HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817149Generated: October 30, 2026
Methyl 3-aminopyrazinecarboxylate → 3-Aminopyrazine-2-carbaldehyde
https://huagongshe.com/reaction/1817149
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 3-aminopyrazinecarboxylate | HCID 72669 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-Aminopyrazine-2-carbaldehyde | HCID 15274931 | 34% |
Reaction Steps
Methyl-3-aminopyrazine-2-carboxylate (11 g) was dissolved in THF and cooled to −78° C. Diisobutylaluminum hydride (1M in hexanes, 250 mL) was added, and the reaction stirred at −78° C. for 4 hours. The reaction was then warmed to 0° C. for one hour before being quenched slowly by addition of 1M hydrochloric acid. Ethyl acetate was added and the layers separated. The organic layer was dried over magnesium sulfate, filtered and concentrated. The residue was triturated in hexanes to afford title compound (3.0 g, 34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598251B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-72aa06987f2b428ca5bc3609a46a03b4 |
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| Source note | uspto-grants-2009_10 |
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