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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1174118Erstellt: 27. Oktober 2026

Ethyl bromopyruvate → Ethyl 2-pyridin-2-yl-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/1174118

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl bromopyruvateHCID 66144—
EduktPyridine-2-carbothioamideHCID 1549499—
LösungsmittelEthanolHCID 702—
ProduktEthyl 2-pyridin-2-yl-1,3-thiazole-4-carboxylateHCID 1008276135,4%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

A solution of the product of Example 3H (25.4 mmol) in ethanol (50 mL) was treated with ethyl bromopyruvate (3 mL, 23.9 mmol) and molecular sieves (10 g, 3 Å), heated at reflux for 16 hours, cooled to 25° C., filtered and concentrated. The concentrate was partitioned between ethyl acetate and saturated NaHCO3, and the organic phase was washed with brine, dried over MgSO4, filtered and concentrated. The residue was chromatographed on silica gel eluting with 0-25% ethyl acetate in dichloromethane to give the title compound (1.98 g, 33% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07834043B2
Quelldatensatzuspto-grants-2010_11
ORD IDord-7a125277526f45339d6f7ae805fcaa7b
Quellennotizuspto-grants-2010_11