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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247018Generated: October 30, 2026

Potassium Carbonate → (S)-N-{3-[4-(4-(Prop-2-yn-1-yl)-4-hydroxypiperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide

https://huagongshe.com/reaction/2247018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantAmmonium ChlorideHCID 25517—
ReactantN-[(5S)-3-[3-fluoro-4-(4-oxopiperidinyl)phenyl]-2-oxo-5-oxazolidinyl]methylacetamideHCID 54375226—
ReactantHCID 178506808HCID 178506808—
SolventTetrahydrofuranHCID 8028—
Product(S)-N-{3-[4-(4-(Prop-2-yn-1-yl)-4-hydroxypiperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamideHCID 1174959519%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A mixture of lithio(trimethylsilyl)acetylene (1.72 mmol) and (S)-N-{3-[4-(4-oxo-piperidin-1-yl)-3-fluorophenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide (1.72 mmol) in tetrahydrofuran (10 ml) was stirred at a temperature −78° C. for 15 minutes. It was allowed to come to room temperature and further stirred for 18 hours. The reaction mixture was then stirred with aqueous solution of ammonium chloride, the reaction mixture was extracted with ethyl acetate (3×40 ml). The removal of the solvent provided a residue, which was stirred in aqueous methanolic (15 ml) solution of potassium carbonate (1.72 mmol) for 3 hours. The solvent was removed and the residual mass was purified by column chromatography over silica gel to provide title compound in 19% yield. M.P. 166-167° C. and MS (M+1)=376 (MH+, 100%) M.F.=C19H22FN3O4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687627B2
Source datasetuspto-grants-2010_03
ORD IDord-390733df9c69438e8afeb15ed0c065d8
Source noteuspto-grants-2010_03