Mc. Hosur et al., SYNTHESIS AND ANTIMICROBIAL ACTIVITY OF BRIDGEHEAD NITROGEN-HETEROCYCLES - REACTIONS OF 3-N-METHYL IPERIDINO-4-AMINO-5-MERCAPTO-4(H)-1,2,4-TRIAZOLES/, Indian journal of chemistry. Sect. B: organic chemistry, including medical chemistry, 34(8), 1995, pp. 707-712
The reactions of piperidino-4-amino-5-mercapto-4(H)-1,2,4-triazoles (1
a-f) with various aliphatic/aromatic acids (2a-f-10a-f), cyanogen brom
ide (11a-f), carbon disulphide (12a-f), alpha-haloketones (13a-f-14a-f
), benzoin (15a-f), dimedone (16a-f), chloroacetic acid (17a-f), hydra
zine hydrate (18a-f) and methyl iodide (19a-f) are described. The char
acterisation of products has been done on the basis of elemental analy
sis, IR, NMR and mass spectral data. All the newly synthesised compoun
ds have been screened for antimicrobial activity against bacteria S. a
ureus, E. coli and fungi C. albicans, A. averanthus. Results of antimi
crobial screening have shown that compounds having 3-N-methyl/ethyl/(a
lpha-methyl)ethylpiperidino moiety at position-3 of 1,2,4-triazole nuc
leus exhibit significant antifugal activity against both the fungal st
rains.