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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596087Generated: October 29, 2026

Sodium Carbonate → Methyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoate

https://huagongshe.com/reaction/596087

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-Amino-3-chloropyrazineHCID 276224—
Reactant3-Fluoro-4-methoxycarbonylphenylboronic acid, pinacol esterHCID 22171528—
CatalystHCID 178418807HCID 178418807—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductMethyl 4-(3-aminopyrazin-2-yl)-2-fluorobenzoateHCID 118045820111.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a mixture of 3-chloropyrazin-2-amine (5 g, 38.6 mmol) in DME (160 mL) and aq. 2 M sodium carbonate (40 mL, 80 mmol) was added methyl 2-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate (12.97 g, 46.3 mmol) followed by PdCl2(dppf)-CH2Cl2 adduct (3.15 g, 3.86 mmol). The reaction mixture was purged with N2 and heated in an oil bath at 100° C. for 3-4 h. The reaction mixture was partitioned between ethylacetate and water. The organic layer was separated, washed with brine, dried over sodium sulfate, filtered and evaporated. The crude was triturated with DCM. Solid observed was filtered, washed with ether and dried under reduced pressure to provide product as an off white solid. Filtrate was purified by flash chromatography eluting with 0-50-80% EtOAc/heptane to provide 10.6 g of product in 93% yield. LCMS (m/z): 248.1 (MH+), 0.563 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-80f8d6ffad4f497d9efd08d49c5d3705
Source noteuspto-grants-2016_01