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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >ALKYLATION OF 4,5-DICHLOROPYRIDAZIN-6-ONE WITH ALPHA,OMEGA-DIBROMOALKANES 4,5-DICHLORO-1-(OMEGA-BROMOALKYL)PYRIDAZIN-5-ONES
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ALKYLATION OF 4,5-DICHLOROPYRIDAZIN-6-ONE WITH ALPHA,OMEGA-DIBROMOALKANES 4,5-DICHLORO-1-(OMEGA-BROMOALKYL)PYRIDAZIN-5-ONES

机译:4,5-二氯吡嗪-6-与α,ω-二溴代烷基的烷基化4,5-二氯-1-(ω-溴代烷基)吡嗪-5的烷基化

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摘要

Alkylations of 4,5-dichloropyridazin-6-one (1) with dibromoalkanes 2 or 3 in the presence of potassium carbonate or tetrabutylammonium bromide/potassium hydroxide were investigated under restricted condition. Reactions of 1 with 2 or 3, except for 2b and 3b, in the presence of potassium carbonate or tetrabutylammonium bromide/potassium hydroxide gave only the N-alkylation products 3 and/or 4. Alkylation of 1 with 2b or 3b in the presence of potassium carbonate yielded the N-alkylation products 3b and/or 4b and the O-alkylation product 5 as the main product, whereas treatment of 1 with 2b or 3b in the presence of tetrabutylammonium bromide/potassium hydroxide afforded selectively the N-alkylation products 3b and/or 4b. [References: 10]
机译:在限制条件下,研究了碳酸钾或溴化四丁基铵/氢氧化钾存在下4,5-二氯哒嗪-6-(1)与二溴代烷烃2或3的烷基化。在碳酸钾或四丁基溴化铵/氢氧化钾的存在下,1与2或3的反应(除2b和3b以外)仅产生N-烷基化产物3和/或4。碳酸钾产生N-烷基化产物3b和/或4b,O-烷基化产物5作为主要产物,而在溴化四丁铵/氢氧化钾存在下用2b或3b处理1选择性地得到N-烷基化产物3b。和/或4b。 [参考:10]

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