HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324372Generated: October 29, 2026
m-Chloroperbenzoic acid → HCID 22004598, compound
https://huagongshe.com/reaction/324372
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 22004591 | HCID 22004591 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22004598 | HCID 22004598 | 110.9% |
Reaction Steps
A solution of 3-{benzyl-[6-methyl-3-methylsulfanyl-1-(2,4,6-trichlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]-amino}propanol (42 mg, 0.077 mmol) and m-chloroperbenzoic acid (14 mg, 0.081 mmol) in 0.5 ml of methylene chloride was stirred at room temperature for 3 hours. The mixture was quenched with water and saturated sodium thiosulfate, and extracted with methylene chloride. The organic layer was washed with saturated sodium bicarbonate, dried and concentrated to give an oil which was purified through silica gel column chromatography using 2% methanol in chloroform as eluent to give 46 mg of the title compound as a white glass form. 1H NMR (CDCl3): 1.88(m,2H), 2.54(s,3H), 2.73(s,3H), 3.5-3.7(m,4H), 4.3(m,1H), 5.15(ABq,JAB=16Hz,2H), 7.2-7.4(m,5H), 8.47(ABq,2H)ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06218397B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-8beb598696e84ee298ccca0f0d785553 |
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| Source note | uspto-grants-2001_04 |
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