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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401457Generated: October 30, 2026

(6-Fluoro-5-methylpyridin-3-yl)boronic acid → 6-(6-Fluoro-5-methylpyridin-3-yl) imidazo[1,2-a]pyridine-3-carbaldehyde

https://huagongshe.com/reaction/401457

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(6-Fluoro-5-methylpyridin-3-yl)boronic acidHCID 17750247—
Reactant6-Bromoimidazo[1,2-a]pyridine-3-carbaldehydeHCID 21345676—
Product6-(6-Fluoro-5-methylpyridin-3-yl) imidazo[1,2-a]pyridine-3-carbaldehydeHCID 8667060544%

Reaction Steps

The title compound was prepared by following the procedure as described for Intermediate 1 using 6-bromoimidazo[1,2-a]pyridine-3-carbaldehyde and 6-fluoro-5-methylpyridin-3-ylboronic acid. Yield: 44%; 1H NMR (DMSO-d6; 300 MHz): δ10.0 (s, 1H), 9.59 (s, 1H), 8.58-8.00 (m, 5H), 2.24 (s, 3H), MS: m/z 256(M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741932B2
Source datasetuspto-grants-2014_06
ORD IDord-a85e0c38be014b8b947e50ae0e69dff4
Source noteuspto-grants-2014_06