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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366695Generated: November 3, 2026

4-Methylmorpholine → (2S)-1-(phenylmethyl)-2-(1-pyrrolidinylcarbonyl)piperidine

https://huagongshe.com/reaction/1366695

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPiperidineHCID 8082—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-Benzyl-L-proline hydrochlorideHCID 57367734—
SolventDichloromethaneHCID 6344—
Product(2S)-1-(phenylmethyl)-2-(1-pyrrolidinylcarbonyl)piperidineHCID 6693627140.1%

Reaction Steps

1-(Phenylmethyl)-L-proline hydrochloride (2.0 g, 8.247 mmol) and HOBt (1.34 g, 9.928 mmol) were dissolved in CH2Cl2 (50 mL), and 4-methylmorpholine (2.72 mL, 24.822 mmol), piperidine (0.981 mL, 9.929 mmol), and EDCI (1.906 g, 9.928 mmol) were added to this solution. After stirring overnight, the solution was washed with water (50 mL), and the aqueous layer was extracted with CH2Cl2 (3×50 mL). The combined organic layers were dried over anhydrous MgSO4 and concentrated in vacuo to provide (2S)-1-(phenylmethyl)-2-(1-pyrrolidinylcarbonyl)piperidine (0.901 g, 40%). LCMS: (M+H)+: 273.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-6178d18268e24c79b11e6c0f04b26a34
Source noteuspto-grants-2011_02