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Note | Regular issue | Vol 78, No. 12, 2009, pp.3065-3072
Published online, 17th September, 2009
DOI: 10.3987/COM-09-11806
Heteroarylamination and Heteroarylsulfidation of 2-Chloro-1-azaazulenes

Eiko Yoshioka, Kazuya Koizumi, Shinya Yamazaki, Hiroyuki Fujii, and Noritaka Abe*

*Graduate School of Medicine, Yamaguchi University, 1677-1 Yoshida, Yamaguchi 753-8512, Japan


Heteroarylamination and heteroarylsulfidation of 2-chloro-1-azaazulenes (1) were investigated. Palladium catalyzed coupling of 2-amino-1-azaazulenes (2) with 1 underwent to give bis(1-azaazulen-2-yl)amine derivatives in good yields, but the reaction of 2-mercapto-1-azaazulenes (4) with 1 did not give good results in the same conditions. The reaction of 4 with 1 under basic conditions gave bis(1-azaazulen-2-yl) sulfide derivatives in good yields. Heteroarylamino-substitution was proceeded on the reaction of 4-amino-3-mercapto-4H-1,2,4-triazoles (6) with 1 in BuOH under reflux, whereas heteroarylsulfido-substitution was proceeded on the reaction of 6 with 1 in the presence of NaH in dioxane.