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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428416Generated: November 2, 2026

4-(4-Amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamide → 4-[4-({[4-bromo-3-(pentafluoro-lambda6-sulfanyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamide

https://huagongshe.com/reaction/1428416

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Amino-3-fluorophenoxy)-N-methylpyridine-2-carboxamideHCID 46835219—
Reactant1-Bromo-4-isocyanato-2-(pentafluoro-lambda6-sulfanyl)benzeneHCID 86701291—
SolventDichloromethaneHCID 6344—
Product4-[4-({[4-bromo-3-(pentafluoro-lambda6-sulfanyl)phenyl]carbamoyl}amino)-3-fluorophenoxy]-N-methylpyridine-2-carboxamideHCID 57520888—

Reaction Steps

The crude 1-bromo-4-isocyanato-2-(pentafluoro-λ6-sulfanyl)benzene was dissolved in DCM (70 mL). 4-(4-amino-3-fluorophenoxy)-N-methylpicolinamide (1.75 g, 6.71 mmol, 0.8 eq) was added at room temperature under N2. The mixture was stirred at room temperature for about 30 min, a lot of solid precipitated. DCM (30 mL) was added and made the mixture stirred at room temperature for 18 hrs. The solid was collected by filtration, washed with DCM (50 mL), and dried under high vacuum to afford 2.9 g of the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937088B2
Source datasetuspto-grants-2015_01
ORD IDord-accd4d28638e4e0fbfd07cded7444d3d
Source noteuspto-grants-2015_01