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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595925Generated: October 31, 2026

N-bromobutanimide → 4-(6-Amino-5-bromopyridin-3-yl)-1-methylpyrrolidin-2-one

https://huagongshe.com/reaction/595925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(6-Aminopyridin-3-yl)-1-methylpyrrolidin-2-oneHCID 118047020—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product4-(6-Amino-5-bromopyridin-3-yl)-1-methylpyrrolidin-2-oneHCID 118045587—

Reaction Steps

To 4-(6-aminopyridin-3-yl)-1-methylpyrrolidin-2-one (90 mg, 0.377 mmol) in Acetonitrile 3 mL) in ice bath was added NBS (60.3 mg, 0.339 mmol). The reaction mixture was stirred in ice bath for 15 min and room temperature for 30 min. LC-MS shows mixture of SM and product. Added 0.1 equiv. more of NBS and stirred another 1h at room temperature. Reaction mixture was diluted with EtOAc and added 2 mL of Satd sodium bicarbonate. Stirred 10 min. The organic layer was separated, dried over sodium sulfate, filtered and evaporated. Proceed for next step (73%). LCMS (m/z): 270.2/272.2 (MH+), 0.302 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-2ce8528b38cf46b690634c6c82f7413d
Source noteuspto-grants-2016_01