HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 67846132, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 67643248 | HCID 67643248 | — |
| Solvent | Isobutyramide | HCID 68424 | — |
| Product | HCID 67846132 | HCID 67846132 | — |
Reaction Steps
2 g of the compound obtained in Example 2 and 2 ml of methyl iodide were dissolved in dimethylacetoamide, and stirred overnight at room temperature. The reaction mixture was concentrated to dryness under reduced pressure and 10 ml of 2N sodium hydroxide solution was added thereto. The solution was refluxed for one hour with heating. After cooling to room temperature, the solution was neutralized with 2N HCl and applied on Amberlite XAD-7 column. The column was washed with water and eluted with 50% (V/V) aqueous solution of methanol. The eluate was concentrated to dryness under reduced pressure and recrystallized from ethyl acetate to give 1.8 g of N6,2',3'-O-trimethyladenosine (Compound 60).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05705491 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-f1b997bcf49b49dfbd27e849b0f777bc |
| Source note | uspto-grants-1998_01 |