Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749703Generated: November 4, 2026

Formaldehyde → HCID 71278598, compound

https://huagongshe.com/reaction/1749703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPiperazin-2-oneHCID 231360—
ReactantHCID 1777704HCID 1777704—
SolventEthanolHCID 702—
ProductHCID 71278598HCID 7127859828%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of (Z)-2-[(1H-indol-3-yl)methylene]-6-hydroxybenzofuran-3(2H)-one (0.030 g, 0.11 mmol) obtained in Example A1, Step 1 in ethanol (3.0 mL) was added with 2-oxopiperazine (0.013 g, 0.13 mmol), and 37% aqueous formaldehyde (0.011 g, 0.13 mmol), and the mixture was stirred overnight at 80° C. in a sealed tube. The solvent was evaporated under reduced pressure, and then the residue was subjected to silica gel column chromatography (aminopropyl silica was used, eluted with chloroform/methanol (90:10)) to obtain (Z)-4({2-[(1H-indol-3-yl)methylene]-6-hydroxy-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazin-2-one (0.012 g, 28%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-766c0f078407499db6cb449028903e20
Source noteuspto-grants-2015_10