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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858563Generated: October 30, 2026

4-Methylmorpholine → HCID 58762593, compound

https://huagongshe.com/reaction/858563

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant2-Oxo-1-pyrrolidinepropanoic acidHCID 3146688—
ReactantHCID 178419650HCID 178419650—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58762593HCID 5876259315%

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Chloro-4-6-dimethoxy-1,3,5-triazine (2.68 g, 15.2 mmol) and N-methylmorpholine (4.2 mL, 38.1 mmol) were added to a solution of 3-(2-Oxo-pyrrolidin-1-yl)-propionic acid (2 g, 12.7 mmol, from Step 1) in THF (35 mL). After 1 h the reaction mixture was filtered through a glass frit to remove a white precipitate. The filtrate was treated with copper iodide (2.4 g, 12.7 mmol), cooled to 0° C. and then cyclopentyl magnesium bromide (6.35 mL, 12.7 mmol, 2M in ether) was added. After 4 h the resulting black mixture was quenched with saturated NH4Cl and extracted with CH2Cl2. The organic layers were washed with 1 N HCl, saturated NaHCO3, brine, dried over Na2SO4 and concentrated. The residue was purifed by silica gel chromatography (75% EtOAc in hexanes then 5% MeOH in CH2Cl2) to give the title compound as a yellow oil. (0.4 g, 15% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148226B2
Source datasetuspto-grants-2006_12
ORD IDord-f966936e3fb84293961b9b2a9e0e786a
Source noteuspto-grants-2006_12