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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 69084Erstellt: 24. Oktober 2026

Sodium Iodide → HCID 86675785, Verbindung

https://huagongshe.com/de/reaction/69084

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium IodideHCID 5238—
EduktDiisopropylethylamineHCID 81531—
Edukt6-Bromo-2-chloro-3-(chloromethyl)quinolineHCID 17039790—
EduktHCID 178516143HCID 178516143—
LösungsmittelWaterHCID 962—
LösungsmittelCeric ammonium nitrateHCID 180504—
ProduktHCID 86675785HCID 86675785—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

6-Bromo-2-chloro-3-(chloromethyl)quinoline (0.60 g, 2.1 mmol), 6-(trifluoromethyl)-4-pyrimidinol (0.34 g, 2.1 mmol), DIEA (0.54 ml, 3.1 mmol) and sodium iodide (0.31 g, 2.1 mmol) were suspended in CAN (50 mL) and heated to 70° C. for 1 h. The reaction was cooled, diluted with water (100 mL) and extracted with EtOAc (200 mL). After drying with magnesium sulfate the organic was evaporated to dryness under reduced pressure. Purification using low pressure silica chromatography (0-10% methanol in DCM gradient) to give the desired 6-bromo-2-chloro-3-((6-(trifluoromethyl)pyrimidin-4-yloxy)methyl)quinoline. Step 2 and 3: The product from step 1 was taken through a procedure similar to that described in steps 3 and 4 of Example 9, to provide the titled compound, o-tolyl-3-((6-(trifluoromethyl)pyrimidin-4-yloxy)methyl)quinolin-2-amine. (ESI, pos. ion) m/z: 411 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822485B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-2ba94ad31aea429aaca5434b4d9dc5cd
Quellennotizuspto-grants-2014_09