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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1783784Generated: October 26, 2026

Triethylamine → 3-morpholin-4-yl-N-pyridin-2-ylmethyl-propionamide

https://huagongshe.com/reaction/1783784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant2-PyridinemethanamineHCID 19509—
ReactantOxalyl chlorideHCID 65578—
Reactant4-Morpholinepropanoic acid, methyl esterHCID 101373—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product3-morpholin-4-yl-N-pyridin-2-ylmethyl-propionamideHCID 6882973379.1%

Reaction Steps

To a solution of methyl 4-morpholinepropionate (5.0 g, 28.9 mmol) in MeOH (25 mL) was added 2N NaOH (17.3 mL, 34.6 mmol). The mixture was stirred for 1 h then concentrated in vacuo. The residue was suspended in dichloromethane (125 mL) and DMF (30 μL) was added followed by oxalylchloride (10 mL, 115.6 mmol). The mixture was allowed to stir for 2 h. then concentrated in vacuo. The resulting solid was added portion-wise to a solution of 2-(aminomethyl)pyridine (2.88 mL, 28.2 mmol) and triethylamine (9.0 mL, 64.86 mmol) in dichloromethane (200 mL). The mixture was stirred at ambient temperature for 1 h. then washed with water (300 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated to yield 3-morpholin-4-yl-N-pyridin-2-ylmethyl-propionamide (5.56 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501438B2
Source datasetuspto-grants-2009_03
ORD IDord-5233a06d34af41338ead7aec562398df
Source noteuspto-grants-2009_03