Synthesis of 2-Hydroxy-3-nitro/amino-5-methyl-α-substituted Thiocarbamidoacetophenones

被引：0

作者：

Aswale, S. R. ^{[1
]}

Aswale, S. S. ^{[1
]}

Gawhale, N. D. ^{[2
]}

Kodape, M. M. ^{[3
]}

机构：

[1] Lokmanya Tilak Mahavidyalaya, Dept Chem, Wani 442304, India

[2] BP Sci Coll, Dept Chem, Digras 445203, India

[3] St Gadge Baba Amravati Univ, Dept Chem, Amravati 444602, India

来源：

ASIAN JOURNAL OF CHEMISTRY | 2012年 / 24卷 / 12期

关键词：

2-Hydroxy-3-nitro/amino-5-methyl-alpha-bromoacetophenone; Thioureas; Acetone-ethanol medium; MYCOBACTERIUM-TUBERCULOSIS COMPLEX; ACETOPHENONES; DERIVATIVES; INHIBITION;

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The interactions of 2-hydroxy-3-nitro/amino-5-methyl-alpha-bromoacetophenone (1) with various thioureas (5a-f) in 1:1 molar proportion in acetone-ethanol medium on water bath for 6 h in round bottom flask to synthesis new series of 2-hydroxy-3-nitro/amino-5-methyl-alpha-substituted thiocarbamidoacetophenones (6a-f). The synthesized compounds in these reaction conditions have been characterized on the basis of conventional elemental analysis, chemical characteristic and IR, NMR spectral data.

引用

页码：5800 / 5802

页数：3

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