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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium caroate | HCID 15793144 | — |
| Reactant | Methanol--water (1/1) | HCID 22242641 | — |
| Reactant | 3-(4-methoxybenzyl)-9-(methylsulfanyl)-6,7-dihydro-3H-pyrazolo[4',3':5,6]pyrido[4,3-f]quinazoline | HCID 59490419 | — |
| Product | 3-(4-Methoxybenzyl)-9-(methylsulfonyl)-6,7-dihydro-3h-pyrazolo[4',3':5,6]pyrido[4,3-f]quinazoline | HCID 59490463 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263610B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-08dd2d0d8bb64b818a30a80b5929cb9f |
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| Source note | uspto-grants-2012_09 |
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