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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638977Generated: November 2, 2026

Triethylamine → 4-Chloro-6-methoxy-1,5-naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/638977

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Chloro-6-(methyloxy)-1,5-naphthyridine-3-carboxamideHCID 68576737—
SolventDichloromethaneHCID 6344—
Product4-Chloro-6-methoxy-1,5-naphthyridine-3-carbonitrileHCID 6857910191.1%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-chloro-6-(methyloxy)-1,5-naphthyridine-3-carboxamide (647 mg, 2.7 mmol) in anhydrous DCM (2 mL) with triethyamine (2 mL) at 0° C. was added trifluororacetic anhydride (1 mL) slowly. The resulting solution was warmed up to 25° C. and stirred for 1 h. The mixture was partitioned between CHCl and H2O. The aqueous layer was extracted several times with CHCl. The organic fractions were combined, concentrated and purified with column chromatography (silica, 0-25% ethyl acetate/hexane) affording the title compound as an off-white solid (540 mg, 91%): LC/MS (ES) m/e 220 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691850B2
Source datasetuspto-grants-2010_04
ORD IDord-6e07b8488a3e49a1857584c7cca8b7f9
Source noteuspto-grants-2010_04