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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595911Generated: November 1, 2026

N-bromobutanimide → 5-(6-Amino-5-bromopyridin-3-yl)piperidin-2-one

https://huagongshe.com/reaction/595911

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant5-(6-Aminopyridin-3-yl)piperidin-2-oneHCID 118045436—
SolventAcetonitrileHCID 6342—
Product5-(6-Amino-5-bromopyridin-3-yl)piperidin-2-oneHCID 118046352—

Reaction Steps

To a solution of 5-(6-aminopyridin-3-yl)piperidin-2-one (132 mg, 0.690 mmol) in Acetonitrile (8.00 mL) was added NBS (98 mg, 0.552 mmol) at 0° C. The reaction mixture was stirred for 30 min upon warming-up to room temperature. LCMS 0.28 min, MH+270/272; 0.7 min, MH+400.1/402.1 (SEM protected one). After quenched with Na2S2O3 solution, the reaction mixture was extracted with EtOAc, which was washed with NaHCO3 solution and brine. The organic layer was dried over anhydrous Na2SO4, filtered off, concentrated in vacuo. The crude 5-(6-amino-5-bromopyridin-3-yl)piperidin-2-one was used for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-07f3a6fb310940799de8d032032ca477
Source noteuspto-grants-2016_01