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1.
Pharmazie ; 53(11): 748-51, 1998 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-9853356

RESUMEN

The pyrazolo[3,4-b]pyridine derivatives 3 could be prepared by condensing compounds 1 with the 3-aminopyrazolone derivative 2. The pyrazolo[5,2-b]-1,3-oxazine derivative 11 and polyfunctionally substituted 1,4-dihydropyridines 15, 18 were also synthesized. Some of the obtained compounds were tested for their antimicrobial activity.


Asunto(s)
Antiinfecciosos/síntesis química , Pirazoles/síntesis química , Antibacterianos , Antiinfecciosos/farmacología , Bacterias/efectos de los fármacos , Recuento de Colonia Microbiana , Hongos/efectos de los fármacos , Pirazoles/farmacología
2.
Pol J Pharmacol Pharm ; 38(1): 99-106, 1986.
Artículo en Inglés | MEDLINE | ID: mdl-3763489

RESUMEN

2-Hydroxyquinoline-4-hydrazide was condensed with some aromatic aldehydes and acetophenones to give the hydrazones 1a-h. It was also reacted with HCOOH, PhCOCl and p-CH3O-PhCOCl to afford 2a-c. Cyclization of 2b was completed by using PPA, POCl3 and/or P2S5, which gave compounds 3, 4, and 6 respectively. Reaction of 4 with some amines gave the corresponding derivatives 5a-f. The thiosemicarbazide 7 was cyclized under acid and basic condition to give the thiadiazolyl-8 and triazolyl-10 derivatives.


Asunto(s)
Antibacterianos/síntesis química , Quinolinas/síntesis química , Antifúngicos/síntesis química , Bacterias/efectos de los fármacos , Fenómenos Químicos , Química , Quinolinas/farmacología
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