HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064934Generated: October 30, 2026
Nitrogen → 1-(5,5-Difluoro-hexyl)-1H-pyrazol-4-ylamine
https://huagongshe.com/reaction/2064934
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitrogen | HCID 947 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 1-(5,5-difluoro-hexyl)-4-nitro-1H-pyrazole | HCID 66928574 | — |
| Catalyst | Iron | HCID 23925 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(5,5-Difluoro-hexyl)-1H-pyrazol-4-ylamine | HCID 66929172 | — |
Reaction Steps
In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a mixture of 1-(5,5-difluoro-hexyl)-4-nitro-1H-pyrazole (400 mg, 1.72 mmol), iron powder (290 mg, 5.15 mmol) and NH4Cl (463 mg, 8.58 mmol) in a mixture of EtOH (8.0 mL) and water (4.0 mL) was stirred at 75° C. for 40 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (30 mL) was added followed by 1M NaOH (30 mL). The aq. layer was extracted with CH2Cl2 (2×30 mL) and the combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as a deep red oil. LC-MS-conditions 02: tR=0.60 min; [M+H]+=204.27.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08288419B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-e350799d642a4ccb85ffdffbfcca6c59 |
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| Source note | uspto-grants-2012_10 |
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