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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219250Generated: October 31, 2026

Triethylamine → N-(8-Chloro-1,5-naphthyridin-3-yl)-2-methoxyacetamide

https://huagongshe.com/reaction/219250

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethoxyacetyl chlorideHCID 96623—
Reactant8-Chloro-1,5-naphthyridin-3-amineHCID 57691347—
SolventDichloromethaneHCID 6344—
ProductN-(8-Chloro-1,5-naphthyridin-3-yl)-2-methoxyacetamideHCID 5769126675%

Reaction Steps

A round bottom flask under nitrogen was charged with 8-chloro-1,5-naphthyridin-3-amine (41 mg, 0.23 mmol), triethylamine (64 μl, 0.46 mmol), and dichloromethane (1 mL). To this was added 2-methoxyacetyl chloride (42 μl, 0.46 mmol) dropwise via syringe and reaction allowed to stir overnight at room temperature. Next day reaction mixture was diluted with dichloromethane and washed with aqueous sodium bicarbonate solution. Layers separated and organic layer dried over sodium sulfate to afford yellow oil. This was purified by ISCO silica gel chromatography (2-5% MeOH/DCM) to afford N-(8-chloro-1,5-naphthyridin-3-yl)-2-methoxyacetamide (43 mg, 75% yield) as light yellow solid. MS[M+H]=251.9. Calc'd for C11H10ClN3O2=251.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198448B2
Source datasetuspto-grants-2012_06
ORD IDord-1fcef3bd26a441e9a8c0e5f57ca07956
Source noteuspto-grants-2012_06