JP2004507540A5 - - Google Patents

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Publication number
JP2004507540A5
JP2004507540A5 JP2002523894A JP2002523894A JP2004507540A5 JP 2004507540 A5 JP2004507540 A5 JP 2004507540A5 JP 2002523894 A JP2002523894 A JP 2002523894A JP 2002523894 A JP2002523894 A JP 2002523894A JP 2004507540 A5 JP2004507540 A5 JP 2004507540A5
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JP
Japan
Prior art keywords
formula
alkyl
compound
contacting
compound according
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.)
Granted
Application number
JP2002523894A
Other languages
English (en)
Japanese (ja)
Other versions
JP4146721B2 (ja
JP2004507540A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/EP2001/009688 external-priority patent/WO2002018379A2/en
Publication of JP2004507540A publication Critical patent/JP2004507540A/ja
Publication of JP2004507540A5 publication Critical patent/JP2004507540A5/ja
Application granted granted Critical
Publication of JP4146721B2 publication Critical patent/JP4146721B2/ja
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

JP2002523894A 2000-08-31 2001-08-22 7−オキソ−ピリドピリミジン類 Expired - Fee Related JP4146721B2 (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US22957700P 2000-08-31 2000-08-31
PCT/EP2001/009688 WO2002018379A2 (en) 2000-08-31 2001-08-22 7-oxo pyridopyrimidines

Publications (3)

Publication Number Publication Date
JP2004507540A JP2004507540A (ja) 2004-03-11
JP2004507540A5 true JP2004507540A5 (enExample) 2005-03-17
JP4146721B2 JP4146721B2 (ja) 2008-09-10

Family

ID=22861834

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2002523894A Expired - Fee Related JP4146721B2 (ja) 2000-08-31 2001-08-22 7−オキソ−ピリドピリミジン類

Country Status (18)

Country Link
EP (1) EP1315727B1 (enExample)
JP (1) JP4146721B2 (enExample)
KR (1) KR100582325B1 (enExample)
CN (2) CN1303072C (enExample)
AR (1) AR033996A1 (enExample)
AT (1) ATE298751T1 (enExample)
AU (2) AU1214702A (enExample)
BR (1) BR0113590A (enExample)
CA (1) CA2420122A1 (enExample)
DE (1) DE60111752T2 (enExample)
ES (1) ES2243568T3 (enExample)
GT (1) GT200100190A (enExample)
MX (1) MXPA03001733A (enExample)
PA (1) PA8527401A1 (enExample)
PE (1) PE20020524A1 (enExample)
UY (1) UY26920A1 (enExample)
WO (1) WO2002018379A2 (enExample)
ZA (1) ZA200301078B (enExample)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20040103972A (ko) * 2002-04-19 2004-12-09 스미스클라인 비참 코포레이션 신규 화합물
WO2004060346A2 (en) 2002-12-30 2004-07-22 Angiotech International Ag Drug delivery from rapid gelling polymer composition
US20070020234A1 (en) * 2003-07-07 2007-01-25 Vande Woude George F Inhibition of tumor angiogenesis by combination of thrombospondin-1 and inhibitors of vascular endothelial growth factor
WO2005105097A2 (en) * 2004-04-28 2005-11-10 Gpc Biotech Ag Pyridopyrimidines for treating inflammatory and other diseases
EA200801607A1 (ru) * 2004-06-15 2008-10-30 Пфайзер Инк. Производные бензимидазолонкарбоновой кислоты
US20090306380A1 (en) * 2005-04-25 2009-12-10 Shigeyoshi Nishino Process for preparing 4-amino-2-alkylthio-5-pyrimidinecarbaldehyde
JP2006321749A (ja) * 2005-05-19 2006-11-30 Ube Ind Ltd 2−シアノマロンアルデヒドのアルカリ金属塩の製法
EP1981886B1 (en) 2006-01-31 2009-08-12 F.Hoffmann-La Roche Ag 7h-pyrido[3,4-d]pyrimidin-8-ones, their manufacture and use as protein kinase inhibitors
WO2008055842A1 (en) * 2006-11-09 2008-05-15 F. Hoffmann-La Roche Ag Substituted 6-phenyl-pyrido [2,3-d] pyrimidin-7-one derivatives as kinase inhibitors and methods for using the same
CA2690327A1 (en) 2007-06-15 2008-12-18 Thomas P. Cleary A novel process for the preparation of 3-amino-pentan-1,5-diol
CN102648200A (zh) * 2009-10-09 2012-08-22 亚弗克希斯公司 用于治疗cns病症的8-乙基-6-(芳基)吡啶并[2,3-d]嘧啶-7(8h)-酮
US20120184542A1 (en) 2011-01-19 2012-07-19 Kevin Anderson Pyrido pyrimidines
WO2013142382A1 (en) * 2012-03-22 2013-09-26 Genosco Substituted pyridopyrimidine compounds and their use as flt3 inhibitors
MY181020A (en) 2013-03-15 2020-12-16 Sanofi Sa Heteroaryl compounds and uses thereof
TWI647220B (zh) 2013-03-15 2019-01-11 美商西建卡爾有限責任公司 雜芳基化合物及其用途
MA38393B1 (fr) 2014-03-13 2018-11-30 Sanofi Sa Composés hétéroaryle et utilisations associées
ES2927715T3 (es) 2017-10-05 2022-11-10 Fulcrum Therapeutics Inc Inhibidores de la quinasa p38 reducen la expresión de dux4 y de los genes que le siguen para el tratamiento de la FSHD
WO2020052349A1 (zh) * 2018-09-14 2020-03-19 上海和誉生物医药科技有限公司 Fgfr抑制剂、其制备方法和应用
CN115960098B (zh) * 2020-09-11 2026-04-10 上海凌达生物医药有限公司 一类含氮稠环类化合物的制备方法和用途

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6183168A (ja) * 1984-09-28 1986-04-26 Ube Ind Ltd 2−メルカプト−4−アミノ−5−ホルミルピリミジンおよびその製法
IL117923A (en) * 1995-05-03 2000-06-01 Warner Lambert Co Anti-cancer pharmaceutical compositions containing polysubstituted pyrido¬2,3-d¾pyrimidine derivatives and certain such novel compounds
WO1997044321A1 (en) * 1996-05-20 1997-11-27 Merck & Co., Inc. Antagonists of gonadotropin releasing hormone
US5945422A (en) * 1997-02-05 1999-08-31 Warner-Lambert Company N-oxides of amino containing pyrido 2,3-D! pyrimidines
US6184226B1 (en) * 1998-08-28 2001-02-06 Scios Inc. Quinazoline derivatives as inhibitors of P-38 α
KR100571339B1 (ko) * 2000-08-31 2006-04-17 에프. 호프만-라 로슈 아게 세포증식 억제제로서의 7-옥소 피리도피리미딘

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