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HRID 1364532Erstellt: 24. Oktober 2026

Pyridine → N-(4-amino-5-cyano-6-phenylpyridin-2-yl)-2-(2,5-dimethoxyphenyl)acetamide

https://huagongshe.com/de/reaction/1364532

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
Edukt(2,5-Dimethoxyphenyl)acetyl chlorideHCID 596088—
Edukt4,6-Diamino-2-phenyl-nicotinonitrileHCID 66920608—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(4-amino-5-cyano-6-phenylpyridin-2-yl)-2-(2,5-dimethoxyphenyl)acetamideHCID 6692072412%

Reaktionsschritte

To a solution of 50 mg (0.24 mmol) of 4,6-diamino-2-phenyl-nicotinonitrile in 2 mL of CH2Cl2 was added 150 mg (0.70 mmol) of (2,5-dimethoxyphenyl)acetyl chloride (Example 68A), then 100 μL (1.23 mmol) of pyridine. The mixture was stirred at ambient temperature for 10 minutes then the solvent was removed under reduced pressure. The residue was taken up in 10 mL of ethyl acetate, then extracted with 1 M HCl(aq.) (2×5 mL), saturated NaHCO3(aq) (2×5 mL), and brine (1×5 mL), dried over MgSO4, filtered, and concentrated to an oil. This was purified via silica gel chromatography, eluting with 40% ethyl acetate:hexanes to provide 11 mg (12%) of a white solid. 1H NMR (300 MHz, d6-DMSO) δ 10.43 (m, 1H), 7.75 (m, 2H), 7.51 (m, 4H), 6.99 (m, 2H), 6.91 (m, 1H), 6.81 (m, 2H), 3.69 (m, 8H); MS (ESI) m/e 389 (M+H)+, 387 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07888374B2
Quelldatensatzuspto-grants-2011_02
ORD IDord-4ceea1b837974e7aa6d452ed54598519
Quellennotizuspto-grants-2011_02