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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1749887Generated: November 1, 2026

HCID 71278867, compound → HCID 178487199, compound

https://huagongshe.com/reaction/1749887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71278867HCID 71278867—
ReactantHCID 178520025HCID 178520025—
CatalystPiperidineHCID 8082—
SolventMethanolHCID 887—
ProductHCID 178487199HCID 17848719985%

Reaction Conditions

Temperature60 °C

Reaction Steps

A solution of tert-butyl 4-[1-(6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl)-ethyl]piperazine-1-carboxylate (0.091 g, 0.24 mmol) in methanol (3.0 mL) was added with 1H-indazole-3-carboxaldehyde (0.039 g, 0.27 mmol). Then, the mixture was added with 5 drops of piperidine, and then the mixture was stirred at 60° C. for 1 hour. 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 (100:0→97:3)) to obtain tert-butyl (Z)-4-(1-{2-[(1H-indazol-3-yl)methylene]-6-methoxy-3-oxo-2,3-dihydrobenzofuran-7-yl}ethyl)piperazine-1-carboxylate (0.10 g, 85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156827B2
Source datasetuspto-grants-2015_10
ORD IDord-21d27cd9b26841ae8e67e0cd89ad60a1
Source noteuspto-grants-2015_10