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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446759Generated: October 25, 2026

Trimethylsilylacetylene → 2-Bromo-5-trimethylsilanylethynyl-pyrazine

https://huagongshe.com/reaction/446759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant2-Bromo-5-iodopyrazineHCID 21931200—
CatalystPalladiumHCID 23938—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
Solventtriethylamine N,N-dimethylformamideHCID 22056947—
Product2-Bromo-5-trimethylsilanylethynyl-pyrazineHCID 57497686—

Reaction Steps

Reaction of a mixture of 2-bromo-5-iodo-pyrazine and copper (1) iodide under inert conditions in an appropriate solvent and base e.g. DMF/Et3N with ethynyl-trimethyl-silane using a palladium catalyst e.g. Pd(PPh3)4 at room temperature gives 2-Bromo-5-trimethylsilanylethynyl-pyrazine. This material can be used without further purification and reacted to form 6-bromo-2-trimethylsilanyl-pyrazolo[1,5-a]pyrazine using O-(mesitylenesulfonyl)hydroxylamine to form the N-amino adduct. This can then be cyclised by reacting with base e.g. K2CO3 to form pyrazolopyrazine core (Scheme 6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481531B2
Source datasetuspto-grants-2013_07
ORD IDord-c34d6f58a99c472fa4ffd4f8f00f6c89
Source noteuspto-grants-2013_07