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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474361Generated: November 4, 2026

4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-one → 5-(1-hydroxy-2-{4-[2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-yl}ethyl)-4-methyl-2-benzofuran-1(3H)-one

https://huagongshe.com/reaction/1474361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-methyl-5-(oxiran-2-yl)isobenzofuran-1(3H)-oneHCID 55270555—
Reactant4-methyl-5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-oneHCID 59568688—
SolventEthanolHCID 702—
Product5-(1-hydroxy-2-{4-[2-(4-methyl-1-oxo-1,3-dihydro-2-benzofuran-5-yl)ethyl]piperazine-1-yl}ethyl)-4-methyl-2-benzofuran-1(3H)-oneHCID 49804478—

Reaction Conditions

Temperature150 °C

Reaction Steps

4-Methyl-5-oxiran-2-yl-2-benzofuran-1(3H)-one (60 mg, 0.31 mmol, 1.2 mmol) and 4-methyl-5-(2-piperazin-1-ylethyl)-2-benzofuran-1(3H)-one (68 mg, 0.26 mmol, 1.0 eq) were suspended in ethanol (5 ml) in a microwave tube. The tube was capped, degassed under vacuum, and purged with nitrogen gas. The mixture was heated to 150° C. for 30 min under microwave irradiation. The mixture was then concentrated and purified by flash column chromatography (0-10% MeOH/DCM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018211B2
Source datasetuspto-grants-2015_04
ORD IDord-04671f86f73244c8bc2d87c778c3a1d9
Source noteuspto-grants-2015_04