Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25385Erstellt: 24. Oktober 2026

Pyridine → HCID 22319544, Verbindung

https://huagongshe.com/de/reaction/25385

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktBenzoyl chlorideHCID 7412—
Edukt3-Amino-5-nitroindazoleHCID 3136655—
LösungsmittelWaterHCID 962—
ProduktHCID 22319544HCID 22319544—

Reaktionsschritte

N-(5-Nitro-1H-indazol-3-yl)benzamide can be obtained in the following way: 0.39 ml of benzoyl chloride is added dropwise to a solution, cooled to 0° C., of 0.6 g of 3-amino-5-nitro-1H-indazole and of 5 ml of pyridine. The medium is brought back to a temperature in the region of 20° C. and maintained with stirring for 18 hours. After addition of 20 ml of distilled water, the medium is extracted with 20 ml and 10 ml of ethyl acetate. The organic phases are pooled, dried over magnesium sulfate, filtered and concentrated by evaporation under reduced pressure. The residue thus obtained is purified by chromatography on a silica column with a dichloromethane/methanol (99/1 by volume) mixture as eluent. 0.9 g of N-(5-nitro-1H-indazol-3-yl)benzamide is thus obtained in the form of an orange solid melting at 231° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858638B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-b32628b6c1cb473093f6eeb51a7dbc2f
Quellennotizuspto-grants-2005_02