Synthesis of 3-bromo-4-isobutyloxyphenyl carbothioamide
Authors
Qinqin Wang, Yuping Guo, Min Wang, WuFu Zhu, Shan Xu
Corresponding Author
Qinqin Wang
Available Online December 2015.
- DOI
- 10.2991/mmeceb-15.2016.157How to use a DOI?
- Keywords
- 3-bromo-4-isobutyloxyphenyl carbothioamide, Synthesis
- Abstract
3-bromo-4-isobutyloxyphenyl carbothioamide 1 is an important intermediate in many biologically active compounds such as febuxostat. In this work, a rapid synthetic method for compound 1 was established. The compound 1 was synthesized from the commercially available 4-hydroxybenzonitrile 2 through three steps including bromination, oxyalkylation and thioamidation. The structure was confirmed by MS and 1HNMR. Furthermore, the synthetic method was optimized. The total yield of the three steps was 49.2%.
- Copyright
- © 2016, the Authors. Published by Atlantis Press.
- Open Access
- This is an open access article distributed under the CC BY-NC license (http://creativecommons.org/licenses/by-nc/4.0/).
Cite this article
TY - CONF AU - Qinqin Wang AU - Yuping Guo AU - Min Wang AU - WuFu Zhu AU - Shan Xu PY - 2015/12 DA - 2015/12 TI - Synthesis of 3-bromo-4-isobutyloxyphenyl carbothioamide BT - Proceedings of the 2015 2nd International Conference on Machinery, Materials Engineering, Chemical Engineering and Biotechnology PB - Atlantis Press SP - 794 EP - 797 SN - 2352-5401 UR - https://doi.org/10.2991/mmeceb-15.2016.157 DO - 10.2991/mmeceb-15.2016.157 ID - Wang2015/12 ER -