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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1838819Generated: October 25, 2026

Sodium Hydroxide → 2-(Methoxymethyl)thiazolo[4,5-c]quinoline

https://huagongshe.com/reaction/1838819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantMethoxyacetyl chlorideHCID 96623—
Reactant3-Aminoquinoline-4-thiolHCID 178507990—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventMethoxyacetic AcidHCID 12251—
Product2-(Methoxymethyl)thiazolo[4,5-c]quinolineHCID 22648259—

Reaction Conditions

Temperature140 °C

Reaction Steps

Methoxyacetyl chloride (1.8 mL) was added to a mixture of 3-aminoquinoline-4-thiol (2.8 g) in methoxyacetic acid (15 mL). The reaction was heated at about 140° C. for 1 hour and then allowed to cool to ambient temperature. The reaction mixture was diluted with a small amount of water, made basic with 10% sodium hydroxide and then extracted with dichloromethane (300 mL). The extract was washed with sodium bicarbonate, washed with water, dried over magnesium sulfate and then concentrated under vacuum to provide crude product as a dark oil. The oil was dissolved in dichloromethane and then placed on a layer of silica gel. The silica gel was eluted with 1:1 hexane:ethyl acetate. The eluant was concentrated under vacuum to provide 2.3 g of 2-(methoxymethyl)thiazolo[4,5-c]quinoline as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677334B2
Source datasetuspto-grants-2004_01
ORD IDord-72e811f5fcee43ccba3d93c80efe3435
Source noteuspto-grants-2004_01