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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1994411Generated: October 30, 2026

Trimethylsilyl iodide → HCID 59134035, compound

https://huagongshe.com/reaction/1994411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 68693749HCID 68693749—
SolventAcetonitrileHCID 6342—
ProductHCID 59134035HCID 5913403586.6%

Reaction Steps

103 mg (0.517 mmol) of iodotrimethylsilane were added to a solution of 104 mg (0.129 mmol) of benzyl 4-[6-(4-chlorobenzyl)-1-(2,4-dichlorobenzenesulfonyl)-8-isopropyl-4,7-dioxooctahydropyrazino[1,2-a]pyrimidin-3-ylcarbamoyl]piperidine-1-carboxylate in 2.5 ml of acetonitrile at room temperature with stirring. After 2 hours, the mixture was concentrated. The residue was purified on a Varian Bond-Elut SCX ion exchange cartridge (elution with methanol, then with 3N—NH3 in methanol). The purified amine was converted into the hydrochloride salt. 75 mg of the desired compound were obtained. LC/MS (expected monoisotopic MW=669.13; measured value (M+H)=670)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07652007B2
Source datasetuspto-grants-2010_01
ORD IDord-d22e67cbe53f48049e60cc2d67e7e88f
Source noteuspto-grants-2010_01