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HRID 1589564作成日:2026年10月27日

1,8-Diazabicyclo(5.4.0)undec-7-ene → 7-(2,5-Diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/1589564

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物1-Ethyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acidHCID 800521—
反応物2,5-Diazabicyclo(2.2.2)octane dihydrochlorideHCID 22924390—
溶媒AcetonitrileHCID 6342—
生成物7-(2,5-Diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acidHCID 1356579543.4%

反応手順

A solution of 0.52 g (2.0 mmole) of 1-ethyl-6,7-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 0.37 g (2.0 mmole) of 2,5-diazabicyclo(2.2.2)octane dihydrochloride [P. A. Sturm et al., J. Med. Chem., 17, 481 (1974)], 0.90 ml (6.0 mmole) of 1,8-diazabicyclo[5.4.0]undec-7-ene and 25 ml of acetonitrile was heated under reflux for 21 hours. The reaction mixture was filtered and the filtrate was evaporated to dryness. The residue was recrystallized from ethanol to give 0.30 g of the title compound, mp 270°-272°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04571396
出典データセットuspto-grants-1986_02
ORD IDord-9cd97c866e664a92aa9f435b7db69aaf
出典メモuspto-grants-1986_02