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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46202Generated: October 28, 2026

Trimethylsilyl iodide → HCID 46889774, compound

https://huagongshe.com/reaction/46202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
Reactant2-(6-(2-Chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)pyridazin-3-yl)-5-methyloxazoleHCID 67287339—
SolventAcetonitrileHCID 6342—
ProductHCID 46889774HCID 4688977411.7%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-(6-(2-chloro-5-((2S,3S,4R,5R,6R)-3,4,5-tris(benzyloxy)-6-(benzyloxymethyl)-tetrahydro-2H-pyran-2-yl)benzyl)pyridazin-3-yl)-5-methyloxazole (1.2 mmol) from Step 2 in acetonitrile (5 mL) was added Iodotrimethylsilane (3 mL). The resulting reaction mixture was heated to 50° C. overnight. After cooling to 0° C., the reaction quenched with methanol and concentrated in vacuo. Purification by reverse phase preparative HPLC (Gilson®, SunFire™ Prep, 5 to 50% acetonitrile in water gradient) provided the title compound (62 mg, 0.14 mmol, 11%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541380B2
Source datasetuspto-grants-2013_09
ORD IDord-a4f933002906477da2381c4258aed56a
Source noteuspto-grants-2013_09