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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297551Generated: October 30, 2026

Dichloromethane → HCID 482680, compound

https://huagongshe.com/reaction/2297551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 482668HCID 482668—
ReactantSodium BicarbonateHCID 516892—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 482680HCID 48268068.5%

Reaction Steps

To a solution of the 1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(4-phenacyl-1-piperazinyl)-quinoline-3-carboxylic acid (0.44 g, 1 mmole) [H. Kondo et. al., J. Med. Chem., 29, 2020 (1986)] in absolute methanol (20 ml) was added a solution of hydroxylamine hydrochloride (0.14 g, 2 mmol) and sodium bicarbonate (0.17 g, 2 mmol) in water (2 ml). The mixture was heated at reflux for 36 hr and allowed to cool to room temperature. CH2Cl2 (50 ml) was added, and the layers were separated. The organic phase was washed successively with water and brine, dried over Na2SO4, filtered and concentrated in vacuo to give a solid which was purified by flash column chromatography (silica gel, with CH2Cl2/methanol (10:1) as the eluant) and crystillization from CH2Cl2/methanol (5:1) to give 1-ethyl-6-fluoro-4-oxo-7-[4-(2-hydroxyimino-2-phenylethyl)-1-piperazinyl]-1,4-dihydroquinoline-3-carboxylic acid as an off-white amorphous solid (0.31 g, 68%). Mp: 203° C. (dec). 1H NMR (DMSO-d6) δ 1.38 (t, 3H, J=7.2), 2.64 and 3.25 (two m, 8H), 3.43 and 3.73 (two s, 2 H), 4.56 (q, 2H, J=7.2), 7.15 (d, 1H, J=7.2), 7.36-7.79 (m, 5H), 7.88 (d, 1H, J=13.2), 8.92 (s, 1H), 10.99 and 11.48 (two s, 1H), 15.07 (br s, 1H). Anal. Calcd. for C24H25FN4O4•1.5 H2O: C, 60.10; H, 5.89; N, 11.68. Found: C, 60.19; H, 5.81; N, 11.64.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492373B2
Source datasetuspto-grants-2002_12
ORD IDord-c00a9a79fc5e482197b633402d69e44f
Source noteuspto-grants-2002_12