GT200500008A - Intermediarios de quinolina como inhibidores de receptores de tirosina quinasas y la sintesis de los mismos - Google Patents
Intermediarios de quinolina como inhibidores de receptores de tirosina quinasas y la sintesis de los mismosInfo
- Publication number
- GT200500008A GT200500008A GT200500008A GT200500008A GT200500008A GT 200500008 A GT200500008 A GT 200500008A GT 200500008 A GT200500008 A GT 200500008A GT 200500008 A GT200500008 A GT 200500008A GT 200500008 A GT200500008 A GT 200500008A
- Authority
- GT
- Guatemala
- Prior art keywords
- inhibitors
- thirosine
- intermediaries
- quinoline
- synthesis
- Prior art date
Links
- 108091000080 Phosphotransferase Proteins 0.000 title abstract 2
- 239000003112 inhibitor Substances 0.000 title abstract 2
- 102000020233 phosphotransferase Human genes 0.000 title abstract 2
- SMWDFEZZVXVKRB-UHFFFAOYSA-N Quinoline Chemical compound N1=CC=CC2=CC=CC=C21 SMWDFEZZVXVKRB-UHFFFAOYSA-N 0.000 title 2
- 230000015572 biosynthetic process Effects 0.000 title 1
- 238000003786 synthesis reaction Methods 0.000 title 1
- 150000001875 compounds Chemical class 0.000 abstract 2
- 230000001413 cellular effect Effects 0.000 abstract 1
- 230000003463 hyperproliferative effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
- C07D215/16—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D215/48—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
- C07D215/54—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/14—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D295/155—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals with the ring nitrogen atoms and the carbon atoms with three bonds to hetero atoms separated by carbocyclic rings or by carbon chains interrupted by carbocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Abstract
LA PRESENTE INVENCION SE REFIERE A UN METODO DE PREPARACION DE COMPUESTOS DE FORMULA GENERAL I EN LA QUE PG,A,G,LG,R1,R4, SON GRUPOS FUNCIONALES DESCRITOS EN EL EXPEDIENTE. ESTOS COMPUESTOS SON INHIBIDORES DE RECEPTORES DE TIROSINA QUINASAS POR LO QUE SON DE UTILIDAD PRINCIPALMENTE EN TRASTORNOS CELULARES HIPERPROLIFERATIVOS.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US53732904P | 2004-01-16 | 2004-01-16 |
Publications (1)
Publication Number | Publication Date |
---|---|
GT200500008A true GT200500008A (es) | 2005-08-16 |
Family
ID=34807094
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GT200500008A GT200500008A (es) | 2004-01-16 | 2005-01-14 | Intermediarios de quinolina como inhibidores de receptores de tirosina quinasas y la sintesis de los mismos |
Country Status (20)
Country | Link |
---|---|
US (2) | US7432377B2 (es) |
EP (1) | EP1711467A2 (es) |
KR (1) | KR20060123545A (es) |
CN (1) | CN1930128A (es) |
AR (1) | AR047424A1 (es) |
AU (1) | AU2005206541A1 (es) |
BR (1) | BRPI0520812A2 (es) |
CA (1) | CA2553729A1 (es) |
CR (1) | CR8530A (es) |
EC (1) | ECSP066773A (es) |
GT (1) | GT200500008A (es) |
MY (1) | MY136959A (es) |
NO (1) | NO20063501L (es) |
PA (1) | PA8621501A1 (es) |
PE (1) | PE20050896A1 (es) |
RU (1) | RU2006127414A (es) |
SG (1) | SG149817A1 (es) |
TW (1) | TW200526219A (es) |
UA (1) | UA85698C2 (es) |
WO (1) | WO2005070890A2 (es) |
Families Citing this family (38)
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WO2005070890A2 (en) | 2004-01-16 | 2005-08-04 | Wyeth | Quinoline intermediates of receptor tyrosine kinase inhibitors and the synthesis thereof |
KR20080016604A (ko) * | 2005-05-25 | 2008-02-21 | 와이어쓰 | 6-알킬아미노퀴놀린 유도체의 합성 방법 |
RU2007143161A (ru) * | 2005-05-25 | 2009-07-10 | Вайет (Us) | Способы синтеза замещенных 3-цианохинов и их продуктов |
CN101180269A (zh) * | 2005-05-25 | 2008-05-14 | 惠氏公司 | 制备3-氰基-喹啉的方法和由其制得的中间体 |
TW200808728A (en) * | 2006-05-23 | 2008-02-16 | Wyeth Corp | Method of preparing 4-halogenated quinoline intermediates |
US8093246B2 (en) * | 2006-12-14 | 2012-01-10 | Lexicon Pharmaceuticals, Inc. | O-linked pyrimidin-4-amine-based compounds, compositions comprising them, and methods of their use to treat cancer |
PE20090717A1 (es) | 2007-05-18 | 2009-07-18 | Smithkline Beecham Corp | Derivados de quinolina como inhibidores de la pi3 quinasa |
US8063220B2 (en) | 2007-06-22 | 2011-11-22 | Richter Gedeon Nyrt. | Sulfonyl-quinoline derivatives |
SI2300013T1 (en) | 2008-05-21 | 2018-03-30 | Adriad Pharmacaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
US9273077B2 (en) | 2008-05-21 | 2016-03-01 | Ariad Pharmaceuticals, Inc. | Phosphorus derivatives as kinase inhibitors |
US8338439B2 (en) | 2008-06-27 | 2012-12-25 | Celgene Avilomics Research, Inc. | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
US11351168B1 (en) | 2008-06-27 | 2022-06-07 | Celgene Car Llc | 2,4-disubstituted pyrimidines useful as kinase inhibitors |
DK2361248T3 (en) | 2008-06-27 | 2019-01-14 | Celgene Car Llc | Heteroberl compounds and uses thereof |
AU2009314631B2 (en) | 2008-11-12 | 2014-07-31 | Takeda Pharmaceutical Company Limited | Pyrazinopyrazines and derivatives as kinase inhibitors |
EP3144298A1 (en) | 2010-08-10 | 2017-03-22 | Celgene Avilomics Research, Inc. | Besylate salt of a btk inhibitor |
JP5956999B2 (ja) | 2010-11-01 | 2016-07-27 | セルジーン アヴィロミクス リサーチ, インコーポレイテッド | ヘテロアリール化合物およびその使用 |
MX2013004894A (es) | 2010-11-01 | 2013-10-17 | Celgene Avilomics Res Inc | Compuestos heterociclicos y usos de los mismos. |
US8796255B2 (en) | 2010-11-10 | 2014-08-05 | Celgene Avilomics Research, Inc | Mutant-selective EGFR inhibitors and uses thereof |
JP5999177B2 (ja) | 2011-05-04 | 2016-09-28 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Egfr発動性がんの細胞増殖阻害用化合物 |
AR088570A1 (es) | 2011-10-28 | 2014-06-18 | Celgene Avilomics Res Inc | Metodos para tratar una enfermedad o trastorno relacionado con la tirosina quinasa de bruton |
JP6317319B2 (ja) | 2012-03-15 | 2018-04-25 | セルジーン シーエーアール エルエルシー | 上皮成長因子受容体キナーゼ阻害剤の固体形態 |
MX356179B (es) | 2012-03-15 | 2018-05-17 | Celgene Avilomics Res Inc | Sales de un inhibidor de cinasa del receptor del factor de crecimiento epidermico. |
JP6469567B2 (ja) | 2012-05-05 | 2019-02-13 | アリアド・ファーマシューティカルズ・インコーポレイテッド | Egfr発動性がんの細胞増殖阻害用化合物 |
EP2935226A4 (en) | 2012-12-21 | 2016-11-02 | Celgene Avilomics Res Inc | HETEROARYL COMPOUNDS AND USES THEREOF |
CN105188371A (zh) | 2013-02-08 | 2015-12-23 | 西建阿维拉米斯研究公司 | Erk抑制剂及其用途 |
US9611283B1 (en) | 2013-04-10 | 2017-04-04 | Ariad Pharmaceuticals, Inc. | Methods for inhibiting cell proliferation in ALK-driven cancers |
US9492471B2 (en) | 2013-08-27 | 2016-11-15 | Celgene Avilomics Research, Inc. | Methods of treating a disease or disorder associated with Bruton'S Tyrosine Kinase |
US9415049B2 (en) | 2013-12-20 | 2016-08-16 | Celgene Avilomics Research, Inc. | Heteroaryl compounds and uses thereof |
ES2741785T3 (es) | 2014-08-13 | 2020-02-12 | Celgene Car Llc | Formas y composiciones de un inhibidor de ERK |
US9708272B2 (en) | 2014-08-29 | 2017-07-18 | Tes Pharma S.R.L. | Inhibitors of α-amino-β-carboxymuconic acid semialdehyde decarboxylase |
US10463226B2 (en) * | 2014-09-01 | 2019-11-05 | Electrolux Appliances Aktiebolag | Support assembly |
WO2017062500A2 (en) | 2015-10-05 | 2017-04-13 | The Trustees Of Columbia University In The City Of New York | Activators of autophagic flux and phospholipase d and clearance of protein aggregates including tau and treatment of proteinopathies |
CN105503720B (zh) * | 2015-12-31 | 2018-07-03 | 重庆威鹏药业有限公司 | 来那替尼中间体的制备方法 |
CN107501175A (zh) * | 2017-07-25 | 2017-12-22 | 广州大学 | 一种喹啉衍生物的合成方法 |
CN107417612A (zh) * | 2017-07-25 | 2017-12-01 | 广州大学 | 一种喹啉衍生物的合成方法 |
CN107501174A (zh) * | 2017-07-25 | 2017-12-22 | 广州大学 | 一种喹啉衍生物的合成方法 |
JP7256823B2 (ja) | 2018-04-18 | 2023-04-12 | コンステレーション・ファーマシューティカルズ・インコーポレイテッド | メチル修飾酵素のモジュレーター、その組成物および使用 |
CA3100977A1 (en) | 2018-05-21 | 2019-11-28 | Constellation Pharmaceuticals, Inc. | Modulators of methyl modifying enzymes, compositions and uses thereof |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
UA73073C2 (uk) | 1997-04-03 | 2005-06-15 | Уайт Холдінгз Корпорейшн | Заміщені 3-ціанохіноліни, спосіб їх одержання та фармацевтична композиція |
WO1998054156A1 (en) | 1997-05-28 | 1998-12-03 | Rhone-Poulenc Rorer Pharmaceuticals, Inc. | QUINOLINE AND QUINOXALINE COMPOUNDS WHICH INHIBIT PLATELET-DERIVED GROWTH FACTOR AND/OR P56lck TYROSINE KINASES |
US6245760B1 (en) | 1997-05-28 | 2001-06-12 | Aventis Pharmaceuticals Products, Inc | Quinoline and quinoxaline compounds which inhibit platelet-derived growth factor and/or p56lck tyrosine kinases |
US6297258B1 (en) | 1998-09-29 | 2001-10-02 | American Cyanamid Company | Substituted 3-cyanoquinolines |
BRPI9914164B8 (pt) | 1998-09-29 | 2021-05-25 | American Cyanamid Co | compostos de 3-ciano quinolina |
GB9910577D0 (en) | 1999-05-08 | 1999-07-07 | Zeneca Ltd | Chemical compounds |
EP1294709A2 (en) | 2000-01-28 | 2003-03-26 | AstraZeneca AB | Quinoline derivatives and their use as aurora 2 kinase inhibitors |
WO2002036570A1 (en) | 2000-11-02 | 2002-05-10 | Astrazeneca Ab | 4-substituted quinolines as antitumor agents |
UA77200C2 (en) | 2001-08-07 | 2006-11-15 | Wyeth Corp | Antineoplastic combination of cci-779 and bkb-569 |
AU2003224482A1 (en) * | 2002-04-30 | 2003-11-17 | Korea Research Institute Of Chemical Technology | Quinoline derivatives as caspase-3 inhibitor, preparation for producing the same and pharmaceutical composition comprising the same |
CL2004000016A1 (es) | 2003-01-21 | 2005-04-15 | Wyeth Corp | Compuesto derivado de cloruro de 4-amino-2-butenoilo o una sal farmaceuticamente aceptable del mismo; procedimiento para preparar dicho compuesto, util como intermediario en la sintesis de compuestos inhibidores de proteina quinasa tirosina. |
US7365203B2 (en) * | 2003-09-15 | 2008-04-29 | Wyeth | Process for the synthesis of 6-amino-4-(3-chloro-4-fluoro-phenylamino)-7-ethoxy-quinoline-3-carbonitrile |
WO2005070890A2 (en) | 2004-01-16 | 2005-08-04 | Wyeth | Quinoline intermediates of receptor tyrosine kinase inhibitors and the synthesis thereof |
GB0509224D0 (en) | 2005-05-05 | 2005-06-15 | Chroma Therapeutics Ltd | Inhibitors of intracellular enzymatic activity |
-
2005
- 2005-01-14 WO PCT/US2005/001384 patent/WO2005070890A2/en active Application Filing
- 2005-01-14 RU RU2006127414/04A patent/RU2006127414A/ru not_active Application Discontinuation
- 2005-01-14 TW TW094101148A patent/TW200526219A/zh unknown
- 2005-01-14 CN CNA2005800077483A patent/CN1930128A/zh active Pending
- 2005-01-14 US US11/036,408 patent/US7432377B2/en not_active Expired - Fee Related
- 2005-01-14 CA CA002553729A patent/CA2553729A1/en not_active Abandoned
- 2005-01-14 GT GT200500008A patent/GT200500008A/es unknown
- 2005-01-14 SG SG200900078-7A patent/SG149817A1/en unknown
- 2005-01-14 PA PA20058621501A patent/PA8621501A1/es unknown
- 2005-01-14 EP EP05711511A patent/EP1711467A2/en not_active Withdrawn
- 2005-01-14 BR BRPI0520812-2A patent/BRPI0520812A2/pt not_active IP Right Cessation
- 2005-01-14 UA UAA200609099A patent/UA85698C2/ru unknown
- 2005-01-14 KR KR1020067016319A patent/KR20060123545A/ko not_active Application Discontinuation
- 2005-01-14 AU AU2005206541A patent/AU2005206541A1/en not_active Withdrawn
- 2005-01-15 MY MYPI20050166A patent/MY136959A/en unknown
- 2005-01-17 AR ARP050100169A patent/AR047424A1/es unknown
- 2005-01-17 PE PE2005000069A patent/PE20050896A1/es not_active Application Discontinuation
-
2006
- 2006-07-24 CR CR8530A patent/CR8530A/es not_active Application Discontinuation
- 2006-08-01 NO NO20063501A patent/NO20063501L/no not_active Application Discontinuation
- 2006-08-16 EC EC2006006773A patent/ECSP066773A/es unknown
-
2008
- 2008-08-28 US US12/200,120 patent/US20090030197A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
PE20050896A1 (es) | 2005-11-14 |
EP1711467A2 (en) | 2006-10-18 |
WO2005070890A3 (en) | 2005-11-03 |
CA2553729A1 (en) | 2005-08-04 |
BRPI0520812A2 (pt) | 2009-10-06 |
SG149817A1 (en) | 2009-02-27 |
KR20060123545A (ko) | 2006-12-01 |
US20090030197A1 (en) | 2009-01-29 |
US7432377B2 (en) | 2008-10-07 |
AU2005206541A1 (en) | 2005-08-04 |
RU2006127414A (ru) | 2008-02-27 |
UA85698C2 (ru) | 2009-02-25 |
US20050159446A1 (en) | 2005-07-21 |
MY136959A (en) | 2008-12-31 |
TW200526219A (en) | 2005-08-16 |
AR047424A1 (es) | 2006-01-18 |
WO2005070890A2 (en) | 2005-08-04 |
NO20063501L (no) | 2006-09-28 |
CR8530A (es) | 2008-09-23 |
CN1930128A (zh) | 2007-03-14 |
PA8621501A1 (es) | 2005-08-10 |
ECSP066773A (es) | 2006-11-16 |
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