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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 593211Generated: November 1, 2026

Diisopropylamine → HCID 89444279, compound

https://huagongshe.com/reaction/593211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylamineHCID 7912—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 89437205HCID 89437205—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89444279HCID 8944427980%

Reaction Steps

A solution of methyl 4-[(5-bromopyrazin-2-yl)amino]-4-oxo-butanoate (A2, 1.0 g, 3.5 mmol), copper iodide (0.17 mmol, 0.033 g), diisopropylamine (4.2 mmol, 0.42 g, 0.59 mL) and palladium(II)bis(triphenylphosphine)dichloride (0.17 mmol, 0.12 g) in tetrahydrofuran (30 mL) was degassed with Ar. Then ethynyl(trimethyl)silane (7.60 mmol, 0.75 g, 1.1 mL) was added slowly and the mixture was stirred overnight. The mixture was filtered through a pad of celite which was washed with ethyl acetate and filtrate was concentrated under reduced pressure. The product was purified by flash chromatography (ethyl acetate/cyclohexane: 1/99→99/1) to give methyl 4-oxo-4-[[5-(2-trimethylsilylethynyl)pyrazin-2-yl]amino]butanoate (E, 0.85 g, 2.8 mmol, 80% Yield). 1H NMR (400 MHz, CDCl3) 9.46 (1H, s), 9.00 (1H, s), 8.33 (1H, s), 3.71 (3H, s), 2.88-2.75 (2H, m), 0.20 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09241489B2
Source datasetuspto-grants-2016_01
ORD IDord-d760143028304bd49deec570863bd054
Source noteuspto-grants-2016_01