Metal-Free Rapid Synthesis of 2-Aroylamino Naphtho[1,2-d]thiazoles

被引:1
作者
Liu, Tianbao [1 ]
Peng, Yanfen [1 ]
Gui, Meifang [1 ]
Zhang, Min [1 ]
机构
[1] Chizhou Univ, Anhui Higher Educ Inst, Key Lab Micronano Powder & Adv Energy Mat, Dept Chem & Mat Engn, Chizhou 247000, Anhui, Peoples R China
基金
中国国家自然科学基金;
关键词
naphtho[1,2-d]thiazole; thiourea; iodosobenzene diacetate; metal-free; CYANINE DYE; INTRAMOLECULAR CYCLIZATION; BOND FORMATION; FLUORESCENT; REACTIVITY; ENAMINONES; DNA;
D O I
10.6023/cjoc201904029
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A novel and efficient approach has been developed to synthesize 2-aroylamino naphtho[1,2-d]thiazole compounds through the reaction between 3-[1-(4-substituted naphthyl)]-1-aroylthiourea and iodosobenzene diacetate (IBD) under ambient air. A library of naphtho[1,2-d]thiazole derivatives having a variety of substituents has been synthesized. A plausible reaction pathway has been predicted. This reaction offers a metal-free synthesis, broad substrate scope, easily accessible reactants, excellent regioselectivity, room temperature reaction conditions under ambient air. The reported method is the efficient approach for the synthesis of naphtho[1,2-d]thiazole derivatives.
引用
收藏
页码:3199 / 3206
页数:8
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