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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182256Generated: October 30, 2026

Trimethylsilyl iodide → HCID 22477326, compound

https://huagongshe.com/reaction/2182256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 22477636HCID 22477636—
SolventAcetonitrileHCID 6342—
ProductHCID 22477326HCID 2247732666.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 2-(6-benzyloxy-5-methoxy-1-methyl-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine [1.24 g, Reference Example 13(p)] in acetonitrile (100 mL) was treated with iodotrimethylsilane (820 μl). The reaction mixture was stirred at 50° C. for 2 hours and then concentrated in vacuo. The residue was treated with water (40 mL) and the mixture was extracted three times with dichloromethane (100 mL). The combined organic phases were washed with brine (40 mL), then dried over magnesium sulfate and then evaporated. The residue was subjected to flash column chromatography on silica eluting with a mixture of cyclohexane and ethyl acetate (1:1, v/v) to give the title compound (686 mg) as a white foam. TLC: RF=0.27 (cyclohexane/ethyl acetate: 1/1). MS: EI (70 eV); m/z=447 M+.(45%); 292 (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897207B2
Source datasetuspto-grants-2005_05
ORD IDord-939820a6d6484d57b99719c093c74a7d
Source noteuspto-grants-2005_05