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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807725Generated: November 1, 2026

Potassium Fluoride → (S)-1-(2-Fluoro-4-(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)-piperazine-1-carbonyl)phenyl)-3-(1-hydroxybutan-2-yl)urea

https://huagongshe.com/reaction/1807725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium FluorideHCID 522689—
Reactant(S)-1-(4-(4-(4-(2-(tert-Butyldimethylsilyloxy)-1,1,1,3,3,3-hexafluoropropan-2-yl)benzyl)-piperazine-1-carbonyl)-2-fluorophenyl)-3-(1-hydroxybutan-2-yl)ureaHCID 59175877—
SolventTetrahydrofuranHCID 8028—
Product(S)-1-(2-Fluoro-4-(4-(4-(1,1,1,3,3,3-hexafluoro-2-hydroxypropan-2-yl)benzyl)-piperazine-1-carbonyl)phenyl)-3-(1-hydroxybutan-2-yl)ureaHCID 5917584973.5%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirring solution of (S)-1-(4-(4-(4-(2-(tert-butyldimethylsilyloxy)-1,1,1,3,3,3-hexafluoropropan-2-yl)benzyl)piperazine-1-carbonyl)-2-fluorophenyl)-3-(1-hydroxybutan-2-yl)urea (0.303 mmol, 215 mg) in tetrahydrofuran (1 mL) was added potassium fluoride (50% weight on celite) (1.517 mmol, 176 mg). The resulting suspension was heated to 80° C. for 48 hours. The reaction mixture was filtered through celite and concentrated under vacuum. The resulting residue was purified by SCX chromatography to afford the title compound (132.4 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357679B2
Source datasetuspto-grants-2013_01
ORD IDord-2dfad7203da5422e86e0f6c63f8280cd
Source noteuspto-grants-2013_01