HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-bromo-1-methylpyrimidin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-2(1H)-pyrimidinone | HCID 101494 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-bromo-1-methylpyrimidin-2(1H)-one | HCID 139707 | — |
Reaction Steps
A mixture of 5-bromopyrimidin-2(1H)-one (3 g), methyliodide (1.1 mL) and K2CO3 (2.4 g) in N,N-dimethylformamide (60 mL) is stirred for 5 hours at room temperature. The mixture is filtered and the mother liquor is concentrated. The residue is partitioned between water and dichloromethane. The organic phase is washed with brine, dried (MgSO4) and concentrated to give the title compound. Yield: 385 mg; LC (method 9): tR=0.25 min; Mass spectrum (ESI+): m/z=189 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08642585B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-da26afe45c084e588889ca5a8671f02c |
| Source note | uspto-grants-2014_02 |