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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 473216Erstellt: 25. Oktober 2026

Toluene → 8-Cyclopropyl-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline

https://huagongshe.com/reaction/473216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTolueneHCID 1140—
EduktPotassium Phosphate, TribasicHCID 62657—
EduktCyclopropylboronic acidHCID 2760897—
Edukt8-Bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazolineHCID 66609469—
KatalysatorDichlorobis(tricyclohexylphosphine)pallium (II)HCID 11050900—
LösungsmittelWaterHCID 962—
Produkt8-Cyclopropyl-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazolineHCID 6660981684%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a mixture of 8-bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline from Example 35 step B (200 mg, 0.5 mmol), dichlorobis(tricyclohexylphosphine)palladium(II) (37 mg, 0.05 mmol), cyclopropylboronic acid (65 mg, 0.75 mmol) and K3PO4 (371 mg, 1.75 mmol) were added toluene (6 mL) and water (0.5 mL). The reaction vessel was evacuated and flushed with argon (3×), and then the mixture was heated at 100° C. for 4 h. The mixture was concentrated under reduced pressure onto Celite and the residue was purified by silica gel chromatography eluting with 10-50% EtOAc/hexanes to afford impure 8-cyclopropyl-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline (150 mg, 84%) which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633207B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-4b691892610748fdaab7fcdc1a140446
Quellennotizuspto-grants-2014_01