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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 416611Erstellt: 23. Oktober 2026

Ethyl 2-aminothiazole-4-carboxylate → Ethyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylate

https://huagongshe.com/de/reaction/416611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2-aminothiazole-4-carboxylateHCID 73216—
Edukt2-Bromo-2'-nitroacetophenoneHCID 244025—
LösungsmittelMethyl Ethyl KetoneHCID 6569—
ProduktEthyl 6-(2-nitrophenyl)imidazo[2,1-b]thiazole-3-carboxylateHCID 2523252279,4%

Reaktionsschritte

In a typical run, 2.1 g of ethyl 2-aminothiazole-4-carboxylate (Combi-Blocks, 0.0123 mol) was mixed with 25 mL of methyl ethyl ketone along with 2-bromo-2′-nitroacetophenone (3.0 g, 0.0123 mol). The reaction mixture was stirred under reflux for 18 hours. It was then cooled to room temperature and filtered to remove some of the solids. The filtrate was concentrated to afford 3.10 g of 6-(2-nitro-phenyl)-imidazo[2,1-b]thiazole-3-carboxylic acid ethyl ester (MS, M++H=318).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08088928B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-f11f0e9818664a20991016afb4914dc7
Quellennotizuspto-grants-2012_01