HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655587Generated: October 31, 2026
Bromine → Methyl 3-bromopyrazine-2-carboxylate
https://huagongshe.com/reaction/1655587
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromine | HCID 24408 | — |
| Reactant | Methyl 3-aminopyrazinecarboxylate | HCID 72669 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 3-bromopyrazine-2-carboxylate | HCID 13318551 | 46% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05250548 |
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| Source dataset | uspto-grants-1993_10 |
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| ORD ID | ord-78181a2919d845e28601c0d06eeda450 |
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| Source note | uspto-grants-1993_10 |
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