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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15302Generated: October 25, 2026

Formaldehyde → Methyl 2-[3-chloro-6-(methoxy)-1,5-naphthyridin-4-yl]-2-propenoate

https://huagongshe.com/reaction/15302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl [3-chloro-6-(methyloxy)-[1,5]naphthyridin-4-yl]acetateHCID 57707490—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventWaterHCID 962—
SolventCyclohexaneHCID 8078—
ProductMethyl 2-[3-chloro-6-(methoxy)-1,5-naphthyridin-4-yl]-2-propenoateHCID 5748686889%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methyl[3-chloro-6-(methyloxy)-1,5-naphthyridin-4-yl]acetate (43.3 g, 162 mmol), benzyltriethylammonium chloride (71.2 g, 313 mmol), potassium carbonate (42 g, 304 mmol) and paraformaldehyde (42 g) in cyclohexane (1060 ml) was heated at 80° C. for 24 h, cooled and treated with ethyl acetate and water. After separation, the aqueous was extracted with ethyl acetate. The combined organic phases were dried and the solvent was removed. The residue was subjected to column chromatography on silica gel using hexane/15% ethyl acetate to provide the desired compound (40.2 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07732461B2
Source datasetuspto-grants-2010_06
ORD IDord-8a5f8952a0f6427990cce09d7e945dcd
Source noteuspto-grants-2010_06