JP6086326B2 - 二環式ヘテロアリールキナーゼ阻害剤および使用方法 - Google Patents
二環式ヘテロアリールキナーゼ阻害剤および使用方法 Download PDFInfo
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- JP6086326B2 JP6086326B2 JP2013512166A JP2013512166A JP6086326B2 JP 6086326 B2 JP6086326 B2 JP 6086326B2 JP 2013512166 A JP2013512166 A JP 2013512166A JP 2013512166 A JP2013512166 A JP 2013512166A JP 6086326 B2 JP6086326 B2 JP 6086326B2
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- pyrrolo
- phenyl
- pyridin
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- 0 C*1CCN(Cc(cc2)ccc2-c2cnc3[n]cc(*)c3c2)CC1 Chemical compound C*1CCN(Cc(cc2)ccc2-c2cnc3[n]cc(*)c3c2)CC1 0.000 description 8
- SQZXFMCDIDWEGL-UHFFFAOYSA-N O=C(Nc(c1n2)ncc2Br)N1c(cc1)cc2c1[nH]cc2 Chemical compound O=C(Nc(c1n2)ncc2Br)N1c(cc1)cc2c1[nH]cc2 SQZXFMCDIDWEGL-UHFFFAOYSA-N 0.000 description 2
- YAEZGCXSMFMCKO-UHFFFAOYSA-N CC(N1CCN(Cc(cc2)ccc2-c(cc23)cnc2[nH]cc3-c(cc2)ccc2C(N)=O)CC1)=O Chemical compound CC(N1CCN(Cc(cc2)ccc2-c(cc23)cnc2[nH]cc3-c(cc2)ccc2C(N)=O)CC1)=O YAEZGCXSMFMCKO-UHFFFAOYSA-N 0.000 description 1
- ATUHZRKVLIURIP-JLHYYAGUSA-N CC/C(/c(nc1)ccc1O)=C(/C)\NC(C)NC=C Chemical compound CC/C(/c(nc1)ccc1O)=C(/C)\NC(C)NC=C ATUHZRKVLIURIP-JLHYYAGUSA-N 0.000 description 1
- LJKNFQFQRCENRD-OTKHNXBGSA-N CC/C=C(\C=N/CCc1ccc(CN2CCN(C)CC2)cc1)/OC Chemical compound CC/C=C(\C=N/CCc1ccc(CN2CCN(C)CC2)cc1)/OC LJKNFQFQRCENRD-OTKHNXBGSA-N 0.000 description 1
- CYEYLYGHCOHIDC-UHFFFAOYSA-N CC1(C)OB(c2ccc(CN3CCN(C)CC3)cc2)OC1(C)C Chemical compound CC1(C)OB(c2ccc(CN3CCN(C)CC3)cc2)OC1(C)C CYEYLYGHCOHIDC-UHFFFAOYSA-N 0.000 description 1
- XYQKORCSGIMICJ-UHFFFAOYSA-N CCC(NC(C)=C)=N Chemical compound CCC(NC(C)=C)=N XYQKORCSGIMICJ-UHFFFAOYSA-N 0.000 description 1
- PVOAHINGSUIXLS-UHFFFAOYSA-N CN1CCNCC1 Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 description 1
- GSBVSBOARGLTSS-UHFFFAOYSA-N CNc(cc1)ncc1-c(cc12)cnc1[nH]cc2-c(cc1)cc2c1[nH]cc2 Chemical compound CNc(cc1)ncc1-c(cc12)cnc1[nH]cc2-c(cc1)cc2c1[nH]cc2 GSBVSBOARGLTSS-UHFFFAOYSA-N 0.000 description 1
- UJUKZEQXNMDNMB-ZDLGFXPLSA-N COc(cc(cc1OC)-c(cc2/C3=C/Cc4ccccc4)cnc2NC3=O)c1OC Chemical compound COc(cc(cc1OC)-c(cc2/C3=C/Cc4ccccc4)cnc2NC3=O)c1OC UJUKZEQXNMDNMB-ZDLGFXPLSA-N 0.000 description 1
- GNZKXRXWADXJOQ-UHFFFAOYSA-N COc(cc(cc1OC)-c(cc23)cnc2[nH]cc3-c2cnc(N)nc2)c1OC Chemical compound COc(cc(cc1OC)-c(cc23)cnc2[nH]cc3-c2cnc(N)nc2)c1OC GNZKXRXWADXJOQ-UHFFFAOYSA-N 0.000 description 1
- BNUYPQOBSWQDMG-UHFFFAOYSA-N COc(cc(cc1OC)-c(cc23)cnc2[nH]cc3I)c1OC Chemical compound COc(cc(cc1OC)-c(cc23)cnc2[nH]cc3I)c1OC BNUYPQOBSWQDMG-UHFFFAOYSA-N 0.000 description 1
- NAVNICSNKNRXON-UHFFFAOYSA-N COc(cc(cc1OC)-c(cc2C34CCCC3)cnc2NC4=O)c1OC Chemical compound COc(cc(cc1OC)-c(cc2C34CCCC3)cnc2NC4=O)c1OC NAVNICSNKNRXON-UHFFFAOYSA-N 0.000 description 1
- KDUPSKIOLZENPU-UHFFFAOYSA-N COc(cc(cc1OC)-c(cc2C3CC4CC4)cnc2NC3=O)c1OC Chemical compound COc(cc(cc1OC)-c(cc2C3CC4CC4)cnc2NC3=O)c1OC KDUPSKIOLZENPU-UHFFFAOYSA-N 0.000 description 1
- CZWFHBMRVMLUGV-UHFFFAOYSA-N COc(cc(cc1OC)-c(nc23)cnc2[nH]cc3-c(cc2)cc3c2[nH]cc3)c1OC Chemical compound COc(cc(cc1OC)-c(nc23)cnc2[nH]cc3-c(cc2)cc3c2[nH]cc3)c1OC CZWFHBMRVMLUGV-UHFFFAOYSA-N 0.000 description 1
- PXEBCKJMBGGJJQ-UHFFFAOYSA-N COc1cc(-c(cc2C3(CC4CC4)CC4CC4)cnc2NC3=O)cc(OC)c1OC Chemical compound COc1cc(-c(cc2C3(CC4CC4)CC4CC4)cnc2NC3=O)cc(OC)c1OC PXEBCKJMBGGJJQ-UHFFFAOYSA-N 0.000 description 1
- ONQVGGQQYPYXMG-UHFFFAOYSA-N C[BrH]c1nc(Br)cnc1N Chemical compound C[BrH]c1nc(Br)cnc1N ONQVGGQQYPYXMG-UHFFFAOYSA-N 0.000 description 1
- MESKXSBOVFFYPL-VUUHIHSGSA-N C[C@H](C(CC=C1/C2=S\Cc3cnccc3)N=C1NC2=O)OC Chemical compound C[C@H](C(CC=C1/C2=S\Cc3cnccc3)N=C1NC2=O)OC MESKXSBOVFFYPL-VUUHIHSGSA-N 0.000 description 1
- GBOCZYXBZCQRQO-UHFFFAOYSA-N Cc([n](c(c1c2)ncc2-c2ccc(CN3CCN(C)CC3)cc2)S(c(cc2)ccc2Cl)=O)c1-c(nc1)ccc1OC Chemical compound Cc([n](c(c1c2)ncc2-c2ccc(CN3CCN(C)CC3)cc2)S(c(cc2)ccc2Cl)=O)c1-c(nc1)ccc1OC GBOCZYXBZCQRQO-UHFFFAOYSA-N 0.000 description 1
- RRJOBQPONVPISS-UHFFFAOYSA-N Cc([n](c(c1c2)ncc2Br)S(c2ccc(C)cc2)=O)c1-c(nc1)ccc1OC Chemical compound Cc([n](c(c1c2)ncc2Br)S(c2ccc(C)cc2)=O)c1-c(nc1)ccc1OC RRJOBQPONVPISS-UHFFFAOYSA-N 0.000 description 1
- QJZUKDFHGGYHMC-UHFFFAOYSA-N O=Cc1cnccc1 Chemical compound O=Cc1cnccc1 QJZUKDFHGGYHMC-UHFFFAOYSA-N 0.000 description 1
Classifications
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- 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
- A61K31/437—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 five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
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- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
- A61K31/444—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring heteroatom, e.g. amrinone
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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- 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
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- 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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- Animal Behavior & Ethology (AREA)
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- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Neurology (AREA)
- Biomedical Technology (AREA)
- Epidemiology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Hematology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Pain & Pain Management (AREA)
- Immunology (AREA)
- Psychiatry (AREA)
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Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34769410P | 2010-05-24 | 2010-05-24 | |
| US61/347,694 | 2010-05-24 | ||
| PCT/US2011/037758 WO2011149950A2 (en) | 2010-05-24 | 2011-05-24 | Bicyclic heteroaryl kinase inhibitors and methods of use |
Publications (3)
| Publication Number | Publication Date |
|---|---|
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| EP2576549A2 (en) | 2013-04-10 |
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| NZ603644A (en) | 2014-10-31 |
| CN103153994A (zh) | 2013-06-12 |
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