Department of chemistry, Indian Institute of Technology Madras , Chennai 600036, Tamil Nadu, India.
Org Lett. 2017 Apr 7;19(7):1670-1673. doi: 10.1021/acs.orglett.7b00462. Epub 2017 Mar 23.
An efficient protocol is described for the synthesis of 2-acylbenzo[b]thiophenes from easily accessible 2-iodochalcones through α-C-H functionalization using Cu(OAc) catalyst and xanthate as sulfur source. Less reactive 2-bromochalcones also yielded the corresponding 2-acylbenzothiophenes in good yield. The reaction proceeds via in situ incorporation of sulfur followed by copper-catalyzed cyclization to generate 2-acylbenzothiophenes without external acyl source. The synthetic importance is showcased by synthesis of 1-(5-hydroxybenzothiophene-2-yl)ethanone, which is a known pre-mRNA splicing modulator.
本文描述了一种从易得的 2-碘查耳酮通过α-C-H 官能化反应,使用 Cu(OAc)催化剂和黄原酸盐作为硫源合成 2-酰基苯并[b]噻吩的有效方法。反应活性较低的 2-溴查耳酮也以良好的收率得到了相应的 2-酰基苯并[b]噻吩。该反应通过原位引入硫,然后进行铜催化环化,生成 2-酰基苯并[b]噻吩,无需外部酰基源。通过合成已知的 pre-mRNA 剪接调节剂 1-(5-羟基苯并[b]噻吩-2-基)乙酮,展示了该合成方法的重要性。