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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 857974Generated: October 30, 2026

Hydrogen Peroxide → Thiazolo[4,5-c]quinoline

https://huagongshe.com/reaction/857974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178527812HCID 178527812—
CatalystSodium HydroxideHCID 14798—
SolventWaterHCID 962—
ProductThiazolo[4,5-c]quinolineHCID 306677844.3%

Reaction Steps

Thiazolo[4,5-c]quinoline-2-thiol (8.7 g, 0.04 mole) was suspended in a solution of sodium hydroxide (1.4 g, 0.04 mole) in water. A few drops of 50% sodium hydroxide were added to the suspension until most of the solid dissolved. Hydrogen peroxide (13.5 mL of 30%, 0.08 mole) was added dropwise over a period of 30 minutes while maintaining the temperature of the reaction mixture at 25–35° C. with a cold water bath. The bath was removed and the reaction mixture was stirred for 15 minutes. Sulfuric acid (2.5 g of 95.98%) was added dropwise to the reaction mixture. After 30 minutes the reaction was made basic (pH 9–9.5) with 50% sodium hydroxide. The reaction mixture was acidified (pH 2.5) with hydrochloric acid, a tan solid precipitated. The mixture was then heated on a steam bath for 15 minutes and the precipitate dissolved. The solution was allowed to cool to ambient temperature and a precipitate formed. The mixture was made basic (pH 9) with 50% sodium hydroxide. The resulting oily product was extracted with ethyl acetate. The extracts were combined, washed with water, dried over magnesium sulfate and then concentrated under vacuum to provide 3.3 g of thiazolo[4,5-c]quinoline as a tan solid, m.p. 104.4–105° C. Analysis: Calculated for C10H6N2S: % C, 64.19; % H, 3.25; % N, 15.04; Found: % C, 64.15; % H, 3.26; % N, 14.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148232B2
Source datasetuspto-grants-2006_12
ORD IDord-1a18bc35c59545c4994042c9c4d7ac85
Source noteuspto-grants-2006_12