157834-12-3Relevant academic research and scientific papers
Recyclable Heterogeneous Palladium-Catalyzed Cyclocarbonylation of 2-Iodoanilines with Acyl Chlorides in the Biomass-Derived Solvent 2-Methyltetrahydrofuran
Hao, Wenyan,Xu, Zhaotao,Zhou, Zebiao,Cai, Mingzhong
, p. 8522 - 8532 (2020)
A highly efficient, green palladium-catalyzed cyclocarbonylation of 2-iodoanilines with acyl chlorides has been developed that proceeds smoothly in a biomass-derived solvent 2-methyltetrahydrofuran with N,N-diisopropylethylamine as base at 100 °C under 20 bar of carbon monoxide using an 2-aminoethylamino-modified MCM-41-anchored palladium acetate complex [2N-MCM-41-Pd(OAc)2] as a heterogeneous catalyst, yielding a wide variety of 2-substituted 4H-3,1-benzoxazin-4-one derivatives in good to excellent yields. This supported palladium catalyst could be facilely obtained by a two-step procedure from easily available starting materials and readily recovered via a simple filtration process and recycled at least 8 times without any apparent decrease in catalytic efficiency. The developed methodology not only avoids the use of toxic solvents such as tetrahydrofuran and dimethylformamide but also solves the basic problem of expensive palladium catalyst recovery and reuse and prevents effectively palladium contamination of the desired product.
A simple synthesis of 2-substituted-4H-3,1-benzoxazin-4-ones by palladium-catalyzed cyclocarbonylation of o-iodoanilines with acid chlorides
Larksarp, Chitchamai,Alper, Howard
, p. 1619 - 1622 (2008/02/10)
(matrix presented). One-pot reaction of o-iodoanilines with acid chlorides and carbon monoxide, in the presence of a palladium catalyst and diisopropylethylamine, regioselectively affords 2-substituted-4H-3,1-benzoxazin-4-ones in good to excellent yields. The reaction is believed to proceed via in situ amide formation from an o-iodoaniline and an acid chloride, followed by oxidative addition to Pd(0), CO insertion, and intramolecular cyclization to form the 2-substituted-4H-3,1-benzoxazin-4-one derivatives.
Synthesis and anticonvulsant activity of some new 3-(p-sulfamoylphenyl)-4(3H)-quinazolinones
El-Naser Ossman,El-Sayed Barakat
, p. 915 - 919 (2007/10/02)
In view of their expected anticonvulsant property, a series of 3-(p-sulfamoylphenyl)-4(3H)-quinazolinone derivatives (V) were synthesized by condensation of sulfanilamide with various 4H-3,1-benzoxazin-4-ones (III). Some 2-amido-N-(p-sulfamoylphenyl) benz
