AR116909A1 - Derivados bicíclicos - Google Patents
Derivados bicíclicosInfo
- Publication number
- AR116909A1 AR116909A1 ARP190103665A ARP190103665A AR116909A1 AR 116909 A1 AR116909 A1 AR 116909A1 AR P190103665 A ARP190103665 A AR P190103665A AR P190103665 A ARP190103665 A AR P190103665A AR 116909 A1 AR116909 A1 AR 116909A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- chroman
- carboxamide
- naphthyridine
- dichlorophenyl
- Prior art date
Links
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 122
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 33
- 229910052739 hydrogen Inorganic materials 0.000 abstract 25
- 239000001257 hydrogen Substances 0.000 abstract 25
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 25
- -1 -CHO Chemical group 0.000 abstract 20
- 229910052736 halogen Inorganic materials 0.000 abstract 16
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 15
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 15
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 abstract 14
- 229910052757 nitrogen Inorganic materials 0.000 abstract 13
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 12
- 125000001424 substituent group Chemical group 0.000 abstract 12
- 125000005843 halogen group Chemical group 0.000 abstract 11
- 229910052760 oxygen Inorganic materials 0.000 abstract 10
- 229910052717 sulfur Inorganic materials 0.000 abstract 10
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 8
- 150000002367 halogens Chemical group 0.000 abstract 7
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 abstract 6
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 6
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 125000003545 alkoxy group Chemical group 0.000 abstract 4
- 125000003118 aryl group Chemical group 0.000 abstract 4
- 125000004043 oxo group Chemical group O=* 0.000 abstract 4
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000005842 heteroatom Chemical group 0.000 abstract 3
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 2
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 abstract 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 abstract 2
- 125000006163 5-membered heteroaryl group Chemical group 0.000 abstract 2
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 2
- JVPLUVNNWQOXJW-IBGZPJMESA-N ClC1=CC=CC(=C1Cl)C1=CN=CC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC=CC(=C1Cl)C1=CN=CC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 JVPLUVNNWQOXJW-IBGZPJMESA-N 0.000 abstract 2
- 101001043818 Mus musculus Interleukin-31 receptor subunit alpha Proteins 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 125000001153 fluoro group Chemical group F* 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- LCCRVUGAKMYOFL-FQEVSTJZSA-N 4-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-8-(dimethylamino)-6H-pyrido[2,3-d]pyridazine-7-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C1=CC=NC=2C1=CNN(C=2N(C)C)C(=O)N[C@H]1CCOC2=CC=CC=C12 LCCRVUGAKMYOFL-FQEVSTJZSA-N 0.000 abstract 1
- JEHOIUWCOWFECR-QFIPXVFZSA-N 4-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-8-morpholin-4-yl-6H-pyrido[2,3-d]pyridazine-7-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C1=CC=NC=2C1=CNN(C=2N1CCOCC1)C(=O)N[C@H]1CCOC2=CC=CC=C12 JEHOIUWCOWFECR-QFIPXVFZSA-N 0.000 abstract 1
- BQTLPFWLTUKQPM-NRFANRHFSA-N 4-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-8-(dimethylamino)-6H-pyrido[2,3-d]pyridazine-7-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C1=CC=NC=2C1=CNN(C=2N(C)C)C(=O)N[C@H]1CCOC2=CC=CC=C12 BQTLPFWLTUKQPM-NRFANRHFSA-N 0.000 abstract 1
- AARPNLNVDKENJH-IBGZPJMESA-N 4-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-8-(dimethylamino)pyrido[3,2-d]pyrimidine-7-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C=1C2=C(N=CN=1)C(=C(C=N2)C(=O)N[C@H]1CCOC2=CC=CC=C12)N(C)C AARPNLNVDKENJH-IBGZPJMESA-N 0.000 abstract 1
- PTYIDYYVKFVCNZ-QHCPKHFHSA-N 4-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-8-morpholin-4-yl-6H-pyrido[2,3-d]pyridazine-7-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C1=CC=NC=2C1=CNN(C=2N1CCOCC1)C(=O)N[C@H]1CCOC2=CC=CC=C12 PTYIDYYVKFVCNZ-QHCPKHFHSA-N 0.000 abstract 1
- VSHVSOSWLUHWNB-NRFANRHFSA-N 4-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-8-morpholin-4-ylpyrido[3,2-d]pyrimidine-7-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C=1C2=C(N=CN=1)C(=C(C=N2)C(=O)N[C@H]1CCOC2=CC=CC=C12)N1CCOCC1 VSHVSOSWLUHWNB-NRFANRHFSA-N 0.000 abstract 1
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 abstract 1
- BVXQMIIJTPAIQM-IBGZPJMESA-N 7-chloro-8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=CN=C2C(=C(C=NC2=C1C1=C(C(=CC=C1)Cl)Cl)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C BVXQMIIJTPAIQM-IBGZPJMESA-N 0.000 abstract 1
- MIJPYMJCEYGNNF-NRFANRHFSA-N 7-chloro-8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-morpholin-4-yl-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=CN=C2C(=C(C=NC2=C1C1=C(C(=CC=C1)Cl)Cl)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1 MIJPYMJCEYGNNF-NRFANRHFSA-N 0.000 abstract 1
- GBKUCZCNVHVMFM-FQEVSTJZSA-N 7-chloro-8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=CN=C2C(=C(C=NC2=C1C1=CC(=CC(=C1)Cl)Cl)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C GBKUCZCNVHVMFM-FQEVSTJZSA-N 0.000 abstract 1
- MYPHJKZPXLIZBN-IBGZPJMESA-N 7-chloro-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-8-(2,3,5-trifluorophenyl)-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=CN=C2C(=C(C=NC2=C1C1=C(C(=CC(=C1)F)F)F)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C MYPHJKZPXLIZBN-IBGZPJMESA-N 0.000 abstract 1
- MFGDSIAYQCUTTO-NRFANRHFSA-N 7-chloro-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-morpholin-4-yl-8-(2,3,5-trifluorophenyl)-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=CN=C2C(=C(C=NC2=C1C1=C(C(=CC(=C1)F)F)F)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1 MFGDSIAYQCUTTO-NRFANRHFSA-N 0.000 abstract 1
- CUYYGFUGQMTZLL-FQEVSTJZSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-1,7-naphthyridine-3-carboxamide Chemical compound CN(C)C1=C2C=CN=C(C3=C(Cl)C(Cl)=CC=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 CUYYGFUGQMTZLL-FQEVSTJZSA-N 0.000 abstract 1
- XCOSGCUCYATSHK-IBGZPJMESA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-5-fluoro-1,7-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1N=CC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)F XCOSGCUCYATSHK-IBGZPJMESA-N 0.000 abstract 1
- MNLATFKKAOZKTJ-FQEVSTJZSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-5-methoxy-1,6-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1C=NC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)OC MNLATFKKAOZKTJ-FQEVSTJZSA-N 0.000 abstract 1
- AUNBSVLIOSGPSM-IBGZPJMESA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-5-methoxy-1,7-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1N=CC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)OC AUNBSVLIOSGPSM-IBGZPJMESA-N 0.000 abstract 1
- REDBHBKTFLQOAG-IBGZPJMESA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-7-fluoro-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1C(=CN=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)F REDBHBKTFLQOAG-IBGZPJMESA-N 0.000 abstract 1
- QSFRVQQPONIHFJ-IBGZPJMESA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-7-methoxy-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1C(=CN=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)OC QSFRVQQPONIHFJ-IBGZPJMESA-N 0.000 abstract 1
- JDULLCYQDSPZKV-FQEVSTJZSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-7-methoxy-1,6-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1C(=NC=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)OC JDULLCYQDSPZKV-FQEVSTJZSA-N 0.000 abstract 1
- KASIFTAJEGASTK-QFIPXVFZSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-morpholin-4-yl-1,7-naphthyridine-3-carboxamide Chemical compound ClC1=CC=CC(=C1Cl)C1=NC=CC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 KASIFTAJEGASTK-QFIPXVFZSA-N 0.000 abstract 1
- ANXFCBLSBHVKGH-IBGZPJMESA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-oxo-1H-1,6-naphthyridine-3-carboxamide Chemical compound ClC1=C(Cl)C(C2=CN=CC3=C2NC=C(C3=O)C(=O)N[C@@H]2C3=CC=CC=C3OCC2)=CC=C1 ANXFCBLSBHVKGH-IBGZPJMESA-N 0.000 abstract 1
- PJVICOLDDUDLHP-NRFANRHFSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-5-fluoro-4-morpholin-4-yl-1,7-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1N=CC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1)F PJVICOLDDUDLHP-NRFANRHFSA-N 0.000 abstract 1
- OIMUCOJIVQVTOL-QFIPXVFZSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-5-methoxy-4-morpholin-4-yl-1,6-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1C=NC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1)OC OIMUCOJIVQVTOL-QFIPXVFZSA-N 0.000 abstract 1
- MQIAZODYOPOYCQ-NRFANRHFSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-5-methoxy-4-morpholin-4-yl-1,7-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1N=CC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1)OC MQIAZODYOPOYCQ-NRFANRHFSA-N 0.000 abstract 1
- AHRDUZRCJBGACA-NRFANRHFSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-7-fluoro-4-morpholin-4-yl-1,5-naphthyridine-3-carboxamide Chemical compound FC1=CN=C2C(N=CC(C(=O)N[C@H]3CCOC4=C3C=CC=C4)=C2N2CCOCC2)=C1C1=C(Cl)C(Cl)=CC=C1 AHRDUZRCJBGACA-NRFANRHFSA-N 0.000 abstract 1
- BZQQHOFWOCXPDM-NRFANRHFSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-7-methoxy-4-morpholin-4-yl-1,5-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1C(=CN=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1)OC BZQQHOFWOCXPDM-NRFANRHFSA-N 0.000 abstract 1
- RJRBGTUZKUYQJH-QFIPXVFZSA-N 8-(2,3-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-7-methoxy-4-morpholin-4-yl-1,6-naphthyridine-3-carboxamide Chemical compound ClC1=C(C=CC=C1Cl)C=1C(=NC=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1)OC RJRBGTUZKUYQJH-QFIPXVFZSA-N 0.000 abstract 1
- NTQJEXTTWISVGS-NRFANRHFSA-N 8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-1,7-naphthyridine-3-carboxamide Chemical compound CN(C)C1=C2C=CN=C(C3=CC(Cl)=CC(Cl)=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 NTQJEXTTWISVGS-NRFANRHFSA-N 0.000 abstract 1
- UYSRTNFGWNZJSA-NRFANRHFSA-N 8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-5-methoxy-1,6-naphthyridine-3-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C=1C=NC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)OC UYSRTNFGWNZJSA-NRFANRHFSA-N 0.000 abstract 1
- UTYSGKBUOYRGOM-FQEVSTJZSA-N 8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-7-methoxy-1,5-naphthyridine-3-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C=1C(=CN=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)OC UTYSGKBUOYRGOM-FQEVSTJZSA-N 0.000 abstract 1
- NMRJRCJADOLTDU-NRFANRHFSA-N 8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-7-methoxy-1,6-naphthyridine-3-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C=1C(=NC=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N(C)C)OC NMRJRCJADOLTDU-NRFANRHFSA-N 0.000 abstract 1
- XQFJFPQLCFMQLO-QHCPKHFHSA-N 8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-morpholin-4-yl-1,7-naphthyridine-3-carboxamide Chemical compound ClC1=CC(=CC(Cl)=C1)C1=NC=CC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 XQFJFPQLCFMQLO-QHCPKHFHSA-N 0.000 abstract 1
- BVUHIKFTPPYQLP-QHCPKHFHSA-N 8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-5-methoxy-4-morpholin-4-yl-1,6-naphthyridine-3-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C=1C=NC(=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1)OC BVUHIKFTPPYQLP-QHCPKHFHSA-N 0.000 abstract 1
- UJFCZLRUDQDPTE-QHCPKHFHSA-N 8-(3,5-dichlorophenyl)-N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-7-methoxy-4-morpholin-4-yl-1,6-naphthyridine-3-carboxamide Chemical compound ClC=1C=C(C=C(C=1)Cl)C=1C(=NC=C2C(=C(C=NC=12)C(=O)N[C@H]1CCOC2=C1C=CC=C2)N1CCOCC1)OC UJFCZLRUDQDPTE-QHCPKHFHSA-N 0.000 abstract 1
- LDYRLLDEMDCGSN-AWEZNQCLSA-N BrC1=C2NC=C(C(=O)N[C@H]3CCOC4=CC=CC=C34)C(=O)C2=CN=C1 Chemical compound BrC1=C2NC=C(C(=O)N[C@H]3CCOC4=CC=CC=C34)C(=O)C2=CN=C1 LDYRLLDEMDCGSN-AWEZNQCLSA-N 0.000 abstract 1
- VFGVRRYIDNWASM-NRFANRHFSA-N CN(C)C1=C2C=NC=C(C3=C(Cl)C(Cl)=CC=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound CN(C)C1=C2C=NC=C(C3=C(Cl)C(Cl)=CC=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 VFGVRRYIDNWASM-NRFANRHFSA-N 0.000 abstract 1
- UHHLJTPGZQZPNE-QFIPXVFZSA-N CN(C)C1=C2C=NC=C(C3=CC(Cl)=CC(Cl)=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound CN(C)C1=C2C=NC=C(C3=CC(Cl)=CC(Cl)=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 UHHLJTPGZQZPNE-QFIPXVFZSA-N 0.000 abstract 1
- LVKRNUHFZXOGMG-FQEVSTJZSA-N CN(C)C1=C2N=CC=C(C3=C(Cl)C(Cl)=CC=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound CN(C)C1=C2N=CC=C(C3=C(Cl)C(Cl)=CC=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 LVKRNUHFZXOGMG-FQEVSTJZSA-N 0.000 abstract 1
- CTYURYOIUXWAKQ-NRFANRHFSA-N CN(C)C1=C2N=CC=C(C3=CC(Cl)=CC(Cl)=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound CN(C)C1=C2N=CC=C(C3=CC(Cl)=CC(Cl)=C3)C2=NC=C1C(=O)N[C@H]1CCOC2=CC=CC=C12 CTYURYOIUXWAKQ-NRFANRHFSA-N 0.000 abstract 1
- SPWJKTDOBQYHEB-FQEVSTJZSA-N ClC1=CC(=CC(Cl)=C1)C1=C2NC=C(C(=O)N[C@H]3CCOC4=CC=CC=C34)C(=O)C2=CN=C1 Chemical compound ClC1=CC(=CC(Cl)=C1)C1=C2NC=C(C(=O)N[C@H]3CCOC4=CC=CC=C34)C(=O)C2=CN=C1 SPWJKTDOBQYHEB-FQEVSTJZSA-N 0.000 abstract 1
- CSNUXPHIUYICGA-IBGZPJMESA-N ClC1=CC(=CC(Cl)=C1)C1=CC=NC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC(=CC(Cl)=C1)C1=CC=NC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 CSNUXPHIUYICGA-IBGZPJMESA-N 0.000 abstract 1
- QQEAQCMPNBMZTD-QHCPKHFHSA-N ClC1=CC(=CC(Cl)=C1)C1=CC=NC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC(=CC(Cl)=C1)C1=CC=NC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 QQEAQCMPNBMZTD-QHCPKHFHSA-N 0.000 abstract 1
- DSRMMFGUQBCHQB-FQEVSTJZSA-N ClC1=CC(=CC(Cl)=C1)C1=CN=CC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC(=CC(Cl)=C1)C1=CN=CC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 DSRMMFGUQBCHQB-FQEVSTJZSA-N 0.000 abstract 1
- WYTCOXIJHFVUTE-DEOSSOPVSA-N ClC1=CC(=CC(Cl)=C1)C1=CN=CC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC(=CC(Cl)=C1)C1=CN=CC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 WYTCOXIJHFVUTE-DEOSSOPVSA-N 0.000 abstract 1
- VNYQELJFLPSJBO-SFHVURJKSA-N ClC1=CC=CC(=C1Cl)C1=CC=NC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC=CC(=C1Cl)C1=CC=NC2=C(Cl)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 VNYQELJFLPSJBO-SFHVURJKSA-N 0.000 abstract 1
- QHSBOLXENZGAII-QFIPXVFZSA-N ClC1=CC=CC(=C1Cl)C1=CC=NC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC=CC(=C1Cl)C1=CC=NC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 QHSBOLXENZGAII-QFIPXVFZSA-N 0.000 abstract 1
- PNAKBLGLMXNOPO-QHCPKHFHSA-N ClC1=CC=CC(=C1Cl)C1=CN=CC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 Chemical compound ClC1=CC=CC(=C1Cl)C1=CN=CC2=C(N3CCOCC3)C(=CN=C12)C(=O)N[C@H]1CCOC2=CC=CC=C12 PNAKBLGLMXNOPO-QHCPKHFHSA-N 0.000 abstract 1
- NYUGTVSWJHTTOF-IBGZPJMESA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-5-fluoro-8-(2,3,5-trifluorophenyl)-1,7-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(N=CC(=C2C=1N(C)C)F)C1=C(C(=CC(=C1)F)F)F NYUGTVSWJHTTOF-IBGZPJMESA-N 0.000 abstract 1
- PGXUHTKLTFUYLF-IBGZPJMESA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-5-methoxy-8-(2,3,5-trifluorophenyl)-1,7-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(N=CC(=C2C=1N(C)C)OC)C1=C(C(=CC(=C1)F)F)F PGXUHTKLTFUYLF-IBGZPJMESA-N 0.000 abstract 1
- WAMHOJDKUCLTFQ-IBGZPJMESA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-7-fluoro-8-(2,3,5-trifluorophenyl)-1,5-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(C(=CN=C2C=1N(C)C)F)C1=C(C(=CC(=C1)F)F)F WAMHOJDKUCLTFQ-IBGZPJMESA-N 0.000 abstract 1
- GOSOOTRYSYAWOT-IBGZPJMESA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-(dimethylamino)-7-methoxy-8-(2,3,5-trifluorophenyl)-1,5-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(C(=CN=C2C=1N(C)C)OC)C1=C(C(=CC(=C1)F)F)F GOSOOTRYSYAWOT-IBGZPJMESA-N 0.000 abstract 1
- FLACYJGMEGFKDH-QFIPXVFZSA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-morpholin-4-yl-8-(2,3,5-trichlorophenyl)-1,7-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=CC=CC=C12)NC(=O)C=1C=NC2=C(N=CC=C2C=1N1CCOCC1)C1=C(C(=CC(=C1)Cl)Cl)Cl FLACYJGMEGFKDH-QFIPXVFZSA-N 0.000 abstract 1
- FBTILQNQGVEJPB-QFIPXVFZSA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-4-morpholin-4-yl-8-(2,3,5-trifluorophenyl)-1,7-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(N=CC=C2C=1N1CCOCC1)C1=C(C(=CC(=C1)F)F)F FBTILQNQGVEJPB-QFIPXVFZSA-N 0.000 abstract 1
- UPJACOKSBDADEO-NRFANRHFSA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-5-fluoro-4-morpholin-4-yl-8-(2,3,5-trifluorophenyl)-1,7-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(N=CC(=C2C=1N1CCOCC1)F)C1=C(C(=CC(=C1)F)F)F UPJACOKSBDADEO-NRFANRHFSA-N 0.000 abstract 1
- UYXFBKMKCNDXOJ-NRFANRHFSA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-5-methoxy-4-morpholin-4-yl-8-(2,3,5-trifluorophenyl)-1,7-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(N=CC(=C2C=1N1CCOCC1)OC)C1=C(C(=CC(=C1)F)F)F UYXFBKMKCNDXOJ-NRFANRHFSA-N 0.000 abstract 1
- ZUYZFUKHZIFVJK-NRFANRHFSA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-7-fluoro-4-morpholin-4-yl-8-(2,3,5-trifluorophenyl)-1,5-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(C(=CN=C2C=1N1CCOCC1)F)C1=C(C(=CC(=C1)F)F)F ZUYZFUKHZIFVJK-NRFANRHFSA-N 0.000 abstract 1
- RIARNFNFBWFFEQ-NRFANRHFSA-N N-[(4S)-3,4-dihydro-2H-chromen-4-yl]-7-methoxy-4-morpholin-4-yl-8-(2,3,5-trifluorophenyl)-1,5-naphthyridine-3-carboxamide Chemical compound O1CC[C@@H](C2=C1C=CC=C2)NC(=O)C=1C=NC2=C(C(=CN=C2C=1N1CCOCC1)OC)C1=C(C(=CC(=C1)F)F)F RIARNFNFBWFFEQ-NRFANRHFSA-N 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 abstract 1
- 125000005553 heteroaryloxy group Chemical group 0.000 abstract 1
- 125000002911 monocyclic heterocycle group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/4353—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
- A61K31/4375—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/47—Quinolines; Isoquinolines
- A61K31/472—Non-condensed isoquinolines, e.g. papaverine
- A61K31/4725—Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5375—1,4-Oxazines, e.g. morpholine
- A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
- C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
- C07D311/68—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with nitrogen atoms directly attached in position 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- 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
- C07D405/02—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 containing two hetero rings
- C07D405/12—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 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D493/00—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
- C07D493/04—Ortho-condensed systems
-
- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
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- 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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
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- Chemical & Material Sciences (AREA)
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- Veterinary Medicine (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicación 1: Un compuesto de fórmula (1), en donde n es 0 ó 1; X¹ se selecciona del grupo que consiste en N y CR¹; X² se selecciona del grupo que consiste en N y CR²; X³ se selecciona del grupo que consiste en N y CR³; X⁴ se selecciona del grupo que consiste en N y CR⁴; X⁵ se selecciona del grupo que consiste en N y CR⁵; X⁶ se selecciona del grupo que consiste en N y CR⁶; en donde al menos uno de X¹, X², X³, y X⁵ es N o en donde ninguno de X¹, X², X³, X⁴, X⁵, y X⁶ es N; G es el grupo de fórmula (1); Y¹ se selecciona del grupo que consiste en CR⁸R⁹, O, S y NR¹⁰; Y² se selecciona del grupo que consiste en CR⁸R⁹, O, S, y NR¹⁰; en donde al menos uno de los grupos Y¹ o Y² es CR⁸R⁹; Z¹ se selecciona del grupo que consiste en N, O, S, y CR¹¹; Z² se selecciona del grupo que consiste en cero, N, y CR¹¹; Z³ se selecciona del grupo que consiste en cero, N y CR¹¹; Z⁴ se selecciona del grupo que consiste en N, O, S, y CR¹¹; en donde no más de 2 de Z¹, Z², Z³, y Z⁴ son N y en donde solo uno de Z¹ y Z⁴ es O ó S, Z² es cero solo cuando Z¹ es O ó S, y Z³ es cero solo cuando Z⁴ es O ó S; R¹ se selecciona del grupo que consiste en hidrógeno, halógeno, hidroxilo, -SH, -S-alquilo C₁₋₄, -S(O)(alquilo C₁₋₄), -S(O)₂(alquilo C₁₋₄), ciano, alquilo C₁₋₄, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -B(OR¹²)(OR¹³) en donde R¹² se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, R¹³ se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, o R¹² y R¹³ junto con los átomos de oxígeno a los cuales están unidos forman un anillo de 5 a 7 miembros que está opcionalmente sustituido con 1 a 4 alquilo C₁₋₄; -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂; R² se selecciona del grupo que consiste en hidrógeno, halógeno, hidroxilo, -SH, -S-alquilo C₁₋₄, -S(O)(alquilo C₁₋₄), -S(O)₂(alquilo C₁₋₄), ciano, alquilo C₁₋₄, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -B(OR¹²)(OR¹³) en donde R¹² se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, R¹³ se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, o R¹² y R¹³ junto con los átomos de oxígeno a los cuales están unidos forman un anillo de 5 a 7 miembros que está opcionalmente sustituido con 1 a 4 alquilo C₁₋₄; -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂; R³ se selecciona del grupo que consiste en hidrógeno, halógeno, hidroxilo, -SH, -S-alquilo C₁₋₄, -S(O)(alquilo C₁₋₄), -S(O)₂(alquilo C₁₋₄), ciano, alquilo C₁₋₄, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -B(OR¹²)(OR¹³) en donde R¹² se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, R¹³ se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, o R¹² y R¹³ junto con los átomos de oxígeno a los cuales están unidos forman un anillo de 5 a 7 miembros que está opcionalmente sustituido con 1 a 4 alquilo C₁₋₄; -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂; R⁴ se selecciona del grupo que consiste en halógeno, ciano, -CHO, hidroxilo, alquilo C₁₋₄, alquenilo C₂₋₄, alquinilo C₂₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alquilo C₁₋₄ sustituido con alcoxi C₁₋₄, bencilo opcionalmente sustituido con 1 a 5 átomos de halógeno, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), -N(alquilo C₁₋₄)₂, -NH(cicloalquilo C₃₋₆), -N(alquil C₁₋₄)(cicloalquilo C₃₋₆), -NH(heterocicloalquilo de 4 a 7 miembros), -N(alquilo C₁₋₄)(heterocicloalquilo de 4 a 7 miembros), -N(alquil C₁₋₄)(cicloalquilo C₃₋₆), -N(alquil C₁₋₄)(alcoxi C₁₋₄), -C(O)NH(alquilo C₁₋₄), -C(O)N(alquilo C₁₋₄)₂, -NHSO₂(alquilo C₁₋₄), -S-alquilo C₁₋₄, -S(O)alquilo C₁₋₄, -SO₂-alquilo C₁₋₄, -B(OR¹²)(OR¹³) en donde R¹² se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, R¹³ se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, o R¹² y R¹³ junto con los átomos de oxígeno a los cuales están unidos forman un anillo de 5 a 7 miembros que está opcionalmente sustituido con 1 a 4 alquilo C₁₋₄; arilo de 6 ó 10 miembros; y un heterociclo monocíclico seleccionado del grupo de heterocicloalquilo de 4 a 7 miembros, heteroarilo de 5 miembros que tiene al menos un átomo de nitrógeno a través del cual el anillo heteroarilo de 5 miembros se conecta al resto de la molécula; heteroarilo de 6 miembros que tiene al menos un átomo de nitrógeno; cada uno del anillo arilo, heterocicloalquilo, y heteroarilo en R⁴ está opcionalmente sustituido con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, ciano, nitro, hidroxilo, oxo, alquilo C₁₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), -N(alquilo C₁₋₄)₂, -NH(cicloalquilo C₃₋₆), -N(alquil C₁₋₄)(cicloalquilo C₃₋₆), -NHSO₂(alquilo C₁₋₄), -S-alquilo C₁₋₄, -S(O)alquilo C₁₋₄, -SO₂-alquilo C₁₋₄, -S(O)-halógenoalquilo C₁₋₄ y -SO₂-halógenoalquilo C₁₋₄; y en donde cada alquilo C₁₋₄, cicloalquilo C₃₋₆ y alcoxi C₁₋₄ en R⁴ puede estar opcionalmente sustituido con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, hidroxilo, -NH₂, -NH(alquilo C₁₋₄), -N(alquilo C₁₋₄)₂, ciano, carboxilo, carbamoílo, alcoxicarbonilo C₁₋₄, -C(O)NH(alquilo C₁₋₄), -C(O)N(alquilo C₁₋₄)₂, y alcoxi C₁₋₄; R⁵ se selecciona del grupo que consiste en hidrógeno, halógeno, hidroxilo, -SH, -S-alquilo C₁₋₄, -S(O)(alquilo C₁₋₄), -S(O)₂(alquilo C₁₋₄), ciano, alquilo C₁₋₄, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -B(OR¹²)(OR¹³) en donde R¹² se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, R¹³ se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, o R¹² y R¹³ junto con los átomos de oxígeno a los cuales están unidos forman un anillo de 5 a 7 miembros que está opcionalmente sustituido con 1 a 4 alquilo C₁₋₄; -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂; R⁶ se selecciona del grupo que consiste en hidrógeno, halógeno, hidroxilo, -SH, -S-alquilo C₁₋₄, -S(O)(alquilo C₁₋₄), -S(O)₂(alquilo C₁₋₄), ciano, alquilo C₁₋₄, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -B(OR¹²)(OR¹³) en donde R¹² se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, R¹³ se selecciona, cada vez, del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆, o R¹² y R¹³ junto con los átomos de oxígeno a los cuales están unidos forman un anillo de 5 a 7 miembros que está opcionalmente sustituido con 1 a 4 alquilo C₁₋₄; -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂; R⁷ se selecciona del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆ opcionalmente sustituido con 1 a 5 átomos de halógeno, -C(H)O, alquenilo C₂₋₄, alquinilo C₂₋₄, halógenoalquilo C₁₋₄, y alcoxi C₁₋₄; R⁸ se selecciona, cada vez, independientemente del grupo que consiste en hidrógeno, fluoro, y alquilo C₁₋₄; R⁹ se selecciona, cada vez, independientemente del grupo que consiste en hidrógeno, fluoro, y alquilo C₁₋₄; R¹⁰ se selecciona del grupo que consiste en hidrógeno y alquilo C₁₋₄; R¹¹ se selecciona, cada vez, independientemente del grupo que consiste en hidrógeno, halógeno, hidroxilo, ciano, alquilo C₁₋₄, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, cicloalquilo C₃₋₆, -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂; y Q se selecciona del grupo que consiste en arilo de 6 ó 10 miembros opcionalmente sustituido con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, ciano, nitro, hidroxilo, alquilo C₁₋₄, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, cicloalquilo C₃₋₆, -NH₂, -NH(alquilo C₁₋₄), -N(alquilo C₁₋₄)₂, -NH(cicloalquilo C₃₋₆), -N(alquil C₁₋₄)(cicloalquilo C₃₋₆), -NHSO₂(alquilo C₁₋₄), -S-alquilo C₁₋₄, -S(O)alquilo C₁₋₄, -SO₂-alquilo C₁₋₄, -S(O)-halógenoalquilo C₁₋₄ y -SO₂-halógenoalquilo C₁₋₄, en donde el arilo de 6 ó 10 miembros está opcionalmente fusionado con un heterocicloalquilo de 4 a 7 miembros que tiene 1 ó 2 heteroátomos seleccionados del grupo O, S, y N y en donde los carbonos del heterocicloalquilo están opcionalmente sustituidos con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo halógeno, ciano, nitro, hidroxilo, oxo, alquilo C₁₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂ y cualquier N en el heterocicloalquilo está, siempre que la valencia lo permita, sustituido con un sustituyente seleccionado del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆; heteroarilo de 5 a 10 miembros que tiene 1 ó 2 heteroátomos seleccionados del grupo O, S, y N y en donde los carbonos del heteroarilo de 5 a 10 miembros están opcionalmente sustituidos con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, ciano, nitro, hidroxilo, alquilo C₁₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂ y cualquier N en el heteroarilo, siempre que la valencia lo permita, está opcionalmente sustituido con un sustituyente seleccionado del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆; un heterocicloalquilo de 4 a 7 miembros que tiene 1 ó 2 heteroátomos seleccionados del grupo O, S, N, en donde el heterocicloalquilo está opcionalmente benzo-fusionado, en donde los carbonos del heterocicloalquilo de 4 a 7 miembros o heterocicloalquilo de 4 a 7 miembros opcionalmente benzo-fusionado están opcionalmente sustituidos con 1, 2, 3, ó 4 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, ciano, nitro, hidroxilo, oxo, alquilo C₁₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), y -N(alquilo C₁₋₄)₂ y cualquier N en el heterocicloalquilo está opcionalmente sustituido con un sustituyente seleccionado del grupo que consiste en hidrógeno, alquilo C₁₋₄, y cicloalquilo C₃₋₆; ariloxi de 6 ó 10 miembros opcionalmente sustituido con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, ciano, nitro, hidroxilo, alquilo C₁₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), -N(alquilo C₁₋₄)₂, -NH(cicloalquilo C₃₋₆), -N(alquil C₁₋₄)(cicloalquilo C₃₋₆), -NHSO₂(alquilo C₁₋₄), -S-alquilo C₁₋₄, -S(O)alquilo C₁₋₄, -SO₂-alquilo C₁₋₄, -S(O)-halógenoalquilo C₁₋₄ y -SO₂-halógenoalquilo C₁₋₄; ariltio-oxi de 6 ó 10 miembros opcionalmente sustituido con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, ciano, nitro, hidroxilo, alquilo C₁₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), -N(alquilo C₁₋₄)₂, -NH(cicloalquilo C₃₋₆), -N(alquil C₁₋₄)(cicloalquilo C₃₋₆), -NHSO₂(alquilo C₁₋₄), -S-alquilo C₁₋₄, -S(O)alquilo C₁₋₄, -SO₂-alquilo C₁₋₄, -S(O)-halógenoalquilo C₁₋₄ y - SO₂-halógenoalquilo C₁₋₄; y heteroariloxi de 5 a 10 miembros opcionalmente sustituido con 1, 2 ó 3 sustituyentes independientemente seleccionados del grupo que consiste en halógeno, ciano, nitro, hidroxilo, oxo, alquilo C₁₋₄, cicloalquilo C₃₋₆, halógenoalquilo C₁₋₄, alcoxi C₁₋₄, -NH₂, -NH(alquilo C₁₋₄), -N(alquilo C₁₋₄)₂, -NH(cicloalquilo C₃₋₆), -N(alquil C₁₋₄)(cicloalquilo C₃₋₆), -NHSO₂(alquilo C₁₋₄), -S-alquilo C₁₋₄, -S(O)alquilo C₁₋₄, -SO₂-alquilo C₁₋₄, -S(O)-halógenoalquilo C₁₋₄ y -SO₂-halógenoalquilo C₁₋₄; excluyendo los compuestos: N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(dimetilamino)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(dimetilamino)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; 4-cloro-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-1,6-naftiridin-3-carboxamida; 8-bromo-N-[(4S)-croman-4-il]-4-oxo-1,4-dihidro-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-oxo-1,4-dihidro-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-oxo-1,4-dihidro-1,6-naftiridin-3-carboxamida; 4-cloro-N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-1,6-naftiridin-3-carboxamida; 4-cloro-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(dimetilamino)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(dimetilamino)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(morfolin-4-il)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(morfolin-4-il)-1,6-naftiridin-3-carboxamida; 4-cloro-N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-1,5-naftiridin-3-carboxamida; 4-cloro-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-1,5-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; 8-cloro-4-(3,5-diclorofenil)-N-[(4S)-croman-4-il]pirido[3,2-d]pirimidin-7-carboxamida; 4-(3,5-diclorofenil)-N-[(4S)-croman-4-il]-8-(dimetilamino)-pirido[3,2-d]pirimidin-7-carboxamida; 4-(3,5-diclorofenil)-N-[(4S)-croman-4-il]-8-(morfolin-4-il)-pirido[3,2-d]pirimidin-7-carboxamida; 8-bromo-4-cloro-4-N-[(4S)-croman-4-il]cinnolin-3-carboxamida; 8-bromo-4-N-[(4S)-croman-4-il]-4-(dimetilamino)cinnolin-3-carboxamida; 8-bromo-4-N-[(4S)-croman-4-il]-4-metoxicinnolin-3-carboxamida; 8-(3,5-diclorofenil)-4-N-[(4S)-croman-4-il]-4-(dimetilamino)cinnolin-3-carboxamida; 8-(3-clorofenil)-4-N-[(4S)-croman-4-il]-4-(dimetilamino)cinnolin-3-carboxamida; 8-(2,3-diclorofenil)-4-N-[(4S)-croman-4-il]-4-(dimetilamino)cinnolin-3-carboxamida; 8-(3,4-difluorofenil)-4-N-[(4S)-croman-4-il]-4-(dimetilamino)cinnolin-3-carboxamida; 8-(3,5-diclorofenil)-4-N-[(4S)-croman-4-il]-4-metoxicinnolin-3-carboxamida; 8-(3-clorofenil)-4-N-[(4S)-croman-4-il]-4-metoxicinnolin-3-carboxamida; 8-(2,3-diclorofenil)-4-N-[(4S)-croman-4-il]-4-metoxicinnolin-3-carboxamida; 8-(3,4-fluorofenil)-4-N-[(4S)-croman-4-il]-4-metoxicinnolin-3-carboxamida; 8-cloro-4-(2,3-diclorofenil)-N-[(4S)-croman-4-il]pirido[3,2-d]piridazin-7-carboxamida; 4-(2,3-diclorofenil)-N-[(4S)-croman-4-il]-8-(dimetilamino)-pirido[3,2-d]piridazin-7-carboxamida; 4-(2,3-diclorofenil)-N-[(4S)-croman-4-il]-8-(morfolin-4-il)-pirido[3,2-d]piridazin-7-carboxamida; 4-(3,5-diclorofenil)-N-[(4S)-croman-4-il]-8-(dimetilamino)-pirido[3,2-d]piridazin-7-carboxamida; 4-(3,5-diclorofenil)-N-[(4S)-croman-4-il]-8-(morfolin-4-il)-pirido[3,2-d]piridazin-7-carboxamida; N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3,5-triclorofenil)-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-5-fluoro-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-5-fluoro-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-5-metoxi-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-5-fluoro-4-(dimetilamino)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-5-metoxi-4-(dimetilamino)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-5-fluoro-4-(dimetilamino)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-5-metoxi-4-(dimetilamino)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-5-metoxi-4-(morfolin-4-il)-1,7-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-5-metoxi-4-(dimetilamino)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-7-metoxi-4-(morfolin-4-il)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-7-metoxi-4-(dimetilamino)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-7-metoxi-4-(dimetilamino)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-7-metoxi-4-(morfolin-4-il)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-5-metoxi-4-(morfolin-4-il)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-5-metoxi-4-(morfolin-4-il)-1,6-naftiridin-3-carboxamida; N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-5-metoxi-4-(dimetilamino)-1,6-naftiridin-3-carboxamida; 7-cloro-N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-cloro-N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; 7-cloro-N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-cloro-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-cloro-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; 7-metoxi-N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-fluoro-N-[(4S)-croman-4-il]-8-(3,5-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-metoxi-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-metoxi-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; 7-metoxi-N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-metoxi-N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; 7-fluoro-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; 7-fluoro-N-[(4S)-croman-4-il]-8-(2,3-diclorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; 7-fluoro-N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-4-(dimetilamino)-1,5-naftiridin-3-carboxamida; y 7-fluoro-N-[(4S)-croman-4-il]-8-(2,3,5-trifluorofenil)-4-(morfolin-4-il)-1,5-naftiridin-3-carboxamida; o una sal del mismo.
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| US201862781073P | 2018-12-18 | 2018-12-18 |
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| AR (1) | AR116909A1 (es) |
| AU (1) | AU2019401442B2 (es) |
| BR (1) | BR112021012016A2 (es) |
| CA (1) | CA3122105A1 (es) |
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| SG11202012922VA (en) | 2018-07-09 | 2021-01-28 | Boehringer Ingelheim Animal Health Usa Inc | Anthelminthic heterocyclic compounds |
| US20220064159A1 (en) * | 2018-12-18 | 2022-03-03 | Elanco Tiergesundheit Ag | Bicyclic derivatives |
| CA3133100A1 (en) | 2019-03-19 | 2020-09-24 | Boehringer Ingelheim Animal Health USA Inc. | Anthelmintic aza-benzothiophene and aza-benzofuran compounds |
| BR112021024726A2 (pt) | 2019-06-07 | 2022-01-18 | Elanco Tiergesundheit Ag | Novos derivados bicíclicos |
| TWI865563B (zh) * | 2019-07-30 | 2024-12-11 | 德商拜耳動物保健有限公司 | 新穎異喹啉衍生物 |
| CN115667221A (zh) * | 2020-04-09 | 2023-01-31 | 拜耳动物保健有限责任公司 | 作为驱虫化合物的取代的稠合嗪类 |
| CR20220665A (es) | 2020-05-29 | 2023-07-19 | Boehringer Ingelheim Pharma | Compuestos heterocíclicos como anthelmínticos |
| EP4247809A2 (en) | 2020-11-18 | 2023-09-27 | Elanco Tiergesundheit AG | N-(2,3-dihydro-1,4-benzoxazin-4-yl)-3-isopropyl-7-(2,3,5-trifluorophenyl)benzo-thiophene-2-carboxamide derivatives and similar compounds for the treatment of heartworm infections |
| CN116685584A (zh) * | 2020-11-18 | 2023-09-01 | 礼蓝动物保健有限公司 | 用于治疗心丝虫感染的n-(2,3-二氢-1,4-苯并噁嗪-4-基)-3-异丙基-7-(2,3,5-三氟苯基)苯并噻吩-2-甲酰胺衍生物和类似化合物 |
| TW202237600A (zh) * | 2020-12-04 | 2022-10-01 | 瑞士商禮藍動物保健股份有限公司 | 雙環衍生物 |
| CN116888124A (zh) * | 2020-12-04 | 2023-10-13 | 礼蓝动物保健有限公司 | 二环衍生物 |
| AU2021395477A1 (en) * | 2020-12-11 | 2023-06-22 | Intervet International B.V. | Anthelmintic compounds comprising a thienopyridine structure |
| WO2022122987A1 (en) * | 2020-12-11 | 2022-06-16 | Intervet International B.V. | Anthelmintic compounds comprising a pyridine structure |
| US20250340562A1 (en) * | 2021-06-30 | 2025-11-06 | The General Hospital Corporation | Chromane imaging ligands |
| EP4148052A1 (en) * | 2021-09-09 | 2023-03-15 | Bayer Animal Health GmbH | New quinoline derivatives |
| PE20250675A1 (es) | 2021-11-01 | 2025-03-04 | Boehringer Ingelheim Vetmedica Gmbh | Compuestos de pirrolopiridazina como antihelminticos |
| US11484825B1 (en) * | 2021-12-20 | 2022-11-01 | Next Carbon Solutions, Llc | Devices, systems, facilities and processes for carbon capture optimization in industrial facilities |
| WO2024213752A1 (en) | 2023-04-14 | 2024-10-17 | Elanco Animal Health Gmbh | Long-term prevention and/or treatment of a disease by slo-1 inhibitors |
| WO2025027117A1 (en) | 2023-08-02 | 2025-02-06 | Intervet International B.V. | Carboxamide-4-quinoline compounds with anthelmintic activity |
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| SG11201903059SA (en) * | 2016-11-11 | 2019-05-30 | Bayer Animal Health Gmbh | New anthelmintic quinoline-3-carboxamide derivatives |
| PL3585791T3 (pl) | 2017-04-27 | 2025-03-17 | Elanco Animal Health Gmbh | Nowe pochodne bicyklicznego pirazolu |
| PE20200608A1 (es) | 2017-06-30 | 2020-03-10 | Bayer Animal Health Gmbh | Nuevos derivados de azaquinolina |
| KR20200036909A (ko) | 2017-08-04 | 2020-04-07 | 바이엘 애니멀 헬스 게엠베하 | 연충에 의한 감염을 치료하기 위한 퀴놀린 유도체 |
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| KR20210106502A (ko) | 2021-08-30 |
| AU2019401442B2 (en) | 2022-10-20 |
| WO2020131629A1 (en) | 2020-06-25 |
| MX2021007538A (es) | 2021-10-13 |
| NZ777370A (en) | 2024-11-29 |
| EP3897843A1 (en) | 2021-10-27 |
| JP2022514571A (ja) | 2022-02-14 |
| BR112021012016A2 (pt) | 2021-09-08 |
| CN113474044A (zh) | 2021-10-01 |
| AU2019401442A1 (en) | 2021-07-15 |
| US20220064160A1 (en) | 2022-03-03 |
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