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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719975Generated: October 30, 2026

Diisopropylethylamine → 5-(2-Methylprop-1-en-1-yl)pyrazin-2-amine

https://huagongshe.com/reaction/719975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantLithium ChlorideHCID 433294—
Reactant2-Amino-5-bromopyrazineHCID 599539—
ReactantTributyl(2-methylprop-1-enyl)stannaneHCID 11759721—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product5-(2-Methylprop-1-en-1-yl)pyrazin-2-amineHCID 2189729426%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of the crude isobutenyltri-n-butyltin (6.90 g, 58 purity), 2-amino-5-bromopyrazine (1.92 g, 11 mmol), and N,N-diisopropylethylamine (5 mL) in N,N-dimethylformamide (50 mL) was treated with lithium chloride (2.0 g) and tetrakis(triphenylphosphine)palladium(0) (381 mg, 0.33 mmol). The mixture was stirred at 130° C. for 4 h, at which time, thin layer chromatography indicated complete consumption of the starting material. The mixture was concentrated in vacuo. The residue was treated with a saturated aqueous potassium fluoride solution and then extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230–400 mesh, 1.5/1 hexanes/ethyl acetate) afforded 2-amino-5-(2,2-dimethylvinyl)-pyrazine (420 mg, 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132425B2
Source datasetuspto-grants-2006_11
ORD IDord-82edf9a5ea144812907b8b8bcc1b70a6
Source noteuspto-grants-2006_11