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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 386059Erstellt: 26. Oktober 2026

Trimethylsilylmethyl Azide → 2-Bromo-6-{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}pyridine

https://huagongshe.com/reaction/386059

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrimethylsilylmethyl AzideHCID 150751—
Edukt2-Bromo-6-ethynylpyridineHCID 12970532—
EduktSodium AscorbateHCID 23667548—
LösungsmittelWaterHCID 962—
Lösungsmitteltert-ButanolHCID 6386—
LösungsmittelSodium BicarbonateHCID 516892—
Produkt2-Bromo-6-{1-[(trimethylsilyl)methyl]-1H-1,2,3-triazol-4-yl}pyridineHCID 59525901—

Reaktionsschritte

2-Bromo-6-ethynylpyridine (Example 465, Step 1) (350 mg, 1.92 mmol) and trimethylsilylmethyl azide (323 mg, 2.50 mmol) were combined in t-BuOH (4.0 mL) and water (3.0 mL). CuSO4.5H2O (24 mg, 0.096 mmol) in water (0.50 mL) was added, followed by sodium ascorbate (76 mg, 0.39 mmol) in water (0.50 mL). The reaction was stirred at room temperature overnight, diluted with saturated NaHCO3, and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered, and evaporated to a yellow residue that was purified by flash chromatography (0-50% EtOAc/hexanes) to afford the title compound as a colorless solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367706B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-2302a702b83c454e84c00efd094b899a
Quellennotizuspto-grants-2013_02