[EN] NOVEL 2-PIPERIDIN-1-YL-ACETAMIDE COMPOUNDS FOR USE AS TANKYRASE INHIBITORS [FR] NOUVEAUX COMPOSÉS 2-PIPERIDIN-1-YL-ACETAMIDE UTILISABLES EN TANT QU'INHIBITEURS DE TANKYRASE
[EN] BENZOXAZINONE DERIVATIVES FOR THE TREATMENT OF GLYTL MEDIATED DISORDERS<br/>[FR] DÉRIVÉS DE BENZOXAZINONE POUR TRAITER DES TROUBLES INDUITS PAR GLYTL
申请人:GLAXO GROUP LTD
公开号:WO2011012622A1
公开(公告)日:2011-02-03
The present invention relates to benzoxazinone derivatives, processes for their preparation, pharmaceutical compositions and medicaments containing them and to their use in treating disorders mediated by GlyT1, including neurological and neuropsychiatric disorders, in particular psychoses, dementia or attention deficit disorder.
NOVEL 2-PIPERIDIN-1-YL-ACETAMIDE COMPOUNDS FOR USE AS TANKYRASE INHIBITORS
申请人:Cheung Atwood Kim
公开号:US20150025070A1
公开(公告)日:2015-01-22
The present invention provides for compounds of formula (I):
wherein R
1
-R
5
and L are defined herein. The present invention also provides for pharmaceutical compositions and combinations comprising a compound of formula (I) as well as for the use of such compounds as tankyrase inhibitors and in the treatment of Wnt signaling and tankyrase 1 and 2 signaling related disorders which include, but are not limited to, cancer.
2-piperidin-1-yl-acetamide compounds for use as tankyrase inhibitors
申请人:Cheung Atwood Kim
公开号:US09181266B2
公开(公告)日:2015-11-10
The present invention provides for compounds of formula (I):
wherein R1-R5 and L are defined herein. The present invention also provides for pharmaceutical compositions and combinations comprising a compound of formula (I) as well as for the use of such compounds as tankyrase inhibitors and in the treatment of Wnt signaling and tankyrase 1 and 2 signaling related disorders which include, but are not limited to, cancer.
A novel ring transformation of oxazinones and azetidinones into pyrimidinones
作者:Shinichi Kawamura、Yuzuru Sanemitsu
DOI:10.1021/jo00054a026
日期:1993.1
Azetidinones or oxazinones, being easily prepared from enamines and acyl isocyanates, were transformed into highly substituted 4(3H)-pyrimidinones upon treatment with ammonium acetate. This novel ring transformation was also accomplished through a one-pot reaction without isolation of the adduct.