区域选择性
化学
对映选择合成
产量(工程)
组合化学
生物化学
催化作用
材料科学
冶金
作者
Ian M. Armitage,Eric L. Elliott,Frederick A. Hicks,Marianne Langston,Ashley McCarron,Quentin J. McCubbin,Erin M. O’Brien,Matt Stirling,Lei Zhu
标识
DOI:10.1021/acs.oprd.5b00209
摘要
A practical synthesis of a novel NEDD8-activating enzyme (NAE) inhibitor pevonedistat (MLN4924) is described. Key steps include an enantioselective synthesis of an amino-diol cyclopentane intermediate containing three chiral centers and a novel, regioselective sulfamoylation using N-(tert-butoxycarbonyl)-N-[(triethylenediammonium)sulfonyl]azanide. The linear process, involving six solid isolations, has been carried out in multiple cGMP productions on 15–30 kg scale to produce pevonedistat in 98% (a/a) chemical purity and 25% overall yield.
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