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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 985991Generated: November 1, 2026

Ammonium Chloride → 6-(2-methoxypyrid-5-yl)-2-(1H)-quinolone

https://huagongshe.com/reaction/985991

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant5-Bromo-2-methoxypyridineHCID 2734895—
ReactantEthylenediaminetetraacetic acid disodium saltHCID 13020083—
Reactant6-Iodoquinolin-2(1H)-oneHCID 13836184—
ReactantHCID 178418306HCID 178418306—
CatalystZincchlorideHCID 3007855—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventPentaneHCID 8003—
SolventTetrahydrofuranHCID 8028—
Product6-(2-methoxypyrid-5-yl)-2-(1H)-quinoloneHCID 13836190—

Reaction Steps

A solution of 5-bromo-2-methoxypyridine (1.50 g) in tetrahydrofuran (THF) (10 cm3) was stirred at -70° under nitrogen during the addition of t-butyllithium (8.0 cm3 of a 2.0M solution in pentane). After 10 minutes a solution of anhydrous zinc chloride (1.09 g) in tetrahydrofuran (THF) (10 cm3) was added and the mixture was allowed to warm to room temperature over 1 hour. A suspension of 6-iodo-2-(1H)-quinolone (0.813 g) and tetrakis (triphenylphosphine) palladium(O) (0.03 g) in THF (10 cm3) was then added and the mixture was heated under reflux for 3 hours. Saturated ammonium chloride solution (1 cm3) was added to the cooled mixture followed by a solution of ethylenediaminetetraacetic acid disodium salt (6.0 g) in water (100 cm3). Chloroform (100 cm3) and methanol (30 cm3) were added and the mixture was warmed until all the solid material dissolved. The phases were separated, the aqueous layer was further extracted with chloroform:methanol 9:1 (3×50 cm3), and the combined and dried (MgSO4) extracts were concentrated in vacuo to afford a solid which was recrystallised from isopropanol to give 6-(2-methoxypyrid-5-yl)-2-(1H)-quinolone, m.p. 248°-252°, (0.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04710507
Source datasetuspto-grants-1987_12
ORD IDord-d29d0c1739bd4c3aa47026f322aea51f
Source noteuspto-grants-1987_12