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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473631Generated: October 30, 2026

Water → N-(4-(3-Iodopyridin-2-yloxy)phenyl)pyridin-2-amine

https://huagongshe.com/reaction/473631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant2-Chloro-3-iodopyridineHCID 2735743—
Reactant4-(Pyridin-2-ylamino)phenolHCID 21262571—
SolventDimethyl SulfoxideHCID 679—
ProductN-(4-(3-Iodopyridin-2-yloxy)phenyl)pyridin-2-amineHCID 59373959—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 250-mL round-bottomed flask was added 2-chloro-3-iodopyridine (5.32 g, 22.22 mmol), 4-(pyridin-2-ylamino)phenol (4.96 g, 26.6 mmol) and cesium carbonate (11.27 g, 34.6 mmol) in DMSO (100 mL) and the reaction was heated at 80° C. overnight. The reaction was cooled to rt and poured into water (400 mL). The solution was extracted with EtOAc (4×100 mL) and the combined organic layers were washed with brine and dried over Na2SO4. The solution was filtered, evaporated onto silica gel and purified by flash chromatography (Isco, (330 gram)) eluting with 2M NH3 in MeOH:CH2Cl2 (0:1→1:19). The material was dissolved in MeOH, evaporated onto silica gel and further purified by flash chromatography (Isco (330 gram)) eluting with EtOAc:hexanes (0:1→3:1) to give a white amorphous solid. MS (ESI, pos. ion) m/z: 389.9. IC50 (uM)=0.2284.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08637500B2
Source datasetuspto-grants-2014_01
ORD IDord-c95da350112849abba2d5baac6340481
Source noteuspto-grants-2014_01