Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387117Generated: November 2, 2026

Trimethylsilyl iodide → HCID 21182795, compound

https://huagongshe.com/reaction/1387117

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 21182999HCID 21182999—
SolventDichloromethaneHCID 6344—
ProductHCID 21182795HCID 2118279537.3%

Reaction Steps

The 379 mg of 6-benzyloxy-2-[4-[2-(1-pyrrolidinyl)ethoxy]phenyl]benzo[b]thiophen-3-yl 3-[(methoxycarbonyl)(methyl)amino]-4-(1-pyrrolidinylmethyl)phenyl ketone (Part G) was dissolved in 5.5 mL of dry CH2Cl2. To the solution was added 0.31 mL of trimethylsilyl iodide. The reaction mixture was stirred for 5.5 h. The reaction was quenched with 0.3 mL of MeOH and the mixture was concentrated to dryness under reduced pressure. Purification by flash chromatography (silica gel, 5% to 8% [10% conc NH4OH/MeOH]/CH2Cl2) afforded 130 mg (0.201 mmol, 37%) of a yellow foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-394de76fe0b3469c8ca834688fc81b83
Source noteuspto-grants-2001_07