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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297322Generated: October 30, 2026

4-Hydroxybenzylamine → 4-{[(3-Amino-6-bromopyrazin-2-yl)amino]methyl}phenol

https://huagongshe.com/reaction/1297322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-HydroxybenzylamineHCID 97472—
Reactant2-Amino-3,5-dibromopyrazineHCID 620004—
SolventDimethyl SulfoxideHCID 679—
Product4-{[(3-Amino-6-bromopyrazin-2-yl)amino]methyl}phenolHCID 2482042811.7%

Reaction Steps

A solution of 3,5-dibromo-pyrazin-2-ylamine (220 mg, 0.87 mmol) and 4-aminomethyl-phenol (225.0 mg, 1.83 mmol) in DMSO (2.5 mL) was heated at 98° C. under nitrogen for 24 hours. HPLC showed that 35% of product was formed and 40% of starting material presented. The reaction solution was partitioned between EtOAc and water. After condensation of organic layer, the residue was purified on a silica gel column eluting with 3% methanol in dichloromethane to provide 4-[(3-amino-6-bromo-pyrazin-2-ylamino)-methyl]-phenol (30 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250417B2
Source datasetuspto-grants-2007_07
ORD IDord-f54413153dba4639ab1ace9cd9bb69ca
Source noteuspto-grants-2007_07