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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548703Generated: October 30, 2026

Sodium Thiosulfate → HCID 15949498, compound

https://huagongshe.com/reaction/548703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 15949403HCID 15949403—
SolventAcetonitrileHCID 6342—
ProductHCID 15949498HCID 1594949841.6%

Reaction Steps

A solution of N-(1-ethyl-1H-pyrazol-3-yl)-3-{[(1S)-1-methyl-2-(methyloxy)ethyl]oxy}-5-[(4-methyl-5-oxo-2,3,4,5-tetrahydro-1,4-benzoxazepin-8-yl)oxy]benzamide (125 mg, 0.25 mmol) in acetonitrile (5 mL) was treated with trimethylsilyl iodide (0.178 mL) drop wise and stirred at RT under argon for 2.5 hours. Aqueous sodium thiosulphate solution (30 mL) was added to quench the reaction and the mixture was extracted with ethyl acetate (3×30 mL). The combined organic extracts were dried (MgSO4), filtered and evaporated to give a yellow oil. Purification was carried out by column chromatography on silica, eluting with 50-100% ethyl acetate in isohexane, to give the desired compound as a pale yellow foam (50 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943607B2
Source datasetuspto-grants-2011_05
ORD IDord-c8c4d1e9fa0147fb80fe99e0b363766b
Source noteuspto-grants-2011_05