HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 305Erstellt: 24. Oktober 2026
4-(Trifluoromethyl)benzylamine → 6-[[4-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamide
https://huagongshe.com/de/reaction/305
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-(Trifluoromethyl)benzylamine | HCID 76804 | — |
| Edukt | 6-Chloronicotinamide | HCID 80456 | — |
| Reagenz | Sodium t-butoxide | HCID 23676156 | — |
| Katalysator | Binap, (A+-)- | HCID 634876 | — |
| Katalysator | Palladium (II) acetate | HCID 4144353 | — |
| Lösungsmittel | 1,2-Dimethoxyethane | HCID 8071 | — |
| Produkt | 6-[[4-(Trifluoromethyl)phenyl]methylamino]pyridine-3-carboxamide | HCID 78915650 | 7,4% |
Reaktionsschritte
To a stirred solution of 6-chloronicotinamide (0.053 g, 0.34 mmol), 2,2'-bis(diphenylphosphino)-1,1'-binaphthyl (0.021 g, 0.03 mmol), sodium 2-methylpropan-2-olate (0.065 g, 0.68 mmol) and diacetoxypalladium (7.60 mg, 0.03 mmol) in DME (1 mL) was added (4-(trifluoromethyl)phenyl)methanamine (0.097 mL, 0.68 mmol). The reaction was run in microwave at 100 °C for 4h. The compound was purified by preparative HPLC on a Kromasil C8 column (10 µm 250x20 ID mm) using a gradient of 51-55% acetonitrile in H2O/ACN/FA 95/5/0.2 buffer, over 25 minutes with a flow of 19 mL/min. The compounds were detected by UV at 270nm. 6-(4-(trifluoromethyl)benzylamino)nicotinamide (7.40 mg, 7.40 %) was obtained.
Herkunft & Nachweise
| Quelldatensatz | 750 AstraZeneca ELN dataset |
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| ORD ID | ord-92bacb0740454b4398d7f3969518ce26 |
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| Quellennotiz | 750 AstraZeneca ELN dataset |
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