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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297562Generated: October 30, 2026

Hydroxyamine hydrochloride → HCID 86585219, compound

https://huagongshe.com/reaction/2297562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydroxyamine hydrochlorideHCID 443297—
ReactantHCID 482669HCID 482669—
ProductHCID 86585219HCID 86585219—

Reaction Steps

1-Ethyl-6-fluoro-7-{4-[2-(4-chlorophenyl)-2-hydroxy-iminoethyl]-1-piperazinyl}-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid was prepared from 1-ethyl-6-fluoro-7-{4-[2-(4-chlorophenyl)-2-oxoethyl]-1-piperazinyl}-4-oxo-1,4-dihydro-3-quinolinecarboxylic acid (0.24 g, 0.5 mmole) and hydroxylamine hydrochloride (0.07 g, 1 mmol) by a method similar to that described for Example 3 (73% yield). 1H NMR (DMSO-d6) δ 1.39 (t, 3H, J=7.0), 2.61 and 3.24 (two m, 8H), 3.44 and 3.73 (two s, 2H), 4.56 (q, 2H, J=7.0), 7.24 and 7.78 (two m, 5H), 7.89 (d, 1H, J=13.4), 8.93 (s, 1H), 11.03 and 11.49 (two s, 1 H), 15.35 (br s, 1H). Anal. Calcd. for C24H24FClN4O4•0.25 H2O: C, 58.66; H, 5.02; N, 11.40. Found: C, 58.48; H, 5.01; N, 11.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492373B2
Source datasetuspto-grants-2002_12
ORD IDord-759a83c668c447ad8b1e9e45914c6c8d
Source noteuspto-grants-2002_12