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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383414Generated: November 2, 2026

2-Amino-6-fluorobenzylamine → [1,6]Naphthyridine-2-carboxylic acid (trans-2-phenyl-cyclopropyl)-amide

https://huagongshe.com/reaction/1383414

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-6-fluorobenzylamineHCID 578998—
Reactant1,6-Naphthyridine-2-carboxylic acidHCID 735908—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantN-(2-amino-6-fluorobenzyl)-2-[1,6]naphthyridinecarboxamideHCID 18621328—
SolventDimethylformamideHCID 6228—
Product[1,6]Naphthyridine-2-carboxylic acid (trans-2-phenyl-cyclopropyl)-amideHCID 5728000694%

Reaction Steps

Compound #16 N-(2-amino-6-fluorobenzyl)-2-[1,6]naphthyridinecarboxamide 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. Flash 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 numberUS06255318B1
Source datasetuspto-grants-2001_07
ORD IDord-a2ff9ea586d846c2b30b8a6db54029d2
Source noteuspto-grants-2001_07