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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425911Generated: October 26, 2026

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

https://huagongshe.com/reaction/425911

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 crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106197B2
Source datasetuspto-grants-2012_01
ORD IDord-e92353001d6d40ff81a529730b262d62
Source noteuspto-grants-2012_01