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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 547467Generated: October 30, 2026

Triethylamine → 3,5-Bis-trimethylsilanylethynyl-pyrazin-2-ylamine

https://huagongshe.com/reaction/547467

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Amino-3,6-dibromopyrazineHCID 51051665—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product3,5-Bis-trimethylsilanylethynyl-pyrazin-2-ylamineHCID 8663360082.7%

Reaction Steps

Trimethylsilylacetylene (11.1 mL, 80 mmol) was added to a solution of 2-amino-3,6-dibromopyrazine (5.06 g, 20 mmol), Pd(PPh3)2Cl2 (0.140 g, 0.20 mmol), triethylamine (11.4 mL, 80 mmol) and copper(I) iodide (0.114 g, 0.60 mmol) in 50 mL of tetrahydrofuran at 0-5° C. The reaction mixture was allowed to warm to RT and stirred for 64 h. Additional trimethylsilylacetylene (5.6 mL, 40 mmol), Pd(PPh3)2Cl2 (0.140 g, 0.20 mmol) and copper(I) iodide (0.114 g, 0.60 mmol) were added, and the mixture was stirred at 50° C. for 22 h then allowed to cool to RT. The mixture was diluted with 200 mL of ethyl acetate and 200 mL of hexanes, then sequentially washed with three 200 mL portions of water and 200 mL of a sat. aq. NaHCO3 solution, dried over MgSO4, filtered and concentrated to a residue. Silica gel chromatography (0->25% EtOAc/hexanes) afforded 4.36 g (76%) of 3,5-bis-trimethylsilanylethynyl-pyrazin-2-ylamine as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939531B2
Source datasetuspto-grants-2011_05
ORD IDord-0a4e2282fefb46cba0c97779cead2bd4
Source noteuspto-grants-2011_05