2017
DOI: 10.4236/oalib.1103526
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The Uses of 2-Amino-4-Phenylthiazole in the Synthesis of Coumarin, Pyran, Pyridine and Thiazole Derivatives with Antitumor Activities

Abstract: The thiazole derivative 3 was used for a series of heterocyclization reaction to produce pyran, pyridine and thiazole derivatives. The cytotoxicity of the newly synthesized compounds was studied against the six cancer cell lines namely NUGC, HR, DLD1, HA22T, HEPG2, MCF, HONE1 and normal fibroblast cells (WI38). The results showed that most of the synthesized compounds were of high potency. Among the tested compounds, 2-Amino-4-(4-chlorophenyl)-6-(4-phenylthiazol-2-yl)-4H-pyran-3,5-dicarbonitrile 17b showed the… Show more

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Cited by 4 publications
(3 citation statements)
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“…Condensation of 13 with three types of substituted benzaldehydes (namely, benzaldehyde 4-chlorobenzaldehyde or 4-methoxybenzaldehyde) produced the corresponding benzylidene derivatives 14 . In addition, when compound 13 reacted with salicylaldehyde, it gave the coumarin derivative 15 ( Scheme 3 ) [ 31 ].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…Condensation of 13 with three types of substituted benzaldehydes (namely, benzaldehyde 4-chlorobenzaldehyde or 4-methoxybenzaldehyde) produced the corresponding benzylidene derivatives 14 . In addition, when compound 13 reacted with salicylaldehyde, it gave the coumarin derivative 15 ( Scheme 3 ) [ 31 ].…”
Section: Resultsmentioning
confidence: 99%
“…Furthermore, the multi-component reaction of 13 with substituted benzaldehydes and thiourea produced the pyrimidine scaffolds 20 . 2-Amino-4-(4-chlorophenyl)-6-(4-phenylthiazol-2-yl)-4 H -pyran-3,5-dicarbonitrile ( 17 , X = Cl) indicated the maximum cytotoxicity among the synthesized compounds towards six cancer cell lines [ 31 ].…”
Section: Resultsmentioning
confidence: 99%
“…Also, they prepared N-phenylthiourea, N-cyanoacetyl, arylidene, aryl hydrazone, and pyrimidine derivatives, but were exhibited moderate activity (Fig. 10) [75].…”
Section: Modification Of 2-amine To 2-alkylaminomentioning
confidence: 99%