Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667108Generated: November 2, 2026

1-(Bis(4-fluorophenyl)methyl)piperazine → HCID 57393322, compound

https://huagongshe.com/reaction/1667108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(Bis(4-fluorophenyl)methyl)piperazineHCID 152932—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-(2-Oxo-3,3-diphenylpyrrolidin-1-yl)acetic acidHCID 67359013—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 57393322HCID 57393322—

Reaction Steps

To a solution of 1-(bis(4-fluorophenyl)methyl)piperazine (0.29 g, 1.00 mmol) in dichloromethane (20 mL) under nitrogen was added 2-(2-oxo-3,3-diphenylpyrrolidin-1-yl)acetic acid (Example 1C, 0.30 g, 1.00 mmol) followed by N1-((ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride (0.38 g, 2.00 mmol) and N,N-dimethylpyridin-4-amine (0.61 mg, 0.005 mmol). The reaction mixture was stirred overnight at room temperature. The reaction was concentrated, and the residue was partitioned in ethyl acetate/water (8:2, 400 mL). The organic layer was washed with water followed by brine, dried over magnesium sulfate, filtered, and concentrated. Silica gel chromatography eluting with ethyl acetate/hexane (1:1) gave the title compound. 1H NMR (300 MHz, DMSO-d6) δ ppm 7.42-7.47 (m, 4H), 7.21-7.33 (m, 10H), 7.11-7.17 (m, 4H), 4.41 (s, 1H), 4.14-4.15 (br s, 2H), 3.37-3.47 (m, 4H), 3.35 (t, J=6.6 Hz, 2H), 2.71 (t, J=6.5 Hz, 2H), 2.21-2.26 (m, 4H); MS (DCI+) m/z 566 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044069B2
Source datasetuspto-grants-2011_10
ORD IDord-b9260aed72ae410994ea6636b2ffd714
Source noteuspto-grants-2011_10