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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 869157Generated: October 30, 2026

Trimethylsilyl iodide → HCID 67451810, compound

https://huagongshe.com/reaction/869157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 67454077HCID 67454077—
SolventMethanolHCID 887—
SolventAcetonitrileHCID 6342—
ProductHCID 67451810HCID 6745181088%

Reaction Steps

Benzyl 2-(5-(6-((1-(3-fluoropyridin-2-yl)cyclobutyl)methylamino)pyridazin-3-yl)-1H-indazol-3-ylamino)ethylcarbamate (48 mg, 84 μmol) was dissolved in acetonitrile (5 mL), and TMSI (0.5 mL) was added. The reaction was stirred for 15 min, diluted with methanol (15 mL), concentrated, and was directly purified by reverse phase column chromatography to yield 20 mg (88%) of N1-(5-(6-((1-(3-fluoropyridin-2-yl)cyclobutyl)methylamino)pyridazin-3-yl)-1H-indazol-3-yl)ethane-1,2-diamine as a yellow solid, m/z=433 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969346B2
Source datasetuspto-grants-2015_03
ORD IDord-68db51973d244a919404f57efbe15a91
Source noteuspto-grants-2015_03