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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 707275Erstellt: 26. Oktober 2026

Water → 2-(Methylsulfonyl)thiazolo[5,4-b]pyridine

https://huagongshe.com/reaction/707275

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktPotassium PermanganateHCID 516875—
Edukt2-(Methylthio)thiazolo[5,4-b]pyridineHCID 699840—
LösungsmittelAcetic AcidHCID 176—
Produkt2-(Methylsulfonyl)thiazolo[5,4-b]pyridineHCID 360450320,1%

Reaktionsschritte

To a stirred, room temperature solution of 2-(methylthio)thiazolo[5,4-b]pyridine (182 mg, 1.0 mmol) in acetic acid (10 mL) was added a solution of potassium permanganate (47.3 mg, 0.3 mmol) in water (6 mL) dropwise. The reaction mixture was stirred at room temperature for 16 h. LCMS showed incomplete conversion. Additional KMnO4 (158 mg) was mixed in and stirred for another 5 h. LCMS showed complete conversion. The reaction mixture was quenched with aqueous sodium sulfite. The resulting mixture was vigorously stirred at room temperature overnight. The resulting solution was partitioned between EtOAc and saturated Na2CO3. The aqueous layer was extracted with ethyl acetate, dried (Na2SO4), and concentrated. To the residue was added aq. Na2CO3 until the pH reaches 7. The precipitate formed was collected by filtration, dried to give 2-(methylsulfonyl)thiazolo[5,4-b]pyridine (43 mg, 0.201 mmol, 20.10% yield) as a tan solid. 1H NMR (300 MHz, CHLOROFORM-d) δ ppm 3.42 (s, 3 H) 7.62 (dd, J=8.40, 4.60 Hz, 1 H) 8.47 (dd, J=8.33, 1.46 Hz, 1 H) 8.75-8.84 (m, 1H). EST (M+1) 214.9.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09174992B2
Quelldatensatzuspto-grants-2015_11
ORD IDord-52fceaeb7d9140889103e9e33fbf4d89
Quellennotizuspto-grants-2015_11