NO313330B1 - Antiviralt aktive heterocykliske azaheksanderivater - Google Patents
Antiviralt aktive heterocykliske azaheksanderivater Download PDFInfo
- Publication number
- NO313330B1 NO313330B1 NO19984900A NO984900A NO313330B1 NO 313330 B1 NO313330 B1 NO 313330B1 NO 19984900 A NO19984900 A NO 19984900A NO 984900 A NO984900 A NO 984900A NO 313330 B1 NO313330 B1 NO 313330B1
- Authority
- NO
- Norway
- Prior art keywords
- phenyl
- formula
- amino
- tert
- methoxycarbonyl
- Prior art date
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- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 title description 93
- 125000000623 heterocyclic group Chemical group 0.000 title description 11
- 150000001875 compounds Chemical class 0.000 claims description 431
- -1 prazinyl Chemical group 0.000 claims description 264
- 239000000203 mixture Substances 0.000 claims description 137
- 238000000034 method Methods 0.000 claims description 127
- 239000002253 acid Substances 0.000 claims description 122
- 125000006239 protecting group Chemical group 0.000 claims description 103
- 238000006243 chemical reaction Methods 0.000 claims description 102
- 150000003839 salts Chemical class 0.000 claims description 79
- 125000000217 alkyl group Chemical group 0.000 claims description 73
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 46
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 43
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 37
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 31
- 125000000524 functional group Chemical group 0.000 claims description 29
- 238000002360 preparation method Methods 0.000 claims description 26
- 229910052799 carbon Inorganic materials 0.000 claims description 17
- 125000003754 ethoxycarbonyl group Chemical group C(=O)(OCC)* 0.000 claims description 17
- 230000001177 retroviral effect Effects 0.000 claims description 17
- 125000001544 thienyl group Chemical group 0.000 claims description 17
- 101000898643 Candida albicans Vacuolar aspartic protease Proteins 0.000 claims description 16
- 101000898783 Candida tropicalis Candidapepsin Proteins 0.000 claims description 16
- 101000898784 Cryphonectria parasitica Endothiapepsin Proteins 0.000 claims description 16
- 101000933133 Rhizopus niveus Rhizopuspepsin-1 Proteins 0.000 claims description 16
- 101000910082 Rhizopus niveus Rhizopuspepsin-2 Proteins 0.000 claims description 16
- 101000910079 Rhizopus niveus Rhizopuspepsin-3 Proteins 0.000 claims description 16
- 101000910086 Rhizopus niveus Rhizopuspepsin-4 Proteins 0.000 claims description 16
- 101000910088 Rhizopus niveus Rhizopuspepsin-5 Proteins 0.000 claims description 16
- 101000898773 Saccharomyces cerevisiae (strain ATCC 204508 / S288c) Saccharopepsin Proteins 0.000 claims description 16
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 16
- 125000003831 tetrazolyl group Chemical group 0.000 claims description 16
- 125000000335 thiazolyl group Chemical group 0.000 claims description 15
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 14
- 125000004076 pyridyl group Chemical group 0.000 claims description 14
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 14
- 201000010099 disease Diseases 0.000 claims description 13
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims description 13
- 125000003373 pyrazinyl group Chemical group 0.000 claims description 12
- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 0.000 claims description 11
- 125000001424 substituent group Chemical group 0.000 claims description 11
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 10
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 10
- 125000001541 3-thienyl group Chemical group S1C([H])=C([*])C([H])=C1[H] 0.000 claims description 10
- 241001465754 Metazoa Species 0.000 claims description 10
- 125000004432 carbon atom Chemical group C* 0.000 claims description 10
- 150000002429 hydrazines Chemical class 0.000 claims description 10
- 125000004442 acylamino group Chemical group 0.000 claims description 8
- 125000003545 alkoxy group Chemical group 0.000 claims description 8
- 230000002401 inhibitory effect Effects 0.000 claims description 8
- 229910052740 iodine Inorganic materials 0.000 claims description 8
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims description 8
- 239000008194 pharmaceutical composition Substances 0.000 claims description 7
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 claims description 6
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 claims description 6
- 125000000852 azido group Chemical class *N=[N+]=[N-] 0.000 claims description 4
- 239000003937 drug carrier Substances 0.000 claims description 4
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000003814 drug Substances 0.000 claims description 3
- 238000005932 reductive alkylation reaction Methods 0.000 claims description 3
- 229910052703 rhodium Inorganic materials 0.000 claims description 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 claims description 2
- OPZSFSBOEOXKKY-QUAHOIDUSA-N methyl n-[(2s)-1-[2-[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-4-phenylbutyl]-2-[[4-(1,3-thiazol-2-yl)phenyl]methyl]hydrazinyl]-3,3-dimethyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=CN=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 OPZSFSBOEOXKKY-QUAHOIDUSA-N 0.000 claims description 2
- CRANYLJCHUZXPB-ZSEJKAPFSA-N methyl n-[(2s)-1-[2-[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-4-phenylbutyl]-2-[[4-(1,3-thiazol-5-yl)phenyl]methyl]hydrazinyl]-3-methyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@@H]([C@@H](O)CN(NC(=O)[C@H](C(C)C)NC(=O)OC)CC=1C=CC(=CC=1)C=1SC=NC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 CRANYLJCHUZXPB-ZSEJKAPFSA-N 0.000 claims description 2
- ASYGQLSJYNDTKH-XFTNXAEASA-N methyl n-[(2s)-1-[[(2s,3s)-3-hydroxy-4-[[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-[[4-(1,3-thiazol-2-yl)phenyl]methyl]amino]-1-phenylbutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)OC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=CN=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 ASYGQLSJYNDTKH-XFTNXAEASA-N 0.000 claims description 2
- UVESUYYZXCTSSA-ZSEJKAPFSA-N methyl n-[(2s)-1-[[(2s,3s)-3-hydroxy-4-[[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-[[4-(1,3-thiazol-5-yl)phenyl]methyl]amino]-1-phenylbutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)OC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=NC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 UVESUYYZXCTSSA-ZSEJKAPFSA-N 0.000 claims description 2
- BFKMYBHUMHOWJH-YVHASNINSA-N methyl n-[(2s)-1-[[(2s,3s)-3-hydroxy-4-[[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-[[4-(2-methyltetrazol-5-yl)phenyl]methyl]amino]-1-phenylbutan-2-yl]amino]-3,3-dimethyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)[C@@H](O)CN(CC=1C=CC(=CC=1)C1=NN(C)N=N1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 BFKMYBHUMHOWJH-YVHASNINSA-N 0.000 claims description 2
- AHIMZZXNXYKPCH-LCXJGUJVSA-N methyl n-[(2s,3s)-1-[2-[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-4-phenylbutyl]-2-[[4-(1,3-thiazol-5-yl)phenyl]methyl]hydrazinyl]-3-methyl-1-oxopentan-2-yl]carbamate Chemical compound C([C@@H]([C@@H](O)CN(NC(=O)[C@@H](NC(=O)OC)[C@@H](C)CC)CC=1C=CC(=CC=1)C=1SC=NC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 AHIMZZXNXYKPCH-LCXJGUJVSA-N 0.000 claims description 2
- HUUSFDUFQRSWAH-GUTFHCGTSA-N methyl n-[(2s,3s)-1-[[(2s,3s)-3-hydroxy-4-[[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-[[4-(1,3-thiazol-2-yl)phenyl]methyl]amino]-1-phenylbutan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)[C@@H](C)CC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=CN=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 HUUSFDUFQRSWAH-GUTFHCGTSA-N 0.000 claims description 2
- ZQHIWOJIDTYSKQ-LCXJGUJVSA-N methyl n-[(2s,3s)-1-[[(2s,3s)-3-hydroxy-4-[[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-[[4-(1,3-thiazol-5-yl)phenyl]methyl]amino]-1-phenylbutan-2-yl]amino]-3-methyl-1-oxopentan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)[C@@H](C)CC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=NC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 ZQHIWOJIDTYSKQ-LCXJGUJVSA-N 0.000 claims description 2
- 150000002118 epoxides Chemical class 0.000 claims 1
- JFYUUFVUMXSOIH-RTNMLALUSA-N methyl n-[(2s)-1-[2-[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-4-phenylbutyl]-2-[(4-pyridin-2-ylphenyl)methyl]hydrazinyl]-3-methyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@@H]([C@@H](O)CN(NC(=O)[C@H](C(C)C)NC(=O)OC)CC=1C=CC(=CC=1)C=1N=CC=CC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 JFYUUFVUMXSOIH-RTNMLALUSA-N 0.000 claims 1
- VYMKRRDHEOUFPR-YDPTYEFTSA-N methyl n-[(2s)-1-[2-[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3-methylbutanoyl]amino]-4-phenylbutyl]-2-[(4-pyridin-2-ylphenyl)methyl]hydrazinyl]-3-methyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)OC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=CC=1)NC(=O)[C@@H](NC(=O)OC)C(C)C)C1=CC=CC=C1 VYMKRRDHEOUFPR-YDPTYEFTSA-N 0.000 claims 1
- VJVDUCVRWNDZEP-RTNMLALUSA-N methyl n-[(2s)-1-[[(2s,3s)-3-hydroxy-4-[[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-[(4-pyridin-2-ylphenyl)methyl]amino]-1-phenylbutan-2-yl]amino]-3-methyl-1-oxobutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)OC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=CC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 VJVDUCVRWNDZEP-RTNMLALUSA-N 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 334
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 300
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 225
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 174
- 239000000243 solution Substances 0.000 description 131
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 126
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 118
- 229910001868 water Inorganic materials 0.000 description 118
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 113
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 88
- 238000001704 evaporation Methods 0.000 description 77
- 230000008020 evaporation Effects 0.000 description 77
- 238000004128 high performance liquid chromatography Methods 0.000 description 70
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 69
- 235000002639 sodium chloride Nutrition 0.000 description 62
- 238000004809 thin layer chromatography Methods 0.000 description 61
- 238000004992 fast atom bombardment mass spectroscopy Methods 0.000 description 56
- 239000011541 reaction mixture Substances 0.000 description 53
- 239000012074 organic phase Substances 0.000 description 50
- 239000007858 starting material Substances 0.000 description 48
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 44
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 43
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 42
- 125000004453 alkoxycarbonyl group Chemical group 0.000 description 39
- 239000008346 aqueous phase Substances 0.000 description 36
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 35
- 239000002904 solvent Substances 0.000 description 35
- 238000002844 melting Methods 0.000 description 34
- 230000008018 melting Effects 0.000 description 34
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 33
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 33
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 30
- NPZTUJOABDZTLV-UHFFFAOYSA-N hydroxybenzotriazole Substances O=C1C=CC=C2NNN=C12 NPZTUJOABDZTLV-UHFFFAOYSA-N 0.000 description 30
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 29
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 28
- YEDUAINPPJYDJZ-UHFFFAOYSA-N 2-hydroxybenzothiazole Chemical compound C1=CC=C2SC(O)=NC2=C1 YEDUAINPPJYDJZ-UHFFFAOYSA-N 0.000 description 28
- 241000208199 Buxus sempervirens Species 0.000 description 28
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 description 27
- 229920006395 saturated elastomer Polymers 0.000 description 27
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 25
- 238000006722 reduction reaction Methods 0.000 description 25
- NWPRXAIYBULIEI-RXMQYKEDSA-N (2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoic acid Chemical compound COC(=O)N[C@H](C(O)=O)C(C)(C)C NWPRXAIYBULIEI-RXMQYKEDSA-N 0.000 description 24
- SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 24
- 239000012267 brine Substances 0.000 description 24
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 23
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 23
- 238000001816 cooling Methods 0.000 description 23
- 239000012299 nitrogen atmosphere Substances 0.000 description 23
- 230000009467 reduction Effects 0.000 description 23
- 239000011734 sodium Substances 0.000 description 23
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 23
- 239000002585 base Substances 0.000 description 22
- 238000005160 1H NMR spectroscopy Methods 0.000 description 21
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 21
- 150000007513 acids Chemical class 0.000 description 21
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 21
- 239000003054 catalyst Substances 0.000 description 21
- 210000004027 cell Anatomy 0.000 description 21
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 21
- 125000003277 amino group Chemical group 0.000 description 19
- 239000003921 oil Substances 0.000 description 19
- 235000019198 oils Nutrition 0.000 description 19
- 238000003756 stirring Methods 0.000 description 19
- LVEYOSJUKRVCCF-UHFFFAOYSA-N 1,3-bis(diphenylphosphino)propane Chemical compound C=1C=CC=CC=1P(C=1C=CC=CC=1)CCCP(C=1C=CC=CC=1)C1=CC=CC=C1 LVEYOSJUKRVCCF-UHFFFAOYSA-N 0.000 description 18
- ZAFNJMIOTHYJRJ-UHFFFAOYSA-N Diisopropyl ether Chemical compound CC(C)OC(C)C ZAFNJMIOTHYJRJ-UHFFFAOYSA-N 0.000 description 18
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 18
- 238000004440 column chromatography Methods 0.000 description 18
- 239000000047 product Substances 0.000 description 18
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 18
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 17
- 239000012300 argon atmosphere Substances 0.000 description 17
- 238000009835 boiling Methods 0.000 description 17
- 108010037444 diisopropylglutathione ester Proteins 0.000 description 17
- 235000019253 formic acid Nutrition 0.000 description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 17
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 16
- 150000008064 anhydrides Chemical class 0.000 description 16
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 16
- 239000003795 chemical substances by application Substances 0.000 description 16
- 150000002148 esters Chemical class 0.000 description 16
- 229910052736 halogen Inorganic materials 0.000 description 16
- 229910052739 hydrogen Inorganic materials 0.000 description 16
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 15
- 241000713772 Human immunodeficiency virus 1 Species 0.000 description 15
- 150000002367 halogens Chemical class 0.000 description 15
- 229910052757 nitrogen Inorganic materials 0.000 description 15
- 239000000725 suspension Substances 0.000 description 15
- 238000012360 testing method Methods 0.000 description 15
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 15
- CEFVHPDFGLDQKU-YFKPBYRVSA-N (2s)-2-(methoxycarbonylamino)-3-methylbutanoic acid Chemical compound COC(=O)N[C@@H](C(C)C)C(O)=O CEFVHPDFGLDQKU-YFKPBYRVSA-N 0.000 description 14
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 14
- 229910004298 SiO 2 Inorganic materials 0.000 description 14
- 241000700605 Viruses Species 0.000 description 14
- 239000000460 chlorine Substances 0.000 description 14
- 238000002425 crystallisation Methods 0.000 description 14
- 230000008025 crystallization Effects 0.000 description 14
- 239000003112 inhibitor Substances 0.000 description 14
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 13
- 150000001298 alcohols Chemical class 0.000 description 13
- 150000001299 aldehydes Chemical class 0.000 description 13
- 229940024606 amino acid Drugs 0.000 description 13
- 235000001014 amino acid Nutrition 0.000 description 13
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 13
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 13
- 238000005984 hydrogenation reaction Methods 0.000 description 13
- 208000030507 AIDS Diseases 0.000 description 12
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- 239000004480 active ingredient Substances 0.000 description 12
- 150000001413 amino acids Chemical class 0.000 description 12
- LVKROKMNCYTCHK-WDSKDSINSA-N (2s,3s)-2-(methoxycarbonylamino)-3-methylpentanoic acid Chemical compound CC[C@H](C)[C@@H](C(O)=O)NC(=O)OC LVKROKMNCYTCHK-WDSKDSINSA-N 0.000 description 11
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 11
- 108010016183 Human immunodeficiency virus 1 p16 protease Proteins 0.000 description 11
- 125000003118 aryl group Chemical group 0.000 description 11
- 230000015572 biosynthetic process Effects 0.000 description 11
- 238000000921 elemental analysis Methods 0.000 description 11
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- 125000006633 tert-butoxycarbonylamino group Chemical group 0.000 description 1
- SYGUPSZLTHDFLR-ZXRKZBAXSA-N tert-butyl n-[[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3-methylbutanoyl]amino]-4-phenylbutyl]-[(4-pyrazin-2-ylphenyl)methyl]amino]carbamate Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)OC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=NC=1)NC(=O)OC(C)(C)C)C1=CC=CC=C1 SYGUPSZLTHDFLR-ZXRKZBAXSA-N 0.000 description 1
- LMBCPHKLPKAOLG-NSVAZKTRSA-N tert-butyl n-[[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3-methylbutanoyl]amino]-4-phenylbutyl]-[[4-(1,3-thiazol-5-yl)phenyl]methyl]amino]carbamate Chemical compound C([C@H](NC(=O)[C@H](C(C)C)NC(=O)OC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=NC=1)NC(=O)OC(C)(C)C)C1=CC=CC=C1 LMBCPHKLPKAOLG-NSVAZKTRSA-N 0.000 description 1
- JYOZTTQRPKIKGR-IOZSVJQTSA-N tert-butyl n-[[(2s,3s)-2-hydroxy-3-[[(2s,3s)-2-(methoxycarbonylamino)-3-methylpentanoyl]amino]-4-phenylbutyl]-[(4-pyrazin-2-ylphenyl)methyl]amino]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)[C@@H](C)CC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=NC=1)NC(=O)OC(C)(C)C)C1=CC=CC=C1 JYOZTTQRPKIKGR-IOZSVJQTSA-N 0.000 description 1
- VHOWTDFESBALAN-ACNFANBVSA-N tert-butyl n-[[(2s,3s)-2-hydroxy-3-[[(2s,3s)-2-(methoxycarbonylamino)-3-methylpentanoyl]amino]-4-phenylbutyl]-[[4-(1,3-thiazol-2-yl)phenyl]methyl]amino]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)[C@@H](C)CC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=CN=1)NC(=O)OC(C)(C)C)C1=CC=CC=C1 VHOWTDFESBALAN-ACNFANBVSA-N 0.000 description 1
- WCBACWWVDAZIKL-NGSUXZSRSA-N tert-butyl n-[[(2s,3s)-2-hydroxy-3-[[(2s,3s)-2-(methoxycarbonylamino)-3-methylpentanoyl]amino]-4-phenylbutyl]-[[4-(1,3-thiazol-5-yl)phenyl]methyl]amino]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)[C@@H](C)CC)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1SC=NC=1)NC(=O)OC(C)(C)C)C1=CC=CC=C1 WCBACWWVDAZIKL-NGSUXZSRSA-N 0.000 description 1
- NDVQOJIYRRIPDZ-UPVQGACJSA-N tert-butyl n-[[(2s,3s)-2-hydroxy-4-phenyl-3-[(2,2,2-trifluoroacetyl)amino]butyl]-[(4-pyrazin-2-ylphenyl)methyl]amino]carbamate Chemical compound C([C@@H]([C@@H](O)CN(NC(=O)OC(C)(C)C)CC=1C=CC(=CC=1)C=1N=CC=NC=1)NC(=O)C(F)(F)F)C1=CC=CC=C1 NDVQOJIYRRIPDZ-UPVQGACJSA-N 0.000 description 1
- CSPWQNVBBHOUNJ-VXKWHMMOSA-N tert-butyl n-[[(2s,3s)-2-hydroxy-4-phenyl-3-[(2,2,2-trifluoroacetyl)amino]butyl]-[[4-(1,3-thiazol-5-yl)phenyl]methyl]amino]carbamate Chemical compound C([C@@H]([C@@H](O)CN(NC(=O)OC(C)(C)C)CC=1C=CC(=CC=1)C=1SC=NC=1)NC(=O)C(F)(F)F)C1=CC=CC=C1 CSPWQNVBBHOUNJ-VXKWHMMOSA-N 0.000 description 1
- CLRHAGPFYFWYKY-BLFWRVEASA-N tert-butyl n-[amino-(4-pyridin-2-ylphenyl)methyl]-n-[(2s,3s)-2-hydroxy-3-[[(2s)-2-(methoxycarbonylamino)-3,3-dimethylbutanoyl]amino]-4-phenylbutyl]carbamate Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)[C@@H](O)CN(C(N)C=1C=CC(=CC=1)C=1N=CC=CC=1)C(=O)OC(C)(C)C)C1=CC=CC=C1 CLRHAGPFYFWYKY-BLFWRVEASA-N 0.000 description 1
- 125000001981 tert-butyldimethylsilyl group Chemical group [H]C([H])([H])[Si]([H])(C([H])([H])[H])[*]C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- QSUJAUYJBJRLKV-UHFFFAOYSA-M tetraethylazanium;fluoride Chemical compound [F-].CC[N+](CC)(CC)CC QSUJAUYJBJRLKV-UHFFFAOYSA-M 0.000 description 1
- WHRNULOCNSKMGB-UHFFFAOYSA-N tetrahydrofuran thf Chemical compound C1CCOC1.C1CCOC1 WHRNULOCNSKMGB-UHFFFAOYSA-N 0.000 description 1
- WROMPOXWARCANT-UHFFFAOYSA-N tfa trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.OC(=O)C(F)(F)F WROMPOXWARCANT-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 150000003555 thioacetals Chemical class 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- 230000001052 transient effect Effects 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- VAVYFBVYRHOIDI-UHFFFAOYSA-N tricopper;dioxido(dioxo)chromium;oxygen(2-);dihydrate Chemical compound O.O.[O-2].[O-2].[Cu+2].[Cu+2].[Cu+2].[O-][Cr]([O-])(=O)=O VAVYFBVYRHOIDI-UHFFFAOYSA-N 0.000 description 1
- PNQBEPDZQUOCNY-UHFFFAOYSA-N trifluoroacetyl chloride Chemical compound FC(F)(F)C(Cl)=O PNQBEPDZQUOCNY-UHFFFAOYSA-N 0.000 description 1
- 125000000025 triisopropylsilyl group Chemical group C(C)(C)[Si](C(C)C)(C(C)C)* 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-UHFFFAOYSA-N 0.000 description 1
- HRXKRNGNAMMEHJ-UHFFFAOYSA-K trisodium citrate Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O HRXKRNGNAMMEHJ-UHFFFAOYSA-K 0.000 description 1
- 229940038773 trisodium citrate Drugs 0.000 description 1
- YFNGWGVTFYSJHE-UHFFFAOYSA-K trisodium;phosphonoformate Chemical compound [Na+].[Na+].[Na+].OP(O)(=O)C([O-])=O.OP(O)(=O)C([O-])=O.OP(O)(=O)C([O-])=O YFNGWGVTFYSJHE-UHFFFAOYSA-K 0.000 description 1
- 239000012588 trypsin Substances 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- 238000002211 ultraviolet spectrum Methods 0.000 description 1
- 229960005486 vaccine Drugs 0.000 description 1
- 125000002114 valyl group Chemical group 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000029812 viral genome replication Effects 0.000 description 1
- 229940087450 zerit Drugs 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/24—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D213/36—Radicals substituted by singly-bound nitrogen atoms
- C07D213/42—Radicals substituted by singly-bound nitrogen atoms having hetero atoms attached to the substituent nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C271/06—Esters of carbamic acids
- C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
- C07C271/10—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C271/22—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/02—Compounds containing any of the groups, e.g. carbazates
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C281/00—Derivatives of carbonic acid containing functional groups covered by groups C07C269/00 - C07C279/00 in which at least one nitrogen atom of these functional groups is further bound to another nitrogen atom not being part of a nitro or nitroso group
- C07C281/02—Compounds containing any of the groups, e.g. carbazates
- C07C281/04—Compounds containing any of the groups, e.g. carbazates the other nitrogen atom being further doubly-bound to a carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/12—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D257/00—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms
- C07D257/02—Heterocyclic compounds containing rings having four nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D257/04—Five-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/22—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D277/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
- C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
- C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
- C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
- C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
- C07D333/20—Radicals substituted by singly bound hetero atoms other than halogen by nitrogen atoms
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Oncology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Tropical Medicine & Parasitology (AREA)
- AIDS & HIV (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pyridine Compounds (AREA)
- Heterocyclic Compounds Containing Sulfur Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Epoxy Compounds (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Indole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH101896 | 1996-04-22 | ||
CH2997 | 1997-01-08 | ||
CH22397 | 1997-01-31 | ||
PCT/EP1997/001860 WO1997040029A1 (en) | 1996-04-22 | 1997-04-14 | Antivirally active heterocyclic azahexane derivatives |
Publications (3)
Publication Number | Publication Date |
---|---|
NO984900D0 NO984900D0 (no) | 1998-10-21 |
NO984900L NO984900L (no) | 1998-12-21 |
NO313330B1 true NO313330B1 (no) | 2002-09-16 |
Family
ID=27171723
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO19984900A NO313330B1 (no) | 1996-04-22 | 1998-04-14 | Antiviralt aktive heterocykliske azaheksanderivater |
NO2005010C NO2005010I1 (no) | 1996-04-22 | 2005-04-13 | Azaheksansulfat |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NO2005010C NO2005010I1 (no) | 1996-04-22 | 2005-04-13 | Azaheksansulfat |
Country Status (28)
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EP (1) | EP0900210B1 (da) |
JP (1) | JP3174347B2 (da) |
CN (3) | CN1082508C (da) |
AR (1) | AR006720A1 (da) |
AT (1) | ATE288903T1 (da) |
AU (1) | AU706183B2 (da) |
BR (1) | BR9701877A (da) |
CA (3) | CA2250840C (da) |
CY (1) | CY2596B2 (da) |
CZ (1) | CZ296135B6 (da) |
DE (2) | DE122005000003I1 (da) |
DK (1) | DK0900210T3 (da) |
EA (1) | EA001794B1 (da) |
ES (1) | ES2238720T3 (da) |
FR (1) | FR05C0030I2 (da) |
HK (2) | HK1018788A1 (da) |
HU (1) | HU224125B1 (da) |
IL (1) | IL126381A (da) |
LU (1) | LU91189I2 (da) |
MY (1) | MY114457A (da) |
NL (1) | NL300203I2 (da) |
NO (2) | NO313330B1 (da) |
NZ (3) | NZ509045A (da) |
PT (1) | PT900210E (da) |
SI (1) | SI0900210T1 (da) |
SK (1) | SK285048B6 (da) |
TW (1) | TW409125B (da) |
WO (1) | WO1997040029A1 (da) |
Families Citing this family (39)
Publication number | Priority date | Publication date | Assignee | Title |
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US6087383A (en) * | 1998-01-20 | 2000-07-11 | Bristol-Myers Squibb Company | Bisulfate salt of HIV protease inhibitor |
US6251906B1 (en) | 1998-05-15 | 2001-06-26 | Abbott Laboratories | Retroviral protease inhibiting compounds |
EP1077977A1 (en) * | 1998-05-15 | 2001-02-28 | Abbott Laboratories | Retroviral protease inhibiting compounds |
EP0976736A1 (en) * | 1998-07-29 | 2000-02-02 | SUMIKA FINE CHEMICALS Co., Ltd. | Production method of 2-(p-alkylphenyl)pyridine compound |
EP0979820B1 (en) | 1998-08-07 | 2003-05-07 | SUMIKA FINE CHEMICALS Co., Ltd. | 2-Phenylpyridine derivatives and production method thereof |
US6207715B1 (en) | 1998-12-09 | 2001-03-27 | American Home Products Corporation | Alpha-methylbenzyl-containing thiourea inhibitors of herpes viruses containing a substituted phenylene-diamine group |
US6255349B1 (en) | 1998-12-09 | 2001-07-03 | American Home Products Corporation | Alph-methylbenzyl-containing thiourea inhibitors of herpes viruses containing a phenylenediamine group |
US6197803B1 (en) | 1998-12-09 | 2001-03-06 | American Home Products Corporation | Heterocyclic carboxamide-containing thiourea inhibitors of herpes viruses containing phenylenediamine group |
US6335350B1 (en) | 1998-12-09 | 2002-01-01 | American Home Products Corporation | Acetamide and substituted acetamide-containing thiourea inhibitors of herpes viruses |
JP4222671B2 (ja) | 1999-02-15 | 2009-02-12 | 住友化学株式会社 | ヒドラジン誘導体の製造方法 |
IT1313664B1 (it) * | 1999-10-12 | 2002-09-09 | Norpharma S P A | Processo per la preparazione di un composto aril-piridinico. |
JP4278316B2 (ja) * | 2000-07-14 | 2009-06-10 | 住友化学株式会社 | ヒドラジン誘導体の製造方法 |
US6365745B1 (en) | 2000-07-14 | 2002-04-02 | Sumika Fine Chemicals Co., Ltd. | Method for producing hydrazine derivative |
EP1546106A1 (en) | 2002-10-02 | 2005-06-29 | Euticals Prime European Therapeutical S.P.A | Process for the preparation of aryl-pyridyl compounds |
CA2510006C (en) * | 2002-12-06 | 2012-02-07 | Vertex Pharmaceuticals Incorporated | Compositions comprising a combination of diphenyl urea impdh inhibitors and apoptosis-inducing anti-cancer agents |
ITMI20032338A1 (it) * | 2003-11-28 | 2005-05-29 | Dinamite Dipharma S P A In Forma A Bbreviata Diph | Composti feniltetrazolici. |
CN1980666B (zh) * | 2004-05-04 | 2011-03-30 | 布里斯托尔-迈尔斯斯奎布公司 | 制备阿扎那韦硫酸氢盐的方法和新的形式 |
CA2594395A1 (en) | 2005-02-10 | 2006-08-17 | Medivir Ab | Hiv protease inhibitors |
ES2574831T3 (es) * | 2006-07-21 | 2016-06-22 | Gilead Sciences, Inc. | Inhibidores de la proteasa antivirales |
BRPI0823520A2 (pt) | 2007-06-12 | 2013-12-17 | Concert Pharmaceuticals Inc | Composto derivado de azapeptídeos e composição farmacêutica contendo o mesmo |
WO2009130534A1 (en) * | 2008-04-24 | 2009-10-29 | Oxyrane (Pty) Ltd. | Process for synthesizing atazanavir |
EP2272830A1 (en) | 2009-06-18 | 2011-01-12 | Esteve Química, S.A. | Preparation process of an antivirally heterocyclic azahexane derivative |
EP2272831A1 (en) | 2009-06-26 | 2011-01-12 | Prime European Therapeuticals S.p.A. | Process for the preparation of arylpyridinyl compounds |
WO2011037467A1 (en) | 2009-09-28 | 2011-03-31 | Stichting Katholieke Universiteit | Atazanavir for treating inflammatory diseases |
WO2011080562A1 (en) | 2009-12-29 | 2011-07-07 | Hetero Research Foundation | Novel aza-peptides containing 2,2-disubstituted cyclobutyl and/or substituted alkoxy benzyl derivatives as antivirals |
WO2011107843A2 (en) * | 2010-03-01 | 2011-09-09 | Lupin Limited | Process for the preparation of atazanavir sulfate substantially free of diastereomers |
EP2621472A1 (en) | 2010-09-28 | 2013-08-07 | Ratiopharm GmbH | Dry processing of atazanavir |
US20140343290A1 (en) * | 2011-07-27 | 2014-11-20 | Rakesh Kumar Singh | Process for the preparation of atazanavir or its bisulfate salt |
US9227990B2 (en) | 2012-10-29 | 2016-01-05 | Cipla Limited | Antiviral phosphonate analogues and process for preparation thereof |
CN104250224A (zh) * | 2013-06-28 | 2014-12-31 | 上海威智医药科技有限公司 | 阿扎那韦富马酸盐及其制备和应用 |
CN104163787A (zh) * | 2014-08-08 | 2014-11-26 | 山东威智医药工业有限公司 | 阿扎那韦及其硫酸盐的制备方法 |
CN107459496B (zh) * | 2016-06-03 | 2022-07-19 | 华东理工大学 | 噻唑类衍生物在治疗病毒感染中的应用 |
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CN107245052A (zh) * | 2017-06-21 | 2017-10-13 | 连云港杰瑞药业有限公司 | 一种阿扎那韦制备方法 |
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CN109251165B (zh) * | 2018-10-02 | 2022-09-23 | 国药集团川抗制药有限公司 | 阿扎那韦达二4-氨基苯磺酸盐及其制备方法 |
CN109574916A (zh) * | 2018-12-29 | 2019-04-05 | 常州吉恩药业有限公司 | 阿扎那韦中间体2-[4-(2-吡啶基)苄基]-肼羧酸叔丁酯的工业化生产方法 |
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CN113603634B (zh) * | 2021-08-06 | 2023-03-21 | 江苏八巨药业有限公司 | 一种阿扎那韦中间体的制备方法 |
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IE20010533A1 (en) * | 1990-11-20 | 2003-03-05 | Abbott Lab | Intermediates for preparing retroviral protease inhibiting compounds |
DE59207226D1 (de) * | 1991-07-03 | 1996-10-31 | Ciba Geigy Ag | Pharmakologisch wirksame Hydrazinderivate und Verfahren zu deren Herstellung |
DE59303870D1 (de) * | 1992-12-23 | 1996-10-24 | Ciba Geigy Ag | Antiretrovirale hydrazinderivate |
DK0727419T3 (da) * | 1992-12-29 | 2002-06-10 | Abbott Lab | Mellemprodukter til fremstilling af forbindelser, som inhiberer retroviral protease |
US5461067A (en) * | 1993-02-25 | 1995-10-24 | Abbott Laboratories | Retroviral protease inhibiting compounds |
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