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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929359Generated: October 26, 2026

N-bromobutanimide → (2-Amino-5-bromopyridin-3-yl)(6-bromopyridin-2-yl)methanone

https://huagongshe.com/reaction/1929359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 57690673HCID 57690673—
Product(2-Amino-5-bromopyridin-3-yl)(6-bromopyridin-2-yl)methanoneHCID 5769061657.2%

Reaction Steps

To a suspension of (2-aminopyridin-3-yl)(6-bromopyridin-2-yl)methanone (5.76 g, 20.7 mmol) in acetonirile (120 ml) was added N-bromosuccinimide (4.05 g, 22.77 mmol). The resulting mixture was stirred at room temperature for 1 hour before mixture was concentrated in vacuo to approximately 20 ml. The solid was then collected by filtration and washed with minimal acetonitrile and dried to leave title compound as a brown solid (4.23 g, 57%). 1H NMR (DMSO-d6) 7.93-7.89 (4H, m), 8.03-7.99 (1H, m), 8.22 (1H, d), 8.36 (1H, d). ES+ 357.99.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188071B2
Source datasetuspto-grants-2012_05
ORD IDord-3d1c334b5a8a4c5cade6271e175a2fe5
Source noteuspto-grants-2012_05