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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1423075Generated: November 2, 2026

Potassium Carbonate → HCID 52933352, compound

https://huagongshe.com/reaction/1423075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethanesulfonamideHCID 72879—
Reactanttrans-N,N'-dimethyl-1,2-cyclohexanediamineHCID 2733821—
ReactantHCID 86672836HCID 86672836—
Catalystcopper(II) trifluoromethanesulfonateHCID 2734996—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 52933352HCID 52933352—

Reaction Conditions

Temperature125 °C

Reaction Steps

To a mixture of 6-cyano-1-(4-fluorophenyl)-1H-indole-4-carboxylic acid (6-bromo-pyridin-3-ylmethyl)-amide (75 mg, 0.17 mmol), methanesulfonamide (81 mg, 0.85 mmol), copper (II) trifluoromethanesulfonate (105 mg, 0.290 mmol), trans-N,N′-dimethylcyclohexane-1,2-diamine (55.2 μL, 0.35 mmol) and potassium carbonate (247 mg, 1.79 mmol) in a sealed tube is added NMP (2.5 mL). The solution is degassed with argon for 3 minutes. The reaction is warmed at 125° C. in a microwave reactor. After 40 minutes, the reaction is diluted with saturated aqueous potassium carbonate (15 mL) and extracted with EtOAc (2×15 mL). The combined organic layers are washed with brine (2×15 mL), dried over magnesium sulfate and concentrated in vacuo. The residue is purified by preparative reversed phase HPLC to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927550B2
Source datasetuspto-grants-2015_01
ORD IDord-f78fcd3bd3f24016a15c3b391584d1ec
Source noteuspto-grants-2015_01