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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383406Generated: October 31, 2026

4-Chlorobenzylamine → HCID 15923149, compound

https://huagongshe.com/reaction/1383406

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzylamineHCID 66036—
Reactant1,6-Naphthyridine-2-carboxylic acidHCID 735908—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantHCID 178526939HCID 178526939—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 15923149HCID 1592314994%

Reaction Steps

To a stirring mixture of 2-[1,6]naphthyridinecarboxylic acid (50 mg, 0.287 mmol) in anhydrous DMF (6.3 mL) at room temperature was added sequentially-hydroxybenzotriazole hydrate (42.7 mg, 0.316 mmol), 4-chlorobenzyl amine (53.5 μL, 0.431 mmol) 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 and the resulting residue was re-dissolved in CH2Cl2 (50 mL). The organic layer was washed with aqueous NaHCO3, dried over anhydrous Na2SO4, and concentrated to give the crude mixture. Flash column chromatography of the crude (50% hexane/ethyl acetate to 100% ethyl acetate) afforded the desired product as a white solid (80.3 mg, 94%): m.p. 110-111° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255318B1
Source datasetuspto-grants-2001_07
ORD IDord-cf440162538d4d37aa13ae33b4de962d
Source noteuspto-grants-2001_07