HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 7-Bromo-2-methylsulfanyl-1,3-benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-Bromobenzo[D]thiazole-2-thiol | HCID 11850771 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-Bromo-2-methylsulfanyl-1,3-benzothiazole | HCID 66760618 | — |
Reaction Steps
Potassium carbonate (67 mg, 0.49 mmol) was added to a solution of 7-bromo-1,3-benzothiazole-2(3H)-thione (100 mg, 0.41 mmol) in DMF (5 mL). The mixture was stirred at room temperature for 30 min. Methyl iodide (25 μL, 0.41 mmol) was added and the resulting mixture was stirred at room temperature for 30 min. EtOAc was added the separated organic fraction was washed with water and brine, dried over sodium sulfate, and concentrated. The title compound thus obtained was used without further purification. MS (ESI): 260.34, 262.32 [M+H]+; HPLC tR=1.54 min (HPLC: Anayltical—2 min).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08378104B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-3c50b97598664657871d1c3bcc18f2be |
| Source note | uspto-grants-2013_02 |