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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384193Generated: November 2, 2026

2-Amino-3-bromo-5-methylpyrazine → 3-Methoxy-5-methyl-2-pyrazinamine

https://huagongshe.com/reaction/1384193

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-bromo-5-methylpyrazineHCID 9899043—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
Product3-Methoxy-5-methyl-2-pyrazinamineHCID 1070189475%

Reaction Steps

2-Amino-3-bromo-5-methylpyrazine (0.374 g) was added to a freshly prepared solution of sodium methoxide in methanol (made by addition of sodium (0.115 g) to methanol (6 ml)). The reaction was heated under reflux for 18 hours, cooled to ambient temperature and the solvent removed by evaporation. Water (5 ml) was added to the residue and extracted with dichloromethane (3×20 ml). The combined organic extracts were dried (MgSO4) and the solvent removed by evaporation. The residue was purified by chromatography on silica gel, eluting with dichloromethane to give 2-amino-3-methoxy-5-methylpyrazine as a white crystalline solid (0.208 g, 75%), m.p. 67-69° C.; mass spectrum (+ve CI): 140 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258817B1
Source datasetuspto-grants-2001_07
ORD IDord-2e77fb7910e24599b75cef2f170dd761
Source noteuspto-grants-2001_07