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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1356071Erstellt: 26. Oktober 2026

Sodium Carbonate → 2-Amino-4-(4-methyl-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile

https://huagongshe.com/reaction/1356071

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
Edukt2-Amino-4-chloro-6-methylsulfanyl-pyrimidine-5-carbonitrileHCID 18507260—
Edukt2-(4-Methyl-furan-2-yl)-benzo[1,3,2]dioxaboroleHCID 18507588—
KatalysatorTetrakis(triphenylphosphine)palladiumHCID 11979704—
LösungsmittelBenzeneHCID 241—
Produkt2-Amino-4-(4-methyl-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrileHCID 1850749147%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

To a stirred suspension of 2.19 g (10.9 mmol) 2-amino-4-chloro-6-methylsulfanyl-pyrimidine-5-carbonitrile in 40 ml benzene at room temperature were added 2,40 g (12.0 mmol) 2-(4-methyl-furan-2-yl)-benzo[1,3,2]dioxaborole, 252mg (0.22 mmol) tetrakis(triphenylphosphine)palladium(O) and 11 ml (22.0 mmol) 2M aqueous sodium carbonate. The reaction mixture was heated at 90° C. for 16 h, then concentrated in vacuo. Chromatography (1/3 ethyl acetate/hexane then 1/1 ethyl acetate/hexane) afforded 1.26 g (47%) 2-amino-4-(4-methyl-furan-2-yl)-6-methylsulfanyl-pyrimidine-5-carbonitrile as a light yellow crystalline solid. EI-MS m/e (%): 246 (M+, 61), 245 ([M—H]+, 100).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06586441B2
Quelldatensatzuspto-grants-2003_07
ORD IDord-b629dd33f06e4fe5846ff2e1d6e33a8f
Quellennotizuspto-grants-2003_07