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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413935Generated: November 3, 2026

Ethanol → HCID 13787391, compound

https://huagongshe.com/reaction/2413935

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Methoxybenzoic AcidHCID 7478—
ReactantHCID 13787376HCID 13787376—
SolventWaterHCID 962—
ProductHCID 13787391HCID 1378739141%

Reaction Conditions

Temperature4 °C

Reaction Steps

The procedure is analogous to that described in Example 1, but starting with 4-methoxybenzoic acid (6.1 g), N,N'-carbonyldiimidazole (6.5 g) and 2-amino-7-anilino-1,8-naphthyridine (7 g). The product obtained by precipitation in water (12 g) is dissolved in boiling ethanol (140 cc). After cooling for 1 hour at 4° C., the crystallized solid is separated by filtration, washed with ethanol (10 cc), and dried at 45° C. under reduced pressure (0.07 kPa). N-(7-Anilino-1,8-naphthyridin-2-yl)-4-methoxybenzamide (4.5 g), m.p. 245° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04720500
Source datasetuspto-grants-1988_01
ORD IDord-5a797eaf26f74792a71249d689b533c1
Source noteuspto-grants-1988_01