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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-aminopyrazinecarboxylateHCID 72669—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventTetrahydrofuranHCID 8028—
Product3-Aminopyrazine-2-carbaldehydeHCID 1527493134%

Reaction Conditions

Temperature-78 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598251B2
Source datasetuspto-grants-2009_10
ORD IDord-72aa06987f2b428ca5bc3609a46a03b4
Source noteuspto-grants-2009_10