戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2291275作成日:2026年10月27日

2-Methylpiperazine → 3-Quinolinecarboxylic acid, 1,4-dihydro-5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-4-oxo-

https://huagongshe.com/reaction/2291275

反応式

関与物質

役割名称HCID仕込み量
反応物2-MethylpiperazineHCID 66057—
反応物5-Amino-1-cyclopropyl-6,7,8-trifluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 13910947—
溶媒PyridineHCID 1049—
生成物3-Quinolinecarboxylic acid, 1,4-dihydro-5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-4-oxo-HCID 306668488.3%

反応手順

A mixture of 5-amino-1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.25 g), 2-methylpiperazine (2.0 g), and pyridine (13 ml) was heated at 105°-110° C. for 1 hour with stirring. The reaction mixture was evaporated to dryness under reduced pressure and water was added to the residue. The mixture was extracted with chloroform and the extract was dried. After evaporation of chloroform, ethanol was added to the residue. The resulting crystals were filtered and recrystallized from chloroform-ethanol to give 5-amino-1-cyclopropyl-6,8-difluoro-7-(3-methyl-1-piperazinyl)-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (1.4 g), m.p. 251°-253° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04795751
出典データセットuspto-grants-1989_01
ORD IDord-7575f8ad516d41479d5f0b19a63d9fe6
出典メモuspto-grants-1989_01