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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1932373Generated: November 2, 2026

Hydrogen Peroxide → HCID 67142183, compound

https://huagongshe.com/reaction/1932373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 67141825HCID 67141825—
SolventAcetic AcidHCID 176—
ProductHCID 67142183HCID 67142183—

Reaction Conditions

Temperature60 °C

Reaction Steps

Hydrogen peroxide (50 wt. %, 100 μl) was added to a solution of 2-(1-allyl-3-methylsulfinyl-2-methyl-1H-pyrrolo[2,3-c]pyridin-7-yl)-1,2,3,4-tetrahydroisoquinoline hydrochloride (30 mg, 0.07 mmol) prepared in Example 632 in acetic acid (3 ml). The reaction mixture was stirred for 1 hour at 60° C., cooled to room temperature, basified with a potassium carbonate solution, and then extracted with dichloromethane. The organic layer was dried on anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography. The resulting product was dissolved in ethyl ether, saturated with hydrochloric acid gas, and then filtered to give 8 mg of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188114B2
Source datasetuspto-grants-2012_05
ORD IDord-c1bf4bddef2549e78917334c024784c2
Source noteuspto-grants-2012_05