90797-73-2Relevant articles and documents
Synthetic method of 4,5-disubstituted-2-aminothiazole compound
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Paragraph 0051; 0053-0057; 0089-0092, (2018/09/08)
The invention discloses a synthetic method of a 4,5-disubstituted-2-aminothiazole compound. The synthetic method sequentially comprises the following steps: 1) making a nitro-epoxy compound react withammonium thiocyanate in the presence of a solvent and an alkali catalyst at the temperature of 40-/+5 DEG C for 10 to 14 hours; 2) adding water into reaction liquid prepared in the step 1), extracting the mixture with ethyl acetate, washing a prepared organic layer, drying the organic layer, and performing concentration with a rotary evaporator; 3) performing silica gel column chromatography on the concentrate prepared in the step 2) to obtain the 4,5-disubstituted-2-aminothiazole compound. The method for synthesizing the 4,5-disubstituted-2-aminothiazole compound disclosed by the invention has the characteristics of adoption of readily-available raw materials, mild reaction conditions, high yield, convenience in post treatment and the like.
One-pot three-component protocol for the synthesis of substituted 2-aminothiazoles
Guo, Shanshan,Zhao, Donghong,Zhu, Yue,Yu, Yongping,Chen, Wenteng,Zhang, Guolin
supporting information, p. 1758 - 1764 (2017/09/23)
Substituted 2-aminothiazoles have been synthesized from α-nitro-epoxides, cyanamide, and sodium sulfide through a facile, three-component, and ecofriendly protocol with good to excellent yields. This reaction was achieved at room temperature without any additives. A possible mechanism has also been proposed.
Preparation method of 4,5-disubstituted-2-substituted aminothiazole compound
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Paragraph 0056; 0057; 0058; 0059; 0060-0064; 0094-0098, (2016/10/10)
The invention discloses a preparation method of a 4,5-disubstituted-2-substituted aminothiazole compound. The preparation method comprises steps as follows: 1), nitro epoxy compounds and thiourea compounds react at the room temperature for 4-8 h in the pr