Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750018Generated: November 3, 2026

Tert-butyl 4-[(3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate → HCID 178452294, compound

https://huagongshe.com/reaction/1750018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-[(3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylateHCID 60155978—
ReactantHCID 178520050HCID 178520050—
CatalystPiperidineHCID 8082—
SolventMethanolHCID 887—
ProductHCID 178452294HCID 17845229448%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of tert-butyl 4-[(3-oxo-2,3-dihydrobenzofuran-7-yl)methyl]piperazine-1-carboxylate (0.0442 g, 0.133 mmol) synthesized in Example B45, Step 3 in methanol (3 mL) was added with 1H-pyrazolo[3,4-b]pyridine-3-carboxaldehyde (0.0206 g, 0.140 mmol) and piperidine (7 drops), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was concentrated, and the resulting residue was purified by silica gel column chromatography (chloroform/methanol) to obtain tert-butyl (Z)-4-({2-[(1H-pyrazolo[3,4-b]pyridin-3-yl)methylene]-3-oxo-2,3-dihydrobenzofuran-7-yl}methyl)piperazine-1-carboxylate (0.0292 g, 48%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-7a03441f2af74b8d9896069f5fcf2041
Source noteuspto-grants-2015_10