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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750012Generated: November 3, 2026

Piperidine → HCID 178487159, compound

https://huagongshe.com/reaction/1750012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 71278755HCID 71278755—
ReactantHCID 178520025HCID 178520025—
SolventMethanolHCID 887—
ProductHCID 178487159HCID 17848715991.8%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of tert-butyl 4-[4-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)-2-methylbut-3-yn-2-yl]piperazine-1-carboxylate (0.113 g, 0.273 mmol) in methanol (1 mL) was added with 1H-indazole-3-carboxaldehyde (0.0399 g, 0.273 mmol) and piperidine (0.0186 g, 0.218 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 (Z)-4-(4-{2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}-2-methylbut-3-yn-2-yl)piperazine-1-carboxylate (0.136 g, 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-b2f421c320d4473d96e9c52797adccbf
Source noteuspto-grants-2015_10