4-Methyltetrahydropyran as a Convenient Alternative Solvent for Olefin Metathesis Reaction: Model Studies and Medicinal Chemistry Applications
Author(s) -
Tomasz Nienałtowski,
Paweł Krzesiński,
Marcel E. Baumert,
Aleksandra Skoczeń,
Ewa Suska-Kauf,
Jolanta Pawłowska,
Anna Kajetanowicz,
Karol Grela
Publication year - 2020
Publication title -
acs sustainable chemistry and engineering
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.878
H-Index - 109
ISSN - 2168-0485
DOI - 10.1021/acssuschemeng.0c06668
Subject(s) - chemistry , context (archaeology) , olefin metathesis , combinatorial chemistry , metathesis , salt metathesis reaction , organic chemistry , catalysis , derivative (finance) , solvent , polymerization , polymer , paleontology , financial economics , economics , biology
A number of metathesis reactions were successfully conducted in 4-methyltetrahydropyran, including both standard model dienes, as well as more complex substrates, such as analogues of biologically active compounds and active pharmaceutical ingredients. To place this solvent in a context of pharmaceutical R + D, larger-scale syntheses of SUAM 1221, a prolyl endopeptidase inhibitor with potential application in Alzheimer disease treatment, and a derivative of sildenafil, an analogue of the popular Viagra drug, were executed. In the latter case, despite all the setup being made in air, the metathesis reaction at a 33 g scale proceeded very well with relatively low catalyst loading and without need of aqueous workup or column chromatography.
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