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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 455187Erstellt: 24. Oktober 2026

1-Chloro-2-isocyanato-4-(trifluoromethyl)benzene → HCID 59454495, Verbindung

https://huagongshe.com/de/reaction/455187

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Chloro-2-isocyanato-4-(trifluoromethyl)benzeneHCID 2733263—
EduktN-[6-(3-aminophenoxy)-7-cyano-1,3-benzothiazol-2-yl]acetamideHCID 86644686—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelEthyl AcetateHCID 8857—
ProduktHCID 59454495HCID 5945449574%

Reaktionsschritte

N-[6-(3-Aminophenoxy)-7-cyano-1,3-benzothiazol-2-yl]acetamide (150 mg, 0.462 mmol) produced in Example 12(ii) was dissolved in N,N-dimethylformamide (2 mL), 1-chloro-2-isocyanato-4-(trifluoromethyl)benzene (90 μL, 0.60 mmol) was added, and the mixture was stirred at room temperature for 12 hr. The reaction mixture was diluted with ethyl acetate (10 mL), washed successively with 5% aqueous sodium hydrogen carbonate solution (5 mL) and saturated brine (5 mL), and dried over anhydrous sodium sulfate. Insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/n-hexane=40/60→100/0), and the obtained solution was concentrated under reduced pressure. The residue was crystallized from ethanol to give the title compound (186 mg, 74%) as a white powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08497274B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-900e56ff63cb424ab7ae36930faf679e
Quellennotizuspto-grants-2013_07