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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1861814Generated: November 4, 2026

2-Amino-6-fluorobenzylamine → N-(2-amino-6-fluorobenzyl)-2-[1,6]naphthyridinecarboxamide

https://huagongshe.com/reaction/1861814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-fluorobenzylamineHCID 578998—
Reactant1,6-Naphthyridine-2-carboxylic acidHCID 735908—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
SolventDimethylformamideHCID 6228—
ProductN-(2-amino-6-fluorobenzyl)-2-[1,6]naphthyridinecarboxamideHCID 1862132894%

Reaction Steps

To a stirring mixture of 2-[1,6]naphthyridinecarboxylic acid (50 mg, 0.287 mmol) in anhydrous DMF (1.0 mL) at room temperature was added sequentially 1-hydroxybenzotriazole hydrate (42.7 mg, 0.316 mmol), 2-amino-6-fluorobenzylamine (60.0 μL) and 1-(3-dimethylaminopropyl)-3-ethylcarboiimide hydrochloride (61.8 mg, 0.316 mmol). The resulting mixture was allowed to stir at room temperature overnight and it was found to be clear. The solvent was removed under vacuum. 1Flash column chromatography of the residue (50% hexane/ethyl acetate to 100% ethyl acetate) afforded the desired product as a white solid (80.0 mg, 94%): m.p. 165 (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06534520B2
Source datasetuspto-grants-2003_03
ORD IDord-6c8a693373d04ae4ba22b45281aa59f6
Source noteuspto-grants-2003_03