HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1508628Generated: October 30, 2026
Trimethylsilyl triflate → HCID 89975769, compound
https://huagongshe.com/reaction/1508628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethylsilyl triflate | HCID 65367 | — |
| Reactant | N,O-bis(trimethylsilyl)acetamide | HCID 6913588 | — |
| Reactant | HCID 24851310 | HCID 24851310 | — |
| Reactant | Cytosine | HCID 178418229 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 89975769 | HCID 89975769 | 30.6% |
Reaction Steps
0.44 mL of N,O-bis(trimethylsilyl)acetamide was added to a suspension of 208 mg of 1-O-acetyl-2,3,5-tri-O-benzoyl-4-thio-β-D-ribofuranose and 67 mg of cytosine in 2.0 mL of acetonitrile, and the obtained mixture was then stirred at 60° C. for 1 hour. Thereafter, 0.22 mL of trimethylsilyl trifluoromethanesulfonate was added to the reaction mixture, and the obtained mixture was then stirred at 80° C. for 4 hours. Thereafter, ethyl acetate was added to the reaction mixture, and the thus obtained mixture was then washed with a saturated sodium hydrogen carbonate aqueous solution. After that, the solvent was distilled away under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate/methanol=1/0 to 4/1), so as to obtain 70 mg of 1-(2,3,5-tri-O-benzoyl-4-thio-β-D-ribofuranosyl)cytosine in the form of a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221865B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-2c14c5b89e8f43a0a6d5e5978f02ccdc |
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| Source note | uspto-grants-2015_12 |
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