HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 627689Generated: October 30, 2026
Dimethylformamide → Methyl 6-chloro-3-methylpyrazine-2-carboxylate
https://huagongshe.com/reaction/627689
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Methyl 3-methyl-1-oxidopyrazin-1-ium-2-carboxylate;methyl 3-methyl-4-oxidopyrazin-4-ium-2-carboxylate | HCID 86728143 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 6-chloro-3-methylpyrazine-2-carboxylate | HCID 57992035 | 106% |
| Product | Methyl 5-chloro-3-methylpyrazine-2-carboxylate | HCID 72218580 | 48.1% |
Reaction Steps
A solution of mixture of 2-(methoxycarbonyl)-3-methylpyrazine 1-oxide compound with 3-(methoxycarbonyl)-2-methylpyrazine 1-oxide (1:1) (5.1 g, 15.17 mmol) in toluene (50 mL) was cooled to 0° C. To the mixture was added phosphorus oxychloride (2.78 ml, 30.3 mmol) under nitrogen followed by n,n′-dimethylformamide (0.117 ml, 1.517 mmol). The reaction mixture was stirred at room temperature for 4 h and then was heated to 65° C. for 18 h. The mixture was cooled to room temperature, diluted with EtOAc and washed with saturated NaHCO3 solution. The aqueous layer was back-extracted with EtOAc. The combined organic extracts were dried (MgSO4), filtered and concentrated in vacuo. The mixture was purified with ISCO (0% to 50% EtOAc/Hexanes) to afford both isomers: methyl 5-chloro-3-methylpyrazine-2-carboxylate (0.68 g, 48.1% yield) and methyl 6-chloro-3-methylpyrazine-2-carboxylate (1.5 g, 106% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09309263B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-302116827bbc4f6da8e88938c8ff13c7 |
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| Source note | uspto-grants-2016_04 |
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