KR20140059268A - 아미노-치환된 이미다조피리다진 - Google Patents
아미노-치환된 이미다조피리다진 Download PDFInfo
- Publication number
- KR20140059268A KR20140059268A KR1020147008395A KR20147008395A KR20140059268A KR 20140059268 A KR20140059268 A KR 20140059268A KR 1020147008395 A KR1020147008395 A KR 1020147008395A KR 20147008395 A KR20147008395 A KR 20147008395A KR 20140059268 A KR20140059268 A KR 20140059268A
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- imidazo
- benzofuran
- pyridazin
- oxy
- 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.)
- Ceased
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- -1 Amino-substituted imidazopyridazines Chemical class 0.000 title claims abstract description 262
- 238000000034 method Methods 0.000 claims abstract description 119
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 38
- 238000011282 treatment Methods 0.000 claims abstract description 33
- 201000010099 disease Diseases 0.000 claims abstract description 23
- 239000004480 active ingredient Substances 0.000 claims abstract description 19
- 238000002360 preparation method Methods 0.000 claims abstract description 14
- 150000001875 compounds Chemical class 0.000 claims description 279
- 239000000203 mixture Substances 0.000 claims description 138
- 125000001424 substituent group Chemical group 0.000 claims description 105
- 125000005843 halogen group Chemical group 0.000 claims description 93
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 80
- 150000003839 salts Chemical class 0.000 claims description 69
- 229910052799 carbon Inorganic materials 0.000 claims description 59
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 58
- 125000004942 pyridazin-6-yl group Chemical group N1=NC=CC=C1* 0.000 claims description 55
- 125000003118 aryl group Chemical group 0.000 claims description 53
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 46
- 206010028980 Neoplasm Diseases 0.000 claims description 45
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 43
- 239000012453 solvate Substances 0.000 claims description 38
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical compound BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 31
- 150000001204 N-oxides Chemical class 0.000 claims description 30
- 125000001072 heteroaryl group Chemical group 0.000 claims description 27
- 125000006584 (C3-C10) heterocycloalkyl group Chemical group 0.000 claims description 20
- 239000003814 drug Substances 0.000 claims description 20
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 claims description 20
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 19
- 239000000460 chlorine Substances 0.000 claims description 18
- 229910052801 chlorine Inorganic materials 0.000 claims description 17
- 229910052794 bromium Inorganic materials 0.000 claims description 16
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 15
- KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 15
- 229910052740 iodine Inorganic materials 0.000 claims description 15
- 206010027476 Metastases Diseases 0.000 claims description 14
- 125000003003 spiro group Chemical group 0.000 claims description 14
- 230000004083 survival effect Effects 0.000 claims description 13
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 12
- 230000009401 metastasis Effects 0.000 claims description 11
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 claims description 10
- 208000003174 Brain Neoplasms Diseases 0.000 claims description 10
- 230000004663 cell proliferation Effects 0.000 claims description 10
- 235000019253 formic acid Nutrition 0.000 claims description 10
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 230000028993 immune response Effects 0.000 claims description 9
- 230000037361 pathway Effects 0.000 claims description 9
- 230000001413 cellular effect Effects 0.000 claims description 8
- 230000028709 inflammatory response Effects 0.000 claims description 8
- 125000003107 substituted aryl group Chemical group 0.000 claims description 8
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical group OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 claims description 8
- 206010025323 Lymphomas Diseases 0.000 claims description 7
- 208000000453 Skin Neoplasms Diseases 0.000 claims description 7
- 230000010261 cell growth Effects 0.000 claims description 7
- 239000003085 diluting agent Substances 0.000 claims description 7
- 208000032839 leukemia Diseases 0.000 claims description 7
- 208000008839 Kidney Neoplasms Diseases 0.000 claims description 5
- 239000002246 antineoplastic agent Substances 0.000 claims description 5
- 230000000973 chemotherapeutic effect Effects 0.000 claims description 5
- 208000028149 female reproductive system neoplasm Diseases 0.000 claims description 5
- 230000001404 mediated effect Effects 0.000 claims description 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 4
- 208000001976 Endocrine Gland Neoplasms Diseases 0.000 claims description 4
- 201000003793 Myelodysplastic syndrome Diseases 0.000 claims description 4
- 208000007097 Urinary Bladder Neoplasms Diseases 0.000 claims description 4
- 201000011523 endocrine gland cancer Diseases 0.000 claims description 4
- 210000003734 kidney Anatomy 0.000 claims description 4
- 230000035755 proliferation Effects 0.000 claims description 4
- 238000011321 prophylaxis Methods 0.000 claims description 4
- 201000004477 skin sarcoma Diseases 0.000 claims description 4
- 210000003932 urinary bladder Anatomy 0.000 claims description 4
- 206010029098 Neoplasm skin Diseases 0.000 claims description 3
- 230000024932 T cell mediated immunity Effects 0.000 claims description 3
- 210000000481 breast Anatomy 0.000 claims description 3
- 230000006806 disease prevention Effects 0.000 claims description 3
- 208000037841 lung tumor Diseases 0.000 claims description 3
- 208000023958 prostate neoplasm Diseases 0.000 claims description 3
- USMIFXDDQHVDHD-UHFFFAOYSA-N 1-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-methylpropan-2-amine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OCC(C)(N)C)=CC2=C1 USMIFXDDQHVDHD-UHFFFAOYSA-N 0.000 claims description 2
- OSBGMACOIDTJTO-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-(oxolan-3-yl)ethanamine Chemical compound C1=CC2=NC=C(C=3OC4=CC=CC=C4C=3)N2N=C1OC(CN)C1CCOC1 OSBGMACOIDTJTO-UHFFFAOYSA-N 0.000 claims description 2
- ZQBPSJFVZVCZKU-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-cyclopropylethanamine Chemical compound C1=CC2=NC=C(C=3OC4=CC=CC=C4C=3)N2N=C1OC(CN)C1CC1 ZQBPSJFVZVCZKU-UHFFFAOYSA-N 0.000 claims description 2
- OTPOGFWDXGTVHV-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-4-methylpentan-1-amine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OC(CN)CC(C)C)=CC2=C1 OTPOGFWDXGTVHV-UHFFFAOYSA-N 0.000 claims description 2
- MZQPJGSTVGHBDD-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxyethanamine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OCCN)=CC2=C1 MZQPJGSTVGHBDD-UHFFFAOYSA-N 0.000 claims description 2
- RQMSEQXVSMKOLK-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxypropane-1,3-diamine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OC(CN)CN)=CC2=C1 RQMSEQXVSMKOLK-UHFFFAOYSA-N 0.000 claims description 2
- FTFLGRLUOMVAAC-UHFFFAOYSA-N 4-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-methylbutan-2-amine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OCCC(C)(N)C)=CC2=C1 FTFLGRLUOMVAAC-UHFFFAOYSA-N 0.000 claims description 2
- AGDWSMNMYNYZQH-UHFFFAOYSA-N 4-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxybutan-1-amine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OCCCCN)=CC2=C1 AGDWSMNMYNYZQH-UHFFFAOYSA-N 0.000 claims description 2
- HTJDQJBWANPRPF-UHFFFAOYSA-N Cyclopropylamine Chemical compound NC1CC1 HTJDQJBWANPRPF-UHFFFAOYSA-N 0.000 claims description 2
- 208000032612 Glial tumor Diseases 0.000 claims description 2
- 206010018338 Glioma Diseases 0.000 claims description 2
- 210000004556 brain Anatomy 0.000 claims description 2
- QLRAZPPSOATMKB-RHSMWYFYSA-N (1r,2r)-2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxycyclohexan-1-amine Chemical compound N[C@@H]1CCCC[C@H]1OC1=NN2C(C=3OC4=CC=CC=C4C=3)=CN=C2C=C1 QLRAZPPSOATMKB-RHSMWYFYSA-N 0.000 claims 1
- CJXDHBGTYIJIMW-QGZVFWFLSA-N (1s)-2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-1-(4-chlorophenyl)ethanamine Chemical compound C1([C@@H](COC2=NN3C(C=4OC5=CC=CC=C5C=4)=CN=C3C=C2)N)=CC=C(Cl)C=C1 CJXDHBGTYIJIMW-QGZVFWFLSA-N 0.000 claims 1
- DQQCXFUUJRYTMD-QGZVFWFLSA-N (1s)-2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-1-phenylethanamine Chemical compound C1([C@@H](COC2=NN3C(C=4OC5=CC=CC=C5C=4)=CN=C3C=C2)N)=CC=CC=C1 DQQCXFUUJRYTMD-QGZVFWFLSA-N 0.000 claims 1
- NSQSAXGFNPZJMA-QGZVFWFLSA-N (1s)-2-[3-(5-chloro-1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-1-phenylethanamine Chemical compound C1([C@@H](COC2=NN3C(C=4OC5=CC=C(Cl)C=C5C=4)=CN=C3C=C2)N)=CC=CC=C1 NSQSAXGFNPZJMA-QGZVFWFLSA-N 0.000 claims 1
- BCUZWVGODXHEOL-BBRMVZONSA-N (1s,2s)-2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxycyclopentan-1-amine Chemical compound N[C@H]1CCC[C@@H]1OC1=NN2C(C=3OC4=CC=CC=C4C=3)=CN=C2C=C1 BCUZWVGODXHEOL-BBRMVZONSA-N 0.000 claims 1
- JOLVRVLCKKGOQJ-FQEVSTJZSA-N (2r)-2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-phenylethanamine Chemical compound C1([C@@H](OC2=NN3C(C=4OC5=CC=CC=C5C=4)=CN=C3C=C2)CN)=CC=CC=C1 JOLVRVLCKKGOQJ-FQEVSTJZSA-N 0.000 claims 1
- CMDIADSAZCFCCT-LLVKDONJSA-N (2r)-2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxypropan-1-amine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)O[C@@H](CN)C)=CC2=C1 CMDIADSAZCFCCT-LLVKDONJSA-N 0.000 claims 1
- IFEKINMXPHDXRH-UHFFFAOYSA-N 1-[[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxymethyl]cyclobutan-1-amine Chemical compound C1=CC2=NC=C(C=3OC4=CC=CC=C4C=3)N2N=C1OCC1(N)CCC1 IFEKINMXPHDXRH-UHFFFAOYSA-N 0.000 claims 1
- OLUBNFKIAWVZDO-UHFFFAOYSA-N 1-cyclopropyl-2-[3-(4-methoxy-1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxyethanamine Chemical compound C=1C=2C(OC)=CC=CC=2OC=1C(N1N=2)=CN=C1C=CC=2OCC(N)C1CC1 OLUBNFKIAWVZDO-UHFFFAOYSA-N 0.000 claims 1
- XHMSRGDEBWJLBE-UHFFFAOYSA-N 2-(oxan-2-yl)ethanamine Chemical compound NCCC1CCCCO1 XHMSRGDEBWJLBE-UHFFFAOYSA-N 0.000 claims 1
- PRSSWDWEJRSSQB-UHFFFAOYSA-N 2-[2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxyethoxy]ethanamine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OCCOCCN)=CC2=C1 PRSSWDWEJRSSQB-UHFFFAOYSA-N 0.000 claims 1
- KCOJAJMFSMVAEL-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-1-pyridin-3-ylethanamine Chemical compound C1=CC2=NC=C(C=3OC4=CC=CC=C4C=3)N2N=C1OCC(N)C1=CC=CN=C1 KCOJAJMFSMVAEL-UHFFFAOYSA-N 0.000 claims 1
- UNZKJXCLZWPNAF-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-(2,4-difluorophenyl)ethanamine Chemical compound C1=CC2=NC=C(C=3OC4=CC=CC=C4C=3)N2N=C1OC(CN)C1=CC=C(F)C=C1F UNZKJXCLZWPNAF-UHFFFAOYSA-N 0.000 claims 1
- BUEXJQAIHMRUJG-UHFFFAOYSA-N 2-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-(3-propan-2-yloxyphenyl)ethanamine Chemical compound CC(C)OC1=CC=CC(C(CN)OC2=NN3C(C=4OC5=CC=CC=C5C=4)=CN=C3C=C2)=C1 BUEXJQAIHMRUJG-UHFFFAOYSA-N 0.000 claims 1
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- YCFARJHAUUFOKT-UHFFFAOYSA-N 2-[3-(4-methoxy-1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxyethanamine Chemical compound C1=CC(OCCN)=NN2C(C=3OC=4C=CC=C(C=4C=3)OC)=CN=C21 YCFARJHAUUFOKT-UHFFFAOYSA-N 0.000 claims 1
- IJTRNKUOPXFLMC-UHFFFAOYSA-N 2-[3-(5-methoxy-1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxyethanamine Chemical compound C1=CC(OCCN)=NN2C(C=3OC4=CC=C(C=C4C=3)OC)=CN=C21 IJTRNKUOPXFLMC-UHFFFAOYSA-N 0.000 claims 1
- TUHUFIDQZKLMBA-UHFFFAOYSA-N 3-[3-(1-benzofuran-2-yl)imidazo[1,2-b]pyridazin-6-yl]oxy-2-methylpropan-1-amine Chemical compound C1=CC=C2OC(C3=CN=C4C=CC(=NN43)OCC(CN)C)=CC2=C1 TUHUFIDQZKLMBA-UHFFFAOYSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- 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
- A61K31/50—Pyridazines; Hydrogenated pyridazines
- A61K31/5025—Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Epidemiology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Oncology (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Fats And Perfumes (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP11180129.6 | 2011-09-06 | ||
| EP11180129 | 2011-09-06 | ||
| EP11182440 | 2011-09-23 | ||
| EP11182440.5 | 2011-09-23 | ||
| EP12179902.7 | 2012-08-09 | ||
| EP12179902 | 2012-08-09 | ||
| PCT/EP2012/067264 WO2013034570A1 (en) | 2011-09-06 | 2012-09-05 | Amino-substituted imidazopyridazines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20140059268A true KR20140059268A (ko) | 2014-05-15 |
Family
ID=47831558
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020147008395A Ceased KR20140059268A (ko) | 2011-09-06 | 2012-09-05 | 아미노-치환된 이미다조피리다진 |
Country Status (36)
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US9730929B2 (en) | 2011-06-01 | 2017-08-15 | Bayer Intellectual Property Gmbh | Substituted aminoimidazopyridazines |
| UA117092C2 (uk) | 2011-09-06 | 2018-06-25 | Байєр Інтеллектуал Проперті Гмбх | Амінозаміщені імідазопіридазини |
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