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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264153Generated: October 30, 2026

Sodium Methoxide → Methyl 3-methoxypyrazine-2-carboxylate

https://huagongshe.com/reaction/2264153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantMethyl 3-bromopyrazine-2-carboxylateHCID 13318551—
SolventMethanolHCID 887—
ProductMethyl 3-methoxypyrazine-2-carboxylateHCID 21418987—

Reaction Steps

To a solution of 2 g of methyl 3-bromopyrazine-2-carboxylate (prepared as described by J. H. Jones, W. H. Holtz, E. J. C. Cragoe, J. Med. Chem., 1969, 12, 285-287) in 50 mL of methanol was added 4 mL of 30% NaOMe in methanol. After stirring 30 min the reaction was quenched with 6 mL of acetic acid and concentrated under reduced pressure. The residue was partitioned between 50 mL ethyl acetate and 50 mL saturated NaHCO3, the extract dried over MgSO4. Concentration under reduced pressure gave a white crystalline solid: MS (m+1)=169.1; 1H NMR (400 MHz, CDCl3) 8.3 (m, 2H), 4.1 (s, 3H), 4.0 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855201B2
Source datasetuspto-grants-2010_12
ORD IDord-f3a82a8a5dec4be69935fba377aaef3b
Source noteuspto-grants-2010_12