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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2105311Generated: October 31, 2026

Triethylamine → HCID 24760790, compound

https://huagongshe.com/reaction/2105311

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTrimethylsilylacetyleneHCID 66111—
ReactantHCID 11246214HCID 11246214—
CatalystTriphenylphosphineHCID 11776—
CatalystCopper iodideHCID 83717—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 24760790HCID 2476079085%

Reaction Steps

2-[2-(3-(R)-Amino-piperidin-1-yl)-5-bromo-6-oxo-6H-pyrimidin-1-ylmethyl]-benzonitrile (189 mg, 0.49 mmol), trimethylsilylacetylene (103 μL, 0.73 mmol), triphenylphosphine (4 mg, 0.02 mmol), and triethylamine (102 μL, 0.73 mmol) were stirred in THF (4 mL) in a flask purged with nitrogen. Dichlorobis(triphenylphosphine)palladium(II) (17 mg, 0.024 mmol) was added, and after 10 min copper iodide (2 mg) was added. The reaction stirred for 18 h at r.t. The solution was diluted with EtOAc, washed with brine, dried (MgSO4), and concentrated in vacuo. Purification by silica gel chromatography (5% MeOH/CHCl3) gave 168 mg (85%) of the title compound as a clear oil. MS (ES) [m+H] calc'd for C22H27N5OSi, 406; found 406.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07579357B2
Source datasetuspto-grants-2009_08
ORD IDord-fdfed85cce4742079be51faba1b58263
Source noteuspto-grants-2009_08