HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Methanesulfonate → 4,6-diiodo-N-methylpyrimidin-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Methanesulfonate | HCID 4156 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4,6-Diiodopyrimidin-5-amine | HCID 11810154 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4,6-diiodo-N-methylpyrimidin-5-amine | HCID 25186362 | — |
Reaction Steps
To a solution of 4,6-diiodopyrimidin-5-amine (1.0 g) in tetrahydrofuran (10 mL) was added sodium hydride (60%, 138 mg) under ice-cooling. The mixture was stirred at room temperature for 30 min. To the reaction system was added dropwise a solution of methyl methanesulfonate (0.256 mL) in tetrahydrofuran (4.0 mL). The mixture was stirred at room temperature for 3 hrs and ethyl acetate was added. The mixture washed with water and saturated brine and dried over magnesium sulfate. After concentration under reduced pressure, the residue was separated and purified by silica gel column chromatography (hexane:ethyl acetate=9:1→3:1) to give the title compound (600 mg) as pale-yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07507740B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-72c172c741374100bf28532885c01fb5 |
| Source note | uspto-grants-2009_03 |