Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile

A pyrimidinethione derivative namely, 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile, was readily synthesized and reacted with carbon electrophiles in an attempt to synthesize selected fused heterocycles. The reactivity of 6-(1,3-diphenyl-1H-pyrazol-4-yl)...

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Main Authors: Ramadan Sayed K., El-Helw Eman A. E., Sallam Hanan A.
Format: Article
Language:English
Published: De Gruyter 2019-11-01
Series:Heterocyclic Communications
Subjects:
Online Access:https://doi.org/10.1515/hc-2019-0008
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spelling doaj-f8238899570b4533934653ddcff9e8182021-09-06T19:19:48ZengDe GruyterHeterocyclic Communications2191-01972019-11-0125110711510.1515/hc-2019-0008Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrileRamadan Sayed K.0El-Helw Eman A. E.1Sallam Hanan A.2Chemistry Department, Faculty of Science, Ain Shams University, Abassia, Cairo 11566, EgyptChemistry Department, Faculty of Science, Ain Shams University, Abassia, Cairo 11566, EgyptChemistry Department, Faculty of Science, Ain Shams University, Abassia, Cairo 11566, EgyptA pyrimidinethione derivative namely, 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile, was readily synthesized and reacted with carbon electrophiles in an attempt to synthesize selected fused heterocycles. The reactivity of 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile was investigated towards selected nitrogen nucleophiles. Thiation and hydrolysis reactions of the tetrahydropyrimidine derivative were investigated. Antitumor and antimicrobial activity evaluation of some of the synthesized products exhibited promising results.https://doi.org/10.1515/hc-2019-0008antitumor and antimicrobial activitycarbon electrophilestetrahydropyrimidinethiationthiazolopyrimidine
collection DOAJ
language English
format Article
sources DOAJ
author Ramadan Sayed K.
El-Helw Eman A. E.
Sallam Hanan A.
spellingShingle Ramadan Sayed K.
El-Helw Eman A. E.
Sallam Hanan A.
Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile
Heterocyclic Communications
antitumor and antimicrobial activity
carbon electrophiles
tetrahydropyrimidine
thiation
thiazolopyrimidine
author_facet Ramadan Sayed K.
El-Helw Eman A. E.
Sallam Hanan A.
author_sort Ramadan Sayed K.
title Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile
title_short Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile
title_full Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile
title_fullStr Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile
title_full_unstemmed Cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile
title_sort cytotoxic and antimicrobial activities of some novel heterocycles employing 6-(1,3-diphenyl-1h-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile
publisher De Gruyter
series Heterocyclic Communications
issn 2191-0197
publishDate 2019-11-01
description A pyrimidinethione derivative namely, 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile, was readily synthesized and reacted with carbon electrophiles in an attempt to synthesize selected fused heterocycles. The reactivity of 6-(1,3-diphenyl-1H-pyrazol-4-yl)-4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidine-5-carbonitrile was investigated towards selected nitrogen nucleophiles. Thiation and hydrolysis reactions of the tetrahydropyrimidine derivative were investigated. Antitumor and antimicrobial activity evaluation of some of the synthesized products exhibited promising results.
topic antitumor and antimicrobial activity
carbon electrophiles
tetrahydropyrimidine
thiation
thiazolopyrimidine
url https://doi.org/10.1515/hc-2019-0008
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