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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 235814Generated: November 1, 2026

Ethanol → HCID 20217519, compound

https://huagongshe.com/reaction/235814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant2,6-Difluorobenzoic acidHCID 9796—
Reactant7-Chloro-1,8-naphthyridin-2-amineHCID 85199—
SolventWaterHCID 962—
ProductHCID 20217519HCID 2021751948.2%

Reaction Conditions

Temperature4 °C

Reaction Steps

The procedure is similar to that described in Example 1, but starting with 2,6-difluorobenzoic acid (12.1 g), N,N'-carbonyldiimidazole (12.3 g) and 2-amino-7-chloro-1,8-naphthyridine (8.5 g). The product produced by precipitation in water (6.8 g; m.p. 215° C.) is dissolved in boiling ethanol (450 cc). After 4 hours' cooling at 4° C., the crystallised solid is separated by filtration washed with ethanol (3×15 cc) and dried at 40° C. under reduced pressure (0.067 kPa). N-(7-chloro-1,8-naphthyridin-2-yl)-2,6-difluorobenzamide (7.3 g) is produced, m.p. 242° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04642308
Source datasetuspto-grants-1987_02
ORD IDord-081965effdeb47199976257e68bdc672
Source noteuspto-grants-1987_02