Development of a Scalable and Safer Synthesis of Diazeniumdiolates

Although diazeniumdiolates (DAZDs) and the synthetic methods to access DAZDs were discovered over 50 years ago, the current methodology is not safe, has a limited substrate scope, and is not amenable to large-scale production. For example, a recent investigation utilizing the standard methodology to...

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Veröffentlicht in:Organic process research & development 2020-09, Vol.24 (9), p.1602-1608
Hauptverfasser: Zhong, Yong-Li, Muzzio, Daniel J, Weisel, Mark, Zhang, Li, Humphrey, Guy R, Maloney, Kevin M, Campos, Kevin R
Format: Artikel
Sprache:eng
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Zusammenfassung:Although diazeniumdiolates (DAZDs) and the synthetic methods to access DAZDs were discovered over 50 years ago, the current methodology is not safe, has a limited substrate scope, and is not amenable to large-scale production. For example, a recent investigation utilizing the standard methodology to prepare DAZDs resulted in two unexpected explosions, highlighting the need for safer and more practical chemistry. Recently, we have reported a general, scalable, safer, and high-yielding methodology adaptable to large-scale synthesis of diazeniumdiolates in water using a calcium hydroxide base. Herein, we report the full account for the development of the reaction. The merit of this strategy is evidenced by the highly efficient and safer preparation of a key DAZD intermediate, on the kilogram scale, needed for the preparation of MK-8150 (1), a novel O2-alkylated diazeniumdiolate NO donor under investigation as a potent and significant blood-pressure-lowering drug candidate.
ISSN:1083-6160
1520-586X
DOI:10.1021/acs.oprd.0c00067