HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192914Generated: November 1, 2026
Water → Methyl 5-(((allyloxy)carbonyl)amino)pyrazine-2-carboxylate
https://huagongshe.com/reaction/2192914
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Allyl chloroformate | HCID 18052 | — |
| Reactant | Methyl 5-aminopyrazine-2-carboxylate | HCID 14536427 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 5-(((allyloxy)carbonyl)amino)pyrazine-2-carboxylate | HCID 59570895 | — |
Reaction Steps
To a solution of methyl 5-aminopyrazine-2-carboxylate (2 g) in dichloromethane (20 mL) were added pyridine (36.4 mL) and allyl chloroformate (25.2 mL) in 4 divided portions respectively, under ice-cooling, followed by stirring at room temperature overnight. To the reaction mixture was added water under ice-cooling, followed by extraction with ethyl acetate. The organic layer was sequentially washed with 1 M hydrochloric acid, saturated aqueous sodium bicarbonate, and saturated brine. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The obtained solid was collected by filtration while washing with a solvent (hexane:ethyl acetate=3:1) to obtain methyl 5-{[(allyloxy)carbonyl]amino}pyrazine-2-carboxylate (481 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329707B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-5f0e2b42efed48c28445b77afe091370 |
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| Source note | uspto-grants-2012_12 |
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