Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | HCID 86662596 | HCID 86662596 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | WS-070117 | HCID 45377904 | 24.8% |
Reaction Steps
To a solution of O2′,O3′,O5′-tri-acetyl-6-chloroadenosine (5.4 g) in absolute ethanol (30 mL) were added 3-aminophenol (4.28 g) and dry triethylamine (3.96 g), and the mixture was refluxed 8 h at 60° C. The solution was allowed to cool and was concentrated in vacuo and the residue was chromatographed (ethyl acetate:petroleumether=2:1) to give O2′,O3′,O5′-tri-acetyl-N6-(3-hydroxylphenyl)adenosine as a white solid (1.51 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08435962B2 |
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| Source dataset | uspto-grants-2013_05 |
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| ORD ID | ord-b3e931a7a7fd45df86909c6e31f6978f |
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| Source note | uspto-grants-2013_05 |
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