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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1257848Generated: November 4, 2026

6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amine → 6-[2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl]methylquinoxaline

https://huagongshe.com/reaction/1257848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-(4-Bromo-3-fluorophenyl)-1,2,4-triazin-3-amineHCID 57516523—
Reactant2-Chloro-3-quinoxalin-6-ylpropanalHCID 62395537—
Solventtert-ButanolHCID 6386—
Product6-[2-(4-Bromo-3-fluorophenyl)imidazo[1,2-b][1,2,4]triazin-7-yl]methylquinoxalineHCID 6722443962%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 2-chloro-3-quinoxalin-6-ylpropanal (110 mg, 0.52 mmol), and 6-(4-bromo-3-fluorophenyl)-1,2,4-triazin-3-amine (140 mg, 0.52 mmol) in tert-butyl alcohol (4 mL) was stirred at 110° C. overnight. After cooling to RT, it was concentrated and purified by chromatography on silica gel with EtOAc in Hexane (0-40%) to afford the desired product (140 mg, 62%). LCMS: (M+H)=435.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461330B2
Source datasetuspto-grants-2013_06
ORD IDord-6a79b37cf99a47cc8a60d0c4e23d126f
Source noteuspto-grants-2013_06