HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730705Generated: October 25, 2026
Potassium Carbonate → Tert-butyl 4-(3-chloropyridin-2-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/730705
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,3-Dichloropyridine | HCID 16988 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Catalyst | Copper | HCID 23978 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl 4-(3-chloropyridin-2-yl)piperazine-1-carboxylate | HCID 11630777 | — |
Reaction Steps
A mixture of 2,3-dichloropyridine (10 g, 67.5 mmol, Aldrich), tert-butyl 1-piperazinecarboxylate (12.58 g, 67.5 mmol, Aldrich), copper powder (0.5 g, 7.8 mmol) and K2CO3 (9.33 g, 67.5 mmol) in DMF (100 mL) was stirred at 120° C. for 16 h. The reaction mixture was cooled to room temperature, concentrated in vacuo and the residue was dissolved in EtOAc (200 mL). The organic solution was washed with saturated aqueous solution of NaHCO3 (50 mL) and brine (50 mL), dried over Na2SO4, and filtered. The solvent was removed in vacuo and the residue was purified by silica gel column chromatography, eluting with 15% EtOAc/hexane, to give the title compound as an orange oil. MS (ESI, pos. ion) m/z: 298 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582761B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-8ec3d2d97ed5457598894e4b83e37840 |
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| Source note | uspto-grants-2009_09 |
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