HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307793Generated: November 1, 2026
3,5-Dibromopyridine → Tert-butyl 4-(5-bromopyridin-3-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/2307793
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3,5-Dibromopyridine | HCID 69369 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Tert-butyl 4-(5-bromopyridin-3-yl)piperazine-1-carboxylate | HCID 11653049 | — |
Reaction Steps
A solution of the 3,5-dibromo-pyridine (12.8 g, 68.8 mmol) and piperazine-1-carboxylic acid tert butyl ester (10 g, 42.4 mmol) in 200 mL of dioxane was treated with Pd2(dba)3 (5 g, 5.5 mmol), 2-(di-tbutyl-phosphino)biphenyl (4 g, 13.4 mmol), and sodium t-butoxide (7.2 g, 75 mmol). The reaction was heated to 95° C. for 8 h then cooled and filtered through celite. The mixture was evaporated and the residue was purified by flash column chromatography on silica gel, eluting with a solvent gradient of 1:4 ethyl acetate/hexane to 100% ethyl acetate. Recovered 2.9 g of product (20%). MS (ESI) m/z 344 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06831175B2 |
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| Source dataset | uspto-grants-2004_12 |
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| ORD ID | ord-b0ab05137684442bb98b6abe41667324 |
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| Source note | uspto-grants-2004_12 |
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