Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334785Generated: October 27, 2026

2-Amino-3-bromopyridine → 8-Bromo-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine

https://huagongshe.com/reaction/334785

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-3-bromopyridineHCID 817700—
Reactant1-Bromo-6-(trimethylsilyl)hex-5-yn-2-oneHCID 86086769—
Product8-Bromo-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridineHCID 6659832061.3%

Reaction Steps

The title compound was prepared in accordance with the general method of Example 223(D), from 3-bromopyridin-2-amine (280 mg, 1.60 mmol) and 1-bromo-6-(trimethylsilyl)hex-5-yn-2-one (compound 223(C), 870 mg, 3.5 mmol). The crude residue was purified over silicagel chromatography (prepacked 25 g silicagel column, DCM/MeOH: from 100/0 to 98/2 as eluent) to afford 315 mg of 8-bromo-2-(4-(trimethylsilyl)but-3-ynyl)-imidazo[1,2-a]pyridine (Yield: 61%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883826B2
Source datasetuspto-grants-2014_11
ORD IDord-da3bb06cdf1f4b44b2350e2e40ecea5e
Source noteuspto-grants-2014_11