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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370713Generated: November 3, 2026

Iodoethane → HCID 13477662, compound

https://huagongshe.com/reaction/370713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTriethylamineHCID 8471—
Reactant1-Ethyl-6-fluoro-7-(3-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid--hydrogen chloride (1/1)HCID 3062436—
SolventDimethylformamideHCID 6228—
ProductHCID 13477662HCID 1347766248.1%

Reaction Steps

A solution of 1.00 g of 1-ethyl-6-fluoro-1,4-dihydro-7-(3-methyl-1-piperazinyl)-4-oxoquinoline-3-carboxylic acid hydrochloride, 1.29 g of ethyl iodide and 1.09 g of triethylamine in 20 ml of N,N-dimethylformamide was heated at 70° to 80° C. for 1.5 hours. The solvent of the reaction mixture was evaporated and the residue was acidified with 50% aqueous acetic acid. The solution was neutralized with 20% aqueous sodium hydroxide and the precipitate was filtered. The precipitate was chromatographed on silica gel using chloroform-methanol (9:1) as eluent to give 0.47 g of the title compound as colorless crystalls, which was recrystallized from a mixture of chloroform and methanol as colorless needles, M.p. 203°-205° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528287
Source datasetuspto-grants-1985_07
ORD IDord-a92f15e714c14af3b947ab4eb76e57cd
Source noteuspto-grants-1985_07