EA201101042A1 - Производные бензотиазолона - Google Patents
Производные бензотиазолонаInfo
- Publication number
- EA201101042A1 EA201101042A1 EA201101042A EA201101042A EA201101042A1 EA 201101042 A1 EA201101042 A1 EA 201101042A1 EA 201101042 A EA201101042 A EA 201101042A EA 201101042 A EA201101042 A EA 201101042A EA 201101042 A1 EA201101042 A1 EA 201101042A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- benzothiazolone
- derivatives
- tumors
- compounds
- formula
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/10—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- 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
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/04—Antineoplastic agents specific for metastasis
-
- 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
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/60—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings condensed with carbocyclic rings or ring systems
- C07D277/62—Benzothiazoles
- C07D277/68—Benzothiazoles 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 in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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)
- Oncology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Hematology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Соединения формулы I, в которой R, R, R, R, R, R, Е, Е', Е'' и Е''' имеют значения, указанные в п.1, являются ингибиторами тирозинкиназ, в особенности Met киназы, и могут применяться, среди прочего, для лечения опухолей.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE102009003975A DE102009003975A1 (de) | 2009-01-07 | 2009-01-07 | Benzothiazolonderivate |
PCT/EP2009/008756 WO2010078905A1 (de) | 2009-01-07 | 2009-12-08 | Benzothiazolonderivate |
Publications (2)
Publication Number | Publication Date |
---|---|
EA201101042A1 true EA201101042A1 (ru) | 2012-01-30 |
EA021067B1 EA021067B1 (ru) | 2015-03-31 |
Family
ID=41600341
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201101042A EA021067B1 (ru) | 2009-01-07 | 2009-12-08 | Производные бензотиазолона |
Country Status (16)
Country | Link |
---|---|
US (1) | US8877751B2 (ru) |
EP (1) | EP2373635A1 (ru) |
JP (1) | JP5653933B2 (ru) |
KR (1) | KR20110102504A (ru) |
CN (1) | CN102272112A (ru) |
AR (1) | AR074989A1 (ru) |
AU (1) | AU2009336847B2 (ru) |
BR (1) | BRPI0923602A2 (ru) |
CA (1) | CA2748908C (ru) |
DE (1) | DE102009003975A1 (ru) |
EA (1) | EA021067B1 (ru) |
IL (1) | IL213827A (ru) |
MX (1) | MX2011007232A (ru) |
SG (1) | SG172424A1 (ru) |
WO (1) | WO2010078905A1 (ru) |
ZA (1) | ZA201105779B (ru) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2015011290A (es) * | 2013-02-28 | 2015-12-03 | Novartis Ag | Formulacion que comprende un compuesto de benzotiazolona. |
EP2933245A1 (en) * | 2014-04-17 | 2015-10-21 | Bayer Technology Services GmbH | Oxidative carbonylation of amino aryl compounds by aryl formates |
US10750742B2 (en) | 2015-12-22 | 2020-08-25 | Syngenta Participations Ag | Pesticidally active pyrazole derivatives |
WO2020156453A1 (zh) * | 2019-02-01 | 2020-08-06 | 南京明德新药研发有限公司 | 作为c-Met抑制剂的含嘧啶基团的三并环类化合物 |
CN115583939A (zh) * | 2022-11-04 | 2023-01-10 | 苏州莱安医药化学技术有限公司 | 一种特泊替尼中间体的合成方法 |
Family Cites Families (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB9624482D0 (en) | 1995-12-18 | 1997-01-15 | Zeneca Phaema S A | Chemical compounds |
ATE237596T1 (de) | 1996-02-13 | 2003-05-15 | Astrazeneca Ab | Chinazolinderivate und deren verwendung als vegf hemmer |
PT885198E (pt) | 1996-03-05 | 2002-06-28 | Astrazeneca Ab | Derivados de 4-anilinoquinazolina |
GB9718972D0 (en) | 1996-09-25 | 1997-11-12 | Zeneca Ltd | Chemical compounds |
GB9714249D0 (en) | 1997-07-08 | 1997-09-10 | Angiogene Pharm Ltd | Vascular damaging agents |
GB9900334D0 (en) | 1999-01-07 | 1999-02-24 | Angiogene Pharm Ltd | Tricylic vascular damaging agents |
GB9900752D0 (en) | 1999-01-15 | 1999-03-03 | Angiogene Pharm Ltd | Benzimidazole vascular damaging agents |
AU2001258628A1 (en) | 2000-05-31 | 2001-12-11 | Astrazeneca Ab | Indole derivatives with vascular damaging activity |
RU2003103603A (ru) | 2000-07-07 | 2004-08-20 | Энджиоджен Фармасьютикалз Лимитед (Gb) | Производные колхинола в качестве ингибиторов ангиогенеза |
CN1255391C (zh) | 2000-07-07 | 2006-05-10 | 安吉奥金尼药品有限公司 | 作为血管破坏剂的colchinol衍生物 |
AU2002303892A1 (en) | 2001-05-30 | 2002-12-09 | Jingrong Cui | 5-aralkylsulfonyl-3- (pyrrol-2-ylmethylidene)-2-indolinone derivatives as kinase inhibitors |
AU2002313249B2 (en) | 2001-06-22 | 2008-08-21 | Kirin Pharma Kabushiki Kaisha | Quinoline derivative and quinazoline derivate inhibiting self-phosphorylation of hepatocytus proliferator receptor, and medicinal composition containing the same |
WO2003037349A1 (en) | 2001-10-31 | 2003-05-08 | Merck Patent Gmbh | Type 4 phosphodiesterase inhibitors and uses thereof |
DE60329990D1 (de) | 2002-03-08 | 2009-12-24 | Merck & Co Inc | Mitotische kinesin-hemmer |
JP2007516180A (ja) | 2003-07-02 | 2007-06-21 | スゲン,インコーポレイティド | c−Met阻害薬としてのアリールメチルトリアゾロおよびイミダゾピラジン類 |
SI2392564T1 (sl) | 2003-09-26 | 2014-02-28 | Exelixis, Inc. | c-Met modulatorji in postopki uporabe |
US7977345B2 (en) | 2004-07-02 | 2011-07-12 | Exelixis, Inc. | c-MET modulators and method of use |
DE102004036581A1 (de) | 2004-07-28 | 2006-03-23 | Robert Bosch Gmbh | Verfahren zum Betreiben eines Hybridantriebs und Vorrichtung zur Durchführung des Verfahrens |
CH697191A5 (de) | 2004-07-29 | 2008-06-25 | Biospectra Ag | Mehrfach-Bioreaktorvorrichtung. |
EP1621785A1 (en) | 2004-07-30 | 2006-02-01 | Mecos Traxler AG | Method and apparatus for controlling a magnetic bearing device |
PL1784396T3 (pl) | 2004-08-26 | 2011-05-31 | Pfizer | Związki aminoheteroarylowe podstawione pirazolem jako inhibitory kinazy białkowej |
JP2008524246A (ja) | 2004-12-16 | 2008-07-10 | タケダ サン ディエゴ インコーポレイテッド | ヒストンデアセチラーゼ阻害剤 |
JP2008533122A (ja) | 2005-03-18 | 2008-08-21 | オーキッド ケミカルズ アンド ファーマシューティカルズ リミテッド | 新規なチロシン誘導体 |
DE102005038537A1 (de) | 2005-08-16 | 2007-02-22 | Merck Patent Gmbh | 1-Acyldihydropyrazolderivate |
DE102005055354A1 (de) * | 2005-11-21 | 2007-10-31 | Merck Patent Gmbh | Substituierte 5-Phenyl-3,6-dihydro-2-oxo-6H-[1,3,4]thiadiazine |
DE102007026341A1 (de) * | 2007-06-06 | 2008-12-11 | Merck Patent Gmbh | Benzoxazolonderivate |
-
2009
- 2009-01-07 DE DE102009003975A patent/DE102009003975A1/de not_active Withdrawn
- 2009-12-08 BR BRPI0923602A patent/BRPI0923602A2/pt not_active IP Right Cessation
- 2009-12-08 EA EA201101042A patent/EA021067B1/ru not_active IP Right Cessation
- 2009-12-08 CN CN200980153630XA patent/CN102272112A/zh active Pending
- 2009-12-08 EP EP09768335A patent/EP2373635A1/de not_active Withdrawn
- 2009-12-08 KR KR1020117018354A patent/KR20110102504A/ko not_active Application Discontinuation
- 2009-12-08 CA CA2748908A patent/CA2748908C/en active Active
- 2009-12-08 US US13/143,467 patent/US8877751B2/en not_active Expired - Fee Related
- 2009-12-08 WO PCT/EP2009/008756 patent/WO2010078905A1/de active Application Filing
- 2009-12-08 AU AU2009336847A patent/AU2009336847B2/en not_active Ceased
- 2009-12-08 MX MX2011007232A patent/MX2011007232A/es not_active Application Discontinuation
- 2009-12-08 JP JP2011544794A patent/JP5653933B2/ja not_active Expired - Fee Related
- 2009-12-08 SG SG2011047552A patent/SG172424A1/en unknown
-
2010
- 2010-01-06 AR ARP100100015A patent/AR074989A1/es not_active Application Discontinuation
-
2011
- 2011-06-28 IL IL213827A patent/IL213827A/en active IP Right Grant
- 2011-08-05 ZA ZA2011/05779A patent/ZA201105779B/en unknown
Also Published As
Publication number | Publication date |
---|---|
IL213827A0 (en) | 2011-07-31 |
EP2373635A1 (de) | 2011-10-12 |
JP5653933B2 (ja) | 2015-01-14 |
US20110269756A1 (en) | 2011-11-03 |
CA2748908C (en) | 2017-10-24 |
MX2011007232A (es) | 2011-08-03 |
BRPI0923602A2 (pt) | 2016-01-12 |
US8877751B2 (en) | 2014-11-04 |
CN102272112A (zh) | 2011-12-07 |
AU2009336847B2 (en) | 2015-12-10 |
IL213827A (en) | 2015-05-31 |
CA2748908A1 (en) | 2010-07-15 |
EA021067B1 (ru) | 2015-03-31 |
AR074989A1 (es) | 2011-03-02 |
ZA201105779B (en) | 2012-04-25 |
AU2009336847A1 (en) | 2011-08-25 |
WO2010078905A1 (de) | 2010-07-15 |
DE102009003975A1 (de) | 2010-07-08 |
JP2012514610A (ja) | 2012-06-28 |
SG172424A1 (en) | 2011-07-28 |
KR20110102504A (ko) | 2011-09-16 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM |