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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916589Generated: November 2, 2026

1-Pyrrolidineethanamine → 5-Bromo-N-[2-(pyrrolidin-1-yl)ethyl]pyridin-2-amine

https://huagongshe.com/reaction/1916589

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PyrrolidineethanamineHCID 1344—
ReactantPotassium CarbonateHCID 11430—
Reactant2,5-DibromopyridineHCID 69353—
ReactantBinap, (A+-)-HCID 634876—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product5-Bromo-N-[2-(pyrrolidin-1-yl)ethyl]pyridin-2-amineHCID 62642748—

Reaction Steps

13.8 g (100.0 mmol) K2CO3, 79 mg (0.12 mmol) 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl and 28 mg (0.12 mmol) Pd(OAc)2 are added successively to a solution of 1.5 g (6.33 mmol) 2,5-dibromopyridine and 0.98 mL (7.60 mmol) 1-(2-aminoethyl)-pyrrolidine in 60 mL toluene. The reaction is refluxed for 40 h. The solvent is eliminated i.vac. and the residue is taken up in 150 mL EtOAc and 100 mL water. The organic phase is dried over Na2SO4 and the solvent is eliminated i.vac. Purification is carried out by column chromatography on silica gel (gradient: EtOAc/MeOH/NH3 19:1:0.1 to EtOAc/MeOH/NH3 9:1:0.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618132B2
Source datasetuspto-grants-2013_12
ORD IDord-7129f45d21e24b6fb1a6b29c9ffb5bd5
Source noteuspto-grants-2013_12