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HRID 222941Erstellt: 23. Oktober 2026

Biphenyl → 4-(5-amino-2-methylphenyl)-8-(2,6-difluorophenyl)-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one

https://huagongshe.com/de/reaction/222941

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBiphenylHCID 7095—
EduktTriethylamineHCID 8471—
Edukt3-Iodo-p-toluidineHCID 118889—
EduktPinacolboraneHCID 6364989—
Edukt4-Chloro-2-methylsulfanyl-8-(2,6-difluorophenyl)-8H-pyrido[2,3-d]pyrimidin-7-oneHCID 11951513—
EduktBarium hydroxide, octahydrateHCID 17749109—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelWaterHCID 962—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt4-(5-amino-2-methylphenyl)-8-(2,6-difluorophenyl)-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-oneHCID 5921267980,3%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a solution of 3-iodo-4-methylaniline (110.0 mg, 0.47 mmol) in dioxane (1.0 mL) was added (under argon) triethylamine (0.26 mL, 1.86 mmol), palladium diacetate (5.2 mg, 0.023 mmol), 2-(dicyclophexyl phosphino) biphenyl (33.0 mg, 0.093 mmol), and pinacolborane (0.20 mL, 1.40 mmol). The mixture was stirred at about 80° C. for about 1 hour, cooled to room temperature (rt), and added with water (0.2 mL), barium hydroxide octahydrate (440.0 mg, 1.40 mmol) and 4-chloro-8-(2,6-difluorophenyl)-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one (180.0 mg, 0.47 mmol). The mixture was heated at about 100° C. under stirring for about 1 hour, cooled to room temperature, filtered through celite, and diluted with brine (5.0 mL). The mixture was then extracted with CH2Cl2 (3×10 mL). The combined organic phases were dried over Na2SO4, filtered, and concentrated. Purification via the CombiFlash system then afforded the title compound (155.0 mg, 75%): LC-MS m/z 411 (M+H)+, 2.60 min (ret. time).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207176B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-b35000c270a04566af2d6062f5ff9a44
Quellennotizuspto-grants-2012_06