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dc.contributor.authorAhlqvist, Grace P.
dc.contributor.authorMcGeough, Catherine P.
dc.contributor.authorSenanayake, Chris
dc.contributor.authorArmstrong, Joseph D.
dc.contributor.authorYadaw, Ajay
dc.contributor.authorRoy, Sarabindu
dc.contributor.authorAhmad, Saeed
dc.contributor.authorSnead, David R.
dc.contributor.authorJamison, Timothy F
dc.date.accessioned2021-06-02T20:45:43Z
dc.date.available2021-06-02T20:45:43Z
dc.date.issued2021-04
dc.date.submitted2021-02
dc.identifier.issn2470-1343
dc.identifier.issn2470-1343
dc.identifier.urihttps://hdl.handle.net/1721.1/130900
dc.description.abstractMolnupiravir (MK-4482, EIDD-2801) is a promising orally bioavailable drug candidate for the treatment of COVID-19. Herein, we describe a supply-centered and chromatography-free synthesis of molnupiravir from cytidine, consisting of two steps: a selective enzymatic acylation followed by transamination to yield the final drug product. Both steps have been successfully performed on a decagram scale: the first step at 200 g and the second step at 80 g. Overall, molnupiravir has been obtained in a 41% overall isolated yield compared to a maximum 17% isolated yield in the patented route. This route provides many advantages to the initial route described in the patent literature and would decrease the cost of this pharmaceutical should it prove safe and efficacious in ongoing clinical trials.en_US
dc.description.sponsorshipNational Science Foundation (Grant 1745302)en_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/acsomega.1c00772en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceACSen_US
dc.titleProgress Toward a Large-Scale Synthesis of Molnupiravir (MK-4482, EIDD-2801) from Cytidineen_US
dc.typeArticleen_US
dc.identifier.citationAhlqvist, Grace P. et al. "Progress Toward a Large-Scale Synthesis of Molnupiravir (MK-4482, EIDD-2801) from Cytidine." ACS Omega 6, 15 (April 2021): 10396–10402. © 2021 The Authorsen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalACS Omegaen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2021-06-02T16:25:15Z
dspace.orderedauthorsAhlqvist, GP; McGeough, CP; Senanayake, C; Armstrong, JD; Yadaw, A; Roy, S; Ahmad, S; Snead, DR; Jamison, TFen_US
dspace.date.submission2021-06-02T16:25:16Z
mit.journal.volume6en_US
mit.journal.issue15en_US
mit.licensePUBLISHER_CC
mit.metadata.statusComplete


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