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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911133Generated: October 26, 2026

Dimethyl Sulfoxide → HCID 57756228, compound

https://huagongshe.com/reaction/911133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantCesium carbonateHCID 10796—
Reactant4-(2-chloropyridin-3-yl)-N-methylpyridin-2-amineHCID 16108983—
ReactantHCID 178507770HCID 178507770—
ProductHCID 57756228HCID 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 numberUS08022221B2
Source datasetuspto-grants-2011_09
ORD IDord-363b4085b12046a796d2c45b70781d58
Source noteuspto-grants-2011_09