HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026759Generated: November 3, 2026
Cyclobutylamine → N-{1-[2-(4-Fluorophenyl)pyridin-4-yl]ethyl}cyclobutaneamine
https://huagongshe.com/reaction/1026759
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyclobutylamine | HCID 75645 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-[2-(4-Fluorophenyl)pyridin-4-yl]ethanone | HCID 86690483 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-{1-[2-(4-Fluorophenyl)pyridin-4-yl]ethyl}cyclobutaneamine | HCID 86690484 | 97.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729271B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-0e2248f51d54413a915473444cabf1c7 |
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| Source note | uspto-grants-2014_05 |
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