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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1667756Erstellt: 26. Oktober 2026

Epichlorohydrin → 4-(3-Chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide

https://huagongshe.com/reaction/1667756

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEpichlorohydrinHCID 7835—
EduktPotassium CarbonateHCID 11430—
Edukt4-(3-Chloro-phenyl)-2-(6-hydroxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amideHCID 67445498—
KatalysatorPotassium IodideHCID 4875—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-(3-Chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amideHCID 8664283475%

Reaktionsschritte

A mixture of 0.037 g (0.1 mmole) of 4-(3-chloro-phenyl)-2-(6-hydroxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide (I.25d), 0.5 mL of dimethylformamide, 0.069 g (0.5 mmole) of potassium carbonate, 0.001 g of potassium iodide and 0.012 mL (0.15 mmole) of 2-chloromethyl-oxirane was heated at 100 degrees for 3 hours. The mixture was concentrated under reduced pressure, diluted with 20 mL of water and the resulting precipitate collected by filtration. The solid was triturated with diethyl ether to give 0.032 g of 4-(3-chloro-phenyl)-2-(6-oxiranylmethoxy-benzoimidazol-1-yl)-thiazole-5-carboxylic acid amide (I.39a) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08044213B2
Quelldatensatzuspto-grants-2011_10
ORD IDord-43e8fccbc30f4b768f6fca37b6fdf341
Quellennotizuspto-grants-2011_10