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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1724688Erstellt: 26. Oktober 2026

Nitric Acid → Ethyl 5-nitro-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/1724688

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
Eduktethyl 1H-indazole-3-carboxylateHCID 78251—
LösungsmittelSulfuric AcidHCID 1118—
ProduktEthyl 5-nitro-1H-indazole-3-carboxylateHCID 1268936853%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

Ethyl indazole-3-carboxylate (73.7 mmol) was dissolved in 20 mL concentrated sulfuric acid and the reaction mixture was cooled to 0° C. A mixture of concentrated sulfuric acid (12 mL) and 70% nitric acid (12 mL) was added dropwise over the course of 1 h. The mixture was stirred for an additional 1 h at 0° C. and was poured onto of crushed ice (200 g). The solid was collected by vacuum filtration, washed with several portions of water and dried in vacuo. The dried solid was suspended in 250 mL acetonitrile and the mixture was heated at reflux for 2 h. The mixture was allowed to cool to room temperature and the solid was collected and dried in vacuo to provide ethyl 5-nitroindazole-3-carboxylate (53%) as a colorless solid. The acid, obtained by basic hydrolysis, was coupled with the bicyclobase according to procedure A.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07488737B2
Quelldatensatzuspto-grants-2009_02
ORD IDord-35869c7c38fa4b6dbbfaa9e689f47cf2
Quellennotizuspto-grants-2009_02