in the form of injection solutions, drops or juices, as semi-solid dosage forms in the form of granules, tablets, pellets, patches, capsules, patches / spray patches or aerosols ,
  • excipients etc. as well as the amounts to be used depend on whether the drug is oral, peroral, parenteral, intravenous, intraperitoneal, intradermal, intramuscular, nasal, buccal, rectal or topical, for example on the skin, mucous membranes or in the eyes, to be applied.
  • preparations in the form of tablets, dragees, capsules, granules, drops, juices and syrups are suitable; for parenteral, topical and inhalative administration, solutions, suspensions, Constituable dry preparations and sprays.
  • Substituted compounds according to the invention in a depot, in dissolved form or in a plaster, optionally with the addition of main-promoting agents, are suitable percutaneous agents
  • Substituted compounds according to the invention may also be present in parenteral
  • the amount of drug to be administered to the patient varies depending on the weight of the patient, the mode of administration, the indication and the severity of the disease. Usually 0.00005 to 50 mg / kg, in particular 0.01 to 5 mg / kg of at least one compound according to the invention are administered.
  • a substituted compound according to the invention present is optionally present as a pure diastereomer and / or enantiomer, as a racemate or as a non-equimolar or equimolar mixture of the diastereomers and / or enantiomers.
  • the person skilled in suitable methods for the separation of stereoisomers are known.
  • substituted compounds according to the invention can be used in particular for the preparation of a medicament for the treatment of pain, in particular of acute, visceral, neuropathic or chronic pain or inflammatory pain.
  • Another object of the invention is therefore the use of at least one substituted compound according to the invention for the manufacture of a medicament for the treatment of pain, in particular of acute, visceral, neuropathic or chronic pain.
  • a specific embodiment of the present invention is the use of at least one of the substituted compounds of the invention for the manufacture of a medicament for the treatment of inflammatory pain.
  • the invention also provides the use of at least one substituted compound according to the invention for the treatment of pain, in particular of acute, visceral, neuropathic or chronic pain or inflammatory pain.
  • Another object of the invention is the use of at least one substituted according to the invention for the manufacture of a medicament for the treatment of diabetes, respiratory diseases, for example bronchial asthma, allergies, COPD / chronic obstructive pulmonary disease or cystic fibrosis; inflammatory bowel disease, for example, ulcerative colitis or CD / Crohn's disease;
  • neurological diseases for example multiple sclerosis, neurodegenerative diseases, fibrotic diseases, inflammation of the skin, for example atopic dermatitis, psoriasis or bacterial infections; rheumatic diseases,
  • rheumatoid arthritis or osteoarthritis for example rheumatoid arthritis or osteoarthritis; septic shock;
  • Reperfusion syndrome for example after heart attack or stroke, obesity; and as an angiogenesis inhibitor.
  • the invention also provides the use of at least one substituted compound according to the invention for the treatment of one of the aforementioned indications.
  • a substituted compound used is present as a pure diastereomer and / or enantiomer, as a racemate or as a non-equimolar or equimolar mixture of the diastereomers and / or enantiomers.
  • Another object of the invention is a method for the treatment, in particular in one of the aforementioned indications, of a non-human mammal or human, which requires a treatment of the corresponding indication, by administering a therapeutically effective dose of a substituted compound or a medicament according to the invention.
  • Another object of the invention is a method for the treatment of pain, in particular one of the aforementioned types of pain, a non-human mammal or human, or a treatment, in particular pain, especially of acute, visceral, neuropathic or chronic pain or
  • Inflammatory pain is required by administering a therapeutically effective dose of a substituted compound of the invention or a pharmaceutical composition of the invention.
  • Another object of the invention is a process for the preparation of
  • Aryl zinc compounds e.g. after (Ref No. 5) Takahashi, Hideki; Inagaki, Shinya; Nishihara, Yasushi; Shibata, Takanori; Takagi, Kentaro; Organic Letters; Vol. 8; (2006); p. 3037-3040, from aldehydes e.g. after (Ref No. 6) Kotake, Yoshihiko; lijima, Atsumi; Yoshimatsu, Kentaro; Tamai, Naoko; Ozawa, Yoichi; et al .; Journal of Medicinal Chemistry; Vol. 37; (1994); p. 1616-1624, from arylboronic acids e.g. after (Ref No. 7) Horiguchi, Hakaru; Tsurugi, Hayato;
  • ester derivatives of (I) are obtained by these methods, which are then converted to the step (j) in the acids (I).
  • Acids of the general formula (II) can be prepared by methods known from the literature, e.g. by oxidation (Ref No. 10) Matveeva, E. D .; Podrugina, T.A .; Zefirova, O. N .; Alekseyev, A. S .; Bachurin, S. O .; Pellicciari, R .; Zefirov, N.S .; Russian Journal of Organic Chemistry; vol. 38; (2002); p. 1764-1768, by carbonyl insertion (Ref. No. 11) WO2005 / 95387 (A1) and (Ref No. 12) Takeuchi, Ryo; Yasue, Hiroyuki; Journal of Organic Chemistry; Vol.
  • step (d) acids of the general formula (II) are prepared by a literature method (see (a) Protecting Groups, Philip J. Kocienski, Thieme, Stuttgart, 3rd Revised Edition (14 February 2005) (b) Protective Groups in Organic Synthesis, Theodora W. Greene and Peter GM Wuts, Wiley &Sons; 4th Edition (October 30, 2006)) into an ester preferably selected from the group consisting of methyl, ethyl, isopropyl and tert-butyl esters of the general formula (III), transferred.
  • step (e) ketones of the general formula (III) are dissolved in at least one solvent, preferably selected from the group consisting of water, dichloromethane,
  • At least one inorganic base preferably selected from the group consisting of potassium hydride, potassium carbonate, sodium carbonate, cesium carbonate, sodium hydroxide, and sodium acetate, or an organic base, preferably selected from the group consisting of triethylamine, diisopropylethylamine and pyridine, at temperatures of preferably -15 ° C to 100 ° C to give compounds of general formula (IV).
  • step (f) hydroxylamines of the general formula (IV) in at least one
  • Solvent preferably selected from the group consisting of dichloromethane, chloroform, dimethylformamide, diethyl ether, dioxane, tetrahydrofuran, water, methanol, ethanol and isopropanol with at least one reducing agent preferably selected from the group consisting of lithium aluminum hydride, sodium borohydride, lithium borohydride, sodium, sodium amalgam and zinc optionally in the presence of at least one acid or Lewis acid, preferably selected from the group consisting of hydrochloric acid, sulfuric acid, acetic acid and titanium tetrachloride at temperatures of preferably -15 ° C to 100 ° C to give compounds having the general formula (VI).
  • at least one reducing agent preferably selected from the group consisting of lithium aluminum hydride, sodium borohydride, lithium borohydride, sodium, sodium amalgam and zinc optionally in the presence of at least one acid or Lewis acid, preferably selected from the group consisting of hydrochloric acid, sulfuric acid, acetic acid and titanium
  • hydroxylamines of the general formula (IV) in step (f) may also be present in at least one solvent, preferably selected from the group consisting of chloroform, ethyl acetate, dimethylformamide, diethyl ether, dioxane, tetrahydrofuran,
  • at least one catalyst preferably selected from the group consisting of rhodium on carbon, palladium on carbon, palladium black, Raney nickel and platinum oxide
  • at least one acid Preferably selected from the group consisting of hydrochloric acid, sulfuric acid and acetic acid at temperatures of preferably 0 ° C to 50 ° C are converted to compounds having the general formula (VI).
  • Step (k) are obtained, wherein Pg preferably Boc corresponds.
  • Pg preferably Boc corresponds.
  • Tetra hydrofu ran dimethyl sulfoxide, methanol and ethanol or mixtures of these
  • step (g) amines of the general formula (VI) are prepared by a literature method (see (a) Protecting Groups, Philip J. Kocienski, Thieme, Stuttgart, 3rd Revised Edition (14 February 2005) (b) Protective Groups in Organic Synthesis, Theodora W. Greene and Peter GM Wuts, Wiley &Sons; 4th Edition (October 30, 2006)) with appropriate protecting groups (Pg), preferably selected from the group consisting of tert-butyloxycarbonyl (Boc) and benzylcarbamate (Cbz) Mistake.
  • Pg protecting groups
  • step (h) are amines of general formula (VI) or (XII), in at least one solvent, preferably selected from the group consisting of dichloromethane, acetonitrile, dimethylformamide, diethyl ether, dioxane, tetrahydrofuran, methanol, Ethanol and isopropanol with acid chlorides or sulfonyl chlorides, in the presence of at least one inorganic base, preferably selected from the group consisting of
  • Potassium carbonate and cesium carbonate or an organic base, preferably selected from the group consisting of triethylamine, diisopropylethylamine and pyridine and optionally with the addition of 4- (dimethylamino) pyridine or 1-hydroxybenzotriazole, at temperatures of preferably -15 ° C to 50 ° C. converted into compounds of the general formula (VII) or (IX).
  • step (h) instead of the carboxylic acid chlorides and the corresponding carboxylic acids are used.
  • R'OH wherein R 'has the meaning given above, are used in at least one
  • Solvent preferably selected from the group consisting of dichloromethane,
  • Cesium carbonate or an organic base, preferably selected from the group consisting of triethylamine, diisopropylethylamine and pyridine and optionally with the addition of 4- (dimethylamino) pyridine or 1-hydroxybenzotriazole to give compounds having the general formula (VII) or (IX) ,
  • Cyclic amidic systems are synthesized in step (h) in analogy to rules known from the literature, e.g. (Ref 14) Bioorganic & Medicinal Chemistry Letters 17 (2007) 428-433 and (ref 15) Bioorganic & Medicinal Chemistry Letters 17 (2007) 424-427.
  • the step (h) can be carried out in two steps.
  • first the amines of the general forms (VI) or (XII) are converted into the corresponding alkylated amines before the second step is carried out analogously to the above-described methods 1) or 2) for the step (h).
  • the alkylated amines are either by
  • Reaction of the amines of the general forms (VI) or (XII) with aldehydes or ketones in at least one organic solvent preferably from the group consisting of diethyl ether, tetrahydrofuran, methanol, ethanol, dichloroethane, dichloromethane and toluene, with the addition of at least a reducing agent, preferably from the group consisting of borane-pyridine complex, sodium borohydride, sodium triacetoxyborohydride, sodium cyanoborohydride and triethylsilane optionally in the presence of at least one acid, preferably selected from the group consisting of formic acid, acetic acid, hydrochloric acid and trifluoroacetic acid at temperatures of preferably -70 ° C to 100 ° C, or by reacting the amines of the general forms (VI) or (XII) with halides, preferably bromides or iodides, or sulfonates, preferably mesy
  • At least one suitable base preferably sodium hydride or
  • Potassium carbonate in at least one organic solvent, preferably from the group consisting of THF, DMSO and DMF at temperatures of preferably -70 ° C to 100 ° C.
  • step (i) compounds of the general formula (V) or (VII) are dissolved in at least one solvent, preferably selected from the group consisting of water,
  • Dimetylformamide, dioxane and dimethyl sulfoxide with an inorganic base preferably selected from the group consisting of lithium hydroxide, sodium hydroxide, potassium hydroxide, Kaliumtertbutanolat, lithium propanethiolate and sodium phenylselenolat, optionally with the addition of HMPA or lithium chloride or with a Lewis acid, preferably selected from the group consisting of trimethylsilyl chloride, boron tribromide and
  • Aluminum trichloride optionally with the addition of thiols, sodium iodide or lithium chloride, reacted at temperatures of preferably 0 ° C to 100 ° C to give compounds of general formula (VIII) or (X).
  • step () compounds of the general formula (X) or (VIII) in at least one solvent, preferably selected from the group consisting of
  • step (k) the amine protecting groups (Pg) are prepared from molecules of the general formula (XI) by a method known from the literature (see (a) Protecting Groups, Philip J. Kocienski, Thieme, Stuttgart, 3rd Revised Edition (February 14, 2005) (b) Protective Groups in Organic Synthesis, Theodora W. Greene and Peter GM Wuts, Wiley &Sons; 4th Edition (30.
  • step (k) the compounds of general formula (XI) in at least one solvent, preferably selected from the group consisting of water, methanol, ethanol, isopropanol, diethyl ether, tetrahydrofuran, acetonitrile, dioxane, Dimetylformamid and dimethyl sulfoxide with an acid, preferably selected from the group consisting of trifluoroacetic acid, sulfuric acid and hydrochloric acid or acetyl chloride / methanol at temperatures of preferably 0 ° C to 80 ° C to
  • step (o) the amine protecting groups (Pg) (preferably Boc, Cbz, Bn, PMB) are prepared from the corresponding compounds by a method known from the literature (see (a) Protecting Groups, Philip J. Kocienski, Thieme, Stuttgart, 3rd Revised Edition (February 14, 2005) (b) Protective Groups in Organic Synthesis, Theodora W. Greene and Peter GM Wuts, Wiley &Sons; 4th Edition (October 30, 2006)).
  • Pg amine protecting groups
  • step (o) the corresponding compounds are in at least one solvent, preferably selected from the group consisting of water, methanol, ethanol, isopropanol, diethyl ether, tetrahydrofuran, acetonitrile, dioxane, dimethylformamide and dimethyl sulfoxide with an acid , preferably selected from the group consisting of trifluoroacetic acid, sulfuric acid and hydrochloric acid or
  • Acetyl chloride / methanol reacted at temperatures of preferably 0 ° C to 80 ° C to the corresponding deprotected compounds.
  • step (I) compounds of general formula (XIII) in at least one
  • Solvent preferably selected from the group consisting of ethanol, methanol, n-butanol, iso-propanol, 2-butanone, DMSO, diethyl ether, water, benzene, toluene, THF, DCM, acetonitrile, acetone, DMF and pentane with boronic acids, iodide , Bromide, chloride or mesylate compounds, optionally with the addition of at least one base, preferably selected from the group consisting of potassium hydroxide, sodium hydroxide,
  • potassium carbonate optionally in aqueous or alcoholic solution, potassium carbonate,
  • Sodium ethoxide, sodium tert-butoxide and diisopropylethylamine optionally with the addition of an adjuvant, preferably selected from the group consisting of 18-crown-6, 15-crown-5, terabutylammonium bromide or sulphate,
  • Benzyltriethyiammonium chloride, 1-n-butyl-3-methylimidazolium tetrafluoroborate and DMAP optionally with the use of a catalyst, preferably selected from the group consisting of Pd (pyclohexyl 3 ) 2 Cl 2 , Pd 2 (dba) 3l Ni (OAc) 2 , Cu (OAc ) 2 , optionally using a ligand, preferably selected from the group consisting of P (o-tolyl) 3 , P (1, 1'-bis (diphenylphosphino) ferrocene, 2,2'-bipyridine, P (tri-o-tolylphosphine) 3 to Implemented compounds of general formula (XIV).
  • a catalyst preferably selected from the group consisting of Pd (pyclohexyl 3 ) 2 Cl 2 , Pd 2 (dba) 3l Ni (OAc) 2 , Cu (OAc ) 2
  • compounds of the general formula (XIV) are obtained by reacting compounds of the general formula (XIII) with iodide, bromide, chloride or mesylate compounds under Buchwald-Hartwig conditions.
  • step (m) will be compounds of general formula (XIII) with aldehydes of the general formula R b CHO, or ketones of the general formula R b COR ° wherein R b and R c have the abovementioned meanings, in at least one organic
  • Solvent preferably from the group consisting of diethyl ether, tetrahydrofuran, methanol, ethanol, dichloroethane, dichloromethane and toluene, with the addition of at least one reducing agent, preferably from the group consisting of borane-pyridine complex, sodium borohydride, sodium triacetoxyborohydride, sodium cyanoborohydride and triethylsilane, optionally in the presence at least one acid, preferably selected from the group consisting of formic acid, acetic acid, hydrochloric acid and trifluoroacetic acid at temperatures of preferably -70 ° C to 100 ° C to give compounds of general formula (XVI).
  • at least one reducing agent preferably from the group consisting of borane-pyridine complex, sodium borohydride, sodium triacetoxyborohydride, sodium cyanoborohydride and triethylsilane
  • at least one acid preferably selected from the group consisting of formic acid, ace
  • step (n) amines of the general formula (XIII), in at least one
  • Solvents preferably selected from the group consisting of dichloromethane, acetonitrile, dimethylformamide, diethyl ether, dioxane, tetrahydrofuran, methanol, ethanol and isopropanol with acid chlorides R d COCI, or sulfonyl chlorides R d S0 2 CI, or isocyanates R d NCO wherein R d has the abovementioned meaning, in the presence of at least one inorganic base, preferably selected from the group consisting of
  • Potassium carbonate and cesium carbonate or an organic base, preferably selected from the group consisting of triethylamine, diisopropylethylamine and pyridine and optionally with the addition of 4- (dimethylamino) pyridine or 1-hydroxybenzotriazole, at temperatures of preferably -15 ° C to 50 ° C. converted into compounds of general formula (XVIII).
  • step (n) instead of the carboxylic acid chlorides and the
  • R d C0 2 H, wherein R d has the meaning given above, in at least one
  • Solvent preferably selected from the group consisting of dichloromethane,
  • Cesium carbonate, or an organic base preferably selected from the group consisting of triethylamine, diisopropylethylamine and pyridine and optionally with the addition of 4- (dimethylamino) pyridine or 1-hydroxybenzotriazole to give compounds of general formula (XVIII).
  • step (p) compounds of the general formula (XX) with amines of the general formula R e NHR f in which R e and R f have the abovementioned meanings, in at least one organic solvent, preferably from the group consisting of diethyl ether, tetrahydrofuran, Methanol, ethanol, dichloroethane, dichloromethane and toluene, with the addition of at least one reducing agent, preferably from the group consisting of borane-pyridine complex, sodium borohydride, sodium triacetoxyborohydride,
  • step (q) will be compounds of general formula (XX) in at least one organic solvent, preferably from the group consisting of diethyl ether, tetrahydrofuran, methanol, ethanol, dichloroethane, dichloromethane and toluene, with the addition of at least one reducing agent, preferably from the group consisting of
  • Sodium cyanoborohydride, diborane, and triethylsilane Selectride ® optionally in the presence of at least one acid, preferably selected from the group consisting of formic acid, acetic acid, hydrochloric acid and trifluoroacetic acid at temperatures of preferably -25 ° C to 100 ° C to give compounds of the general formula (XXIII) implemented.
  • step (r) compounds of general formula (XXIII) are converted to compounds of general formula (XXIV) by introduction of a suitable leaving group, such as, for example, halogen or mesylate, and subsequent reaction with alcohols.
  • a suitable leaving group such as, for example, halogen or mesylate
  • Trifluoromethylsulfonyl chloride Trifluoromethylsulfonyl chloride, tolylsulfonyl chloride and at least one base, preferably selected from the group consisting of cesium carbonate, calcium carbonate,
  • Potassium carbonate, triethylamine, diisopropylethylamine and pyridine are converted at temperatures of preferably 0 ° C to 80 ° C in the corresponding mesylates.
  • These are in at least one solvent, preferably selected from the group consisting of dichloromethane, dioxane, diethyl ether, tetrahydrofuran, acetonitrile, toluene and
  • step (r) compounds of the general formula (XXIV) in a
  • Mitsunobu reaction can be prepared from compounds of general formula (XXIV).
  • stage (r) can be carried out analogously to stage (t).
  • step (s) the carbonyl compounds (XX) with organometallics, typically Li or Mg organyls (Grignard) in solvents such as toluene, benzene, hexane, pentane, THF or diethyl ether, optionally with the addition of, for example CeCl 3 to the tertiary alcohols (XXVI) implemented.
  • organometallics typically Li or Mg organyls (Grignard) in solvents such as toluene, benzene, hexane, pentane, THF or diethyl ether, optionally with the addition of, for example CeCl 3 to the tertiary alcohols (XXVI) implemented.
  • step (u) compounds of the general formula (XXVI) in at least one solvent, preferably selected from the group consisting of methanol, ethanol, isopropanol, dichloromethane, dioxane, diethyl ether, dimethyl sulfoxide, tetrahydrofuran, acetonitrile and dimethylformamide in the presence of at least one acid, preferably selected from the group consisting of formic acid, acetic acid, hydrochloric acid,
  • the agonistic or antagonistic action of substances may be due to bradykinin
  • Receptor 1 (B1 R) of the human and rat species can be determined by the following assay.
  • the intracellular Ca 2+ increase after administration of a B1 R agonist by means of a Ca + -sensitive dye (type Fluo-4, Molecular Probes Europe BV, Leiden Netherlands) in the Fluorescent Imaging Plate Reader (FLIPR, Molecular Devices, Sunnyvale, USA) and / or Novostar (BMG Labtech GmbH, Offenburg, Germany).

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EP11761012.1A 2010-09-22 2011-09-21 Substituierte benzamid-verbindungen Withdrawn EP2619178A1 (de)

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Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW201217312A (en) * 2010-09-22 2012-05-01 Gruenenthal Gmbh Substituted benzamide compounds
US9034874B2 (en) * 2012-07-20 2015-05-19 Novartis Ag Carbamate/urea derivatives
MX2020005736A (es) * 2013-04-12 2021-06-14 Obschestvo S Ogranichennoi Otvetstvennostiyu Pharmenterprises Derivados de glutarimida, uso de los mismos, composicion farmaceutica basada en los mismos y metodos para producir derivados de glutarimida.
WO2014186704A2 (en) * 2013-05-17 2014-11-20 N30 Pharmaceuticals, Inc. Novel compounds for the treatment of cystic fibrosis
RU2678571C1 (ru) * 2013-12-19 2019-01-30 Эйсай Ар Энд Ди Менеджмент Ко., Лтд. Терапевтическое и/или профилактическое средство, содержащее производное 1-индансульфамида, против боли
JP6535007B2 (ja) 2013-12-20 2019-06-26 インスティテュート オブ ファーマコロジー アンド トキシコロジー アカデミー オブ ミリタリー メディカル サイエンシズ ピー．エル．エー．チャイナ 新規ピペリジンカルボキサミド化合物、その調製方法及び使用
ES2958391T3 (es) 2014-11-06 2024-02-08 Bial R&D Invest S A Imidazo[1,5-a]pirimidinas sustituidas y su uso en el tratamiento de trastornos médicos
WO2016073895A1 (en) 2014-11-06 2016-05-12 Lysosomal Therapeutics Inc. Substituted pyrazolo(1,5-a)pyrimidines and their use in the treatment of medical disorders
EP3215509B1 (en) 2014-11-06 2020-02-26 Lysosomal Therapeutics Inc. Substituted pyrrolo[1,2-a]pyrimidines and their use in the treatment of medical disorders
CN105175272A (zh) * 2015-08-31 2015-12-23 吴玲 制备r-5-溴-1-氨基茚满的方法
EP3440083A4 (en) 2016-04-06 2019-09-18 Lysosomal Therapeutics Inc. IMIDAZO [1,5-A] PYRIMIDINYL-CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDER
EP3440080A4 (en) 2016-04-06 2020-01-22 Lysosomal Therapeutics Inc. PYRAZOLO [1,5-A] PYRIMIDINYL CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS
JP7034935B2 (ja) 2016-04-06 2022-03-14 リソソーマル・セラピューティクス・インコーポレイテッド ピロロ［１，２－ａ］ピリミジニルカルボキサミド化合物および医学的障害の処置におけるその使用
KR102530515B1 (ko) 2016-05-05 2023-05-09 비알 - 알&디 인베스트먼츠, 에스.에이. 치환된 이미다조[1,2-b]피리다진, 치환된 이미다조[1,5-b]피리다진, 관련 화합물, 및 의학적 장애의 치료에서의 그의 용도
EP3452455A4 (en) 2016-05-05 2019-11-13 Lysosomal Therapeutics Inc. SUBSTITUTED IMDAZO [1,2-] PYRIDINES, SUBSTITUTED IMIDAZO [1,2-] PYRAZINES, RELATED COMPOUNDS AND THEIR USE IN THE TREATMENT OF ILLNESSES
CN106279114B (zh) * 2016-08-04 2019-01-29 东南大学 一种Taladegib的合成方法
JOP20190156B1 (ar) * 2016-12-23 2023-09-17 Bayer Pharma AG أميدات عطرية لحمض الكربوكسيليك بصفتها مضادات لمستقبلة البراديكينين b1
EP3366683A1 (en) 2017-02-28 2018-08-29 Acousia Therapeutics GmbH Cyclic amides, acteamides and ureas useful as potassium channel openers
AU2019232437A1 (en) 2018-03-07 2020-10-08 Bayer Aktiengesellschaft Identification and use of ERK5 inhibitors
CN114933568A (zh) * 2022-05-24 2022-08-23 抚州润泰药业有限公司 一种4,6-二甲基-2-甲磺酰基嘧啶的制备方法

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000012077A1 (en) * 1998-09-01 2000-03-09 Bristol-Myers Squibb Company Potassium channel inhibitors and method
BRPI0411673A (pt) * 2003-06-20 2006-08-08 Amgen Inc composto, sal farmaceuticamente aceitável, composição farmacêutica, e, uso de um composto
US20090253908A1 (en) 2004-03-11 2009-10-08 Glaxo Group Limited Novel m3 muscarinic acetylchoine receptor antagonists
EP1740579B1 (en) 2004-03-24 2015-08-19 AbbVie Inc. Tricyclic pyrazole kinase inhibitors
JP2008537953A (ja) * 2005-04-15 2008-10-02 エラン ファーマシューティカルズ，インコーポレイテッド ブラジキニンｂ１受容体拮抗作用に有用な新規化合物
WO2007101007A2 (en) 2006-02-23 2007-09-07 Neurogen Corporation Aryl sulfonyl heterocycles
WO2007140383A2 (en) 2006-05-30 2007-12-06 Neurogen Corporation Spirocyclic sulfonamides and related compounds
CA2664810A1 (en) 2006-09-29 2008-04-10 Gruenenthal Gmbh Substituted sulfonamide derivatives
WO2008046573A1 (de) 2006-10-16 2008-04-24 Grünenthal GmbH Substituierte sulfonamid-derivate als bradykinin 1 rezeptor modulatoren
TW201217312A (en) * 2010-09-22 2012-05-01 Gruenenthal Gmbh Substituted benzamide compounds

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2012038081A1 *

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US20120071461A1 (en) 2012-03-22
US8680159B2 (en) 2014-03-25
AR083167A1 (es) 2013-02-06
AU2011304666A1 (en) 2013-05-02
JP2013540750A (ja) 2013-11-07
TW201217312A (en) 2012-05-01
WO2012038081A1 (de) 2012-03-29
MX2013003309A (es) 2013-04-29
CA2811796A1 (en) 2012-03-29
CL2013000787A1 (es) 2013-09-23
EA201300388A1 (ru) 2014-01-30
CN103097354A (zh) 2013-05-08
IL225350A0 (en) 2013-06-27
ECSP13012519A (es) 2013-05-31
CO6700838A2 (es) 2013-06-28
PE20131350A1 (es) 2013-12-08
BR112013008667A2 (pt) 2016-06-21

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