JP2014534976A5 - - Google Patents
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- JP2014534976A5 JP2014534976A5 JP2014540459A JP2014540459A JP2014534976A5 JP 2014534976 A5 JP2014534976 A5 JP 2014534976A5 JP 2014540459 A JP2014540459 A JP 2014540459A JP 2014540459 A JP2014540459 A JP 2014540459A JP 2014534976 A5 JP2014534976 A5 JP 2014534976A5
- Authority
- JP
- Japan
- Prior art keywords
- ethyl
- quinolin
- pyridin
- thieno
- cyclopropyl
- 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.)
- Pending
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- -1 1,2-ethenediyl Chemical group 0.000 claims 89
- 150000001875 compounds Chemical class 0.000 claims 41
- 229910052739 hydrogen Inorganic materials 0.000 claims 38
- 239000001257 hydrogen Substances 0.000 claims 36
- 229910052757 nitrogen Inorganic materials 0.000 claims 27
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 26
- 125000005842 heteroatom Chemical group 0.000 claims 26
- 229910052760 oxygen Inorganic materials 0.000 claims 26
- 229910052717 sulfur Inorganic materials 0.000 claims 25
- 150000002431 hydrogen Chemical class 0.000 claims 23
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 20
- 229920006395 saturated elastomer Polymers 0.000 claims 18
- 229910052799 carbon Inorganic materials 0.000 claims 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 17
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 17
- 229910052736 halogen Inorganic materials 0.000 claims 16
- 150000002367 halogens Chemical class 0.000 claims 16
- 125000004432 carbon atom Chemical group C* 0.000 claims 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 13
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 13
- 125000001424 substituent group Chemical group 0.000 claims 13
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 12
- 239000011737 fluorine Substances 0.000 claims 12
- 229910052731 fluorine Inorganic materials 0.000 claims 12
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 10
- 125000004159 quinolin-2-yl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C([H])C(*)=NC2=C1[H] 0.000 claims 10
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 claims 10
- 241000124008 Mammalia Species 0.000 claims 9
- 125000001072 heteroaryl group Chemical group 0.000 claims 9
- 125000000623 heterocyclic group Chemical group 0.000 claims 9
- 125000004618 benzofuryl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 8
- 125000002911 monocyclic heterocycle group Chemical group 0.000 claims 8
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 7
- 125000002837 carbocyclic group Chemical group 0.000 claims 7
- 150000001204 N-oxides Chemical class 0.000 claims 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 6
- 239000000651 prodrug Substances 0.000 claims 6
- 229940002612 prodrug Drugs 0.000 claims 6
- 150000003839 salts Chemical class 0.000 claims 6
- ASNUDELVENWRMB-UHFFFAOYSA-N 3-pyridin-4-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CC=NC=C1 ASNUDELVENWRMB-UHFFFAOYSA-N 0.000 claims 5
- 150000004677 hydrates Chemical class 0.000 claims 5
- VDBNYAPERZTOOF-UHFFFAOYSA-N isoquinolin-1(2H)-one Chemical compound C1=CC=C2C(=O)NC=CC2=C1 VDBNYAPERZTOOF-UHFFFAOYSA-N 0.000 claims 5
- 125000002950 monocyclic group Chemical group 0.000 claims 5
- IJAPPYDYQCXOEF-UHFFFAOYSA-N phthalazin-1(2H)-one Chemical compound C1=CC=C2C(=O)NN=CC2=C1 IJAPPYDYQCXOEF-UHFFFAOYSA-N 0.000 claims 5
- 239000000126 substance Substances 0.000 claims 5
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 4
- CYQLXLAJVANNIE-UHFFFAOYSA-N 8-pyridin-4-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CC=NC=C1 CYQLXLAJVANNIE-UHFFFAOYSA-N 0.000 claims 4
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 4
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 4
- 125000004430 oxygen atom Chemical group O* 0.000 claims 4
- 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 claims 3
- RROZJMWKQNSJOL-UHFFFAOYSA-N 3-pyrimidin-5-yl-5-(2-quinolin-2-ylcyclopropyl)thieno[3,2-c]pyridin-4-one Chemical compound C1=2C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC=2SC=C1C1=CN=CN=C1 RROZJMWKQNSJOL-UHFFFAOYSA-N 0.000 claims 3
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 3
- DUPNPBCUJHMSFZ-UHFFFAOYSA-N 5h-thieno[3,2-c]pyridin-4-one Chemical compound O=C1NC=CC2=C1C=CS2 DUPNPBCUJHMSFZ-UHFFFAOYSA-N 0.000 claims 3
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims 3
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 239000000460 chlorine Substances 0.000 claims 3
- 125000004122 cyclic group Chemical group 0.000 claims 3
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 3
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
- 125000004528 pyrimidin-5-yl group Chemical group N1=CN=CC(=C1)* 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- DBEXXZREBNIVIE-UHFFFAOYSA-N 1-[1-oxo-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-8-yl]piperidine-4-carbonitrile Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1N1CCC(C#N)CC1 DBEXXZREBNIVIE-UHFFFAOYSA-N 0.000 claims 2
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 2
- LCSGWIUZBNBGDL-UHFFFAOYSA-N 8-(2-fluoropyridin-4-yl)-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C1=NC(F)=CC(C=2C=3C(=O)N(C4C(C4)C=4N=C5C=CC=CC5=CC=4)C=CC=3C=CC=2)=C1 LCSGWIUZBNBGDL-UHFFFAOYSA-N 0.000 claims 2
- XPPXUDVPZXZMHC-UHFFFAOYSA-N 8-morpholin-4-yl-2-(2-quinolin-2-ylcyclopropyl)isoquinolin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1N1CCOCC1 XPPXUDVPZXZMHC-UHFFFAOYSA-N 0.000 claims 2
- MQKXIURELWPBHC-UHFFFAOYSA-N 8-pyridin-4-yl-2-(2-quinolin-2-ylcyclopropyl)phthalazin-1-one Chemical compound C=12C(=O)N(C3C(C3)C=3N=C4C=CC=CC4=CC=3)N=CC2=CC=CC=1C1=CC=NC=C1 MQKXIURELWPBHC-UHFFFAOYSA-N 0.000 claims 2
- KPOZQDBDLQTIGV-GHRIWEEISA-N 8-pyridin-4-yl-2-[(e)-2-quinolin-2-ylethenyl]isoquinolin-1-one Chemical compound C=12C(=O)N(\C=C\C=3N=C4C=CC=CC4=CC=3)C=CC2=CC=CC=1C1=CC=NC=C1 KPOZQDBDLQTIGV-GHRIWEEISA-N 0.000 claims 2
- 208000028698 Cognitive impairment Diseases 0.000 claims 2
- KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 claims 2
- 125000003545 alkoxy group Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 2
- 125000003354 benzotriazolyl group Chemical group N1N=NC2=C1C=CC=C2* 0.000 claims 2
- 125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 claims 2
- 208000010877 cognitive disease Diseases 0.000 claims 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 2
- 125000002541 furyl group Chemical group 0.000 claims 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000002883 imidazolyl group Chemical group 0.000 claims 2
- 125000003453 indazolyl group Chemical group N1N=C(C2=C1C=CC=C2)* 0.000 claims 2
- 125000001041 indolyl group Chemical group 0.000 claims 2
- 125000002183 isoquinolinyl group Chemical group C1(=NC=CC2=CC=CC=C12)* 0.000 claims 2
- 125000001624 naphthyl group Chemical group 0.000 claims 2
- 125000002971 oxazolyl group Chemical group 0.000 claims 2
- 239000001301 oxygen Substances 0.000 claims 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 2
- 125000003226 pyrazolyl group Chemical group 0.000 claims 2
- 125000002206 pyridazin-3-yl group Chemical group [H]C1=C([H])C([H])=C(*)N=N1 0.000 claims 2
- 125000004076 pyridyl group Chemical group 0.000 claims 2
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 2
- 125000000168 pyrrolyl group Chemical group 0.000 claims 2
- 125000002294 quinazolinyl group Chemical group N1=C(N=CC2=CC=CC=C12)* 0.000 claims 2
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 claims 2
- 201000000980 schizophrenia Diseases 0.000 claims 2
- 125000003003 spiro group Chemical group 0.000 claims 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- 125000001544 thienyl group Chemical group 0.000 claims 2
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- ATGDQZMISIVOEX-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-4,8-dipyridin-4-ylphthalazin-1-one Chemical compound C12=CC=CC(C=3C=CN=CC=3)=C2C(=O)N(CCC=2N=C3C=CC=CN3C=2)N=C1C1=CC=NC=C1 ATGDQZMISIVOEX-UHFFFAOYSA-N 0.000 claims 1
- HLTZFJMZKQGXKH-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-4-morpholin-4-ylphthalazin-1-one Chemical compound C12=CC=CC=C2C(=O)N(CCC=2N=C3C=CC=CN3C=2)N=C1N1CCOCC1 HLTZFJMZKQGXKH-UHFFFAOYSA-N 0.000 claims 1
- PZVOUFFDRRBEIU-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-4-pyrimidin-5-ylphthalazin-1-one Chemical compound C12=CC=CC=C2C(=O)N(CCC=2N=C3C=CC=CN3C=2)N=C1C1=CN=CN=C1 PZVOUFFDRRBEIU-UHFFFAOYSA-N 0.000 claims 1
- RVGGBBZQPFBCDN-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-5-morpholin-4-ylphthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=C1N1CCOCC1 RVGGBBZQPFBCDN-UHFFFAOYSA-N 0.000 claims 1
- BGHVTPXKDAVZDD-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-5-pyridin-3-ylphthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=C1C1=CC=CN=C1 BGHVTPXKDAVZDD-UHFFFAOYSA-N 0.000 claims 1
- YDEQSCDRKVMILG-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-5-pyridin-4-ylphthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=C1C1=CC=NC=C1 YDEQSCDRKVMILG-UHFFFAOYSA-N 0.000 claims 1
- VEUACMGMFIDCST-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-5-pyrimidin-5-ylphthalazin-1-one Chemical compound C1=CC=C2C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=C1C1=CN=CN=C1 VEUACMGMFIDCST-UHFFFAOYSA-N 0.000 claims 1
- FJJZNBZJFQVYRT-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1,2,3,6-tetrahydropyridin-4-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1=CCNCC1 FJJZNBZJFQVYRT-UHFFFAOYSA-N 0.000 claims 1
- LEDAISWHEVRGMO-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1,2-oxazolidin-2-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N1CCCO1 LEDAISWHEVRGMO-UHFFFAOYSA-N 0.000 claims 1
- KGMRCSFKZMMGRS-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1,3-oxazol-2-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1=NC=CO1 KGMRCSFKZMMGRS-UHFFFAOYSA-N 0.000 claims 1
- IXMPEMSGOMZKGC-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1-methylpyrazol-3-yl)phthalazin-1-one Chemical compound CN1C=CC(C=2C=3C(=O)N(CCC=4N=C5C=CC=CN5C=4)N=CC=3C=CC=2)=N1 IXMPEMSGOMZKGC-UHFFFAOYSA-N 0.000 claims 1
- OOLMPGZFHBLLPN-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1-methylpyrazol-4-yl)phthalazin-1-one Chemical compound C1=NN(C)C=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 OOLMPGZFHBLLPN-UHFFFAOYSA-N 0.000 claims 1
- NZAAMDAAXLPMLH-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(1h-pyrazol-5-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C=1C=CNN=1 NZAAMDAAXLPMLH-UHFFFAOYSA-N 0.000 claims 1
- BRHKMKBJJNZXQM-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2,2,6,6-tetrafluoromorpholin-4-yl)phthalazin-1-one Chemical compound C1C(F)(F)OC(F)(F)CN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 BRHKMKBJJNZXQM-UHFFFAOYSA-N 0.000 claims 1
- SKTBUCLTFLIQBW-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-methoxypyrimidin-5-yl)phthalazin-1-one Chemical compound C1=NC(OC)=NC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 SKTBUCLTFLIQBW-UHFFFAOYSA-N 0.000 claims 1
- GOPOXQNQVLGYPW-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-methylpyrimidin-5-yl)phthalazin-1-one Chemical compound C1=NC(C)=NC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 GOPOXQNQVLGYPW-UHFFFAOYSA-N 0.000 claims 1
- SAWLWXZQBGYFCB-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-oxa-6-azaspiro[3.3]heptan-6-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N(C1)CC21COC2 SAWLWXZQBGYFCB-UHFFFAOYSA-N 0.000 claims 1
- ZUIMMYOMYAIPIS-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-oxa-7-azaspiro[3.4]octan-7-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N(C1)CCC21COC2 ZUIMMYOMYAIPIS-UHFFFAOYSA-N 0.000 claims 1
- GUGMALZEBFWGRM-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-oxa-7-azaspiro[3.5]nonan-7-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1N(CC1)CCC21COC2 GUGMALZEBFWGRM-UHFFFAOYSA-N 0.000 claims 1
- KCDUNKDGHMAWFN-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(2-oxo-1,3-dihydroindol-6-yl)phthalazin-1-one Chemical compound C1=CC=CC2=NC(CCN3N=CC=4C=CC=C(C=4C3=O)C3=CC=C4CC(NC4=C3)=O)=CN21 KCDUNKDGHMAWFN-UHFFFAOYSA-N 0.000 claims 1
- NVDGEXVYORQXAV-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(3-methoxypyridin-4-yl)phthalazin-1-one Chemical compound COC1=CN=CC=C1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 NVDGEXVYORQXAV-UHFFFAOYSA-N 0.000 claims 1
- DZDFVQFBSZHODZ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(4-methylpiperazin-1-yl)phthalazin-1-one Chemical compound C1CN(C)CCN1C1=CC=CC2=C1C(=O)N(CCC=1N=C3C=CC=CN3C=1)N=C2 DZDFVQFBSZHODZ-UHFFFAOYSA-N 0.000 claims 1
- GHKGNRPMXWTDJJ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(morpholin-4-ylmethyl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1CN1CCOCC1 GHKGNRPMXWTDJJ-UHFFFAOYSA-N 0.000 claims 1
- QYDOEPJNJJZBJP-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxan-3-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCCOC1 QYDOEPJNJJZBJP-UHFFFAOYSA-N 0.000 claims 1
- HOKNXJOOGBPPNC-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxan-4-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1CCOCC1 HOKNXJOOGBPPNC-UHFFFAOYSA-N 0.000 claims 1
- CAJOMULDHTXCCJ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxan-4-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCOCC1 CAJOMULDHTXCCJ-UHFFFAOYSA-N 0.000 claims 1
- DXCMCCZFNKZAMD-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxetan-3-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1COC1 DXCMCCZFNKZAMD-UHFFFAOYSA-N 0.000 claims 1
- MFNGOWHRKORXFO-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxetan-3-ylmethylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NCC1COC1 MFNGOWHRKORXFO-UHFFFAOYSA-N 0.000 claims 1
- BYBQUXPEWFXGOZ-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxetan-3-yloxy)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1OC1COC1 BYBQUXPEWFXGOZ-UHFFFAOYSA-N 0.000 claims 1
- PWXUZKKXTLUZSF-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxolan-3-yl)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1C1CCOC1 PWXUZKKXTLUZSF-UHFFFAOYSA-N 0.000 claims 1
- YGMWDYMNXOAZCG-UHFFFAOYSA-N 2-(2-imidazo[1,2-a]pyridin-2-ylethyl)-8-(oxolan-3-ylamino)phthalazin-1-one Chemical compound C=12C(=O)N(CCC=3N=C4C=CC=CN4C=3)N=CC2=CC=CC=1NC1CCOC1 YGMWDYMNXOAZCG-UHFFFAOYSA-N 0.000 claims 1
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| WO2014200885A1 (en) * | 2013-06-11 | 2014-12-18 | Janssen Pharmaceutica Nv | PDE10a INHIBITORS FOR THE TREATMENT OF TYPE II DIABETES |
| US9193736B2 (en) | 2013-06-11 | 2015-11-24 | Janssen Pharmaceutica, Nv | PDE 10a inhibitors for the treatment of type II diabetes |
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- 2012-10-29 US US13/663,008 patent/US9273068B2/en not_active Expired - Fee Related
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- 2012-11-08 CA CA2852604A patent/CA2852604A1/en not_active Abandoned
- 2012-11-08 EP EP12784578.2A patent/EP2776418B1/en not_active Not-in-force
- 2012-11-08 ES ES12784578T patent/ES2620531T3/es active Active
- 2012-11-08 SG SG11201402142VA patent/SG11201402142VA/en unknown
- 2012-11-08 JP JP2014540459A patent/JP2014534976A/ja active Pending
- 2012-11-08 KR KR1020147015427A patent/KR20140097318A/ko not_active Withdrawn
- 2012-11-08 CN CN201280052929.8A patent/CN104053654A/zh active Pending
- 2012-11-08 AR ARP120104208A patent/AR088801A1/es unknown
- 2012-11-08 HK HK15101856.4A patent/HK1201519A1/xx unknown
- 2012-11-08 WO PCT/EP2012/072150 patent/WO2013068470A1/en not_active Ceased
- 2012-11-08 PH PH1/2014/500877A patent/PH12014500877A1/en unknown
- 2012-11-08 AU AU2012334074A patent/AU2012334074A1/en not_active Abandoned
- 2012-11-08 PE PE2014000642A patent/PE20141938A1/es not_active Application Discontinuation
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