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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108690Generated: October 30, 2026

Methanol → 5-(4-Nitro-phenyl)-furan-2-carboxylic acid (1-aza-bicyclo[2.2.2]oct-3-yl)-amide

https://huagongshe.com/reaction/2108690

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantQuinuclidine, 3-amino-, dihydrochlorideHCID 197853—
Reactant5-(4-nitrophenyl)furan-2-carbonyl ChlorideHCID 3829983—
ReactantSodium MethoxideHCID 10942334—
SolventDichloromethaneHCID 6344—
Product5-(4-Nitro-phenyl)-furan-2-carboxylic acid (1-aza-bicyclo[2.2.2]oct-3-yl)-amideHCID 4840026—

Reaction Steps

A mixture of (±)3-aminoquinuclidine dihydrochloride, methanol (250 ml), sodium methoxide (5.1 g, 95 mmol) was stirred at reflux for 1 hour. The mixture was evaporated and was mixed with methanol (150 ml) and dichloromethane (100 ml) was added and cooled on ice, and 5-(4-nitrophenyl)-2-furoyl chloride (11.2 g, 44.5 mmol), solved in dichloromethane (200 ml) was added drop-wise at 0° C. The mixture was stirred at room temperature for 21 hours. The mixture was evaporated, water (200 ml) was added and the pH was adjusted to 8.5 with triethylamine. The mixture was extracted with ethyl acetate (3×200 ml) and the pure product was isolated as free base. Yield 5.0 g (33%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514450B2
Source datasetuspto-grants-2009_04
ORD IDord-0f8b4a7839d343c9b4aa5ae50993071d
Source noteuspto-grants-2009_04