HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040372Generated: October 30, 2026
N-bromobutanimide → Methyl 5-amino-6-bromopyrazine-2-carboxylate
https://huagongshe.com/reaction/1040372
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 5-aminopyrazine-2-carboxylate | HCID 14536427 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Water ethylacetate | HCID 22728543 | — |
| Product | Methyl 5-amino-6-bromopyrazine-2-carboxylate | HCID 29983315 | 78.3% |
Reaction Steps
Add 1.79 g (10.05 mmol) of N-bromosuccinimide to a solution of 1.4 g (9.14 mmol) of methyl 5-aminopyrazine-2-carboxylate in 10 mL of acetonitrile. Stir the reaction mixture for 2 h at 20° C. then distribute in 100 mL of EtOAc/water 1:1 mixture. Wash the organic phase with 2×50 mL of water, dry over Na2SO4 and concentrate under reduced pressure. Purify the residue obtained by silica gel column chromatography, eluting with a cyclohexane/EtOAc gradient from 0 to 50% of EtOAc. After concentration under reduced pressure, we obtain 1.66 g of methyl 5-amino-6-bromopyrazine-2-carboxylate in the form of yellow wax.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08552201B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-c650f43a3d7c4499b5767d2488d3d667 |
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| Source note | uspto-grants-2013_10 |
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