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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1402832Erstellt: 25. Oktober 2026

5-chloro-2-(chloromethyl)-1H-1,3-benzodiazole → Ethyl n-[(5-chloro-2-benzimidazolyl)methyl]-n-(4-chlorophenyl)glycinate

https://huagongshe.com/reaction/1402832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt5-chloro-2-(chloromethyl)-1H-1,3-benzodiazoleHCID 271286—
EduktGlycine, N-(4-chlorophenyl)-, ethyl esterHCID 302644—
EduktSodium BicarbonateHCID 516892—
LösungsmittelDimethylformamideHCID 6228—
ProduktEthyl n-[(5-chloro-2-benzimidazolyl)methyl]-n-(4-chlorophenyl)glycinateHCID 6675958222,6%

Reaktionsbedingungen

Temperatur150 °C

Reaktionsschritte

The mixture of ethyl N-(4-chlorophenyl)glycinate (0.43 g), 5-chloro-2-chloromethylbenzimidazole (0.4 g), and sodium bicarbonate (0.17 g) in N,N-dimethylformamide (2 ml) was stirred at 150° C. for 0.5 h. After cooling to rt the mixture was poured into saturated sodium bicarbonate solution (50 ml) and extracted twice with EtOAc (40 ml). The combined organic layers were washed with 10% sodium carbonate solution (40 ml) and water (40 ml) and dried (sodium sulfate). After concentration the crude (0.66 g) was purified by flash chromatography (dichloromethane/1% methanol) on silica gel to provide an orange solid. The solid was further purified by trituration with diethyl ether to give ethyl N-[(5-chloro-2-benzimidazolyl)methyl]-N-(4-chlorophenyl)glycinate (0.17 g) as a light orange crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08912186B2
Quelldatensatzuspto-grants-2014_12
ORD IDord-9831c1577fc64d46b7bb4e74cd716567
Quellennotizuspto-grants-2014_12