JP2004534826A5 - - Google Patents

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Publication number

JP2004534826A5

JP2004534826A5 JP2003507091A JP2003507091A JP2004534826A5 JP 2004534826 A5 JP2004534826 A5 JP 2004534826A5 JP 2003507091 A JP2003507091 A JP 2003507091A JP 2003507091 A JP2003507091 A JP 2003507091A JP 2004534826 A5 JP2004534826 A5 JP 2004534826A5

Authority

JP

Japan

Prior art keywords

pyrrolo

methyl

indol

pyridin

methoxy

Prior art date

2002-06-20

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.)

Granted

Links

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• 150000001875 compounds Chemical class 0.000 claims 129
• 125000000217 alkyl group Chemical group 0.000 claims 79
• -1 cyclic acetal Chemical class 0.000 claims 76
• 125000001072 heteroaryl group Chemical group 0.000 claims 55
• 229910052739 hydrogen Inorganic materials 0.000 claims 48
• 239000001257 hydrogen Substances 0.000 claims 48
• 125000004093 cyano group Chemical group *C#N 0.000 claims 47
• 125000003118 aryl group Chemical group 0.000 claims 45
• 125000005843 halogen group Chemical group 0.000 claims 40
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 40
• 239000000651 prodrug Substances 0.000 claims 36
• 229940002612 prodrug Drugs 0.000 claims 36
• 150000003839 salts Chemical class 0.000 claims 36
• 239000012453 solvate Substances 0.000 claims 36
• 150000001204 N-oxides Chemical class 0.000 claims 33
• 239000002253 acid Substances 0.000 claims 30
• 125000000592 heterocycloalkyl group Chemical group 0.000 claims 28
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 24
• 150000002431 hydrogen Chemical class 0.000 claims 24
• 125000003342 alkenyl group Chemical group 0.000 claims 22
• 125000000753 cycloalkyl group Chemical group 0.000 claims 22
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 17
• 125000001424 substituent group Chemical group 0.000 claims 12
• 125000003545 alkoxy group Chemical group 0.000 claims 10
• 125000001475 halogen functional group Chemical group 0.000 claims 10
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 9
• 239000003814 drug Substances 0.000 claims 9
• 125000001041 indolyl group Chemical group 0.000 claims 9
• 238000004519 manufacturing process Methods 0.000 claims 9
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 8
• 125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims 8
• 125000003302 alkenyloxy group Chemical group 0.000 claims 8
• 150000001408 amides Chemical class 0.000 claims 8
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 8
• 125000002252 acyl group Chemical group 0.000 claims 7
• ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 claims 6
• 125000003710 aryl alkyl group Chemical group 0.000 claims 6
• 125000004446 heteroarylalkyl group Chemical group 0.000 claims 6
• 125000005885 heterocycloalkylalkyl group Chemical group 0.000 claims 6
• 229910052760 oxygen Inorganic materials 0.000 claims 6
• 229910052717 sulfur Inorganic materials 0.000 claims 6
• 125000005530 alkylenedioxy group Chemical group 0.000 claims 5
• 230000003197 catalytic effect Effects 0.000 claims 5
• 239000003112 inhibitor Substances 0.000 claims 5
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 5
• RPOHBQMVRIVWKP-UHFFFAOYSA-N 1-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxypropan-2-ol Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OCC(O)C)=CC2=C1 RPOHBQMVRIVWKP-UHFFFAOYSA-N 0.000 claims 4
• DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 claims 4
• 206010003246 arthritis Diseases 0.000 claims 4
• XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 4
• 238000000034 method Methods 0.000 claims 4
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 4
• 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 4
• 125000000168 pyrrolyl group Chemical group 0.000 claims 4
• QBUASRVBPRBVRJ-UHFFFAOYSA-N 1-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxycyclobutane-1-carboxamide Chemical compound C=1C=C2N(C)C=C(C=3NC4=NC=CC=C4C=3)C2=CC=1OC1(C(N)=O)CCC1 QBUASRVBPRBVRJ-UHFFFAOYSA-N 0.000 claims 3
• RVHRALDRJAGLNN-UHFFFAOYSA-N 1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indole-6-carboxylic acid Chemical compound C12=CC=C(C(O)=O)C=C2N(C)C=C1C1=CC2=CC=CN=C2N1 RVHRALDRJAGLNN-UHFFFAOYSA-N 0.000 claims 3
• FTJGHPGHUSLQAK-UHFFFAOYSA-N 2-(5-methoxy-1-methylindol-3-yl)-1h-pyrrolo[2,3-b]pyridine-4-carbonitrile Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC)=CC2=C1C#N FTJGHPGHUSLQAK-UHFFFAOYSA-N 0.000 claims 3
• JODRAEBPOHRJGI-UHFFFAOYSA-N 2-[1-methyl-5-(2h-tetrazol-5-yl)indol-3-yl]-1h-pyrrolo[2,3-b]pyridine Chemical compound C=1C=C2N(C)C=C(C=3NC4=NC=CC=C4C=3)C2=CC=1C=1N=NNN=1 JODRAEBPOHRJGI-UHFFFAOYSA-N 0.000 claims 3
• SWSNYMMQZWVXAI-UHFFFAOYSA-N 3-(4-chloro-1h-pyrrolo[2,3-b]pyridin-2-yl)-1-methylindole-5-carboxylic acid Chemical compound C12=CC(C(O)=O)=CC=C2N(C)C=C1C1=CC2=C(Cl)C=CN=C2N1 SWSNYMMQZWVXAI-UHFFFAOYSA-N 0.000 claims 3
• BQBOHCHMCHLMDK-UHFFFAOYSA-N 3-(4-cyano-1h-pyrrolo[2,3-b]pyridin-2-yl)-1-methylindole-5-carboxylic acid Chemical compound C12=CC(C(O)=O)=CC=C2N(C)C=C1C1=CC2=C(C#N)C=CN=C2N1 BQBOHCHMCHLMDK-UHFFFAOYSA-N 0.000 claims 3
• WSECXIQXQRTLLK-UHFFFAOYSA-N 3-(4-cyano-1h-pyrrolo[2,3-b]pyridin-2-yl)-n-(2-hydroxy-2-methylpropyl)-1-methylindole-5-carboxamide Chemical compound C12=CC(C(=O)NCC(C)(C)O)=CC=C2N(C)C=C1C1=CC2=C(C#N)C=CN=C2N1 WSECXIQXQRTLLK-UHFFFAOYSA-N 0.000 claims 3
• CBSWBKLIQDUSCA-UHFFFAOYSA-N 3-[4-(3,5-dimethyl-1,2-oxazol-4-yl)-1h-pyrrolo[2,3-b]pyridin-2-yl]-1h-indole-5-carboxylic acid Chemical compound CC1=NOC(C)=C1C1=CC=NC2=C1C=C(C=1C3=CC(=CC=C3NC=1)C(O)=O)N2 CBSWBKLIQDUSCA-UHFFFAOYSA-N 0.000 claims 3
• CYGVUQDIFRECJA-UHFFFAOYSA-N 4-[2-(5-methoxy-1-methylindol-3-yl)-1h-pyrrolo[2,3-b]pyridin-4-yl]-3,5-dimethyl-1,2-oxazole Chemical compound C12=CC(OC)=CC=C2N(C)C=C1C(NC1=NC=C2)=CC1=C2C=1C(C)=NOC=1C CYGVUQDIFRECJA-UHFFFAOYSA-N 0.000 claims 3
• MIJMZVTYIXYSDK-UHFFFAOYSA-N 6-(5-methoxy-1-methylindol-3-yl)-5h-pyrrolo[2,3-b]pyrazine Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC)=CC2=N1 MIJMZVTYIXYSDK-UHFFFAOYSA-N 0.000 claims 3
• UGHVSNVFYBZSLH-UHFFFAOYSA-N [1-[1-methyl-3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indol-5-yl]oxycyclobutyl]methanol Chemical compound C=1C=C2N(C)C=C(C=3NC4=NC=CN=C4C=3)C2=CC=1OC1(CO)CCC1 UGHVSNVFYBZSLH-UHFFFAOYSA-N 0.000 claims 3
• 125000000304 alkynyl group Chemical group 0.000 claims 3
• 208000027866 inflammatory disease Diseases 0.000 claims 3
• TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Natural products OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-UHFFFAOYSA-N 0.000 claims 3
• AMECZOITPGYJEM-UHFFFAOYSA-N n-(1-hydroxy-2-methylpropan-2-yl)-2-(5-methoxy-1-methylindol-3-yl)-1h-pyrrolo[2,3-b]pyridine-4-carboxamide Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC)=CC2=C1C(=O)NC(C)(C)CO AMECZOITPGYJEM-UHFFFAOYSA-N 0.000 claims 3
• 125000004076 pyridyl group Chemical group 0.000 claims 3
• JWHOQZUREKYPBY-UHFFFAOYSA-N rubonic acid Natural products CC1(C)CCC2(CCC3(C)C(=CCC4C5(C)CCC(=O)C(C)(C)C5CC(=O)C34C)C2C1)C(=O)O JWHOQZUREKYPBY-UHFFFAOYSA-N 0.000 claims 3
• 125000003831 tetrazolyl group Chemical group 0.000 claims 3
• MUQFTYHVZUPXES-CYBMUJFWSA-N (2r)-3-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxypropane-1,2-diol Chemical compound C12=CC(OC[C@H](O)CO)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 MUQFTYHVZUPXES-CYBMUJFWSA-N 0.000 claims 2
• SAYAZSFRHPSZLZ-CYBMUJFWSA-N (2r)-3-[6-methoxy-1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxypropane-1,2-diol Chemical compound C1=CN=C2NC(C3=CN(C)C=4C=C(C(=CC=43)OC[C@H](O)CO)OC)=CC2=C1 SAYAZSFRHPSZLZ-CYBMUJFWSA-N 0.000 claims 2
• ZUHZMIKTWRJJLA-UHFFFAOYSA-N 1-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]ethanone Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)C(=O)C)=CC2=C1 ZUHZMIKTWRJJLA-UHFFFAOYSA-N 0.000 claims 2
• AZEKOCYKHUJNKS-UHFFFAOYSA-N 1-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxycyclobutane-1-carboxylic acid Chemical compound C=1C=C2N(C)C=C(C=3NC4=NC=CC=C4C=3)C2=CC=1OC1(C(O)=O)CCC1 AZEKOCYKHUJNKS-UHFFFAOYSA-N 0.000 claims 2
• VGGBMWRHJWCWBG-UHFFFAOYSA-N 1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-n-(1h-1,2,4-triazol-5-yl)indole-6-carboxamide Chemical compound C1=C2N(C)C=C(C=3NC4=NC=CC=C4C=3)C2=CC=C1C(=O)NC=1N=CNN=1 VGGBMWRHJWCWBG-UHFFFAOYSA-N 0.000 claims 2
• AVNBDKGXTGVKOZ-UHFFFAOYSA-N 1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-ol Chemical compound C12=CC(O)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 AVNBDKGXTGVKOZ-UHFFFAOYSA-N 0.000 claims 2
• UVGZNKUGQAZSFE-UHFFFAOYSA-N 1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indole-5-carboxamide Chemical compound C12=CC(C(N)=O)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 UVGZNKUGQAZSFE-UHFFFAOYSA-N 0.000 claims 2
• KYWSGFFFDGCSES-UHFFFAOYSA-N 1-methyl-3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indol-5-ol Chemical compound C12=CC(O)=CC=C2N(C)C=C1C1=CC2=NC=CN=C2N1 KYWSGFFFDGCSES-UHFFFAOYSA-N 0.000 claims 2
• NCODGTKJFCNVAH-UHFFFAOYSA-N 1-methyl-3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indole-5-carboxylic acid Chemical compound C12=CC(C(O)=O)=CC=C2N(C)C=C1C1=CC2=NC=CN=C2N1 NCODGTKJFCNVAH-UHFFFAOYSA-N 0.000 claims 2
• KELLLGDNFSNCIO-UHFFFAOYSA-N 2-(2-phenyl-1h-pyrrolo[2,3-b]pyridin-3-yl)acetonitrile Chemical compound N1C2=NC=CC=C2C(CC#N)=C1C1=CC=CC=C1 KELLLGDNFSNCIO-UHFFFAOYSA-N 0.000 claims 2
• GZRCWJUTTURNJO-UHFFFAOYSA-N 2-(5,6-dimethoxy-1-methylindol-3-yl)-1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC(C=3C=4C=C(C(=CC=4N(C)C=3)OC)OC)=CC2=C1 GZRCWJUTTURNJO-UHFFFAOYSA-N 0.000 claims 2
• VZLHVQTYCPRPHS-UHFFFAOYSA-N 2-(5-methoxy-1-methylindol-3-yl)-1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC)=CC2=C1 VZLHVQTYCPRPHS-UHFFFAOYSA-N 0.000 claims 2
• LPOOZQNTAHNETD-UHFFFAOYSA-N 2-(5-methoxy-1-methylindol-3-yl)-4-phenyl-1h-pyrrolo[2,3-b]pyridine Chemical compound C12=CC(OC)=CC=C2N(C)C=C1C(NC1=NC=C2)=CC1=C2C1=CC=CC=C1 LPOOZQNTAHNETD-UHFFFAOYSA-N 0.000 claims 2
• FKDHQBOTZUDZEJ-UHFFFAOYSA-N 2-(5-methoxy-1-methylindol-3-yl)-4-pyridin-3-yl-1h-pyrrolo[2,3-b]pyridine Chemical compound C12=CC(OC)=CC=C2N(C)C=C1C(NC1=NC=C2)=CC1=C2C1=CC=CN=C1 FKDHQBOTZUDZEJ-UHFFFAOYSA-N 0.000 claims 2
• CIDALPHOFCAXQR-UHFFFAOYSA-N 2-(5-methoxy-1h-indol-3-yl)-1h-pyrrolo[2,3-b]pyridine-4-carbonitrile Chemical compound C1=CN=C2NC(C3=CNC4=CC=C(C=C43)OC)=CC2=C1C#N CIDALPHOFCAXQR-UHFFFAOYSA-N 0.000 claims 2
• MCEGXLZIVNTQAG-UHFFFAOYSA-N 2-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxyacetic acid Chemical compound C12=CC(OCC(O)=O)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 MCEGXLZIVNTQAG-UHFFFAOYSA-N 0.000 claims 2
• NGRLVNLOYHSCOT-UHFFFAOYSA-N 2-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxyethanol Chemical compound C12=CC(OCCO)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 NGRLVNLOYHSCOT-UHFFFAOYSA-N 0.000 claims 2
• COKIRTGHADVGEP-UHFFFAOYSA-N 2-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxypropan-1-ol Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC(CO)C)=CC2=C1 COKIRTGHADVGEP-UHFFFAOYSA-N 0.000 claims 2
• FPFNTCBEXLWOSS-UHFFFAOYSA-N 2-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxypropanoic acid Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC(C)C(O)=O)=CC2=C1 FPFNTCBEXLWOSS-UHFFFAOYSA-N 0.000 claims 2
• MCTZIYPXXHBZEW-UHFFFAOYSA-N 2-[1-methyl-5-(2-methyltetrazol-5-yl)indol-3-yl]-1h-pyrrolo[2,3-b]pyridine Chemical compound CN1N=NC(C=2C=C3C(C=4NC5=NC=CC=C5C=4)=CN(C)C3=CC=2)=N1 MCTZIYPXXHBZEW-UHFFFAOYSA-N 0.000 claims 2
• BJBMPYZXKSTFJM-UHFFFAOYSA-N 2-[5-(1-methoxypropan-2-yloxy)-1-methylindol-3-yl]-1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC(C)COC)=CC2=C1 BJBMPYZXKSTFJM-UHFFFAOYSA-N 0.000 claims 2
• AKSKFTWNVYJOKH-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(2-methylquinolin-4-yl)acetamide Chemical compound C1=CN=C2NC(C3=CN(CC(=O)NC=4C5=CC=CC=C5N=C(C)C=4)C4=CC=C(C=C43)OC)=CC2=C1 AKSKFTWNVYJOKH-UHFFFAOYSA-N 0.000 claims 2
• VAJOSPMTARTPKN-UHFFFAOYSA-N 2-[5-methoxy-3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indol-1-yl]-1-morpholin-4-ylethanone Chemical compound C1=C(C=2NC3=NC=CN=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)N1CCOCC1 VAJOSPMTARTPKN-UHFFFAOYSA-N 0.000 claims 2
• SMCLLQQYFYBQQL-UHFFFAOYSA-N 2-[5-methoxy-3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indol-1-yl]ethanol Chemical compound C1=CN=C2NC(C3=CN(CCO)C4=CC=C(C=C43)OC)=CC2=N1 SMCLLQQYFYBQQL-UHFFFAOYSA-N 0.000 claims 2
• JHUWLGXCOIMHHQ-UHFFFAOYSA-N 3-(1h-pyrrolo[2,3-b]pyridin-2-yl)-1h-indole-5-carboxylic acid Chemical compound C1=CN=C2NC(C3=CNC4=CC=C(C=C43)C(=O)O)=CC2=C1 JHUWLGXCOIMHHQ-UHFFFAOYSA-N 0.000 claims 2
• HIWPOKJDACYAFJ-UHFFFAOYSA-N 3-(4-methoxy-1h-pyrrolo[2,3-b]pyridin-2-yl)-1-methylindole-5-carboxylic acid Chemical compound C1=C(C(O)=O)C=C2C(C=3NC=4N=CC=C(C=4C=3)OC)=CN(C)C2=C1 HIWPOKJDACYAFJ-UHFFFAOYSA-N 0.000 claims 2
• KERGNDFCTBAMGA-UHFFFAOYSA-N 3-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxypropan-1-ol Chemical compound C12=CC(OCCCO)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 KERGNDFCTBAMGA-UHFFFAOYSA-N 0.000 claims 2
• MUQFTYHVZUPXES-UHFFFAOYSA-N 3-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]oxypropane-1,2-diol Chemical compound C12=CC(OCC(O)CO)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 MUQFTYHVZUPXES-UHFFFAOYSA-N 0.000 claims 2
• BZGCYSXNPHENAB-UHFFFAOYSA-N 3-[1-methyl-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-5-yl]propanoic acid Chemical compound C12=CC(CCC(O)=O)=CC=C2N(C)C=C1C1=CC2=CC=CN=C2N1 BZGCYSXNPHENAB-UHFFFAOYSA-N 0.000 claims 2
• VEKQEFMQDFQZSJ-UHFFFAOYSA-N 3-[3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indol-1-yl]propan-1-ol Chemical compound C12=CC=CC=C2N(CCCO)C=C1C1=CC2=NC=CN=C2N1 VEKQEFMQDFQZSJ-UHFFFAOYSA-N 0.000 claims 2
• LIZDNKRMTCXMAV-UHFFFAOYSA-N 3-[4-(3,5-dimethyl-1,2-oxazol-4-yl)-1h-pyrrolo[2,3-b]pyridin-2-yl]-1-methylindole-5-carboxylic acid Chemical compound CC1=NOC(C)=C1C1=CC=NC2=C1C=C(C=1C3=CC(=CC=C3N(C)C=1)C(O)=O)N2 LIZDNKRMTCXMAV-UHFFFAOYSA-N 0.000 claims 2
• BSONOAQXFAIGPB-UHFFFAOYSA-N 3-[5-methoxy-3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indol-1-yl]propan-1-ol Chemical compound C1=CN=C2NC(C3=CN(CCCO)C4=CC=C(C=C43)OC)=CC2=N1 BSONOAQXFAIGPB-UHFFFAOYSA-N 0.000 claims 2
• YHKXZXWIOPNPDS-UHFFFAOYSA-N 3-[[1-methyl-3-(5h-pyrrolo[2,3-b]pyrazin-6-yl)indole-5-carbonyl]amino]propanoic acid Chemical compound C12=CC(C(=O)NCCC(O)=O)=CC=C2N(C)C=C1C1=CC2=NC=CN=C2N1 YHKXZXWIOPNPDS-UHFFFAOYSA-N 0.000 claims 2
• JJTVNLBIXOXIQR-UHFFFAOYSA-N 4-[2-(5-methoxy-1h-indol-3-yl)-1h-pyrrolo[2,3-b]pyridin-4-yl]-3,5-dimethyl-1,2-oxazole Chemical compound C12=CC(OC)=CC=C2NC=C1C(NC1=NC=C2)=CC1=C2C=1C(C)=NOC=1C JJTVNLBIXOXIQR-UHFFFAOYSA-N 0.000 claims 2
• LMHHYPOKWRDJTP-UHFFFAOYSA-N 4-chloro-2-(5-methoxy-1-methylindol-3-yl)-1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC)=CC2=C1Cl LMHHYPOKWRDJTP-UHFFFAOYSA-N 0.000 claims 2
• AZZIWMRQTCNYEQ-UHFFFAOYSA-N 4-chloro-2-(5-methoxy-1h-indol-3-yl)-1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC(C3=CNC4=CC=C(C=C43)OC)=CC2=C1Cl AZZIWMRQTCNYEQ-UHFFFAOYSA-N 0.000 claims 2
• JFFMPLDYSOUBPW-UHFFFAOYSA-N 4-methoxy-2-(5-methoxy-1-methylindol-3-yl)-1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC(C3=CN(C)C4=CC=C(C=C43)OC)=CC2=C1OC JFFMPLDYSOUBPW-UHFFFAOYSA-N 0.000 claims 2
• QFSGJFOPYOPYRB-UHFFFAOYSA-N 4-methoxy-2-(5-methoxy-1h-indol-3-yl)-1h-pyrrolo[2,3-b]pyridine Chemical compound C1=CN=C2NC(C3=CNC4=CC=C(C=C43)OC)=CC2=C1OC QFSGJFOPYOPYRB-UHFFFAOYSA-N 0.000 claims 2
• OPIPFYKXYNLMGL-UHFFFAOYSA-N 6-(1-methyl-4-phenylpyrrol-3-yl)-5h-pyrrolo[2,3-b]pyrazine Chemical compound C=1N(C)C=C(C=2NC3=NC=CN=C3C=2)C=1C1=CC=CC=C1 OPIPFYKXYNLMGL-UHFFFAOYSA-N 0.000 claims 2
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• DYJCPBAQGVSXMD-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(2-phenylsulfanylethyl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NCCSC1=CC=CC=C1 DYJCPBAQGVSXMD-UHFFFAOYSA-N 0.000 claims 1
• ZJRMHCBWQNCDCN-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(2-piperidin-1-ylethyl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NCCN1CCCCC1 ZJRMHCBWQNCDCN-UHFFFAOYSA-N 0.000 claims 1
• XBGORNDCEPLSDY-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(2-pyridin-4-ylethyl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NCCC1=CC=NC=C1 XBGORNDCEPLSDY-UHFFFAOYSA-N 0.000 claims 1
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• GAQSDLALUSQSCO-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(3-methylbutan-2-yl)acetamide Chemical compound C1=CN=C2NC(C3=CN(CC(=O)NC(C)C(C)C)C4=CC=C(C=C43)OC)=CC2=C1 GAQSDLALUSQSCO-UHFFFAOYSA-N 0.000 claims 1
• UDCRMLPEZMWHKH-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(3-methylbutyl)acetamide Chemical compound C1=CN=C2NC(C3=CN(CC(=O)NCCC(C)C)C4=CC=C(C=C43)OC)=CC2=C1 UDCRMLPEZMWHKH-UHFFFAOYSA-N 0.000 claims 1
• IFOXNFQUBVQIBF-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(3-oxo-1,2-oxazolidin-4-yl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NC1CONC1=O IFOXNFQUBVQIBF-UHFFFAOYSA-N 0.000 claims 1
• SBRQMBKXTAWGCK-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(3-phenylmethoxypyridin-2-yl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NC1=NC=CC=C1OCC1=CC=CC=C1 SBRQMBKXTAWGCK-UHFFFAOYSA-N 0.000 claims 1
• RUQQVNMGWNCECS-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(3-pyrrolidin-1-ylpropyl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NCCCN1CCCC1 RUQQVNMGWNCECS-UHFFFAOYSA-N 0.000 claims 1
• BGIPIZFHVWJSCZ-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(4-morpholin-4-ylphenyl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NC(C=C1)=CC=C1N1CCOCC1 BGIPIZFHVWJSCZ-UHFFFAOYSA-N 0.000 claims 1
• RODKSYLFQRPFDT-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(4-phenylbutan-2-yl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NC(C)CCC1=CC=CC=C1 RODKSYLFQRPFDT-UHFFFAOYSA-N 0.000 claims 1
• KUTAWJWZJYRUQB-UHFFFAOYSA-N 2-[5-methoxy-3-(1h-pyrrolo[2,3-b]pyridin-2-yl)indol-1-yl]-n-(oxolan-2-ylmethyl)acetamide Chemical compound C1=C(C=2NC3=NC=CC=C3C=2)C2=CC(OC)=CC=C2N1CC(=O)NCC1CCCO1 KUTAWJWZJYRUQB-UHFFFAOYSA-N 0.000 claims 1
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