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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026759Generated: November 2, 2026

Cyclobutylamine → N-{1-[2-(4-Fluorophenyl)pyridin-4-yl]ethyl}cyclobutaneamine

https://huagongshe.com/reaction/1026759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutylamineHCID 75645—
ReactantSodium BicarbonateHCID 516892—
Reactant1-[2-(4-Fluorophenyl)pyridin-4-yl]ethanoneHCID 86690483—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
ProductN-{1-[2-(4-Fluorophenyl)pyridin-4-yl]ethyl}cyclobutaneamineHCID 8669048497.8%

Reaction Steps

Titanium(IV) isopropoxide (1.85 g) was added to a solution of cyclobutylamine (930 mg) in methanol (10 mL), and the mixture was stirred at room temperature for 10 min. A solution of 1-[2-(4-fluorophenyl)pyridin-4-yl]ethanone (350 mg) in methanol (5 mL) was added thereto and the mixture was stirred at room temperature overnight. Saturated sodium hydrogen carbonate solution was added to the reaction mixture, which was then filtered through Celite, and the solvent was distilled off under reduced pressure. After extracting with chloroform, the organic phase was separated out, and the solvent was distilled off under reduced pressure. The resulting residue was purified by column chromatography (NH silica gel cartridge, hexane:ethyl acetate=98:2-80:20) to afford the title compound (430 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729271B2
Source datasetuspto-grants-2014_05
ORD IDord-0e2248f51d54413a915473444cabf1c7
Source noteuspto-grants-2014_05