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取代3-氨基嘧啶及其噻吩磺酰脲衍生物的合成和除草活性

Synthesis of Substituted 2 Aminopyrimidines and Their Derivatives of 2 Thiophenesulfonylureas
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摘要 采用克莱森缩合反应合成了6个β-二羰基化合物(Ⅰ),Ⅰ与胍的缩合环化反应等合成了7个取代2-氨基嘧啶(Ⅱ),Ⅱ与2-噻吩磺酰异氰酸酯反应合成了5个含不同取代嘧啶环的2-噻吩磺酰脲(Ⅲ),Ⅱ和Ⅲ中有8个为首次合成,其结构经IR,1HNMR,元素分析等测试确证,并初步测定了部分化合物的除草活性。 Using Claisen condensation six β dicarbonyl compounds have been synthesized. The compounds reacted with guanidine carbonate to give seven various subatituted 2 aminopyrimidines. Five N′ (substitutedpyrimidin 2 ly) 2 thiophenesulfonylureas are synthesized by nucleophilic addition of 2 aminopyrimidines with 2 thiophenesulfonyl isocyanate. Among them eight were unreported. The structures of substituted 2 aminopyrimidines and their 2 thiophenesulfonylurea derivatives have been confirmed by IR, 1H NMR and elemental analysis,and their herbicidal activities have been tested.
出处 《合成化学》 CAS CSCD 1998年第4期413-417,共5页 Chinese Journal of Synthetic Chemistry
基金 湖北省自然科学基金
关键词 氨基嘧啶 噻吩磺酰脲 衍生物 除草剂 β Dicarbonyl compounds, 2 Aminopyrimidine, 2 Thiophenesulfonylurea, Synthesis, Herbicidal activity.
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