HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1685524Erstellt: 25. Oktober 2026
Triethylamine → 5-bromo-N-(3,5-difluorophenyl)nicotinamide
https://huagongshe.com/reaction/1685524
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Oxalyl chloride | HCID 65578 | — |
| Edukt | 5-Bromonicotinic acid | HCID 88707 | — |
| Edukt | 3,5-Difluoroaniline | HCID 96595 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 5-bromo-N-(3,5-difluorophenyl)nicotinamide | HCID 41601149 | 93% |
Reaktionsschritte
Oxalyl chloride (1.2 mL) and DMF (25 μL) were added to 5-bromonicotinic acid (1.0 g, 4.95 mmol) suspended in CH2Cl2 (30 mL). The resulting mixture was stirred at room temperature for 12 min. It was then concentrated to dryness and azeotroped with toluene. The residual was then dissolved in toluene (30 mL). 3,5-Difluoroaniline (1.0 g, 7.8 mmol) was added followed by triethylamine (1.1 mL, 7.5 mmol). The resulting suspension was stirred at room temperature for 10 min. The reaction mixture was taken in 5% acetic acid(aq) (300 mL) and extracted with ethyl acetate (2×200 mL). The combined organic extract was washed with 1.0 M Na2CO3(aq) (2×100 mL) and brine. The organic layers were combined, dried (Na2SO4) and concentrated to dryness to provide the title compound (1.4 g, 93%). MS (APCI) m/z 313, 315 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08148408B2 |
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| Quelldatensatz | uspto-grants-2012_04 |
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| ORD ID | ord-f52c81fc79e24d85b3f93f6952166dde |
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| Quellennotiz | uspto-grants-2012_04 |
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