Enamine rearrangement of pyrimidinium salts Part XI: Novel synthesis of some pyrazolo and triazolopyrimidine derivatives
Alexandria Journal of Pharmaceutical Sciences. 1994; 8 (2): 150-3
en Inglés
| IMEMR
| ID: emr-31608
ABSTRACT
The pyrazolo [1,5-a] pyrimidine derivatives IV and VI underwent pyrimidine ring opening, then recyclized when heated with aqueous alcoholic alkali solution to give the corresponding pyrazolo [3,4-b] pyridine V and VII, respectively. In a similar manner, the triazolo [4,3-a] pyrimidine VIII underwent recyclization to the corresponding triazolo [1,5-a] pyrimidine IX
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Índice:
IMEMR (Mediterraneo Oriental)
Asunto principal:
Pirimidinas
Idioma:
Inglés
Revista:
Alex. J. Pharm. Sci.
Año:
1994
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