HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403569Generated: October 26, 2026
tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/2403569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 3-Bromo-2-methylpyridine | HCID 1201003 | — |
| Reactant | Sodium tert-butoxide | HCID 45051916 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate | HCID 68106327 | 98% |
Reaction Steps
3-Bromo-2-methylpyridine (500 mg) and tert-butyl piperazine-1-carboxylate (650 mg) were dissolved in toluene (7.5 ml), and (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one_palladium (3:2) (40 mg), 1,1′-binaphthalene-2,2′-diylbis(diphenylphosphine) (18 mg), and 2-methylpropan-2-ol sodium (391 mg) were added thereto in this order under a nitrogen atmosphere, followed by warming to 100° C. and stirring overnight. The reaction mixture was subjected to liquid separation with CHCl3 and water, the organic layer was dried over Na2SO4, and then the solvent was evaporated. The obtained residue was purified by silica gel column chromatography (CHCl3 to 5% MeOH/CHCl3) to obtain tert-butyl 4-(2-methylpyridin-3-yl)piperazine-1-carboxylate (790 mg) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802679B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-98cadd563f1c443daa2dfa7faf16755c |
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| Source note | uspto-grants-2014_08 |
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