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HRID 223155作成日:2026年10月26日

Formaldehyde → 1-Ethyl-6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-1,8-naphthyridine-3-carboxylic acid

https://huagongshe.com/reaction/223155

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物EnoxacinHCID 3229—
溶媒Formic AcidHCID 284—
生成物1-Ethyl-6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-1,8-naphthyridine-3-carboxylic acidHCID 3057926—

反応手順

To a solution of 37% formalin (12 ml) and formic acid (18 ml) was added 6.0 g of 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-1,8-naphthyridine-3-carboxylic acid, and the mixture was heated at 120°-125° C. for 4 hours with stirring. The mixture was then concentrated to dryness under reduced pressure. The residue was adjusted to pH 8 by addition of aqueous 7% sodium bicarbonate, and extracted with chloroform. The extract was dried and the solvent was evaported. The crystalline residue was recrystallized from a mixture of dichloromethane and ethanol to give 5.0 g of 1-ethyl-6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-4-oxo-1,8-naphthyridine-3-carboxylic acid, m.p. 228°-230° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04352803
出典データセットuspto-grants-1982_10
ORD IDord-525b78df7e5f4a399ec6385f43ca3aba
出典メモuspto-grants-1982_10