Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916174Generated: November 1, 2026

Triethylamine → Methyl-(5-trimethylsilanylethynyl-pyridin-2-yl)-amine

https://huagongshe.com/reaction/1916174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant5-Bromo-N-methylpyridin-2-amineHCID 15645663—
CatalystHCID 178418476HCID 178418476—
SolventTetrahydrofuranHCID 8028—
SolventCyclohexaneHCID 8078—
SolventEthyl AcetateHCID 8857—
ProductMethyl-(5-trimethylsilanylethynyl-pyridin-2-yl)-amineHCID 66705950—

Reaction Steps

The title compound is synthesized according to general procedure GP2 starting from 4.3 g (23.0 mmol) 5-bromo-2-methylamino-pyridine and 4.5 mL (32.2 mmol) 1-trimethylsilyl-ethyne using 134 mg (0.71 mmol) CuI, 601 mg (2.3 mmol) triphenylphosphine, 420 mg (0.60 mmol) PdCl2(PPh3)2 and 32 mL (101 mmol) triethylamine in 40 mL dry THF. For the work-up the reaction mixture is diluted with ethyl acetate and small amounts of cyclohexane, the organic phase is extracted with water and brine. The product is purified by chromatography on silica gel using a hexane/ethyl acetate gradient. Yield: 4.0 g (85%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618111B2
Source datasetuspto-grants-2013_12
ORD IDord-97bfa2f87c0141ce84cca0ebc7c8e601
Source noteuspto-grants-2013_12