EP1601357A4 - HETEROCYCLIC KINASE INHIBITORS: METHODS OF USE AND SYNTHESIS - Google Patents
HETEROCYCLIC KINASE INHIBITORS: METHODS OF USE AND SYNTHESISInfo
- Publication number
- EP1601357A4 EP1601357A4 EP04719237A EP04719237A EP1601357A4 EP 1601357 A4 EP1601357 A4 EP 1601357A4 EP 04719237 A EP04719237 A EP 04719237A EP 04719237 A EP04719237 A EP 04719237A EP 1601357 A4 EP1601357 A4 EP 1601357A4
- Authority
- EP
- European Patent Office
- Prior art keywords
- synthesis
- methods
- kinase inhibitors
- heterocyclic kinase
- heterocyclic
- 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.)
- Withdrawn
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/02—Immunomodulators
-
- 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
- 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
- C07D405/14—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 three or more hetero rings
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US45345703P | 2003-03-10 | 2003-03-10 | |
| US453457P | 2003-03-10 | ||
| US46091003P | 2003-04-07 | 2003-04-07 | |
| US460910P | 2003-04-07 | ||
| US46302503P | 2003-04-15 | 2003-04-15 | |
| US463025P | 2003-04-15 | ||
| US50271003P | 2003-09-12 | 2003-09-12 | |
| US502710P | 2003-09-12 | ||
| PCT/US2004/007286 WO2004080463A1 (en) | 2003-03-10 | 2004-03-10 | Heterocyclic kinase inhibitors: methods of use and synthesis |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EP1601357A1 EP1601357A1 (en) | 2005-12-07 |
| EP1601357A4 true EP1601357A4 (en) | 2007-10-03 |
Family
ID=32996376
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP04719237A Withdrawn EP1601357A4 (en) | 2003-03-10 | 2004-03-10 | HETEROCYCLIC KINASE INHIBITORS: METHODS OF USE AND SYNTHESIS |
Country Status (5)
| Country | Link |
|---|---|
| EP (1) | EP1601357A4 (en) |
| JP (1) | JP2006519846A (en) |
| CA (1) | CA2518398A1 (en) |
| MX (1) | MXPA05009722A (en) |
| WO (1) | WO2004080463A1 (en) |
Families Citing this family (75)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TWI328009B (en) | 2003-05-21 | 2010-08-01 | Glaxo Group Ltd | Quinoline derivatives as phosphodiesterase inhibitors |
| MY179032A (en) | 2004-10-25 | 2020-10-26 | Cancer Research Tech Ltd | Ortho-condensed pyridine and pyrimidine derivatives (e.g.purines) as protein kinase inhibitors |
| MX2007011453A (en) | 2005-04-22 | 2008-02-12 | Alantos Pharmaceuticals Holding Inc | Dipeptidyl peptidase-iv inhibitors. |
| EP1931657B1 (en) | 2005-08-17 | 2013-12-25 | Merck Sharp & Dohme Corp. | Novel high affinity quinoline-based kinase ligands |
| DK3421471T3 (en) | 2006-04-25 | 2021-06-14 | Astex Therapeutics Ltd | PURIN AND DEAZAPURIN DERIVATIVES AS PHARMACEUTICAL COMPOUNDS |
| US7511063B2 (en) * | 2006-08-16 | 2009-03-31 | Schering Corporation | High affinity quinoline-based kinase ligands |
| US7964732B2 (en) | 2006-11-17 | 2011-06-21 | Pfizer Inc. | Substituted bicyclocarboxyamide compounds |
| AU2007329064C1 (en) | 2006-12-07 | 2013-01-17 | F. Hoffmann-La Roche Ag | 2-Aminoquinolines as 5-HT(5A) receptor antagonists |
| MX2009009793A (en) | 2007-03-14 | 2009-10-16 | Ranbaxy Lab Ltd | Pyrazolo (3, 4-b) pyridine derivatives as phosphodiesterase inhibitors. |
| PE20090717A1 (en) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | QUINOLINE DERIVATIVES AS PI3 KINASE INHIBITORS |
| JP2010528007A (en) * | 2007-05-23 | 2010-08-19 | メルク・シャープ・エンド・ドーム・コーポレイション | Cyclopropylpyrrolidine orexin receptor antagonist |
| JP2010536872A (en) * | 2007-08-22 | 2010-12-02 | アラーガン、インコーポレイテッド | Therapeutic quinoline and naphthalene derivatives |
| MX2010003001A (en) * | 2007-09-27 | 2010-04-01 | Hoffmann La Roche | Quinoline derivatives as 5ht5a receptor antagonists. |
| PT2201012E (en) | 2007-10-11 | 2014-09-04 | Astrazeneca Ab | Pyrrolo[2,3-d]pyrimidin derivatives as protein kinase b inhibitors |
| EP2202228B1 (en) | 2007-10-15 | 2014-12-10 | Takeda Pharmaceutical Company Limited | Amide compounds and use of the same |
| CN101903384A (en) | 2007-11-02 | 2010-12-01 | 沃泰克斯药物股份有限公司 | [1H-Pyrazolo[3,4-B]pyridin-4-yl]-phenyl or -pyridin-2-yl derivatives as protein kinase Cθ inhibitors |
| WO2009095752A1 (en) * | 2008-01-29 | 2009-08-06 | Glenmark Pharmaceuticals, S.A. | Fused pyrazole derivatives as cannabinoid receptor modulators |
| JP2011513350A (en) * | 2008-03-05 | 2011-04-28 | エフ.ホフマン−ラ ロシュ アーゲー | 2-Aminoquinolines |
| BRPI0910253A2 (en) * | 2008-03-07 | 2015-09-29 | Hoffmann La Roche | 2-aminoquinoline derivatives |
| WO2009109502A1 (en) * | 2008-03-07 | 2009-09-11 | F. Hoffmann-La Roche Ag | 2-aminoquinolines |
| AU2009224760A1 (en) | 2008-03-12 | 2009-09-17 | F. Hoffmann-La Roche Ag | 2-Aminoquinolines as 5-HT5A receptor antagonists |
| GB0812969D0 (en) | 2008-07-15 | 2008-08-20 | Sentinel Oncology Ltd | Pharmaceutical compounds |
| CN105601619A (en) | 2009-02-27 | 2016-05-25 | 埃姆比特生物科学公司 | JAK kinase modulating compounds and methods of use thereof |
| EA201171098A1 (en) * | 2009-03-02 | 2012-04-30 | Сертрис Фармасьютикалз, Инк. | 8-SUBSTITUTE QUINOLINES AND RELATED ANALOGUES AS SIRTUIN MODULATORS |
| US10253020B2 (en) | 2009-06-12 | 2019-04-09 | Abivax | Compounds for preventing, inhibiting, or treating cancer, AIDS and/or premature aging |
| KR20120051643A (en) * | 2009-06-12 | 2012-05-22 | 쏘시에떼 스플리코 | Compounds useful for treating premature aging in particular progeria |
| ES2575154T3 (en) * | 2009-12-17 | 2016-06-24 | Merck Sharp & Dohme Corp. | Positive allosteric modulators of the quinoline amide M1 receptor |
| KR20120125267A (en) | 2010-01-29 | 2012-11-14 | 베링거 인겔하임 인터내셔날 게엠베하 | Substituted naphthyridines and their use as syk kinase inhibitors |
| EP2582676B1 (en) | 2010-06-15 | 2016-12-14 | Merck Sharp & Dohme Corp. | Tetrahydroquinoline amide m1 receptor positive allosteric modulators |
| AR082733A1 (en) * | 2010-08-27 | 2012-12-26 | Gruenenthal Gmbh | 2-AMINO-QUINOLINA-3-CARBOXAMIDS REPLACED AS MODULATORS OF KCNQ2 / 3 |
| CA2810024A1 (en) | 2010-09-01 | 2012-03-08 | Ambit Biosciences Corporation | Quinazoline compounds and methods of use thereof |
| EP2489663A1 (en) | 2011-02-16 | 2012-08-22 | Almirall, S.A. | Compounds as syk kinase inhibitors |
| WO2012122370A2 (en) | 2011-03-08 | 2012-09-13 | Eutropics Pharmaceuticals, Inc. | Compositions and methods useful for treating diseases |
| HRP20191927T1 (en) | 2011-04-01 | 2020-01-10 | Astrazeneca Ab | THERAPEUTIC TREATMENT |
| CA2834062A1 (en) | 2011-05-10 | 2012-11-15 | Merck Sharp & Dohme Corp. | Pyridyl aminopyridines as syk inhibitors |
| EP2706853B1 (en) | 2011-05-10 | 2017-06-14 | Merck Sharp & Dohme Corp. | Aminopyrimidines as syk inhibitors |
| US9145391B2 (en) | 2011-05-10 | 2015-09-29 | Merck Sharp & Dohme Corp. | Bipyridylaminopyridines as Syk inhibitors |
| KR101986484B1 (en) | 2011-07-26 | 2019-06-10 | 베링거 인겔하임 인터내셔날 게엠베하 | Substituted quinolines and their use as medicaments |
| WO2013052391A1 (en) | 2011-10-05 | 2013-04-11 | Merck Sharp & Dohme Corp. | PHENYL CARBOXAMIDE-CONTAINING SPLEEN TYROSINE KINASE (Syk) INHIBITORS |
| US9216173B2 (en) | 2011-10-05 | 2015-12-22 | Merck Sharp & Dohme Corp. | 2-Pyridyl carboxamide-containing spleen tyrosine kinase (SYK) inhibitors |
| US8987456B2 (en) | 2011-10-05 | 2015-03-24 | Merck Sharp & Dohme Corp. | 3-pyridyl carboxamide-containing spleen tyrosine kinase (SYK) inhibitors |
| PL2785349T5 (en) | 2011-11-30 | 2023-01-30 | Astrazeneca Ab | Combination treatment of cancer |
| AU2013204533B2 (en) | 2012-04-17 | 2017-02-02 | Astrazeneca Ab | Crystalline forms |
| WO2013192128A1 (en) | 2012-06-20 | 2013-12-27 | Merck Sharp & Dohme Corp. | Imidazolyl analogs as syk inhibitors |
| US20150133450A1 (en) | 2012-06-20 | 2015-05-14 | Eutropics Pharmaceuticals, Inc. | Methods and compositions useful for treating diseases involving bcl-2 family proteins with quinoline derivatives |
| WO2013192125A1 (en) | 2012-06-20 | 2013-12-27 | Merck Sharp & Dohme Corp. | Pyrazolyl derivatives as syk inhibitors |
| US9376418B2 (en) | 2012-06-22 | 2016-06-28 | Merck Sharp & Dohme Corp. | Substituted pyridine spleen tyrosine kinase (SYK) inhibitors |
| WO2013192088A1 (en) | 2012-06-22 | 2013-12-27 | Merck Sharp & Dohme Corp. | SUBSTITUTED DIAZINE AND TRIAZINE SPLEEN TYROSINE KINASE (Syk) INHIBITORS |
| WO2014031438A2 (en) | 2012-08-20 | 2014-02-27 | Merck Sharp & Dohme Corp. | SUBSTITUTED PHENYL SPLEEN TYROSINE KINASE (Syk) INHIBITORS |
| US9586931B2 (en) | 2012-09-28 | 2017-03-07 | Merck Sharp & Dohme Corp. | Triazolyl derivatives as Syk inhibitors |
| WO2014081953A1 (en) | 2012-11-21 | 2014-05-30 | Richard David J | Methods and compositions useful for treating diseases involving bcl-2 family proteins with isoquinoline and quinoline derivatives |
| EP2757161A1 (en) | 2013-01-17 | 2014-07-23 | Splicos | miRNA-124 as a biomarker of viral infection |
| US10732182B2 (en) | 2013-08-01 | 2020-08-04 | Eutropics Pharmaceuticals, Inc. | Method for predicting cancer sensitivity |
| EP3063302B1 (en) | 2013-10-30 | 2019-12-04 | Eutropics Pharmaceuticals, Inc. | Methods for determining chemosensitivity and chemotoxicity |
| US9670196B2 (en) | 2013-12-20 | 2017-06-06 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as Spleen Tyrosine Kinase inhibitors |
| EP3082807B1 (en) | 2013-12-20 | 2018-07-04 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| WO2015095445A1 (en) | 2013-12-20 | 2015-06-25 | Merck Sharp & Dohme Corp. | Thiazole-substituted aminoheteroaryls as spleen tyrosine kinase inhibitors |
| WO2015138273A1 (en) | 2014-03-13 | 2015-09-17 | Merck Sharp & Dohme Corp. | 2-pyrazine carboxamides as spleen tyrosine kinase inhibitors |
| EP2974729A1 (en) | 2014-07-17 | 2016-01-20 | Abivax | Quinoline derivatives for use in the treatment of inflammatory diseases |
| ES2707125T3 (en) * | 2014-10-31 | 2019-04-02 | Genoscience Pharma Sas | 2,4-diamino-quinoline substituted as new anticancer agents |
| SI3452465T1 (en) | 2016-05-04 | 2021-04-30 | Genoscience Pharma | Substituted 2, 4-diamino-quinoline derivatives for use in the treatment of proliferative diseases |
| US11091460B2 (en) * | 2017-06-14 | 2021-08-17 | Chia Tai Tianqing Pharmaceutical Group Co., Ltd. | Syk inhibitor and use method therefor |
| EP3658560A4 (en) * | 2017-07-25 | 2021-01-06 | Crinetics Pharmaceuticals, Inc. | SOMATOSTATIN MODULATORS AND USES OF THESE LATEST |
| EP3620164A1 (en) * | 2018-09-05 | 2020-03-11 | Genoscience Pharma SAS | Substituted 2,4 diamino-quinoline as new medicament for fibrosis, autophagy and cathepsins b (ctsb), l (ctsl) and d (ctsd) related diseases |
| CN113166106B (en) * | 2018-12-14 | 2022-07-08 | 正大天晴药业集团股份有限公司 | Salt of Syk inhibitor and crystal form thereof |
| EP3669873A1 (en) | 2018-12-20 | 2020-06-24 | Abivax | Quinoline derivatives for use ine the traeatment of inflammation diseases |
| US11691971B2 (en) | 2020-06-19 | 2023-07-04 | Incyte Corporation | Naphthyridinone compounds as JAK2 V617F inhibitors |
| US11753413B2 (en) | 2020-06-19 | 2023-09-12 | Incyte Corporation | Substituted pyrrolo[2,1-f][1,2,4]triazine compounds as JAK2 V617F inhibitors |
| WO2022006456A1 (en) | 2020-07-02 | 2022-01-06 | Incyte Corporation | Tricyclic pyridone compounds as jak2 v617f inhibitors |
| RS66978B1 (en) | 2020-07-02 | 2025-07-31 | Incyte Corp | Tricyclic urea compounds as jak2 v617f inhibitors |
| US11661422B2 (en) | 2020-08-27 | 2023-05-30 | Incyte Corporation | Tricyclic urea compounds as JAK2 V617F inhibitors |
| US11919908B2 (en) | 2020-12-21 | 2024-03-05 | Incyte Corporation | Substituted pyrrolo[2,3-d]pyrimidine compounds as JAK2 V617F inhibitors |
| WO2022182839A1 (en) | 2021-02-25 | 2022-09-01 | Incyte Corporation | Spirocyclic lactams as jak2 v617f inhibitors |
| EP4440570A1 (en) * | 2021-12-01 | 2024-10-09 | Institut National de la Santé et de la Recherche Médicale (INSERM) | Irap inhibitors for use in the treatment of inflammatory diseases |
| KR20240163688A (en) | 2022-03-17 | 2024-11-19 | 인사이트 코포레이션 | Tricyclic urea compounds as JAK2 V617F inhibitors |
Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE537104C (en) * | 1926-05-04 | 1933-03-17 | Chem Ind Basel | Process for the preparation of substituted quinolinecarboxamides |
| DE858698C (en) * | 1951-02-09 | 1952-12-08 | Basf Ag | Process for the preparation of pyridine and quinoline derivatives |
| GB811957A (en) * | 1956-03-01 | 1959-04-15 | Geigy Ag J R | Improvements relating to 2-hydroxy-4-arylamino-quinolines |
| WO1998018782A1 (en) * | 1996-10-28 | 1998-05-07 | Celltech Therapeutics Limited | 2-pyrimidineamine derivatives and processes for their preparation |
| WO2002014269A2 (en) * | 2000-08-16 | 2002-02-21 | Neurogen Corporation | 2,4-substituted pyridine derivatives |
| WO2003078404A1 (en) * | 2002-03-15 | 2003-09-25 | Novartis Ag | Pyrimidine derivatives |
| WO2004002960A1 (en) * | 2002-06-27 | 2004-01-08 | Schering Aktiengesellschaft | Substituted quinoline ccr5 receptor antagonists |
| WO2004081531A2 (en) * | 2003-03-10 | 2004-09-23 | Schering Corporation | Ligand analysis |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2472066A (en) * | 1949-06-07 | Z-arylamino-x-halogenoqtjinolines | ||
| FR6103M (en) * | 1967-02-22 | 1968-06-10 | ||
| US3755332A (en) * | 1971-07-01 | 1973-08-28 | Ciba Geigy Corp | Substituted 4 indazolaminoquinolines |
| FR2538388B1 (en) * | 1982-12-24 | 1985-06-21 | Pharmuka Lab | NOVEL NAPHTHALENE- OR AZANAPHTHALENECARBOXAMIDE DERIVATIVES, PROCESSES FOR THEIR PREPARATION AND THEIR USE AS MEDICAMENTS |
| JPH05310702A (en) * | 1992-05-06 | 1993-11-22 | Kyowa Hakko Kogyo Co Ltd | Anti-inflammatory agent, immunomodulating agent and quinoline-2,4-dicarboxylic acid diamide derivative |
| EP0975345A1 (en) * | 1997-11-26 | 2000-02-02 | Cerebrus Pharmaceuticals Limited | (-)-mefloquine to block purinergic receptors and to treat movement or neurodegenerative disorders |
| US6303593B1 (en) * | 1999-03-02 | 2001-10-16 | Merck & Co., Inc. | 3-thienyl and 3-furanyl pyrrolidine modulators of chemokine receptor activity |
| AU6051800A (en) * | 1999-06-16 | 2001-01-02 | University Of Iowa Research Foundation, The | Antagonism of immunostimulatory cpg-oligonucleotides by 4-aminoquinolines and other weak bases |
| US6593324B2 (en) * | 2000-03-01 | 2003-07-15 | Orion Corporation | Dervatives of quinoline as alpha-2 antagonists |
| US6900226B2 (en) * | 2000-09-06 | 2005-05-31 | Hoffman-La Roche Inc. | Neuropeptide Y antagonists |
| CN100376557C (en) * | 2001-05-21 | 2008-03-26 | 霍夫曼-拉罗奇有限公司 | Quinoline derivatives as ligands for neuropeptide Y receptors |
| GB0118479D0 (en) * | 2001-07-28 | 2001-09-19 | Astrazeneca Ab | Novel compounds |
| SE0102858D0 (en) * | 2001-08-27 | 2001-08-27 | Astrazeneca Ab | N-type calcium channel antagonists for the treatment of pain |
-
2004
- 2004-03-10 CA CA002518398A patent/CA2518398A1/en not_active Abandoned
- 2004-03-10 WO PCT/US2004/007286 patent/WO2004080463A1/en not_active Ceased
- 2004-03-10 JP JP2006507031A patent/JP2006519846A/en active Pending
- 2004-03-10 MX MXPA05009722A patent/MXPA05009722A/en not_active Application Discontinuation
- 2004-03-10 EP EP04719237A patent/EP1601357A4/en not_active Withdrawn
Patent Citations (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE537104C (en) * | 1926-05-04 | 1933-03-17 | Chem Ind Basel | Process for the preparation of substituted quinolinecarboxamides |
| DE858698C (en) * | 1951-02-09 | 1952-12-08 | Basf Ag | Process for the preparation of pyridine and quinoline derivatives |
| GB811957A (en) * | 1956-03-01 | 1959-04-15 | Geigy Ag J R | Improvements relating to 2-hydroxy-4-arylamino-quinolines |
| WO1998018782A1 (en) * | 1996-10-28 | 1998-05-07 | Celltech Therapeutics Limited | 2-pyrimidineamine derivatives and processes for their preparation |
| WO2002014269A2 (en) * | 2000-08-16 | 2002-02-21 | Neurogen Corporation | 2,4-substituted pyridine derivatives |
| WO2003078404A1 (en) * | 2002-03-15 | 2003-09-25 | Novartis Ag | Pyrimidine derivatives |
| WO2004002960A1 (en) * | 2002-06-27 | 2004-01-08 | Schering Aktiengesellschaft | Substituted quinoline ccr5 receptor antagonists |
| WO2004081531A2 (en) * | 2003-03-10 | 2004-09-23 | Schering Corporation | Ligand analysis |
Non-Patent Citations (5)
| Title |
|---|
| HASEBE, M.; ET AL., TETRAHEDRON LETTERS, vol. 29, no. 48, 1988, pages 6287 - 6290, XP002445489 * |
| ILLUMINATI, G.; GILMAN, H., J. AM. CHEM. SOC., vol. 71, 1949, pages 3349 - 3351, XP002445491 * |
| SARGENT, H., J. AM. CHEM. SOC., vol. 68, 1964, pages 2688 - 2692, XP002445490 * |
| See also references of WO2004080463A1 * |
| WEISS, M.J.; HAUSER, C.R., J. AM. CHEM. SOC., vol. 71, 1949, pages 2026 - 2027, XP002445492 * |
Also Published As
| Publication number | Publication date |
|---|---|
| CA2518398A1 (en) | 2004-09-23 |
| JP2006519846A (en) | 2006-08-31 |
| WO2004080463A1 (en) | 2004-09-23 |
| MXPA05009722A (en) | 2006-03-09 |
| EP1601357A1 (en) | 2005-12-07 |
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