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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
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 67387134HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815869B2
Source datasetuspto-grants-2014_08
ORD IDord-a9066b9a88914e34afc274434ab0eac5
Source noteuspto-grants-2014_08