Hexachlorocyclotriphosphazene (HCCP)-Mediated Direct Formation of Thioethers and Ethers from Quinazolin-4(3H)-ones

被引:7
|
作者
Hu, Baoxiang [1 ]
Zhang, Xiaochu [1 ]
Sheng, Lili [1 ]
Guo, Ming [2 ]
Shen, Zhenlu [1 ]
Hu, Xinquan [1 ]
Sun, Nan [1 ]
Mo, Weimin [1 ]
机构
[1] Zhejiang Univ Technol, Coll Chem Engn & Mat Sci, State Key Lab Breeding Base Green Chem Synth Tech, Hangzhou 310014, Zhejiang, Peoples R China
[2] Zhejiang Agr & Forestry Univ, Dept Chem, Linan 311300, Peoples R China
关键词
quinazolin-4(3H)-ones; hexachlorocyclotriphosphazene; 4-arylthioquinazolines; 4-aryloxyquinazolines; 4-alkoxyquinazolines; PARASITE PLASMODIUM-FALCIPARUM; BIOLOGICAL EVALUATION; POTENT; INHIBITORS; AGENTS; QUINAZOLINES; DERIVATIVES; DISCOVERY; UREAS; IDENTIFICATION;
D O I
10.3390/molecules18055580
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A hexachlorocyclotriphosphazene (HCCP)-mediated direct formation of quinazoline (thio) ethers from quinazolin-4(3H)-ones has been developed. Treatment of quinazolin-4(3H)-ones with HCCP, diisopropylethylamine (DIPEA), and thiophenols resulted in formation of the corresponding 4-arylthioquinazoline derivatives in moderate to excellent yields. This method has also been utilized to prepare 4-aryloxyquinazoline and 4-alkoxyquinazoline derivatives using phenols and sodium alkoxides as the nucleophiles.
引用
收藏
页码:5580 / 5593
页数:14
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