HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 415022Generated: October 25, 2026
1-(3-fluorobenzyl)-5-nitro-1H-indazole → 1-(3-Fluorobenzyl)-1H-indazol-5-amine
https://huagongshe.com/reaction/415022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(3-fluorobenzyl)-5-nitro-1H-indazole | HCID 21966490 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-(3-Fluorobenzyl)-1H-indazol-5-amine | HCID 7147073 | — |
Reaction Steps
Follow modified procedure from WO 99/35146. 1-(3-Fluoro-benzyl)-5-nitro-1H-indazole (2.49 g, 9.2 mmol) is suspended in 40 ml absolute EtOH and Pt/C (5%, wet, 150 mg) is added. The reaction mixture is stirred and heated at 60° C. under a hydrogen atmosphere (balloon). Roughly 4 hours into the reaction LC/MS reveals the formation of substantial amounts of product. The mixture is filtered through Celite and concentrated under reduced pressure. Yield: 2.01 g (90.8%) of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088766B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-ff116f94cb45417cb577c54f4cff4800 |
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| Source note | uspto-grants-2012_01 |
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