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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749992Generated: October 31, 2026

Piperidine → HCID 178487152, compound

https://huagongshe.com/reaction/1749992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTert-butyl 4-[4-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)but-3-enyl]piperidine-1-carboxylateHCID 86682079—
ReactantHCID 178520025HCID 178520025—
SolventMethanolHCID 887—
ProductHCID 178487152HCID 17848715284%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of tert-butyl 4-[4-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)but-3-enyl]piperidine-1-carboxylate (0.0265 g, 0.0660 mmol) in methanol (3 mL) was added with 1H-indazole-3-carboxaldehyde (0.00964 g, 0.0660 mmol) and piperidine (0.0800 mL, 0.810 mmol), 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-((Z)-4-{(Z)-2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}but-3-enyl)piperidine-1-carboxylate (0.0293 g, 84%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-0e5327ef6c6347f191c2e0a562bb5f29
Source noteuspto-grants-2015_10