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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235822Generated: October 30, 2026

Ethanol → HCID 20217548, compound

https://huagongshe.com/reaction/235822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Methoxybenzoic AcidHCID 7478—
ReactantHCID 20217549HCID 20217549—
SolventWaterHCID 962—
ProductHCID 20217548HCID 2021754875.9%

Reaction Conditions

Temperature4 °C

Reaction Steps

The procedure is similar to that described in Example 1, but starting with 4-methoxybenzoic acid (19.8 g), N,N'-carbonyldiimidazole (21.1 g) and 2-amino-7-ethoxy-1,8-naphthyridine (18.5 g). The product produced by precipitation in water (28.9 g; m.p. 144° C.) is dissolved in boiling ethanol (280 cc). After 3 hours' cooling at 4° C., the crystallised solid is separated by filtration, washed with ethanol (2×10 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7-ethoxy-1,8-naphthyridin-2-yl)-4-methoxybenzamide (24 g) is produced, m.p. 152° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642308
Source datasetuspto-grants-1987_02
ORD IDord-b5e31651597a4c1aaf5cc5d4940023ce
Source noteuspto-grants-1987_02