著者
石綺 孝義 鈴江 清吾 入倉 勉
出版者
公益社団法人 日本化学会
雑誌
日本化学会誌(化学と工業化学) (ISSN:03694577)
巻号頁・発行日
vol.1985, no.10, pp.2054-2056, 1985-10-10 (Released:2011-05-30)
参考文献数
11
被引用文献数
3

Reaction of 2, 3, 4, 5-tetrafluoro-1-nitrobenzene [4] with N-(ethoxycarbonyl)piperazine in aqueous ethanol gave 4-(4-ethoxycarbonyl-1-piperazinyl)-2, 3, 5-trifluoro-1-nitrobenzene [5] in 89% yield, which could be quantitatively converted into its 2-cyclopropylamino derivative [6]. Malonate [7] prepared from [6] and diethyl ethoxymethylenemalonate in 73% yield, was cyclized in the reaction with acetic anhydride and conc. sulfuric acid, accompanying elimination of the nitro group, to give [8] in 41% yield. Saponification of [8] gave quinolonecarboxylic acid [3] which possesses potent antibacterial activity both in vivo and in vitro, in 92% yield.

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J-STAGE Articles - フルオロキノロンカルボン酸の新規合成法 石綺 孝義, 鈴江 清吾, 入倉 勉 杏林製薬株式会社中央研究所 日本化学会誌(化学と工業化学) 1985 年 1985 巻 10 号 p. 2054-2056 https://t.co/S31o9T8GyU

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