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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507851Generated: October 27, 2026

2-Piperidone → 2-(3-Methoxypropoxy)-N-{3-methyl-2(S)-[2-oxo-5(S)-(2-oxopiperidin-1-ylmethyl)-oxazolidin-4(S)-ylmethyl]butyl}benzamide

https://huagongshe.com/reaction/507851

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PiperidoneHCID 12665—
ReactantPotassium tert-butoxideHCID 23665647—
Reactanttert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)-(R)-oxiranylpentyl)-carbamateHCID 86613450—
SolventDimethyl SulfoxideHCID 679—
Product2-(3-Methoxypropoxy)-N-{3-methyl-2(S)-[2-oxo-5(S)-(2-oxopiperidin-1-ylmethyl)-oxazolidin-4(S)-ylmethyl]butyl}benzamideHCID 68623980—

Reaction Steps

A mixture of 0.115 g of piperidin-2-one, 0.136 g of potassium tert-butoxide in 3 ml of dimethyl sulphoxide is stirred at room temperature over 30 minutes, admixed with 0.26 g of tert-butyl (3(S)-{[2-(3-methoxypropoxy)benzoylamino]methyl}-4-methyl-1(S)—(R)-oxiranylpentyl)-carbamate (Example 1b) and subsequently stirred further at room temperature overnight. The reaction mixture is poured onto ice-water and extracted with tert-butyl methyl ether (2×). The combined organic phases are washed successively with water and brine, dried over sodium sulphate and concentrated by evaporation. The title compound is identified from the residue by means of flash chromatography (SiO2 60F) on the basis of the Rf value.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786307B2
Source datasetuspto-grants-2010_08
ORD IDord-787a7e4668c44104b35774cb236b783b
Source noteuspto-grants-2010_08