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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2361039Generated: October 30, 2026

Dimethyl Sulfoxide → 4-(2-(5-aminopyridin-2-yloxy)pyridin-3-yl)-N-methylpyridin-2-amine

https://huagongshe.com/reaction/2361039

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantCesium carbonateHCID 10796—
Reactant4-(2-chloropyridin-3-yl)-N-methylpyridin-2-amineHCID 16108983—
ReactantHCID 178507770HCID 178507770—
Product4-(2-(5-aminopyridin-2-yloxy)pyridin-3-yl)-N-methylpyridin-2-amineHCID 57756228—

Reaction Steps

In a microwave vial, 5-aminopyridin-2-ol (125 mg, 1.14 mmol) was dissolved in DMSO (0.910 mL, 0.228 mmol) and cesium carbonate (445 mg, 1.37 mmol) was added. The vial was capped with a septum and the reaction was stirred at RT for 25 minutes until a paste was formed. Then 4-(2-chloropyridin-3-yl)-N-methylpyridin-2-amine (50 mg, 0.23 mmol) was added and the vial was sealed and heated to 180° C. in Personal Chemistry Microwave for 15 min. The mixture was extracted with EtOAc, organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The product was purified by column chromatography on silica gel using 60:40 DCM:(90:10:1 DCM:MeOH:NH4OH to flush out top spots, then 50:50 DCM:(90:10:1 DCM:MeOH:NH4OH) to collect the product. Green solid, 4-(2-(5-aminopyridin-2-yloxy)pyridin-3-yl)-N-methylpyridin-2-amine was obtained. MS m/z=294 [M+1]+. Calcd for C16H15N5O: 293.13.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686155B2
Source datasetuspto-grants-2014_04
ORD IDord-cc437bd7fbb647f9b71a48a424c0cb2f
Source noteuspto-grants-2014_04