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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 392329Generated: October 26, 2026

Methyl 3-methoxy-6-nitro-2-pyrazinecarboxylate → Methyl 6-amino-3-methoxy-2-pyrazinecarboxylate

https://huagongshe.com/reaction/392329

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 3-methoxy-6-nitro-2-pyrazinecarboxylateHCID 22662794—
ReactantHCID 178418361HCID 178418361—
CatalystPalladium on calcium carbonateHCID 17803853—
SolventAcetic AcidHCID 176—
ProductMethyl 6-amino-3-methoxy-2-pyrazinecarboxylateHCID 2266284371.8%

Reaction Steps

At room temperature and under a pressure of 1 atmosphere, hydrogen gas was introduced into a mixture of 24.3 g of methyl 3-methoxy-6-nitro-2-pyrazinecarboxylate, 480 mL of acetic acid and 1.2 g of lead-poisoned palladium-calcium carbonate until the mixture became showing no further absorption of hydrogen. After filtering off insoluble matter from the reaction mixture, the solvent was removed under reduced pressure, and the solid product thus obtained was washed with ethyl acetate and diethyl ether. Thus, 15.0 g of methyl 6-amino-3-metoxy-2-pyrazinecarboxylate was obtained as a solid product. Furthermore, the solvent was removed from the filtrate under reduced pressure to obtain a solid product, and the solid product was washed with ethyl acetate to obtain 2.3 g of methyl 6-amino-3-methoxy-2-pyrazinecarboxylate as a solid product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06800629B2
Source datasetuspto-grants-2004_10
ORD IDord-d607e4676fc845f4bdd82f325eb24bc2
Source noteuspto-grants-2004_10