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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591584Generated: October 30, 2026

Methanesulfonic Acid → 2-(1H-pyrazol-1-yl)-9H-carbazole

https://huagongshe.com/reaction/591584

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
Reactant2-(1H-pyrazol-1-yl)-9-(tetrahydro-2H-pyran-2-yl)-9H-carbazoleHCID 71060607—
SolventMethanolHCID 887—
Product2-(1H-pyrazol-1-yl)-9H-carbazoleHCID 7106027090%

Reaction Steps

5 mmol of 2-(1H-pyrazol-1-yl)-9-(tetrahydro-2H-pyran-2-yl)-9H-carbazole was dissolved in 100 mL of methanol before 25 mmol of methylsulfonic acid was added slowly. The solution was stirred at room temperature for 2 hours, then at 50° C. for 2 hours further. The reaction was cooled, quenched with sodium bicarbonate, and separated between dichloromethane and water. The water was washed twice with dichloromethane, the organic fractions combined and washed once with brine. The organic fraction was then dried with magnesium sulfate, filtered, and the filtrate concentrated under reduced pressure. The resulting solid was subjected to column chromatography, using silica and dichloromethane/ethyl acetate as the eluent. After concentration under reduced pressure, 2-(1H-pyrazol-1-yl)-9H-carbazole was isolated in 90% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238668B2
Source datasetuspto-grants-2016_01
ORD IDord-2cd9177c44cd495bb5542befb1dd4ede
Source noteuspto-grants-2016_01