Synthesis of indeno [1,2-d]pyrimidin-5-ones and their fluorescence in solid state
Synthesis of indeno [1,2-d]pyrimidin-5-ones and their fluorescence in solid state
复制标题
茚并[1,2-d]嘧啶-5-酮的合成及其固态荧光
DOI:
10.1002/jhet.887
复制
发表时间:
2016
影响因子:
2.4
通讯作者:
Y. Tominaga
中科院分区:
文献类型:
--
作者:
M. Hagimori;K. Yokota;A. Fukuda;Y. Nishimura;R. Satodani;B.C. Wang;H.H. Wei;S.L. Wang;Y. Shigemitsu;Y. Tominaga
New fluorescent compounds, 2‐substituted indeno[1,2‐d]pyrimidin‐5‐ones (3a,3b,3c,3d) were synthesized in good yield by the reaction of 2‐[bis(methylsulfanyl)methylene]indan‐1,3‐dione (1) with the respective amidine derivatives [guanidine carbonate (2a), acetamidine hydrochloride (2b),S‐methylisothiourea sulfate (2c), andS‐benzylisothiourea sulfate (2d)]. 4‐Substituted amino‐2‐aminoindeno[1,2‐d]pyrimidin‐5‐ones (7b,7c,7d) were synthesized by a one‐pot reaction of1,2aand the respective amine compounds (4b,4c,4d) in pyridine. These fused pyrimidine derivatives showed fluorescence in the solid state.