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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403509Generated: November 2, 2026

2-Bromopyridine → (S)-tert-butyl 2-methyl-4-(pyridin-2-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1403509

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl (2S)-2-methylpiperazine-1-carboxylateHCID 10081508—
SolventDimethyl SulfoxideHCID 679—
Product(S)-tert-butyl 2-methyl-4-(pyridin-2-yl)piperazine-1-carboxylateHCID 7066534147%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of tert-butyl (2S)-2-methylpiperazine-1-carboxylate (8 g, 39.94 mmol) in DMSO (25 ml) was added 2-bromopyridine (6.594 g, 41.74 mmol), and DIEA (15.48 g, 119.78 mmol). After stirring 2 days at 120° C., the resulting solution was quenched by the addition of DCM (200 ml), washed with water (3×300 ml), dried over anhydrous magnesium sulfate and concentrated under reduced pressure to afford a residue, which was purified via silica gel chromatography (3% ethyl acetate in petroleum ether) to afford (S)-tert-butyl 2-methyl-4-(pyridin-2-yl)piperazine-1-carboxylate as a red oil (5.2 g, 47%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-0eca1fcfc8ac4cda9fac2206d9eefbd9
Source noteuspto-grants-2014_12