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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766732Generated: October 31, 2026

N-bromobutanimide → 5-Bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine

https://huagongshe.com/reaction/1766732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant3-(2,6-Dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamineHCID 21111400—
SolventAcetonitrileHCID 6342—
Product5-Bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamineHCID 2111148551%

Reaction Conditions

Temperature0 °C

Reaction Steps

5-bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine was prepared following procedure 1. A stirring solution of 3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine (9.07 g, 0.03 mol) in acetonitrile was cooled to 0° C. using an ice bath. To this solution was added NBS (5.33 g, 0.03 mol) portionwise. The reaction was stirred at 0° C. for 15 min. The reaction was concentrated to dryness under vacuum. The resulting dark oil was dissolved in EtOAc (500 mL), and purified via silica gel chromatography. The solvents were then removed in vacuo to yield 5-bromo-3-(2,6-dichloro-3-fluoro-benzyloxy)-pyridin-2-ylamine (5.8 g, 0.015 mol, 51%) as a white crystaline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230098B2
Source datasetuspto-grants-2007_06
ORD IDord-9804539b13084a53843e23ecd0c5ff58
Source noteuspto-grants-2007_06