新产品编号:1093671
Chemical Name: N-(4-Methoxy-2,3-dihydro-1H-phenalen-2-yl)acetamide
项目整合开发状态: Biological Testing
项目研究机构: ADIR (Originator)
合成路线:2-Methoxynaphthalene (I) was condensed with bis(N-phenyl-chloromethylimine) (II) using AlCl3 to give 3-methoxyacenaphthene-quinone (III),which was oxidized with H2O2 to afford the naphthalic anhydride (IV).After acid hydrolysis of (IV) and methylation with dimethyl sulfate,the resulting diester (V) was reduced with LiAlH4 to yield diol (VI),which was transformed into dibromide (VII) by means of PBr3.Condensation of (VII) with diethyl malonate (VIII) provided the phenalene dicarboxylate ester (IX).Then,basic hydrolysis of (IX) followed by decarboxylation of the diacid furnished the phenalene-2-carboxylic acid (X).Amine (XIV) was obtained from acid (X) by formation of the acyl azide (XII) through the mixed anhydride (XI),followed by Curtius rearrangement to the corresponding isocyanate (XIII) and acid hydrolysis.Finally,amine (XIV) was acetylated with acetic anhydride to provide the target acetamide.
📌 参考资料/链接:
参考文献标题:Melatonergic properties of the (+)- and (-)-enanti
文献作者:Jellimann,C.; Mathe-Allainmat,M.; Andrieux,J.; Renard,P.; Delagrange,P.; Langlois,M.
参考来源:J Med Chem 1999,42(6),1100