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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 45405Erstellt: 23. Oktober 2026

Pyridine → Ethyl 2-benzamido-4-methylthiazole-5-carboxylate

https://huagongshe.com/de/reaction/45405

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktBenzoyl chlorideHCID 7412—
EduktEthyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 2-benzamido-4-methylthiazole-5-carboxylateHCID 68399197%

Reaktionsschritte

To a solution of ethyl 2-amino-4-methylthiazole-5-carboxylate (2.00 g, 10.00 mmol) in anhydrous dichloromethane (40 mL) was added pyridine (2.50 g, 32.00 mmol), followed by the addition of benzoyl chloride (1.90 g, 13.00 mmol) dropwise. The reaction mixture was stirred at ambient temperature for 18 h, then washed sequentially with 1 N hydrochloric acid (15 mL), saturated aqueous sodium bicarbonate (2×15 mL), and water (15 mL), dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo. The residue was purified by column chromatography to afford the title compound as a white solid in 97% yield (3.0 g); 1H NMR (CDCl3, 300 MHz) δ 11.35 (s, br, 1H), 7.89 (d, J=7.4 Hz, 2H), 7.59 (t, J=7.4 Hz, 1H), 7.47 (t, J=7.6 Hz, 2H), 4.29 (q, J=7.1 Hz, 2H), 2.28 (s, 3H), 1.35 (t, J=7.1 Hz, 3H); MS (ES+) m/z 291.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08541457B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-a688f488a9d64955b03427bc47f03263
Quellennotizuspto-grants-2013_09