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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1654822Generated: October 31, 2026

2-Amino-3-Hydroxypyridine → 3-[(4-Fluorophenyl)methoxy]pyridin-2-amine

https://huagongshe.com/reaction/1654822

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-HydroxypyridineHCID 28114—
Reactant4-Fluorobenzyl bromideHCID 68021—
CatalystTrioctylmethylammonium chlorideHCID 21218—
SolventDichloromethaneHCID 6344—
SolventSodium HydroxideHCID 14798—
Product3-[(4-Fluorophenyl)methoxy]pyridin-2-amineHCID 2728377—

Reaction Steps

A mixture of 4-fluorobenzyl bromide (75 g, 0.396 mol) and 2-amino-3-hydroxypyridine (39.6 g, 0.36 mol) in 40% aqueous sodium hydroxide solution (250 ml) and dichloromethane (250 ml) was treated with Adogen 464 (5 ml) and stirred vigorously at room temperature for 16 hours. The aqueous layer was extracted with dichloromethane and the combined organic layers washed with water, dried and evaporated. Chromatography (silica gel, chloroform) gave the product as an oil which later solidified (45.4 g, 49%), m.p. 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05409943
Source datasetuspto-grants-1995_04
ORD IDord-9b9cfb3ff04544aea650dd30b7ba810f
Source noteuspto-grants-1995_04