RU2010125220A - Ненуклеозидные ингибиторы обратной транскриптазы - Google Patents
Ненуклеозидные ингибиторы обратной транскриптазы Download PDFInfo
- Publication number
- RU2010125220A RU2010125220A RU2010125220/04A RU2010125220A RU2010125220A RU 2010125220 A RU2010125220 A RU 2010125220A RU 2010125220/04 A RU2010125220/04 A RU 2010125220/04A RU 2010125220 A RU2010125220 A RU 2010125220A RU 2010125220 A RU2010125220 A RU 2010125220A
- Authority
- RU
- Russia
- Prior art keywords
- alkyl
- independently
- haloalkyl
- pyridin
- chloro
- Prior art date
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- 229940042402 non-nucleoside reverse transcriptase inhibitor Drugs 0.000 title 1
- 239000002726 nonnucleoside reverse transcriptase inhibitor Substances 0.000 title 1
- 229910052799 carbon Inorganic materials 0.000 claims abstract 43
- 125000001424 substituent group Chemical group 0.000 claims abstract 38
- 150000001875 compounds Chemical class 0.000 claims abstract 26
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract 26
- 150000002367 halogens Chemical class 0.000 claims abstract 20
- 239000000651 prodrug Substances 0.000 claims abstract 20
- 229940002612 prodrug Drugs 0.000 claims abstract 20
- 150000003839 salts Chemical class 0.000 claims abstract 20
- 229910052736 halogen Inorganic materials 0.000 claims abstract 18
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims abstract 12
- 229910052717 sulfur Inorganic materials 0.000 claims abstract 12
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract 10
- 125000003342 alkenyl group Chemical group 0.000 claims abstract 10
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims abstract 8
- 125000003118 aryl group Chemical group 0.000 claims abstract 7
- 229920006395 saturated elastomer Polymers 0.000 claims abstract 7
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims abstract 6
- 101100273648 Mus musculus Ccna2 gene Proteins 0.000 claims abstract 4
- 125000004452 carbocyclyl group Chemical group 0.000 claims abstract 4
- 125000000081 (C5-C8) cycloalkenyl group Chemical group 0.000 claims abstract 3
- 125000002619 bicyclic group Chemical group 0.000 claims abstract 3
- 125000000217 alkyl group Chemical group 0.000 claims 139
- 229910052739 hydrogen Inorganic materials 0.000 claims 35
- -1 1-azetidinyl Chemical group 0.000 claims 24
- JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 claims 12
- 229910052794 bromium Inorganic materials 0.000 claims 12
- 229910052801 chlorine Inorganic materials 0.000 claims 12
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 12
- 125000005842 heteroatom Chemical group 0.000 claims 10
- 125000001624 naphthyl group Chemical group 0.000 claims 10
- 229910052731 fluorine Inorganic materials 0.000 claims 8
- 125000003709 fluoroalkyl group Chemical group 0.000 claims 8
- 125000000623 heterocyclic group Chemical group 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 6
- 125000001188 haloalkyl group Chemical group 0.000 claims 6
- 125000001072 heteroaryl group Chemical group 0.000 claims 6
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
- GMCYQWDQLIDMII-UHFFFAOYSA-N 3-(3,5-dichlorophenoxy)-1-(2h-pyrazolo[3,4-b]pyridin-3-ylmethyl)-4-(trifluoromethyl)pyridin-2-one Chemical compound FC(F)(F)C=1C=CN(CC=2C3=CC=CN=C3NN=2)C(=O)C=1OC1=CC(Cl)=CC(Cl)=C1 GMCYQWDQLIDMII-UHFFFAOYSA-N 0.000 claims 4
- KHIUGRYFNXHUBT-UHFFFAOYSA-N 3-[1-[(6-amino-2h-pyrazolo[3,4-b]pyridin-3-yl)methyl]-4-chloro-2-oxopyridin-3-yl]oxy-5-chlorobenzonitrile;2,2,2-trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F.N=1NC2=NC(N)=CC=C2C=1CN(C1=O)C=CC(Cl)=C1OC1=CC(Cl)=CC(C#N)=C1 KHIUGRYFNXHUBT-UHFFFAOYSA-N 0.000 claims 4
- CVAURPNMBSXXSS-UHFFFAOYSA-N 3-chloro-5-[2-oxo-1-(2h-pyrazolo[3,4-b]pyridin-3-ylmethyl)-4-(trifluoromethyl)pyridin-3-yl]oxybenzonitrile Chemical compound FC(F)(F)C=1C=CN(CC=2C3=CC=CN=C3NN=2)C(=O)C=1OC1=CC(Cl)=CC(C#N)=C1 CVAURPNMBSXXSS-UHFFFAOYSA-N 0.000 claims 4
- XUIZIBCKVKBTGV-UHFFFAOYSA-N 3-chloro-5-[4-methyl-2-oxo-1-[2-(2h-pyrazolo[3,4-b]pyridin-3-yl)ethyl]pyridin-3-yl]oxybenzonitrile Chemical compound CC=1C=CN(CCC=2C3=CC=CN=C3NN=2)C(=O)C=1OC1=CC(Cl)=CC(C#N)=C1 XUIZIBCKVKBTGV-UHFFFAOYSA-N 0.000 claims 4
- 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 4
- 125000000753 cycloalkyl group Chemical group 0.000 claims 4
- 125000002883 imidazolyl group Chemical group 0.000 claims 4
- 125000004122 cyclic group Chemical group 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 3
- 125000002733 (C1-C6) fluoroalkyl group Chemical group 0.000 claims 2
- 125000004214 1-pyrrolidinyl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- ATGKQOUKJPVTKE-UHFFFAOYSA-N 2-[3-(3-chloro-5-cyanophenoxy)-2-oxo-4-(trifluoromethyl)pyridin-1-yl]-n-[(2-chlorophenyl)methyl]-n-methylacetamide Chemical compound C1=CC(C(F)(F)F)=C(OC=2C=C(C=C(Cl)C=2)C#N)C(=O)N1CC(=O)N(C)CC1=CC=CC=C1Cl ATGKQOUKJPVTKE-UHFFFAOYSA-N 0.000 claims 2
- TXIDGJNYVPGVEG-UHFFFAOYSA-N 3-[[6-[2-(6-amino-2h-pyrazolo[3,4-b]pyridin-3-yl)ethyl]-3-chloro-2-oxo-1h-pyridin-4-yl]oxy]-5-chlorobenzonitrile Chemical compound N=1NC2=NC(N)=CC=C2C=1CCC(NC(=O)C=1Cl)=CC=1OC1=CC(Cl)=CC(C#N)=C1 TXIDGJNYVPGVEG-UHFFFAOYSA-N 0.000 claims 2
- ABOZXYNAPFTBHX-UHFFFAOYSA-N 3-chloro-5-[4,5-dichloro-2-oxo-1-(2h-pyrazolo[3,4-b]pyridin-3-ylmethyl)pyridin-3-yl]oxybenzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC=2C(N(CC=3C4=CC=CN=C4NN=3)C=C(Cl)C=2Cl)=O)=C1 ABOZXYNAPFTBHX-UHFFFAOYSA-N 0.000 claims 2
- YMRUCOCNLHJFRC-UHFFFAOYSA-N 3-chloro-5-[4-methyl-2-oxo-1-(2h-pyrazolo[3,4-b]pyridin-3-ylmethyl)pyridin-3-yl]oxybenzonitrile Chemical compound CC=1C=CN(CC=2C3=CC=CN=C3NN=2)C(=O)C=1OC1=CC(Cl)=CC(C#N)=C1 YMRUCOCNLHJFRC-UHFFFAOYSA-N 0.000 claims 2
- RRYPCILBOZGVEJ-UHFFFAOYSA-N 3-chloro-5-[5-chloro-2-[2-(2h-pyrazolo[3,4-b]pyridin-3-yl)ethyl]pyridin-4-yl]oxybenzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC=2C(=CN=C(CCC=3C4=CC=CN=C4NN=3)C=2)Cl)=C1 RRYPCILBOZGVEJ-UHFFFAOYSA-N 0.000 claims 2
- GIOABAWLXRZDTF-UHFFFAOYSA-N 3-chloro-5-[[2-oxo-6-[2-(2h-pyrazolo[3,4-b]pyridin-3-yl)ethyl]-1h-pyridin-4-yl]oxy]benzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC2=CC(=O)NC(CCC=3C4=CC=CN=C4NN=3)=C2)=C1 GIOABAWLXRZDTF-UHFFFAOYSA-N 0.000 claims 2
- MEFSIZQEXHEOCA-UHFFFAOYSA-N 3-chloro-5-[[3,5-dichloro-2-oxo-6-[2-(2h-pyrazolo[3,4-b]pyridin-3-yl)ethyl]-1h-pyridin-4-yl]oxy]benzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC2=C(C(=O)NC(CCC=3C4=CC=CN=C4NN=3)=C2Cl)Cl)=C1 MEFSIZQEXHEOCA-UHFFFAOYSA-N 0.000 claims 2
- KDKUQACKJMWZJZ-UHFFFAOYSA-N 3-chloro-5-[[3-chloro-2-oxo-6-(2h-pyrazolo[3,4-b]pyridin-3-ylmethylamino)-1h-pyridin-4-yl]oxy]benzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC2=C(C(=O)NC(NCC=3C4=CC=CN=C4NN=3)=C2)Cl)=C1 KDKUQACKJMWZJZ-UHFFFAOYSA-N 0.000 claims 2
- GZVLIXZYBWGUTC-UHFFFAOYSA-N 3-chloro-5-[[3-chloro-2-oxo-6-[(2-oxo-3h-benzimidazol-1-yl)methyl]-1h-pyridin-4-yl]oxy]benzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC2=C(C(=O)NC(CN3C(NC4=CC=CC=C43)=O)=C2)Cl)=C1 GZVLIXZYBWGUTC-UHFFFAOYSA-N 0.000 claims 2
- NCPJKBVDFNPLLG-UHFFFAOYSA-N 3-chloro-5-[[3-chloro-2-oxo-6-[2-(2h-pyrazolo[3,4-b]pyridin-3-yl)ethyl]-1h-pyridin-4-yl]oxy]benzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC2=C(C(=O)NC(CCC=3C4=CC=CN=C4NN=3)=C2)Cl)=C1 NCPJKBVDFNPLLG-UHFFFAOYSA-N 0.000 claims 2
- 208000030507 AIDS Diseases 0.000 claims 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 2
- 208000035473 Communicable disease Diseases 0.000 claims 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical group C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 claims 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims 2
- 208000015181 infectious disease Diseases 0.000 claims 2
- 125000002950 monocyclic group Chemical group 0.000 claims 2
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 claims 2
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 2
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 claims 2
- 238000011321 prophylaxis Methods 0.000 claims 2
- 239000003419 rna directed dna polymerase inhibitor Substances 0.000 claims 2
- 238000011282 treatment Methods 0.000 claims 2
- YIQIGLZIZPIAGP-UHFFFAOYSA-N 1-[(3-methyl-4-phenoxypyridin-2-yl)methyl]benzimidazole Chemical compound C1=CN=C(CN2C3=CC=CC=C3N=C2)C(C)=C1OC1=CC=CC=C1 YIQIGLZIZPIAGP-UHFFFAOYSA-N 0.000 claims 1
- RHQXZNCCZYCFFV-UHFFFAOYSA-N 2-[3-(3-bromo-5-chlorophenoxy)-2-oxo-4-(trifluoromethyl)pyridin-1-yl]-n-(2-chloro-4-sulfamoylphenyl)acetamide Chemical compound ClC1=CC(S(=O)(=O)N)=CC=C1NC(=O)CN1C(=O)C(OC=2C=C(Br)C=C(Cl)C=2)=C(C(F)(F)F)C=C1 RHQXZNCCZYCFFV-UHFFFAOYSA-N 0.000 claims 1
- IMRGEQIRLWFLPC-UHFFFAOYSA-N 2-[3-(3-chloro-5-cyanophenoxy)-2-oxo-4-(trifluoromethyl)pyridin-1-yl]-n-(2-chloro-4-sulfamoylphenyl)acetamide Chemical compound ClC1=CC(S(=O)(=O)N)=CC=C1NC(=O)CN1C(=O)C(OC=2C=C(C=C(Cl)C=2)C#N)=C(C(F)(F)F)C=C1 IMRGEQIRLWFLPC-UHFFFAOYSA-N 0.000 claims 1
- YXVABPSUOVOEJJ-UHFFFAOYSA-N 2-methyl-6-[(6-phenoxypyridin-2-yl)methyl]pyridine Chemical compound CC1=CC=CC(CC=2N=C(OC=3C=CC=CC=3)C=CC=2)=N1 YXVABPSUOVOEJJ-UHFFFAOYSA-N 0.000 claims 1
- FTFUKUWGDBEIJI-UHFFFAOYSA-N 3-chloro-5-[3-chloro-2,5-difluoro-6-(2h-pyrazolo[3,4-b]pyridin-3-ylmethylamino)pyridin-4-yl]oxybenzonitrile Chemical compound ClC=1C(F)=NC(NCC=2C3=CC=CN=C3NN=2)=C(F)C=1OC1=CC(Cl)=CC(C#N)=C1 FTFUKUWGDBEIJI-UHFFFAOYSA-N 0.000 claims 1
- ZSDYTNJSFLYICM-UHFFFAOYSA-N 3-chloro-5-[4-chloro-2-oxo-1-(2h-pyrazolo[3,4-b]pyridin-3-ylmethyl)pyridin-3-yl]oxybenzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC=2C(N(CC=3C4=CC=CN=C4NN=3)C=CC=2Cl)=O)=C1 ZSDYTNJSFLYICM-UHFFFAOYSA-N 0.000 claims 1
- CCEYNDRKIOXUGP-UHFFFAOYSA-N 3-chloro-5-[[3-chloro-2-oxo-6-(2h-pyrazolo[3,4-b]pyridin-3-ylmethyl)-1h-pyridin-4-yl]oxy]benzonitrile Chemical compound N#CC1=CC(Cl)=CC(OC2=C(C(=O)NC(CC=3C4=CC=CN=C4NN=3)=C2)Cl)=C1 CCEYNDRKIOXUGP-UHFFFAOYSA-N 0.000 claims 1
- CBFKUUGIHWKPLR-UHFFFAOYSA-N 5-[2-oxo-1-(2h-pyrazolo[3,4-b]pyridin-3-ylmethyl)-4-(trifluoromethyl)pyridin-3-yl]oxybenzene-1,3-dicarbonitrile Chemical compound FC(F)(F)C=1C=CN(CC=2C3=CC=CN=C3NN=2)C(=O)C=1OC1=CC(C#N)=CC(C#N)=C1 CBFKUUGIHWKPLR-UHFFFAOYSA-N 0.000 claims 1
- 241000282326 Felis catus Species 0.000 claims 1
- 108010078851 HIV Reverse Transcriptase Proteins 0.000 claims 1
- 229940099797 HIV integrase inhibitor Drugs 0.000 claims 1
- 229940122313 Nucleoside reverse transcriptase inhibitor Drugs 0.000 claims 1
- PCNDJXKNXGMECE-UHFFFAOYSA-N Phenazine Chemical group C1=CC=CC2=NC3=CC=CC=C3N=C21 PCNDJXKNXGMECE-UHFFFAOYSA-N 0.000 claims 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical group C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000003443 antiviral agent Substances 0.000 claims 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 claims 1
- 125000002618 bicyclic heterocycle group Chemical group 0.000 claims 1
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 1
- 239000003814 drug Substances 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 239000002835 hiv fusion inhibitor Substances 0.000 claims 1
- 239000003084 hiv integrase inhibitor Substances 0.000 claims 1
- 239000004030 hiv protease inhibitor Substances 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 238000010348 incorporation Methods 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 claims 1
- 239000002777 nucleoside Substances 0.000 claims 1
- 150000003833 nucleoside derivatives Chemical class 0.000 claims 1
- 125000002971 oxazolyl group Chemical group 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000003226 pyrazolyl group Chemical group 0.000 claims 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Chemical group COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 125000000335 thiazolyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000006574 non-aromatic ring group Chemical group 0.000 abstract 1
- 0 *N(C(N=I(C=C1)=C)=C1N1N)C1=O Chemical compound *N(C(N=I(C=C1)=C)=C1N1N)C1=O 0.000 description 3
- RBJOYUAKTJHSNU-UHFFFAOYSA-N NN(c(cccn1)c1O1)C1=O Chemical compound NN(c(cccn1)c1O1)C1=O RBJOYUAKTJHSNU-UHFFFAOYSA-N 0.000 description 1
- SBMSLRMNBSMKQC-UHFFFAOYSA-N NN1CCCC1 Chemical compound NN1CCCC1 SBMSLRMNBSMKQC-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D401/02—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 containing two hetero rings
- C07D401/06—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 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Virology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Tropical Medicine & Parasitology (AREA)
- Molecular Biology (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- AIDS & HIV (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US376907P | 2007-11-20 | 2007-11-20 | |
| US61/003,769 | 2007-11-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| RU2010125220A true RU2010125220A (ru) | 2011-12-27 |
Family
ID=40336474
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| RU2010125220/04A RU2010125220A (ru) | 2007-11-20 | 2008-11-14 | Ненуклеозидные ингибиторы обратной транскриптазы |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8404856B2 (https=) |
| EP (1) | EP2222661B1 (https=) |
| JP (1) | JP5539216B2 (https=) |
| KR (1) | KR20100088142A (https=) |
| CN (1) | CN101952274A (https=) |
| AU (1) | AU2008326784B2 (https=) |
| BR (1) | BRPI0820162A2 (https=) |
| CA (1) | CA2705834A1 (https=) |
| IL (1) | IL205386A0 (https=) |
| MX (1) | MX2010005483A (https=) |
| RU (1) | RU2010125220A (https=) |
| WO (1) | WO2009067166A2 (https=) |
Families Citing this family (19)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010026075A1 (en) * | 2008-09-04 | 2010-03-11 | F. Hoffmann-La Roche Ag | Pyridine derivatives as inhibitors of hiv-i reverse transcriptase |
| EP2491033A4 (en) * | 2009-10-20 | 2013-03-13 | Eiger Biopharmaceuticals Inc | AZAINDAZOLES FOR THE TREATMENT OF FLAVIVIRIDAE VIRUS INFECTION |
| SI2924034T1 (sl) * | 2010-03-30 | 2017-05-31 | Merck Canada Inc. | Farmacevtski sestavek, ki obsega nenukleozidni inhibitor reverzne transkriptaze |
| EP2558093A4 (en) * | 2010-04-08 | 2013-10-02 | Merck Sharp & Dohme | PRODRUGS OF HIV INVERTER TRANSCRIPTASE INHIBITOR |
| CA2882947A1 (en) * | 2012-09-26 | 2014-04-03 | Merck Sharp & Dohme Corp. | Crystalline form of a reverse transcriptase inhibitor |
| JO3470B1 (ar) | 2012-10-08 | 2020-07-05 | Merck Sharp & Dohme | مشتقات 5- فينوكسي-3h-بيريميدين-4-أون واستخدامها كمثبطات ناسخ عكسي ل hiv |
| BR112015012843B8 (pt) * | 2012-12-05 | 2023-04-25 | Merck Sharp & Dohme | Método para sintetizar o composto |
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| US20220242847A1 (en) * | 2019-05-22 | 2022-08-04 | Merck Sharp & Dohme Corp. | Pyridinone derivatives as selective cytotoxic agents against hiv infected cells |
| CN110066273A (zh) * | 2019-06-05 | 2019-07-30 | 山东大学 | 一种含三氮唑环的单芳基嘧啶类hiv-1逆转录酶抑制剂及其制备方法与应用 |
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| IL99731A0 (en) * | 1990-10-18 | 1992-08-18 | Merck & Co Inc | Hydroxylated pyridine derivatives,their preparation and pharmaceutical compositions containing them |
| CA2160928C (en) * | 1993-07-28 | 2005-07-05 | Garry Fenton | Compounds as pde iv and tnf inhibitors |
| BR9909976A (pt) | 1998-04-27 | 2000-12-26 | Centre Nat Rech Scient | Composto, processo para a obtenção de compostos, derivado litiado, composições farmacêuticas, e, processos de tratamento de doenças relacionadas com hiv e de tratamento de infecção de hiv |
| GB9910577D0 (en) | 1999-05-08 | 1999-07-07 | Zeneca Ltd | Chemical compounds |
| SE9904045D0 (sv) | 1999-11-09 | 1999-11-09 | Astra Ab | Compounds |
| WO2001056990A2 (en) | 2000-02-03 | 2001-08-09 | Eli Lilly And Company | Pyridine derivates as potentiators of glutamate receptors |
| EP1317450B1 (en) | 2000-09-15 | 2006-11-22 | Vertex Pharmaceuticals Incorporated | Pyrazole compounds useful as protein kinase inhibitors |
| ATE319706T1 (de) * | 2000-09-19 | 2006-03-15 | Centre Nat Rech Scient | Pyridinon und pyridinethion-derivate mit hiv- hemmenden eigenschaften |
| GB0129260D0 (en) | 2001-12-06 | 2002-01-23 | Eisai London Res Lab Ltd | Pharmaceutical compositions and their uses |
| RS52392B (sr) * | 2002-02-14 | 2013-02-28 | Pharmacia Corporation | Supstituisani piridinoni kao modulatori p38 map kinaze |
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| AU2006303367A1 (en) | 2005-10-19 | 2007-04-26 | F. Hoffmann-La Roche Ag | N-phenyl phenylacetamide non-nucleoside reverse transcriptase inihibitors |
| WO2007045573A1 (en) | 2005-10-19 | 2007-04-26 | F. Hoffmann-La Roche Ag | Phenyl-acetamide nnrt inhibitors |
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| TW200831085A (en) | 2006-12-13 | 2008-08-01 | Merck & Co Inc | Non-nucleoside reverse transcriptase inhibitors |
| WO2008098143A2 (en) * | 2007-02-08 | 2008-08-14 | Trius Therapeutics | Antimicrobial compounds and methods of use |
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2008
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- 2008-11-14 US US12/742,159 patent/US8404856B2/en active Active
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| MX2010005483A (es) | 2010-06-11 |
| AU2008326784A1 (en) | 2009-05-28 |
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| IL205386A0 (en) | 2010-12-30 |
| KR20100088142A (ko) | 2010-08-06 |
| CA2705834A1 (en) | 2009-05-28 |
| AU2008326784B2 (en) | 2014-04-24 |
| EP2222661B1 (en) | 2016-04-20 |
| BRPI0820162A2 (pt) | 2019-09-24 |
| CN101952274A (zh) | 2011-01-19 |
| EP2222661A2 (en) | 2010-09-01 |
| JP2011503230A (ja) | 2011-01-27 |
| US20100256181A1 (en) | 2010-10-07 |
| WO2009067166A2 (en) | 2009-05-28 |
| JP5539216B2 (ja) | 2014-07-02 |
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