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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2064938Generated: October 29, 2026

Nitrogen → 1-(5,5-Difluoro-hexyl)-1H-pyrazol-3-ylamine

https://huagongshe.com/reaction/2064938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAmmonium ChlorideHCID 25517—
Reactant1-(5,5-difluoro-hexyl)-3-nitro-1H-pyrazoleHCID 66929022—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product1-(5,5-Difluoro-hexyl)-1H-pyrazol-3-ylamineHCID 66928304—

Reaction Conditions

Temperature75 °C

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)-3-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 yellow oil. LC-MS-conditions 02: tR=0.66 min; [M+H]+=204.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288419B2
Source datasetuspto-grants-2012_10
ORD IDord-89d89928f31f4fbb88acffa75b90ffae
Source noteuspto-grants-2012_10