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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720001Generated: October 30, 2026

Sodium Carbonate → 5-(Thiophen-3-yl)pyrazin-2-amine

https://huagongshe.com/reaction/720001

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantThiophene-3-boronic acidHCID 581760—
Reactant2-Amino-5-bromopyrazineHCID 599539—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventEthyl AcetateHCID 8857—
Product5-(Thiophen-3-yl)pyrazin-2-amineHCID 1165123569%

Reaction Steps

A mixture of 2-amino-5-bromopyrazine (500 mg, 2.874 mmol), dichlorobis(triphenylphosphine)palladium(II) (290 mg, 0.413 mmol), 3-thiopheneboronic acid (500 mg, 3.908 mmol), and a saturated aqueous sodium carbonate solution (4 mL) in ethylene glycol dimethyl ether (8 mL) and ethanol (8 mL) was heated under reflux for 45 min. The reaction mixture was then cooled, diluted with ethyl acetate, and washed with water and a saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo. Biotage chromatography (FLASH 40M, Silica, 1/1 hexanes/ethyl acetate) afforded 5-thiophen-3-yl-pyrazin-2-ylamine (351.3 mg, 69%) as a light purple solid: EI-HRMS m/e calcd for C8H7N3S (M+) 177.0361, found 177.0358.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132425B2
Source datasetuspto-grants-2006_11
ORD IDord-ec7d06e4bd9240bb9bb9468fed880497
Source noteuspto-grants-2006_11