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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | N-Methylbenzeneethanamine | HCID 11503 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | HCID 58872694 | HCID 58872694 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 2-(N-methylphenethylamino)-6-phenylpyrimidine-4-carboxamide | HCID 15603546 | 51,7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08822451B2 |
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| Quelldatensatz | uspto-grants-2014_09 |
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| ORD ID | ord-0539cb802972482dbf0f1709587fadb3 |
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| Quellennotiz | uspto-grants-2014_09 |
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