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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1612637Erstellt: 25. Oktober 2026

Pyridine → Acibenzolar Acid Impurity 21

https://huagongshe.com/reaction/1612637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktTrifluoroacetic anhydrideHCID 9845—
EduktBenzo-1,2,3-thiadiazole-7-carboxylic acid amideHCID 22403364—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktAcibenzolar Acid Impurity 21HCID 22182879—

Reaktionsbedingungen

Temperatur3 °C

Reaktionsschritte

4.0 g (0.022 mol) of benzo-1,2,3-thiadiazol-7-ylcarboxylic acid amide are dissolved in 35 ml of tetrahydrofuran, and 3.6 ml (0.045 mol) of pyridine are added. The batch is then cooled to 3° C. and a solution of 3.9 ml (0.028 mol) of trifluoroacetic acid anhydride in 12 ml of tetrahydrofuran is added dropwise. The reaction mixture is subsequently stirred for 22 hours at room temperature and then poured onto ice/water and extracted twice with ethyl acetate. The extracts are washed with water, dried over magnesium sulfate and filtered through a layer of silica gel. Concentration by evaporation gives 3.5 g (99% of the theoretical yield) of crystalline product having a melting point of 119°-122° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05190928
Quelldatensatzuspto-grants-1993_03
ORD IDord-01b3f64fe80a49e69c45dd9ae52a6bfd
Quellennotizuspto-grants-1993_03