HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334371Generated: October 27, 2026
Methyl morpholine oxide → 4-(7-(Bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-1-(hydroxymethyl)cyclohexanol
https://huagongshe.com/reaction/334371
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | Acetonitrile acetone water | HCID 18799168 | — |
| Reactant | 5-(4-methylenecyclohexyl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine | HCID 66583923 | — |
| Catalyst | Osmium Tetroxide | HCID 30318 | — |
| Product | 4-(7-(Bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-1-(hydroxymethyl)cyclohexanol | HCID 66583932 | — |
Reaction Steps
To a slurry of 5-(4-methylenecyclohexyl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)pyrazolo[1,5-a]pyrimidin-7-amine (4.89 g, 10.0 mmol) in Acetone/H2O/MeCN (60/20/20) was added NMO (4.15 mL, 20 mmol), followed by OsO4 (2.5 wt. % in tBuOH) (6.27 mL, 0.50 mmol) at rt. The resulting reaction mixture was stirred at rt overnight. Organic solvent were evaporated and the aqueous residue was extracted with EtOAc three times, dried over Na2SO4 and concentrated to afford 4-(7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)pyrazolo[1,5-a]pyrimidin-5-yl)-1-(hydroxymethyl)cyclohexanol as a pale brownish oil (5.52 g), which was used without further purification. HPLC-MS TR=2.48 min (UV 254 nm, 5 min method); mass calculated for formula C25H46N4O4Si2 522.3, observed LCMS m/z 523.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883801B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-64dd15f359ce432e85ac7ff9925b32a0 |
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| Source note | uspto-grants-2014_11 |
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