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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2069123Generated: November 2, 2026

Diisopropylethylamine → 2-methoxy-N-(4-(4-nitrophenoxy)pyridin-2-yl)acetamide

https://huagongshe.com/reaction/2069123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantMethoxyacetyl chlorideHCID 96623—
Reactant4-(4-Nitrophenoxy)pyridin-2-amineHCID 22936716—
SolventDichloromethaneHCID 6344—
Product2-methoxy-N-(4-(4-nitrophenoxy)pyridin-2-yl)acetamideHCID 7092174192.6%

Reaction Steps

To a solution of 4-(4-nitrophenoxy)pyridin-2-amine [US Pat Appl 2008319188, Production Example 53] (0.60 g, 2.60 mmol) and DIPEA (0.680 μL, 3.89 mmol) in DCM (15.0 mL) under nitrogen at 0° C. was added 2-methoxyacetyl chloride (225 μL, 3.89 mmol) dropwise over 5 min. The reaction was maintained at RT for 16 hr and was quenched by the addition of a 1% solution of NH3 in MeOH (10 mL). The mixture was evaporated in vacuo and the residue was taken up into DCM (50 mL) and was washed with water (25 mL) and brine (25 mL), and then dried (MgSO4) and evaporated in vacuo. The residue was purified by flash column chromatography (SiO2, EtOAc in DCM, 0-30%, gradient elution) to afford 2-methoxy-N-(4-(4-nitrophenoxy)pyridin-2-yl)acetamide as a white solid (0.73 g, 92%); Rt 1.88 min (Method 2); m/z 304 (M+H)+ (ES+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08299074B2
Source datasetuspto-grants-2012_10
ORD IDord-3442da9e5af541859f8b47a776c7c0aa
Source noteuspto-grants-2012_10