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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 365894Erstellt: 25. Oktober 2026

Triethylamine → 3-(1-Boc-2-(s)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridine

https://huagongshe.com/reaction/365894

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTrimethylsilylacetyleneHCID 66111—
Edukt3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromo-6-chloropyridineHCID 22872667—
KatalysatorHCID 178418397HCID 178418397—
KatalysatorHCID 178505377HCID 178505377—
LösungsmittelTolueneHCID 1140—
Produkt3-(1-Boc-2-(s)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridineHCID 2296182775%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 3-(1-BOC-2-(S)-azetidinylmethoxy)-5-bromo-6-chloropyridine (1.0 g, 2.6 mmol) in toluene (20 mL) was added NEt3 (1 mL), copper (I) iodine (50 mg, 10%), tetrakis(triphenylphosphine)palladium (0) (305 mg, 10%) and (trimethylsilyl)acetylene (0.45 mL, 3.18 mmol). The reaction mixture was stirred and heated at 100° C. for 16 h. Solvent was evaporated and the residue was chromatographed (silica gel; hexane/EtoAc, 5:1 to 2:1) to afford an oil (770 mg, 74%): 1H NMR (CDCl3, 300 MHz) δ 1.42 (s, 9H), 2.20-2.40 (m, 2H), 3.80-3.92 (m, 2H), 4.10 (m, 1H), 4.30 (m, 1H), 4.50 (m, 1H), 7.37 (d, 1H, J=3.0 Hz), 8.05 (d, 1H, J=3.0 Hz); MS (CI/NH3) m/z 395 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06127386
Quelldatensatzuspto-grants-2000_10
ORD IDord-612e7439e0e449bba3d5cef409ba9ff5
Quellennotizuspto-grants-2000_10