HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 633Erstellt: 23. Oktober 2026
N-Ethylaniline → 5-bromo-N-ethyl-4-methoxy-N-phenylpyrimidin-2-amine
https://huagongshe.com/de/reaction/633
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-Ethylaniline | HCID 7670 | — |
| Edukt | 5-Bromo-2-iodo-4-methoxypyrimidine | HCID 84819520 | — |
| Reagenz | Sodium 2-methylbutan-2-olate | HCID 2733478 | — |
| Katalysator | 1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine) | HCID 636044 | — |
| Katalysator | Palladium (II) acetate | HCID 4144353 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 5-bromo-N-ethyl-4-methoxy-N-phenylpyrimidin-2-amine | HCID 106998693 | 70,78% |
Reaktionsschritte
5-bromo-2-iodo-4-methoxypyrimidine (0.086 g, 0.27 mmol), diacetoxypalladium (2.78 mg, 0.01 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) - XantPhos (7.16 mg, 0.01 mmol) and sodium 2-methylbutan-2-olate (0.055 g, 0.50 mmol) and di((3S,5S,7S)-adamantan-1-yl)(butyl)phosphine (8.88 mg, 0.02 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 100°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
| Quelldatensatz | 750 AstraZeneca ELN dataset |
|---|
| ORD ID | ord-3df00475fe9d41898bd3503e3b2ed03d |
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| Quellennotiz | 750 AstraZeneca ELN dataset |
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