Synthesis of 4-(N-pyridyl carboxamido)-5-mercapto-3-substituted-1.2.4-triazoles for possible antitubercular activity

R.H. Udupi, A.R. Bhat

Research output: Contribution to journalArticle

26 Citations (Scopus)

Abstract

Potassium β acyl dithio-carbazinates (4a-r) were obtained by condensation of acid hydrazides (3a-r) with carbon disulphide in ethanolic potassium hydroxide. On heating (4a-r) and isonicotinic acid hydrazide (INH) 4-(N-pyridy carboxamide)-5-mercapto-3-substituted-1,2,4-triazoles (5a-r) were obtained. These compounds were screened for antimicrobial activity.
Original languageUndefined/Unknown
Pages (from-to)41-44
Number of pages4
JournalIndian Journal of Heterocyclic Chemistry
Volume6
Issue number1
Publication statusPublished - 1996

Cite this

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title = "Synthesis of 4-(N-pyridyl carboxamido)-5-mercapto-3-substituted-1.2.4-triazoles for possible antitubercular activity",
abstract = "Potassium β acyl dithio-carbazinates (4a-r) were obtained by condensation of acid hydrazides (3a-r) with carbon disulphide in ethanolic potassium hydroxide. On heating (4a-r) and isonicotinic acid hydrazide (INH) 4-(N-pyridy carboxamide)-5-mercapto-3-substituted-1,2,4-triazoles (5a-r) were obtained. These compounds were screened for antimicrobial activity.",
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Synthesis of 4-(N-pyridyl carboxamido)-5-mercapto-3-substituted-1.2.4-triazoles for possible antitubercular activity. / Udupi, R.H.; Bhat, A.R.

In: Indian Journal of Heterocyclic Chemistry, Vol. 6, No. 1, 1996, p. 41-44.

Research output: Contribution to journalArticle

TY - JOUR

T1 - Synthesis of 4-(N-pyridyl carboxamido)-5-mercapto-3-substituted-1.2.4-triazoles for possible antitubercular activity

AU - Udupi, R.H.

AU - Bhat, A.R.

N1 - cited By 23

PY - 1996

Y1 - 1996

N2 - Potassium β acyl dithio-carbazinates (4a-r) were obtained by condensation of acid hydrazides (3a-r) with carbon disulphide in ethanolic potassium hydroxide. On heating (4a-r) and isonicotinic acid hydrazide (INH) 4-(N-pyridy carboxamide)-5-mercapto-3-substituted-1,2,4-triazoles (5a-r) were obtained. These compounds were screened for antimicrobial activity.

AB - Potassium β acyl dithio-carbazinates (4a-r) were obtained by condensation of acid hydrazides (3a-r) with carbon disulphide in ethanolic potassium hydroxide. On heating (4a-r) and isonicotinic acid hydrazide (INH) 4-(N-pyridy carboxamide)-5-mercapto-3-substituted-1,2,4-triazoles (5a-r) were obtained. These compounds were screened for antimicrobial activity.

M3 - Article

VL - 6

SP - 41

EP - 44

JO - Indian Journal of Heterocyclic Chemistry

JF - Indian Journal of Heterocyclic Chemistry

SN - 0971-1627

IS - 1

ER -