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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 634Erstellt: 23. Oktober 2026

N-Ethylaniline → 5-bromo-N-ethyl-4-methoxy-N-phenylpyrimidin-2-amine

https://huagongshe.com/de/reaction/634

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-EthylanilineHCID 7670—
Edukt5-Bromo-2-iodo-4-methoxypyrimidineHCID 84819520—
ReagenzSodium 2-methylbutan-2-olateHCID 2733478—
KatalysatorPalladium (II) acetateHCID 4144353—
KatalysatorBis(adamantan-1-yl)(butyl)phosphaneHCID 11371790—
LösungsmittelTolueneHCID 1140—
Produkt5-bromo-N-ethyl-4-methoxy-N-phenylpyrimidin-2-amineHCID 10699869353,74%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

5-bromo-2-iodo-4-methoxypyrimidine (0.086 g, 0.27 mmol), diacetoxypalladium (2.78 mg, 0.01 mmol), di((3S,5S,7S)-adamantan-1-yl)(butyl)phosphine (8.88 mg, 0.02 mmol) and sodium 2-methylbutan-2-olate (0.033 g, 0.30 mmol) were added to a micro vial. Then N-ethylaniline (0.031 mL, 0.25 mmol) in toluene (1.5 mL) was added to the reaction mixture. The vial was sealed and evacuated and flushed with nitrogen and then stirred at 60°C o/n. LC/MS showed product formation. The reaction mixture was cooled to rt and then filtered over celite. The crude product was diluted with 25 ml of DCM and then washed with sat. NaHCO3 followed by brine. The organic phase was dried over a phase separator and then concentrated to dryness. **No LC/MS data due to database failure over three months and was only saved locally on LC/MS computer and pdf-files seems to be deleted on machine. Not used in further reactions.**

Herkunft & Nachweise

Quelldatensatz750 AstraZeneca ELN dataset
ORD IDord-8bbed4d3f8cb496989e49be7e55b89ca
Quellennotiz750 AstraZeneca ELN dataset