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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47107Generated: October 30, 2026

Hydrogen Peroxide → 7,7-Dimethyl-2-(2-methoxy-4-methylsulfinyl-phenyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione

https://huagongshe.com/reaction/47107

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
Reactant7,7-dimethyl-2-(2-methoxy-4-methylmercapto-phenyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dioneHCID 70610149—
SolventAcetic AcidHCID 176—
SolventAmmoniaHCID 222—
SolventWaterHCID 962—
Product7,7-Dimethyl-2-(2-methoxy-4-methylsulfinyl-phenyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dioneHCID 70610826—

Reaction Steps

5.1 gm of 7,7-dimethyl-2-(2-methoxy-4-methylmercapto-phenyl)-5H,7H-imidazo[4,5-h]isoquinoline-4,6-dione were reacted in 100 ml of 70% acetic acid with 1.7 gm of 30% hydrogen peroxide, and the mixture was allowed to stand for 50 hours at room temperature (the first 3 hours while stirring). After 18 and again after 26 hours 1.3 gm of 30% hydrogen peroxide were added. The reaction mixture was then diluted with water, and ammonia was added until alkaline reaction. The precipitate was suction-filtered off and the filtrate was extracted twice with chloroform. The combined chloroform phases were evaporated, and the evaporation residue was combined with the precipitate. The thus obtained product was purified on a silicagel column (eluant: chloroform/acetone 19:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04176184
Source datasetuspto-grants-1979_11
ORD IDord-6e2f49757df540dbb47a68a6ced2992a
Source noteuspto-grants-1979_11