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HRID 256315作成日:2026年10月27日

Ciprofloxacin → 1-Cyclopropyl-6-fluoro-1,4-dihydro-7-[4-(5-methyl-2-oxo-1,3-dioxol-4-yl-methyl)-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acid

https://huagongshe.com/reaction/256315

反応式

関与物質

役割名称HCID仕込み量
反応物CiprofloxacinHCID 2764—
反応物Potassium BicarbonateHCID 516893—
反応物4-(Bromomethyl)-5-methyl-1,3-dioxol-2-oneHCID 10774141—
溶媒DimethylformamideHCID 6228—
生成物1-Cyclopropyl-6-fluoro-1,4-dihydro-7-[4-(5-methyl-2-oxo-1,3-dioxol-4-yl-methyl)-1-piperazinyl]-4-oxo-3-quinolinecarboxylic acidHCID 13673272—

反応手順

1.15 g (3.5 mmoles) of 1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinolinecarboxylic acid are stirred in 20 ml of dimethylformamide with 0.85 g (4.4 mmoles) of 4-bromomethyl-5-methyl-1,3-dioxol-2-one and 0.42 g (4.2 mmoles) of powdered potassium bicarbonate for 3 days, while cooling with ice. The mixture is concentrated in vacuo, the residue is stirred with 20 ml of water, the resulting greasy product is dissolved in methanol and the solution is filtered. The filtrate is left to stand at room temperature for 2 days and the colorless crystals which have precipitated are isolated.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04703047
出典データセットuspto-grants-1987_10
ORD IDord-a73071cede0544c8b4b53d87ab259d7d
出典メモuspto-grants-1987_10