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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 68299Erstellt: 24. Oktober 2026

N-Methylbenzeneethanamine → 2-(N-methylphenethylamino)-6-phenylpyrimidine-4-carboxamide

https://huagongshe.com/de/reaction/68299

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-MethylbenzeneethanamineHCID 11503—
EduktDiisopropylethylamineHCID 81531—
EduktHCID 58872694HCID 58872694—
Lösungsmittel1,4-DioxaneHCID 31275—
Produkt2-(N-methylphenethylamino)-6-phenylpyrimidine-4-carboxamideHCID 1560354651,7%

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

2-Methanesulfonyl-6-phenylpyrimidine-4-carboxamide (70 mg, 0.25 mmol), 1,4-dioxane (4 mL), DIPEA (0.3 mL, 2.0 mmol) and N-methylphenethylamine (82 mg, 0.6 mmol) were added to a 8 mL vial. The vial was sealed and heated at 85° C. for two days. The reaction mixture was allowed to cool to room temperature, and the solvent then removed by centrifugal evaporation. The residue was purified by preparative HPLC to afford 43 mg of 2-(N-methylphenethylamino)-6-phenylpyrimidine-4-carboxamide. 1H NMR (CDCl3, 300 MHz) δ 8.14 (m, 2H), 7.74 (s, 1H), 7.67 (br s, 1H), 7.47 (m, 3H), 7.25 (m, 5H), 5.79 (br s, 1H), 3.95 (t, J=6.9 Hz, 2H), 3.21 (s, 3H), 2.97 (t, J=6.9 Hz, 2H). HPLC ret. time 3.25 min, 10-100% CH3CN, 5 min run. ESI-MS m/z 333.3 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08822451B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-0539cb802972482dbf0f1709587fadb3
Quellennotizuspto-grants-2014_09