HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 1-{4-[(4-chlorobenzyl)oxy]benzyl}-4-[4-(4-fluorophenyl)piperazin-yl]-6-methoxy-1,3,5-triazin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-{4-[(4-Chlorobenzyl)oxy]benzyl}-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione | HCID 117839829 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-{4-[(4-chlorobenzyl)oxy]benzyl}-4-[4-(4-fluorophenyl)piperazin-yl]-6-methoxy-1,3,5-triazin-2(1H)-one | HCID 117839773 | 7% |
Reaction Steps
To an N,N-dimethylformamide solution (4 mL) of a crude product (0.69 mmol) of 3-{4-[(4-chlorobenzyl)oxy]benzyl}-6-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazine-2,4(1H,3H)-dione, potassium carbonate (332 mg, 2.40 mmol) and methyl iodide (137 μL, 2.20 mmol) were added at room temperature and the resultant mixture was stirred at room temperature for 1 day. After the completion of the reaction, the reaction solution was concentrated under reduced pressure and the resultant residue was purified by silica gel column chromatography to obtain the title compound (26 mg, two step yield: 7%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403798B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-5698fc973458407b8bcccda1bfa7cbbc |
| Source note | uspto-grants-2016_08 |