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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1624130Generated: November 2, 2026

(Trifluoromethyl)trimethylsilane → HCID 74222541, compound

https://huagongshe.com/reaction/1624130

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Trifluoromethyl)trimethylsilaneHCID 552549—
ReactantTetrabutylammonium FluorideHCID 2724141—
ReactantHCID 86717958HCID 86717958—
SolventTetrahydrofuranHCID 8028—
ProductHCID 74222541HCID 742225418%

Reaction Steps

430 mg of 8-[(2,6-difluorobenzyl)oxy]-2-methyl-N-[(2R)-1-oxohexan-2-yl]imidazo[1,2-a]pyridine-3-carboxamide (1.05 mmol) were initially charged in 30 ml of dry THF, and 194 μl of trimethylsilyl trifluoromethane (1.24 mmol) and 621 μl of tetrabutylammonium fluoride solution (1.0 M in THF; 0.62 mmol) were successively added dropwise at 0° C. The reaction mixture was slowly warmed to RT, and stirring was continued overnight. The mixture was then concentrated and the residue was taken up in ethyl acetate, washed with saturated aqueous sodium bicarbonate solution, dried, filtered and concentrated. Preparative HPLC separation (Method 9) afforded 41 mg of the target compound, which was once more purified by HPLC (Method 10). This gave 28.4 mg of the target compound. The diastereomer ratio was about 3:1 (1H NMR integration).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08778964B2
Source datasetuspto-grants-2014_07
ORD IDord-d4dce23f4ade4df080e499c683ed2f48
Source noteuspto-grants-2014_07