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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189316Generated: November 1, 2026

3,5-Difluoropyridin-2-amine → 6,8-Difluoro-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/1189316

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Difluoropyridin-2-amineHCID 2783238—
Reactant1-Bromo-6-(trimethylsilyl)hex-5-yn-2-oneHCID 86086769—
Product6,8-Difluoro-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridineHCID 6659851049.1%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 223(D), from 3,5-difluoropyridin-2-amine (492 mg, 3.78 mmol) and 1-bromo-6-(trimethylsilyl)hex-5-yn-2-one (compound 223(C), 1.87 mg, 7.56 mmol). The crude residue was purified over silicagel chromatography (prepacked 25 g silicagel column, from DCM/Cyclohexane:70/30 to DCM/MeOH: 95/5 as eluent) to afford 517 mg of 6,8-difluoro-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine (Yield: 49%) as a brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08674106B2
Source datasetuspto-grants-2014_03
ORD IDord-f186e30142a24f4c943f18b2064b7906
Source noteuspto-grants-2014_03