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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1784010Generated: October 30, 2026

4-Methylmorpholine → 2-Methoxy-N-(6-methylpyridin-3-yl)methyl-4-nitrobenzamide

https://huagongshe.com/reaction/1784010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant4-Nitro-o-anisic acidHCID 75776—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(6-Methylpyridin-3-yl)methanamineHCID 12214337—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-Methoxy-N-(6-methylpyridin-3-yl)methyl-4-nitrobenzamideHCID 57589991—

Reaction Steps

2-Methoxy-4-nitrobenzoic acid (293 mg, 1.49 mmol) is dissolved in DMF (2 mL) and 4-methylmorpholine (220 μL, 3.0 mmol) and TBTU (1.79 g, 1.7 mmol) are added. The mixture is stirred at rt for 30 min and C-(6-methylpyridin-3-yl)methylamine (400 mg, 3.27 mmol) is added. Stirring is continued at rt for 12 h. DCM (10 mL) is added and the organic phase is washed with Na2CO3 (5% aq.), HCl (3% aq.) and water, and then dried over Na2SO4. After evaporation of the solvents, the residue is triturated with ether-hexane to afford the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07501411B2
Source datasetuspto-grants-2009_03
ORD IDord-43a1ea37067d45fc96a9ae3ea13df240
Source noteuspto-grants-2009_03