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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877834Generated: October 30, 2026

Trimethylsilyl iodide → HCID 68291912, compound

https://huagongshe.com/reaction/877834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 68350417HCID 68350417—
SolventAcetonitrileHCID 6342—
ProductHCID 68291912HCID 68291912105.5%

Reaction Steps

Iodotrimethylsilane (0.134 mL, 0.938 mmol) was added dropwise to a solution of (3S,4R)-benzyl 4-((6-bromo-3-carbamoylpyrrolo[1,2-b]pyridazin-4-yl)amino)-3-fluoro-3-methylpyrrolidine-1-carboxylate (115 mg, 0.235 mmol) in acetonitrile (3 mL). After 1 h at room temperature, the mixture was quenched with methanol (1 mL) and concentrated in vacuo. The solid residue was triturated with diethyl ether (3 mL) and filtered. The filter cake was rinsed with diethyl ether and dried under vacuum to give crude 6-bromo-4-(((3R,4S)-4-fluoro-4-methylpyrrolidin-3-yl)amino)pyrrolo[1,2-b]pyridazine-3-carboxamide hydroiodide (120 mg), which was used in the next step without further purification. MS (ES+) m/z: 356.0 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987268B2
Source datasetuspto-grants-2015_03
ORD IDord-19a5cca40d7c4f5d9622beffb57221fa
Source noteuspto-grants-2015_03