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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 393601Erstellt: 24. Oktober 2026

Sodium Bicarbonate → HCID 22646584, Verbindung

https://huagongshe.com/de/reaction/393601

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukt5-Benzyloxy-2-fluoro-4-methylphenolHCID 21991049—
EduktHCID 22646522HCID 22646522—
EduktPotassium tert-butoxideHCID 23665647—
LösungsmittelDimethyl SulfoxideHCID 679—
LösungsmittelWaterHCID 962—
ProduktHCID 22646584HCID 2264658463%

Reaktionsbedingungen

Temperatur160 °C

Reaktionsschritte

4-Chloro-6-cyano-7-(2-methoxyethoxy)quinoline (187 mg, 0.71 mmol), (prepared as described for the starting material in Example 1 but with an aqueous sodium hydrogen carbonate work up), was added to a solution of 5-benzyloxy-2-fluoro-4-methylphenol (248 mg, 1 mmol), (prepared as described for the starting material in Example 3), and potassium t-butoxide (120 mg, 1 mmol) in DMSO (5 ml) and the mixture then heated at 160° C. for 1.5 hours. The mixture was diluted with water and extracted with ethyl acetate. The organic layer was separated, washed with brine, dried (MgSO4) and the solvent removed by evaporation. The residue was purified by column chromatography eluting with methylene chloride/ethyl acetate (55/45) followed by preparative reverse-phase HPLC eluting with aqueous ammonium carbonate (2 g/1, adjusted to pH7 with carbon dioxide) and methanol (20/80) to give 4-(5-benzyloxy-2-fluoro-4-methylphenoxy)-6-cyano-7-(2-methoxyethoxy)quinoline (204 mg, 63%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06809097B1
Quelldatensatzuspto-grants-2004_10
ORD IDord-694d6787e78e4946aa91d24d25588844
Quellennotizuspto-grants-2004_10