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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188813Generated: October 29, 2026

Methyl 4-aminobenzoate → Benzoic acid, 4-(2-pyrazinylamino)-, methyl ester

https://huagongshe.com/reaction/2188813

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-aminobenzoateHCID 12082—
ReactantChloropyrazineHCID 73277—
SolventEthyl AcetateHCID 8857—
ProductBenzoic acid, 4-(2-pyrazinylamino)-, methyl esterHCID 5899382890%

Reaction Conditions

Temperature150 °C

Reaction Steps

Into a 250 mL roundbottom flask, was placed methyl 4-aminobenzoate (vii) (10 g, 66.23 mmol) followed by the addition of 2-chloropyrazine (75.9 g, 665.79 mmol). The resulting solution was stirred at 150° C. for 4 hours. The reaction progress was monitored by TLC (EtOAc/PE=1:2). After completion, the reaction was cooled to room temperature and the undissolved material was filtered off. The filtration was dissolved in 400 mL of water and the pH was adjustmented to 9 by the addition of Na2CO3. The resulting solution was extracted four times with 800 mL of EtOAc and the organic layers were combined and dried over Na2SO4. Removal of the solvent and volatile components from the organic layer under reduced pressure provided the crude product methyl 4-(pyrazin-2-ylamino)benzoate (viii) (13.6 g, 90% yield) as a yellow solid which was used directly in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324219B2
Source datasetuspto-grants-2012_12
ORD IDord-c96e2a751b0c47f79ce34eb0f2d4eb16
Source noteuspto-grants-2012_12