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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktCinchomeronic acidHCID 10273—
EduktBenzenebutanamineHCID 83242—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
LösungsmittelDimethylformamideHCID 6228—
ProduktPyridine-3,4-dicarboxylic acid bis-[(4-phenyl-butyl)-amide]HCID 18727498102,8%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135483B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-07c346cc24784912b7e31b67701a9b9d
Quellennotizuspto-grants-2006_11