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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368374Generated: November 1, 2026

Ethyl Acetate → Methyl 3-(bis(tert-butoxycarbonyl)amino)-6-methoxypyrazine-2-carboxylate

https://huagongshe.com/reaction/2368374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 3-(bis(tert-butoxycarbonyl)amino)-6-bromopyrazine-2-carboxylateHCID 86660188—
SolventMethanolHCID 887—
ProductMethyl 3-(bis(tert-butoxycarbonyl)amino)-6-methoxypyrazine-2-carboxylateHCID 70097371—

Reaction Steps

To a solution of methyl 3-(bis(tert-butoxycarbonyl)amino)-6-bromopyrazine-2-carboxylate (500 mg, 1.16 mmol; example A-10, step 1) in MeOH (10 ml) was added sodium methoxide (30%; 280 μl, 1.5 mmol) at room temperature and stirring was continued at r.t. for 2 h. The reaction mixture was poured into ethyl acetate (75 ml) and extracted with potassium hydrogen sulfate (10%). The organic phase was washed with water and brine and the aqueous layers were back-extracted with ethyl acetate. The organic layers were dried and evaporated and the product was obtained after purification by silica gel chromatography using a heptane/ethyl acetate gradient as colorless solid (320 mg, 71%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703768B2
Source datasetuspto-grants-2014_04
ORD IDord-70ce65673c0c4c26b757d1c02a51d767
Source noteuspto-grants-2014_04