ES2850298T3 - Agonistas muscarínicos - Google Patents
Agonistas muscarínicos Download PDFInfo
- Publication number
- ES2850298T3 ES2850298T3 ES16750223T ES16750223T ES2850298T3 ES 2850298 T3 ES2850298 T3 ES 2850298T3 ES 16750223 T ES16750223 T ES 16750223T ES 16750223 T ES16750223 T ES 16750223T ES 2850298 T3 ES2850298 T3 ES 2850298T3
- Authority
- ES
- Spain
- Prior art keywords
- ethyl
- carboxylate
- amino
- piperidin
- azaspiro
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000000472 muscarinic agonist Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 244
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 61
- 125000005842 heteroatom Chemical group 0.000 claims abstract description 52
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 51
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 49
- 150000003839 salts Chemical class 0.000 claims abstract description 40
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 37
- 239000001257 hydrogen Substances 0.000 claims abstract description 37
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 37
- 125000001153 fluoro group Chemical group F* 0.000 claims abstract description 35
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract description 34
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 31
- 101100440695 Dictyostelium discoideum corB gene Proteins 0.000 claims abstract description 13
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract 6
- -1 methoxyethyl Chemical group 0.000 claims description 43
- 238000011282 treatment Methods 0.000 claims description 31
- 208000002193 Pain Diseases 0.000 claims description 28
- 208000010877 cognitive disease Diseases 0.000 claims description 25
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 20
- 208000024827 Alzheimer disease Diseases 0.000 claims description 17
- 239000008194 pharmaceutical composition Substances 0.000 claims description 13
- 208000004296 neuralgia Diseases 0.000 claims description 12
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 9
- 201000000980 schizophrenia Diseases 0.000 claims description 8
- 208000028017 Psychotic disease Diseases 0.000 claims description 7
- 230000001154 acute effect Effects 0.000 claims description 6
- 208000021722 neuropathic pain Diseases 0.000 claims description 6
- 206010065390 Inflammatory pain Diseases 0.000 claims description 5
- 208000005298 acute pain Diseases 0.000 claims description 5
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 5
- RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims description 5
- 230000002981 neuropathic effect Effects 0.000 claims description 5
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 5
- DYWSVUBJGFTOQC-UHFFFAOYSA-N xi-2-Ethylheptanoic acid Chemical compound CCCCCC(CC)C(O)=O DYWSVUBJGFTOQC-UHFFFAOYSA-N 0.000 claims description 5
- 208000000094 Chronic Pain Diseases 0.000 claims description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 230000001684 chronic effect Effects 0.000 claims description 4
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 4
- 125000006001 difluoroethyl group Chemical group 0.000 claims description 4
- BAMIVLQHRMXJCT-UHFFFAOYSA-N ethyl 2-[4-[N-(2-hydroxyethyl)anilino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound OCCN(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C1=CC=CC=C1 BAMIVLQHRMXJCT-UHFFFAOYSA-N 0.000 claims description 4
- 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 206010012335 Dependence Diseases 0.000 claims description 3
- 208000016285 Movement disease Diseases 0.000 claims description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
- VKFQKBQCZDKESK-BFWBPSQCSA-N 1,1-dideuterioethyl 2-[4-[acetyl(ethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound [2H]C([2H])(C)OC(=O)N1CCC2(CC(C2)N2CCC(CC2)N(CC)C(C)=O)C1 VKFQKBQCZDKESK-BFWBPSQCSA-N 0.000 claims description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 claims description 2
- 208000009829 Lewy Body Disease Diseases 0.000 claims description 2
- 201000002832 Lewy body dementia Diseases 0.000 claims description 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 2
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 2
- DENIOJOWKAHBLK-UHFFFAOYSA-N methyl 6-[4-[acetyl(ethyl)amino]piperidin-1-yl]-2-azaspiro[3.4]octane-2-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(CN(C2)C(=O)OC)CC1)CC DENIOJOWKAHBLK-UHFFFAOYSA-N 0.000 claims description 2
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004076 pyridyl group Chemical group 0.000 claims description 2
- WPMFQLSQCJTBEQ-UHFFFAOYSA-N ethyl 2-[4-[acetyl(2,2-difluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)F WPMFQLSQCJTBEQ-UHFFFAOYSA-N 0.000 claims 2
- VKFQKBQCZDKESK-UHFFFAOYSA-N ethyl 2-[4-[acetyl(ethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC VKFQKBQCZDKESK-UHFFFAOYSA-N 0.000 claims 2
- FQFHZPRZMDSMHO-UHFFFAOYSA-N ethyl 2-[4-[acetyl(propan-2-yl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C(C)C FQFHZPRZMDSMHO-UHFFFAOYSA-N 0.000 claims 2
- QAEDMODSSPENIU-UHFFFAOYSA-N ethyl 2-[4-[ethyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F QAEDMODSSPENIU-UHFFFAOYSA-N 0.000 claims 2
- RIMWNZKIPXMYEJ-UHFFFAOYSA-N ethyl 6-[4-[acetyl(ethyl)amino]piperidin-1-yl]-2-azaspiro[3.3]heptane-2-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(CN(C2)C(=O)OCC)C1)CC RIMWNZKIPXMYEJ-UHFFFAOYSA-N 0.000 claims 2
- HVWQDZXGENBEOE-UHFFFAOYSA-N methyl 2-[4-[acetyl(ethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OC)CC HVWQDZXGENBEOE-UHFFFAOYSA-N 0.000 claims 2
- 125000004777 2-fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 1
- DEVGBHIRAQTUGQ-UHFFFAOYSA-N ethyl 2-[4-(N-acetylanilino)piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C1=CC=CC=C1 DEVGBHIRAQTUGQ-UHFFFAOYSA-N 0.000 claims 1
- QZWSMKFGACEYIR-UHFFFAOYSA-N ethyl 2-[4-[1,3-oxazol-5-ylmethyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound O1C=NC=C1CN(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F QZWSMKFGACEYIR-UHFFFAOYSA-N 0.000 claims 1
- IFCFJEHXSVGNLM-UHFFFAOYSA-N ethyl 2-[4-[2,2-difluoroethyl(ethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound FC(CN(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC)F IFCFJEHXSVGNLM-UHFFFAOYSA-N 0.000 claims 1
- KBCLRXWZJBDKFY-UHFFFAOYSA-N ethyl 2-[4-[2-cyanoethyl(ethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(#N)CCN(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC KBCLRXWZJBDKFY-UHFFFAOYSA-N 0.000 claims 1
- IEXAYTYUPLNVRB-UHFFFAOYSA-N ethyl 2-[4-[2-hydroxyethyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound OCCN(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F IEXAYTYUPLNVRB-UHFFFAOYSA-N 0.000 claims 1
- VESJZUSKCLFGGY-UHFFFAOYSA-N ethyl 2-[4-[2-methoxyethoxycarbonyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound COCCOC(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F VESJZUSKCLFGGY-UHFFFAOYSA-N 0.000 claims 1
- FVYXYBBHZBJCGN-UHFFFAOYSA-N ethyl 2-[4-[2-methoxyethyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound COCCN(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F FVYXYBBHZBJCGN-UHFFFAOYSA-N 0.000 claims 1
- AJIPGNUNWQKPLB-UHFFFAOYSA-N ethyl 2-[4-[acetyl(1,3-oxazol-2-ylmethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC=1OC=CN=1 AJIPGNUNWQKPLB-UHFFFAOYSA-N 0.000 claims 1
- IHDIFCVTKQXRAQ-UHFFFAOYSA-N ethyl 2-[4-[acetyl(1,3-oxazol-5-ylmethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1=CN=CO1 IHDIFCVTKQXRAQ-UHFFFAOYSA-N 0.000 claims 1
- IMUSKSAETTZKRP-UHFFFAOYSA-N ethyl 2-[4-[acetyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F IMUSKSAETTZKRP-UHFFFAOYSA-N 0.000 claims 1
- VSVLCRYOODVWKN-UHFFFAOYSA-N ethyl 2-[4-[acetyl(2,2-difluoropropyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(C)(F)F VSVLCRYOODVWKN-UHFFFAOYSA-N 0.000 claims 1
- IIKLTKOTICGSHO-UHFFFAOYSA-N ethyl 2-[4-[acetyl(2-methylpropyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(C)C IIKLTKOTICGSHO-UHFFFAOYSA-N 0.000 claims 1
- XERIXDZUYYSFEH-UHFFFAOYSA-N ethyl 2-[4-[acetyl(benzyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1=CC=CC=C1 XERIXDZUYYSFEH-UHFFFAOYSA-N 0.000 claims 1
- VDSFLLFTIGTSQR-UHFFFAOYSA-N ethyl 2-[4-[acetyl(cyclobutyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C1CCC1 VDSFLLFTIGTSQR-UHFFFAOYSA-N 0.000 claims 1
- FVPDTALLKLIYQG-UHFFFAOYSA-N ethyl 2-[4-[acetyl(cyclopropyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C1CC1 FVPDTALLKLIYQG-UHFFFAOYSA-N 0.000 claims 1
- SVLHLBHIUNWCMN-UHFFFAOYSA-N ethyl 2-[4-[acetyl(cyclopropylmethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1CC1 SVLHLBHIUNWCMN-UHFFFAOYSA-N 0.000 claims 1
- AKMJTLPVZKVNIU-UHFFFAOYSA-N ethyl 2-[4-[acetyl(methoxy)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)OC AKMJTLPVZKVNIU-UHFFFAOYSA-N 0.000 claims 1
- SAFIHWQOWRRICH-UHFFFAOYSA-N ethyl 2-[4-[acetyl(propyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CCC SAFIHWQOWRRICH-UHFFFAOYSA-N 0.000 claims 1
- CCYRTQQNMHMENO-UHFFFAOYSA-N ethyl 2-[4-[acetyl(pyridin-2-yl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C1=NC=CC=C1 CCYRTQQNMHMENO-UHFFFAOYSA-N 0.000 claims 1
- FCOAFBBUXYFPAK-UHFFFAOYSA-N ethyl 2-[4-[acetyl-(1-methylcyclobutyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C1(CCC1)C FCOAFBBUXYFPAK-UHFFFAOYSA-N 0.000 claims 1
- PILNFZIFLFVQPU-UHFFFAOYSA-N ethyl 2-[4-[acetyl-(2-fluoro-2-methylpropyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(C)(C)F PILNFZIFLFVQPU-UHFFFAOYSA-N 0.000 claims 1
- VANWBDHFIIUKMP-UHFFFAOYSA-N ethyl 2-[4-[acetyl-(2-methoxy-2-methylpropyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(C)(C)OC VANWBDHFIIUKMP-UHFFFAOYSA-N 0.000 claims 1
- JUAGSSRTFSGQJY-UHFFFAOYSA-N ethyl 2-[4-[acetyl-(3,3-difluorocyclobutyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C1CC(C1)(F)F JUAGSSRTFSGQJY-UHFFFAOYSA-N 0.000 claims 1
- PGLYVFIAVMEQQB-UHFFFAOYSA-N ethyl 2-[4-[acetyl-[(1-hydroxycyclobutyl)methyl]amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1(CCC1)O PGLYVFIAVMEQQB-UHFFFAOYSA-N 0.000 claims 1
- TUHPFUYSYSSQQU-UHFFFAOYSA-N ethyl 2-[4-[acetyl-[(1-methylcyclobutyl)methyl]amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1(CCC1)C TUHPFUYSYSSQQU-UHFFFAOYSA-N 0.000 claims 1
- JCJDXODXSDSFRB-UHFFFAOYSA-N ethyl 2-[4-[acetyl-[(3-methyloxetan-3-yl)methyl]amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1(COC1)C JCJDXODXSDSFRB-UHFFFAOYSA-N 0.000 claims 1
- BLVNUODAEUSGOK-UHFFFAOYSA-N ethyl 2-[4-[benzyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C1=CC=CC=C1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F BLVNUODAEUSGOK-UHFFFAOYSA-N 0.000 claims 1
- FITQVJNEHAHEIS-UHFFFAOYSA-N ethyl 2-[4-[cyclobutyl(2-hydroxyethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CCC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CCO FITQVJNEHAHEIS-UHFFFAOYSA-N 0.000 claims 1
- ILUWJPLKMCKEJB-UHFFFAOYSA-N ethyl 2-[4-[cyclopropyl(1,2-oxazol-3-ylmethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1=NOC=C1 ILUWJPLKMCKEJB-UHFFFAOYSA-N 0.000 claims 1
- KIWSFBGYSVMWTB-UHFFFAOYSA-N ethyl 2-[4-[cyclopropyl(2,2,2-trifluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(F)(F)F KIWSFBGYSVMWTB-UHFFFAOYSA-N 0.000 claims 1
- MVEHFDVQYBTNOI-UHFFFAOYSA-N ethyl 2-[4-[cyclopropyl(2-hydroxyethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CCO MVEHFDVQYBTNOI-UHFFFAOYSA-N 0.000 claims 1
- KQZBDQNYHJXNBH-UHFFFAOYSA-N ethyl 2-[4-[cyclopropyl(2-methoxyethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CCOC KQZBDQNYHJXNBH-UHFFFAOYSA-N 0.000 claims 1
- YYJNZBVFFCOMNB-UHFFFAOYSA-N ethyl 2-[4-[cyclopropyl(propanoyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C(CC)=O YYJNZBVFFCOMNB-UHFFFAOYSA-N 0.000 claims 1
- NLWSZNPZMBIXGK-UHFFFAOYSA-N ethyl 2-[4-[cyclopropyl-(2,2,2-trifluoroacetyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)C(C(F)(F)F)=O NLWSZNPZMBIXGK-UHFFFAOYSA-N 0.000 claims 1
- ZVHKYEICUGBCFV-UHFFFAOYSA-N ethyl 2-[4-[cyclopropyl-(2-methoxy-2-oxoethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C1(CC1)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC(=O)OC ZVHKYEICUGBCFV-UHFFFAOYSA-N 0.000 claims 1
- ZMPZNGOJYRJGQP-UHFFFAOYSA-N ethyl 2-[4-[dimethylcarbamoyl(ethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound CN(C(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC)C ZMPZNGOJYRJGQP-UHFFFAOYSA-N 0.000 claims 1
- RJGTTYYLXOGRPI-UHFFFAOYSA-N ethyl 2-[4-[ethoxycarbonyl(ethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)OC(=O)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC RJGTTYYLXOGRPI-UHFFFAOYSA-N 0.000 claims 1
- KPUBNIWBBIXZLW-UHFFFAOYSA-N ethyl 2-[4-[ethyl(1,3-oxazol-5-ylmethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CC1=CN=CO1 KPUBNIWBBIXZLW-UHFFFAOYSA-N 0.000 claims 1
- FBFBZWSGCSSKKS-UHFFFAOYSA-N ethyl 2-[4-[ethyl(2-fluoroethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CCF FBFBZWSGCSSKKS-UHFFFAOYSA-N 0.000 claims 1
- BJVZCSXEFGXUEL-UHFFFAOYSA-N ethyl 2-[4-[ethyl(2-methylsulfonylethyl)amino]piperidin-1-yl]-6-azaspiro[3.4]octane-6-carboxylate Chemical compound C(C)N(C1CCN(CC1)C1CC2(C1)CN(CC2)C(=O)OCC)CCS(=O)(=O)C BJVZCSXEFGXUEL-UHFFFAOYSA-N 0.000 claims 1
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- PWQLFIKTGRINFF-UHFFFAOYSA-N tert-butyl 4-hydroxypiperidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCC(O)CC1 PWQLFIKTGRINFF-UHFFFAOYSA-N 0.000 description 1
- IGSFTWJIBCDRRD-UHFFFAOYSA-N tert-butyl 4-propanoylpiperidine-1-carboxylate Chemical compound CCC(=O)C1CCN(C(=O)OC(C)(C)C)CC1 IGSFTWJIBCDRRD-UHFFFAOYSA-N 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
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- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
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Classifications
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/451—Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
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- C07D401/00—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
- 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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- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
- 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
- C07D401/08—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 alicyclic rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
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- Public Health (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Neurology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Psychiatry (AREA)
- Hospice & Palliative Care (AREA)
- Epidemiology (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Rheumatology (AREA)
- Addiction (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
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| GBGB1513742.5A GB201513742D0 (en) | 2015-08-03 | 2015-08-03 | Muscarinic agonists |
| PCT/GB2016/052386 WO2017021730A1 (en) | 2015-08-03 | 2016-08-03 | Muscarinic agonists |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2850298T3 true ES2850298T3 (es) | 2021-08-26 |
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| ES20213929T Active ES2980578T3 (es) | 2015-08-03 | 2016-08-03 | Agonistas muscarínicos |
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| Application Number | Title | Priority Date | Filing Date |
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| ES20213929T Active ES2980578T3 (es) | 2015-08-03 | 2016-08-03 | Agonistas muscarínicos |
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| AU (1) | AU2016302048B2 (https=) |
| BR (1) | BR112018002279B1 (https=) |
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| ES (2) | ES2850298T3 (https=) |
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| AU2012338581B2 (en) | 2011-11-18 | 2016-12-08 | Nxera Pharma Uk Limited | Muscarinic M1 receptor agonists |
| GB201404922D0 (en) | 2014-03-19 | 2014-04-30 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| PE20181366A1 (es) | 2015-08-03 | 2018-08-27 | Bristol Myers Squibb Co | Compuestos heterociclicos utiles como moduladores de factor de necrosis tumoral (tnf) alfa |
| CN108026050B (zh) | 2015-08-03 | 2021-04-30 | 格兰马克药品股份有限公司 | 作为RORγ调节剂的新型化合物 |
| GB201513743D0 (en) | 2015-08-03 | 2015-09-16 | Heptares Therapeutics Ltd | Muscarinic agonists |
| GB201513742D0 (en) | 2015-08-03 | 2015-09-16 | Heptares Therapeutics Ltd | Muscarinic agonists |
| GB201519352D0 (en) | 2015-11-02 | 2015-12-16 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| WO2017107089A1 (en) | 2015-12-23 | 2017-06-29 | Merck Sharp & Dohme Corp. | 3- (1h-pyrazol-4-yl) pyridineallosteric modulators of the m4 muscarinic acetylcholine receptor |
| US10329289B2 (en) | 2015-12-23 | 2019-06-25 | Merck Sharp & Dohme Corp. | 6,7-dihydro-5H-pyrrolo[3,4-B]pyridin-5-one allosteric modulators of the M4 muscarinic acetylcholine receptor |
| GB201617454D0 (en) | 2016-10-14 | 2016-11-30 | Heptares Therapeutics Limited | Pharmaceutical compounds |
| WO2018112842A1 (en) | 2016-12-22 | 2018-06-28 | Merck Sharp & Dohme Corp. | 6,6-fused heteroaryl piperidine ether allosteric modulators of m4 muscarinic acetylcholine receptor |
| WO2018112843A1 (en) | 2016-12-22 | 2018-06-28 | Merck Sharp & Dohme Corp. | Heteroaryl piperidine ether allosteric modulators of the m4 muscarinic acetylcholine receptor |
| WO2019000237A1 (en) | 2017-06-27 | 2019-01-03 | Merck Sharp & Dohme Corp. | ALLOSTERIC MODULATORS OF 3- (1H-PYRAZOL-4-YL) PYRIDINE FROM THE M4 ACETYLCHOLINE MUSCARINIC RECEPTOR |
| WO2019000238A1 (en) | 2017-06-27 | 2019-01-03 | Merck Sharp & Dohme Corp. | 5- (PYRIDIN-3-YL) OXAZOLE ALLOSTERIC MODULATORS OF M4 ACETYLCHOLINE MUSCARINIC RECEPTOR |
| WO2019000236A1 (en) | 2017-06-27 | 2019-01-03 | Merck Sharp & Dohme Corp. | ALLOSTERIC MODULATORS OF 3- (1H-PYRAZOL-4-YL) PYRIDINE FROM THE M4 ACETYLCHOLINE MUSCARINIC RECEPTOR |
| US12600726B2 (en) | 2017-07-12 | 2026-04-14 | Vanderbilt University | Antagonists of the muscarinic acetylcholine receptor M4 |
| JP7166331B2 (ja) * | 2017-08-01 | 2022-11-07 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | 中間体化合物及び方法 |
| WO2019079410A1 (en) | 2017-10-17 | 2019-04-25 | Vanderbilt University | ANTAGONISTS OF THE MUSCARINIC RECEPTOR OF ACETYLCHOLINE M4 |
| IL310346A (en) | 2017-10-20 | 2024-03-01 | Univ Vanderbilt | Muscarinic acetylcholine M4 receptor antagonists |
| EP3732163A4 (en) * | 2017-12-20 | 2021-07-14 | Vanderbilt University | MUSCARIN M4 ACETYLCHOLIN RECEPTOR ANTAGONISTS |
| EP4219464A1 (en) | 2018-03-23 | 2023-08-02 | Pfizer Inc. | Piperazine azaspiro derivaves |
| GB201810239D0 (en) | 2018-06-22 | 2018-08-08 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB201810245D0 (en) * | 2018-06-22 | 2018-08-08 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB201819960D0 (en) | 2018-12-07 | 2019-01-23 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB201819961D0 (en) | 2018-12-07 | 2019-01-23 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| GB202020191D0 (en) | 2020-12-18 | 2021-02-03 | Heptares Therapeutics Ltd | Pharmaceutical compounds |
| KR20220079921A (ko) * | 2019-10-09 | 2022-06-14 | 노파르티스 아게 | M4 작용제로서의 2-아자스피로[3.4]옥탄 유도체 |
| PE20221454A1 (es) | 2019-10-09 | 2022-09-21 | Novartis Ag | Derivados de 2-azaespiro[3.4]octano como agonistas de m4 |
| WO2023114224A1 (en) | 2021-12-13 | 2023-06-22 | Sage Therapeutics, Inc. | Combination of muscarinic receptor positive modulators and nmda positive allosteric modulators |
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| NZ570497A (en) * | 2006-02-22 | 2011-09-30 | Vertex Pharma | Spiro condensed 4,4'-quinilino-piperidines derivatives as modulators of muscarinic receptors |
| UY31672A1 (es) * | 2008-02-28 | 2009-09-30 | "agonistas de receptores muscarínicos composiciones farmacéuticas métodos de tratamiento de los mismos, y procedimientos para su preparación" | |
| US20130197027A1 (en) * | 2010-03-10 | 2013-08-01 | Craig Lindsley | Heterocyclyl-azabicyclo[3.2.1]octane analogs as selective m1 agonists and methods of making and using same |
| AU2012338581B2 (en) * | 2011-11-18 | 2016-12-08 | Nxera Pharma Uk Limited | Muscarinic M1 receptor agonists |
| BR112015006029B1 (pt) * | 2012-09-18 | 2022-01-25 | Heptares Therapeutics Limited | Compostos aza bicíclicos como agonistas de receptor m1 muscarínicos, composição farmacêutica compreendendo ditos compostos e uso dos mesmos para tratar um distúrbio cognitivo ou distúrbio psicótico ou para tratar ou reduzir a gravidade de dores agudas, crônicas, neuropáticas ou inflamatórias |
| KR102352388B1 (ko) | 2014-02-06 | 2022-01-17 | 헵테얼즈 테라퓨틱스 리미티드 | 무스카린성 m1 수용체 및/또는 m4 수용체 작용제로서 바이사이클릭 아자 화합물 |
| PE20181366A1 (es) | 2015-08-03 | 2018-08-27 | Bristol Myers Squibb Co | Compuestos heterociclicos utiles como moduladores de factor de necrosis tumoral (tnf) alfa |
| CN108026050B (zh) | 2015-08-03 | 2021-04-30 | 格兰马克药品股份有限公司 | 作为RORγ调节剂的新型化合物 |
| GB201513742D0 (en) * | 2015-08-03 | 2015-09-16 | Heptares Therapeutics Ltd | Muscarinic agonists |
| AR105556A1 (es) | 2015-08-03 | 2017-10-18 | Hoffmann La Roche | Derivados de etinilo |
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2018
- 2018-01-21 IL IL257064A patent/IL257064A/en unknown
- 2018-02-01 US US15/886,057 patent/US10167272B2/en active Active
- 2018-02-01 CL CL2018000292A patent/CL2018000292A1/es unknown
- 2018-02-02 ZA ZA2018/00715A patent/ZA201800715B/en unknown
- 2018-02-02 PH PH12018500259A patent/PH12018500259A1/en unknown
- 2018-02-26 CO CONC2018/0002060A patent/CO2018002060A2/es unknown
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2019
- 2019-05-21 US US16/418,354 patent/US11091456B2/en active Active
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