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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043174Generated: October 26, 2026

N-bromobutanimide → Methyl 2-(6-amino-5-bromopyridin-3-yloxy)-4-fluorobenzoate

https://huagongshe.com/reaction/1043174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-(6-aminopyridin-3-yloxy)-4-fluorobenzoateHCID 67226188—
SolventDimethylformamideHCID 6228—
ProductMethyl 2-(6-amino-5-bromopyridin-3-yloxy)-4-fluorobenzoateHCID 67226738—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of EXAMPLE 318B (1.6 g) in N,N-dimethylformamide (50 mL) was cooled to 0° C., followed by the addition of N-bromosuccinimide (1.195 g) in N,N-dimethylformamide (10 mL) solution. The reaction mixture was stirred at 0° C. for 1 hour, and quenched with ice-cold saturated NaHCO3 aqueous solution. The reaction mixture was extracted with ethyl acetate. The combined organic phase was washed with water and brine, dried over anhydrous sodium sulfate, filtered, and concentrated. The crude material was purified using flash column purification with 30-40% ethyl acetate/hexane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557983B2
Source datasetuspto-grants-2013_10
ORD IDord-b8e07de85a7f46c0a93517d3e87ed05b
Source noteuspto-grants-2013_10