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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413313Generated: October 29, 2026

Tetrabutylammonium Fluoride → HCID 59063640, compound

https://huagongshe.com/reaction/413313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant(R)-N-[5-(1-(tert-Butyl-dimethyl-silanyloxy)-2-{2-[4-(2-methyl-thiazol-4-yl)-phenoxy]-ethylamino}-ethyl)-pyridin-2-yl]-acetamideHCID 69743740—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59063640HCID 5906364083.4%

Reaction Steps

To a solution of (R)-N-[5-(1-(tert-butyl-dimethyl-silanyloxy)-2-{2-[4-(2-methyl-thiazol-4-yl)-phenoxy]-ethylamino}-ethyl)-pyridin-2-yl]-acetamide (115 mg, 0.218 mmol) in tetrahydrofuran (1.5 mL) was added tetrabutylammonium fluoride (1.0 M in tetrahydrofuran, 0.65 mL, 0.65 mmol) at room temperature. The resulting solution was allowed to stir for about two and one-half hours, and the reaction mixture was then partitioned between ethyl acetate and water. The pH of the mixture was adjusted to about 10-11, and the aqueous phase was then extracted with ethyl acetate. The combined organic extracts were washed with brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The resulting crude material was purified by column chromatography (methylene chloride to 20% methanol/methylene chloride) to afford 75 mg (83%) of the desired product. LRMS ([M+1]+): 413.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566377B2
Source datasetuspto-grants-2003_05
ORD IDord-d5bc922983cb4c19a1a7894614d258df
Source noteuspto-grants-2003_05