Synthesis of a Unique Isoindoline/Tetrahydroisoquinoline-based Tricyclic Sultam Library Utilizing a Heck-aza-Michael Strategy

The synthesis of a unique isoindoline- and tetrahydroisoquinoline (THIQ)-containing tricyclic sultam library, utilizing a Heck-aza-Michael (HaM) strategy is reported. Both isoindoline and THIQ rings are installed through a Heck reaction on a vinylsulfonamide, followed by one-pot deprotection and int...

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Veröffentlicht in:ACS combinatorial science 2012-03, Vol.14 (3), p.211-217
Hauptverfasser: Zang, Qin, Javed, Salim, Porubsky, Patrick, Ullah, Farman, Neuenswander, Benjamin, Lushington, Gerald H, Basha, Fatima Z, Organ, Michael G, Hanson, Paul R
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Sprache:eng
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Zusammenfassung:The synthesis of a unique isoindoline- and tetrahydroisoquinoline (THIQ)-containing tricyclic sultam library, utilizing a Heck-aza-Michael (HaM) strategy is reported. Both isoindoline and THIQ rings are installed through a Heck reaction on a vinylsulfonamide, followed by one-pot deprotection and intramolecular aza-Michael reaction. Subsequent cyclization with either paraformaldehyde condensation or 1,1′-carbonyldiimidazole coupling generates a variety of tricyclic sultams. Overall, a 160-member library of these sultams, together with their isoindolines/THIQ and secondary sulfonamides precursors, were constructed using this strategy.
ISSN:2156-8952
2156-8944
DOI:10.1021/co200181x