Dergiler / Turkish Journal of Chemistry / 2012 / Cilt: 36 - Sayı: 1

Synthesis of linezolid-like molecules and evaluation of their antimicrobial activities

Sayfa
37–53
Yayın Tarihi
2012-01-01
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The antimicrobial activity study revealed that all compounds showed good antitubercular activities.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:3-Fluoro-4-(morpholin-4-yl)aniline (2), prepared from 3,4-difluoronitrobenzene, was converted to the corresponding Schiff base (3) by treatment with indol-3-carbaldehyde.
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Temel Bulgular & Veri:The treatment of thiourea 4 and carbothioamide derivatives 9 with ethyl bromoacetate or 4-substituted phenacyl bromides generated the corresponding thiazolidinone (5 and 13) and thiazoline (6 and 12) derivatives, respectively.
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Sonuç & Katkı:The antimicrobial activity study revealed that all compounds showed good antitubercular activities.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:3-Thiazole · 4-thiadiazole · 4-triazole

Özet

3-Fluoro-4-(morpholin-4-yl)aniline (2), prepared from 3,4-difluoronitrobenzene, was converted to the corresponding Schiff base (3) by treatment with indol-3-carbaldehyde. The treatment of thiourea 4 and carbothioamide derivatives 9 with ethyl bromoacetate or 4-substituted phenacyl bromides generated the corresponding thiazolidinone (5 and 13) and thiazoline (6 and 12) derivatives, respectively. The acidic or basic treatment of carbothioamide 9 produced 1,3,4-thiadiazole (11) or 1,2,4-triazole (10) compounds, respectively. The structural assignments of the new compounds were based on elemental analysis and spectral (IR, 1H-NMR, 13C-NMR, and LC-MS) data. The antimicrobial activity study revealed that all compounds showed good antitubercular activities.

Abstract

3-Fluoro-4-(morpholin-4-yl)aniline (2), prepared from 3,4-difluoronitrobenzene, was converted to the corresponding Schiff base (3) by treatment with indol-3-carbaldehyde. The treatment of thiourea 4 and carbothioamide derivatives 9 with ethyl bromoacetate or 4-substituted phenacyl bromides generated the corresponding thiazolidinone (5 and 13) and thiazoline (6 and 12) derivatives, respectively. The acidic or basic treatment of carbothioamide 9 produced 1,3,4-thiadiazole (11) or 1,2,4-triazole (10) compounds, respectively. The structural assignments of the new compounds were based on elemental analysis and spectral (IR, 1H-NMR, 13C-NMR, and LC-MS) data. The antimicrobial activity study revealed that all compounds showed good antitubercular activities.

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Bu Makaleye Atıf Yap

BAŞOĞLU, S., YOLAL, M., DEMİRBA&#, A., BEKTAŞ, H. (2012). Synthesis of linezolid-like molecules and evaluation of their antimicrobial activities. Turkish Journal of Chemistry, Cilt: 36 - Sayı: 1, 37–53. https://ajindex.com/articles/185271

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