HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → HCID 86761231, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | HCID 86761226 | HCID 86761226 | — |
| Reactant | HCID 131728575 | HCID 131728575 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86761231 | HCID 86761231 | 80.4% |
Reaction Steps
The above-obtained 3′,5′-bis-O-(tert-butyldimethylsilyl)-6-O-diphenylcarbamoyl-2-N-methylthiocarbamoyldeoxyguanosine (900 mg, 1.17 mmol) was azeotroped with anhydrous tetrahydrofuran three times and dissolved in anhydrous tetrahydrofuran (6.0 mL), and triethylamine 3 hydrogen fluoride (574 μL, 3.51 mmol) was added thereto. The mixture was stirred at room temperature overnight, and then toluene (5 mL) was added thereto. The solvent was evaporated under reduced pressure. To the residue, methanol (5 mL) and hexane (25 mL) were added for precipitation. The resulting precipitate was purified by filtration to give 6-O-diphenylcarbamoyl-2-N-methylthiocarbamoyldeoxyguanosine (504 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07851157B1 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-8c7eacf5367f4e24b5a7151454483938 |
| Source note | uspto-grants-2010_12 |