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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894261Generated: October 30, 2026

4,4-Dimethylpiperidin-2-one → 1-(5-Bromo-pyrazin-2-yl)-4,4-dimethyl-pyrrolidin-2-one

https://huagongshe.com/reaction/1894261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4-Dimethylpiperidin-2-oneHCID 12202097—
Reactant2-Bromo-5-iodopyrazineHCID 21931200—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product1-(5-Bromo-pyrazin-2-yl)-4,4-dimethyl-pyrrolidin-2-oneHCID 5751678153.2%

Reaction Steps

To a well stirred suspension of 2-bromo-5-iodopyrazine (300 mg, 1.05 mmol), 4,4-dimethylpiperidin-2-one (155 mg, 1.37 mmol, 1.3 equiv.) and 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene (xantphos) (24.4 mg, 0.042 mmol, 0.04 equiv.) in 4 ml of toluene were added under argon atmosphere tris(dibenzylideneacetone)dipalladium(0) (Pd2(dba)3), (19.3 mg, 0.021 mmol, 0.02 equiv.) and the mixture was stirred for 5 hours at 100° C. The crude mixture was adsorbed on silicagel and purified by flash chromatography over a 20 g silicagel column using a 2:1 heptane/ethyl acetate mixture as eluant. The title compound (151 mg, 53% yield) was obtained as a white solid, MS: m/e=270.1, 272.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513273B2
Source datasetuspto-grants-2013_08
ORD IDord-86e4b31a179d4f9ab29cfdd5f337d04b
Source noteuspto-grants-2013_08