HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189271Generated: October 26, 2026
Cesium carbonate → 1-(4-(6-Nitropyridin-3-YL)piperazin-1-YL)ethan-1-one
https://huagongshe.com/reaction/2189271
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 5-Bromo-2-nitropyridine | HCID 817620 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-(6-Nitropyridin-3-YL)piperazin-1-YL)ethan-1-one | HCID 4780686 | 53.9% |
Reaction Steps
To a mixture of 5-bromo-2-nitropyridine (406 mg, 2 mmol) and 1-acetylpiperazine (256 mg, 2 mmol) in toluene (5 mL) is added Cs2CO3, then Pd2(dba)3 (74 mg, 0.08 mmol) and BINAP (100 mg, 0.16 mmol) are added. The mixture is degassed, and heated at 100° C. for 16 hours. Then the mixture is cooled down to room temperature, diluted with EtOAc, and filtered through celite. The filtrate is concentrated under reduced pressure. The crude product is purified by column chromatography (SiO2, MeOH:CH2Cl2=0.7:99.3 to 6:93) to give 270 mg of the title compound as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08324225B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-f6e4a121a91e43aea060ec5808bd5e65 |
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| Source note | uspto-grants-2012_12 |
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