戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 248464作成日:2026年10月26日

7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid → 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(phenoxymethyl)-1-piperazinyl]-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/248464

反応式

関与物質

役割名称HCID仕込み量
反応物7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 483169—
反応物3-PhenoxymethylpiperazineHCID 19763604—
溶媒PyridineHCID 1049—
生成物1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(phenoxymethyl)-1-piperazinyl]-3-quinolinecarboxylic acidHCID 1483935546.9%

反応条件

温度130 °C

反応手順

A mixture of 2 g of 3-phenoxymethylpiperazine and 701 mg of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid in 10 ml of pyridine was heated under argon in a pressure bottle at 130° C. for 18 hours. The solvents were removed and the residue chromatographed on silica gel, eluting with chloroform:methanol (9:1). The appropriate fractions were combined, evaporated, triturated with methanol and ether, then dried, giving 519 mg of the desired compound, mp 198°-200° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05210193
出典データセットuspto-grants-1993_05
ORD IDord-b8fee752830b4340872bb1e8ffe1ea49
出典メモuspto-grants-1993_05