An efficient synthetic route has been described for the alkylation of 1$H$-indole, 1$H$-benzimidazole, and 1$H$-benzotriazole. This approach features the alkylation of heteroaromatics through in situ generated enones from ketonic Mannich bases under metal-free conditions. A series of alkylated heteroaromatics have been synthesized via the K10 catalyzed alkylation reactions of these heteroaromatics with a variety of ketonic Mannich bases. Environmentally benign K10 catalyst, water-mediated mild reaction conditions, and the efficient synthesis of alkylated products are the advantages of this alkylation method.
Mannich base, alkylation reaction of 1$H$-indole 1$H$-benzimidazole and 1$H$-benzotriazole, K10, environmentally friendly synthesis
SEYİTDANLIOĞLU, PINAR; HANASHALHALSHAHABY, ESSAM HAMIED AHMED; and ÜNALEROĞLU, CANAN
"An efficient water-mediated synthetic route for the alkylation of heteroarenes,"
Turkish Journal of Chemistry: Vol. 42:
6, Article 11.
Available at: https://journals.tubitak.gov.tr/chem/vol42/iss6/11