作者
Takeo Sasaki,Kenzo Yahata,Minetaka Isomura,Isao Ōhashi,Takashi Fukuyama,Yusuke Miyashita,Yuzo Watanabe,Norio Murai,Masaaki Matsuda,Atsushi Kamada,Yosuke Kaburagi,Kazunobu Kira,Kentaro Iso,Yuki Sato,Fumiyoshi Matsuura,Yasunobu Matsumoto,Hiroshi Azuma,Daisuke Iida,Tasuku Ishida,W. Itano,Seiji Nagao,Masashi Seki,Akihiko Yamamoto,Yuji Yamamoto,Naoto Yoneda,Masayuki Matsukura,Osamu Asano,Akio Kayano,Katsuya Tagami,Takashi Owa,Yoshito Kishi
摘要
Process development of E7130 Drug Substance, which is a novel anticancer drug candidate, is described. To accomplish rapid delivery of such a large and structurally complex drug substance for first-in-human (FIH) clinical trial, close collaboration among medicinal chemistry, process chemistry, and academia teams was required. The successful establishment of a suitable synthetic route in a concise time frame while negotiating challenging chemical reactions (e.g., asymmetric catalytic Nozaki–Hiyama–Kishi (NHK) reaction and Zr/Ni-mediated ketone coupling reaction) is described herein. Experience with the development of eribulin mesylate was helpful in anticipating and overcoming the chemical and logistical challenges encountered in the E7130 project. Based on this background, more than 10 g of E7130 Drug Substance has been successfully manufactured under Good Manufacturing Practice (GMP) controls within 1.5 years after the medicinal chemistry team succeeded in the first total synthesis.