HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730747Generated: October 29, 2026
Water → Tert-butyl 4-(3,5,6-trifluoropyridin-2-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/730747
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,3,5,6-Tetrafluoropyridine | HCID 137749 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Tert-butyl 4-(3,5,6-trifluoropyridin-2-yl)piperazine-1-carboxylate | HCID 67398573 | — |
Reaction Steps
A mixture of 2,3,5,6-tetrafluoropyridine (755 mg, 5 mmol, Aldrich), 1-Boc-piperazine (558 mg, 3 mmol, Aldrich) and N,N-diisopropylethylamine (1 mL, 5.8 mmol, Aldrich) in NMP (5 mL) was heated at 150° C. for 16 h. The reaction mixture was cooled to room temperature, water (25 mL) was added, and the mixture was extracted with EtOAc (2×40 mL). The combined organic phases were washed with brine (50 mL), then dried over Na2SO4 and filtered. The filtrate was concentrated in vacuo and the residue was purified by silica gel column chromatography, eluting with 20% EtOAc/hexane to give the title compound as a white solid. MS (ESI, pos. ion) m/z: 318 (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-e1c5ce74141c4cd1ac37d5ade23b85ee |
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| Source note | uspto-grants-2009_09 |
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