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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747101Generated: October 25, 2026

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

https://huagongshe.com/reaction/747101

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactantethyl 1H-indazole-3-carboxylateHCID 78251—
SolventSulfuric AcidHCID 1118—
ProductEthyl 5-nitro-1H-indazole-3-carboxylateHCID 1268936853%

Reaction Conditions

Temperature0 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396833B2
Source datasetuspto-grants-2008_07
ORD IDord-c61aef33cfe44b9bbabc0cfb772115d7
Source noteuspto-grants-2008_07