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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485461Generated: October 30, 2026

Potassium Carbonate → Methyl-3-((6-methoxy-3-nitropyridin-2-yl)amino)-2-methylpropanoate

https://huagongshe.com/reaction/1485461

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-6-methoxy-3-nitropyridineHCID 2795029—
ReactantMethyl 3-amino-2-methylpropanoateHCID 10486829—
SolventTetrahydrofuranHCID 8028—
ProductMethyl-3-((6-methoxy-3-nitropyridin-2-yl)amino)-2-methylpropanoateHCID 7097845798%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 2-chloro-6-methoxy-3-nitropyridine (3 g, 15.91 mmol) in tetrahydrofuran (20 mL) was added methyl-3-amino-2-methylpropanoate (2.05 g, 17.50 mmol) and potassium carbonate (4.40 g, 31.82 mmol). The mixture was stirred at 50° C. for 12 hours. The reaction mixture was concentrated in vacuo and washed with water (20 mL), extracted with acetic ester (20 mL×3). The combined organic phase was dried by anhydrous sodium sulphate, and then filtered. The filtrate was concentrated and purified by column chromatograph silica gel (elute: dichloromethane/Methanol: 100:1→80:1) to give methyl-3-((6-methoxy-3-nitropyridin-2-yl)amino)-2-methylpropanoate (4.2 g, 97%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09422292B2
Source datasetuspto-grants-2016_08
ORD IDord-c3dd6a517e164204930206a102c71e5a
Source noteuspto-grants-2016_08