JP2011527994A5 - - Google Patents

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Publication number
JP2011527994A5
JP2011527994A5 JP2011517773A JP2011517773A JP2011527994A5 JP 2011527994 A5 JP2011527994 A5 JP 2011527994A5 JP 2011517773 A JP2011517773 A JP 2011517773A JP 2011517773 A JP2011517773 A JP 2011517773A JP 2011527994 A5 JP2011527994 A5 JP 2011527994A5
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JP
Japan
Prior art keywords
alkyl
physiologically acceptable
ring
formula
compound
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JP2011517773A
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English (en)
Japanese (ja)
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JP5449346B2 (ja
JP2011527994A (ja
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Priority claimed from PCT/EP2009/004770 external-priority patent/WO2010006704A1/en
Publication of JP2011527994A publication Critical patent/JP2011527994A/ja
Publication of JP2011527994A5 publication Critical patent/JP2011527994A5/ja
Application granted granted Critical
Publication of JP5449346B2 publication Critical patent/JP5449346B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2011517773A 2008-07-15 2009-07-02 Edg−1受容体アゴニストとしてのオキサゾロピリミジン類 Expired - Fee Related JP5449346B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP08290694.2 2008-07-15
EP08290694 2008-07-15
PCT/EP2009/004770 WO2010006704A1 (en) 2008-07-15 2009-07-02 Oxazolopyrimidines as edg-1 receptor agonists

Publications (3)

Publication Number Publication Date
JP2011527994A JP2011527994A (ja) 2011-11-10
JP2011527994A5 true JP2011527994A5 (enExample) 2012-07-26
JP5449346B2 JP5449346B2 (ja) 2014-03-19

Family

ID=39967817

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2011517773A Expired - Fee Related JP5449346B2 (ja) 2008-07-15 2009-07-02 Edg−1受容体アゴニストとしてのオキサゾロピリミジン類

Country Status (20)

Country Link
US (1) US8735387B2 (enExample)
EP (2) EP2583720A1 (enExample)
JP (1) JP5449346B2 (enExample)
KR (1) KR20110042286A (enExample)
CN (1) CN102159582B (enExample)
AR (1) AR072496A1 (enExample)
AU (1) AU2009270511B2 (enExample)
BR (1) BRPI0915781A2 (enExample)
CA (1) CA2730843A1 (enExample)
CL (1) CL2011000071A1 (enExample)
CO (1) CO6331436A2 (enExample)
IL (1) IL210639A0 (enExample)
MA (1) MA32455B1 (enExample)
MX (1) MX2011000211A (enExample)
NZ (1) NZ590377A (enExample)
RU (1) RU2503680C2 (enExample)
TW (1) TW201016707A (enExample)
UY (1) UY31981A (enExample)
WO (1) WO2010006704A1 (enExample)
ZA (1) ZA201008786B (enExample)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TWI485153B (zh) 2010-01-13 2015-05-21 Sanofi Aventis 2,5,7-經取代唑并嘧啶衍生物
TWI478929B (zh) 2010-01-13 2015-04-01 Sanofi Aventis 含2,5,7-經取代唑并嘧啶環之羧酸衍生物
AR079885A1 (es) * 2010-01-14 2012-02-29 Sanofi Aventis Derivados de oxazolo[5,4-d]pirimidina 2,5-sustituidos utiles para el tratamiento del sindrome del pie diabetico(dfs), composiciones farmaceuticas que los contienen y proceso para prepararlos.
PT2523962E (pt) * 2010-01-14 2014-02-06 Sanofi Sa Derivados de ácidos carboxílicos com um anel oxazolopirimidina substituído em 2,5
MY156476A (en) * 2010-01-14 2016-02-26 Sanofi Sa Heterocyclic carboxylic acid derivatives having a 2,5-substituted oxazolopyrimidine ring
CN102791691B (zh) 2010-03-12 2015-06-03 日本曹达株式会社 含有吡啶环的化合物、及卤代甲基吡啶衍生物以及四唑基肟衍生物的制造方法
US9321787B2 (en) 2011-07-07 2016-04-26 Sanofi Carboxylic acid derivatives having an oxazolo[5,4-d]pyrimidine ring
US8735402B2 (en) * 2011-07-07 2014-05-27 Sanofi Cycloalkyloxycarboxylic acid derivatives
US8907093B2 (en) * 2011-07-07 2014-12-09 Sanofi Carboxylic acid derivatives having an oxazolo[4,5-c]pyridine ring
US8580816B2 (en) * 2011-07-07 2013-11-12 Sanofi Carboxylic acid derivatives having an oxazolo[5,4-b]pyridine ring
EP2847200B1 (en) * 2012-04-26 2017-03-29 Bristol-Myers Squibb Company Imidazothiadiazole derivatives as protease activated receptor 4 (par4) inhibitors for treating platelet aggregation
JP6073464B2 (ja) * 2012-04-26 2017-02-01 ブリストル−マイヤーズ スクイブ カンパニーBristol−Myers Squibb Company 血小板凝集を治療するためのプロテアーゼ活性化受容体4(par4)阻害剤としてのイミダゾチアジアゾールおよびイミダゾピラジン誘導体
US10577308B2 (en) 2015-03-26 2020-03-03 The Florey Institute Sodium channel modulators
CN117529325A (zh) * 2021-04-21 2024-02-06 纳特科药品有限公司 制备7-(吗啉基)-2-(N-哌嗪基)甲基噻吩并[2,3-c]吡啶衍生物的改进方法

Family Cites Families (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3679682A (en) * 1970-04-23 1972-07-25 Fmc Corp CERTAIN 5H-ISOXAZOLO{8 5,4-d{9 PYRIMIDIN-4-ONES
US7294633B2 (en) * 2001-05-14 2007-11-13 Novartis Ag Oxazolo-and furopyrimidines and their use in medicaments against tumors
CA2472680A1 (en) 2002-01-18 2003-07-31 Merck & Co., Inc. Selective s1p1/edg1 receptor agonists
WO2004096813A1 (en) 2003-04-25 2004-11-11 University College Cardiff Consultants Limited Heterocyclic compounds for use in the treatment of viral infections
AU2004234067B2 (en) * 2003-04-30 2008-02-28 Novartis Ag Aminopropanol derivatives as sphingosine-1-phosphate receptor modulators
BRPI0410439A (pt) * 2003-05-19 2006-06-06 Irm Llc compostos e composições imunossupressoras
EP1666468A4 (en) 2003-09-09 2007-03-21 Ono Pharmaceutical Co CRF ANTAGONISTS AND HETEROBICYCLIC COMPOUNDS
AU2004299456B2 (en) 2003-12-17 2010-10-07 Merck Sharp & Dohme Corp. (3,4-disubstituted)propanoic carboxylates as S1P (Edg) receptor agonists
US20050165029A1 (en) 2004-01-13 2005-07-28 Ambit Biosciences Corporation Pyrrolopyrimidine derivatives and analogs and their use in the treatment and prevention of diseases
WO2005123677A1 (en) 2004-06-16 2005-12-29 Actelion Pharmaceuticals Ltd 4-carbonyl substituted 1,1,2-trimethyl-1a,4,5,5a-tetrahydro-1h-4-aza-cyclopropa'a!pentalene derivatives as agonists for the g-protein-coupled receptor s1p1/edg1 and immunosuppressive agents
WO2006010379A1 (en) 2004-07-29 2006-02-02 Actelion Pharmaceuticals Ltd. Novel thiophene derivatives as immunosuppressive agents
JP2008517915A (ja) 2004-10-22 2008-05-29 メルク エンド カムパニー インコーポレーテッド S1p受容体アゴニストとしての2−(アリール)アザシクリルメチルカルボキシレート、スルホネート、ホスホネート、ホスフィネート及びヘテロ環
JP2009520688A (ja) * 2005-11-23 2009-05-28 エピックス デラウェア, インコーポレイテッド S1p受容体調節化合物およびそれらの使用
EP1900729A1 (en) * 2006-09-15 2008-03-19 Novartis AG Benzoxazoles and oxazolopyridines being useful as Janus kinases inhibitors

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