HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 4-(5-Bromothiophen-2-yl)-2-methylsulfanylpyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 178527860 | HCID 178527860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 4-(5-Bromothiophen-2-yl)-2-methylsulfanylpyrimidine | HCID 2820534 | 88.6% |
Reaction Steps
4-(5-Bromothiophen-2-yl)-pyrimidine thiol (2.5 g, 9.15 mmol) was completely dissolved in 14.8 mL DI water and 2.4 mL 4 N NaOH. The mixture was diluted with EtOH (25 mL) and MeI (0.598 mL, 9.61 mmol) was added. The reaction was stirred 18 hours. The yellow solids were collected by filtration, washed with EtOH and dried to afford 4-(5-Bromothiophen-2-yl)-2-methylsulfanyl-pyrimidine (2.32 g, 88.6%) as a pale yellow solid. MS: m/z 287 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803806B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-72a7db485f6342fa8c41bb88a3caf18d |
| Source note | uspto-grants-2010_09 |