CA2897678A1 - Heteroaryl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds - Google Patents
Heteroaryl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds Download PDFInfo
- Publication number
- CA2897678A1 CA2897678A1 CA2897678A CA2897678A CA2897678A1 CA 2897678 A1 CA2897678 A1 CA 2897678A1 CA 2897678 A CA2897678 A CA 2897678A CA 2897678 A CA2897678 A CA 2897678A CA 2897678 A1 CA2897678 A1 CA 2897678A1
- Authority
- CA
- Canada
- Prior art keywords
- tautomer
- compound
- thiazin
- hexahydropyrano
- difluorophenyl
- 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.)
- Abandoned
Links
- QRXWUHYBXASSFN-UHFFFAOYSA-N 1,2,4,4a,5,6-hexahydropyrano[3,4-d][1,3]thiazin-2-amine Chemical class O1CCC2CSC(N)NC2=C1 QRXWUHYBXASSFN-UHFFFAOYSA-N 0.000 title description 5
- 150000001875 compounds Chemical class 0.000 claims abstract description 289
- 238000000034 method Methods 0.000 claims abstract description 101
- 150000003839 salts Chemical class 0.000 claims abstract description 79
- 238000011282 treatment Methods 0.000 claims abstract description 47
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 11
- -1 cyano, methyl Chemical group 0.000 claims description 103
- WADGHWKXQZVKFK-UHFFFAOYSA-N thiazin-2-amine Chemical compound NN1SC=CC=C1 WADGHWKXQZVKFK-UHFFFAOYSA-N 0.000 claims description 73
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 38
- 208000024827 Alzheimer disease Diseases 0.000 claims description 27
- 102100021257 Beta-secretase 1 Human genes 0.000 claims description 26
- 101710150192 Beta-secretase 1 Proteins 0.000 claims description 26
- 239000001257 hydrogen Substances 0.000 claims description 26
- 229910052739 hydrogen Inorganic materials 0.000 claims description 26
- 125000001424 substituent group Chemical group 0.000 claims description 25
- 229910052799 carbon Inorganic materials 0.000 claims description 24
- 206010012601 diabetes mellitus Diseases 0.000 claims description 19
- 125000001072 heteroaryl group Chemical group 0.000 claims description 18
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims description 17
- 125000001153 fluoro group Chemical group F* 0.000 claims description 16
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 15
- 230000002401 inhibitory effect Effects 0.000 claims description 15
- 239000003814 drug Substances 0.000 claims description 14
- 230000005764 inhibitory process Effects 0.000 claims description 14
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 13
- 125000005842 heteroatom Chemical group 0.000 claims description 12
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 12
- 208000015122 neurodegenerative disease Diseases 0.000 claims description 11
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 11
- 238000004519 manufacturing process Methods 0.000 claims description 10
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000004216 fluoromethyl group Chemical group [H]C([H])(F)* 0.000 claims description 8
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 8
- 230000004770 neurodegeneration Effects 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 229910052736 halogen Inorganic materials 0.000 claims description 7
- 150000002367 halogens Chemical class 0.000 claims description 7
- 102000004169 proteins and genes Human genes 0.000 claims description 7
- 108090000623 proteins and genes Proteins 0.000 claims description 7
- 125000003226 pyrazolyl group Chemical group 0.000 claims description 7
- 125000001425 triazolyl group Chemical group 0.000 claims description 7
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 6
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 6
- 125000004076 pyridyl group Chemical group 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims description 6
- 125000000842 isoxazolyl group Chemical group 0.000 claims description 5
- 125000001715 oxadiazolyl group Chemical group 0.000 claims description 5
- 125000002971 oxazolyl group Chemical group 0.000 claims description 5
- 125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
- 239000003085 diluting agent Substances 0.000 claims description 4
- 125000005494 pyridonyl group Chemical group 0.000 claims description 4
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 3
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 claims description 3
- 125000004857 imidazopyridinyl group Chemical group N1C(=NC2=C1C=CC=N2)* 0.000 claims description 3
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 3
- JCKADNLKXNAZNU-YCELRVBUSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(4-fluoro-1-methylpyrazol-3-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound CN1C=C(F)C([C@@H]2OC[C@@]3(N=C(N)SC[C@@H]3C2)C=2C(=CC(F)=CC=2)F)=N1 JCKADNLKXNAZNU-YCELRVBUSA-N 0.000 claims description 2
- OAQHRRNHJUTEMP-VDYXNGCNSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(5-methoxypyrimidin-2-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound N1=CC(OC)=CN=C1[C@@H]1OC[C@]2(C=3C(=CC(F)=CC=3)F)N=C(N)SC[C@@H]2C1 OAQHRRNHJUTEMP-VDYXNGCNSA-N 0.000 claims description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
- 230000002265 prevention Effects 0.000 claims description 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 5
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 4
- LOMSVYYCZMWWKZ-LCUABVJFSA-N (4ar,6r,8as)-6-[4-(difluoromethyl)-1,3-oxazol-2-yl]-8a-(2,4-difluorophenyl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1([C@@H]2OC[C@@]3(N=C(SC[C@@H]3C2)N)C=2C(=CC(F)=CC=2)F)=NC(C(F)F)=CO1 LOMSVYYCZMWWKZ-LCUABVJFSA-N 0.000 claims 1
- YRPCKZFYHRQIQN-JNHRWOMLSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(1-methyltriazol-4-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound N1=NN(C)C=C1[C@@H]1OC[C@]2(C=3C(=CC(F)=CC=3)F)N=C(N)SC[C@@H]2C1 YRPCKZFYHRQIQN-JNHRWOMLSA-N 0.000 claims 1
- MISNYDXFQSWHAX-MOFZMDFASA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(2-methoxypyridin-4-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1=NC(OC)=CC([C@@H]2OC[C@@]3(N=C(N)SC[C@@H]3C2)C=2C(=CC(F)=CC=2)F)=C1 MISNYDXFQSWHAX-MOFZMDFASA-N 0.000 claims 1
- XKJDNQQRKWLMAK-IRWQIABSSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(2-methylpyridin-4-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1=NC(C)=CC([C@@H]2OC[C@@]3(N=C(N)SC[C@@H]3C2)C=2C(=CC(F)=CC=2)F)=C1 XKJDNQQRKWLMAK-IRWQIABSSA-N 0.000 claims 1
- NXWRDGYXAULZIN-XZOAIXRZSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(2-methylpyrimidin-5-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1=NC(C)=NC=C1[C@@H]1OC[C@]2(C=3C(=CC(F)=CC=3)F)N=C(N)SC[C@@H]2C1 NXWRDGYXAULZIN-XZOAIXRZSA-N 0.000 claims 1
- RHOCNDGDVTUWRH-JNHRWOMLSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(2-methyltriazol-4-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound CN1N=CC([C@@H]2OC[C@@]3(N=C(N)SC[C@@H]3C2)C=2C(=CC(F)=CC=2)F)=N1 RHOCNDGDVTUWRH-JNHRWOMLSA-N 0.000 claims 1
- YSSIVDQDOKWLPW-YCELRVBUSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(5-fluoro-1-methylpyrazol-3-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1=C(F)N(C)N=C1[C@@H]1OC[C@]2(C=3C(=CC(F)=CC=3)F)N=C(N)SC[C@@H]2C1 YSSIVDQDOKWLPW-YCELRVBUSA-N 0.000 claims 1
- WWPKMTNUNPCENN-LSKLOWJMSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(5-fluoropyridin-3-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1([C@@H]2OC[C@@]3(N=C(SC[C@@H]3C2)N)C=2C(=CC(F)=CC=2)F)=CN=CC(F)=C1 WWPKMTNUNPCENN-LSKLOWJMSA-N 0.000 claims 1
- UHEMQQDCLNXFOB-WILYLXEWSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(5-methoxypyridin-3-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound COC1=CN=CC([C@@H]2OC[C@@]3(N=C(N)SC[C@@H]3C2)C=2C(=CC(F)=CC=2)F)=C1 UHEMQQDCLNXFOB-WILYLXEWSA-N 0.000 claims 1
- ULVIMNOZDYOJLV-VAHXTSCQSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(5-methyl-1,2,4-oxadiazol-3-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound O1C(C)=NC([C@@H]2OC[C@@]3(N=C(N)SC[C@@H]3C2)C=2C(=CC(F)=CC=2)F)=N1 ULVIMNOZDYOJLV-VAHXTSCQSA-N 0.000 claims 1
- VHXQPAJVUGIRHC-LSKLOWJMSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-(5-methylpyrazin-2-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1=NC(C)=CN=C1[C@@H]1OC[C@]2(C=3C(=CC(F)=CC=3)F)N=C(N)SC[C@@H]2C1 VHXQPAJVUGIRHC-LSKLOWJMSA-N 0.000 claims 1
- MCIIOYNNPPTDHU-KEMVTONXSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-([1,3]oxazolo[4,5-c]pyridin-2-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1([C@@]23N=C(SC[C@@H]2C[C@@H](OC3)C=2OC3=CC=NC=C3N=2)N)=CC=C(F)C=C1F MCIIOYNNPPTDHU-KEMVTONXSA-N 0.000 claims 1
- OTIZLFDINUQJQA-FUVFPRGESA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-([1,3]oxazolo[5,4-c]pyridin-2-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1([C@@]23N=C(SC[C@@H]2C[C@@H](OC3)C=2OC3=CN=CC=C3N=2)N)=CC=C(F)C=C1F OTIZLFDINUQJQA-FUVFPRGESA-N 0.000 claims 1
- PESSOXMFWBNOSU-CXMBCZLWSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-[1-(2,2,2-trifluoroethyl)pyrazol-4-yl]-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C=1([C@@H]2OC[C@@]3(N=C(SC[C@@H]3C2)N)C=2C(=CC(F)=CC=2)F)C=NN(CC(F)(F)F)C=1 PESSOXMFWBNOSU-CXMBCZLWSA-N 0.000 claims 1
- JYDYMWJEZLKIBS-JZVSSPTHSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-[1-(trideuteriomethyl)pyrazol-4-yl]-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1=NN(C([2H])([2H])[2H])C=C1[C@@H]1OC[C@]2(C=3C(=CC(F)=CC=3)F)N=C(N)SC[C@@H]2C1 JYDYMWJEZLKIBS-JZVSSPTHSA-N 0.000 claims 1
- SREYUNASIGFXOS-ZLXGRDSLSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-imidazo[1,2-a]pyridin-6-yl-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1([C@@]23N=C(SC[C@@H]2C[C@@H](OC3)C2=CN3C=CN=C3C=C2)N)=CC=C(F)C=C1F SREYUNASIGFXOS-ZLXGRDSLSA-N 0.000 claims 1
- AGVSEJHWLJHZMN-CXMBCZLWSA-N (4ar,6r,8as)-8a-(2,4-difluorophenyl)-6-pyrimidin-5-yl-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1([C@@H]2OC[C@@]3(N=C(SC[C@@H]3C2)N)C=2C(=CC(F)=CC=2)F)=CN=CN=C1 AGVSEJHWLJHZMN-CXMBCZLWSA-N 0.000 claims 1
- VHXQPAJVUGIRHC-DPZKZMLUSA-N (4as,6s,8ar)-8a-(2,4-difluorophenyl)-6-(5-methylpyrazin-2-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C1=NC(C)=CN=C1[C@H]1OC[C@@]2(C=3C(=CC(F)=CC=3)F)N=C(N)SC[C@H]2C1 VHXQPAJVUGIRHC-DPZKZMLUSA-N 0.000 claims 1
- AWKVMOUMPQXDPO-NPQNXCPHSA-N (4r,4ar,6r,8as)-8a-(2,4-difluorophenyl)-4-methyl-6-(1-methylpyrazol-4-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound C=1([C@@H]2OC[C@@]3(N=C(N)S[C@@H]([C@@H]3C2)C)C=2C(=CC(F)=CC=2)F)C=NN(C)C=1 AWKVMOUMPQXDPO-NPQNXCPHSA-N 0.000 claims 1
- JIAYOIBUKDISBO-IYPIGGPWSA-N (4s,4ar,6r,8as)-8a-(2,4-difluorophenyl)-4-(fluoromethyl)-6-(3-methyl-1,2-oxazol-5-yl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-2-amine Chemical compound O1N=C(C)C=C1[C@@H]1OC[C@]2(C=3C(=CC(F)=CC=3)F)N=C(N)S[C@H](CF)[C@@H]2C1 JIAYOIBUKDISBO-IYPIGGPWSA-N 0.000 claims 1
- KBYFSXJKVKUVGM-YCELRVBUSA-N 2-[(4ar,6r,8as)-2-amino-8a-(2,4-difluorophenyl)-4a,5,6,8-tetrahydro-4h-pyrano[3,4-d][1,3]thiazin-6-yl]-1,3-oxazole-4-carbonitrile Chemical compound C1([C@@H]2OC[C@@]3(N=C(SC[C@@H]3C2)N)C=2C(=CC(F)=CC=2)F)=NC(C#N)=CO1 KBYFSXJKVKUVGM-YCELRVBUSA-N 0.000 claims 1
- 230000015572 biosynthetic process Effects 0.000 abstract description 135
- 238000003786 synthesis reaction Methods 0.000 abstract description 133
- 239000000543 intermediate Substances 0.000 abstract description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 441
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 300
- 239000000243 solution Substances 0.000 description 226
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 169
- 239000000047 product Substances 0.000 description 142
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 118
- 239000011541 reaction mixture Substances 0.000 description 116
- 238000005160 1H NMR spectroscopy Methods 0.000 description 114
- 239000000203 mixture Substances 0.000 description 109
- 238000004895 liquid chromatography mass spectrometry Methods 0.000 description 102
- 239000007787 solid Substances 0.000 description 100
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 96
- 229920006395 saturated elastomer Polymers 0.000 description 82
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 81
- 239000012044 organic layer Substances 0.000 description 79
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 77
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- 238000006243 chemical reaction Methods 0.000 description 67
- 229910052938 sodium sulfate Inorganic materials 0.000 description 67
- 235000011152 sodium sulphate Nutrition 0.000 description 67
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- 238000010898 silica gel chromatography Methods 0.000 description 60
- GQHTUMJGOHRCHB-UHFFFAOYSA-N 2,3,4,6,7,8,9,10-octahydropyrimido[1,2-a]azepine Chemical compound C1CCCCN2CCCN=C21 GQHTUMJGOHRCHB-UHFFFAOYSA-N 0.000 description 59
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 24
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- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 20
- 239000002904 solvent Substances 0.000 description 20
- 239000000463 material Substances 0.000 description 19
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 18
- 229910052757 nitrogen Inorganic materials 0.000 description 17
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Classifications
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- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/54—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 sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/542—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 sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
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- 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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- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
- C07D513/04—Ortho-condensed systems
Landscapes
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
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- Psychiatry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361764185P | 2013-02-13 | 2013-02-13 | |
| US61/764,185 | 2013-02-13 | ||
| PCT/IB2014/058760 WO2014125394A1 (en) | 2013-02-13 | 2014-02-03 | HETEROARYL-SUBSTITUTED HEXAHYDROPYRANO [3,4-d][1,3] THIAZIN-2-AMINE COMPOUNDS |
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| CA2897678A1 true CA2897678A1 (en) | 2014-08-21 |
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| CA2897678A Abandoned CA2897678A1 (en) | 2013-02-13 | 2014-02-03 | Heteroaryl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds |
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| US (3) | US8865706B2 (cg-RX-API-DMAC7.html) |
| EP (1) | EP2956458B1 (cg-RX-API-DMAC7.html) |
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| TW (1) | TW201443064A (cg-RX-API-DMAC7.html) |
| UY (1) | UY35320A (cg-RX-API-DMAC7.html) |
| WO (1) | WO2014125394A1 (cg-RX-API-DMAC7.html) |
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| EP2751116B1 (en) | 2011-08-31 | 2016-10-12 | Pfizer Inc | Hexahydropyrano [3,4-d][1,3]thiazin-2-amine compounds |
| WO2013164730A1 (en) * | 2012-05-04 | 2013-11-07 | Pfizer Inc. | Heterocyclic substituted hexahydropyrano [3,4-d] [1,3] thiazin- 2 -amine compounds as inhibitors of app, bace1 and bace 2. |
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- 2014-02-03 WO PCT/IB2014/058760 patent/WO2014125394A1/en not_active Ceased
- 2014-02-03 EP EP14704927.4A patent/EP2956458B1/en not_active Not-in-force
- 2014-02-11 TW TW103104416A patent/TW201443064A/zh unknown
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| AR094762A1 (es) | 2015-08-26 |
| US20140228356A1 (en) | 2014-08-14 |
| US20140364426A1 (en) | 2014-12-11 |
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| US20150224110A1 (en) | 2015-08-13 |
| EP2956458B1 (en) | 2017-08-09 |
| US8865706B2 (en) | 2014-10-21 |
| EP2956458A1 (en) | 2015-12-23 |
| WO2014125394A1 (en) | 2014-08-21 |
| UY35320A (es) | 2014-09-30 |
| TW201443064A (zh) | 2014-11-16 |
| JP2016507551A (ja) | 2016-03-10 |
| US9045499B2 (en) | 2015-06-02 |
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