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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852780Generated: October 30, 2026

Chlorotrimethylsilane → HCID 178517977, compound

https://huagongshe.com/reaction/852780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantLithium diisopropylamideHCID 2724682—
ReactantSelectfluorHCID 2724933—
ReactantHCID 178517976HCID 178517976—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178517977HCID 178517977—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A dry 100 mL round-bottomed flask was charged with 5-cyclopentyl-2-(2-fluorophenylamino)thiazol-4(5H)-one (0.200 g, 0.717 mmol) and 6.0 mL of THF. This solution was cooled to −78° C., and LDA (2.0 M in THF/heptane/ethyl benzene, 1.43 mL, 2.86 mmol) was added. The resulting brown solution was allowed to stir at that temperature for 1 h, then TMSCl (0.623 g, 0.725 mL, 5.74 mmol) was added. The solution was warmed to room temperature and allowed to stir for an additional 1 h. The solution was concentrated in vacuo to remove the volatiles and then redissolved in 10 mL of CH3CN. Selectfluor (0.508 g, 1.43 mmol) was added at room temperature, and the resulting solution was stirred for 2 h. The reaction was quenched with saturated aqueous NaHCO3, and the resulting mixture was thoroughly extracted with CH2Cl2. This combined organic extracts were dried and concentrated in vacuo to give an oil which was purified by column chromatography (100% to 70% hexanes/30% ethyl acetate) to give the title compound as a colorless oil. Mass Spec (M+H)+; 297.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253196B2
Source datasetuspto-grants-2007_08
ORD IDord-a76c341eaa364f629cf0518846328717
Source noteuspto-grants-2007_08