Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368317Generated: November 2, 2026

Triethylamine → 3-Amino-6-furan-2-yl-pyrazine-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/2368317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethyl 3-Amino-6-bromopyrazine-2-carboxylateHCID 227251—
ReactantFuran-2-boronic acidHCID 2734357—
Catalystpalladium(II) acetateHCID 167845—
Catalyst1,1`-Bis(diphenylphosphino)ferroceneHCID 15241612—
SolventDimethylformamideHCID 6228—
Product3-Amino-6-furan-2-yl-pyrazine-2-carboxylic acid methyl esterHCID 7009885760.3%

Reaction Steps

A mixture of Pd(OAc)2 (146 mg, 0.7 mmol) and 1,1-bis(diphenylphosphino)ferrocene (478 mg, 0.9 mmol) in DMF (65 ml) under an argon atmosphere was stirred at 50° for 15 min and cooled to rt. The reaction mixture was evacuated, then flushed with argon. 3-Amino-6-bromopyrazine-2-carboxylic acid methyl ester (5.0 g, 21.5 mmol), 2-furanboronic acid (2.65 g, 23.7 mmol) and triethylamine (4.3 ml) were added. The reaction mixture was again evacuated, then flushed with argon. The mixture was heated at 90° overnight. After cooling to rt, the black mixture was concentrated to dryness. The residue was dissolved in dichloromethane (800 ml), washed with water, dried over MgSO4, filtered and evaporated. The crude product was purified by silica gel chromatography using a n-heptane/EtOAc gradient for elution, providing the title compound as yellow solid (2.84 g, 60%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703768B2
Source datasetuspto-grants-2014_04
ORD IDord-b396e672f299443bb52173721f2f7e94
Source noteuspto-grants-2014_04