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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168535Generated: November 1, 2026

Formaldehyde → Ethyl 8-Fluoro-1-((hydroxymethyl)(methyl)amino)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/1168535

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantEthyl 1-((tert-Butoxycarbonyl)(methyl)amino)-8-fluoro-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 12083058—
SolventWaterHCID 962—
ProductEthyl 8-Fluoro-1-((hydroxymethyl)(methyl)amino)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 12083060113.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of ethyl 1-((tert-butoxycarbonyl)(methyl)amino)-8-fluoro-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate (Preparation 35, 0.200 g), 37% aqueous formaldehyde (4.0 mL), and water (2.0 mL) is heated in an oil bath for 2.5 h at 85° C. The mixture is cooled, diluted with ice water (30 mL), and the resulting precipitate is collected, rinsed with ice water and partially air dried. The solid is dissolved in a mixture of acetone and CH2Cl2, dried (Na2SO4), and concentrated at reduced pressure to yield 0.194 g (90%) of the title compound as a white solid. Physical characteristics: MS (ESI+) m/z 421 (M+H)+; TLC (silica gel GF): Rf=0.32 acetone/CH2Cl2 (1/4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06624159B2
Source datasetuspto-grants-2003_09
ORD IDord-91f4aae8d499475c94f0fdaf0046fb96
Source noteuspto-grants-2003_09