HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2408848Generated: October 31, 2026
Benzyl piperazine-1-carboxylate → HCID 67387134, compound
https://huagongshe.com/reaction/2408848
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzyl piperazine-1-carboxylate | HCID 643495 | — |
| 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 67387134 | HCID 67387134 | — |
Reaction Steps
To a solution of 2-(2-oxo-3,3-diphenylpyrrolidin-1-yl)acetic acid (0.29 g, 1.0 mmol, Example 21C) in CH2Cl2 (15 mL) was added benzyl piperazine-1-carboxylate (0.22 g, 1.0 mmol) under nitrogen. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.38 g, 2.0 mmol) and 4-(dimethylamino)pyridine (0.012 g, 0.1 mmol) were added, and the reaction mixture was stirred overnight at room temperature. The organic layer was washed with water and brine, dried over MgSO4, filtered, and concentrated. The crude product was purified by chromatography on silica gel (Analogix Intelliflash 280; CH3OH/CH2Cl2, 2:98 eluant) to yield the title compound. 1H NMR (300 MHz, CDCl3) δ ppm 7.43-7.16 (m, 15H), 5.14 (s, 2H), 4.19 (s, 2H), 3.64-3.23 (m, 10H), 2.81 (t, J=6.5, 2H); MS (DCI+) m/z 414 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815869B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-a9066b9a88914e34afc274434ab0eac5 |
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| Source note | uspto-grants-2014_08 |
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