BR112016030787B1 - Entidade química, composição farmacêutica e seu uso - Google Patents
Entidade química, composição farmacêutica e seu uso Download PDFInfo
- Publication number
- BR112016030787B1 BR112016030787B1 BR112016030787-9A BR112016030787A BR112016030787B1 BR 112016030787 B1 BR112016030787 B1 BR 112016030787B1 BR 112016030787 A BR112016030787 A BR 112016030787A BR 112016030787 B1 BR112016030787 B1 BR 112016030787B1
- Authority
- BR
- Brazil
- Prior art keywords
- methyl
- amino
- pyrimidin
- carbonyl
- thienyl
- Prior art date
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- 150000005829 chemical entities Chemical class 0.000 title claims abstract description 171
- 239000008194 pharmaceutical composition Substances 0.000 title claims abstract description 15
- 150000003839 salts Chemical class 0.000 claims abstract description 77
- 150000001875 compounds Chemical class 0.000 claims abstract description 55
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 524
- GBLRQXKSCRCLBZ-YVQAASCFSA-N (1R,2S,1'R,2'S)-doxacurium Chemical compound COC1=C(OC)C(OC)=CC(C[C@H]2[N@+](CCC3=C2C(=C(OC)C(OC)=C3)OC)(C)CCCOC(=O)CCC(=O)OCCC[N@@+]2(C)[C@@H](C3=C(OC)C(OC)=C(OC)C=C3CC2)CC=2C=C(OC)C(OC)=C(OC)C=2)=C1 GBLRQXKSCRCLBZ-YVQAASCFSA-N 0.000 claims description 400
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 399
- 229910052739 hydrogen Inorganic materials 0.000 claims description 328
- 239000001257 hydrogen Substances 0.000 claims description 328
- -1 cyano, amino Chemical group 0.000 claims description 298
- 125000004527 pyrimidin-4-yl group Chemical group N1=CN=C(C=C1)* 0.000 claims description 297
- IIACRCGMVDHOTQ-UHFFFAOYSA-M sulfamate Chemical compound NS([O-])(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-M 0.000 claims description 192
- 125000001931 aliphatic group Chemical group 0.000 claims description 156
- 125000000623 heterocyclic group Chemical group 0.000 claims description 149
- 150000002431 hydrogen Chemical class 0.000 claims description 141
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 126
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 111
- LXRZVMYMQHNYJB-UNXOBOICSA-N [(1R,2S,4R)-4-[[5-[4-[(1R)-7-chloro-1,2,3,4-tetrahydroisoquinolin-1-yl]-5-methylthiophene-2-carbonyl]pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound CC1=C(C=C(S1)C(=O)C1=C(N[C@H]2C[C@H](O)[C@@H](COS(N)(=O)=O)C2)N=CN=C1)[C@@H]1NCCC2=C1C=C(Cl)C=C2 LXRZVMYMQHNYJB-UNXOBOICSA-N 0.000 claims description 108
- 229910052736 halogen Inorganic materials 0.000 claims description 106
- 150000002367 halogens Chemical group 0.000 claims description 102
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 98
- 229910052731 fluorine Inorganic materials 0.000 claims description 97
- 239000011737 fluorine Substances 0.000 claims description 96
- 125000003118 aryl group Chemical group 0.000 claims description 93
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 88
- 238000000634 powder X-ray diffraction Methods 0.000 claims description 76
- 229910052757 nitrogen Inorganic materials 0.000 claims description 73
- 239000000460 chlorine Substances 0.000 claims description 67
- 229910052801 chlorine Inorganic materials 0.000 claims description 67
- 229910052760 oxygen Inorganic materials 0.000 claims description 66
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 65
- 125000001072 heteroaryl group Chemical group 0.000 claims description 63
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 62
- 125000005842 heteroatom Chemical group 0.000 claims description 60
- 229910052799 carbon Inorganic materials 0.000 claims description 59
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 54
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 52
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 51
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 48
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 48
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 42
- 229910052717 sulfur Inorganic materials 0.000 claims description 40
- 150000001721 carbon Chemical group 0.000 claims description 39
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 38
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 34
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims description 32
- 229910052794 bromium Inorganic materials 0.000 claims description 30
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 29
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 29
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 29
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 28
- 125000004428 fluoroalkoxy group Chemical group 0.000 claims description 27
- 125000002947 alkylene group Chemical group 0.000 claims description 26
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 25
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 24
- 239000001301 oxygen Chemical group 0.000 claims description 24
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 23
- 239000011593 sulfur Chemical group 0.000 claims description 23
- 206010028980 Neoplasm Diseases 0.000 claims description 22
- 125000001424 substituent group Chemical group 0.000 claims description 22
- 201000011510 cancer Diseases 0.000 claims description 20
- 238000002360 preparation method Methods 0.000 claims description 20
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 17
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 16
- 125000000217 alkyl group Chemical group 0.000 claims description 16
- 125000000325 methylidene group Chemical group [H]C([H])=* 0.000 claims description 16
- 239000003814 drug Substances 0.000 claims description 12
- 125000001153 fluoro group Chemical group F* 0.000 claims description 12
- 229910052703 rhodium Inorganic materials 0.000 claims description 12
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 10
- 125000004008 6 membered carbocyclic group Chemical group 0.000 claims description 8
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 8
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000002883 imidazolyl group Chemical group 0.000 claims description 6
- 125000001041 indolyl group Chemical group 0.000 claims description 5
- 125000005647 linker group Chemical group 0.000 claims description 5
- 125000001544 thienyl group Chemical group 0.000 claims description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 2
- 229940079593 drug Drugs 0.000 claims description 2
- BTXCHYCUHBGRMK-UHFFFAOYSA-N amino sulfamate Chemical compound NOS(N)(=O)=O BTXCHYCUHBGRMK-UHFFFAOYSA-N 0.000 claims 21
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 13
- QWODOYQWTQYIQP-UHFFFAOYSA-N cyclopentyl sulfamate Chemical compound NS(=O)(=O)OC1CCCC1 QWODOYQWTQYIQP-UHFFFAOYSA-N 0.000 claims 5
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 claims 4
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 claims 3
- FIYXUOWXHWJDAM-UHFFFAOYSA-N methyl sulfamate Chemical compound COS(N)(=O)=O FIYXUOWXHWJDAM-UHFFFAOYSA-N 0.000 claims 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 3
- 125000004938 5-pyridyl group Chemical group N1=CC=CC(=C1)* 0.000 claims 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 2
- DXASQZJWWGZNSF-UHFFFAOYSA-N n,n-dimethylmethanamine;sulfur trioxide Chemical group CN(C)C.O=S(=O)=O DXASQZJWWGZNSF-UHFFFAOYSA-N 0.000 claims 2
- 125000003107 substituted aryl group Chemical group 0.000 claims 2
- 125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 claims 2
- YVWMYFBCZXSSIW-UHFFFAOYSA-N 2-(4-phosphonooxyphenyl)acetic acid Chemical compound OC(=O)CC1=CC=C(OP(O)(O)=O)C=C1 YVWMYFBCZXSSIW-UHFFFAOYSA-N 0.000 claims 1
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims 1
- AGPKZVBTJJNPAG-WHFBIAKZSA-N L-isoleucine Chemical compound CC[C@H](C)[C@H](N)C(O)=O AGPKZVBTJJNPAG-WHFBIAKZSA-N 0.000 claims 1
- KZSNJWFQEVHDMF-BYPYZUCNSA-N L-valine Chemical compound CC(C)[C@H](N)C(O)=O KZSNJWFQEVHDMF-BYPYZUCNSA-N 0.000 claims 1
- GMWFKCZAZBSPSL-XAMZUMDUSA-N [(1R,2R,3S,4R)-2,3-dihydroxy-4-[[5-(5-phenylfuran-2-carbonyl)pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H]([C@H]([C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC(=CC=1)C1=CC=CC=C1)O)O)(=O)=O GMWFKCZAZBSPSL-XAMZUMDUSA-N 0.000 claims 1
- OLUZHLGPXCAXQN-JTYAGIKBSA-N [(1R,2R,3S,4R)-4-[[2-chloro-5-(5-phenylfuran-2-carbonyl)pyrimidin-4-yl]amino]-2,3-dihydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H]([C@H]([C@@H](C1)NC1=NC(=NC=C1C(=O)C=1OC(=CC=1)C1=CC=CC=C1)Cl)O)O)(=O)=O OLUZHLGPXCAXQN-JTYAGIKBSA-N 0.000 claims 1
- BNUNUBSDPLCMIP-QTRJSKNGSA-N [(1R,2R,3S,4R)-4-[[5-(5-benzylfuran-2-carbonyl)pyrimidin-4-yl]amino]-2,3-dihydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H]([C@H]([C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC(=CC=1)CC1=CC=CC=C1)O)O)(=O)=O BNUNUBSDPLCMIP-QTRJSKNGSA-N 0.000 claims 1
- HQEWNFAQYBRCGY-QTRJSKNGSA-N [(1R,2R,3S,4R)-4-[[5-(5-benzylthiophene-2-carbonyl)pyrimidin-4-yl]amino]-2,3-dihydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H]([C@H]([C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC(=CC=1)CC1=CC=CC=C1)O)O)(=O)=O HQEWNFAQYBRCGY-QTRJSKNGSA-N 0.000 claims 1
- ZRXJRPCREKSXLD-JGZGQIEPSA-N [(1R,2R,3S,4R)-4-[[5-[5-(2-chlorophenyl)furan-2-carbonyl]pyrimidin-4-yl]amino]-2,3-dihydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H]([C@H]([C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC(=CC=1)C1=C(C=CC=C1)Cl)O)O)(=O)=O ZRXJRPCREKSXLD-JGZGQIEPSA-N 0.000 claims 1
- ZCZSYZWFGJGPAH-RKVPGOIHSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-(5-methyl-4-phenylsulfanylthiophene-2-carbonyl)pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC(=C(C=1)SC1=CC=CC=C1)C)O)(=O)=O ZCZSYZWFGJGPAH-RKVPGOIHSA-N 0.000 claims 1
- URWODEDLSUOSKF-QKCSRTOESA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(2-hydroxypropan-2-yl)furan-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl nitrate Chemical compound CC(C)(C1=COC(=C1)C(=O)C2=CN=CN=C2N[C@@H]3C[C@@H]([C@H](C3)O)CO[N+](=O)[O-])O URWODEDLSUOSKF-QKCSRTOESA-N 0.000 claims 1
- KSWJWCOPHNDJIQ-GGPKGHCWSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(2-phenylethyl)thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)CCC1=CC=CC=C1)O)(=O)=O KSWJWCOPHNDJIQ-GGPKGHCWSA-N 0.000 claims 1
- PDKIBWNJLCSCDU-WZRBSPASSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(hydroxymethyl)furan-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC=C(C=1)CO)O)(=O)=O PDKIBWNJLCSCDU-WZRBSPASSA-N 0.000 claims 1
- LHRSDZIFNCMQCE-WZRBSPASSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(hydroxymethyl)thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)CO)O)(=O)=O LHRSDZIFNCMQCE-WZRBSPASSA-N 0.000 claims 1
- SQFDXJWOWULRJS-BZPMIXESSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(methoxymethyl)furan-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC=C(C=1)COC)O)(=O)=O SQFDXJWOWULRJS-BZPMIXESSA-N 0.000 claims 1
- OIQNLHOWKQGOTO-BZPMIXESSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(methoxymethyl)thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)COC)O)(=O)=O OIQNLHOWKQGOTO-BZPMIXESSA-N 0.000 claims 1
- HRJLEENWYWQALR-MDZRGWNJSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(phenoxymethyl)thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)COC1=CC=CC=C1)O)(=O)=O HRJLEENWYWQALR-MDZRGWNJSA-N 0.000 claims 1
- UWVLISLOPZNVBS-MDZRGWNJSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-(phenylsulfanylmethyl)thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)CSC1=CC=CC=C1)O)(=O)=O UWVLISLOPZNVBS-MDZRGWNJSA-N 0.000 claims 1
- RCQSNQIUSRZIBG-SUMDDJOVSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-[(3-iodophenyl)methyl]thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)CC1=CC(=CC=C1)I)O)(=O)=O RCQSNQIUSRZIBG-SUMDDJOVSA-N 0.000 claims 1
- DVKCOVBTUXFBLH-HLIPFELVSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-[(3-methoxyphenyl)methyl]thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)CC1=CC(=CC=C1)OC)O)(=O)=O DVKCOVBTUXFBLH-HLIPFELVSA-N 0.000 claims 1
- HCMUBBHTSFDSRP-GGPKGHCWSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-[(3-methylphenyl)methyl]furan-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC=C(C=1)CC1=CC(=CC=C1)C)O)(=O)=O HCMUBBHTSFDSRP-GGPKGHCWSA-N 0.000 claims 1
- BJSPVARPZQVHCZ-GGPKGHCWSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[4-[(3-methylphenyl)methyl]thiophene-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)CC1=CC(=CC=C1)C)O)(=O)=O BJSPVARPZQVHCZ-GGPKGHCWSA-N 0.000 claims 1
- VSOHAUTWFIIXRU-BREBYQMCSA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[5-(hydroxymethyl)furan-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC(=CC=1)CO)O)(=O)=O VSOHAUTWFIIXRU-BREBYQMCSA-N 0.000 claims 1
- LEKZKECGNGEWBQ-GYSYKLTISA-N [(1R,2S,4R)-2-hydroxy-4-[[5-[5-(methoxymethyl)furan-2-carbonyl]pyrimidin-4-yl]amino]cyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC(=CC=1)COC)O)(=O)=O LEKZKECGNGEWBQ-GYSYKLTISA-N 0.000 claims 1
- CXZVYQZESKGQJG-OYRHQHFDSA-N [(1R,2S,4R)-4-[[5-(4,5-dibenzylfuran-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC(=C(C=1)CC1=CC=CC=C1)CC1=CC=CC=C1)O)(=O)=O CXZVYQZESKGQJG-OYRHQHFDSA-N 0.000 claims 1
- VVAATQOKCQZITB-OYRHQHFDSA-N [(1R,2S,4R)-4-[[5-(4,5-dibenzylthiophene-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC(=C(C=1)CC1=CC=CC=C1)CC1=CC=CC=C1)O)(=O)=O VVAATQOKCQZITB-OYRHQHFDSA-N 0.000 claims 1
- DLCWAGWRPPFZMP-BREBYQMCSA-N [(1R,2S,4R)-4-[[5-(4-acetyl-5-chlorothiophene-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC(=C(C=1)C(C)=O)Cl)O)(=O)=O DLCWAGWRPPFZMP-BREBYQMCSA-N 0.000 claims 1
- DVRGJYPOUNPDBF-BZPMIXESSA-N [(1R,2S,4R)-4-[[5-(4-acetylfuran-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC=C(C=1)C(C)=O)O)(=O)=O DVRGJYPOUNPDBF-BZPMIXESSA-N 0.000 claims 1
- YJYSEDLYNWJECJ-QKCSRTOESA-N [(1R,2S,4R)-4-[[5-(4-acetylthiophene-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC=C(C=1)C(C)=O)O)(=O)=O YJYSEDLYNWJECJ-QKCSRTOESA-N 0.000 claims 1
- JDUOHLXIAXEAQX-CPUCHLNUSA-N [(1R,2S,4R)-4-[[5-(4-benzoyl-5-chlorothiophene-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC(=C(C=1)C(C1=CC=CC=C1)=O)Cl)O)(=O)=O JDUOHLXIAXEAQX-CPUCHLNUSA-N 0.000 claims 1
- LFAHBAQSIFIHRN-KYJSFNMBSA-N [(1R,2S,4R)-4-[[5-(4-benzoylfuran-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1OC=C(C=1)C(C1=CC=CC=C1)=O)O)(=O)=O LFAHBAQSIFIHRN-KYJSFNMBSA-N 0.000 claims 1
- WYLMPZNGCIDRFA-NUJGCVRESA-N [(1R,2S,4R)-4-[[5-(4-benzyl-5-chlorothiophene-2-carbonyl)pyrimidin-4-yl]amino]-2-hydroxycyclopentyl]methyl sulfamate Chemical compound S(N)(OC[C@@H]1[C@H](C[C@@H](C1)NC1=NC=NC=C1C(=O)C=1SC(=C(C=1)CC1=CC=CC=C1)Cl)O)(=O)=O WYLMPZNGCIDRFA-NUJGCVRESA-N 0.000 claims 1
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
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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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- C07F9/02—Phosphorus compounds
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/655—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms
- C07F9/6552—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring
- C07F9/65522—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having oxygen atoms, with or without sulfur, selenium, or tellurium atoms, as the only ring hetero atoms the oxygen atom being part of a six-membered ring condensed with carbocyclic rings or carbocyclic ring systems
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- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6558—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system
- C07F9/65586—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing at least two different or differently substituted hetero rings neither condensed among themselves nor condensed with a common carbocyclic ring or ring system at least one of the hetero rings does not contain nitrogen as ring hetero atom
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| PCT/US2015/038712 WO2016004136A1 (en) | 2014-07-01 | 2015-06-30 | Heteroaryl compounds useful as inhibitors of sumo activating enzyme |
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2015
- 2015-06-30 PT PT158153304T patent/PT3164130T/pt unknown
- 2015-06-30 JP JP2017521031A patent/JP6603712B2/ja active Active
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