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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219245Generated: October 26, 2026

2-Methoxyethanol → 8-Chloro-3-(2-methoxyethoxy)-1,5-naphthyridine

https://huagongshe.com/reaction/219245

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethanolHCID 8019—
ReactantTetrahydrofuranHCID 8028—
ReactantTriphenylphosphineHCID 11776—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant8-Chloro-1,5-naphthyridin-3-olHCID 135743576—
SolventDichloromethaneHCID 6344—
SolventDichloromethane methanolHCID 21226129—
Product8-Chloro-3-(2-methoxyethoxy)-1,5-naphthyridineHCID 5769111855.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

A round bottom flask under nitrogen environment was charged with 8-chloro-1,5-naphthyridin-3-ol (1.05 g, 5.8 mmol), 22.8 g of PS-Triphenylphosphine (loading: 2.2 mmol/g), 2-methoxyethanol (2.2 mL, 27.9 mmol), and THF (29.1 ml, 5814 μmol)/DCM (58.1 mL). Mixture cooled to 0° C. and to this was added DEAD (1.84 mL) dropwise via syringe. Reaction mixture allowed to stir at room temperature for 16 hours. Diluted with 50 mL of 10% MeOH/dichloromethane and resin bound reagent filtered. Filtrate concentrated under reduced pressure and purified by ISCO silica gel chromatography (10-30% EtOAc/Hexanes) to afford 8-chloro-3-(2-methoxyethoxy)-1,5-naphthyridine (770 mg, 55% yield) as white solid. MS [M+H]=238.9. Calc'd for C11H11ClN2O2=238.67. The following compounds were prepared in a similar fashion as 8-chloro-3-(2-methoxyethoxy)-1,5-naphthyridine:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198448B2
Source datasetuspto-grants-2012_06
ORD IDord-76c061bc0722435089b4c4183b839099
Source noteuspto-grants-2012_06