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Process Development and GMP Production of a Potent NAE Inhibitor Pevonedistat
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-butoxycarb...
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Published in: | Organic process research & development 2015-09, Vol.19 (9), p.1299-1307 |
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container_title | Organic process research & development |
container_volume | 19 |
creator | Armitage, Ian Elliott, Eric L Hicks, Frederick Langston, Marianne McCarron, Ashley McCubbin, Quentin J O’Brien, Erin Stirling, Matt Zhu, Lei |
description | 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. |
doi_str_mv | 10.1021/acs.oprd.5b00209 |
format | article |
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title | Process Development and GMP Production of a Potent NAE Inhibitor Pevonedistat |
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