Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168534Generated: October 31, 2026

Water → Ethyl 8-Fluoro-6-iodo-1-(methylamino)-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/1168534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantEthyl 1-((tert-Butoxycarbonyl)(methyl)amino)-8-fluoro-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 12083058—
SolventDichloromethaneHCID 6344—
ProductEthyl 8-Fluoro-6-iodo-1-(methylamino)-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 1208305998%

Reaction Steps

A solution of trifluroacetic acid (6.40 g) in methylene chloride (5 mL) is added dropwise over a 4 minute period to a solution of ethyl 1-((tert-butoxycarbonyl)(methyl)amino)-8-fluoro-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate (Preparation 34, 1.10 g) in methylene chloride (20 mL) at room temperature. After 3.5 h, the mixture is poured into a mixture of saturated sodium bicarbonate solution (125 mL) and water (50 mL), and extracted two times with ethyl acetate. The combined organic extracts are dried (Na2SO4) and concentrated at reduced pressure. The resulting gummy solid is stirred with diethyl ether at room temperature to afford 0.857 g (98%) of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624159B2
Source datasetuspto-grants-2003_09
ORD IDord-6962e63c3a1646fda836dbffdede0ffd
Source noteuspto-grants-2003_09