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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1622349Generated: November 4, 2026

Trimethylsilyl iodide → HCID 45275136, compound

https://huagongshe.com/reaction/1622349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 58378283HCID 58378283—
SolventDichloromethaneHCID 6344—
ProductHCID 45275136HCID 4527513698.3%

Reaction Steps

To a solution of benzyl-4-(1-(3,5-dichloropyridin-4-yl)piperidine-4-carbonyl)piperazine-1-carboxylate 13 (40 mg, 0.080 mmol) in DCM (1 mL), cooled to 0° C. was added trimethylsilyliodide (24 μL, 0.16 mmol) and the solution was stirred at this temperature for 90 min, after which time trimethylsilyl iodide (48 μL, 0.32 mmol) was added and the mixture warmed to room temperature. After stirring for a further 45 min, the solution was concentrated under reduced pressure and the crude product was purified on an SCX-2 cartridge (MeOH followed by 0.5 M NH3 in MeOH) to furnish the title compound as a yellow solid (27 mg, 94%), m.p. 256-258° C.; m/z (ESI) C15H20C12N4NaO requires 365.0906, found [M+Na]+ 365.0909.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778925B2
Source datasetuspto-grants-2014_07
ORD IDord-bea454855ee049fd8c1fd1207a7697d6
Source noteuspto-grants-2014_07