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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 471398Generated: October 26, 2026

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

https://huagongshe.com/reaction/471398

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 numberUS08633183B2
Source datasetuspto-grants-2014_01
ORD IDord-71264766d05b432a907f6194ca01b16a
Source noteuspto-grants-2014_01