HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804002Generated: October 25, 2026
Toluene → 4-(5-Cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/1804002
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Cyclobutylboronic acid | HCID 16217845 | — |
| Reactant | tert-Butyl 4-(5-bromo-3-methylpyridin-2-yl)piperazine-1-carboxylate | HCID 46739269 | — |
| Catalyst | Bis(tricyclohexylphosphine)palladium(II) Dichloride | HCID 11556747 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(5-Cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester | HCID 67380970 | 12.5% |
Reaction Steps
To a mixture of 4-(5-bromo-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (4.8 g), bis(tricyclohexylphosphine)palladium (II) dichloride (515 mg), tripotassium phosphate (16 g) and cyclobutylboronic acid (2.6 g) were added toluene (39 mL) and water (2 mL), and the mixture was refluxed for 8 hr. After cooling, the mixture was extracted with ethyl acetate, washed with saturated brine, and the solvent was evaporated. The residue was purified by column chromatography (hexane:ethyl acetate) to give 4-(5-cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (560 mg). 4-(5-cyclobutyl-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (560 mg) was dissolved in chloroform (1.5 mL), 4N hydrogen chloride/ethyl acetate (1.5 mL) was added, and the mixture was stirred at room temperature overnight. To the reaction mixture was added 1N aqueous sodium hydroxide solution (8 mL), and the mixture was extracted with chloroform. The organic layer was washed with saturated brine, and the solvent was evaporated to give the title compound (350 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08354401B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-7ce875a981d945d4af3c13d85682da8d |
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| Source note | uspto-grants-2013_01 |
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