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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1008826Erstellt: 26. Oktober 2026

Triethylamine → N-(5-Methylpyridin-2-yl)pivalamide

https://huagongshe.com/reaction/1008826

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt2-Amino-5-methylpyridineHCID 15348—
EduktPivaloyl chlorideHCID 62493—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-(5-Methylpyridin-2-yl)pivalamideHCID 418292498,4%

Reaktionsschritte

To a stirred solution of 5-methylpyridin-2-amine (200 g, 1.85 mol) in anhydrous CH2Cl2 (1000 mL) was added dropwise a solution of Et3N (513 mL, 3.70 mol) and 2,2-dimethyl-propionyl chloride (274 mL, 2.22 mol) at 0° C. under N2. The ice bath was removed and stirring was continued at room temperature for 2 hours. The reaction was poured into ice (2000 g). The organic layer was separated and the remaining aqueous layer was extracted with CH2Cl2 (3×). The combined organics were dried over Na2SO4 and evaporated to afford 2,2-dimethyl-N-(5-methyl-pyridin-2-yl)-propionamide (350 g), which was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ 8.12 (d, J=8.4 Hz, 1 H), 8.06 (d, J=1.2 Hz, 1 H), 7.96 (s, 1 H), 7.49 (dd, J=1.6, 8.4 Hz, 1 H), 2.27 (s, 1 H), 1.30 (s, 9 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07973038B2
Quelldatensatzuspto-grants-2011_07
ORD IDord-330f892a6c10477cb7a801661cd8a01d
Quellennotizuspto-grants-2011_07