HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912840Generated: October 29, 2026
Phthalimide potassium salt → tert-Butyl 4-(6-amino-3,5-difluoropyridin-2-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/912840
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phthalimide potassium salt | HCID 24194345 | — |
| Reactant | Tert-butyl 4-(3,5,6-trifluoropyridin-2-yl)piperazine-1-carboxylate | HCID 67398573 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | tert-Butyl 4-(6-amino-3,5-difluoropyridin-2-yl)piperazine-1-carboxylate | HCID 86593828 | — |
Reaction Steps
A mixture of 4-(3,5,6-trifluoro-pyridin-2-yl)-piperazine-1-carboxylic acid tert-butyl ester (1.59 g, 5 mmol, Example 39a), potassium phthalimide (0.93 g, 5 mmol, Aldrich) in DMF (20 mL) was heated at 140° C. with stirring for 16 h. The reaction mixture was cooled to room temperature, diluted with water (60 mL) and extracted with EtOAc (2×70 mL). The combined organic extracts were dried over Na2SO4, and filtered. The filtrate was evaporated and the residue was purified by silica gel column chromatography, eluting with 20% EtOAc in hexane to give the title compound as a yellow solid. MS (ESI, pos. ion) m/z: 315 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08026241B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-3e5d602ceecf4ee3a70a059a46b269d3 |
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| Source note | uspto-grants-2011_09 |
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