首页> 外文期刊>Synthetic Communications >Reaction of 2-oxoindoin-3-ylidene derivatives with heterocyclic enamines.A convenient one-pot synthesis of pyrimido [5,4:5',6']pyrido[2,3-b]-indole-2,4-dione and spiro indolin-2-one-3,5'-pyrido [2,3-d]pyrimidines
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Reaction of 2-oxoindoin-3-ylidene derivatives with heterocyclic enamines.A convenient one-pot synthesis of pyrimido [5,4:5',6']pyrido[2,3-b]-indole-2,4-dione and spiro indolin-2-one-3,5'-pyrido [2,3-d]pyrimidines

机译:2-氧代吲哚-3-吡咯衍生物与杂环烯胺的反应。一锅法合成嘧啶基[5,4:5',6']吡啶[2,3-b]-吲哚-2,4-二酮和螺吲哚-2-2-一-3,5'-吡啶并[2,3-d]嘧啶

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摘要

The reaction of 6-aminouracils 2a,b with 2-oxoindolin-3-ylideneacetophenones 1a-h afforeded Pyrimido[5,4:5',6'] pyrido-[2,3-b]indole-2,4-dones 3 a-k via a regiospecific Michael addition,followed bycyclization.Alternatively,the reaction of 2a with 2-oxoindolin-3-ylidenemalononitriles 6a,b gave rise to regiospecific formation fospiro indolin-2-one-3,5'-pyrido[2,3]d]pyrimidines 7a,b.
机译:6-氨基尿嘧啶2a,b与2-氧代吲哚-3-基亚苯乙酮1a-h的嘧啶基[5,4:5',6']吡啶-[2,3-b]吲哚-2,4-dones反应ak通过区域特异性迈克尔加成反应,然后环化。或者,2a与2-氧代吲哚-3-基亚吡喃二腈6a,b的反应引起区域特异性形成螺螺吲哚-2--2--3,5'-吡啶基[2,3] d]嘧啶7a,b。

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