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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 20548Generated: October 26, 2026

Sodium Thiosulfate → HCID 178469074, compound

https://huagongshe.com/reaction/20548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 59346927HCID 59346927—
SolventAcetonitrileHCID 6342—
ProductHCID 178469074HCID 178469074111.3%

Reaction Steps

Trimethylsilyl iodide (0.27 mL) was added dropwise under argon to a solution of tert-butyl 3-({3-[4-(ethoxycarbonyl)phenoxy]-5-[(1S)-2-methoxy-1-methylethoxy]benzoyl}amino)-1H-pyrazole-1-carboxylate (167 mg, 0.38 mmol) in acetonitrile (5 mL) and stirred at ambient temperature for 16 hours. Sodium thiosulfate solution was added to quench the reaction and the reaction mixture was extracted into ethyl acetate (3×25 mL). Organic phases were combined and dried (MgSO4) and the filtrate was concentrated in vacuo to give a clear oil (180 mg), which was not purified further.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07745475B2
Source datasetuspto-grants-2010_06
ORD IDord-41f61ad5ddc44ea48222b7de70689e06
Source noteuspto-grants-2010_06