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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452294Generated: October 30, 2026

1-(2-Fluorophenyl)piperazine → HCID 16637237, compound

https://huagongshe.com/reaction/452294

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Fluorophenyl)piperazineHCID 70529—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyrazole-1-carboxamidine monohydrochlorideHCID 2734672—
SolventAcetonitrileHCID 6342—
ProductHCID 16637237HCID 1663723797%

Reaction Steps

To a solution of 4-(fluorophenyl)piperazine (100 mg, 0.56 mmol) and diisopropylethylamine (106 μL, 0.61 mmol) in ACN (2 mL) was added 1H-pyrazole-1-carboximidamide hydrochloride (89 mg, 0.61 mmol). The reaction stirred at room temperature overnight. A precipitate formed, which was collected via filtration and washed with ACN to obtain 4-(4-fluorophenyl)piperazine-1-carboximidamide as a white solid (119 mg, 97% yield). 1H NMR. (300 MHz, DMSO-d6): δ 7.77 (br s, 3H), 7.10-6.97 (m, 4H), 3.60 (dd, 4H, J=5.3, 4.7 Hz), 3.14 (dd, 4H, J=5.4, 4.7 Hz); 13C NMR (75.5 MHz, DMSO-d6): δ 157.9 (154.8), 156.3, 147.2, 118.0, 115.5 (115.2), 48.3, 44.7; 19F NMR (282.4 MHz, DMSO-d6): δ−124.70−124.78 (m, 1F); HRMS calcd for C11H15FN4: 223.13535 found 223.1353.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08491868B2
Source datasetuspto-grants-2013_07
ORD IDord-d7e97f505cb8424c91d687511b00cc61
Source noteuspto-grants-2013_07