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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 707274Erstellt: 24. Oktober 2026

Methyl iodide → 2-(Methylthio)thiazolo[5,4-b]pyridine

https://huagongshe.com/de/reaction/707274

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl iodideHCID 6328—
EduktPotassium CarbonateHCID 11430—
EduktHCID 178527801HCID 178527801—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelEthyl AcetateHCID 8857—
Produkt2-(Methylthio)thiazolo[5,4-b]pyridineHCID 699840100%

Reaktionsschritte

To the suspension of thiazolo[5,4-b]pyridine-2-thiol (168 mg, 1.0 mmol) in THF (3.3 ml) was added potassium carbonate (193 mg, 1.4 mmol), followed by iodomethane (68.2 μl, 1.1 mmol) dropwise. The reaction mixture was stirred at room temperature for 16 h. Additional iodomethane were mixed in (40 uL) and stirred at room temperature for another 3 h. LCMS showed reaction was complete. The crude reaction mixture was suspended in ethyl acetate and washed with water, then brine, dried over sodium sulfate, filtered, and concentrated to give 2-(methylthio)thiazolo[5,4-b]pyridine (182 mg, 1.0 mmol, 100% yield) as a tan solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09174992B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-687eaacea0954c2181fa4689a4f58028
Quellennotizuspto-grants-2015_11