Studies on Synthesis of N-1 Fused Heterocyclic Derivatives Using Potassium Carbonate and PEG- 400 as Green Catalyst

Anjali M. Wanegaonkar, M. Bhitre
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Abstract

Due to their synthetic utility and extensive variety of pharmacological effects, indole and benzimidazole, as well as their substituted derivatives, help to draw interest. The N-substituted fused heterocyclic compounds are usually physiologically active and could be employed as antitumor medicines. The various reactions reported that reactions of K2CO3 showing its essentiality for a particular reaction due to its characteristics like solubility in water, mild base character, easy availability, eco-friendly, and nontoxic in nature. In the presence and absence of phase transfer catalyst such as PEG-400 and TEBAC, the effect of the ratio of catalyst used anhydrous K2CO3 for its N-1 alkylation or arylation of indole-3-carboxaldehyde and 2-acetylbenzimidazole is observed. The ratio 1:4 of anhydrous K2CO3 along with PEG-400 gives, ease of catalyst handling, mild reaction conditions and reactions carried out at 10-15oC temperature with excellent yields. The simplicity of the approach makes it attractive for the synthesis of N-fused heterocyclic derivatives that could be employed as biological substitutes.
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碳酸钾和PEG- 400绿色催化剂合成N-1熔融杂环衍生物的研究
由于它们的合成用途和广泛的药理作用,吲哚和苯并咪唑以及它们的取代衍生物有助于引起人们的兴趣。n取代的融合杂环化合物通常具有生理活性,可作为抗肿瘤药物。各种反应报道,由于K2CO3在水中的溶解性、温和的碱性、易获得性、生态友好性和无毒性等特点,K2CO3在特定反应中表现出其重要性。在PEG-400和TEBAC等相转移催化剂存在和不存在的情况下,考察了无水K2CO3催化剂用量对吲哚-3-甲醛和2-乙酰苯并咪唑N-1烷基化或芳化反应的影响。无水K2CO3与PEG-400的比例为1:4,催化剂处理方便,反应条件温和,反应温度为10-15℃,产率高。该方法的简单性使其对可作为生物替代品的n -融合杂环衍生物的合成具有吸引力。
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