HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040374Generated: October 25, 2026
Sodium Carbonate → Methyl 3-amino-6-chloro-5-(2-methylphenyl)pyrazine-2-carboxylate
https://huagongshe.com/reaction/1040374
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 3-amino-5,6-dichloropyrazine-2-carboxylate | HCID 73828 | — |
| Reactant | 2-Methylphenyl boronic acid | HCID 2733267 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Brine ethyl acetate | HCID 131718255 | — |
| Product | Methyl 3-amino-6-chloro-5-(2-methylphenyl)pyrazine-2-carboxylate | HCID 86637366 | 50% |
Reaction Steps
Put 5 g (22.5 mmol) of methyl 3-amino-5,6-dichloropyrazine-2-carboxylate, 3.2 g (23.65 mmol) of 2-methylphenyl boronic acid in 45 mL of anhydrous toluene in a screw-top bottle. After dissolution, add 34 mL (67.6 mmol) of a 2N aqueous solution of sodium carbonate and degas the two-phase mixture for 30 min by bubbling with argon. Then add 1.3 g (1.13 mmol) of Pd(PPh3)4 and stir the reaction mixture vigorously at 110° C. for 48 h. After cooling, distribute the solution in 500 mL of EtOAc/brine 1:1 mixture and extract the aqueous phase again with 4×50 mL of EtOAc. Combine the organic phases, 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 20% of EtOAc. After concentration under reduced pressure, we obtain 2 g of methyl 3-amino-6-chloro-5-(2-methylphenyl)pyrazine-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-1b5160dca7ae4142b9049d34884f05b1 |
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| Source note | uspto-grants-2013_10 |
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