HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183114Generated: October 30, 2026
Hydrazine → 3-(4-Fluorophenyl)-1H-indazole-5-carbonitrile
https://huagongshe.com/reaction/2183114
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 4-Fluoro-3-(4-fluorobenzoyl)benzonitrile | HCID 22480156 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Fluorophenyl)-1H-indazole-5-carbonitrile | HCID 22260670 | — |
Reaction Steps
To a flask containing 4-fluoro-3-{(4-fluorophenyl)carbonyl}benzenecarbonitrile (4.2 g, 0.017 mmol) was added hydrazine monohydrate (15mL) and anhydrous hydrazine (10 mL). In an addition flask the procedure was repeated. Both flasks were allowed to stir overnight exposed to the atmosphere. LCMS confirmed the reactions were complete. To the flasks were added an excess amount of water. The reactions were allowed to stir for two hours. The product of the reactions was collected via a fritted funnel by filtration and combined to yield the title compound. The product was allowed to dry under vacuum and taken on crude into the next step of the synthesis. 1H NMR (DMSO-d6) 8.7 (s, 1H), 8.1 (m, 2H), 7.7-7.8 (m, 2H), 7.3-7.4 (t, 2H), ES-MS m/z 238 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06897231B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-99c46e197b7240ce99c1cbc91428fd6c |
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| Source note | uspto-grants-2005_05 |
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