Synthesis starting from 3-methyl-2-phenyl-5-(3-methyl-2-phenyl-3,4-dehydropiperidyl-6)pyridine. 2-phenyldinicotinic and 4-azafluorenone-2-carboxylic acids

N-Methyl (ethyl, benzoyl, trifluoroacetyl)-substituted 3-methyl-2-phenyl-5-(3′-methyl-2′-phenyl-3′,4′-dehydropiperidyl-6′) pyridines and di(N-oxide) of the correspondingly substituted α,ß-dipyridyl were prepared. A method for synthesizing 2-phenyldinicotinic acid was developed. Cyclodehydration of this acid gave 4-azafluorenone-2-carboxylic acid. Transformations of this acid were carried out with respect to two functional groups. © 1986 Plenum Publishing Corporation.

Publisher
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Number of issue
6
Language
English
Pages
642-646
Status
Published
Volume
22
Year
1986
Organizations
  • 1 P. Lumumba Peoples' Friendship University, Moscow, 117923, Russian Federation
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Other records

Prostakov N.S., Shalimov V.P., Kruglyak E.V., Montenegro Cordova G.B.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 22. 1986. P. 640-642
Belen'kii L.I., Cheskis M.A., Zvolinskii V.P., Obukhov A.E.
Chemistry of Heterocyclic Compounds. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Vol. 22. 1986. P. 654-663