JP2009532428A5 - - Google Patents

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Publication number
JP2009532428A5
JP2009532428A5 JP2009503555A JP2009503555A JP2009532428A5 JP 2009532428 A5 JP2009532428 A5 JP 2009532428A5 JP 2009503555 A JP2009503555 A JP 2009503555A JP 2009503555 A JP2009503555 A JP 2009503555A JP 2009532428 A5 JP2009532428 A5 JP 2009532428A5
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JP
Japan
Prior art keywords
formula
alkyl
methyl
substituted
het
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
JP2009503555A
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English (en)
Japanese (ja)
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JP5167242B2 (ja
JP2009532428A (ja
Filing date
Publication date
Priority claimed from GBGB0607899.2A external-priority patent/GB0607899D0/en
Application filed filed Critical
Publication of JP2009532428A publication Critical patent/JP2009532428A/ja
Publication of JP2009532428A5 publication Critical patent/JP2009532428A5/ja
Application granted granted Critical
Publication of JP5167242B2 publication Critical patent/JP5167242B2/ja
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

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JP2009503555A 2006-04-03 2007-03-30 複素環式誘導体の製造方法 Expired - Fee Related JP5167242B2 (ja)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0607899.2A GB0607899D0 (en) 2006-04-03 2006-04-03 Process for preparing heterocyclic derivatives
GB0607899.2 2006-04-03
PCT/EP2007/053118 WO2007113261A1 (en) 2006-04-03 2007-03-30 Process for preparing heterocyclic derivatives

Publications (3)

Publication Number Publication Date
JP2009532428A JP2009532428A (ja) 2009-09-10
JP2009532428A5 true JP2009532428A5 (https=) 2010-05-27
JP5167242B2 JP5167242B2 (ja) 2013-03-21

Family

ID=36581002

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2009503555A Expired - Fee Related JP5167242B2 (ja) 2006-04-03 2007-03-30 複素環式誘導体の製造方法

Country Status (18)

Country Link
US (2) US20070232808A1 (https=)
EP (1) EP2007747B1 (https=)
JP (1) JP5167242B2 (https=)
KR (1) KR101411124B1 (https=)
CN (1) CN101454308B (https=)
AU (1) AU2007233744B2 (https=)
BR (1) BRPI0710049A2 (https=)
CA (1) CA2648089A1 (https=)
CR (1) CR10351A (https=)
EA (1) EA017304B1 (https=)
ES (1) ES2443219T3 (https=)
GB (1) GB0607899D0 (https=)
IL (1) IL194389A0 (https=)
MA (1) MA30354B1 (https=)
MX (1) MX2008012876A (https=)
NO (1) NO20084414L (https=)
WO (1) WO2007113261A1 (https=)
ZA (1) ZA200808107B (https=)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MD3995C2 (ro) * 2009-05-11 2010-07-31 Государственный Университет Молд0 Utilizare a di(µ-Ofenoxi)-di{[2-(4-aminobenzensulfamido)-5-etil-1,3,4-tiadiazol]-3,5-dibromosalicilidentiosemicarbazonato(-1)-cupru} în calitate de inhibitor al proliferării celulelor T-47D ale cancerului mamar
IT201700041723A1 (it) 2017-04-14 2018-10-14 Italfarmaco Spa Nuovi inibitori selettivi di HDAC6
CN106866657A (zh) * 2017-04-25 2017-06-20 成都倍特药业有限公司 一种麦角新碱的制备方法
US9862675B1 (en) 2017-07-05 2018-01-09 King Fahd University Of Petroleum And Minerals Method of N-formylating amines with a phosphonic anhydride
MX2023001086A (es) 2020-08-07 2023-03-23 Italfarmaco Spa Nuevos inhibidores selectivos de histona desacetilasa 6 (hdac6) basados en oxadiazol.

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020032238A1 (en) * 2000-07-08 2002-03-14 Henning Priepke Biphenylcarboxylic acid amides, the preparation thereof and the use thereof as medicaments
DE10033337A1 (de) * 2000-07-08 2002-01-17 Boehringer Ingelheim Pharma Biphenylcarbonsäureamide, ihre Herstellung und ihre Verwendung als Arzneimittel
WO2002032238A2 (de) * 2000-10-20 2002-04-25 Messmer, Ludwig Hochverdichteter filter tow ballen
PE20051173A1 (es) * 2004-02-23 2006-02-14 Glaxo Group Ltd Compuestos azabiciclico (3.1.0) hexanos como moduladores de receptores de dopamina d3
GB0517193D0 (en) 2005-08-22 2005-09-28 Glaxo Group Ltd Novel use

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