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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1056954Erstellt: 27. Oktober 2026

Water → 4-bromo-6-methyl-1H,6H,7H-pyrrolo[2,3-c]pyridin-7-one

https://huagongshe.com/reaction/1056954

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktSodium HydroxideHCID 14798—
Edukt4-Bromo-1,6-dihydro-6-methyl-1-((4-methylphenyl)sulfonyl)-7H-pyrrolo(2,3-c)pyridin-7-oneHCID 89656304—
LösungsmittelEthanolHCID 702—
Produkt4-bromo-6-methyl-1H,6H,7H-pyrrolo[2,3-c]pyridin-7-oneHCID 57329766108,4%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

A solution of 4-bromo-6-methyl-1-[(4-methylphenyl)sulfonyl]-1,6-dihydro-7H-pyrrolo[2,3-c]pyridin-7-one (5.81 g, 15.2 mmol) in ethanol (100 mL) was treated with 3.0 M sodium hydroxide in water (50.8 mL, 152 mmol) and stirred at 20° C. for 16 h. The reaction mixture was concentrated in vacuo to remove most of the ethanol. The remaining aqueous layer was neutralized with concentrated HCl to pH ˜7 and extracted with ethyl acetate (2×). The combined organic layers were dried with magnesium sulfate, filtered, and concentrated to give the desired product (3.74 g, quantitative) which was used without further purification. LCMS calculated for C8H8BrN2O (M+H)+: m/z=227.0, 229.0. found: 227.0, 228.9.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09399640B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-6681ac83dd14478d98fc7a54cf5cd8d9
Quellennotizuspto-grants-2016_07