首页> 外文期刊>Research Journal of Chemical Sciences >Synthesis, Characterization, of 2H-3-Aryl-3, 4-Dihydro-1,3-Chlorobenzoxazine Derivatives of Benzoxazoline, antimicrobial activity and PC model Computational Studies
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Synthesis, Characterization, of 2H-3-Aryl-3, 4-Dihydro-1,3-Chlorobenzoxazine Derivatives of Benzoxazoline, antimicrobial activity and PC model Computational Studies

机译:苯并恶唑啉的2H-3-芳基-3,4-二氢-1,3-氯苯并恶嗪衍生物的合成,表征,抗菌活性和PC模型计算研究

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The invention comprises benzoxazole-2-carboxylic acid derivatives of the general formula wherein R represents a chlorine atom or an alkyl radical containing 1 to 4 carbon atoms, n is O or an integer of 1 to 4, and Y represents -OR1 or -NR112, wherein R1 represents an alkyl, aralkyl, cycloalkyl, aryl or chloroaryl radical and R11 represents a hydrogen atom or an alkyl, aralkyl or cycloalkyl radical, or -NR112 represents a heterocyclic ring. They may be prepared by causing a 3-chlorobenzoxazine-(1,4)-one-(2) of the general formula to react with ammonia, a strong basic primary or secondary amine, an alcohol, a phenol or a chlorophenol in the presence of an acid binding agent.; The reaction is expediently performed in an inert organic solvent or diluent at -30 DEG to + 200 DEG C. and when one of the reactants is an alcohol it can advantageously be used in excess as the diluent. Specified acid binding agents are the alkali metal and alkaline earth metal hydroxides, carbonates and bicarbonates, but in the case of the reaction with ammonia or an amine an excess thereof can be used instead of the binding agent.; The compounds of the invention may be isolated from the reaction mixture, which may contain the corresponding 3-substituted-benzoxazine-(1,4)-ones-(2) as by-products (see Specification 1,008,266), by, for example, fractional crystallization or preparative chromatography. ALSO:Herbicidal compositions comprise benzoxazole-2-carboxylic acid derivatives of the general formula wherein R represents a chloric atom or an alkyl radical containing 1 to 4 carbon atoms, n is 0 or an integer of 1 to 4, and 7 represents -OR1 or -NR112, where in R1 represents an alkyl, aralkyl, cycloalkyl, aryl or chloroaryl radical and R11 represents a hydrogen atom or an alkyl, aralkyl or cycloalkyl radical, or -NR112 represents a heterocyclic ring.; The compositions may be in the form of p emulsifiable concentrates, spray powders, pastes, soluble powders, dusts or granulates and contain 0.1 to 95% by weight of the active compounds.
机译:本发明包含通式的苯并恶唑-2-羧酸衍生物,其中R代表氯原子或含1-4个碳原子的烷基,n是O或1-4的整数,Y代表-OR1或-NR112 ,其中R 1代表烷基,芳烷基,环烷基,芳基或氯芳基,并且R 11代表氢原子或烷基,芳烷基或环烷基,或-NR 112代表杂环。它们可以通过使通式3-氯苯并恶嗪-(1,4)-一-(2)与氨,强碱性伯或仲胺,醇,酚或氯酚反应而制备。酸结合剂。该反应宜在惰性有机溶剂或稀释剂中于-30℃至+ 200℃下进行,当反应物之一是醇时,可有利地过量使用它作为稀释剂。特定的酸结合剂是碱金属和碱土金属的氢氧化物,碳酸盐和碳酸氢盐,但是在与氨或胺反应的情况下,可以使用过量的酸结合剂代替结合剂。可以例如通过以下方法从反应混合物中分离出本发明的化合物,所述反应混合物可以包含相应的3-取代的苯并恶嗪-(1,4)-一个-(2)作为副产物(参见说明书1,008,266)。分步结晶或制备色谱。 ALSO:除草组合物包含通式的苯并恶唑-2-羧酸衍生物,其中R代表氯原子或含有1-4个碳原子的烷基,n为0或1-4的整数,并且7代表-OR1或-NR112,其中R1代表烷基,芳烷基,环烷基,芳基或氯芳基,R11代表氢原子或烷基,芳烷基或环烷基,或-NR112代表杂环。组合物可以是可乳化的浓缩物,喷雾粉,糊剂,可溶性粉,粉剂或颗粒剂形式,并含有0.1-95重量%的活性化合物。

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