HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1724688Generated: October 26, 2026
Nitric Acid → Ethyl 5-nitro-1H-indazole-3-carboxylate
https://huagongshe.com/reaction/1724688
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | ethyl 1H-indazole-3-carboxylate | HCID 78251 | — |
| Solvent | Sulfuric Acid | HCID 1118 | — |
| Product | Ethyl 5-nitro-1H-indazole-3-carboxylate | HCID 12689368 | 53% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07488737B2 |
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| Source dataset | uspto-grants-2009_02 |
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| ORD ID | ord-35869c7c38fa4b6dbbfaa9e689f47cf2 |
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| Source note | uspto-grants-2009_02 |
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