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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 365915Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/365915

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktTrimethylsilylacetyleneHCID 66111—
Edukt3-(1-Boc-2-(r)-azetidinylmethoxy)-5-bromo-6-chloropyridineHCID 22961807—
KatalysatorHCID 178418397HCID 178418397—
KatalysatorHCID 178505377HCID 178505377—
LösungsmittelTolueneHCID 1140—
Produkt3-(1-Boc-2-(r)-azetidinylmethoxy)-6-chloro-5-(trimethylsilylethynyl)pyridineHCID 2296181062,2%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 3-(1-BOC-2-(R)-azetidinylmethoxy)-6-chloro-5-bromopyridine (660 mg, 1.75 mmol) in toluene (20 mL) was added NEt3 (0.7 mL), copper (I) iodine (33 mg), tetrakis(triphenylphosphine)palladium (0) (201 mg) and (trimethylsilyl)acetylene (0.30 mL, 2.10 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 (430 mg, 62%): 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, (H, 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-0d484c2eeb0f41ee9ddffa78538276ef
Quellennotizuspto-grants-2000_10