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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223369Generated: November 1, 2026

2-Amino-5-chloropyridine → 3-amino-N-(5-chloropyridin-2-yl)-2-naphthamide

https://huagongshe.com/reaction/2223369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-chloropyridineHCID 66174—
Reactant2H-naphtho[2,3-d][1,3]oxazine-2,4(1H)-dioneHCID 294481—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventO-XyleneHCID 7237—
Product3-amino-N-(5-chloropyridin-2-yl)-2-naphthamideHCID 231250198%

Reaction Conditions

Temperature150 °C

Reaction Steps

A suspension of 2H-naphth[2,3-d][1,3]oxazine-2,4(1H)-dione (216 mg) and 2-amino-5-chloropyridine (202 mg) in xylene (5 ml) is stirred at 150° C. for 13 hours, and thereto added 4-dimethylaminopyridine (14.4 mg) and the mixture is stirred at 150° C. for another 3 hours. The reaction solution is concentrated under reduced pressure and the resulting residue is suspended in ethyl acetate, and filtered to remove insoluble materials. The filtrate is concentrated under reduced pressure, and the residue is purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=2/1) to give 3-amino-N-(5-chloropyridin-2-yl)-2-naphthamide (24 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375119B2
Source datasetuspto-grants-2008_05
ORD IDord-c6251bdbe98a4de28a691d45717f2dc2
Source noteuspto-grants-2008_05