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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624429Generated: October 26, 2026

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

https://huagongshe.com/reaction/624429

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 numberUS09303025B2
Source datasetuspto-grants-2016_04
ORD IDord-5d093f678978431bb2b0edb194df9a4d
Source noteuspto-grants-2016_04