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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1040373Generated: November 2, 2026

Sodium Carbonate → Methyl 5-amino-6-[3-(benzyloxy)-4-chlorophenyl]pyrazine-2-carboxylate

https://huagongshe.com/reaction/1040373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantButyldiphenylphosphineHCID 80755—
Reactant(3-(Benzyloxy)-4-chlorophenyl)boronic acidHCID 23005378—
ReactantMethyl 5-amino-6-bromopyrazine-2-carboxylateHCID 29983315—
Catalyst(Bis-benzonitrile)-palladiumHCID 86637365—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventWater ethylacetateHCID 22728543—
ProductMethyl 5-amino-6-[3-(benzyloxy)-4-chlorophenyl]pyrazine-2-carboxylateHCID 6672126750.3%

Reaction Steps

Stir a suspension of 137 mg (0.36 mmol) of (bis-benzonitrile)-palladium II dichloride and 183 mg (0.43 mmol) of diphenylphosphinobutane in 7 mL of toluene under argon for 30 min at room temperature. Then add, while bubbling with argon, 1.66 g (7.15 mmol) of methyl 5-amino-6-bromopyrazine-2-carboxylate, 1.97 g (7.51 mmol) of [3-(benzyloxy)-4-chlorophenyl]boronic acid, 2.4 mL of ethanol and 3.58 mL (7.15 mmol) of a 2N aqueous solution of sodium carbonate. Reflux the reaction mixture for 5 h 30 min and then distribute in 100 mL of a water/EtOAc 1:1 mixture. Wash the organic phase with 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 50 to 100% of EtOAc. After concentration under reduced pressure, we obtain 1.33 g of methyl 5-amino-6-[3-(benzyloxy)-4-chlorophenyl]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-fd77a90a30384fecad8b42b43765f64e
Source noteuspto-grants-2013_10