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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-(Bis(4-fluorophenyl)methyl)piperazine | HCID 152932 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 2-(2-Oxo-3,3-diphenylpyrrolidin-1-yl)acetic acid | HCID 67359013 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57393322 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044069B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-b9260aed72ae410994ea6636b2ffd714 |
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| Source note | uspto-grants-2011_10 |
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