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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009039Generated: October 29, 2026

Triethylamine → 4-Ethyl-5-trimethylsilanylethynyl-thiazol-2-ylamine

https://huagongshe.com/reaction/1009039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAmmonium ChlorideHCID 25517—
ReactantTrimethylsilylacetyleneHCID 66111—
Reactant4-Ethyl-5-iodo-thiazol-2-ylamineHCID 86630954—
CatalystHCID 178418476HCID 178418476—
SolventAcetonitrileHCID 6342—
Product4-Ethyl-5-trimethylsilanylethynyl-thiazol-2-ylamineHCID 86630955—

Reaction Steps

Under a stream of Ar the above prepared 4-ethyl-5-iodo-thiazol-2-ylamine (1.67 g, 6.57 mmol) was dissolved in 40 mL of acetonitrile and treated successively with triethylamine (2.73 mL, 3 eq.), Cul (0.125 g, 0.1 eq.), (Ph3P)2PdCl2 (0.46 g, 0.1 eq.) and ethynyltrimethylsilane (2.73 mL, 3 eq.). The flask was closed with a septum and allowed to stir for 15 h at ambient temperature. The reaction mixture was then poured onto icewater/NH4Cl, twofold extracted with ethyl acetate, washed with water and brine, dried over sodium sulfate, and evaporated to dryness. Flash chromatography (SiO2, hexane/AcOEt=7/3) afforded finally 0.598 g of the title compound as brown viscous oil, contaminated with some des-iodo-compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07973051B2
Source datasetuspto-grants-2011_07
ORD IDord-42b8e34bc556430c8bba6efc986a3565
Source noteuspto-grants-2011_07