CA2979905A1 - Compounds and their use as bace1 inhibitors - Google Patents
Compounds and their use as bace1 inhibitors Download PDFInfo
- Publication number
- CA2979905A1 CA2979905A1 CA2979905A CA2979905A CA2979905A1 CA 2979905 A1 CA2979905 A1 CA 2979905A1 CA 2979905 A CA2979905 A CA 2979905A CA 2979905 A CA2979905 A CA 2979905A CA 2979905 A1 CA2979905 A1 CA 2979905A1
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- Prior art keywords
- hydrogen
- alkyl
- imino
- halogen
- deuterium
- 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
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- 150000001875 compounds Chemical class 0.000 title claims abstract description 273
- 229940125759 BACE1 protease inhibitor Drugs 0.000 title description 35
- 150000003839 salts Chemical class 0.000 claims abstract description 55
- 208000024827 Alzheimer disease Diseases 0.000 claims abstract description 40
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims abstract description 12
- 201000010374 Down Syndrome Diseases 0.000 claims abstract description 10
- 206010064930 age-related macular degeneration Diseases 0.000 claims abstract description 10
- 230000006735 deficit Effects 0.000 claims abstract description 10
- 208000002780 macular degeneration Diseases 0.000 claims abstract description 10
- 239000008194 pharmaceutical composition Substances 0.000 claims abstract description 9
- 206010044688 Trisomy 21 Diseases 0.000 claims abstract description 8
- 230000004770 neurodegeneration Effects 0.000 claims abstract description 8
- 102000013455 Amyloid beta-Peptides Human genes 0.000 claims abstract description 7
- 108010090849 Amyloid beta-Peptides Proteins 0.000 claims abstract description 7
- 206010012289 Dementia Diseases 0.000 claims abstract description 7
- 208000018737 Parkinson disease Diseases 0.000 claims abstract description 7
- 208000035475 disorder Diseases 0.000 claims abstract description 6
- 230000000750 progressive effect Effects 0.000 claims abstract description 6
- 208000000044 Amnesia Diseases 0.000 claims abstract description 5
- 206010059245 Angiopathy Diseases 0.000 claims abstract description 5
- 208000024172 Cardiovascular disease Diseases 0.000 claims abstract description 5
- 208000028698 Cognitive impairment Diseases 0.000 claims abstract description 5
- 208000010412 Glaucoma Diseases 0.000 claims abstract description 5
- 208000026139 Memory disease Diseases 0.000 claims abstract description 5
- 208000029578 Muscle disease Diseases 0.000 claims abstract description 5
- 206010036631 Presenile dementia Diseases 0.000 claims abstract description 5
- 206010039966 Senile dementia Diseases 0.000 claims abstract description 5
- 208000030886 Traumatic Brain injury Diseases 0.000 claims abstract description 5
- 208000010877 cognitive disease Diseases 0.000 claims abstract description 5
- 230000006984 memory degeneration Effects 0.000 claims abstract description 5
- 208000023060 memory loss Diseases 0.000 claims abstract description 5
- 208000015122 neurodegenerative disease Diseases 0.000 claims abstract description 5
- 230000007436 olfactory function Effects 0.000 claims abstract description 5
- 208000024891 symptom Diseases 0.000 claims abstract description 5
- 230000009529 traumatic brain injury Effects 0.000 claims abstract description 5
- 208000001072 type 2 diabetes mellitus Diseases 0.000 claims abstract description 5
- 239000012453 solvate Substances 0.000 claims abstract 39
- 125000000217 alkyl group Chemical group 0.000 claims description 331
- 229910052739 hydrogen Inorganic materials 0.000 claims description 237
- 239000001257 hydrogen Substances 0.000 claims description 237
- 150000002431 hydrogen Chemical group 0.000 claims description 231
- 229910052736 halogen Inorganic materials 0.000 claims description 184
- 150000002367 halogens Chemical group 0.000 claims description 184
- UZVGSSNIUNSOFA-UHFFFAOYSA-N dibenzofuran-1-carboxylic acid Chemical compound O1C2=CC=CC=C2C2=C1C=CC=C2C(=O)O UZVGSSNIUNSOFA-UHFFFAOYSA-N 0.000 claims description 178
- YZCKVEUIGOORGS-OUBTZVSYSA-N Deuterium Chemical group [2H] YZCKVEUIGOORGS-OUBTZVSYSA-N 0.000 claims description 177
- 229910052805 deuterium Inorganic materials 0.000 claims description 177
- 125000003118 aryl group Chemical group 0.000 claims description 139
- 125000001188 haloalkyl group Chemical group 0.000 claims description 132
- 125000001072 heteroaryl group Chemical group 0.000 claims description 128
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 119
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims description 99
- 125000004404 heteroalkyl group Chemical group 0.000 claims description 98
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 88
- 125000000304 alkynyl group Chemical group 0.000 claims description 85
- -1 NR' Inorganic materials 0.000 claims description 83
- 125000003342 alkenyl group Chemical group 0.000 claims description 71
- 239000000651 prodrug Chemical group 0.000 claims description 65
- 229940002612 prodrug Drugs 0.000 claims description 65
- 229910052757 nitrogen Inorganic materials 0.000 claims description 54
- 229910052799 carbon Inorganic materials 0.000 claims description 53
- 150000001721 carbon Chemical class 0.000 claims description 39
- NDOVLWQBFFJETK-UHFFFAOYSA-N 1,4-thiazinane 1,1-dioxide Chemical compound O=S1(=O)CCNCC1 NDOVLWQBFFJETK-UHFFFAOYSA-N 0.000 claims description 37
- 125000003368 amide group Chemical group 0.000 claims description 36
- 125000003277 amino group Chemical group 0.000 claims description 36
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 35
- 102100021257 Beta-secretase 1 Human genes 0.000 claims description 34
- HABIAKDIZVCTLU-UHFFFAOYSA-N 1,3-diazinan-4-one Chemical compound O=C1CCNCN1 HABIAKDIZVCTLU-UHFFFAOYSA-N 0.000 claims description 29
- 125000000623 heterocyclic group Chemical group 0.000 claims description 29
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims description 28
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 27
- 102000034570 NR1 subfamily Human genes 0.000 claims description 27
- 108020001305 NR1 subfamily Proteins 0.000 claims description 27
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 27
- 229910052717 sulfur Inorganic materials 0.000 claims description 27
- 125000006376 (C3-C10) cycloalkyl group Chemical group 0.000 claims description 26
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 25
- 125000005605 benzo group Chemical group 0.000 claims description 25
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 24
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 23
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 23
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 21
- 229910052760 oxygen Inorganic materials 0.000 claims description 19
- 125000005018 aryl alkenyl group Chemical group 0.000 claims description 18
- 125000005015 aryl alkynyl group Chemical group 0.000 claims description 18
- 125000004447 heteroarylalkenyl group Chemical group 0.000 claims description 18
- 125000005312 heteroarylalkynyl group Chemical group 0.000 claims description 18
- IBBMAWULFFBRKK-UHFFFAOYSA-N picolinamide Chemical compound NC(=O)C1=CC=CC=N1 IBBMAWULFFBRKK-UHFFFAOYSA-N 0.000 claims description 17
- VMWNQDUVQKEIOC-CYBMUJFWSA-N apomorphine Chemical compound C([C@H]1N(C)CC2)C3=CC=C(O)C(O)=C3C3=C1C2=CC=C3 VMWNQDUVQKEIOC-CYBMUJFWSA-N 0.000 claims description 16
- 125000002837 carbocyclic group Chemical group 0.000 claims description 15
- 238000000034 method Methods 0.000 claims description 14
- QPJVMBTYPHYUOC-UHFFFAOYSA-N methyl benzoate Chemical compound COC(=O)C1=CC=CC=C1 QPJVMBTYPHYUOC-UHFFFAOYSA-N 0.000 claims description 10
- UQDUPQYQJKYHQI-UHFFFAOYSA-N methyl laurate Chemical compound CCCCCCCCCCCC(=O)OC UQDUPQYQJKYHQI-UHFFFAOYSA-N 0.000 claims description 10
- KXDAEFPNCMNJSK-UHFFFAOYSA-N Benzamide Chemical compound NC(=O)C1=CC=CC=C1 KXDAEFPNCMNJSK-UHFFFAOYSA-N 0.000 claims description 8
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 125000002950 monocyclic group Chemical group 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- 102000003728 Peroxisome Proliferator-Activated Receptors Human genes 0.000 claims description 6
- 108090000029 Peroxisome Proliferator-Activated Receptors Proteins 0.000 claims description 6
- HSEMFIZWXHQJAE-UHFFFAOYSA-N hexadecanamide Chemical compound CCCCCCCCCCCCCCCC(N)=O HSEMFIZWXHQJAE-UHFFFAOYSA-N 0.000 claims description 6
- 241000124008 Mammalia Species 0.000 claims description 5
- 230000002401 inhibitory effect Effects 0.000 claims description 5
- 229940095102 methyl benzoate Drugs 0.000 claims description 5
- 230000007170 pathology Effects 0.000 claims description 5
- QEODWPGJXCSBCR-UHFFFAOYSA-N 5-[2-(ethylcarbamoyl)-4-[3-(trifluoromethyl)pyrazol-1-yl]-1h-pyrrolo[2,3-b]pyridin-5-yl]pyridine-3-carboxylic acid Chemical compound C=1N=C2NC(C(=O)NCC)=CC2=C(N2N=C(C=C2)C(F)(F)F)C=1C1=CN=CC(C(O)=O)=C1 QEODWPGJXCSBCR-UHFFFAOYSA-N 0.000 claims description 4
- 101000894895 Homo sapiens Beta-secretase 1 Proteins 0.000 claims description 4
- UKNRYQULTFHIEA-NRFANRHFSA-N N-[3-[(4S)-2-amino-1,4-dimethyl-6-oxo-5H-pyrimidin-4-yl]-4-chlorophenyl]-5-prop-1-ynylpyridine-2-carboxamide Chemical compound ClC1=C(C=C(C=C1)NC(C1=NC=C(C=C1)C#CC)=O)[C@]1(NC(N(C(C1)=O)C)=N)C UKNRYQULTFHIEA-NRFANRHFSA-N 0.000 claims description 4
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 claims description 4
- 239000000546 pharmaceutical excipient Substances 0.000 claims description 4
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims description 2
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 claims description 2
- CUPOOAWTRIURFT-UHFFFAOYSA-N thiophene-2-carbonitrile Chemical compound N#CC1=CC=CS1 CUPOOAWTRIURFT-UHFFFAOYSA-N 0.000 claims description 2
- 239000012458 free base Substances 0.000 claims 19
- SZEDGFFAIDSOQK-QFIPXVFZSA-N (3R)-3,6,6-trimethyl-3-(9-methyl-6,11-dihydro-5H-benzo[b][1]benzazepin-2-yl)-1,1-dioxo-2H-1,4-thiazin-5-amine Chemical compound N=C1N[C@@](CS(C1(C)C)(=O)=O)(C=1C=CC2=C(NC3=C(CC2)C=CC(=C3)C)C=1)C SZEDGFFAIDSOQK-QFIPXVFZSA-N 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- TYFDPTNOAQWDOO-QFIPXVFZSA-N (3R)-3,6,6-trimethyl-1,1-dioxo-3-(8-prop-1-ynyldibenzothiophen-2-yl)-2H-1,4-thiazin-5-amine Chemical compound NC1=N[C@@](CS(C1(C)C)(=O)=O)(C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1)C TYFDPTNOAQWDOO-QFIPXVFZSA-N 0.000 claims 2
- KYWPORDLBGCZCA-NRFANRHFSA-N (3R)-3,6,6-trimethyl-3-(2-methyl-6,11-dihydro-5H-pyrido[2,3-b][1]benzazepin-9-yl)-1,1-dioxo-2H-1,4-thiazin-5-amine Chemical compound N=C1N[C@@](CS(C1(C)C)(=O)=O)(C=1C=CC2=C(NC3=C(CC2)C=CC(=N3)C)C=1)C KYWPORDLBGCZCA-NRFANRHFSA-N 0.000 claims 2
- FNKAXYGBMALXGW-NRFANRHFSA-N (3R)-3,6,6-trimethyl-3-(9-methyl-5,5-dioxo-6,11-dihydrobenzo[c][1,5]benzothiazepin-2-yl)-1,1-dioxo-2H-1,4-thiazin-5-amine Chemical compound N=C1C(S(C[C@@](N1)(C)C1=CC2=C(S(CC3=C(N2)C=C(C=C3)C)(=O)=O)C=C1)(=O)=O)(C)C FNKAXYGBMALXGW-NRFANRHFSA-N 0.000 claims 2
- KGKREPAGYWRXPP-QFIPXVFZSA-N (3R)-3-(3-fluoro-8-prop-1-ynyldibenzothiophen-2-yl)-3,6,6-trimethyl-1,1-dioxo-2H-1,4-thiazin-5-amine Chemical compound NC1=N[C@](CS(C1(C)C)(=O)=O)(C)C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1F KGKREPAGYWRXPP-QFIPXVFZSA-N 0.000 claims 2
- KWRKQLLZTAYYTI-NRFANRHFSA-N (3R)-5-amino-1,3-dimethyl-3-(8-prop-1-ynyldibenzothiophen-2-yl)-2H-pyrazin-6-one Chemical compound CC#Cc1ccc2sc3ccc(cc3c2c1)[C@]1(C)CN(C)C(=O)C(N)=N1 KWRKQLLZTAYYTI-NRFANRHFSA-N 0.000 claims 2
- YZFSPSBGKUKIIH-LJQANCHMSA-N (4R)-5,5-difluoro-4-methyl-4-(8-prop-1-ynyldibenzothiophen-2-yl)-6H-1,3-oxazin-2-amine Chemical compound FC1([C@](NC(OC1)=N)(C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1)C)F YZFSPSBGKUKIIH-LJQANCHMSA-N 0.000 claims 2
- UDJZDQVQVXPDRT-HSZRJFAPSA-N (6R)-2-amino-6-cyclopropyl-3-methyl-6-(8-prop-1-ynyldibenzothiophen-2-yl)-5H-pyrimidin-4-one Chemical compound CC#Cc1ccc2sc3ccc(cc3c2c1)[C@@]1(CC(=O)N(C)C(N)=N1)C1CC1 UDJZDQVQVXPDRT-HSZRJFAPSA-N 0.000 claims 2
- AYJQECPHSZARBB-NRFANRHFSA-N (6R)-6-(7-fluoro-8-prop-1-ynyldibenzothiophen-2-yl)-6-methyl-4,4-dioxo-4lambda6-thia-7-azaspiro[2.5]oct-7-en-8-amine Chemical compound FC1=CC2=C(C3=C(S2)C=CC(=C3)[C@@]2(CS(C3(CC3)C(N2)=N)(=O)=O)C)C=C1C#CC AYJQECPHSZARBB-NRFANRHFSA-N 0.000 claims 2
- UISDNDOYIIVJRO-NRFANRHFSA-N (6R)-6-methyl-4,4-dioxo-6-(8-prop-1-ynyldibenzothiophen-2-yl)-4lambda6-thia-7-azaspiro[2.5]oct-7-en-8-amine Chemical compound N=C1N[C@@](CS(C11CC1)(=O)=O)(C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1)C UISDNDOYIIVJRO-NRFANRHFSA-N 0.000 claims 2
- RGJTZWPFWJCREO-NRFANRHFSA-N (6S)-2-amino-3,6-dimethyl-6-(8-prop-1-ynyldibenzofuran-2-yl)-5H-pyrimidin-4-one Chemical compound N=C1N[C@@](CC(N1C)=O)(C1=CC2=C(OC3=C2C=C(C=C3)C#CC)C=C1)C RGJTZWPFWJCREO-NRFANRHFSA-N 0.000 claims 2
- DPXVUTUGNIOPIB-SFHVURJKSA-N (6S)-2-amino-3,6-dimethyl-6-[8-(trifluoromethyl)dibenzothiophen-2-yl]-5H-pyrimidin-4-one Chemical compound NC1=N[C@@](CC(N1C)=O)(C1=CC2=C(SC3=C2C=C(C=C3)C(F)(F)F)C=C1)C DPXVUTUGNIOPIB-SFHVURJKSA-N 0.000 claims 2
- WOTUUUZFIWUIGA-QFIPXVFZSA-N (6S)-2-amino-3-(2,2-difluoroethyl)-6-methyl-6-(8-prop-1-ynyldibenzothiophen-2-yl)-5H-pyrimidin-4-one Chemical compound FC(CN1C(N[C@@](CC1=O)(C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1)C)=N)F WOTUUUZFIWUIGA-QFIPXVFZSA-N 0.000 claims 2
- MRVOXMFCXREREJ-QHCPKHFHSA-N (6S)-2-amino-3-(2-methoxyethyl)-6-methyl-6-(8-prop-1-ynyldibenzothiophen-2-yl)-5H-pyrimidin-4-one Chemical compound N=C1N[C@@](CC(N1CCOC)=O)(C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1)C MRVOXMFCXREREJ-QHCPKHFHSA-N 0.000 claims 2
- CQZXFAARULDROS-SFHVURJKSA-N (6S)-2-amino-6-(8-bromodibenzothiophen-2-yl)-3,6-dimethyl-5H-pyrimidin-4-one Chemical compound CN1C(N)=N[C@@](C)(CC1=O)c1ccc2sc3ccc(Br)cc3c2c1 CQZXFAARULDROS-SFHVURJKSA-N 0.000 claims 2
- RJFGEEPBVTVJQR-NRFANRHFSA-N (6S)-2-amino-6-(9,9-difluoro-6-prop-1-ynylfluoren-3-yl)-3,6-dimethyl-5H-pyrimidin-4-one Chemical compound FC1(C2=CC=C(C=C2C=2C=C(C=CC1=2)[C@@]1(CC(N(C(N1)=N)C)=O)C)C#CC)F RJFGEEPBVTVJQR-NRFANRHFSA-N 0.000 claims 2
- MYPHJXVDVQRMEI-DEOSSOPVSA-N (6S)-2-amino-6-(9,9-dimethyl-6-prop-1-ynylfluoren-3-yl)-3,6-dimethyl-5H-pyrimidin-4-one Chemical compound CC#Cc1ccc2c(c1)-c1cc(ccc1C2(C)C)[C@]1(C)CC(=O)N(C)C(N)=N1 MYPHJXVDVQRMEI-DEOSSOPVSA-N 0.000 claims 2
- YLHQLLAHILJOTD-QFIPXVFZSA-N (6S)-2-amino-6-[8-(diethylamino)dibenzothiophen-2-yl]-3,6-dimethyl-5H-pyrimidin-4-one Chemical compound CCN(CC)c1ccc2sc3ccc(cc3c2c1)[C@]1(C)CC(=O)N(C)C(N)=N1 YLHQLLAHILJOTD-QFIPXVFZSA-N 0.000 claims 2
- LSXNEPXGNJUKRN-LJAQVGFWSA-N [(Z)-[(4S)-1,4-dimethyl-6-oxo-4-(8-prop-1-ynyldibenzothiophen-2-yl)-1,3-diazinan-2-ylidene]amino]methyl benzoate Chemical compound C(C1=CC=CC=C1)(=O)OC\N=C\1/N(C(C[C@](N/1)(C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1)C)=O)C LSXNEPXGNJUKRN-LJAQVGFWSA-N 0.000 claims 2
- LQZXSFWASQHLEU-UMSFTDKQSA-N [(Z)-[(4S)-1,4-dimethyl-6-oxo-4-(8-prop-1-ynyldibenzothiophen-2-yl)-1,3-diazinan-2-ylidene]amino]methyl dodecanoate Chemical compound C(CCCCCCCCCCC)(=O)OC\N=C\1/N(C(C[C@](N/1)(C1=CC2=C(SC3=C2C=C(C=C3)C#CC)C=C1)C)=O)C LQZXSFWASQHLEU-UMSFTDKQSA-N 0.000 claims 2
- HFLOJEVMDZVPNT-NVAPDCRFSA-N (3R)-3,6,6-trimethyl-1,1-dioxo-3-[(1R,2R)-2-[(5-prop-1-ynyl-1,2-benzoxazol-3-yl)methyl]cyclopropyl]-2H-1,4-thiazin-5-amine Chemical compound N=C1N[C@@](CS(C1(C)C)(=O)=O)([C@H]1[C@H](C1)CC1=NOC2=C1C=C(C=C2)C#CC)C HFLOJEVMDZVPNT-NVAPDCRFSA-N 0.000 claims 1
- PVWJIGZZQKXFRC-REDKUUPNSA-N (3R)-3,6,6-trimethyl-1,1-dioxo-3-[(1R,2R)-2-[(5-prop-1-ynyl-1-benzothiophen-3-yl)methyl]cyclopropyl]-2H-1,4-thiazin-5-amine Chemical compound N=C1N[C@@](CS(C1(C)C)(=O)=O)([C@H]1[C@H](C1)CC=1C2=C(SC=1)C=CC(=C2)C#CC)C PVWJIGZZQKXFRC-REDKUUPNSA-N 0.000 claims 1
- OZBYFDJFHSRROP-BEFAXECRSA-N (3R)-3,6,6-trimethyl-1,1-dioxo-3-[(3R)-1-(4-prop-1-ynylpyridin-2-yl)pyrrolidin-3-yl]-2H-1,4-thiazin-5-amine Chemical compound N=C1N[C@@](CS(C1(C)C)(=O)=O)([C@H]1CN(CC1)C1=NC=CC(=C1)C#CC)C OZBYFDJFHSRROP-BEFAXECRSA-N 0.000 claims 1
- CJJVOGGLKBNGFN-FQEVSTJZSA-N (3R)-3-[2-(2,4-dimethyl-1,3-oxazol-5-yl)indolizin-7-yl]-3,6,6-trimethyl-1,1-dioxo-2H-1,4-thiazin-5-amine Chemical compound CC=1OC(=C(N=1)C)C=1C=C2C=C(C=CN2C=1)[C@@]1(CS(C(C(N1)=N)(C)C)(=O)=O)C CJJVOGGLKBNGFN-FQEVSTJZSA-N 0.000 claims 1
- IHSBXFYIRGZLBH-FQEVSTJZSA-N (5R)-2,5-dimethyl-1,1-dioxo-5-(8-prop-1-ynyldibenzothiophen-2-yl)-6H-1,2,4-thiadiazin-3-amine Chemical compound CC#Cc1ccc2sc3ccc(cc3c2c1)[C@]1(C)CS(=O)(=O)N(C)C(N)=N1 IHSBXFYIRGZLBH-FQEVSTJZSA-N 0.000 claims 1
- IXONLFNIVJIZSG-KRWDZBQOSA-N (6S)-2-amino-3,6-dimethyl-6-(3-prop-1-ynyl-1H-indol-5-yl)-5H-pyrimidin-4-one Chemical compound N=C1N[C@@](CC(N1C)=O)(C=1C=C2C(=CNC2=CC=1)C#CC)C IXONLFNIVJIZSG-KRWDZBQOSA-N 0.000 claims 1
- LIGAUMZFOCJESW-SFHVURJKSA-N (6S)-2-amino-3,6-dimethyl-6-(3-prop-1-ynylquinolin-6-yl)-5H-pyrimidin-4-one Chemical compound N=C1N[C@@](CC(N1C)=O)(C=1C=C2C=C(C=NC2=CC=1)C#CC)C LIGAUMZFOCJESW-SFHVURJKSA-N 0.000 claims 1
- FPXDGVFYCLFFMH-SFHVURJKSA-N (6S)-2-amino-3,6-dimethyl-6-(6-prop-1-ynylquinolin-3-yl)-5H-pyrimidin-4-one Chemical compound N=C1N[C@@](CC(N1C)=O)(C=1C=NC2=CC=C(C=C2C=1)C#CC)C FPXDGVFYCLFFMH-SFHVURJKSA-N 0.000 claims 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61K31/54—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
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- 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
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
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- 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
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| US10947223B2 (en) | 2016-12-15 | 2021-03-16 | Amgen Inc. | Substituted oxazines as beta-secretase inhibitors |
| CA3047287A1 (en) | 2016-12-15 | 2018-06-21 | Amgen Inc. | Cyclopropyl fused thiazine derivatives as beta-secretase inhibitors and methods of use |
| JP7148518B2 (ja) | 2016-12-15 | 2022-10-05 | アムジエン・インコーポレーテツド | β-セクレターゼ阻害剤としての二環式チアジンおよびオキサジン誘導体ならびに使用方法 |
| MX387729B (es) * | 2016-12-15 | 2025-03-18 | Amgen Inc | Derivados de dióxido de 1,4-tiazina y dióxido 1,2,4-tiadiazina como inhibidores de beta-secretasa y métodos de uso. |
| WO2018112083A1 (en) | 2016-12-15 | 2018-06-21 | Amgen Inc. | Thiazine derivatives as beta-secretase inhibitors and methods of use |
| GB201805816D0 (en) * | 2018-04-06 | 2018-05-23 | Ucb Biopharma Sprl | Therapeutic agents |
| CN109180670A (zh) * | 2018-09-17 | 2019-01-11 | 广东东阳光药业有限公司 | 亚氨基噻二嗪二氧化物衍生物及其用途 |
| CN109180672A (zh) * | 2018-09-29 | 2019-01-11 | 广东东阳光药业有限公司 | 亚氨基噻二嗪二氧化物衍生物及其用途 |
| CN109796447B (zh) * | 2019-01-07 | 2020-03-13 | 广东东阳光药业有限公司 | 亚氨基噻二嗪二氧化物衍生物及其用途 |
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| US7763609B2 (en) | 2003-12-15 | 2010-07-27 | Schering Corporation | Heterocyclic aspartyl protease inhibitors |
| CN101084199A (zh) * | 2004-10-15 | 2007-12-05 | 阿斯利康(瑞典)有限公司 | 取代的氨基化合物及其用途 |
| AU2006307314C1 (en) * | 2005-10-25 | 2011-08-25 | Shionogi & Co., Ltd. | Aminodihydrothiazine derivative |
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| ES2476605T3 (es) * | 2007-04-24 | 2014-07-15 | Shionogi & Co., Ltd. | Derivados de aminohidrotiazina sustituidos con grupos cíclicos |
| EP2161271A1 (en) * | 2008-09-08 | 2010-03-10 | Università Degli Studi Di Milano - Bicocca | Alpha-carboline inhibitors of NMP-ALK, RET, and Bcr-Abl |
| UA108363C2 (uk) * | 2009-10-08 | 2015-04-27 | Похідні імінотіадіазиндіоксиду як інгібітори bace, композиція на їх основі і їх застосування | |
| US8815881B2 (en) * | 2010-08-09 | 2014-08-26 | Hoffmann-La Roche Inc. | 1,4,5,6-tetrahydro-pyrimidin-2-ylamine compounds |
| EP2694489B1 (en) * | 2011-04-07 | 2017-09-06 | Merck Sharp & Dohme Corp. | C5-c6 oxacyclic-fused thiadiazine dioxide compounds as bace inhibitors, compositions, and their use |
| US9145426B2 (en) | 2011-04-07 | 2015-09-29 | Merck Sharp & Dohme Corp. | Pyrrolidine-fused thiadiazine dioxide compounds as BACE inhibitors, compositions, and their use |
| CN103596939A (zh) * | 2011-04-13 | 2014-02-19 | 默沙东公司 | 作为bace抑制剂的5-取代的亚氨基噻嗪类及其单和二氧化物、组合物及其应用 |
| AU2012243329B2 (en) * | 2011-04-13 | 2015-09-17 | Merck Sharp & Dohme Corp. | 5-substituted iminothiazines and their mono-and dioxides as BACE inhibitors,compositions,and their use |
| KR20140054295A (ko) * | 2011-08-22 | 2014-05-08 | 머크 샤프 앤드 돔 코포레이션 | Bace 억제제로서의 2-스피로-치환된 이미노티아진 및 그의 모노- 및 디옥시드, 조성물 및 그의 용도 |
| US9416129B2 (en) * | 2012-10-17 | 2016-08-16 | Merck Sharp & Dohme Corp. | Tricyclic substituted thiadiazine dioxide compounds as BACE inhibitors, compositions and their use |
| CA2825821A1 (en) * | 2013-08-28 | 2015-02-28 | Chiesi Farmaceutici S.P.A. | 1-phenylalkanecarboxylic acid derivatives for the treatment of alzheimer's disease and multiple sclerosis |
| CN104910238B (zh) | 2014-03-14 | 2017-08-11 | 中国科学院上海药物研究所 | 一类五环三萜类化合物及其在制备治疗阿尔兹海默病的药物中的用途 |
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| TW201702240A (zh) | 2017-01-16 |
| JP6765681B2 (ja) | 2020-10-07 |
| WO2016172255A1 (en) | 2016-10-27 |
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