HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 543Erstellt: 24. Oktober 2026
Benzylamine → 4-N-benzyl-2-N-phenylpyridine-2,4-diamine
https://huagongshe.com/de/reaction/543
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | 4-chloro-N-phenylpyridin-2-amine | HCID 23458041 | — |
| Reagenz | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Palladium (II) acetate | HCID 4144353 | — |
| Katalysator | 2-Dicyclohexylphosphino-2',6'-diisopropoxybiphenyl | HCID 16217985 | — |
| Lösungsmittel | Dimethylacetamide | HCID 31374 | — |
| Produkt | 4-N-benzyl-2-N-phenylpyridine-2,4-diamine | HCID 101883688 | 4,83% |
Reaktionsschritte
Phenylmethanamine (57.6 mg, 0.54 mmol), 4-chloro-N-phenylpyridin-2-amine (100 mg, 0.49 mmol) and sodium 2-methylpropan-2-olate (94 mg, 0.98 mmol) were suspended in DMA (2 mL) and sealed into a microwave tube. Nitrogen was bubbled through the reaction mixture for 5 minutes. 2-Dicyclohexylphosphino-2',6'-di- i-propoxy-1,1'-biphenyl (27.4 mg, 0.06 mmol) and diacetoxypalladium (8.78 mg, 0.04 mmol) were added to the reaction mixture and nitrogen was bubbled through the reaction mixture for a further 5 minutes. The reaction was heated thermally to 100 °C for 1.5 hours under nitrogen and cooled to RT. The reaction mixture was neutralised with HCl and purified by ion exchange chromatography, using a 20 g SCX column. The crude product was purified by preparative HPLC (Waters SunFire column, 5µ silica, 50 mm diameter, 100 mm length), using decreasingly polar mixtures of water (containing 0.1% formic acid) and MeCN as eluents. Fractions containing the desired compound were evaporated to dryness N4-benzyl-N2-phenylpyridine-2,4-diamine (6.50 mg, 4.83 %) as an off-white solid.
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-a3160d640f594550bd2649e07be8658f |
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| Quellennotiz | 750 AstraZeneca ELN dataset |
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