HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515979Generated: October 30, 2026
Selenium Dioxide → Methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-formyl-6-(1-methyl-1H-pyrazol-4-yl)pyrimidine-5-carboxylate
https://huagongshe.com/reaction/515979
Participants
| Role | Name | HCID | Charge |
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| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | HCID 67238013 | HCID 67238013 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-formyl-6-(1-methyl-1H-pyrazol-4-yl)pyrimidine-5-carboxylate | HCID 86654705 | — |
Reaction Steps
To a 25 mL round bottom flask was added methyl 2-((1R,2S)-2-(tert-butoxycarbonylamino)cyclohexylamino)-4-methyl-6-(1-methyl-1H-pyrazol-4-yl)pyrimidine-5-carboxylate (0.17 g, 0.382 mmol), selenium dioxide (0.085 g, 0.765 mmol) and dioxane. The reaction mixture was heated at 100° C. overnight, cooled to RT, and filtered through a bed of Celite 545, which was rinsed with MeOH. The solvent was removed to give the title compound as yellowish-brown foam, which was used in the next step without further purification (245 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108970B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-27900a96cfb8493ba4f97682a2cacf4f |
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| Source note | uspto-grants-2015_08 |
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