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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 704317Erstellt: 26. Oktober 2026

Triethylamine → N-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamide

https://huagongshe.com/reaction/704317

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktEthyl AcetateHCID 8857—
Edukt2-Nitrobenzenesulfenyl chlorideHCID 24319—
Edukt4-((5-Chloropyrimidin-2-yl)oxy)-3-methylanilineHCID 14207808—
LösungsmittelTolueneHCID 1140—
ProduktN-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamideHCID 1000036883,6%

Reaktionsschritte

2.0 g of 4-(5 chloro-2-pyrimidinyloxy)-3methylaniline and 0.94 g of triethylamine were dissolved in 20 ml of toluene, and a solution of 1.61 g of 2-nitrobenzenesulfenyl chloride dissolved in 5 ml of toluene was dropwise added thereto at room temperature. The mixture was reacted at room temperature for 1 hour under stirring. After completion of the reaction, ethyl acetate was added to the reaction product, and the ethyl acetate layer was washed with water, dried over Glauber's salt and then purified by column chromatography to obtain 2.76 g of N-[4-(5-chloro-2-pyrimidinyloxy)-3-methylphenyl]-2-nitrobenzenesulfenamide (Intermediate Compound No. 37) (melting point: 74°-85° C.) in a yellow non-crystalline form.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04987135
Quelldatensatzuspto-grants-1991_01
ORD IDord-635377d9a71e459093799c5dc60a7731
Quellennotizuspto-grants-1991_01