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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1837454Erstellt: 27. Oktober 2026

2-(Trimethylstannyl)-1,3-thiazole → Methyl 4-acetamido-3-chloro-6-(2-thiazolyl)pyridine-2-carboxylate

https://huagongshe.com/reaction/1837454

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-(Trimethylstannyl)-1,3-thiazoleHCID 12956641—
EduktMethyl 4-acetamido-3,6-dichloropyridine-2-carboxylateHCID 22677481—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 4-acetamido-3-chloro-6-(2-thiazolyl)pyridine-2-carboxylateHCID 2267734929,6%

Reaktionsschritte

A solution of methyl 4-acetamido-3,6-dichloropyridine-2-carboxylate (1.0 g, 4.05 mmol), 2-(trimethylstannyl)thiazole (2.9 g, 17.3 mmol) and dichlorobis(triphenylphosphine)palladium(II) (0.4 g, 0.6 mmol) in tetrahydrofuran (75 mL) was heated under reflux for four hours. The reaction was diluted with water (100 mL) and extracted with ethyl acetate (2×100 mL). The organic phase was dried (MgSO4) and concentrated. The crude product was purified by column chromatography (50% ethyl acetate in hexane) to give methyl 4-acetamido-3-chloro-6-(2-thiazolyl)pyridine-2-carboxylate (0.38 g, 1.2 mmol), mp 187-8° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06784137B2
Quelldatensatzuspto-grants-2004_08
ORD IDord-2830be1461e74111bc05fa55fd57f14f
Quellennotizuspto-grants-2004_08