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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749999Generated: October 29, 2026

tert-butyl (E)-4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)vinyl]piperidine-1-carboxylate → HCID 178487112, compound

https://huagongshe.com/reaction/1749999

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl (E)-4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)vinyl]piperidine-1-carboxylateHCID 86682082—
ReactantHCID 178520025HCID 178520025—
CatalystPiperidineHCID 8082—
SolventMethanolHCID 887—
ProductHCID 178487112HCID 17848711277%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of tert-butyl (E)-4-[2-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)vinyl]piperidine-1-carboxylate (0.0692 g, 0.185 mmol) in methanol (5 mL) was added with 1H-indazole-3-carboxaldehyde (0.0270 g, 0.185 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 4-((E)-2-{(Z)-2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}vinyl)piperidine-1-carboxylate (0.0712 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-d3849690c80a42ed811bd5ca0c2a9400
Source noteuspto-grants-2015_10