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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1876800Generated: October 27, 2026

1,4-Diiodobutane → (4aRS,5SR,8aRS)-1-benzyl-5-(pyrrolidin-1-yl)perhydroquinoxaline-2,3-dione

https://huagongshe.com/reaction/1876800

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DiiodobutaneHCID 12337—
ReactantSodium BicarbonateHCID 516892—
Reactant(4aRS,5SR,8aRS)-5-amino-1-benzylperhydroquinoxaline-2,3-dioneHCID 68777664—
SolventAcetonitrileHCID 6342—
Product(4aRS,5SR,8aRS)-1-benzyl-5-(pyrrolidin-1-yl)perhydroquinoxaline-2,3-dioneHCID 68777117—

Reaction Steps

(4aRS,5SR,8aRS)-5-Amino-1-benzylperhydroquinoxaline-2,3-dione (3.06 g, 11.2 mmol) was dissolved in CH3CN (300 ml). NaHCO3 (6.4 g, 76.2 mmol) and 1,4-diiodobutane (13.9 g, 44.8 mmol, 5.9 ml) were added and the mixture was heated under reflux for 18 hours. NaHCO3 was separated off with a blue-band filter (Schleicher&Schuell) and the yellow solution was concentrated in vacuo. The solid was taken up in CH2Cl2 and the mixture was extracted by shaking three times with HCl (1 N). The aqueous phase was then brought to pH 8 with NaOH (2 N) and extracted by shaking three times with CH2Cl2. The organic phases were dried over Na2SO4 and evaporated in vacuo. A pale yellow solid was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309725B2
Source datasetuspto-grants-2012_11
ORD IDord-f8523a2b440a489c84e2be6a3be9cf77
Source noteuspto-grants-2012_11