Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178539Generated: October 29, 2026

Dicyclohexylcarbodiimide → 1-[2-(2-{3-[2-Oxo-2-(pyrrolidin-1-yl)ethyl]pyrrolidin-1-yl}ethyl)phenyl]piperidin-2-one

https://huagongshe.com/reaction/2178539

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantPyrrolidineHCID 31268—
ReactantDiisopropylethylamineHCID 81531—
Reactant(1-{2-[2-(2-Oxopiperidin-1-yl)phenyl]ethyl}pyrrolidin-3-yl)acetic acidHCID 89500481—
ReactantHCID 178418300HCID 178418300—
SolventDichloromethaneHCID 6344—
Product1-[2-(2-{3-[2-Oxo-2-(pyrrolidin-1-yl)ethyl]pyrrolidin-1-yl}ethyl)phenyl]piperidin-2-oneHCID 715226577%

Reaction Steps

To (1-{2-[2-(2-oxopiperidin-1-yl)phenyl]ethyl}pyrrolidin-3-yl)acetic acid a14-1 (115 mg, 0.348 mmol, 1 eq) and pyrrolidine (32 μl, 0.382 mmol 1.1 eq) in dichloromethane (5 ml) are added dicyclohexylcarbodiimide (79 mg, 0.82 mmol, 1.1 eq), hydroxybenzotriazole (52 mg, 0.382 mmol, 1.1 eq) and diisopropylethylamine (131 μl, 0.731 mmol, 2.1 eq). The reaction mixture is stirred overnight at room temperature, then filtered and concentrated under reduced pressure. The residue is purified by reverse phase chromatography (gradient: CH3CN/H2O/NH4OH from 30/70/0.1 to 60/40/0.1) to afford 9 mg of 1-[2-(2-{3-[2-oxo-2-(pyrrolidin-1-yl)ethyl]pyrrolidin-1-yl}ethyl)phenyl]piperidin-2-one 86 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067930B2
Source datasetuspto-grants-2015_06
ORD IDord-9889b75340824337a95f65a0c4cd408f
Source noteuspto-grants-2015_06