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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655587Generated: October 31, 2026

Bromine → Methyl 3-bromopyrazine-2-carboxylate

https://huagongshe.com/reaction/1655587

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantMethyl 3-aminopyrazinecarboxylateHCID 72669—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
SolventHydrogen BromideHCID 260—
SolventWaterHCID 962—
ProductMethyl 3-bromopyrazine-2-carboxylateHCID 1331855146%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a rapidly stirring heterogeneous mixture of 3-aminopyrazine-2-carboxylic acid methyl ester (2.00 g, 13.1 mmol) in 48% hydrobromic acid (7.9 mL) cooled to 0° C. was added bromine (2.00 mL, 6.2 g, 38.8 mmol) dropwise over 5 minutes. Then a solution of sodium nitrite (2.27 g, 32.8 mmol) in 9.5 mL of water was added dropwise over 10 minutes. The reaction mixture was stirred at 0° C. for 15-30 minutes and then basified with 60 mL of saturated sodium bicarbonate solution and extracted with ethyl acetate followed by chloroform. The combined organic extracts were dried over magnesium sulfate and concentrated under reduced pressure. The residue obtained was flash chromatographed on silica gel eluting with mixtures of hexane and ethyl acetate to afford the title compound (1.265 g, 46%). m.p. 43.5°-44° C. 1H NMR (CDCl3, 300 MHz) δ 4.04 (s, 3H), 8.50 (bs, 1H), 8.60 (bs, 1H). MS (DCl/NH3) m/e 217/219 (M+H)+, 234/236 (M+H+NH3)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250548
Source datasetuspto-grants-1993_10
ORD IDord-78181a2919d845e28601c0d06eeda450
Source noteuspto-grants-1993_10