HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178476387, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178425471 | HCID 178425471 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 178476387 | HCID 178476387 | 12.2% |
Reaction Steps
To 8-hydroxy-2-(2-hydroxyethylamino)-9-{(6-methyl-3-pyridyl)methyl}adenine (100 mg, 0.32 mmol) prepared by Comparative example 10 in pyridine (1 ml) was added under ice cooling acetic anhydride (0.033 ml, 0.35 mmol), and the mixture was stirred for 3 hours. To the reaction mixture was added sodium hydrogen carbonate solution, and the mixture was extracted with chloroform. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was purified by preparative thin-layer chromatography to give the captioned compound (14 mg, 0.039 mmol, yield: 12%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754728B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-8c28fbe4f7014aed91c0bb7fbed45dc3 |
| Source note | uspto-grants-2010_07 |