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. 2023 Apr;27(2):667-678.
doi: 10.1007/s11030-022-10446-0. Epub 2022 May 19.

Efficient regioselective five-component synthesis of novel thiazolo[3,2-a]pyridine carbohydrazides and oxazolo[3,2-a]pyridine carbohydrazides

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Efficient regioselective five-component synthesis of novel thiazolo[3,2-a]pyridine carbohydrazides and oxazolo[3,2-a]pyridine carbohydrazides

Hadiseh Rouzban et al. Mol Divers. 2023 Apr.

Abstract

Two new categories of fused pyridines include 2H-thiazolo[3,2-a]pyridine-6-carbohydrazides and 2H-oxazolo[3,2-a]pyridine-6-carbohydrazides have been successfully synthesized via five-component cascade reactions using 9-fluorenone, cyanoacetohydrazide, 1,1-bis(methylthio)-2-nitroethene, aromatic aldehydes and cysteamine hydrochloride or ethanol amine as starting materials. This new approach involves a subsequence of key steps: N,S-acetal or N,O-acetal formation, Knoevenagel condensation, Michael addition, tautomerization and N-cyclization. It also has some advantages, such as convenience of operation, tolerance of a wide diversity of functional groups, use of green solvent and ease of purification by washing the crude products with ethanol.

Keywords: Cyanoacetohydrazide; Nitroketene acetal; One-pot reaction; Oxazolopyridine; Thiazolopyridine.

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References

    1. El-Hag Ali G, Khalil AK, Lamphon RQ, El-Maghraby AA (2005) Studies of thiazolopyridines, Part 6: Synthesis and antimicrobial evaluation of some novel thiazolo[3,2-a]pyridine and thiazolo[2′,3′:6,1]-pyrido[2,3-d]pyrimidine derivatives. Phosphor Sulfur Silicon Relat Elem 180:1909–1919 - DOI
    1. El-Maghraby AA, El-Hag Ali G, Ahmed AHA, El-Gaby MSA (2002) Studies on thiazolopyridines. Part 1: antimicrobial activity of some novel fluorinated thiazolo[3,2-a]pyridines and thiazolo[2′,3′:1,6]pyrido[2,3-d]pyrimidines. Phosphor Sulfur Silicon Relat Elem 177:293–302 - DOI
    1. Terzidis MAJ, Stephanatou S, Tsoleridis CA, Terzis A, Raptopoulou CP (2010) Expeditious one-pot synthesis of highly substituted thiazolo[3,2-a]pyridines involving chromones. Tetrahedron 66:947–954 - DOI
    1. Vadivelan S, Sinha BN, Irudayam SJ, Jagarlapudi SA (2007) Virtual screening studies to design potent CDK2-cyclin A inhibitors. J Chem Inf Model 47:1526–1533 - DOI - PubMed
    1. Manhi FM, Soliman GA (1993) Studies with 2-thiazoline-4-one derivatives as potential uterus stimulants. Bull Fac Pharm 31:265–271

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