Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | Sodium Permanganate | HCID 23673458 | — |
| Reactant | HCID 59379929 | HCID 59379929 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 24803339 | HCID 24803339 | — |
Reaction Steps
1-[4-[4-(Cyclohexylsulfanylmethyl)-6-[(3S)-3-methylmorpholin-4-yl]pyrimidin-2-yl]phenyl]-3-methyl-urea (0.35 mmol) was dissolved in 1,4-dioxane (5 mL) and water (1 mL). 3-chloroperbenzoic acid (75%) (121 mg) was added to the solution followed immediately by sodium permanganate (140 mg) and the reactions stirred at RT for 1 hour. Further 3-chloroperbenzoic acid (75%) (121 mg) and sodium permanganate (140 mg) were added and the reactions allowed to stir at RT for 1 hour. Further 3-chloroperbenzoic acid (75%) (121 mg) and sodium permanganate (140 mg) were added and the reactions allowed to stir at RT for another 1 hour then loaded onto a SCX-3 column. The column was washed with methanol and the desired material removed with 7N ammonia in methanol. The crude material was purified by prep-HPLC (basic) to give the desired material (74 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750003B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-ab61751fc55745ef825ba9b1773cb07b |
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| Source note | uspto-grants-2010_07 |
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