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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2422146Generated: November 1, 2026

2-Naphthoic acid → HCID 59514514, compound

https://huagongshe.com/reaction/2422146

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Naphthoic acidHCID 7123—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 59514483HCID 59514483—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59514514HCID 59514514669.2%

Reaction Steps

A mixture of methyl[2-(4-aminobenzyl)-4,6-dichloropyrimidin-5-yl]acetate (0.073 g, 0.23 mmol), 2-naphthoic acid (0.048 g, 0.028 mmol), and WSCI (0.049 g, 0.026 mmol) in anhydrous THF (3 mL) was stirred at room temperature under Ar atmosphere for 10 hours. EtOAc (80 mL) was then introduced and the organic phase was washed sequentially with saturated NaHCO3, water, and brine, dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The crude product thus obtained as a light orange oil was triturated with diisopropyl ether and the separated solids was collected by suction to give methyl {4,6-dichloro-2-[4-(2-naphthoylamino)benzyl]pyrimidin-5-yl}acetate (0.090 g, 78% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960393B2
Source datasetuspto-grants-2011_06
ORD IDord-cdf5425743fb469e8b9efc5059093b75
Source noteuspto-grants-2011_06