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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1913241Generated: November 3, 2026

Water → HCID 86664790, compound

https://huagongshe.com/reaction/1913241

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,6-LutidineHCID 7937—
ReactantSodium ThiosulfateHCID 24477—
ReactantHCID 66733437HCID 66733437—
CatalystOsmium TetroxideHCID 30318—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86664790HCID 8666479092%

Reaction Steps

To 3-(quinolin-3-yl)-N,N-bis((2-(trimethylsilyl)ethoxy)methyl)-5-vinylpyrazolo[1,5-a]pyrimidin-7-amine (Int-8a, 0.7 g, 1.3 mmol) in 1,4-dioxane (10 mL) was added 2.5 wt % OsO4 in 1,4-dioxane (1.0 g, 0.02 mmol), 2,6-lutidine (0.6 mL, 5.2 mmol) and H2O (2 mL), and the resulting mixture was stirred at room temperature for 20 minutes. NaIO4 (0.8 g, 3.81 mmol) was then added and the reaction mixture was stirred at room temperature for 16 hours. L C/MS analysis at that time showed the diol intermediate was still present. Therefore, more NaIO4 (0.3 g, 1.3 mmol) was added, and the reaction mixture was stirred for 12 hours for full conversion to the product. Saturated Na2S2O3 solution (10 mL) was added and the mixture was stirred for 10 minutes. The organics were then extracted with CH2Cl2 (4×40 mL), dried (Na2SO4) and concentrated in vacuo to give 7-(bis((2-(trimethylsilyl)ethoxy)methyl)amino)-3-(quinolin-3-yl)pyrazolo[1,5-a]pyrimidine-5-carbaldehyde (Int-8b) as a yellow solid (0.6 g, 1.2 mmol, 92%). LCMS: 2.67 mins, m/z=550.0 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609675B2
Source datasetuspto-grants-2013_12
ORD IDord-ced4db7a85514a458ca4f6d304b9f638
Source noteuspto-grants-2013_12