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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1478591Generated: November 1, 2026

Triethylamine → tert-Butyl 3-((3-amino-6-bromopyrazin-2-ylamino)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1478591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Amino-3,5-dibromopyrazineHCID 620004—
Reactant1-Boc-3-(aminomethyl)piperidineHCID 2756483—
SolventDimethyl SulfoxideHCID 679—
Producttert-Butyl 3-((3-amino-6-bromopyrazin-2-ylamino)methyl)piperidine-1-carboxylateHCID 8662641526%

Reaction Conditions

Temperature130 °C

Reaction Steps

tert-butyl 3-(aminomethyl)piperidine-1-carboxylate (4.97 g, 22.40 mmol) was dissolved in DMSO (80 ml), and then 3,5-dibromopyrazine-2-amine (8.5 g, 33.60 mmol) and Et3N (6.3 ml) were added, followed by stirring at 130° C. overnight. After the completion of the reaction, the reaction mixture was extracted with H2O, EA, and brine, followed by drying (Na2SO4), filtration, and concentration under reduced pressure, and the residue was purified by column chromatography (EA:Hex=1:1), to give tert-butyl 3-(((3-amino-6-bromopyrazine-2-yl)amino)methyl)piperidine-1-carboxylate (2.19 g, two steps: 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403831B2
Source datasetuspto-grants-2016_08
ORD IDord-f3d96c62a7fc4619acc31183a04d7349
Source noteuspto-grants-2016_08