HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405167Generated: November 1, 2026
Methanol → 3-(Methoxycarbonyl)pyrazine-2-carboxylic acid
https://huagongshe.com/reaction/1405167
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Furo(3,4-b)pyrazine-5,7-dione | HCID 78482 | — |
| Product | 3-(Methoxycarbonyl)pyrazine-2-carboxylic acid | HCID 15207346 | — |
Reaction Steps
A solution of 12.0 g (79.95 mmol) of 2,3-pyrazine dicarboxylic anhydride in 282 mL of MeOH was heated to 65° C. overnight. The reaction mixture was cooled to ambient temperature and concentrated in vacuo. To the obtained residue was added water followed by slow addition of solid NaHCO3. After gas evolution ceased, the aqueous layer was extracted with EtOAc (1×). The aqueous layer was then acidified to pH 2 by addition of conc. HCl. The aqueous layer was extracted with EtOAc (2×) and the combined organics from the second extraction washed with brine (1×). The organic layer was dried over Na2SO4, filtered and concentrated in vacuo to yield 12.41 g (85% crude yield) of 3-(methoxycarbonyl)pyrazine-2-carboxylic acid (Compound 6) as a white powder that was used without further purification: 1H NMR (DMSO, 300 MHz): δppm 8.91 (d, J=2.7 Hz, 1H), 8.89 (d, J=2.7 Hz, 1H), 3.91 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916563B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-b1ac389928c74e7aa33e3dbcbff79009 |
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| Source note | uspto-grants-2014_12 |
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