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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384642Generated: October 29, 2026

2-Amino-5-bromopyrazine → HCID 59613433, compound

https://huagongshe.com/reaction/384642

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-bromopyrazineHCID 599539—
Reactanttert-Butyl(dimethyl)[(prop-2-yn-1-yl)oxy]silaneHCID 3445622—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
ProductHCID 59613433HCID 5961343391%

Reaction Conditions

Temperature60 °C

Reaction Steps

2-Amino-5-bromopyrazine (1.50 g, 8.6 mmol) was dissolved in anhydrous, deoxygenated DMF (24.5 mL) with triethylamine (10.5 mL). Copper(I) iodide (0.33 g, 1.7 mmol), tetrakis(triphenylphosphine)-palladium(0) (0.61 g, 0.51 mmol) and tert-butyldimethyl(prop-2-ynyloxy)silane (1.90 g, 11.2 mmol) were added and the solution was stirred overnight at 60° C., then cooled and partitioned between water and dichloromethane. The aqueous phase was extracted with dichloromethane and the combined organic phases were dried (Na2SO4) and evaporated. The residue was purified by silica chromatography to give 2-amino-5-(3-(tert-butyldimethylsilyloxy)prop-1-ynyl)pyrazine (2.06 g, 91%) as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367658B2
Source datasetuspto-grants-2013_02
ORD IDord-a9694d9ce95a4080ba633b35d4919f5c
Source noteuspto-grants-2013_02