Enamine rearrangement of pyridinium salts part XII rearrangement of 2-alkylpyrimidines to 2-aminopyridines

H.A., Etman; A.A., Fadda

H.A., Etman; A.A., Fadda.

Alexandria Journal of Pharmaceutical Sciences. 1994; 8 (3): 187-191

in English | IMEMR | ID: emr-31638

ABSTRACT

ABSTRACT

In alcoholic methylamine solution, 2-alkylpyrimidines underwent rearrangement to 2-methylaminopyridines. Similarly, in alkaline medium, even a nonquaternized 2-methyl-5-nitropyrimidine formed 2-amino-5-nitropyridine

Subject(s)

Chemistry; Pharmacokinetics

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Index: IMEMR (Eastern Mediterranean) Main subject: Pharmacokinetics / Chemistry Language: English Journal: Alex. J. Pharm. Sci. Year: 1994

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Index: IMEMR (Eastern Mediterranean) Main subject: Pharmacokinetics / Chemistry Language: English Journal: Alex. J. Pharm. Sci. Year: 1994