Beilstein Journal of Organic Chemistry p. 1897 - 1903 (2016)
Update date:2022-08-05
Topics:
Kunishima, Munetaka
Kato, Daiki
Kimura, Nobu
Kitamura, Masanori
Yamada, Kohei
Hioki, Kazuhito
This study describes the synthesis of triazine-based dehydrocondensing reagents substituted by amido substituents and demonstrates their efficiency for dehydrocondensing reactions in MeOH and THF. N-Phenylbenzamido-substituted chlorotriazine is readily converted to a stable, non-hygroscopic triazinylammonium-based dehydrocondensing reagent that is superior to 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride (DMT-MM) in terms of its reactivity in dehydrocondensing reactions.
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