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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358500Generated: November 2, 2026

Trimethylsilyl iodide → HCID 56975984, compound

https://huagongshe.com/reaction/1358500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 57248052HCID 57248052—
SolventChloroformHCID 6212—
ProductHCID 56975984HCID 5697598452.7%

Reaction Steps

To an ice cooled solution of 1-[(2S,3R)-2-benzyloxy-5-(6-chloroindol-1-yl)-3-pentyl]imidazole-4-carboxamide (47.9 mg, 0.110 mmol) in chloroform (5 ml) was added trimethylsilyl iodide (42.6 mg, 0.213 mmol). After 3 minutes, the ice bath was removed, and then stirred at room temperature for 3 hours. The reaction was quenched by addition of methanol. This mixture was extracted with ethyl acetate, and the extracts were washed with brine, dried (sodium sulfate) and evaporated in vacuo. The residue was purified by silica gel (1.5 g) chromatography eluting with chloroform/methanol (50:1 to 10:1) to give 1-[(2S,3R)-5-(6-chloroindol-1-yl)-2-hydroxy-3-pentyl]imidazole-4-carboxamide (20.1 mg, 52.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06596738B1
Source datasetuspto-grants-2003_07
ORD IDord-58a016a26078479a88a5175169dd0201
Source noteuspto-grants-2003_07