立体中心
过程(计算)
芯(光纤)
过程开发
化学
衍生工具(金融)
分子
药物开发
天然产物
杂质
立体化学
立体选择性
组合化学
酶
化学合成
丙二酸
四级碳
反应条件
有机化学
全合成
下游加工
降级(电信)
作者
Yasuhiro Nagato,Yasutaka Baba,Muneo Shoji,Yuko Suzumura,Noriyuki Nakajima
标识
DOI:10.1021/acs.oprd.5c00166
摘要
The novel LpxC inhibitor T-1228 is a candidate drug molecule for multidrug-resistant Gram-negative bacterial infection. This report describes the synthesis of the malonamide derivative,(2S)-2-(4-iodo-N-methylbenzamido)-N1,2-dimethyl-N3-((tetrahydro-2H-pyran-2-yl)oxy)malonamide, containing the quaternary stereogenic core of the novel LpxC inhibitor T-1228 from commercially available diethyl 2-bromo-2-methylmalonate in 8 steps and 2 isolation. The quaternary stereogenic center of the malonamide core was created via enzymatic desymmetrization, by treating the malonic ester derivative, diethyl 2-(((benzyloxy)carbonyl)(methyl)amino)-2-methylmalonate, with porcine liver esterase. To control impurities that could negatively affect the quality of the drug substance, a novel approach for producing the final intermediate, (S)-2-(4-((4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)phenyl)ethynyl)-N-methylbenzamido)-N1-hydroxy-N3,2-dimethylmalonamide, was also developed, in which a selective deprotection reaction was incorporated. Using this newly developed process chemistry route, we have successfully synthesized 38.8 kg of the malonamide derivative and 13.5 kg of the final intermediate.
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