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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098588Generated: November 1, 2026

Trimethylsilylacetylene → HCID 58235284, compound

https://huagongshe.com/reaction/1098588

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant3-Amino-5-bromopyridineHCID 817681—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
ProductHCID 58235284HCID 5823528427%

Reaction Steps

5-Bromopyridin-3-amine (0.94 g, 5.43 mmol), PdCl2(PPh3)2 (0.076 g, 0.109 mmol) and ethynyltrimethylsilane (0.64 g, 6.52 mmol) were combined in TEA (12.0 mL). After stirring for 5 min, CuI (0.010 g, 0.054 mmol) was added. The reaction mixture was flushed with N2 and stirred at RT overnight, followed by at 55° C. overnight. The reaction was filtered and the solid was washed with EtOAc (30 mL). The combined organics were concentrated in vacuo and purified by chromatography to afford 5-(2-(trimethylsilyl)ethynyl)pyridin-3-amine (0.279 g, 27% yield) as a white solid. MS (ESI) m/z: 191.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143293B2
Source datasetuspto-grants-2012_03
ORD IDord-86c143eacbe64d0992ed34f1a9e9411d
Source noteuspto-grants-2012_03