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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1515845Erstellt: 27. Oktober 2026

Trimethylsilylacetylene → 5-Nitro-3-trimethylsilanylethynyl-pyridin-2-ylamine

https://huagongshe.com/reaction/1515845

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylacetyleneHCID 66111—
Edukt2-Amino-3-iodo-5-nitropyridineHCID 11623112—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178479804HCID 178479804—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelTriethylamineHCID 8471—
LösungsmittelDimethylacetamideHCID 31374—
Produkt5-Nitro-3-trimethylsilanylethynyl-pyridin-2-ylamineHCID 1152878970%

Reaktionsschritte

2-Amino-3-iodo-5-nitropyridine (10.0 g, 37.75 mmol) was dissolved in a mixture of triethylamine (250 mL), tetrahydrofuran (40 mL), N,N-dimethylacetamide (80 mL) and the solution was degassed and purged with nitrogen. Trimethylsilylacetylene (8.0 mL, 56.5 mmol), copper(I) iodide (0.145 g, 0.75 mmol) and bis(triphenylphosphino) palladium (II) chloride (0.53 g, 0.75 mmol) were added. The mixture was degassed and purged with nitrogen one more time, then stirred at ambient temperature for 16 h. The precipitate was removed by filtration, and the filtrate was concentrated in vacuo. The residue was purified by flash column chromatography (silica gel from QingDao, 200-300 mesh, 15%-35% ethyl acetate/hexanes) to afford 5-nitro-3-trimethylsilanylethynyl-pyridin-2-ylamine (6.2 g, 70%) as a yellow solid: LC/MS m/e calcd for C10H13N3O2Si [M+H]+ 236.32, observed 236.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08222416B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-d69067af30874b68b609adb255ea63d3
Quellennotizuspto-grants-2012_07