Relevant bibliographies by topics / 1H-Imidazo[4

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Academic literature on the topic '1H-Imidazo[4'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "1H-Imidazo[4"

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Sunitha, Ch, and G. Brahmeshwari. "Design and Synthesis of some novel 3-benzylidene-1H-benzo [4,5]imidazo[2,1-c] [1,4]oxazine-1,4(3H)-dione derivatives and evaluation of their biological activity." Research Journal of Chemistry and Environment 25, no. 11 (2021): 157–69. http://dx.doi.org/10.25303/2511rjce157169.

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A novel series of 3-arylbenzylidene-1H-benzo[4,5] imidazo[2,1-c][1,4]oxazine-1,4(3H)-dione (4a-l) was synthesized in moderate to good yields. The structures of the newly synthesized compounds were confirmed by 1H NMR, 13C NMR mass spectrometry and elemental analysis. The synthesized compounds were evaluated for their anti-bacterial and anti-oxidant activities. Among all the derivatives tested, the compound 3-(3,5- dimethoxy benzylidene)-1H-benzo [4,5]imidazo[2,1- c][1,4]oxazine-1,4-(3H)-dione showed more potent activity and 3-(4-methoxybenzylidene)-1H benzo[4,5] imidazo[2,1-c][1,4]oxazine-1,4(
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Balewski, Łukasz, Franciszek Sączewski, Patrick J. Bednarski, et al. "Synthesis, Structure and Cytotoxicity Testing of Novel 7-(4,5-Dihydro-1H-imidazol-2-yl)-2-aryl-6,7-dihydro-2H-imidazo[2,1-c][1,2,4]triazol-3(5H)-Imine Derivatives." Molecules 25, no. 24 (2020): 5924. http://dx.doi.org/10.3390/molecules25245924.

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The appropriate 1-arylhydrazinecarbonitriles 1a–c are subjected to the reaction with 2-chloro-4,5-dihydro-1H-imidazole (2), yielding 7-(4,5-dihydro-1H-imidazol-2-yl)-2-aryl-6,7-dihydro-2H-imidazo[2,1-c][1,2,4]triazol-3(5H)-imines 3a–c, which are subsequently converted into the corresponding amides 4a–e, 8a–c, sulfonamides 5a–n, 9, ureas 6a–I, and thioureas 7a–d. The structures of the newly prepared derivatives 3a–c, 4a–e, 5a–n, 6a–i, 7a–d, 8a–c, and 9 are confirmed by IR, NMR spectroscopic data, as well as single-crystal X-ray analyses of 5e and 8c. The in vitro cytotoxic potency of these comp
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Zhou, Qifan, Fangyu Du, Yajie Shi, Ting Fang, and Guoliang Chen. "Synthesis and Analysis of 1-Methyl-4-Phenyl-1H-Imidazol-2-Amine." Journal of Chemical Research 42, no. 12 (2018): 608–10. http://dx.doi.org/10.3184/174751918x15414286606248.

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A practical synthetic route to an important pharmaceutical intermediate 1-methyl-4-phenyl-1H-imidazol-2-amine, via a three-step sequence involving cyclisation, hydrolysis and methylation, is reported. In the process of optimisation, a novel chemical entity was isolated and confirmed to be 2,6-diphenyl-1H-imidazo[1,2-a]imidazole by MS, 1H NMR and 13C NMR. The scale-up experiment was carried out to provide 1-methyl-4-phenyl-1H-imidazol-2-amine in 27.4% total yield.
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Shamanth, Sadashivamurthy, Kempegowda Mantelingu, Haruvegowda Kiran Kumar, Hemmige S. Yathirajan, Sabine Foro, and Christopher Glidewell. "Crystal structures of three 6-aryl-2-(4-chlorobenzyl)-5-[(1H-indol-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazoles." Acta Crystallographica Section E Crystallographic Communications 76, no. 1 (2020): 18–24. http://dx.doi.org/10.1107/s2056989019016050.

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Three title compounds, namely, 2-(4-chlorobenzyl)-5-[(1H-indol-3-yl)methyl]-6-phenylimidazo[2,1-b][1,3,4]thiadiazole, C26H19ClN4S, (I), 2-(4-chlorobenzyl)-6-(4-fluorophenyl)-5-[(1H-indol-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole, C26H18ClFN4S, (II), and 6-(4-bromophenyl)-2-(4-chlorobenzyl)-5-[(1H-indol-3-yl)methyl]imidazo[2,1-b][1,3,4]thiadiazole, C26H18BrClN4S, (III), have been prepared using a reductive condensation of indole with the corresponding 6-aryl-2-(4-chlorobenzyl)imidazo[2,1-b][1,3,4]thiadiazole-5-carbaldehydes (aryl = phenyl, 4-fluorophenyl or 4-bromophenyl), and their crystal
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Das, Minati, Mongoli Brahma, Sophy A. Shimray, Francis A. S. Chipem, and G. Krishnamoorthy. "Nanoparticle and surfactant controlled switching between proton transfer and charge transfer reaction coordinates." Physical Chemistry Chemical Physics 24, no. 8 (2022): 4944–56. http://dx.doi.org/10.1039/d1cp02165f.

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6

Sonawane, Vikas D., Raghunath B. Bhosale, Gajanan S. Rashinkar, and Kailas D. Kailas D. "GREEN SYNTHESIS AND BIOLOGICAL SCREENING OF IMIDAZO [2,1-B] THIAZOLE PYRIMIDINES AS POTENT ANTI-BACTERIAL AGENTS." YMER Digital 21, no. 07 (2022): 280–95. http://dx.doi.org/10.37896/ymer21.07/21.

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A series of Imidazo[2,1-b]thiazole pyrmidine derivatives (3a-g-) were designed, synthesized from imidazo[2,1-b]thiazole chalcone derivatives. (2a-g) and Urea in PEG-400 and evaluated for their anti-bacterial potency. Characterization of newly synthesized compounds was done using IR and 1H NMR and Mass spectroscopy. Further Imidazo [2,1-b]thiazole pyrimidine derivatives were subjected to check their anti-bacterial activities against four different strains, viz two Gram +ve bacteria Staphylococcus aureus & Bacillus subtilis and two Gram -ve bacteria Escherichia coli & Pseudomonas aerugin
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Loh, Wan-Sin, Hoong-Kun Fun, Reshma Kayarmar, S. Viveka, and G. K. Nagaraja. "4-Hydrazinyl-1-isobutyl-1H-imidazo[4,5-c]quinoline." Acta Crystallographica Section E Structure Reports Online 67, no. 2 (2011): o406. http://dx.doi.org/10.1107/s1600536811001553.

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Fun, Hoong-Kun, Wan-Sin Loh, Dinesha, Reshma Kayarmar, and G. K. Nagaraja. "1-Isobutyl-4-methoxy-1H-imidazo[4,5-c]quinoline." Acta Crystallographica Section E Structure Reports Online 67, no. 9 (2011): o2331. http://dx.doi.org/10.1107/s1600536811031801.

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Ma, Ling, Liping Lu, and Miaoli Zhu. "2-(4-Methylphenyl)-1H-imidazo[4,5-f][1,10]phenanthroline." Acta Crystallographica Section E Structure Reports Online 67, no. 4 (2011): o864—o865. http://dx.doi.org/10.1107/s1600536811008853.

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10

Glushkov, R. G., N. K. Davydova, and N. B. Marchenko. "Synthesis of 4-methyl-1H-imidazo[4,5-c]quinoline." Chemistry of Heterocyclic Compounds 25, no. 2 (1989): 189–90. http://dx.doi.org/10.1007/bf00479915.

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Book chapters on the topic "1H-Imidazo[4"

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Deshmukh, M. B., S. R. Yankanchi, S. M. Deshmukh, and Bhagawan Patil. "SYNTHESIS AND BIOLOGICAL INVESTIGATIONS OF NEWLY SYNTHESIZED SUBSTITUTED IMIDAZOLE [2, 1-C] [1, 2, 4] TRIAZOLE DERIVATIVES FROM IMIDACLOPRID." In Futuristic Trends in Chemical Material Sciences & Nano Technology Volume 3 Book 1. Iterative International Publishers, Selfypage Developers Pvt Ltd, 2024. http://dx.doi.org/10.58532/v3bdcs1ch7.

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New molecules with promising insecticidal properties like imidazo[2,1-c][124] triazole analogs were synthesized, starting with imidacloprid and bio-assayed. The structures of synthesized molecules were confirmed with diverse modern methods like FT-IR, 1H NMR, 13C NMR, and Mass spectrometry. The synthesized molecules are screened to investigate their insecticidal and anti-bacterial activity. The bioassay screening showed that synthesized compounds chloro (3-(4-chlorophenyl)-7-[(6-chloropyridin-3-yl)methyl]-2,5,6,7-tetrahydro-3H-imidazo [2,1-c] [1,2,4] triazole (4b), the 3-(2-chlorophenyl)-7-[(6
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Conference papers on the topic "1H-Imidazo[4"

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Hosmane, Ramachandra, та Huan-Ming Chen. "Synthesis of 1-(2'-Deoxy-γ-D-ribofuranosyl)-1H-imidazo[4,5-d]pyridazine-4,7(5 H,6H)-dion: a Potentially Beneficial Building Block for Antisense Applications". У The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01926.

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Hosmane, Ramachandra, та Huan-Ming Chen. "Synthesis of 1-(2'-O-Methyl-γ -D-Ribofuranosyl)-1H-imidazo[4,5-d]pyridazine-4,7(5H,6H)-dion: an Attractive Building Block for Antisense and Triple-helical Applications". У The 4th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2000. http://dx.doi.org/10.3390/ecsoc-4-01925.

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Journal articles
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