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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503524Generated: November 1, 2026

4-Aminophenol → 4-(7-Methoxy-1,5-naphthyridin-4-yloxy)benzenamine

https://huagongshe.com/reaction/503524

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant8-Chloro-3-methoxy-1,5-naphthyridineHCID 59427340—
SolventDimethylformamideHCID 6228—
Product4-(7-Methoxy-1,5-naphthyridin-4-yloxy)benzenamineHCID 44185106—

Reaction Steps

Five 20 mL microwave vials were each charged with 4-aminophenol (0.700 mg, 33 mmol) and 3 equivalents of cesium carbonate in 6.0 ml of DMF. The mixture was stirred at RT for 10 minutes. Following addition of 8-chloro-3-methoxy-1,5-naphthyridine (1 g, 26 mmol), the reaction vessels were capped and irradiated at 150° C. for 15 min in the microwave, at which time the reaction was determined complete by LCMS. The mixture was allowed to cool to ambient temperature and material from the five vessels was combined. A deep brown solid crashed out with addition of water. Filtered solids, washed with water and dried overnight in the vacuum oven to afford 4-(7-methoxy-1,5-naphthyridin-4-yloxy)benzenamine as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776857B2
Source datasetuspto-grants-2010_08
ORD IDord-cd70aa3c42fc41999055d438f1182d14
Source noteuspto-grants-2010_08