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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452298Generated: October 29, 2026

Diisopropylethylamine → 4-[4-(2-Fluoro-ethoxy)-phenyl]-piperazine-1-carboxamidine

https://huagongshe.com/reaction/452298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPraxadineHCID 2734673—
Reactant1-[4-(2-Fluoroethoxy)phenyl]piperazineHCID 11492296—
SolventAcetonitrileHCID 6342—
Product4-[4-(2-Fluoro-ethoxy)-phenyl]-piperazine-1-carboxamidineHCID 5947054584.6%

Reaction Steps

To a solution of 1-(4-(2-fluoroethoxy)phenyl)piperazine (50 mg, 0.15 mmol) and diisopropylethylamine (59 μL, 0.34 mmol) in ACN (1 mL) was added 1H-pyrazole-1-carboximidamide (25 mg, 0.17 mmol). The reaction stirred at room temperature for 1 h, monitored by LC-MS. The precipitate was then filtered and washed with ACN to obtain the desired product as a white solid (33.8 mg, 58% yield). 1H NMR (300 MHz, DMSO-d6): δ 7.55 (br s, 3H), 6.95-6.86 (m, 4H), 4.78 (m, 1H), 4.62 (m, 1H), 4.21 (m, 1H), 4.11 (m, 1H), 3.57 (dd, 4H, J=5.2, 4.9 Hz), 3.09 (dd, 4H, J=5.1, 5.0 Hz); 19F NMR (DMSO-d6): δ−222.037 (m, 1F); 13C NMR (75.5 MHz, DMSO-d6): δ 156.0, 152.2, 144.9, 119.2, 115.1, 82.2 (81.1), 67.4 (67.2), 48.9, 44.9; HRMS calcd. for C12H17FN2O: 267.16157 found 267.16146.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08491868B2
Source datasetuspto-grants-2013_07
ORD IDord-db2dd922ec5b45c8ba258717d9bc3572
Source noteuspto-grants-2013_07