EA031201B1 - Соединения имидазопиридазина - Google Patents
Соединения имидазопиридазина Download PDFInfo
- Publication number
- EA031201B1 EA031201B1 EA201700042A EA201700042A EA031201B1 EA 031201 B1 EA031201 B1 EA 031201B1 EA 201700042 A EA201700042 A EA 201700042A EA 201700042 A EA201700042 A EA 201700042A EA 031201 B1 EA031201 B1 EA 031201B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- imidazo
- carboxamide
- pyridazin
- pyridazine
- chloro
- Prior art date
Links
- 150000005233 imidazopyridazines Chemical class 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 157
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 67
- 238000000034 method Methods 0.000 claims abstract description 39
- 150000003839 salts Chemical class 0.000 claims abstract description 28
- 201000010099 disease Diseases 0.000 claims abstract description 24
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 12
- -1 4-chloro-3-fluorophenyl Chemical group 0.000 claims description 329
- XPYGVSPRBCZOBS-UHFFFAOYSA-N 1h-pyridazine-2-carboxamide Chemical compound NC(=O)N1NC=CC=C1 XPYGVSPRBCZOBS-UHFFFAOYSA-N 0.000 claims description 161
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 66
- 102000001708 Protein Isoforms Human genes 0.000 claims description 43
- 108010029485 Protein Isoforms Proteins 0.000 claims description 43
- 125000004566 azetidin-1-yl group Chemical group N1(CCC1)* 0.000 claims description 43
- WSFSSNUMVMOOMR-BJUDXGSMSA-N methanone Chemical compound O=[11CH2] WSFSSNUMVMOOMR-BJUDXGSMSA-N 0.000 claims description 34
- 125000004526 pyridazin-2-yl group Chemical group N1N(C=CC=C1)* 0.000 claims description 32
- DJUSZKBLNSVQLI-UHFFFAOYSA-N imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound N1=CC=CC2=NC(C(=O)N)=CN21 DJUSZKBLNSVQLI-UHFFFAOYSA-N 0.000 claims description 31
- UTCSSFWDNNEEBH-UHFFFAOYSA-N imidazo[1,2-a]pyridine Chemical compound C1=CC=CC2=NC=CN21 UTCSSFWDNNEEBH-UHFFFAOYSA-N 0.000 claims description 25
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 18
- 201000000980 schizophrenia Diseases 0.000 claims description 13
- 208000024827 Alzheimer disease Diseases 0.000 claims description 12
- 208000019901 Anxiety disease Diseases 0.000 claims description 12
- 208000018737 Parkinson disease Diseases 0.000 claims description 12
- 206010061218 Inflammation Diseases 0.000 claims description 11
- 230000004054 inflammatory process Effects 0.000 claims description 11
- 201000006417 multiple sclerosis Diseases 0.000 claims description 11
- PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 claims description 11
- 208000006673 asthma Diseases 0.000 claims description 10
- 208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 claims description 9
- 208000026106 cerebrovascular disease Diseases 0.000 claims description 9
- 206010010744 Conjunctivitis allergic Diseases 0.000 claims description 8
- 208000006011 Stroke Diseases 0.000 claims description 8
- 208000002205 allergic conjunctivitis Diseases 0.000 claims description 8
- 230000036506 anxiety Effects 0.000 claims description 8
- 208000024998 atopic conjunctivitis Diseases 0.000 claims description 8
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 8
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 7
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 7
- 125000004939 6-pyridyl group Chemical group N1=CC=CC=C1* 0.000 claims description 6
- SCHCQOLPISHKOS-UHFFFAOYSA-N N1(CCC1)C(=O)C=1N=C2N(N=CC=C2)C=1C1=CC(=C(C(=C1)F)OC)F Chemical compound N1(CCC1)C(=O)C=1N=C2N(N=CC=C2)C=1C1=CC(=C(C(=C1)F)OC)F SCHCQOLPISHKOS-UHFFFAOYSA-N 0.000 claims description 6
- VFRSADQPWYCXDG-LEUCUCNGSA-N ethyl (2s,5s)-5-methylpyrrolidine-2-carboxylate;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.CCOC(=O)[C@@H]1CC[C@H](C)N1 VFRSADQPWYCXDG-LEUCUCNGSA-N 0.000 claims description 6
- 150000004675 formic acid derivatives Chemical class 0.000 claims description 6
- YOCIPGYKDZCTFU-UHFFFAOYSA-N ClC1=CC=C(C=C1)C1=C(N=C2N1N=CC=C2)C(=O)NC1CC1 Chemical compound ClC1=CC=C(C=C1)C1=C(N=C2N1N=CC=C2)C(=O)NC1CC1 YOCIPGYKDZCTFU-UHFFFAOYSA-N 0.000 claims description 5
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 claims description 5
- GLYPDLWNQYDRTQ-UHFFFAOYSA-N 4-[2-(azetidine-1-carbonyl)imidazo[1,2-b]pyridazin-3-yl]-2,5-difluorobenzonitrile Chemical compound FC1=CC(C#N)=C(F)C=C1C1=C(N=C2C=CC=NN12)C(=O)N1CCC1 GLYPDLWNQYDRTQ-UHFFFAOYSA-N 0.000 claims description 4
- COQGBMKNVJUVAB-UHFFFAOYSA-N 4-[2-(azetidine-1-carbonyl)imidazo[1,2-b]pyridazin-3-yl]-2-fluorobenzonitrile Chemical compound FC1=C(C=CC(=C1)C1=C(N=C2C=CC=NN12)C(=O)N1CCC1)C#N COQGBMKNVJUVAB-UHFFFAOYSA-N 0.000 claims description 4
- GGBPMJVCUHMAJB-UHFFFAOYSA-N 4-[2-(azetidine-1-carbonyl)imidazo[1,2-b]pyridazin-3-yl]-5-fluoro-2-methylbenzonitrile Chemical compound CC1=C(C=C(F)C(=C1)C1=C(N=C2C=CC=NN12)C(=O)N1CCC1)C#N GGBPMJVCUHMAJB-UHFFFAOYSA-N 0.000 claims description 4
- VGOMARAKBZMHJT-UHFFFAOYSA-N ClC1=CC=C(C=C1)C1=C(N=C2C=CC=NN12)C(=O)N1CCCC1 Chemical compound ClC1=CC=C(C=C1)C1=C(N=C2C=CC=NN12)C(=O)N1CCCC1 VGOMARAKBZMHJT-UHFFFAOYSA-N 0.000 claims description 4
- WFFUVTXNYNORQT-UHFFFAOYSA-N O=C(N1CCC1)C1=C(N2N=CC=CC2=N1)C1=CN2N=CN=C2C=C1 Chemical compound O=C(N1CCC1)C1=C(N2N=CC=CC2=N1)C1=CN2N=CN=C2C=C1 WFFUVTXNYNORQT-UHFFFAOYSA-N 0.000 claims description 4
- PKGAXGNVVMHTJZ-UHFFFAOYSA-N [3-(4-chlorophenyl)imidazo[1,2-b]pyridazin-2-yl]-(3,3-difluoroazetidin-1-yl)methanone Chemical compound FC1(F)CN(C1)C(=O)C1=C(N2N=CC=CC2=N1)C1=CC=C(Cl)C=C1 PKGAXGNVVMHTJZ-UHFFFAOYSA-N 0.000 claims description 4
- WJDDXTCEGQNYBD-UHFFFAOYSA-N [3-(4-chlorophenyl)imidazo[1,2-b]pyridazin-2-yl]-(3-methoxyazetidin-1-yl)methanone Chemical compound COC1CN(C1)C(=O)C1=C(N2N=CC=CC2=N1)C1=CC=C(Cl)C=C1 WJDDXTCEGQNYBD-UHFFFAOYSA-N 0.000 claims description 4
- RINAWWCARFNGLM-UHFFFAOYSA-N azetidin-1-yl-(3-pyrazolo[1,5-a]pyrimidin-6-ylimidazo[1,2-b]pyridazin-2-yl)methanone Chemical compound O=C(N1CCC1)C1=C(N2N=CC=CC2=N1)C1=CN2N=CC=C2N=C1 RINAWWCARFNGLM-UHFFFAOYSA-N 0.000 claims description 4
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- IVSBLXFZMFGIAK-UHFFFAOYSA-N azetidin-1-yl-[3-(4-chloro-3-fluorophenyl)imidazo[1,2-b]pyridazin-2-yl]methanone Chemical compound FC1=C(Cl)C=CC(=C1)C1=C(N=C2C=CC=NN12)C(=O)N1CCC1 IVSBLXFZMFGIAK-UHFFFAOYSA-N 0.000 claims description 4
- QELHEVBSVCAUHV-UHFFFAOYSA-N azetidin-1-yl-[3-(5-chloropyridin-3-yl)imidazo[1,2-b]pyridazin-2-yl]methanone Chemical compound ClC1=CC(=CN=C1)C1=C(N=C2C=CC=NN12)C(=O)N1CCC1 QELHEVBSVCAUHV-UHFFFAOYSA-N 0.000 claims description 4
- 230000001404 mediated effect Effects 0.000 claims description 4
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 3
- KNOPWXCBOLJCAA-UHFFFAOYSA-N 3-cyclopropylimidazo[1,2-b]pyridazine-2-carboxamide Chemical compound C1(CC1)C1=C(N=C2N1N=CC=C2)C(=O)N KNOPWXCBOLJCAA-UHFFFAOYSA-N 0.000 claims description 3
- 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 3
- 125000006432 1-methyl cyclopropyl group Chemical group [H]C([H])([H])C1(*)C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 2
- MKZIIZYJPRYKMM-UHFFFAOYSA-N 3-fluoroazetidine-1-carbaldehyde Chemical compound FC1CN(C=O)C1 MKZIIZYJPRYKMM-UHFFFAOYSA-N 0.000 claims description 2
- NJCCFDZQRIVPQK-UHFFFAOYSA-N 4-[2-(azetidine-1-carbonyl)imidazo[1,2-b]pyridazin-3-yl]-2-fluoro-5-methylbenzonitrile Chemical compound CC1=CC(C#N)=C(F)C=C1C1=C(N=C2C=CC=NN12)C(=O)N1CCC1 NJCCFDZQRIVPQK-UHFFFAOYSA-N 0.000 claims description 2
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- 101000988424 Homo sapiens cAMP-specific 3',5'-cyclic phosphodiesterase 4B Proteins 0.000 claims description 2
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- JMTGAAJHYHUEQI-UHFFFAOYSA-N 3-(4-chloro-2,5-difluorophenyl)-N-propan-2-ylimidazo[1,2-b]pyridazine-2-carboxamide Chemical compound CC(C)NC(=O)C1=C(N2N=CC=CC2=N1)C1=CC(F)=C(Cl)C=C1F JMTGAAJHYHUEQI-UHFFFAOYSA-N 0.000 claims 1
- OPBIZTGCIJZSGG-NWDGAFQWSA-N 3-(4-chloro-2-fluorophenyl)-N-[(1R,2S)-2-fluorocyclopropyl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound F[C@H]1C[C@H]1NC(=O)C1=C(N2N=CC=CC2=N1)C1=CC=C(Cl)C=C1F OPBIZTGCIJZSGG-NWDGAFQWSA-N 0.000 claims 1
- XIVVDTJZCTVMFP-QWHCGFSZSA-N 3-(4-chloro-2-methylphenyl)-N-[(1R,2S)-2-fluorocyclopropyl]imidazo[1,2-b]pyridazine-2-carboxamide Chemical compound CC1=CC(Cl)=CC=C1C1=C(N=C2C=CC=NN12)C(=O)N[C@@H]1C[C@@H]1F XIVVDTJZCTVMFP-QWHCGFSZSA-N 0.000 claims 1
- VTRNMYGATDHWOK-UHFFFAOYSA-N 3-(4-chloro-3-fluorophenyl)-N-cyclopropyl-N-methylimidazo[1,2-b]pyridazine-2-carboxamide Chemical compound CN(C1CC1)C(=O)C1=C(N2N=CC=CC2=N1)C1=CC(F)=C(Cl)C=C1 VTRNMYGATDHWOK-UHFFFAOYSA-N 0.000 claims 1
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Applications Claiming Priority (3)
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|---|---|---|---|
| US201462033684P | 2014-08-06 | 2014-08-06 | |
| US201562157129P | 2015-05-05 | 2015-05-05 | |
| PCT/IB2015/055597 WO2016020786A1 (en) | 2014-08-06 | 2015-07-23 | Imidazopyridazine compounds |
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| EA201700042A1 EA201700042A1 (ru) | 2017-07-31 |
| EA031201B1 true EA031201B1 (ru) | 2018-11-30 |
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| EP3172210B1 (en) | 2014-07-24 | 2020-01-15 | Pfizer Inc | Pyrazolopyrimidine compounds |
| PT3177624T (pt) | 2014-08-06 | 2019-07-11 | Pfizer | Compostos de imidazopiridazina |
| CA3015166C (en) * | 2016-02-23 | 2021-08-03 | Pfizer Inc. | 6,7-dihydro-5h-pyrazolo[5,1-b][1,3]oxazine-2-carboxamide compounds |
| EP3824906A1 (en) | 2016-12-21 | 2021-05-26 | Amgen Inc. | Anti-tnf alpha antibody formulations |
| US11370769B2 (en) | 2017-09-07 | 2022-06-28 | Board Of Regents Of The University Of Nebraska | TRPC5 inhibitors and methods of using same |
| EP3773538A1 (en) * | 2018-04-13 | 2021-02-17 | Healx Limited | Treatment of fragile x syndrome |
| US20210393621A1 (en) | 2018-10-26 | 2021-12-23 | The Research Foundation For The State University Of New York | Combination serotonin specific reuptake inhibitor and serotonin 1a receptor partial agonist for reducing l-dopa-induced dyskinesia |
| EP3937942A4 (en) * | 2019-03-15 | 2022-11-16 | Skyhawk Therapeutics, Inc. | COMPOSITIONS AND METHODS FOR CORRECTING ABERRANT SPLICING |
| CR20220160A (es) | 2019-09-16 | 2022-06-16 | Takeda Pharmaceuticals Co | Derivados de piridazin-3(2h)-ona fusionados con azol |
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Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011051342A1 (en) * | 2009-10-30 | 2011-05-05 | Janssen Pharmaceutica Nv | IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS |
Non-Patent Citations (2)
| Title |
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| DONNELL, A.F. ; DOLLINGS, P.J. ; BUTERA, J.A. ; DIETRICH, A.J. ; LIPINSKI, K.K. ; GHAVAMI, A. ; HIRST, W.D.: "Identification of pyridazino[4,5-b]indolizines as selective PDE4B inhibitors", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, PERGAMON, AMSTERDAM, NL, vol. 20, no. 7, 1 April 2010 (2010-04-01), AMSTERDAM, NL, pages 2163 - 2167, XP026971036, ISSN: 0960-894X * |
| NAGANUMA, K. ; OMURA, A. ; MAEKAWARA, N. ; SAITOH, M. ; OHKAWA, N. ; KUBOTA, T. ; NAGUMO, H. ; KODAMA, T. ; TAKEMURA, M. ; OHTSUKA: "Discovery of selective PDE4B inhibitors", BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, PERGAMON, AMSTERDAM, NL, vol. 19, no. 12, 15 June 2009 (2009-06-15), AMSTERDAM, NL, pages 3174 - 3176, XP026138493, ISSN: 0960-894X, DOI: 10.1016/j.bmcl.2009.04.121 * |
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