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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2413924Generated: November 4, 2026

Ethanol → HCID 13787387, compound

https://huagongshe.com/reaction/2413924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant3,4-Dichlorobenzoic acidHCID 5817—
Reactant7-Chloro-1,8-naphthyridin-2-amineHCID 85199—
SolventWaterHCID 962—
ProductHCID 13787387HCID 1378738752.7%

Reaction Conditions

Temperature4 °C

Reaction Steps

The procedure is analogous to that described in Example 1, but starting with 3,4-dichlorobenzoic acid (15.3 g), N,N'-carbonyldiimidazole (12.9 g) and 2-amino-7-chloro-1,8-naphthyridine (8.9 g). The product obtained by precipitation in water (17.6 g; m.p. 228° C.) is dissolved in boiling ethanol (900 cc). After cooling for 2 hours at 4° C., the crystallized solid is separated by filtration, washed with isopropyl ether (2×30 cc) and dried at 40° C. under reduced pressure (0.07 kPa). N-(7-Chloro-1,8-naphthyridin-2-yl)-3,4-dichlorobenzamide (9.2 g), m.p. 230° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04720500
Source datasetuspto-grants-1988_01
ORD IDord-a88e4cca355d4184a467ec9a3d7629ab
Source noteuspto-grants-1988_01