DE69900220T2 - Diaza-spiro[3,5]nonan-Derivate - Google Patents
Diaza-spiro[3,5]nonan-DerivateInfo
- Publication number
- DE69900220T2 DE69900220T2 DE69900220T DE69900220T DE69900220T2 DE 69900220 T2 DE69900220 T2 DE 69900220T2 DE 69900220 T DE69900220 T DE 69900220T DE 69900220 T DE69900220 T DE 69900220T DE 69900220 T2 DE69900220 T2 DE 69900220T2
- Authority
- DE
- Germany
- Prior art keywords
- phenyl
- nonan
- spiro
- diaza
- diazaspiro
- 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.)
- Expired - Lifetime
Links
- YKXOWLUZZIFXMJ-UHFFFAOYSA-N 1,2-diazaspiro[3.5]nonane Chemical class C1NNC11CCCCC1 YKXOWLUZZIFXMJ-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims description 102
- 238000000034 method Methods 0.000 claims description 69
- 239000000203 mixture Substances 0.000 claims description 34
- -1 or C(O)O-C16alkyl Chemical group 0.000 claims description 24
- 108090000622 Nociceptin Proteins 0.000 claims description 18
- 102000048266 Nociceptin Human genes 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 15
- PULGYDLMFSFVBL-SMFNREODSA-N nociceptin Chemical compound C([C@@H](C(=O)N[C@H](C(=O)NCC(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CO)C(=O)N[C@@H](C)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](C)C(=O)N[C@@H](CC(N)=O)C(=O)N[C@@H](CCC(N)=O)C(O)=O)[C@@H](C)O)NC(=O)CNC(=O)CNC(=O)[C@@H](N)CC=1C=CC=CC=1)C1=CC=CC=C1 PULGYDLMFSFVBL-SMFNREODSA-N 0.000 claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 claims description 10
- 239000001257 hydrogen Substances 0.000 claims description 10
- 208000002193 Pain Diseases 0.000 claims description 9
- 239000002253 acid Substances 0.000 claims description 7
- 239000003814 drug Substances 0.000 claims description 6
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 6
- 230000001154 acute effect Effects 0.000 claims description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims description 5
- 201000010099 disease Diseases 0.000 claims description 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 5
- 229910052736 halogen Inorganic materials 0.000 claims description 5
- 150000002367 halogens Chemical group 0.000 claims description 5
- 208000024891 symptom Diseases 0.000 claims description 5
- 208000024827 Alzheimer disease Diseases 0.000 claims description 4
- 208000000044 Amnesia Diseases 0.000 claims description 4
- 208000019901 Anxiety disease Diseases 0.000 claims description 4
- 208000027796 Blood pressure disease Diseases 0.000 claims description 4
- 208000000094 Chronic Pain Diseases 0.000 claims description 4
- 206010010904 Convulsion Diseases 0.000 claims description 4
- 206010012289 Dementia Diseases 0.000 claims description 4
- 208000026139 Memory disease Diseases 0.000 claims description 4
- 208000008589 Obesity Diseases 0.000 claims description 4
- 208000013200 Stress disease Diseases 0.000 claims description 4
- 208000007271 Substance Withdrawal Syndrome Diseases 0.000 claims description 4
- 208000005298 acute pain Diseases 0.000 claims description 4
- 125000003545 alkoxy group Chemical group 0.000 claims description 4
- 230000036506 anxiety Effects 0.000 claims description 4
- 230000004872 arterial blood pressure Effects 0.000 claims description 4
- 230000033228 biological regulation Effects 0.000 claims description 4
- 230000036461 convulsion Effects 0.000 claims description 4
- 206010015037 epilepsy Diseases 0.000 claims description 4
- 230000029142 excretion Effects 0.000 claims description 4
- 208000014674 injury Diseases 0.000 claims description 4
- 230000006984 memory degeneration Effects 0.000 claims description 4
- 208000023060 memory loss Diseases 0.000 claims description 4
- 208000030159 metabolic disease Diseases 0.000 claims description 4
- 230000000926 neurological effect Effects 0.000 claims description 4
- 235000020824 obesity Nutrition 0.000 claims description 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 4
- 230000008733 trauma Effects 0.000 claims description 4
- AJYMZRDFCFFPPR-UHFFFAOYSA-N 7-(1,2,3,4,4a,5,6,7,8,8a-decahydronaphthalen-2-yl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound O=C1CC2(CCN(CC2)C2CC3CCCCC3CC2)N1C1=CC=CC=C1 AJYMZRDFCFFPPR-UHFFFAOYSA-N 0.000 claims description 3
- XFUQQZWGUPWDLW-UHFFFAOYSA-N 7-cyclononyl-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C=1C=CC=CC=1N1C(=O)CC1(CC1)CCN1C1CCCCCCCC1 XFUQQZWGUPWDLW-UHFFFAOYSA-N 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims description 3
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 238000006268 reductive amination reaction Methods 0.000 claims description 3
- VITXVCYZJIGRMI-UHFFFAOYSA-N 7-cyclononyl-1-phenyl-1,7-diazaspiro[3.5]nonane Chemical compound C=1C=CC=CC=1N1CCC1(CC1)CCN1C1CCCCCCCC1 VITXVCYZJIGRMI-UHFFFAOYSA-N 0.000 claims description 2
- GSUUINFTNAGZDH-UHFFFAOYSA-N 7-cyclooctyl-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C=1C=CC=CC=1N1C(=O)CC1(CC1)CCN1C1CCCCCCC1 GSUUINFTNAGZDH-UHFFFAOYSA-N 0.000 claims description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 claims description 2
- YOMSZEJVVGTTDO-KDURUIRLSA-N CC(C)[C@H]1CC[C@H](CC1)N1CCC2(CC(=O)N2c2ccccc2)CC1 Chemical compound CC(C)[C@H]1CC[C@H](CC1)N1CCC2(CC(=O)N2c2ccccc2)CC1 YOMSZEJVVGTTDO-KDURUIRLSA-N 0.000 claims description 2
- MEBVZOCGRFHLIS-BGYRXZFFSA-N CC(C)[C@H]1CC[C@H](CC1)N1CCC2(CCN2c2ccccc2)CC1 Chemical compound CC(C)[C@H]1CC[C@H](CC1)N1CCC2(CCN2c2ccccc2)CC1 MEBVZOCGRFHLIS-BGYRXZFFSA-N 0.000 claims description 2
- YWKGRWMEVBUKGU-BGYRXZFFSA-N OCC1(C(N(C12CCN(CC2)[C@@H]2CC[C@@H](CC2)C(C)C)C2=CC=CC=C2)=O)CO Chemical compound OCC1(C(N(C12CCN(CC2)[C@@H]2CC[C@@H](CC2)C(C)C)C2=CC=CC=C2)=O)CO YWKGRWMEVBUKGU-BGYRXZFFSA-N 0.000 claims description 2
- 125000004094 acenaphthen-1-yl group Chemical group [H]C1=C([H])C2=C3C(=C([H])C([H])=C([H])C3=C1[H])C([H])([H])C2([H])* 0.000 claims description 2
- 125000004129 indan-1-yl group Chemical group [H]C1=C([H])C([H])=C2C(=C1[H])C([H])([H])C([H])([H])C2([H])* 0.000 claims description 2
- 125000004130 indan-2-yl group Chemical group [H]C1=C([H])C([H])=C2C(=C1[H])C([H])([H])C([H])(*)C2([H])[H] 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- MRXZFGVQIFJVOM-UHFFFAOYSA-N 3-cycloheptyl-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C1CNCCC21N(C=1C=CC=CC=1)C(=O)C2C1CCCCCC1 MRXZFGVQIFJVOM-UHFFFAOYSA-N 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 59
- 239000007787 solid Substances 0.000 description 38
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 36
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 34
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 27
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 27
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 26
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 18
- 239000001530 fumaric acid Substances 0.000 description 16
- PVXPBVFOSCAEHS-UHFFFAOYSA-N 1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C=1C=CC=CC=1N1C(=O)CC21CCNCC2 PVXPBVFOSCAEHS-UHFFFAOYSA-N 0.000 description 15
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 13
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- 238000006243 chemical reaction Methods 0.000 description 11
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 10
- 125000000217 alkyl group Chemical group 0.000 description 10
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 238000006722 reduction reaction Methods 0.000 description 9
- 238000000354 decomposition reaction Methods 0.000 description 8
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 8
- 239000000047 product Substances 0.000 description 8
- 239000000741 silica gel Substances 0.000 description 8
- 229910002027 silica gel Inorganic materials 0.000 description 8
- 239000000243 solution Substances 0.000 description 8
- 239000000829 suppository Substances 0.000 description 8
- 210000004027 cell Anatomy 0.000 description 7
- 150000003840 hydrochlorides Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 108010020615 nociceptin receptor Proteins 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- PBIUDEUWYGBHDW-UHFFFAOYSA-N 2-chloro-1-pyridin-3-ylethanone;hydrochloride Chemical compound Cl.ClCC(=O)C1=CC=CN=C1 PBIUDEUWYGBHDW-UHFFFAOYSA-N 0.000 description 5
- FPKISACHVIIMRA-UHFFFAOYSA-N 4-propan-2-ylcyclohexan-1-one Chemical compound CC(C)C1CCC(=O)CC1 FPKISACHVIIMRA-UHFFFAOYSA-N 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 5
- 238000004587 chromatography analysis Methods 0.000 description 5
- 239000007903 gelatin capsule Substances 0.000 description 5
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 5
- 235000019341 magnesium sulphate Nutrition 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 229920002261 Corn starch Polymers 0.000 description 4
- SXVPOSFURRDKBO-UHFFFAOYSA-N Cyclododecanone Chemical compound O=C1CCCCCCCCCCC1 SXVPOSFURRDKBO-UHFFFAOYSA-N 0.000 description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 4
- GUBGYTABKSRVRQ-QKKXKWKRSA-N Lactose Natural products OC[C@H]1O[C@@H](O[C@H]2[C@H](O)[C@@H](O)C(O)O[C@@H]2CO)[C@H](O)[C@@H](O)[C@H]1O GUBGYTABKSRVRQ-QKKXKWKRSA-N 0.000 description 4
- 241000699670 Mus sp. Species 0.000 description 4
- 241000700159 Rattus Species 0.000 description 4
- 239000000556 agonist Substances 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 238000009833 condensation Methods 0.000 description 4
- 230000005494 condensation Effects 0.000 description 4
- 239000008120 corn starch Substances 0.000 description 4
- BAUZLFKYYIVGPM-UHFFFAOYSA-N cyclononanone Chemical compound O=C1CCCCCCCC1 BAUZLFKYYIVGPM-UHFFFAOYSA-N 0.000 description 4
- UMJJFEIKYGFCAT-UHFFFAOYSA-N indan-2-one Chemical compound C1=CC=C2CC(=O)CC2=C1 UMJJFEIKYGFCAT-UHFFFAOYSA-N 0.000 description 4
- 239000008101 lactose Substances 0.000 description 4
- YDCHPLOFQATIDS-UHFFFAOYSA-N methyl 2-bromoacetate Chemical compound COC(=O)CBr YDCHPLOFQATIDS-UHFFFAOYSA-N 0.000 description 4
- 239000002808 molecular sieve Substances 0.000 description 4
- GXETWWCCWKWBEZ-UHFFFAOYSA-N n-phenyl-1-(4-propan-2-ylcyclohexyl)piperidin-4-imine Chemical compound C1CC(C(C)C)CCC1N(CC1)CCC1=NC1=CC=CC=C1 GXETWWCCWKWBEZ-UHFFFAOYSA-N 0.000 description 4
- 239000012071 phase Substances 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 208000020016 psychiatric disease Diseases 0.000 description 4
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- KEDNIKLAILXYCS-UHFFFAOYSA-N 3,3-bis(hydroxymethyl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C1CNCCC11C(CO)(CO)C(=O)N1C1=CC=CC=C1 KEDNIKLAILXYCS-UHFFFAOYSA-N 0.000 description 3
- KOCHSZXXZDBASW-UHFFFAOYSA-N 3-(hydroxymethyl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C1CNCCC11C(CO)C(=O)N1C1=CC=CC=C1 KOCHSZXXZDBASW-UHFFFAOYSA-N 0.000 description 3
- BIMZZJDNYSFXCL-UHFFFAOYSA-N 4-methyl-1,3-dihydroinden-2-one Chemical compound CC1=CC=CC2=C1CC(=O)C2 BIMZZJDNYSFXCL-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- 239000007832 Na2SO4 Substances 0.000 description 3
- 102100028646 Nociceptin receptor Human genes 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 3
- VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 description 3
- 238000003556 assay Methods 0.000 description 3
- 239000002775 capsule Substances 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000008298 dragée Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000001914 filtration Methods 0.000 description 3
- 238000005984 hydrogenation reaction Methods 0.000 description 3
- 150000002466 imines Chemical class 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000012528 membrane Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229910052987 metal hydride Inorganic materials 0.000 description 3
- 150000004681 metal hydrides Chemical class 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- 235000019198 oils Nutrition 0.000 description 3
- 239000012044 organic layer Substances 0.000 description 3
- 239000012074 organic phase Substances 0.000 description 3
- 239000000825 pharmaceutical preparation Substances 0.000 description 3
- 238000010992 reflux Methods 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
- 239000001993 wax Substances 0.000 description 3
- LMMRZFSAWTYZRD-UHFFFAOYSA-N 1-(9-bicyclo[3.3.1]nonanyl)piperidin-4-one Chemical compound C1CC(=O)CCN1C1C2CCCC1CCC2 LMMRZFSAWTYZRD-UHFFFAOYSA-N 0.000 description 2
- RPCBUMMVFDGODE-UHFFFAOYSA-N 1-phenyl-1,7-diazaspiro[3.5]nonan-2-one;hydrochloride Chemical compound Cl.C=1C=CC=CC=1N1C(=O)CC21CCNCC2 RPCBUMMVFDGODE-UHFFFAOYSA-N 0.000 description 2
- QKNYBSVHEMOAJP-UHFFFAOYSA-N 2-amino-2-(hydroxymethyl)propane-1,3-diol;hydron;chloride Chemical compound Cl.OCC(N)(CO)CO QKNYBSVHEMOAJP-UHFFFAOYSA-N 0.000 description 2
- QRGJETBAUPTTQM-UHFFFAOYSA-N 4-anilino-1-(9-bicyclo[3.3.1]nonanyl)piperidine-4-carbonitrile Chemical compound C1CN(C2C3CCCC2CCC3)CCC1(C#N)NC1=CC=CC=C1 QRGJETBAUPTTQM-UHFFFAOYSA-N 0.000 description 2
- WICXQDXKCXTXPF-UHFFFAOYSA-N 7-(2,3,3a,4,5,6-hexahydro-1h-phenalen-1-yl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound O=C1CC2(CCN(CC2)C2C=3C=CC=C4CCCC(C=34)CC2)N1C1=CC=CC=C1 WICXQDXKCXTXPF-UHFFFAOYSA-N 0.000 description 2
- QZBIXFFLYYAZPD-UHFFFAOYSA-N 7-(2,3,3a,4,5,6-hexahydro-1h-phenalen-1-yl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one;hydrochloride Chemical compound Cl.O=C1CC2(CCN(CC2)C2C=3C=CC=C4CCCC(C=34)CC2)N1C1=CC=CC=C1 QZBIXFFLYYAZPD-UHFFFAOYSA-N 0.000 description 2
- NBQABLRWCNTRRC-WLHGVMLRSA-N 7-(2,3,3a,4,5,6-hexahydro-1h-phenalen-1-yl)-1-phenyl-1,7-diazaspiro[3.5]nonane;(e)-but-2-enedioic acid Chemical compound OC(=O)\C=C\C(O)=O.C1CC2(CCN(CC2)C2C=3C=CC=C4CCCC(C=34)CC2)N1C1=CC=CC=C1 NBQABLRWCNTRRC-WLHGVMLRSA-N 0.000 description 2
- MTTCPRUJBRANEU-UHFFFAOYSA-N 7-(2,3-dihydro-1h-inden-2-yl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one;hydrochloride Chemical compound Cl.O=C1CC2(CCN(CC2)C2CC3=CC=CC=C3C2)N1C1=CC=CC=C1 MTTCPRUJBRANEU-UHFFFAOYSA-N 0.000 description 2
- CXFCRYUQUQXBSH-UHFFFAOYSA-N 7-(4-methyl-2,3-dihydro-1h-inden-2-yl)-1-phenyl-1,7-diazaspiro[3.5]nonane;hydrochloride Chemical compound Cl.C1C=2C(C)=CC=CC=2CC1N(CC1)CCC21CCN2C1=CC=CC=C1 CXFCRYUQUQXBSH-UHFFFAOYSA-N 0.000 description 2
- OYHYLAGIYGVBKY-WLHGVMLRSA-N 7-(9-bicyclo[6.2.0]decanyl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one;(e)-but-2-enedioic acid Chemical compound OC(=O)\C=C\C(O)=O.O=C1CC2(CCN(CC2)C2C3CCCCCCC3C2)N1C1=CC=CC=C1 OYHYLAGIYGVBKY-WLHGVMLRSA-N 0.000 description 2
- CAWWHOGXBDZETR-UHFFFAOYSA-N 7-benzyl-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C=1C=CC=CC=1N1C(=O)CC1(CC1)CCN1CC1=CC=CC=C1 CAWWHOGXBDZETR-UHFFFAOYSA-N 0.000 description 2
- UEXPDKKNCBLYTK-UHFFFAOYSA-N 7-benzyl-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one;hydrochloride Chemical compound Cl.C=1C=CC=CC=1N1C(=O)CC1(CC1)CCN1CC1=CC=CC=C1 UEXPDKKNCBLYTK-UHFFFAOYSA-N 0.000 description 2
- YXLRUZCVHBAMMN-UHFFFAOYSA-N 7-benzyl-3,3-bis(hydroxymethyl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one;hydrochloride Chemical compound Cl.C1CN(CC=2C=CC=CC=2)CCC11C(CO)(CO)C(=O)N1C1=CC=CC=C1 YXLRUZCVHBAMMN-UHFFFAOYSA-N 0.000 description 2
- ZUKADAPSNLSKSF-UHFFFAOYSA-N 7-benzyl-3-(hydroxymethyl)-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one;hydrochloride Chemical compound Cl.C1CN(CC=2C=CC=CC=2)CCC11C(CO)C(=O)N1C1=CC=CC=C1 ZUKADAPSNLSKSF-UHFFFAOYSA-N 0.000 description 2
- YNQHGZPSSJWKSX-UHFFFAOYSA-N 7-cycloheptyl-1-phenyl-1,7-diazaspiro[3.5]nonan-2-one Chemical compound C=1C=CC=CC=1N1C(=O)CC1(CC1)CCN1C1CCCCCC1 YNQHGZPSSJWKSX-UHFFFAOYSA-N 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
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- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—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
- 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
- C07D471/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/04—Centrally acting analgesics, e.g. opioids
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/08—Antiepileptics; Anticonvulsants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Child & Adolescent Psychology (AREA)
- Vascular Medicine (AREA)
- Cardiology (AREA)
- Hospice & Palliative Care (AREA)
- Heart & Thoracic Surgery (AREA)
- Addiction (AREA)
- Urology & Nephrology (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP98110804 | 1998-06-12 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE69900220D1 DE69900220D1 (de) | 2001-09-20 |
| DE69900220T2 true DE69900220T2 (de) | 2002-05-08 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE69900220T Expired - Lifetime DE69900220T2 (de) | 1998-06-12 | 1999-06-07 | Diaza-spiro[3,5]nonan-Derivate |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US6113527A (enExample) |
| EP (1) | EP0970957B1 (enExample) |
| JP (1) | JP3286268B2 (enExample) |
| KR (1) | KR100344732B1 (enExample) |
| CN (1) | CN1107066C (enExample) |
| AR (1) | AR019859A1 (enExample) |
| AT (1) | ATE204279T1 (enExample) |
| AU (1) | AU743983B2 (enExample) |
| BR (1) | BR9902651A (enExample) |
| CA (1) | CA2274202A1 (enExample) |
| DE (1) | DE69900220T2 (enExample) |
| DK (1) | DK0970957T3 (enExample) |
| ES (1) | ES2162503T3 (enExample) |
| HR (1) | HRP990188A2 (enExample) |
| HU (1) | HU220894B1 (enExample) |
| ID (1) | ID23304A (enExample) |
| IL (1) | IL130377A0 (enExample) |
| MA (1) | MA26644A1 (enExample) |
| NO (1) | NO312590B1 (enExample) |
| NZ (1) | NZ336189A (enExample) |
| PE (1) | PE20000548A1 (enExample) |
| PL (1) | PL333695A1 (enExample) |
| PT (1) | PT970957E (enExample) |
| SG (1) | SG79259A1 (enExample) |
| SI (1) | SI0970957T1 (enExample) |
| TR (1) | TR199901381A2 (enExample) |
| YU (1) | YU26499A (enExample) |
| ZA (1) | ZA993852B (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030040479A1 (en) * | 2001-07-02 | 2003-02-27 | Omeros Corporation | Rotational intrathecal analgesia method and device |
| JP2005502619A (ja) * | 2001-07-02 | 2005-01-27 | オメロス コーポレイション | オピオイドレセプター様レセプター１アゴニストと交替でオピオイドレセプターアゴニストを投与することを含む、痛覚脱失を生成するための方法 |
| PT1491212E (pt) * | 2002-03-29 | 2012-11-16 | Mitsubishi Tanabe Pharma Corp | Medicamento para distúrbios de sono |
| JP2005289816A (ja) | 2002-05-14 | 2005-10-20 | Banyu Pharmaceut Co Ltd | ベンズイミダゾール誘導体 |
| EA009789B1 (ru) * | 2002-07-05 | 2008-04-28 | Таргасепт, Инк. | N-арилдиазаспирациклические соединения и способы их получения и применения |
| KR20050043935A (ko) * | 2002-09-09 | 2005-05-11 | 얀센 파마슈티카 엔.브이. | Ｏｒｌ-1 수용체 매개 장애의 치료에 유용한 하이드록시 알킬 치환된 1,3,8-트리아자스피로[4.5]데칸-4-온 유도체 |
| GB0323204D0 (en) * | 2003-10-03 | 2003-11-05 | Novartis Ag | Organic compounds |
| US20050228023A1 (en) * | 2003-12-19 | 2005-10-13 | Sri International | Agonist and antagonist ligands of the nociceptin receptor |
| US20060178390A1 (en) * | 2004-08-02 | 2006-08-10 | Alfonzo Jordan | 1,3,8-Triazaspiro[4,5]decan-4-one derivatives useful for the treatment of ORL-1 receptor mediated disorders |
| CA2575461A1 (en) * | 2004-08-20 | 2006-03-02 | Targacept, Inc. | The use of n-aryl diazaspiracyclic compounds in the treatment of addiction |
| US20080247964A1 (en) * | 2006-05-08 | 2008-10-09 | Yuelian Xu | Substituted azaspiro derivatives |
| KR20090083954A (ko) * | 2006-11-28 | 2009-08-04 | 얀센 파마슈티카 엔.브이. | 3-(3-아미노-2-(ｒ)-하이드록시프로필)-1-(4-플루오로페닐)-8-(8-메틸나프탈렌-1-일메틸)-1,3,8-트리아자-스피로[4.5]데칸-4-온의 염 |
| CA2683598C (en) * | 2007-04-09 | 2015-11-17 | Janssen Pharmaceutica Nv | 1,3,8-trisubstituted-1,3,8-triaza-spiro[4.5]decan-4-one derivatives as ligands of the orl-i receptor for the treatment of anxiety and depression |
| KR101704226B1 (ko) | 2015-06-30 | 2017-02-07 | 현대자동차주식회사 | 자동차의 쿼터글라스 어셈블리 |
| TW202340202A (zh) * | 2021-12-22 | 2023-10-16 | 美國加利福尼亞大學董事會 | Gtp酶抑制劑及其用途 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5756743A (en) * | 1996-04-10 | 1998-05-26 | Hoechst Marion Roussel Inc. | Spiro cyclopent b!indole-piperidines! |
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1999
- 1999-06-07 SI SI9930008T patent/SI0970957T1/xx unknown
- 1999-06-07 PT PT99110943T patent/PT970957E/pt unknown
- 1999-06-07 EP EP99110943A patent/EP0970957B1/en not_active Expired - Lifetime
- 1999-06-07 DK DK99110943T patent/DK0970957T3/da active
- 1999-06-07 DE DE69900220T patent/DE69900220T2/de not_active Expired - Lifetime
- 1999-06-07 ES ES99110943T patent/ES2162503T3/es not_active Expired - Lifetime
- 1999-06-07 AT AT99110943T patent/ATE204279T1/de not_active IP Right Cessation
- 1999-06-08 ID IDP990543D patent/ID23304A/id unknown
- 1999-06-08 PE PE1999000487A patent/PE20000548A1/es not_active Application Discontinuation
- 1999-06-08 ZA ZA9903852A patent/ZA993852B/xx unknown
- 1999-06-09 CA CA002274202A patent/CA2274202A1/en not_active Abandoned
- 1999-06-09 SG SG9903066A patent/SG79259A1/en unknown
- 1999-06-09 HU HU9901911A patent/HU220894B1/hu not_active IP Right Cessation
- 1999-06-09 IL IL13037799A patent/IL130377A0/xx unknown
- 1999-06-09 NZ NZ336189A patent/NZ336189A/xx unknown
- 1999-06-10 JP JP16357099A patent/JP3286268B2/ja not_active Expired - Fee Related
- 1999-06-10 AU AU34987/99A patent/AU743983B2/en not_active Ceased
- 1999-06-10 KR KR1019990021485A patent/KR100344732B1/ko not_active Expired - Fee Related
- 1999-06-10 YU YU26499A patent/YU26499A/sh unknown
- 1999-06-10 MA MA25616A patent/MA26644A1/fr unknown
- 1999-06-10 AR ARP990102763A patent/AR019859A1/es active IP Right Grant
- 1999-06-11 US US09/330,851 patent/US6113527A/en not_active Expired - Fee Related
- 1999-06-11 BR BR9902651-1A patent/BR9902651A/pt not_active Application Discontinuation
- 1999-06-11 TR TR1999/01381A patent/TR199901381A2/xx unknown
- 1999-06-11 HR HR98110804.6A patent/HRP990188A2/hr not_active Application Discontinuation
- 1999-06-11 CN CN99108373A patent/CN1107066C/zh not_active Expired - Fee Related
- 1999-06-11 PL PL99333695A patent/PL333695A1/xx unknown
- 1999-06-11 NO NO19992873A patent/NO312590B1/no unknown
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