HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444966Generated: October 30, 2026
Cesium carbonate → HCID 69146057, compound
https://huagongshe.com/reaction/444966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | 1-Allylpiperazine | HCID 806422 | — |
| Reactant | 5-Bromo-2-nitropyridine | HCID 817620 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69146057 | HCID 69146057 | — |
Reaction Steps
315 mg (2.5 mmol) of N-allylpiperazine were dissolved in 5 ml of toluene under an argon atmosphere. 93 mg (0.1 mmol) of tris-(dibenzylideneacetone)-dipalladium(0) (Pd2 dba3), 126 mg (0.2 mmol) of 2,2′-bis-(diphenylphosphino)-1,1′-binaphthyl (BINAP), 1.14 g (3.5 mmol) of cesium carbonate and 515 mg (2.54 mmol) of 5-bromo-2-nitropyridine were then added and the mixture was stirred at 120° C., in a microwave oven, for 4 hours. After the reaction mixture had cooled down to room temperature, a saturated aqueous solution of ammonium chloride was added. After that, the aqueous reaction mixture was extracted three times with in each case 50 ml of ethyl acetate. After the organic phase had been dried over sodium sulfate, the drying agent had been filtered off and the solvent had been evaporated down to dryness, the residue was chromatographed through silica gel using ethyl acetate/methanol (4:1), with 304 mg (46% of theory) of the title compound being obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08476275B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ec471ef36d7f4c5d83d9dedad4aef415 |
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| Source note | uspto-grants-2013_07 |
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