CN101679409B - 双环杂环衍生化合物、其医药组合物和其用途 - Google Patents
双环杂环衍生化合物、其医药组合物和其用途 Download PDFInfo
- Publication number
- CN101679409B CN101679409B CN200780047742.8A CN200780047742A CN101679409B CN 101679409 B CN101679409 B CN 101679409B CN 200780047742 A CN200780047742 A CN 200780047742A CN 101679409 B CN101679409 B CN 101679409B
- Authority
- CN
- China
- Prior art keywords
- phenyl
- pyridin
- group
- base
- imidazo
- 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.)
- Expired - Fee Related
Links
- 0 CC1=C2N=CC(*=C)=CN2CC=C1 Chemical compound CC1=C2N=CC(*=C)=CN2CC=C1 0.000 description 7
- OHTQHZVNZWWYFD-UHFFFAOYSA-N Brc(cn1)ncc1I Chemical compound Brc(cn1)ncc1I OHTQHZVNZWWYFD-UHFFFAOYSA-N 0.000 description 1
- OASOJRLJBDCVNU-UHFFFAOYSA-N Brc1cc2ncc[n]2cc1 Chemical compound Brc1cc2ncc[n]2cc1 OASOJRLJBDCVNU-UHFFFAOYSA-N 0.000 description 1
- NYPYPOZNGOXYSU-UHFFFAOYSA-N Brc1cnccc1 Chemical compound Brc1cnccc1 NYPYPOZNGOXYSU-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N C1CCCCC1 Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- VOPRIKIKYHNQPE-UHFFFAOYSA-N CC([n]1c(ccc(C)c2)c2nc1)=O Chemical compound CC([n]1c(ccc(C)c2)c2nc1)=O VOPRIKIKYHNQPE-UHFFFAOYSA-N 0.000 description 1
- YMXIIVIQLHYKOT-UHFFFAOYSA-N CC1(C)OB(c2cc(N)ccc2)OC1(C)C Chemical compound CC1(C)OB(c2cc(N)ccc2)OC1(C)C YMXIIVIQLHYKOT-UHFFFAOYSA-N 0.000 description 1
- OQZVMYHXMPXXDO-UHFFFAOYSA-N CC1(C)OB(c2cc(Nc3ncc[n]3C)ccc2)OC1(C)C Chemical compound CC1(C)OB(c2cc(Nc3ncc[n]3C)ccc2)OC1(C)C OQZVMYHXMPXXDO-UHFFFAOYSA-N 0.000 description 1
- DPXKWJRFFFMQIE-UHFFFAOYSA-N CN1CCN(Cc2cc(-c3cc4ncc[n]4cc3)ccc2)CC1 Chemical compound CN1CCN(Cc2cc(-c3cc4ncc[n]4cc3)ccc2)CC1 DPXKWJRFFFMQIE-UHFFFAOYSA-N 0.000 description 1
- BANOTGHIHYMTDL-UHFFFAOYSA-N C[n]1c(Br)ncc1 Chemical compound C[n]1c(Br)ncc1 BANOTGHIHYMTDL-UHFFFAOYSA-N 0.000 description 1
- MEQBJJUWDCYIAB-UHFFFAOYSA-N Nc(cccn1)c1Cl Chemical compound Nc(cccn1)c1Cl MEQBJJUWDCYIAB-UHFFFAOYSA-N 0.000 description 1
- OLQLKEGDKARDNO-UHFFFAOYSA-N Nc1c(Nc2ccccc2)nccc1 Chemical compound Nc1c(Nc2ccccc2)nccc1 OLQLKEGDKARDNO-UHFFFAOYSA-N 0.000 description 1
- IHEYHMWRLSPJOC-UHFFFAOYSA-N O=Cc1cc(-c2cc3ncc[n]3cc2)ccc1 Chemical compound O=Cc1cc(-c2cc3ncc[n]3cc2)ccc1 IHEYHMWRLSPJOC-UHFFFAOYSA-N 0.000 description 1
- ONGHBSNRFQKFCR-UHFFFAOYSA-N [AlH2][n]1c(ccc(Br)c2)c2nc1 Chemical compound [AlH2][n]1c(ccc(Br)c2)c2nc1 ONGHBSNRFQKFCR-UHFFFAOYSA-N 0.000 description 1
- YWWQIEUNFFAQBD-UHFFFAOYSA-N [AlH2]c1c(cnc([AlH2])c2)[n]2nc1 Chemical compound [AlH2]c1c(cnc([AlH2])c2)[n]2nc1 YWWQIEUNFFAQBD-UHFFFAOYSA-N 0.000 description 1
- MIYAGMGZOUGESO-UHFFFAOYSA-N [AlH2]c1c[n]2ncc(I)c2cn1 Chemical compound [AlH2]c1c[n]2ncc(I)c2cn1 MIYAGMGZOUGESO-UHFFFAOYSA-N 0.000 description 1
- FMXKGGRGLUTJLQ-UHFFFAOYSA-N [AlH2]c1c[n]2nccc2cn1 Chemical compound [AlH2]c1c[n]2nccc2cn1 FMXKGGRGLUTJLQ-UHFFFAOYSA-N 0.000 description 1
- FGCYBOOOROJQAY-UHFFFAOYSA-N [AlH2]c1cc2ncc[n]2cc1 Chemical compound [AlH2]c1cc2ncc[n]2cc1 FGCYBOOOROJQAY-UHFFFAOYSA-N 0.000 description 1
- UQEANKGXXSENNF-UHFFFAOYSA-N [O-][N+](c(cc(cc1)Br)c1F)=O Chemical compound [O-][N+](c(cc(cc1)Br)c1F)=O UQEANKGXXSENNF-UHFFFAOYSA-N 0.000 description 1
- AGQWNWPWJSILEU-UHFFFAOYSA-N c([n]1-c2ccccc2)nc2c1nccc2 Chemical compound c([n]1-c2ccccc2)nc2c1nccc2 AGQWNWPWJSILEU-UHFFFAOYSA-N 0.000 description 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
- A61K31/437—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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
- Enzymes And Modification Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US87153806P | 2006-12-22 | 2006-12-22 | |
| GB0625827.1 | 2006-12-22 | ||
| GB0625827A GB0625827D0 (en) | 2006-12-22 | 2006-12-22 | New compounds |
| US60/871,538 | 2006-12-22 | ||
| US97958207P | 2007-10-12 | 2007-10-12 | |
| US60/979,582 | 2007-10-12 | ||
| GB0719998.7 | 2007-10-12 | ||
| GB0719998A GB0719998D0 (en) | 2007-10-12 | 2007-10-12 | New compounds |
| PCT/GB2007/004960 WO2008078100A2 (en) | 2006-12-22 | 2007-12-21 | Tricyclic amine derivatives as protein tyrosine kinase inhibitors |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101679409A CN101679409A (zh) | 2010-03-24 |
| CN101679409B true CN101679409B (zh) | 2014-11-26 |
Family
ID=39322759
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200780047742.8A Expired - Fee Related CN101679409B (zh) | 2006-12-22 | 2007-12-21 | 双环杂环衍生化合物、其医药组合物和其用途 |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US8513276B2 (enExample) |
| EP (1) | EP2121687B1 (enExample) |
| JP (1) | JP5442449B2 (enExample) |
| CN (1) | CN101679409B (enExample) |
| AU (1) | AU2007337895C1 (enExample) |
| CA (1) | CA2672213C (enExample) |
| CY (1) | CY1117319T1 (enExample) |
| HR (1) | HRP20151398T1 (enExample) |
| MX (1) | MX2009006704A (enExample) |
| NO (1) | NO342865B1 (enExample) |
| PL (1) | PL2121687T3 (enExample) |
| WO (1) | WO2008078100A2 (enExample) |
Families Citing this family (90)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0420722D0 (en) | 2004-09-17 | 2004-10-20 | Addex Pharmaceuticals Sa | Novel allosteric modulators |
| TWI417095B (zh) | 2006-03-15 | 2013-12-01 | Janssen Pharmaceuticals Inc | 1,4-二取代之3-氰基-吡啶酮衍生物及其作為mGluR2-受體之正向異位性調節劑之用途 |
| CN101679408B (zh) | 2006-12-22 | 2016-04-27 | Astex治疗学有限公司 | 作为fgfr抑制剂的双环杂环化合物 |
| HRP20151398T1 (hr) | 2006-12-22 | 2016-02-12 | Astex Therapeutics Limited | Tricikliäśni derivati amina kao inhibitori protein tirozin kinaze |
| TW200845978A (en) | 2007-03-07 | 2008-12-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives |
| TW200900065A (en) | 2007-03-07 | 2009-01-01 | Janssen Pharmaceutica Nv | 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives |
| AU2008297877C1 (en) | 2007-09-14 | 2013-11-07 | Addex Pharma S.A. | 1,3-disubstituted-4-phenyl-1 H-pyridin-2-ones |
| CN101848893B (zh) | 2007-09-14 | 2012-06-06 | 奥梅-杨森制药有限公司 | 1,3-二取代的4-(芳基-x-苯基)-1h-吡啶-2-酮 |
| EP2203439B1 (en) | 2007-09-14 | 2011-01-26 | Ortho-McNeil-Janssen Pharmaceuticals, Inc. | 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-ý1, 4'¨bipyridinyl-2'-ones |
| GB0720041D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New Compounds |
| GB0720038D0 (en) | 2007-10-12 | 2007-11-21 | Astex Therapeutics Ltd | New compounds |
| CN101861316B (zh) | 2007-11-14 | 2013-08-21 | 奥梅-杨森制药有限公司 | 咪唑并[1,2-a]吡啶衍生物及其作为MGLUR2受体的正变构调节剂的用途 |
| NZ586662A (en) | 2007-12-19 | 2012-08-31 | Vertex Pharma | PYRAZOLO[1,5-a]PYRIMIDINES USEFUL AS JANUS KINASE 2 INHIBITORS |
| GB0810902D0 (en) | 2008-06-13 | 2008-07-23 | Astex Therapeutics Ltd | New compounds |
| WO2010017046A1 (en) | 2008-08-05 | 2010-02-11 | Merck & Co., Inc. | Pyrazolo[1,5-a]pyridines as mark inhibitors |
| JP2011530511A (ja) * | 2008-08-05 | 2011-12-22 | メルク・シャープ・エンド・ドーム・コーポレイション | 治療用化合物 |
| MX2011002042A (es) | 2008-09-02 | 2011-06-20 | Ortho Mcneil Janssen Pharm | Derivados de 3-azabiciclo[3.1.o]hexilo como moduladores de los receptores del glutamato metabotropico. |
| ES2466341T3 (es) | 2008-10-16 | 2014-06-10 | Janssen Pharmaceuticals, Inc. | Derivados de indol y benzomorfolina como moduladores de receptores de glutamato metabotrópicos |
| WO2010060589A1 (en) * | 2008-11-28 | 2010-06-03 | Ortho-Mcneil-Janssen Pharmaceuticals, Inc. | Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors |
| GB0906472D0 (en) * | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| GB0906470D0 (en) * | 2009-04-15 | 2009-05-20 | Astex Therapeutics Ltd | New compounds |
| MY153913A (en) | 2009-05-12 | 2015-04-15 | Janssen Pharmaceuticals Inc | 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors |
| JP5707390B2 (ja) | 2009-05-12 | 2015-04-30 | ジャンセン ファーマシューティカルズ, インコーポレイテッド | 1,2,4−トリアゾロ[4,3−a]ピリジン誘導体およびmGluR2受容体の正のアロステリック調節因子としてのその使用 |
| EP2430022B1 (en) | 2009-05-12 | 2013-11-20 | Janssen Pharmaceuticals, Inc. | 1,2,4-Triazolo[4,3-a]pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders |
| ES2548913T3 (es) | 2009-09-11 | 2015-10-21 | Probiodrug Ag | Derivados heterocíclicos como inhibidores de glutaminil ciclasa |
| FR2950345B1 (fr) * | 2009-09-18 | 2011-09-23 | Sanofi Aventis | Derives acetyleniques de 5-phenyl-pyrazolopyridine, leur preparation et leur application en therapeutique |
| FR2950344B1 (fr) * | 2009-09-18 | 2011-11-25 | Sanofi Aventis | Derives de 5-phenyl-pyrazolopyridine, leur preparation et leur aplication en therapeutique. |
| CN102725292A (zh) * | 2009-11-02 | 2012-10-10 | 雅培制药有限公司 | 作为用于多靶激酶抑制的新构建物的咪唑并吡啶化合物 |
| FR2953520B1 (fr) * | 2009-12-04 | 2011-11-25 | Sanofi Aventis | Derives de diphenyl-pyrazolopyridines, leur preparation et leur application en therapeutique |
| EP2338888A1 (en) * | 2009-12-24 | 2011-06-29 | Almirall, S.A. | Imidazopyridine derivatives as JAK inhibitors |
| UY33213A (es) * | 2010-02-18 | 2011-09-30 | Almirall Sa | Derivados de pirazol como inhibidores de jak |
| EP2360158A1 (en) * | 2010-02-18 | 2011-08-24 | Almirall, S.A. | Pyrazole derivatives as jak inhibitors |
| MX2012012145A (es) * | 2010-04-28 | 2012-11-21 | Daiichi Sankyo Co Ltd | Compuestos [5, 6] heterociclico. |
| AU2011320565A1 (en) * | 2010-10-28 | 2013-05-23 | Innocrin Pharmaceuticals, Inc. | Metalloenzyme inhibitor compounds |
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| PH12013501221A1 (en) * | 2010-12-13 | 2022-03-30 | Array Biopharma Inc | SUBSTITUTED N-(1H-INDAZOL-4-YL)IMIDAZO[1,2-a]PYRIDINE-3-CARBOXAMIDE COMPOUNDS AS TYPE III RECEPTOR TYROSINE KINASE INHIBITORS |
| US8754114B2 (en) | 2010-12-22 | 2014-06-17 | Incyte Corporation | Substituted imidazopyridazines and benzimidazoles as inhibitors of FGFR3 |
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| UA111382C2 (uk) * | 2011-10-10 | 2016-04-25 | Оріон Корпорейшн | Інгібітори протеїнкінази |
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| CA2886187C (en) | 2012-09-28 | 2020-04-14 | Vanderbilt University | Fused heterocyclic compounds as selective bmp inhibitors |
| CN102898426B (zh) * | 2012-11-15 | 2015-04-22 | 江苏先声药业有限公司 | 抑制igf-1r酪氨酸激酶活性的吡啶并吡唑类衍生物 |
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| US9822418B2 (en) | 2013-04-22 | 2017-11-21 | Icahn School Of Medicine At Mount Sinai | Mutations in PDGFRB and NOTCH3 as causes of autosomal dominant infantile myofibromatosis |
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| JO3367B1 (ar) | 2013-09-06 | 2019-03-13 | Janssen Pharmaceutica Nv | مركبات 2،1، 4- ثلاثي زولو [3،4-a] بيريدين واستخدامها بصفة منظمات تفارغية موجبة لمستقبلات ميجلور 2 |
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| US8513276B2 (en) | 2013-08-20 |
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| CA2672213A1 (en) | 2008-07-03 |
| NO342865B1 (no) | 2018-08-20 |
| JP5442449B2 (ja) | 2014-03-12 |
| JP2010513448A (ja) | 2010-04-30 |
| AU2007337895B2 (en) | 2014-01-30 |
| CN101679409A (zh) | 2010-03-24 |
| HRP20151398T1 (hr) | 2016-02-12 |
| CA2672213C (en) | 2016-02-16 |
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