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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580479Generated: October 30, 2026

3-[(ethoxycarbonyl)amino]benzoic acid → HCID 13983397, compound

https://huagongshe.com/reaction/580479

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-[(ethoxycarbonyl)amino]benzoic acidHCID 717662—
Reactant7-methoxy-1,8-Naphthyridin-2-amineHCID 21793027—
SolventWaterHCID 962—
ProductHCID 13983397HCID 1398339758.7%

Reaction Steps

The procedure is similar to that described in Example 2, but starting with 3-ethoxycarbonylaminobenzoic acid (10 g), N,N'-carbonyldiimidazole (7.6 g) and 2-amino-7-methoxy-1,8-naphthyridine (5.95 g). The reaction mixture is then poured into water (1000 cc) and the precipitate formed is separated by filtration, washed with water (10 cc) and dried in the air. On recrystallization in ethyl acetate (100 cc) of the product thereby obtained, N-(7-methoxy-1,8-naphthyridin-2-yl)-3-ethoxycarbonylaminobenzamide (7.3 g), m.p. 120° C., is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04753941
Source datasetuspto-grants-1988_06
ORD IDord-2fa9986e06394ad09bc13329c7a98702
Source noteuspto-grants-1988_06