CA2886322A1 - Antiviral compounds - Google Patents
Antiviral compounds Download PDFInfo
- Publication number
- CA2886322A1 CA2886322A1 CA2886322A CA2886322A CA2886322A1 CA 2886322 A1 CA2886322 A1 CA 2886322A1 CA 2886322 A CA2886322 A CA 2886322A CA 2886322 A CA2886322 A CA 2886322A CA 2886322 A1 CA2886322 A1 CA 2886322A1
- Authority
- CA
- Canada
- Prior art keywords
- alkyl
- independently
- independently selected
- aryl
- optionally substituted
- 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 561
- 230000000840 anti-viral effect Effects 0.000 title abstract 2
- 125000000217 alkyl group Chemical group 0.000 claims description 888
- 125000000623 heterocyclic group Chemical group 0.000 claims description 519
- 125000003118 aryl group Chemical group 0.000 claims description 424
- 125000001188 haloalkyl group Chemical group 0.000 claims description 309
- 125000003710 aryl alkyl group Chemical group 0.000 claims description 308
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 280
- 125000003545 alkoxy group Chemical group 0.000 claims description 270
- 125000005843 halogen group Chemical group 0.000 claims description 251
- -1 -CCl3 Chemical group 0.000 claims description 236
- 125000003342 alkenyl group Chemical group 0.000 claims description 205
- 125000004438 haloalkoxy group Chemical group 0.000 claims description 203
- 229910052739 hydrogen Inorganic materials 0.000 claims description 172
- 239000001257 hydrogen Substances 0.000 claims description 167
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 153
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 152
- 125000000304 alkynyl group Chemical group 0.000 claims description 152
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 148
- 125000004415 heterocyclylalkyl group Chemical group 0.000 claims description 145
- 125000004043 oxo group Chemical group O=* 0.000 claims description 138
- 229910052799 carbon Inorganic materials 0.000 claims description 124
- 125000004966 cyanoalkyl group Chemical group 0.000 claims description 113
- 125000001072 heteroaryl group Chemical group 0.000 claims description 113
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 100
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 80
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 claims description 78
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 73
- 229920006395 saturated elastomer Polymers 0.000 claims description 73
- 125000004963 sulfonylalkyl group Chemical group 0.000 claims description 73
- 125000000392 cycloalkenyl group Chemical group 0.000 claims description 72
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 71
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 71
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 70
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims description 70
- 229910052717 sulfur Inorganic materials 0.000 claims description 69
- 125000000278 alkyl amino alkyl group Chemical group 0.000 claims description 68
- 125000004429 atom Chemical group 0.000 claims description 68
- 150000003839 salts Chemical class 0.000 claims description 68
- 125000004122 cyclic group Chemical group 0.000 claims description 67
- 125000005282 allenyl group Chemical group 0.000 claims description 66
- 125000005129 aryl carbonyl group Chemical group 0.000 claims description 66
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 66
- 125000006517 heterocyclyl carbonyl group Chemical group 0.000 claims description 66
- 150000001721 carbon Chemical group 0.000 claims description 65
- 125000005098 aryl alkoxy carbonyl group Chemical group 0.000 claims description 63
- 125000005099 aryl alkyl carbonyl group Chemical group 0.000 claims description 63
- 229940002612 prodrug Drugs 0.000 claims description 63
- 239000000651 prodrug Substances 0.000 claims description 63
- 125000000033 alkoxyamino group Chemical group 0.000 claims description 61
- 125000004391 aryl sulfonyl group Chemical group 0.000 claims description 57
- 125000001424 substituent group Chemical group 0.000 claims description 57
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims description 53
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 47
- 125000005143 heteroarylsulfonyl group Chemical group 0.000 claims description 46
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims description 45
- 125000005842 heteroatom Chemical group 0.000 claims description 43
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 40
- 125000005159 cyanoalkoxy group Chemical group 0.000 claims description 34
- 125000005180 haloalkoxyalkyloxy group Chemical group 0.000 claims description 34
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 33
- 125000005324 aryloxy alkyloxy group Chemical group 0.000 claims description 33
- 125000005339 cyanocycloalkoxy group Chemical group 0.000 claims description 33
- 125000000000 cycloalkoxy group Chemical group 0.000 claims description 33
- 101100533888 Hypocrea jecorina (strain QM6a) sor4 gene Proteins 0.000 claims description 28
- 101100533877 Hypocrea jecorina (strain QM6a) sor8 gene Proteins 0.000 claims description 28
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims description 28
- 229910052760 oxygen Inorganic materials 0.000 claims description 27
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 27
- 125000002102 aryl alkyloxo group Chemical group 0.000 claims description 20
- 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims description 20
- 229910052757 nitrogen Inorganic materials 0.000 claims description 18
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims description 13
- 125000004686 alkyl sulfanyl alkyl group Chemical group 0.000 claims description 12
- 125000004181 carboxyalkyl group Chemical group 0.000 claims description 11
- 125000005092 alkenyloxycarbonyl group Chemical group 0.000 claims description 10
- 125000004702 alkoxy alkyl carbonyl group Chemical group 0.000 claims description 10
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims description 10
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims description 10
- 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims description 10
- 125000005182 hydroxyalkylcarbonyl group Chemical group 0.000 claims description 10
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims description 9
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims description 9
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 9
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 9
- 101000610557 Homo sapiens U4/U6 small nuclear ribonucleoprotein Prp31 Proteins 0.000 claims description 7
- 101001109965 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 60S ribosomal protein L7-A Proteins 0.000 claims description 7
- 101001109960 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 60S ribosomal protein L7-B Proteins 0.000 claims description 7
- 102100040118 U4/U6 small nuclear ribonucleoprotein Prp31 Human genes 0.000 claims description 7
- 125000002883 imidazolyl group Chemical group 0.000 claims description 7
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 125000004858 cycloalkoxyalkyl group Chemical group 0.000 claims description 6
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims description 5
- 125000002619 bicyclic group Chemical group 0.000 claims description 5
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims description 5
- 125000000165 tricyclic carbocycle group Chemical group 0.000 claims description 5
- 125000000169 tricyclic heterocycle group Chemical group 0.000 claims description 5
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 3
- 125000005127 aryl alkoxy alkyl group Chemical group 0.000 claims description 3
- 125000005326 heteroaryloxy alkyl group Chemical group 0.000 claims description 3
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims description 3
- 125000006163 5-membered heteroaryl group Chemical group 0.000 claims description 2
- 101000726148 Homo sapiens Protein crumbs homolog 1 Proteins 0.000 claims description 2
- 102100027331 Protein crumbs homolog 1 Human genes 0.000 claims description 2
- 101000825534 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 40S ribosomal protein S2 Proteins 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000006626 methoxycarbonylamino group Chemical group 0.000 claims description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 claims 111
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 17
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 claims 13
- 229910020008 S(O) Inorganic materials 0.000 claims 10
- RAHZWNYVWXNFOC-UHFFFAOYSA-N sulfur dioxide Inorganic materials O=S=O RAHZWNYVWXNFOC-UHFFFAOYSA-N 0.000 claims 10
- 125000005018 aryl alkenyl group Chemical group 0.000 claims 8
- 239000008194 pharmaceutical composition Substances 0.000 claims 7
- 208000005176 Hepatitis C Diseases 0.000 claims 6
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 6
- 102000014150 Interferons Human genes 0.000 claims 5
- 108010050904 Interferons Proteins 0.000 claims 5
- 229940079322 interferon Drugs 0.000 claims 5
- 125000002837 carbocyclic group Chemical group 0.000 claims 4
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 239000003814 drug Substances 0.000 claims 4
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 3
- 125000004414 alkyl thio group Chemical group 0.000 claims 3
- 239000003112 inhibitor Substances 0.000 claims 3
- 125000006570 (C5-C6) heteroaryl group Chemical group 0.000 claims 2
- 125000002373 5 membered heterocyclic group Chemical group 0.000 claims 2
- 125000004070 6 membered heterocyclic group Chemical group 0.000 claims 2
- IWUCXVSUMQZMFG-AFCXAGJDSA-N Ribavirin Chemical class N1=C(C(=O)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 IWUCXVSUMQZMFG-AFCXAGJDSA-N 0.000 claims 2
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 claims 2
- 125000005163 aryl sulfanyl group Chemical group 0.000 claims 2
- 125000004104 aryloxy group Chemical group 0.000 claims 2
- 150000001602 bicycloalkyls Chemical group 0.000 claims 2
- 125000004439 haloalkylsulfanyl group Chemical group 0.000 claims 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims 2
- 125000004446 heteroarylalkyl group Chemical group 0.000 claims 2
- 125000005553 heteroaryloxy group Chemical group 0.000 claims 2
- 125000000592 heterocycloalkyl group Chemical group 0.000 claims 2
- 125000004449 heterocyclylalkenyl group Chemical group 0.000 claims 2
- 125000005113 hydroxyalkoxy group Chemical group 0.000 claims 2
- 239000002777 nucleoside Substances 0.000 claims 2
- 229940127073 nucleoside analogue Drugs 0.000 claims 2
- 125000003003 spiro group Chemical group 0.000 claims 2
- 229940124597 therapeutic agent Drugs 0.000 claims 2
- IWUCXVSUMQZMFG-RGDLXGNYSA-N 1-[(2s,3s,4r,5s)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-1,2,4-triazole-3-carboxamide Chemical compound N1=C(C(=O)N)N=CN1[C@@H]1[C@@H](O)[C@@H](O)[C@H](CO)O1 IWUCXVSUMQZMFG-RGDLXGNYSA-N 0.000 claims 1
- TZYVRXZQAWPIAB-FCLHUMLKSA-N 5-amino-3-[(2r,3r,4s,5r)-3,4-dihydroxy-5-(hydroxymethyl)oxolan-2-yl]-4h-[1,3]thiazolo[4,5-d]pyrimidine-2,7-dione Chemical compound O=C1SC=2C(=O)NC(N)=NC=2N1[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1O TZYVRXZQAWPIAB-FCLHUMLKSA-N 0.000 claims 1
- 101001023866 Arabidopsis thaliana Mannosyl-oligosaccharide glucosidase GCS1 Proteins 0.000 claims 1
- 101800001838 Serine protease/helicase NS3 Proteins 0.000 claims 1
- 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 1
- 125000005356 cycloalkylalkenyl group Chemical group 0.000 claims 1
- 125000005357 cycloalkylalkynyl group Chemical group 0.000 claims 1
- 125000005170 cycloalkyloxycarbonyl group Chemical group 0.000 claims 1
- 229940042399 direct acting antivirals protease inhibitors Drugs 0.000 claims 1
- 229940079593 drug Drugs 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000005844 heterocyclyloxy group Chemical group 0.000 claims 1
- 229940047124 interferons Drugs 0.000 claims 1
- 229950003954 isatoribine Drugs 0.000 claims 1
- 238000013160 medical therapy Methods 0.000 claims 1
- 150000003833 nucleoside derivatives Chemical class 0.000 claims 1
- 239000000137 peptide hydrolase inhibitor Substances 0.000 claims 1
- 230000000069 prophylactic effect Effects 0.000 claims 1
- 229960000329 ribavirin Drugs 0.000 claims 1
- HZCAHMRRMINHDJ-DBRKOABJSA-N ribavirin Natural products O[C@@H]1[C@H](O)[C@@H](CO)O[C@H]1N1N=CN=C1 HZCAHMRRMINHDJ-DBRKOABJSA-N 0.000 claims 1
- NHKZSTHOYNWEEZ-AFCXAGJDSA-N taribavirin Chemical compound N1=C(C(=N)N)N=CN1[C@H]1[C@H](O)[C@H](O)[C@@H](CO)O1 NHKZSTHOYNWEEZ-AFCXAGJDSA-N 0.000 claims 1
- 229950006081 taribavirin Drugs 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 238000000034 method Methods 0.000 abstract description 37
- 239000000543 intermediate Substances 0.000 abstract description 9
- 239000000203 mixture Substances 0.000 abstract description 9
- 230000008569 process Effects 0.000 abstract description 6
- 238000002560 therapeutic procedure Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 83
- 239000002253 acid Substances 0.000 description 15
- 238000006243 chemical reaction Methods 0.000 description 14
- 150000002148 esters Chemical class 0.000 description 13
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 13
- 238000003786 synthesis reaction Methods 0.000 description 12
- 229910003827 NRaRb Inorganic materials 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 10
- 239000003153 chemical reaction reagent Substances 0.000 description 10
- 238000000926 separation method Methods 0.000 description 10
- 101001105683 Homo sapiens Pre-mRNA-processing-splicing factor 8 Proteins 0.000 description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 8
- 102100021231 Pre-mRNA-processing-splicing factor 8 Human genes 0.000 description 8
- 101000862778 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) 40S ribosomal protein S3 Proteins 0.000 description 8
- 150000004702 methyl esters Chemical class 0.000 description 7
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 6
- 238000004587 chromatography analysis Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 229910052720 vanadium Inorganic materials 0.000 description 6
- KTVPXOYAKDPRHY-TXICZTDVSA-N 5-O-phosphono-beta-D-ribofuranose Chemical compound O[C@@H]1O[C@H](COP(O)(O)=O)[C@@H](O)[C@H]1O KTVPXOYAKDPRHY-TXICZTDVSA-N 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 5
- 102100036227 Cysteine and histidine-rich protein 1 Human genes 0.000 description 4
- 101000947448 Homo sapiens Cysteine and histidine-rich protein 1 Proteins 0.000 description 4
- 239000007819 coupling partner Substances 0.000 description 4
- 238000006880 cross-coupling reaction Methods 0.000 description 4
- 238000000605 extraction Methods 0.000 description 4
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Substances C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 4
- 230000001404 mediated effect Effects 0.000 description 4
- 229910052763 palladium Inorganic materials 0.000 description 4
- 229910052698 phosphorus Inorganic materials 0.000 description 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 108010002038 rat proteinase inhibitor I Proteins 0.000 description 4
- 229910052703 rhodium Inorganic materials 0.000 description 4
- 230000002378 acidificating effect Effects 0.000 description 3
- 239000012634 fragment Substances 0.000 description 3
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 230000035484 reaction time Effects 0.000 description 3
- 238000006722 reduction reaction Methods 0.000 description 3
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 2
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 101001104102 Homo sapiens X-linked retinitis pigmentosa GTPase regulator Proteins 0.000 description 2
- NFHFRUOZVGFOOS-UHFFFAOYSA-N Pd(PPh3)4 Substances [Pd].C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1.C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 NFHFRUOZVGFOOS-UHFFFAOYSA-N 0.000 description 2
- LOUPRKONTZGTKE-WZBLMQSHSA-N Quinine Chemical compound C([C@H]([C@H](C1)C=C)C2)C[N@@]1[C@@H]2[C@H](O)C1=CC=NC2=CC=C(OC)C=C21 LOUPRKONTZGTKE-WZBLMQSHSA-N 0.000 description 2
- 238000006619 Stille reaction Methods 0.000 description 2
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- 150000001408 amides Chemical class 0.000 description 2
- 150000001499 aryl bromides Chemical class 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 2
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- 229910052731 fluorine Inorganic materials 0.000 description 2
- 238000001640 fractional crystallisation Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000010410 layer Substances 0.000 description 2
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- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
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- WLJVXDMOQOGPHL-UHFFFAOYSA-N phenylacetic acid Chemical compound OC(=O)CC1=CC=CC=C1 WLJVXDMOQOGPHL-UHFFFAOYSA-N 0.000 description 2
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- LPQZERIRKRYGGM-UHFFFAOYSA-N tert-butyl pyrrolidine-1-carboxylate Chemical compound CC(C)(C)OC(=O)N1CCCC1 LPQZERIRKRYGGM-UHFFFAOYSA-N 0.000 description 2
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Natural products C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 2
- 229910052723 transition metal Inorganic materials 0.000 description 2
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- 238000010626 work up procedure Methods 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- NAWXUBYGYWOOIX-SFHVURJKSA-N (2s)-2-[[4-[2-(2,4-diaminoquinazolin-6-yl)ethyl]benzoyl]amino]-4-methylidenepentanedioic acid Chemical compound C1=CC2=NC(N)=NC(N)=C2C=C1CCC1=CC=C(C(=O)N[C@@H](CC(=C)C(O)=O)C(O)=O)C=C1 NAWXUBYGYWOOIX-SFHVURJKSA-N 0.000 description 1
- KIUPCUCGVCGPPA-UHFFFAOYSA-N (5-methyl-2-propan-2-ylcyclohexyl) carbonochloridate Chemical compound CC(C)C1CCC(C)CC1OC(Cl)=O KIUPCUCGVCGPPA-UHFFFAOYSA-N 0.000 description 1
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 1
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-N 0.000 description 1
- DKSYLEFLMUQPDJ-UHFFFAOYSA-N 2-bromo-9,9-difluoro-7-iodofluorene Chemical compound C1=C(I)C=C2C(F)(F)C3=CC(Br)=CC=C3C2=C1 DKSYLEFLMUQPDJ-UHFFFAOYSA-N 0.000 description 1
- XRMDEMQXNXYTFJ-UHFFFAOYSA-N 5,5,5-trifluoro-2-(methoxycarbonylamino)pentanoic acid Chemical compound COC(=O)NC(C(O)=O)CCC(F)(F)F XRMDEMQXNXYTFJ-UHFFFAOYSA-N 0.000 description 1
- 101100080548 Arabidopsis thaliana NRPB1 gene Proteins 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
- 102000014914 Carrier Proteins Human genes 0.000 description 1
- 235000001258 Cinchona calisaya Nutrition 0.000 description 1
- MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 230000005526 G1 to G0 transition Effects 0.000 description 1
- 239000007821 HATU Substances 0.000 description 1
- 101000772173 Homo sapiens Tubby-related protein 1 Proteins 0.000 description 1
- 241000234435 Lilium Species 0.000 description 1
- 238000003820 Medium-pressure liquid chromatography Methods 0.000 description 1
- UUIQMZJEGPQKFD-UHFFFAOYSA-N Methyl butyrate Chemical compound CCCC(=O)OC UUIQMZJEGPQKFD-UHFFFAOYSA-N 0.000 description 1
- QMGVPVSNSZLJIA-UHFFFAOYSA-N Nux Vomica Natural products C1C2C3C4N(C=5C6=CC=CC=5)C(=O)CC3OCC=C2CN2C1C46CC2 QMGVPVSNSZLJIA-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
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- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—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
- 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
- C07D491/10—Spiro-condensed systems
- C07D491/113—Spiro-condensed systems with two or more oxygen atoms as ring hetero atoms in the oxygen-containing ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Virology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Peptides Or Proteins (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
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| US22474509P | 2009-07-10 | 2009-07-10 | |
| US61/224,745 | 2009-07-10 | ||
| US23876009P | 2009-09-01 | 2009-09-01 | |
| US61/238,760 | 2009-09-01 | ||
| CA2761258A CA2761258C (en) | 2009-05-13 | 2010-05-12 | Antiviral compounds |
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| CA2761258A Division CA2761258C (en) | 2009-05-13 | 2010-05-12 | Antiviral compounds |
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| CA2886322A1 true CA2886322A1 (en) | 2010-11-18 |
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| CA2761258A Active CA2761258C (en) | 2009-05-13 | 2010-05-12 | Antiviral compounds |
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| CA2761258A Active CA2761258C (en) | 2009-05-13 | 2010-05-12 | Antiviral compounds |
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