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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506257Generated: October 31, 2026

Sodium Thiosulfate → HCID 178504208, compound

https://huagongshe.com/reaction/1506257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactant2-Iodoxybenzoic acidHCID 108794—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178504209HCID 178504209—
SolventDimethyl SulfoxideHCID 679—
SolventTolueneHCID 1140—
ProductHCID 178504208HCID 17850420866%

Reaction Conditions

Temperature50 °C

Reaction Steps

1-[trans-4-(Hydroxymethyl)cyclohexyl]-7-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[3′,2′:5,6]pyrido[4,3-d]pyrimidine-2,4(3H,7H)-dione (107 mg, 0.240 mmol) in a mixture of toluene (1 mL) and dimethyl sulfoxide (0.25 mL) was mixed with 2-iodoxybenzoic acid (80.9 mg, 0.288 mmol) and stirred at 50° C. for 2 hours. After addition of saturated aqueous sodium thiosulfate and saturated aqueous sodium hydrogen carbonate, the reaction mixture was stirred at room temperature for 30 minutes, and extracted with ethyl acetate, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane=1/1→7/3 (v/v)) to give the title compound as a colorless solid (70.1 mg, yield 66%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-682dfb62b9af4e0a9c933c7f63978539
Source noteuspto-grants-2015_12