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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1422948Generated: October 30, 2026

Trifluoroacetic acid → 4-Benzyloxy-6-methoxy-[1,5]naphthyridin-3-ylamine

https://huagongshe.com/reaction/1422948

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(4-Benzyloxy-6-methoxy-[1,5]naphthyridin-3-yl)-carbamic acid tert-butyl esterHCID 67255694—
SolventDichloromethaneHCID 6344—
Product4-Benzyloxy-6-methoxy-[1,5]naphthyridin-3-ylamineHCID 6725423692.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

Trifluoroacetic acid (10.0 mL, 131.2 mmol, 20.0 eq) is added at 0° C. to a stirred solution of (4-benzyloxy-6-methoxy-[1,5]naphthyridin-3-yl)-carbamic acid tert-butyl ester (2.50 g, 6.55 mmol, 1.0 eq) in dichloromethane (50 mL). After 20 hours stirring at 0° C., the reaction mixture is extracted with dichloromethane (3×200 mL) and water (200 mL) and the pH is adjusted to 12 by the addition of a 1N sodium hydroxide aqueous solution. The combined organic layers are dried over sodium sulfate, filtered and concentrated to afford 4-benzyloxy-6-methoxy-[1,5]naphthyridin-3-ylamine as a light yellow solid (1.70 g, 92% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927541B2
Source datasetuspto-grants-2015_01
ORD IDord-883df7cece1f41299662b47f5c3bd59c
Source noteuspto-grants-2015_01