14 research outputs found
Withdrawal Notice: Ionic Liquid Mediated Synthesis of Schiff bases Bearing Thiazole and Indole Moieties
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Synthesis, characterisation and biological evaluation of 1, 4 disubstituted 1, 2, 3 triazoles
Synthesis of novel antimicrobial 7-But-2-ynyl-1-(substituted-benzyl)-3-methyl-8-morpholin-4-yl-1H -purine-2,6-diones
In this study, we synthesized 7-But-2-ynyl-3-methyl-8-morpholin-4-yl-3,4,5,7-tetrahydro-purine-2,6-diones from 8-Bromo-7-but-2-ynyl-3-methyl-3,4,5,7-tetrahydro-purine-2,6-dione and morpholine using lithium hydroxide and DMSO as a medium. We further coupled 7-But-2-ynyl-3-methyl-8-morpholin-4-yl-3,4,5,7-tetrahydro-purine-2,6-dione with different halo compounds to obtain various derivatives. These synthesized compounds were then tested for their antimicrobial activities against S. aureus, B. subtilis, S. typhi, and E. coli
Synthesis of 3-methyl-4H-benzo[b][1,4]thiazine-2-carboxylates Using CAN as a Catalyst and Its Conversion Into Guanidines
Background:
1,4-benzothiazine carboxylates show wide application in the field of
medicinal chemistry. Therefore, we have designed convenient and efficient method for the synthesis
of 1,4-benzothiazine carboxylates.
Objective:
Synthesis of 1,4-benzothiazine carboxylates and its guanidines by simple and facile
method using efficient catalyst.
Methods:
Derivatives of 1,4-benzothiazine carboxylates were synthesized by cyclocondensing β-
keto esters with 2-aminobenzenethiols using CAN as a catalyst at room temperature. 1,4-benzothiazine
carboxylate, condensed with guanidine hydrochloride in the presence of sodium methoxide
in DMF to obtained new 3-substituted-l-4H-benzo[b][1,4]thiazine-2-carboxyguanidines (88-91%).
Results:
All the products were obtained with good to excellent yields within 40 min. Here, CAN
oxidizes aminothiophenol into disulfide and then nucleophilic attack of enolic form of β-ketoesters
on the disulphide and 1, 4-benzothiazine acetates, were obtained with good yields.
Conclusion:
We have designed convenient and efficient method for the synthesis of 1,4-benzothiazine
carboxylates. Most remarkable features of this cyclocondensation such as use of efficient catalyst
and non-volatile solvent under mild reaction condition to obtain excellent yield.
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