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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-6-methoxy-3-nitropyridine | HCID 2795029 | — |
| Reactant | Methyl 3-amino-2-methylpropanoate | HCID 10486829 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Methyl-3-((6-methoxy-3-nitropyridin-2-yl)amino)-2-methylpropanoate | HCID 70978457 | 98% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09422292B2 |
|---|
| Source dataset | uspto-grants-2016_08 |
|---|
| ORD ID | ord-c3dd6a517e164204930206a102c71e5a |
|---|
| Source note | uspto-grants-2016_08 |
|---|