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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2383408Generated: October 26, 2026

Potassium caroate → 3-(4-Methoxybenzyl)-9-(methylsulfonyl)-6,7-dihydro-3h-pyrazolo[4',3':5,6]pyrido[4,3-f]quinazoline

https://huagongshe.com/reaction/2383408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium caroateHCID 15793144—
ReactantMethanol--water (1/1)HCID 22242641—
Reactant3-(4-methoxybenzyl)-9-(methylsulfanyl)-6,7-dihydro-3H-pyrazolo[4',3':5,6]pyrido[4,3-f]quinazolineHCID 59490419—
Product3-(4-Methoxybenzyl)-9-(methylsulfonyl)-6,7-dihydro-3h-pyrazolo[4',3':5,6]pyrido[4,3-f]quinazolineHCID 5949046377%

Reaction Steps

To a suspension of 3-(4-methoxybenzyl)-9-(methylsulfanyl)-6,7-dihydro-3H-pyrazolo[4′,3′:5,6]pyrido[4,3-f]quinazoline (1.9 g, 4.8 mmol) in 2:1 mixture of methanol-water (100 mL) was added potassium monopersulfate triple salt (Oxone®, 9.2 g, 15 mmol) and the suspension stirred for 18 hours. On completion of the reaction, the mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate (200 mL) and washed with water (2×20 mL), dried using anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the desired product, 3-(4-methoxybenzyl)-9-(methylsulfonyl)-6,7-dihydro-3H-pyrazolo[4′,3′:5,6]pyrido[4,3-f]quinazoline (1.5 g, 77%) as a tan solid. LCMS [M+H]: 422. The compound was used without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08263610B2
Source datasetuspto-grants-2012_09
ORD IDord-08dd2d0d8bb64b818a30a80b5929cb9f
Source noteuspto-grants-2012_09