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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422692Generated: November 1, 2026

Trifluoroacetic acid → 6-Methoxy-1,5-naphthyridin-3-amine

https://huagongshe.com/reaction/1422692

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(6-Methoxy-[1,5]naphthyridine-3-yl)-carbamic acid tert-butyl esterHCID 66747191—
SolventDichloromethaneHCID 6344—
Product6-Methoxy-1,5-naphthyridin-3-amineHCID 6674739621.1%

Reaction Steps

Trifluoroacetic acid (101 mL, 1.32 mol, 20.85 eq) is added to a stirred solution of (6-methoxy-[1,5]naphthyridine-3-yl)-carbamic acid tert-butyl ester (18.2 g, 66.11 mmol, 1.0 eq) in dichloromethane (500 mL). After 19 hours stirring at room temperature, the solution is evaporated to dryness, 6N sodium hydroxide aqueous solution is added to adjust pH to 9˜10 and a lot of solid precipitated. The mixture is extracted with dichloromethane (200 mL) and the residue is extracted with ethyl acetate (3×250 mL). Evaporation of the dichloromethane phase gives 2.44 g of product with 83% purity, which is then purified by column chromatography (silica gel, eluent: dichloromethane:petroleum ether:ethyl acetate, 25:25:2, v/v/v) to afford 6-methoxy-[1,5]naphthyridin-3-ylamino as a light yellow solid (1.95 g with 98% purity). Evaporation of the ethyl acetate phase yields additional 9.88 g of light yellow product with 99% purity. Total: 11.83 g (98% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927542B2
Source datasetuspto-grants-2015_01
ORD IDord-0e548c4260594a32bcffadaa404f6b64
Source noteuspto-grants-2015_01