HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720876Erstellt: 24. Oktober 2026
Triethylamine → Pyridine-3,4-dicarboxylic acid bis-[(4-phenyl-butyl)-amide]
https://huagongshe.com/de/reaction/720876
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Cinchomeronic acid | HCID 10273 | — |
| Edukt | Benzenebutanamine | HCID 83242 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Edukt | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Pyridine-3,4-dicarboxylic acid bis-[(4-phenyl-butyl)-amide] | HCID 18727498 | 102,8% |
Reaktionsschritte
3,4-Pyridinedicarboxylic acid (1 g; 6.0 mmol) is slurried in DMF (50 mL) at ambient temperature. To this reaction mixture is added sequentially 1-hydroxybenzotriazole hydrate (2.43 g; 18.0 mmol), 4-phenylbutylamine (2.08 mL; 13.2 mmol), triethylamine (1.67 mL; 12.0 mmol), and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (2.87 g; 15.0 mmol). The reaction mixture is stirred for 18 hours at ambient temperature. The batch is poured onto ethyl acetate (300 mL), then extracted sequentially with water (100 mL), IN HCl (100 mL), saturated aqueous sodium bicarbonate (50 mL), and brine (50 mL). The organic phase is dried over MgSO4, filtered, and concentrated in vacuo affording the desired product (2.65 g) as a semi-solid. ESMS:MH+ 430.0.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07135483B2 |
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| Quelldatensatz | uspto-grants-2006_11 |
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| ORD ID | ord-07c346cc24784912b7e31b67701a9b9d |
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| Quellennotiz | uspto-grants-2006_11 |
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