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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1935704Generated: October 26, 2026

Water → N-[5-(3-hydroxyphenyl)-2-pyrazinyl]-3-oxospiro[isobenzofuran-1(3H),4'-piperidine]-1'-carboxamide

https://huagongshe.com/reaction/1935704

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant3H-spiro[isobenzofuran-1,4'-piperidin]-3-one hydrochlorideHCID 22380631—
ReactantPhenyl N-[5-(3-hydroxyphenyl)-2-pyrazinyl]carbamateHCID 22660683—
SolventChloroformHCID 6212—
ProductN-[5-(3-hydroxyphenyl)-2-pyrazinyl]-3-oxospiro[isobenzofuran-1(3H),4'-piperidine]-1'-carboxamideHCID 2266074634.7%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of spiro[isobenzofuran-1(3H),4′-piperidine]-3-one hydrochloride (40 mg), phenyl N-[5-(3-hydroxyphenyl)-2-pyrazinyl]carbamate (51 mg) and triethylamine (119 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) and then dried over anhydrous Na2SO4. The concentration of the solvent left a residue, which was purified by column chromatography on silica gel (hexane/ethyl acetate=4/1 to 1/2) followed by recrystallization from ethyl ether-hexane to give the subject compound (24 mg) as colorless crystals (melting point 257-259° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388077B1
Source datasetuspto-grants-2002_05
ORD IDord-36e0424338684c12b4e316664229e734
Source noteuspto-grants-2002_05