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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1047151Generated: October 30, 2026

Ethylene Glycol → 2-Hydroxyethyl 6-bromo-1-ethyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/1047151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantTriphenylphosphineHCID 11776—
Reactantethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Reactant6-Bromo-1-ethyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acidHCID 21529174—
SolventTetrahydrofuranHCID 8028—
Product2-Hydroxyethyl 6-bromo-1-ethyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylateHCID 6874682482%

Reaction Steps

6-Bromo-1-ethyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid (Intermediate 22, 1.7 g, 5.72 mmol), ethane-1,2-diol (1.91 g, 34.34 mmol) and triphenylphosphine (9.0 g, 34.34 mmol) were dissolved in tetrahydrofuran (100 mL). Diethyl azodicarboxylate (DEAD) (4.97 g, 28.61 mol) was added drop wise and the mixture was stirred for 16 h at room temperature. The mixture was concentrated under reduced pressure, and water (100 mL) was added. The aqueous mixture was extracted with ethyl acetate (2×100 mL) and the combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give a crude compound. The crude compound was purified by flash column chromatography over silica gel (100-200 mesh) using eluent gradient of ethyl acetate/petroleum ether: 1:1 to 100:0 to afford 1.6 g (82%) of 2-hydroxyethyl 6-bromo-1-ethyl-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569484B2
Source datasetuspto-grants-2013_10
ORD IDord-bb011c78e9514f88bf1fdaa2d88c75c4
Source noteuspto-grants-2013_10