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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334665Generated: October 29, 2026

2-Bromo-6-(fluoromethyl)pyridine → 6-Fluoro-2-(4-(6-(fluoromethyl)pyridin-2-yl)but-3-ynyl)quinoxaline

https://huagongshe.com/reaction/334665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-(fluoromethyl)pyridineHCID 10241610—
Reactant2-But-3-ynyl-6-fluoro-quinoxalineHCID 86086878—
Product6-Fluoro-2-(4-(6-(fluoromethyl)pyridin-2-yl)but-3-ynyl)quinoxalineHCID 6659812768.2%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 108(C), from 2-bromo-6-(fluoromethyl)-pyridine (43 mg, 0.22 mmol) and 2-but-3-ynyl-6-fluoro-quinoxaline (45 mg, 0.22 mmol). Microwave conditions: 120° C. for 15 minutes. The crude residue was purified by flash chromatography (cyclohexane/AcOEt 3:2) to yield 45 mg (0.15 mmol, 65%) of 6-fluoro-2-(4-(6-(fluoromethyl)pyridin-2-yl)but-3-ynyl)quinoxaline as an orange solid with a purity of 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-e6f34830702648daa4a1ee6012da3e70
Source noteuspto-grants-2014_11