The preparation of 2H‐pyrido[4, 3‐e]‐1, 3‐oxazine‐2, 4(3H)‐dione (II) and the anisoyl, benzoyl, 4‐chlorobenzoyl, trans‐cinnamoyl, 3, 5‐dinitrobenzoyl, 2‐furoyl, and 2‐naphthoyl derivatives substituted at position 3 of II together with their infrared and ultraviolet spectra are described. The 3‐substituted 2 and 4‐(2‐pyridylethyl) and hydroxymethyl derivatives of quinolinimide and cinchomeronimide were also prepared and their spectra recorded.
No takes yet. Share an insight, caveat, or question.
Crum et al. (1966) studied this question.
Synapse has enriched 2 closely related papers on similar clinical questions. Consider them for comparative context: