Synthesis of 5-Chloro-7-iodo-8-quinolinol Sulfate

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A potential anti­cancer agent: 5-chloro-7-iodo-8-hy­droxy­quinolinium dichlorido(5-chloro-7-iodo­quinolin-8-olato-κ2 N,O)palladium(II) dihydrate

The title Pd(II) coordination compound, (C(9)H(6)ClINO)[PdCl(2)(C(9)H(4)ClINO)]·2H(2)O, was prepared as a potential anti-cancer agent. Its structure is ionic and consists of a square-planar [PdCl(2)(CQ)](-) complex anion (CQ is 5-chloro-7-iodo-quinolin-8-olate), with the Pd(II) atom surrounded by two chloride ligands in a cis configuration and one N,O-bidentate CQ mol-ecule, a protonated anion ...

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5-Chloro-8-hydroxy­quinolinium nitrate

The 5-chloro-8-hydroxy-quinolinium cation in the the title ion pair, C(9)H(7)ClNO(+)·NO(3) (-), is approximately coplanar with the nitrate anion [dihedral angle = 16.1 (1)°]. Two ion pairs are hydrogen bonded (2 × O-H⋯O and 2 × N-H⋯O) about a center of inversion, generating an R(4) (4)(14) ring.

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Antifungal activity of 5-, 7-, and 5,7-substituted 2-methyl-8-quinolinols.

2-Methyl-8-quinolinol and sixteen 5-, 7-, and 5,7-substituted derivatives with fluoro, chloro, bromo, iodo, nitro, and amino substituents were tested for in vitro antifungal activity against five fungi, Aspergillus niger, A. oryzae, Trichoderma viride, Myrothecium verrucaria, and Trichophyton mentagrophytes. The 5,7-dichloro and 5,7-dibromo derivatives were the most fungitoxic of the compounds ...

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Spectrophotometric Determination of Tantalum(V) with 5-Iodo-8- -hydroxyquinoline-7-sulphonic Acid

Tantalum(V) reacts with 5-iodo-8-hydroxyquinoline-7-sulphonic acid to form a yellowish coloured complex having maximum absorbance at 405 nm in citric acid medium. The relatively slow reaction at room temperature is completed in 10 minutes at 40 °c. The colour is stable for at least 12 hr. Effects of heating temperature, time, pH, reagent concentration and other variables have been studied. The ...

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Design, synthesis and anti-HIV integrase evaluation of N-(5-chloro-8-hydroxy-2-styrylquinolin-7-yl)benzenesulfonamide derivatives.

Styrylquinoline derivatives are demonstrated to be HIV-1 integrase inhibitors. On the basis of our previous CoMFA analysis of a series of styrylquinoline derivatives, N-[(2-substituted-styryl)-5-chloro-8-hydroxyquinolin-7-yl]-benzenesulfonamide derivatives were designed and synthesized,and their possible HIV IN inhibitory activity was evaluated.

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ژورنال

عنوان ژورنال: Chemical and Pharmaceutical Bulletin

سال: 1973

ISSN: 0009-2363,1347-5223

DOI: 10.1248/cpb.21.911