[Synthesis and antibacterial activity of thiosemicarbazones of 3-acylquinolones].

Ceskoslovenska farmacie Pub Date : 1991-11-01
S Rádl, M Bartonová, L Kovárová
{"title":"[Synthesis and antibacterial activity of thiosemicarbazones of 3-acylquinolones].","authors":"S Rádl,&nbsp;M Bartonová,&nbsp;L Kovárová","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Oxidation of 3-acetyl derivatives of 3-acetyl-1-ethyl-1,4-dihydro-6,7-methylenedioxyquinoline-4-one (VIc) and 3-acetyl-7-chloro-1-ethyl-6-fluoro-1,4-dihydroquinoline-4-one (VId) with selenium dioxide provided the corresponding acids, [1-ethyl-1,4-dihydro-6,7-methylenedioxy-4-oxoquinoline-3-yl]glyoxylic acid (VIe) and [7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-yl]glyoxylic acid (VIf), respectively. Reactions of compounds VIc--VIf with thiosemicarbazide yielded the respective thiosemicarbazones of 3-acetyl-1-ethyl-1,4-dihydro-6,7-methylenedioxyquinoline-4-one (VIIa), 3-acetyl-7-chloro-1-ethyl-6-fluoro-1,4-dihydroquinoline-4-one (VIIb), [1-ethyl-1,4-dihydro-6,7-methylenedioxy-4-oxoquinoline-3-yl]glyoxylic acids (VIId). The compounds showed no significant in vitro antibacterial activity.</p>","PeriodicalId":9871,"journal":{"name":"Ceskoslovenska farmacie","volume":"40 4-5","pages":"145-7"},"PeriodicalIF":0.0000,"publicationDate":"1991-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Ceskoslovenska farmacie","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Oxidation of 3-acetyl derivatives of 3-acetyl-1-ethyl-1,4-dihydro-6,7-methylenedioxyquinoline-4-one (VIc) and 3-acetyl-7-chloro-1-ethyl-6-fluoro-1,4-dihydroquinoline-4-one (VId) with selenium dioxide provided the corresponding acids, [1-ethyl-1,4-dihydro-6,7-methylenedioxy-4-oxoquinoline-3-yl]glyoxylic acid (VIe) and [7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxoquinoline-3-yl]glyoxylic acid (VIf), respectively. Reactions of compounds VIc--VIf with thiosemicarbazide yielded the respective thiosemicarbazones of 3-acetyl-1-ethyl-1,4-dihydro-6,7-methylenedioxyquinoline-4-one (VIIa), 3-acetyl-7-chloro-1-ethyl-6-fluoro-1,4-dihydroquinoline-4-one (VIIb), [1-ethyl-1,4-dihydro-6,7-methylenedioxy-4-oxoquinoline-3-yl]glyoxylic acids (VIId). The compounds showed no significant in vitro antibacterial activity.

[3-酰基喹诺酮类硫代氨基脲的合成及抗菌活性研究]。
用二氧化硒氧化3-乙酰基-1-乙基-1,4-二氢-6,7-亚甲基二氧喹啉-4-酮(VIc)和3-乙酰基-7-氯-1-乙基-6-氟-1,4-二氢喹啉-4-酮(VId)的3-乙酰基衍生物,分别得到相应的酸,[1-乙基-1,4-二氢-6,7-亚甲基二氧基-4-氧喹啉-3-基]乙醛酸(VIe)和[7-氯-1-乙基-6-氟-1,4-二氢-4-氧喹啉-3-基]乙醛酸(VIf)。化合物VIc—VIf与硫代氨基脲反应,分别生成3-乙酰基-1-乙基-1,4-二氢-6,7-亚甲二氧喹啉-4-酮(VIIa)、3-乙酰基-7-氯-1-乙基-6-氟-1,4-二氢喹啉-4-酮(VIIb)、[1-乙基-1,4-二氢-6,7-亚甲二氧基-4-氧喹啉-3-基]乙醛酸(VIId)的硫代氨基氨基脲。这些化合物没有明显的体外抗菌活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信