[EN] CYCLIC DIARYLBORON DERIVATIVES AS NLRP3 INFLAMMASOME INHIBITORS<br/>[FR] DÉRIVÉS DE DIARYLBORON CYCLIQUES UTILISÉS EN TANT QU'INHIBITEURS D'INFLAMMASOME NLRP3
申请人:UNIV MANCHESTER
公开号:WO2017017469A1
公开(公告)日:2017-02-02
Inhibitor compounds are disclosed. The compounds are effective in the treatment of diseases or conditions in which interleukin 1 β activity is implicated. Methods of synthesis of the compounds, as well as pharmaceutical compositions comprising the compounds are also disclosed.
Cyclic diarylboron derivatives as NLRP3 inflammasome inhibitors
申请人:The University of Manchester
公开号:US10570157B2
公开(公告)日:2020-02-25
Inhibitor compounds are disclosed. The compounds are effective in the treatment of diseases or conditions in which interleukin 1 β activity is implicated. Methods of synthesis of the compounds, as well as pharmaceutical compositions comprising the compounds are also disclosed.
The exchange reaction between transition metal(II) acetates and the protic nucleophiles 3-(1-aminoethylidene) pentane-2,4-dione (Hampd) or 3-acetylpentane-2,4-dione (Hacpd) affords the corresponding [M(ampd)(2)] (M = Ni (1), Pd (2)) or [M(acpd)(2)] (M = Mn (5), Fe (6), Ni (7), Cu (8), Pd (9)) complexes in fair to good yields. The reaction is performed in ethanol at room temperature, with addition of sodium carbonate in some cases. This last new synthetic procedure is applied for those complexes which easily undergo an extensive deacylation process. The factors determining the success of the exchange reaction and the resulting N, O or O, O coordination are fully discussed. (C) 2008 Elsevier B.V. All rights reserved.
CYCLIC DIARYLBORON DERIVATIVES AS NLRP3 INFLAMMASOME INHIBITORS
申请人:The University of Manchester
公开号:EP3328868A1
公开(公告)日:2018-06-06
Reactions of β-diketone compounds with nitriles catalyzed by Lewis acids: a simple approach to β-enaminone synthesis