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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2296374Generated: October 31, 2026

Triethylamine → HCID 13146122, compound

https://huagongshe.com/reaction/2296374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Nitrobenzyl bromideHCID 66011—
ReactantHCID 12770893HCID 12770893—
SolventDimethylformamideHCID 6228—
ProductHCID 13146122HCID 1314612281.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)quinoline-3-carboxylic acid hydrochloride (6.7 g), triethylamine (5.45 g), p-nitrobenzylbromide (5.8 g) and dimethylformamide (200 ml) was stirred at 90° C. for 10.5 hrs. The solvent was evaporated off and the residue was treated with water. The solid was filtered, washed with water, dried, and recrystallized from a mixture of dimethylformamide and ethanol to give 6.9 g of 1-ethyl-6,8-difluoro-1,4-dihydro-7-[4-(p-nitrobenzyl)-1-piperazinyl]-4-oxoquinoline-3-carboxylic acid. mp: 241°-242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04429127
Source datasetuspto-grants-1984_01
ORD IDord-f039af4499e34091a0f80f3ed6177c0f
Source noteuspto-grants-1984_01