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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantMethyl 3-amino-5,6-dichloropyrazine-2-carboxylateHCID 73828—
Reactant2-Methylphenyl boronic acidHCID 2733267—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
SolventBrine ethyl acetateHCID 131718255—
ProductMethyl 3-amino-6-chloro-5-(2-methylphenyl)pyrazine-2-carboxylateHCID 8663736650%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552201B2
Source datasetuspto-grants-2013_10
ORD IDord-1b5160dca7ae4142b9049d34884f05b1
Source noteuspto-grants-2013_10