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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2369010Generated: October 30, 2026

Sodium Thiosulfate → HCID 66584820, compound

https://huagongshe.com/reaction/2369010

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantN-IodosuccinimideHCID 120273—
ReactantHCID 66735705HCID 66735705—
SolventAcetonitrileHCID 6342—
ProductHCID 66584820HCID 6658482069%

Reaction Steps

To a solution of 5-(1-(tetrahydro-2H-pyran-4-ylamino)ethyl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (0.17 g, 0.32 mmol) in acetonitrile (15 ml) at 0° C. was added NIS (78 mg, 0.35 mmol) and stirring continued for 10 minutes. LC/MS showed no starting material (M.W=521) remaining. Saturated sodium thiosulfate solution (˜0.5 ml) was added and stirring continued for 5 minutes. After the acetonitrile was rotoevaporated, the aqueous phase was extracted with DCM (25 ml), washed with water (1×5 ml), brine (1×5 ml), dried over MgSO4. Solvent was removed in vacuo and the residue was purified by column chromatography on silica gel. Elution with MeOH/EtOAC (0-20%) gave desired product, 3-iodo-5-(1-(tetrahydro-2H-pyran-4-ylamino)ethyl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (0.14 g, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703784B2
Source datasetuspto-grants-2014_04
ORD IDord-dbc04f3acf31452d9e5b46a38d32cd85
Source noteuspto-grants-2014_04