JP2016512511A5 - - Google Patents
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- Publication number
- JP2016512511A5 JP2016512511A5 JP2016500985A JP2016500985A JP2016512511A5 JP 2016512511 A5 JP2016512511 A5 JP 2016512511A5 JP 2016500985 A JP2016500985 A JP 2016500985A JP 2016500985 A JP2016500985 A JP 2016500985A JP 2016512511 A5 JP2016512511 A5 JP 2016512511A5
- Authority
- JP
- Japan
- Prior art keywords
- butoxy
- tert
- acetic acid
- methylpyrazolo
- pyrimidin
- 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.)
- Ceased
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- 125000000217 alkyl group Chemical group 0.000 claims 24
- -1 benzoimidazolyl Chemical group 0.000 claims 23
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 claims 21
- 125000001424 substituent group Chemical group 0.000 claims 14
- 125000001188 haloalkyl group Chemical group 0.000 claims 13
- 125000001475 halogen functional group Chemical group 0.000 claims 13
- 150000001875 compounds Chemical class 0.000 claims 10
- 125000003342 alkenyl group Chemical group 0.000 claims 9
- 125000003302 alkenyloxy group Chemical group 0.000 claims 8
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims 8
- 125000004438 haloalkoxy group Chemical group 0.000 claims 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 8
- 125000004213 tert-butoxy group Chemical group [H]C([H])([H])C(O*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 7
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 6
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims 6
- 239000003112 inhibitor Substances 0.000 claims 6
- 125000004943 pyrimidin-6-yl group Chemical group N1=CN=CC=C1* 0.000 claims 5
- 208000031886 HIV Infections Diseases 0.000 claims 4
- 108010078851 HIV Reverse Transcriptase Proteins 0.000 claims 4
- 208000037357 HIV infectious disease Diseases 0.000 claims 4
- 125000005336 allyloxy group Chemical group 0.000 claims 4
- 208000033519 human immunodeficiency virus infectious disease Diseases 0.000 claims 4
- 239000002777 nucleoside Substances 0.000 claims 4
- 150000003833 nucleoside derivatives Chemical class 0.000 claims 4
- 239000003419 rna directed dna polymerase inhibitor Substances 0.000 claims 4
- 150000003839 salts Chemical class 0.000 claims 4
- 125000000499 benzofuranyl group Chemical group O1C(=CC2=C1C=CC=C2)* 0.000 claims 3
- 125000004196 benzothienyl group Chemical group S1C(=CC2=C1C=CC=C2)* 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 125000003016 chromanyl group Chemical group O1C(CCC2=CC=CC=C12)* 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- 125000002883 imidazolyl group Chemical group 0.000 claims 3
- 125000001041 indolyl group Chemical group 0.000 claims 3
- 125000001715 oxadiazolyl group Chemical group 0.000 claims 3
- 125000002971 oxazolyl group Chemical group 0.000 claims 3
- 125000003386 piperidinyl group Chemical group 0.000 claims 3
- 125000003226 pyrazolyl group Chemical group 0.000 claims 3
- 125000000335 thiazolyl group Chemical group 0.000 claims 3
- 125000001544 thienyl group Chemical group 0.000 claims 3
- LZOZJWGPUDSKFN-UHFFFAOYSA-N 8-fluoro-5-methyl-3,4-dihydro-2h-chromene Chemical compound O1CCCC2=C1C(F)=CC=C2C LZOZJWGPUDSKFN-UHFFFAOYSA-N 0.000 claims 2
- 208000030507 AIDS Diseases 0.000 claims 2
- 102100035875 C-C chemokine receptor type 5 Human genes 0.000 claims 2
- 101710149870 C-C chemokine receptor type 5 Proteins 0.000 claims 2
- 102100031650 C-X-C chemokine receptor type 4 Human genes 0.000 claims 2
- 229940099797 HIV integrase inhibitor Drugs 0.000 claims 2
- 229940122440 HIV protease inhibitor Drugs 0.000 claims 2
- 101000922348 Homo sapiens C-X-C chemokine receptor type 4 Proteins 0.000 claims 2
- 125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 claims 2
- 230000034303 cell budding Effects 0.000 claims 2
- 125000004093 cyano group Chemical group *C#N 0.000 claims 2
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 2
- 239000003937 drug carrier Substances 0.000 claims 2
- 239000002835 hiv fusion inhibitor Substances 0.000 claims 2
- 239000003084 hiv integrase inhibitor Substances 0.000 claims 2
- 239000004030 hiv protease inhibitor Substances 0.000 claims 2
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 230000035800 maturation Effects 0.000 claims 2
- 239000000203 mixture Substances 0.000 claims 2
- 239000008194 pharmaceutical composition Substances 0.000 claims 2
- CWOLTMOLAIYUFS-XIFFEERXSA-N (2S)-2-[7-(8-fluoro-5-methyl-3,4-dihydro-2H-chromen-6-yl)-5-methyl-2-(6-phenyl-1H-benzimidazol-2-yl)pyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound Cc1nc2cc(nn2c(-c2cc(F)c3OCCCc3c2C)c1[C@H](OC(C)(C)C)C(O)=O)-c1nc2cc(ccc2[nH]1)-c1ccccc1 CWOLTMOLAIYUFS-XIFFEERXSA-N 0.000 claims 1
- JARWJCRLYLIATB-SANMLTNESA-N (2s)-2-[2-(1-benzylpyrazol-4-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C3=CN(CC=4C=CC=CC=4)N=C3)=NN2C=1N1CCC(C)(C)CC1 JARWJCRLYLIATB-SANMLTNESA-N 0.000 claims 1
- OSLZWNQMOQESGQ-VWLOTQADSA-N (2s)-2-[2-(3-benzyl-2-oxoimidazolidin-1-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3C(N(CC=4C=CC=CC=4)CC3)=O)=NN2C=1N1CCC(C)(C)CC1 OSLZWNQMOQESGQ-VWLOTQADSA-N 0.000 claims 1
- RMXYVRPUEQROKQ-SANMLTNESA-N (2s)-2-[2-(3-benzylpyrazol-1-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3N=C(CC=4C=CC=CC=4)C=C3)=NN2C=1N1CCC(C)(C)CC1 RMXYVRPUEQROKQ-SANMLTNESA-N 0.000 claims 1
- RXCWGEDNAQJWCW-QBGQUKIHSA-N (2s)-2-[2-(4-benzyl-2-oxo-1,3-oxazolidin-3-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3C(OCC3CC=3C=CC=CC=3)=O)=NN2C=1N1CCC(C)(C)CC1 RXCWGEDNAQJWCW-QBGQUKIHSA-N 0.000 claims 1
- UUFIOPPDYIQUQS-VWLOTQADSA-N (2s)-2-[2-(4-benzyl-3-chloropyrazol-1-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3N=C(Cl)C(CC=4C=CC=CC=4)=C3)=NN2C=1N1CCC(C)(C)CC1 UUFIOPPDYIQUQS-VWLOTQADSA-N 0.000 claims 1
- APJCPLYCGMOTQA-SANMLTNESA-N (2s)-2-[2-(4-benzylimidazol-1-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3C=C(CC=4C=CC=CC=4)N=C3)=NN2C=1N1CCC(C)(C)CC1 APJCPLYCGMOTQA-SANMLTNESA-N 0.000 claims 1
- IYLUTKNUURMKLM-SANMLTNESA-N (2s)-2-[2-(4-benzylpyrazol-1-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3N=CC(CC=4C=CC=CC=4)=C3)=NN2C=1N1CCC(C)(C)CC1 IYLUTKNUURMKLM-SANMLTNESA-N 0.000 claims 1
- UEMTXTCLWRVXMH-QBGQUKIHSA-N (2s)-2-[2-(5-benzyl-2-oxo-1,3-oxazolidin-3-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3C(OC(CC=4C=CC=CC=4)C3)=O)=NN2C=1N1CCC(C)(C)CC1 UEMTXTCLWRVXMH-QBGQUKIHSA-N 0.000 claims 1
- AMNYYVYPODVSTK-SANMLTNESA-N (2s)-2-[2-(5-benzylpyrazol-1-yl)-7-(4,4-dimethylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3C(=CC=N3)CC=3C=CC=CC=3)=NN2C=1N1CCC(C)(C)CC1 AMNYYVYPODVSTK-SANMLTNESA-N 0.000 claims 1
- MHIXTSDZCWLPNI-VWLOTQADSA-N (2s)-2-[2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-5-methyl-7-(4-methyl-3,6-dihydro-2h-pyridin-1-yl)pyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound C1CC(C)=CCN1C1=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN12 MHIXTSDZCWLPNI-VWLOTQADSA-N 0.000 claims 1
- ICNMTMFUUIWPNH-PMERELPUSA-N (2s)-2-[2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-5-methyl-7-(4-phenyl-3,6-dihydro-2h-pyridin-1-yl)pyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN2C=1N(CC=1)CCC=1C1=CC=CC=C1 ICNMTMFUUIWPNH-PMERELPUSA-N 0.000 claims 1
- WGFWHGVZSUYWMN-DEOSSOPVSA-N (2s)-2-[2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-7-(4-hydroxy-4-methylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN2C=1N1CCC(C)(O)CC1 WGFWHGVZSUYWMN-DEOSSOPVSA-N 0.000 claims 1
- AMCBTFLGLPPAOR-VWLOTQADSA-N (2s)-2-[2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-7-(4-methoxy-4-methylpiperidin-1-yl)-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound C1CC(OC)(C)CCN1C1=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN12 AMCBTFLGLPPAOR-VWLOTQADSA-N 0.000 claims 1
- KFXSYVHURPBUJH-VWLOTQADSA-N (2s)-2-[2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-7-[4-(hydroxymethyl)-4-methylpiperidin-1-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN2C=1N1CCC(C)(CO)CC1 KFXSYVHURPBUJH-VWLOTQADSA-N 0.000 claims 1
- XFFFHJRJTNOYIU-MHZLTWQESA-N (2s)-2-[7-(4,4-dimethylcyclohexyl)-2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN2C=1C1CCC(C)(C)CC1 XFFFHJRJTNOYIU-MHZLTWQESA-N 0.000 claims 1
- WCICUWAODBICEH-VWLOTQADSA-N (2s)-2-[7-(4,4-dimethylpiperidin-1-yl)-2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN2C=1N1CCC(C)(C)CC1 WCICUWAODBICEH-VWLOTQADSA-N 0.000 claims 1
- SFLJSPLNMRWBAV-MHZLTWQESA-N (2s)-2-[7-(4,4-dimethylpiperidin-1-yl)-2-[5-[(4-fluorophenyl)methyl]thiophen-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CC=3)=NN2C=1N1CCC(C)(C)CC1 SFLJSPLNMRWBAV-MHZLTWQESA-N 0.000 claims 1
- KAWLRRIDNLNTEZ-IHZSNKTASA-N (2s)-2-[7-(4,4-dimethylpiperidin-1-yl)-2-[5-[1-(4-fluorophenyl)ethyl]-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound C=1C=C(F)C=CC=1C(C)C(S1)=CN=C1C(=NN12)C=C1N=C(C)C([C@H](OC(C)(C)C)C(O)=O)=C2N1CCC(C)(C)CC1 KAWLRRIDNLNTEZ-IHZSNKTASA-N 0.000 claims 1
- JOIROVAPLYJWCW-SANMLTNESA-N (2s)-2-[7-(4,4-dimethylpiperidin-1-yl)-2-[5-[2-(4-fluorophenyl)ethyl]-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CCC=4C=CC(F)=CC=4)=CN=3)=NN2C=1N1CCC(C)(C)CC1 JOIROVAPLYJWCW-SANMLTNESA-N 0.000 claims 1
- QGIUCHRNNBHRCK-QBGQUKIHSA-N (2s)-2-[7-(4,4-dimethylpiperidin-1-yl)-5-methyl-2-(2-oxo-3-phenoxypyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(N3C(C(OC=4C=CC=CC=4)CC3)=O)=NN2C=1N1CCC(C)(C)CC1 QGIUCHRNNBHRCK-QBGQUKIHSA-N 0.000 claims 1
- VOTWBINOKCQRML-MHZLTWQESA-N (2s)-2-[7-(4-cyclopropyl-4-methylpiperidin-1-yl)-2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound CC(C)(C)O[C@H](C(O)=O)C=1C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN2C=1N(CC1)CCC1(C)C1CC1 VOTWBINOKCQRML-MHZLTWQESA-N 0.000 claims 1
- MDIYXGKYEMEDME-SANMLTNESA-N (2s)-2-[7-(4-ethyl-4-methylpiperidin-1-yl)-2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound C1CC(CC)(C)CCN1C1=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC(C=3SC(CC=4C=CC(F)=CC=4)=CN=3)=NN12 MDIYXGKYEMEDME-SANMLTNESA-N 0.000 claims 1
- YAVQIOMBGSKMCJ-LJAQVGFWSA-N (2s)-2-[7-(8-fluoro-5-methyl-3,4-dihydro-2h-chromen-6-yl)-2-[3-[(4-fluorophenyl)methyl]-1,2,4-oxadiazol-5-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound N=1N2C(C=3C(=C4CCCOC4=C(F)C=3)C)=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC=1C(ON=1)=NC=1CC1=CC=C(F)C=C1 YAVQIOMBGSKMCJ-LJAQVGFWSA-N 0.000 claims 1
- HUECDZXIUWSMDZ-LJAQVGFWSA-N (2s)-2-[7-(8-fluoro-5-methyl-3,4-dihydro-2h-chromen-6-yl)-2-[5-(3-fluorophenyl)-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound N=1N2C(C=3C(=C4CCCOC4=C(F)C=3)C)=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC=1C(S1)=NC=C1C1=CC=CC(F)=C1 HUECDZXIUWSMDZ-LJAQVGFWSA-N 0.000 claims 1
- FWHOVQXUKGGDIE-LJAQVGFWSA-N (2s)-2-[7-(8-fluoro-5-methyl-3,4-dihydro-2h-chromen-6-yl)-2-[5-(4-fluorophenyl)-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound N=1N2C(C=3C(=C4CCCOC4=C(F)C=3)C)=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC=1C(S1)=NC=C1C1=CC=C(F)C=C1 FWHOVQXUKGGDIE-LJAQVGFWSA-N 0.000 claims 1
- RNBBOMASJBJJIZ-PMERELPUSA-N (2s)-2-[7-(8-fluoro-5-methyl-3,4-dihydro-2h-chromen-6-yl)-2-[5-[(4-fluorophenyl)methyl]-1,3-oxazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound N=1N2C(C=3C(=C4CCCOC4=C(F)C=3)C)=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC=1C(O1)=NC=C1CC1=CC=C(F)C=C1 RNBBOMASJBJJIZ-PMERELPUSA-N 0.000 claims 1
- ZKSHDNQVKPHIQJ-PMERELPUSA-N (2s)-2-[7-(8-fluoro-5-methyl-3,4-dihydro-2h-chromen-6-yl)-2-[5-[(4-fluorophenyl)methyl]-1,3-thiazol-2-yl]-5-methylpyrazolo[1,5-a]pyrimidin-6-yl]-2-[(2-methylpropan-2-yl)oxy]acetic acid Chemical compound N=1N2C(C=3C(=C4CCCOC4=C(F)C=3)C)=C([C@H](OC(C)(C)C)C(O)=O)C(C)=NC2=CC=1C(S1)=NC=C1CC1=CC=C(F)C=C1 ZKSHDNQVKPHIQJ-PMERELPUSA-N 0.000 claims 1
- RRZVGDGTWNQAPW-UHFFFAOYSA-N 4-[5-(1-methylpyrazol-4-yl)-3-[2-(1-methylpyrazol-4-yl)ethyl]imidazol-4-yl]benzonitrile Chemical compound C1=NN(C)C=C1CCN1C(C=2C=CC(=CC=2)C#N)=C(C2=CN(C)N=C2)N=C1 RRZVGDGTWNQAPW-UHFFFAOYSA-N 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000002393 azetidinyl group Chemical group 0.000 claims 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 1
- 125000000596 cyclohexenyl group Chemical group C1(=CCCCC1)* 0.000 claims 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 1
- 125000002541 furyl group Chemical group 0.000 claims 1
- 230000005764 inhibitory process Effects 0.000 claims 1
- 125000001786 isothiazolyl group Chemical group 0.000 claims 1
- 125000000842 isoxazolyl group Chemical group 0.000 claims 1
- 125000002757 morpholinyl group Chemical group 0.000 claims 1
- 125000004193 piperazinyl group Chemical group 0.000 claims 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 claims 1
- 125000000168 pyrrolyl group Chemical group 0.000 claims 1
- 230000001225 therapeutic effect Effects 0.000 claims 1
- 238000002560 therapeutic procedure Methods 0.000 claims 1
- 125000001113 thiadiazolyl group Chemical group 0.000 claims 1
- 125000001425 triazolyl group Chemical group 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361779858P | 2013-03-13 | 2013-03-13 | |
| US61/779,858 | 2013-03-13 | ||
| PCT/US2014/022501 WO2014164467A1 (en) | 2013-03-13 | 2014-03-10 | Inhibitors of human immunodeficiency virus replication |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2016512511A JP2016512511A (ja) | 2016-04-28 |
| JP2016512511A5 true JP2016512511A5 (https=) | 2017-04-13 |
Family
ID=50478938
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016500985A Ceased JP2016512511A (ja) | 2013-03-13 | 2014-03-10 | ヒト免疫不全ウイルス複製の阻害剤 |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US9580431B2 (https=) |
| EP (1) | EP2970298A1 (https=) |
| JP (1) | JP2016512511A (https=) |
| CN (1) | CN105189511B (https=) |
| WO (1) | WO2014164467A1 (https=) |
Families Citing this family (24)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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| MX2017015256A (es) | 2015-05-29 | 2018-02-19 | Shionogi & Co | Derivados triciclicos que contienen nitrogeno que tienen actividad inhibidora de la replicacion del virus de inmunodeficiencia adquirida (vih). |
| WO2017006261A1 (en) | 2015-07-06 | 2017-01-12 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| US10221156B2 (en) | 2015-07-08 | 2019-03-05 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| CN107820492A (zh) | 2015-07-09 | 2018-03-20 | Viiv保健英国第五有限公司 | 作为人类免疫缺陷病毒复制抑制剂的吡啶‑3‑基乙酸衍生物 |
| AU2016290205A1 (en) | 2015-07-09 | 2018-01-18 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| BR112018002403A2 (pt) | 2015-08-07 | 2018-09-18 | Viiv Healthcare Uk No 5 Ltd | composto, e, composição útil e método para tratar infecção de hiv |
| AU2016305338A1 (en) | 2015-08-10 | 2018-03-01 | VIIV Healthcare UK (No.5) Limited | Imidazopyridine macrocycles as inhibitors of human immunodeficiency virus replication |
| AR105653A1 (es) | 2015-08-11 | 2017-10-25 | VIIV HEALTHCARE UK (Nº 5) LTD | Derivados del ácido 5-(n-bencil-tetrahidroisoquinolin-6-il)-piridin-3-il acético como inhibidores de la replicación del virus de la inmunodeficiencia humana |
| PT3334723T (pt) | 2015-08-12 | 2019-12-19 | Viiv Healthcare Uk No 5 Ltd | Composto, composição, e, método para tratar infecção por hiv |
| EP3334722A1 (en) | 2015-08-12 | 2018-06-20 | VIIV Healthcare UK (No.5) Limited | 5-(n-fused tricyclic aryl tetrahydroisoquinolin-6-yl) pyridin-3- yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| TW201718537A (zh) * | 2015-08-12 | 2017-06-01 | Ｖｉｉｖ醫療保健英國（Ｎｏ．５）有限公司 | 做為人類免疫缺陷病毒複製抑制劑之吡啶－３－基乙酸衍生物 |
| AU2016307987B2 (en) | 2015-08-20 | 2018-08-30 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| US10407410B2 (en) | 2016-05-11 | 2019-09-10 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| JP2019515000A (ja) | 2016-05-11 | 2019-06-06 | ヴィーブ ヘルスケア ユーケー（ナンバー５）リミテッド | ヒト免疫不全ウイルス複製の阻害剤としてのピリジン−３−イル酢酸誘導体 |
| JP2019515939A (ja) | 2016-05-11 | 2019-06-13 | ヴィーブ ヘルスケア ユーケー（ナンバー５）リミテッド | ヒト免疫不全ウイルス複製の阻害剤としてのピリジン−３−イル酢酸誘導体 |
| JP2020503352A (ja) | 2017-01-03 | 2020-01-30 | ヴィーブ ヘルスケア ユーケー（ナンバー５）リミテッド | ヒト免疫不全ウイルス複製の阻害剤としてのピリジン−３−イル酢酸誘導体 |
| EP3565809A1 (en) | 2017-01-03 | 2019-11-13 | ViiV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| US10234220B2 (en) * | 2017-04-14 | 2019-03-19 | Kent J. Myers | Detachable box magazine with follower retraction member |
| IL276013B2 (en) * | 2018-01-17 | 2024-03-01 | Glaxosmithkline Ip Dev Ltd | Pi4kiiibeta inhibitors |
| WO2019244066A2 (en) | 2018-06-19 | 2019-12-26 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
| WO2020003093A1 (en) | 2018-06-25 | 2020-01-02 | VIIV Healthcare UK (No.5) Limited | Pyridin-3-yl acetic acid derivatives as inhibitors of human immunodeficiency virus replication |
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| DE69922494T2 (de) | 1998-02-04 | 2005-05-25 | Banyu Pharmaceutical Co., Ltd. | Zyklische n-acylamin-derivate |
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| KR20090047450A (ko) | 2006-08-04 | 2009-05-12 | 메르츠 파마 게엠베하 운트 코. 카가아 | 치환된 피라졸로피리미딘, 이의 제조 방법 및 의약품으로서의 이의 용도 |
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| KR20130124291A (ko) | 2010-07-02 | 2013-11-13 | 길리애드 사이언시즈, 인코포레이티드 | Ｈｉｖ 항바이러스 화합물로서의 2-퀴놀리닐-아세트산 유도체 |
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| WO2012066442A1 (en) | 2010-11-15 | 2012-05-24 | Pfizer Limited | Inhibitors of hiv replication |
| JP2013542243A (ja) | 2010-11-15 | 2013-11-21 | カトリーケ ウニヴェルシテイト ルーヴェン | 新規な抗ウイルス性化合物 |
| US8791108B2 (en) * | 2011-08-18 | 2014-07-29 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| US9034882B2 (en) * | 2012-03-05 | 2015-05-19 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
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2014
- 2014-03-10 WO PCT/US2014/022501 patent/WO2014164467A1/en not_active Ceased
- 2014-03-10 EP EP14717006.2A patent/EP2970298A1/en active Pending
- 2014-03-10 CN CN201480026834.8A patent/CN105189511B/zh not_active Expired - Fee Related
- 2014-03-10 JP JP2016500985A patent/JP2016512511A/ja not_active Ceased
- 2014-03-10 US US14/772,146 patent/US9580431B2/en not_active Expired - Fee Related
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