Synthesis of 4H-1,3-benzoxazin-4-ones from 2,2-diazidobenzofuran-3(2H)-ones

被引:1
作者
Prajapati, Ramanand [1 ]
Kumar, Amrendra [1 ]
Kandhikonda, Rajendar [1 ]
Kant, Ruchir [2 ]
Tadigoppula, Narender [1 ]
机构
[1] CSIR Cent Drug Res Inst, Med & Proc Chem Div, Lucknow 226031, Uttar Pradesh, India
[2] CSIR Cent Drug Res Inst, Mol & Struct Biol Div, Lucknow 226031, Uttar Pradesh, India
关键词
4H-1,3-benzoxazin-4-ones; m-CPBA; N-Formylamine solvent as reactant; DNA-PK; PI3K INHIBITION; DOMINO REACTION;
D O I
10.1016/j.tet.2018.12.001
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Benzoxazine derivatives are useful building blocks and display various biological activities. We seren-dipitously discovered and subsequently developed a new one pot method for the synthesis of 2(dimethyl amino)/2-morpholino/2- (piperidin-1-yl)-4H-benzo[e][1,3]oxazin-4-ones from corresponding substituted 2,2-diazidobenzofuran 3(2H) - ones and N-formyl dimethyl amine (DMF)/N-formylmorpholine/N-formylpiperidine using m-CPBA at 100 degrees C in moderate to good yields. We also demonstrated the utility of 4H-benzoxazines for the synthesis of other medicinally important compounds such as 2-hydroxyphenyl substituted 1,2,4-triazoles, unsymmetrical 1,3,5-triazines, and 1,2,4-oxadiazoles. (C) 2018 Elsevier Ltd. All rights reserved.
引用
收藏
页码:374 / 380
页数:7
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