144219-82-9Relevant articles and documents
Convenient one-pot synthesis of N-substituted 3-trifluoroacetyl pyrroles
Zanatta, Nilo,Wouters, Ana D.,Fantinel, Leonardo,Da Silva, Fabio M.,Barichello, Rosemário,Da Silva, Pedro E. A.,Ramos, Daniela F.,Bonacorso, Helio G.,Martins, Marcos A. P.
experimental part, p. 755 - 758 (2009/07/18)
A new one-pot strategy for the synthesis of a series of new N-substituted 3-trifluoroacetyl pyrroles is presented. These compounds were obtained by the reaction of 3-trifluoroacetyl-4,5-dihydrofuran with primary amines, which generated 1,1,1-trifluoro-3-(2-hydroxyethyl)-4-alkylaminobut-3-en-2-one intermediates. In most cases these intermediates were not stable enough to be isolated. Thus, in the same reaction vessel they were directly submitted to oxidation with PCC (Corey's reagent) to furnish 1,1,1-trifluoro-3-(2-ethanal)-4- alkylaminobut-3-en-2-ones, which under reflux underwent intramolecular cyclization to give the desired N-substituted 3-trifluoroacetyl pyrroles, in moderate yields. All of these pyrroles were tested against pan-susceptible Mycobacterium tuberculosis H37Rv and clinical isolates INH- and RMP-resistant strain and some of these compounds showed significant in vitro antimicrobial activity. Georg Thieme Verlag Stuttgart.
A FACILE AND CONVENIENT SYNTHETIC METHOD FOR 3-TRIFLUOROACETYLPYRROLES
Okada, Etsuji,Masuda, Ryoichi,Hojo, Masaru,Yoshida, Reiko
, p. 1435 - 1441 (2007/10/02)
3-Trifluoroacetylpyrroles are easily obtained in excellent yields by oxygen-nitrogen exchange reaction of β-trifluoroacetylvinyl ethers with 2,2-dimethoxyethylamine and subsequent cyclodehydration of the products.
