93075-39-9Relevant academic research and scientific papers
Single step synthesis of 4H-1,4-benzothiazines
Gupta,Kalwania,Kumar
, p. 2343 - 2344 (1984)
Single step synthesis of substituted 4H-1,4-benzothiazines is reported by the condensation and oxidative cyclization of substituted 2-aminobenzenethiol with β-dicarbonyl compounds in DMSO. The structures of the synthesized compounds have been confirmed by their elemental analyses and spectral studies.
Novel synthesis of 1,4-benzothiazines in water accelerated by β-cyclodextrin
Londhe, Balaji S.,Padwal, Sudhakar L.,Bhosale, Manisha R.,Mane, Ramrao A.
, p. 443 - 447 (2016/01/27)
Novel one-pot synthetic protocol has been developed for obtaining 2, 3-disubstituted 1,4-benzothiazines with excellent yields, carrying cyclocondensation of 1,3-dicarbonyl compounds with substituted 2-(2-(2-aminophenyl)disulfanyl)benzenamines, under supra
Facile synthesis of bioactive 4H-[1,4]-benzothiazines under solvent free conditions
Kalwania,Chomal,Choudhary, Savita
, p. 5133 - 5136 (2012/06/18)
An efficient method for synthesis of 4H-[1,4]-benzothiazines under solvent free conditions has been developed. The oxidative condensation of 2-aminobenzenethiols with β-diketones/β-ketoesters in presence of catalytic amount of hydrazine hydrate yields the 4H-[1,4]-benzothiazines. The reaction is accelerated by microwave irradiation under solvent free conditions in presence of an energy transfer agent DMF to get the product in high yield. The 2-aminobenzenethiazole required for the synthesis of 4H-[1,4]-benzothiazines are also obtained by a new method instead of presently used time consuming and low yielding method. The structure of the synthesized compounds has been characterized by IR, NMR, mass spectral studies and elemental analysis.
Baker's yeast catalyzed synthesis of 1,4-benzothiazines, performed under ultrasonication
Pratap, Umesh R.,Jawale, Dhanaji V.,Londhe, Balaji S.,Mane, Ramrao A.
experimental part, p. 94 - 97 (2011/07/07)
An efficient and simple one pot method has been developed for the synthesis of 1,4-benzothiazines by allowing the condensation of 2-aminobenzenethiols and 1,3-dicarbonyls using cheaper biocatalyst, baker's yeast. The role of ultrasonication in the rate expediting of the condensation has been discussed.
Synthesis of a series of 2,3-disubstituted 4H-1,4-benzothiazines and X-ray crystal structure of ethyl 7-chloro-3-methyl-4H-1,4-benzothiazine-2-carboxylate
Dandia, Anshu,Sarawgi, Pritima,Hursthouse, Michael B.,Bingham, Ann L.,Light, Mark E.,Drake, John E.,Ratnani, Raju
, p. 445 - 448 (2007/10/03)
The reaction between 2-aminobenzenethiol and ethyl acetoacetate is studied under a variety of conditions, and a procedure for the exclusive synthesis of 1,4-benzothiazines by the neat reaction of substituted aminothiols with β-ketoesters and β-dicarbonyl compounds in 85-96% yield is described. With microwave heating, even when both the reactants are solid, yields are high, reaction times brief, and work-up easy. A facile reaction is also observed even in a solid-state reaction. The molecular structure of ethyl 7-chloro-3-methyl-4H-1,4-benzothiazine-2-carboxylate (4d) was determined by single-crystal X-ray diffraction.
