EA201201548A1 - Новые способы получения p2x7r антагонистов - Google Patents
Новые способы получения p2x7r антагонистовInfo
- Publication number
- EA201201548A1 EA201201548A1 EA201201548A EA201201548A EA201201548A1 EA 201201548 A1 EA201201548 A1 EA 201201548A1 EA 201201548 A EA201201548 A EA 201201548A EA 201201548 A EA201201548 A EA 201201548A EA 201201548 A1 EA201201548 A1 EA 201201548A1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- new ways
- p2x7r antagonists
- p2x7r
- antagonists
- synthesis
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/40—Nitrogen atoms, not forming part of a nitro radical, e.g. isatin semicarbazone
-
- 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
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/10—Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
- C07D209/14—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Indole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Описаны новые способы синтеза N-замещенных индол-3-ил-алкиламидных соединений, которые действуют в качестве P2X7R антагонистов, причем указанные способы включают перегруппировку промежуточного оксима.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP10162812 | 2010-05-14 | ||
PCT/EP2011/053283 WO2011141194A1 (en) | 2010-05-14 | 2011-03-04 | Novel methods for the preparation of p2x7r antagonists |
Publications (1)
Publication Number | Publication Date |
---|---|
EA201201548A1 true EA201201548A1 (ru) | 2013-05-30 |
Family
ID=43924014
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EA201201548A EA201201548A1 (ru) | 2010-05-14 | 2011-03-04 | Новые способы получения p2x7r антагонистов |
Country Status (13)
Country | Link |
---|---|
US (1) | US20130060047A1 (ru) |
EP (2) | EP2386541A1 (ru) |
JP (1) | JP2013526496A (ru) |
CN (1) | CN102858741A (ru) |
AU (1) | AU2011252351A1 (ru) |
BR (1) | BR112012028850A2 (ru) |
CA (1) | CA2799115A1 (ru) |
EA (1) | EA201201548A1 (ru) |
IL (1) | IL222948A0 (ru) |
MX (1) | MX2012013075A (ru) |
SG (1) | SG185400A1 (ru) |
WO (1) | WO2011141194A1 (ru) |
ZA (1) | ZA201209495B (ru) |
Family Cites Families (59)
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GB832568A (en) * | 1956-08-03 | 1960-04-13 | Clin Byla Ets | Heterocyclic compounds and production thereof |
US2930798A (en) * | 1956-08-03 | 1960-03-29 | Clin Byla Ets | 3-alkanoyl 1-tertiary-amino-alkyl indol oximes and production thereof |
SE9704546D0 (sv) | 1997-12-05 | 1997-12-05 | Astra Pharma Prod | Novel compounds |
SE9704544D0 (sv) | 1997-12-05 | 1997-12-05 | Astra Pharma Prod | Novel compounds |
SE9704545D0 (sv) | 1997-12-05 | 1997-12-05 | Astra Pharma Prod | Novel compounds |
BR0009651A (pt) | 1999-04-09 | 2002-01-08 | Astrazeneca Ab | Composto, processo para a preparação de um composto, composição farmacêutica, uso de um composto, e, método para tratar artrite reumatóide e uma doença obstrutiva das vias aéreas |
SE9901875D0 (sv) | 1999-05-25 | 1999-05-25 | Astra Pharma Prod | Novel compounds |
SE9904505D0 (sv) | 1999-12-09 | 1999-12-09 | Astra Pharma Prod | Novel compounds |
SE9904652D0 (sv) | 1999-12-17 | 1999-12-17 | Astra Pharma Prod | Novel Compounds |
TWI258462B (en) | 1999-12-17 | 2006-07-21 | Astrazeneca Ab | Adamantane derivative compounds, process for preparing the same and pharmaceutical composition comprising the same |
SE9904738D0 (sv) | 1999-12-22 | 1999-12-22 | Astra Pharma Prod | Novel compounds |
GB0013737D0 (en) | 2000-06-07 | 2000-07-26 | Astrazeneca Ab | Novel compounds |
PA8557501A1 (es) | 2001-11-12 | 2003-06-30 | Pfizer Prod Inc | Benzamida, heteroarilamida y amidas inversas |
WO2003042190A1 (en) | 2001-11-12 | 2003-05-22 | Pfizer Products Inc. | N-alkyl-adamantyl derivatives as p2x7-receptor antagonists |
SE0103836D0 (sv) | 2001-11-16 | 2001-11-16 | Astrazeneca Ab | Novel compounds |
WO2003047515A2 (en) | 2001-11-30 | 2003-06-12 | The Government Of The United States Of America, Represented By The Secretary, Department Of Health And Human Services | P2x7 receptor antagonists |
RU2004122409A (ru) | 2001-12-21 | 2005-04-10 | Кинг Фармасьютикалз Рисерч Энд Дивелопмент, Инк. (Us) | Тирозилсодержащие производные и их применение в качестве модуляторов рецепторов р2х7 |
SE0200920D0 (sv) | 2002-03-25 | 2002-03-25 | Astrazeneca Ab | Novel compounds |
CA2506316A1 (en) * | 2002-11-15 | 2004-06-03 | Tibotec Pharmaceuticals Ltd. | Substituted indolepyridinium as anti-infective compounds |
EP1581507A1 (en) | 2002-12-31 | 2005-10-05 | Pfizer Products Inc. | Benzamide inhibitors of the p2x7 receptor |
PA8591801A1 (es) | 2002-12-31 | 2004-07-26 | Pfizer Prod Inc | Inhibidores benzamidicos del receptor p2x7. |
SE0300480D0 (sv) | 2003-02-21 | 2003-02-21 | Astrazeneca Ab | Novel compounds |
DE602004005033T2 (de) | 2003-05-12 | 2007-08-09 | Pfizer Products Inc., Groton | Benzamidinhibitoren des p2x7-rezeptors |
GB0312609D0 (en) | 2003-06-02 | 2003-07-09 | Astrazeneca Ab | Novel compounds |
GB0324498D0 (en) | 2003-07-21 | 2003-11-26 | Aventis Pharma Inc | Heterocyclic compounds as P2X7 ion channel blockers |
SE0302139D0 (sv) | 2003-07-28 | 2003-07-28 | Astrazeneca Ab | Novel compounds |
SE0302192D0 (sv) | 2003-08-08 | 2003-08-08 | Astrazeneca Ab | Novel compounds |
WO2005019182A1 (en) | 2003-08-20 | 2005-03-03 | Bayer Healthcare Ag | Pyrazolylmethylbenzamide derivatives as p2xt-receptor antagonists |
GB2422782A (en) | 2003-10-21 | 2006-08-09 | Inspire Pharmaceuticals Inc | Non-nucleotide compositions and method for treating pain |
JP2007535553A (ja) | 2004-04-29 | 2007-12-06 | アボット・ラボラトリーズ | アミノ−テトラゾール類縁体および使用方法 |
MXPA06013316A (es) * | 2004-05-17 | 2007-02-02 | Tibotec Pharm Ltd | Combinaciones de 1-fenil-1,5-dihidro-pirido-[3,2-b]indol-2-onas sustituidas y otros inhibidores de virus de inmunodeficiencia humana. |
CN1976930B (zh) * | 2004-05-17 | 2011-01-19 | 泰博特克药品有限公司 | 用作抗感染药物的6,7,8,9-取代的1-苯基-1,5-二氢吡啶并(3,2-b)吲哚-2-酮 |
EA012330B1 (ru) * | 2004-05-17 | 2009-08-28 | Тиботек Фармасьютикалз Лтд. | 1-ГЕТЕРОЦИКЛИЛ-1,5-ДИГИДРОПИРИДО[3,2-b]ИНДОЛ-2-ОНЫ |
RU2006146675A (ru) | 2004-06-29 | 2008-07-10 | Пфайзер Продактс Инк. (Us) | Способ получения производных 5-[4-(2-гидроксипропил)-3,5-диоксо-4,5-дигидро-3н-[1,2,4] триазин-2-ил] бензамида снятием защиты с промежуточных продуктов, содержащих защищенный гидроксил |
EP1768965A1 (en) | 2004-06-29 | 2007-04-04 | Pfizer Products Incorporated | Method for preparing 5-¬4-(2-hydroxy-ethyl)-3,5-dioxo-4,5-dihydro-3h-¬1,2,4|-triazin-2-yl|benzamide derivatives with p2x7 inhibiting activity by reaction of the derivative unsubstituted in 4-position of the triazine with an oxiran in the presence of a lewis acid |
US7241776B2 (en) | 2004-08-02 | 2007-07-10 | Abbott Laboratories | Cyanoamidine P2X7 antagonists for the treatment of pain |
SA05260265A (ar) | 2004-08-30 | 2005-12-03 | استرازينيكا ايه بي | مركبات جديدة |
SE0402925D0 (sv) | 2004-11-30 | 2004-11-30 | Astrazeneca Ab | Novel Compounds |
MX2007007424A (es) | 2004-12-24 | 2007-07-17 | Astrazeneca Ab | Derivados de amina. |
JP2008528580A (ja) | 2005-01-27 | 2008-07-31 | アストラゼネカ・アクチエボラーグ | P2x7受容体の阻害剤である新規二環式芳香族化合物 |
US20060211739A1 (en) | 2005-02-08 | 2006-09-21 | Arturo Perez-Medrano | Use of selective P2X7 receptor antagonists |
US7402596B2 (en) | 2005-03-24 | 2008-07-22 | Renovis, Inc. | Bicycloheteroaryl compounds as P2X7 modulators and uses thereof |
WO2006110516A1 (en) | 2005-04-11 | 2006-10-19 | Abbott Laboratories | Acylhydrazide p2x7 antagonists and uses thereof |
WO2006136004A1 (en) | 2005-05-05 | 2006-12-28 | Medicure International Inc. | Inhibition of atp-mediated, p2x7 dependent pathways by pyridoxal-5-phosphaste and vitamin b6 related compounds |
US20090124555A1 (en) | 2005-08-29 | 2009-05-14 | Irma Bernatchez-Lemaire | Use of histogranin and histogranin-like compounds as inhibitors of p2x7 receptor function and as anti-arthritic agents |
WO2007028022A2 (en) | 2005-09-01 | 2007-03-08 | Renovis, Inc. | Novel compounds as p2x7 modulators and uses thereof |
JP2009514864A (ja) | 2005-11-07 | 2009-04-09 | アボット・ラボラトリーズ | P2x7受容体拮抗薬および使用方法 |
JP2009514952A (ja) | 2005-11-09 | 2009-04-09 | アボット・ラボラトリーズ | P2x7受容体拮抗薬としての2−フェニル−2h−ピラゾール誘導体およびそれの使用 |
DK2001474T3 (en) | 2006-03-16 | 2016-05-09 | Second Genome Inc | BICYCLOHETEROARYL COMPOUNDS AS P2X7 MODULATORS AND APPLICATIONS THEREOF |
CA2645652A1 (en) | 2006-03-16 | 2007-09-27 | Renovis, Inc. | Bicycloheteroaryl compounds as p2x7 modulators and uses thereof |
US20100298285A1 (en) | 2006-03-16 | 2010-11-25 | Kelly Michael G | Biclycloheteroaryl Compounds as P2x7 Modulators and Uses Thereof |
WO2007109201A2 (en) | 2006-03-16 | 2007-09-27 | Renovis, Inc. | Bicycloheteroaryl compounds as p2x7 modulators and uses thereof |
CA2645551C (en) | 2006-03-16 | 2016-06-28 | Renovis, Inc. | Bicycloheteroaryl compounds as p2x7 modulators and uses thereof |
TWI464148B (zh) | 2006-03-16 | 2014-12-11 | Evotec Us Inc | 作為p2x7調節劑之雙環雜芳基化合物與其用途 |
GB0611154D0 (en) | 2006-06-06 | 2006-07-19 | Glaxo Group Ltd | Novel receptor antagonists and their methods of use |
JP2009539795A (ja) | 2006-06-06 | 2009-11-19 | グラクソ グループ リミテッド | 疼痛、炎症および神経変性の治療のためのp2x7アンタゴニストとしてのn−(フェニルメチル)−2−(1h−ピラゾール−4−イル)アセトアミド誘導体 |
US20080076924A1 (en) | 2006-06-30 | 2008-03-27 | Patrick Betschmann | Piperazines as P2X7 antagonists |
WO2008003697A1 (en) | 2006-07-06 | 2008-01-10 | Glaxo Group Limited | Substituted n-phenylmethyl -5-oxo-proline-2-amides as p2x7-receptor antagonists and their methods of use |
EP2243772B1 (en) * | 2009-04-14 | 2012-01-18 | Affectis Pharmaceuticals AG | Novel P2X7R antagonists and their use |
-
2011
- 2011-03-04 EP EP11156932A patent/EP2386541A1/en not_active Withdrawn
- 2011-03-04 AU AU2011252351A patent/AU2011252351A1/en not_active Abandoned
- 2011-03-04 CN CN2011800205646A patent/CN102858741A/zh active Pending
- 2011-03-04 CA CA2799115A patent/CA2799115A1/en not_active Abandoned
- 2011-03-04 EP EP11706814A patent/EP2569281A1/en not_active Withdrawn
- 2011-03-04 WO PCT/EP2011/053283 patent/WO2011141194A1/en active Application Filing
- 2011-03-04 US US13/697,666 patent/US20130060047A1/en not_active Abandoned
- 2011-03-04 EA EA201201548A patent/EA201201548A1/ru unknown
- 2011-03-04 BR BR112012028850A patent/BR112012028850A2/pt not_active IP Right Cessation
- 2011-03-04 JP JP2013509476A patent/JP2013526496A/ja not_active Withdrawn
- 2011-03-04 MX MX2012013075A patent/MX2012013075A/es not_active Application Discontinuation
- 2011-03-04 SG SG2012080917A patent/SG185400A1/en unknown
-
2012
- 2012-11-08 IL IL222948A patent/IL222948A0/en unknown
- 2012-12-13 ZA ZA2012/09495A patent/ZA201209495B/en unknown
Also Published As
Publication number | Publication date |
---|---|
SG185400A1 (en) | 2012-12-28 |
BR112012028850A2 (pt) | 2015-09-15 |
JP2013526496A (ja) | 2013-06-24 |
WO2011141194A1 (en) | 2011-11-17 |
EP2569281A1 (en) | 2013-03-20 |
MX2012013075A (es) | 2012-12-17 |
CA2799115A1 (en) | 2011-11-17 |
ZA201209495B (en) | 2013-08-28 |
US20130060047A1 (en) | 2013-03-07 |
AU2011252351A1 (en) | 2012-10-11 |
EP2386541A1 (en) | 2011-11-16 |
IL222948A0 (en) | 2012-12-31 |
CN102858741A (zh) | 2013-01-02 |
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