Synthesis of 7,2′-Dihydroxy-4′,5′-Dimethoxyisoflavanone, a Phytoestrogen with Derma Papilla Cell Proliferative Activity
Taewoo Kim,
Hyun Su Kim,
Jaebong Jang,
Dong-Jun Kim,
Jongkook Lee,
Dongjoo Lee,
Seok-Ho Kim
Affiliations
Taewoo Kim
College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, 120 Haeryong-ro, Pocheon-si, Gyeonggi-do 11160, Korea
Hyun Su Kim
College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, 120 Haeryong-ro, Pocheon-si, Gyeonggi-do 11160, Korea
Jaebong Jang
College of Pharmacy, Korea University, Sejong 30019, Korea
Dong-Jun Kim
College of Pharmacy and Institute of Pharmaceutical Sciences, CHA University, 120 Haeryong-ro, Pocheon-si, Gyeonggi-do 11160, Korea
Jongkook Lee
College of Pharmacy, Kangwon National University, Chuncheon, Gangwon-do 24341, Korea
Dongjoo Lee
College of Pharmacy and Research Institute of Pharmaceutical Science and Technology (RIPST), Ajou University, 206 Worldcup-ro, Yeongtong-gu, Suwon 16499, Korea
Seok-Ho Kim
College of Pharmacy, Kangwon National University, Chuncheon, Gangwon-do 24341, Korea
This paper reports a concise and scalable method for the synthesis of the phytoestrogen 7,2′-dihydroxy-4′,5′-dimethoxyisoflavanone 1 via an optimized synthetic route. Compound 1 was readily obtained in 11 steps and 11% overall yield on a gram scale from commercially available 3,4-dimethoxyphenol. The key features of the synthesis include the construction of the deoxybenzoin unit through a sequence of Claisen rearrangement, oxidative cleavage, and aryllithium addition and the efficient synthesis of the isoflavanone architecture from highly functionalized 2-hydroxyketone.