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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444966Generated: October 30, 2026

Cesium carbonate → HCID 69146057, compound

https://huagongshe.com/reaction/444966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantAmmonium ChlorideHCID 25517—
ReactantBinap, (A+-)-HCID 634876—
Reactant1-AllylpiperazineHCID 806422—
Reactant5-Bromo-2-nitropyridineHCID 817620—
SolventTolueneHCID 1140—
ProductHCID 69146057HCID 69146057—

Reaction Conditions

Temperature120 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476275B2
Source datasetuspto-grants-2013_07
ORD IDord-ec471ef36d7f4c5d83d9dedad4aef415
Source noteuspto-grants-2013_07