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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297563Generated: October 29, 2026

2-Bromo-1-(4-fluorophenyl)ethan-1-one → HCID 10950831, compound

https://huagongshe.com/reaction/2297563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1-(4-fluorophenyl)ethan-1-oneHCID 96749—
Reactant3-Quinolinecarboxylic acid, 1,4-dihydro-6,8-difluoro-1-ethyl-4-oxo-7-(1-piperazinyl)-HCID 113523—
ProductHCID 10950831HCID 10950831—

Reaction Steps

1-Ethyl-6,8-difluoro-7-{4-[2-(4-fluorophenyl)-2-oxoethyl]-1-piperazinyl}-4-oxo-1,4-dihydro-3-quinoline-carboxylic acid was prepared from 1-ethyl-6,8-difluoro-4-oxo-7-(1-piperazinyl)-1,4-dihydro-quinoline-3-carboxylic acid (0.50 g, 1.48 mmole) and 2-bromo-4′-fluoroacetophenone (0.40 g, 1.86 mmole) by a method similar to that described for Example 4 (64% yield). Mp: 170° C. (dec). 1H NMR (DMSO-d6) δ 1.44 (t, 3H, J=7.0), 2.70 and 3.3 (two m, 8H), 3.94 (s, 2H), 4.58 (q, 2H, J=7.0), 7.37 (n, 2H), 7.90 (d, 1H, J=11.8), 8.11 (m, 2H), 8.92 (s, 1H), 14.92 (br s, 1H). Anal. Calcd. for C24H22F3N3O4•0.5 H2O: C, 59.75; H, 4.80; N, 8.71. Found: C, 59.39; H, 4.66; N, 8.62.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492373B2
Source datasetuspto-grants-2002_12
ORD IDord-1e990ce2434d469b9440a39038b7880f
Source noteuspto-grants-2002_12