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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180128Generated: October 30, 2026

Potassium Carbonate → HCID 86590189, compound

https://huagongshe.com/reaction/2180128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidineHCID 10642851—
Reactant4-(4-Fluoro-2-methylindol-5-yloxy)-7-hydroxy-6-methoxycinnolineHCID 135749776—
SolventDimethylformamideHCID 6228—
ProductHCID 86590189HCID 8659018970.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

Under nitrogen a mixture of 4-(4-fluoro-2-methylindol-5-yloxy)-7-hydroxy-6-methoxycinnoline (150 mg, 0.44 mmol), (prepared as described in Example 4), 1-(tert-butoxycarbonyl)-4-(4-methylphenylsulfonyloxymethyl)piperidine (196 mg, 0.53 mmol) and potassium carbonate (122 mg, 0.88 mmol) in DMF (6 ml) was stirred at 100° C. for 2.5 hours. The mixture was filtered, and filtrate was evaporated under vacuum. The residue was purified by column chromatography eluting with methylene chloride followed by methylene chloride/methanol (99/1 and 95/5). The fractions containing the expected product were combined and evaporated. The residue was triturated with a mixture of pentane/ether (1/1) and the solid was filtered, washed with pentane and dried under vacuum to give 7-(1-(tert-butoxycarbonyl)piperidin-4-yl)methoxy)-4-(4-fluoro-2-methylindol-5-yloxy)-6-methoxycinnoline (100 mg, 42%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06887874B2
Source datasetuspto-grants-2005_05
ORD IDord-1c1d425037bf494aa8517c536a0dcc81
Source noteuspto-grants-2005_05