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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1773897Generated: October 31, 2026

Potassium Carbonate → HCID 72695484, compound

https://huagongshe.com/reaction/1773897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Fluorophenylboronic acidHCID 2733986—
ReactantHCID 86703973HCID 86703973—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
ProductHCID 72695484HCID 72695484—

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of 2-iodo-1-methyl-4-(1-methylpiperidin-4-yloxy)-9,10-dihydro-4H-3,10a-diaza-benzo[f]azulene (example 133) (100 mg, 0.23 mmole) in toluene (2 mL) and ethanol (1 mL) in a screw-capped vial are added 3-fluorobenzeneboronic acid (64 mg, 0.46 mmole), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (10 mg) and an 1M aqueous solution of potassium carbonate (0.8 mL). The vial is evacuated and filled with argon. The reaction mixture is stirred at 95° C. for 20 hours. Water is added to the reaction mixture, and the pH is adjusted to 9-10 with 1N aqueous sodium hydroxide. The aqueous phase is extracted three times with ethyl acetate. The pooled organic extracts are dried over magnesium sulphate, filtered and the solvent is removed under reduced pressure. The residue is purified by silica gel chromatography using (CH2Cl2:MeOH:NH4OH) as eluent with a gradient from (95:5:0.1) to (92:8:0.5) to give 2-(3-fluorophenyl)-1-methyl-4-(1-methylpiperidin-4-yloxy)-9,10-dihydro-4H-3,10a-diaza-benzo[f]azulene melting at 132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09255101B2
Source datasetuspto-grants-2016_02
ORD IDord-6dcd4acc17c54c12a0e5c212727fb019
Source noteuspto-grants-2016_02