Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580459Generated: October 30, 2026

2,6-Difluorobenzoic acid → HCID 13983467, compound

https://huagongshe.com/reaction/580459

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-Difluorobenzoic acidHCID 9796—
ReactantHCID 13983447HCID 13983447—
SolventWaterHCID 962—
ProductHCID 13983467HCID 1398346738.9%

Reaction Conditions

Temperature4 °C

Reaction Steps

The procedure is similar to that described in Example 1, but starting with 2,6-difluorobenzoic acid (11.3 g), N,N'-carbonyldiimidazole (12.9 g) and 2-amino-7-(3-dimethylaminopropoxy)-1,8-naphthyridine (11.8 g). The product obtained by precipitation in water followed by drying is dissolved in boiling acetone (450 cc). After 3 hours' cooling at 4° C., the crystallized solid is separated by filtration, washed with acetone (10 cc) and dried at 40° C. under reduced pressure (0.07 kPa). N-[7-(3-Dimethylaminopropoxy)-1,8-naphthyridin-2-yl]-2,6-difluorobenzamide (7.2 g), m.p. 190° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753933
Source datasetuspto-grants-1988_06
ORD IDord-6bfc75c2ea5049c19a712faf42e1b5d5
Source noteuspto-grants-1988_06