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盐酸索他洛尔的合成 被引量:2

Synthesis of Sotalol Hydrochloride
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摘要 以苯胺为原料,经过甲磺酰化、傅克酰基化、异丙胺化和氢化还原得到盐酸索他洛尔产品(Ⅰ),总收率达到75.9%(以苯胺计),化学纯度达到99.8%,最终产物结构通过IR、1HNMR、ESI-MS及元素分析进行表征。该文对甲磺酰化工序的缚酸剂进行研究,确定碳酸氢钠最佳摩尔比为n(碳酸氢钠)∶n(苯胺)=1.1∶1,反应温度为室温,收率为97%;对氢化还原反应的钯炭含量、用量和回收套用进行研究,确定7%钯炭最佳用量为中间体IV投料质量的5%,回收钯炭套用最佳次数为3次。该法合成步骤简便,工艺绿色环保,经济适用,非常适合于产业化大生产。 Sotalol hydrochloride( Ⅰ) was prepared from aniline by methylsulfonylation,Friedel –Crafts acylation,isopropylamination and hydrogen reduction. The total yield was up to 75. 9%( based on aniline),and the purity was 99. 8%. The structure of the product was confirmed by IR,~1HNMR,ESI-MS and elemental analysis. The deacid-reagents in the methylsulfonylation were studied and found that the optimal reaction condition was n( sodium bicarbonate) ∶ n( aniline) = 1. 1 ∶ 1 at ambient temperature with the yield of 97%; The content,amount and recovery of Pd / C in the hydrogen reduction were studied,The optimal weight of 7% Pd / C was 5% of intermediate IV,The optimal reuse number of 7% Pd / C was 3 times. This method is simple,green,economical and suitable for industrial production.
出处 《精细化工》 EI CAS CSCD 北大核心 2016年第1期74-77,共4页 Fine Chemicals
关键词 抗心律失常 Β受体阻断剂 盐酸索他洛尔 医药原料 anti-arhythmia β receptors antagonist sotalol drug materials
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