JP2005504770A5 - - Google Patents

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Publication number
JP2005504770A5
JP2005504770A5 JP2003521232A JP2003521232A JP2005504770A5 JP 2005504770 A5 JP2005504770 A5 JP 2005504770A5 JP 2003521232 A JP2003521232 A JP 2003521232A JP 2003521232 A JP2003521232 A JP 2003521232A JP 2005504770 A5 JP2005504770 A5 JP 2005504770A5
Authority
JP
Japan
Prior art keywords
compound
alkyl
following formula
haloalkyl
independently
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.)
Withdrawn
Application number
JP2003521232A
Other languages
English (en)
Japanese (ja)
Other versions
JP2005504770A (ja
Filing date
Publication date
Application filed filed Critical
Priority claimed from PCT/US2002/027151 external-priority patent/WO2003016309A1/en
Publication of JP2005504770A publication Critical patent/JP2005504770A/ja
Publication of JP2005504770A5 publication Critical patent/JP2005504770A5/ja
Withdrawn legal-status Critical Current

Links

JP2003521232A 2001-08-17 2002-08-13 5−スルホンアミド−8−ヒドロキシ−1,6−ナフチリジン−7−カルボキサミドの製造方法 Withdrawn JP2005504770A (ja)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US31337601P 2001-08-17 2001-08-17
PCT/US2002/027151 WO2003016309A1 (en) 2001-08-17 2002-08-13 Process for preparing 5-sulfonamido-8-hydroxy-1, 6-naphthyridine-7-carboxamides

Publications (2)

Publication Number Publication Date
JP2005504770A JP2005504770A (ja) 2005-02-17
JP2005504770A5 true JP2005504770A5 (enExample) 2006-01-05

Family

ID=23215476

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2003521232A Withdrawn JP2005504770A (ja) 2001-08-17 2002-08-13 5−スルホンアミド−8−ヒドロキシ−1,6−ナフチリジン−7−カルボキサミドの製造方法

Country Status (6)

Country Link
US (1) US20050014780A1 (enExample)
EP (1) EP1427726A1 (enExample)
JP (1) JP2005504770A (enExample)
AR (1) AR036352A1 (enExample)
CA (1) CA2456155A1 (enExample)
WO (1) WO2003016309A1 (enExample)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE430745T1 (de) 2000-10-12 2009-05-15 Merck & Co Inc Aza- und polyaza naphthalenyl karboxamide als inhibitoren der hiv-integrase
EP1558585B1 (en) * 2002-10-04 2013-09-25 Prana Biotechnology Limited Neurologically-active compounds
WO2005028478A1 (en) 2003-09-19 2005-03-31 Gilead Sciences, Inc. Aza-quinolinol phosphonate integrase inhibitor compounds
EP1888581A2 (en) * 2005-05-16 2008-02-20 Gilead Sciences, Inc. Hiv-integrase inhibitor compounds
BRPI0722382A2 (pt) 2006-04-14 2012-06-05 Prana Biotechnology Ltd compostos úteis para o tratamento de cáncer
EP3313420B1 (en) 2015-06-25 2024-03-13 The Children's Medical Center Corporation Methods and compositions relating to hematopoietic stem cell expansion, enrichment, and maintenance
WO2017161001A1 (en) 2016-03-15 2017-09-21 Children's Medical Center Corporation Methods and compositions relating to hematopoietic stem cell expansion
DK4426434T3 (da) 2021-11-02 2025-11-10 Flare Therapeutics Inc Pparg inverse agonists and uses thereof

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH214351A (de) * 1938-08-30 1941-04-15 Cilag Chemisches Ind Lab A G Verfahren zur Darstellung eines Derivates des 2-Aminopyridins.
ATE430745T1 (de) * 2000-10-12 2009-05-15 Merck & Co Inc Aza- und polyaza naphthalenyl karboxamide als inhibitoren der hiv-integrase

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