Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 549053Generated: October 30, 2026

Sodium Iodide → HCID 22477340, compound

https://huagongshe.com/reaction/549053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantHCID 22477493HCID 22477493—
SolventAcetonitrileHCID 6342—
ProductHCID 22477340HCID 2247734058.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

A solution of 2-(5-benzyloxy-6-methoxy-1-methyl-1H-indol-3-yl)-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine [6.26 g, Reference Example 13(e)] in acetonitrile (500 mL) was treated with sodium iodide (4.38 g) followed by trimethylsilyl chloride (3.17 mL). The mixture stirred at 40° C. for 3 hours then treated with further portions of sodium iodide (4.38 g) and trimethylsilyl chloride (3.17 mL). After stirring at 40° C. for a further 12 hours the reaction mixture was evaporated. The residue was treated with water (200 mL) and the mixture was extracted three times with ethyl acetate (200 mL). The combined extracts were dried over magnesium sulfate then evaporated. The residual brown foam was triturated with ethyl acetate and diisopropyl ether to give the title compound (3.04 g) as a light brown solid, m.p. 211-214° C. HPLC (METHOD A): RT=9.30 minutes.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07943616B2
Source datasetuspto-grants-2011_05
ORD IDord-75f93f947f854dc1bbe766277069eb25
Source noteuspto-grants-2011_05