Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1249823Generated: November 2, 2026

Water → 5-fluoro-3-oxo-N-(5-phenyl-2-pyrazinyl)spiro[isobenzo-furan-1(3H),4'-piperidine]-1'-carboxamide

https://huagongshe.com/reaction/1249823

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantPhenyl 5-phenylpyrazin-2-ylcarbamateHCID 9879110—
Reactant5-Fluoro-3H-spiro[isobenzofuran-1,4'-piperidin]-3-one hydrochlorideHCID 22660730—
SolventChloroformHCID 6212—
Product5-fluoro-3-oxo-N-(5-phenyl-2-pyrazinyl)spiro[isobenzo-furan-1(3H),4'-piperidine]-1'-carboxamideHCID 995380196.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-fluorospiro[isobenzofuran-1(3H),4′-piperidine]-3-one hydrochloride (64 mg), phenyl N-(5-phenyl-2-pyrazinyl)carbamate (73 mg) and triethylamine (174 μL) in chloroform (5 mL) was stirred at 80° C. for 2 hours. The reaction mixture was poured into water and extracted with chloroform (20 mL). The organic layer was washed with saturated saline solution (20 mL), then dried over anhydrous Na2SO4 and concentrated. The residue was purified by column chromatography on silica gel (hexane/ethyl acetate=4/1 to 1/2) and recrystallized from ethyl ether-hexane to give the subject compound (100 mg) as colorless crystals (melting point 236-238° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06335345B1
Source datasetuspto-grants-2002_01
ORD IDord-99481ab3215944db8c68ccf51e6bc418
Source noteuspto-grants-2002_01