A solvent-free and catalyst-free reaction of o-aminobenzophenone with aryl isothiocyanates: expedient access to congested 4-phenyl-4-hydroxyquinazolin-2-thione derivatives.

IF 2.9 3区 化学 Q1 CHEMISTRY, ORGANIC
Le Anh Nguyen, Thi Thu Tram Nguyen, Quoc Anh Ngo, Pascal Retailleau, Thanh Binh Nguyen
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引用次数: 0

Abstract

An efficient method to construct 4-phenyl-4-hydroxyquinazolin-2-thiones 3via solvent-free and catalyst-free addition of o-aminobenzophenone 1 with aryl isothiocyanates 2 under thermal conditions has been developed, providing new congested 4-phenyl-4-hydroxyquinazolin-2-thiones 3 in practically quantitative yields via simple purification by filtration/recrystallization. Extension of these conditions to o-aminoacetophenone 4 in place of o-aminobenzophenone 1 led to 4-methylenequinazoline-thione 5 as a result of a subsequent dehydration reaction.

邻氨基二苯甲酮与芳基异硫氰酸酯的无溶剂、无催化剂反应:快速获得拥挤的 4-苯基-4-羟基喹唑啉-2-硫酮衍生物。
通过邻氨基二苯甲酮 1 与芳基异硫氰酸酯 2 在热条件下的无溶剂、无催化剂加成反应,开发出了一种构建 4-苯基-4-羟基喹唑啉-2-硫酮 3 的有效方法,通过过滤/重结晶的简单纯化,可提供新的 4-苯基-4-羟基喹唑啉-2-硫酮 3,产量几乎为定量。将这些条件扩展到邻氨基苯乙酮 4 以代替邻氨基苯甲酮 1,在随后的脱水反应中得到了 4-亚甲基喹唑啉硫酮 5。
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来源期刊
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry 化学-有机化学
CiteScore
5.50
自引率
9.40%
发文量
1056
审稿时长
1.3 months
期刊介绍: The international home of synthetic, physical and biomolecular organic chemistry.
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