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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467720Generated: October 29, 2026

Triethylamine → HCID 70098857, compound

https://huagongshe.com/reaction/467720

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—
ProductHCID 70098857HCID 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 numberUS08623866B2
Source datasetuspto-grants-2014_01
ORD IDord-46b63bfe42534f978af35b45cb6d206a
Source noteuspto-grants-2014_01