HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 1-(4-Chlorobenzyl)-6-(dimethylamino)-4-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazin-2(1H)-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Chloro-4-(chloromethyl)benzene | HCID 7723 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178517893 | HCID 178517893 | — |
| Product | 1-(4-Chlorobenzyl)-6-(dimethylamino)-4-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazin-2(1H)-one | HCID 117840159 | 1% |
Reaction Steps
To an N,N-dimethylformamide solution (5 mL) of 4-[4-(4-fluorophenyl)piperazin-1-yl]-1,3,5-triazin-2(1H)-one (100 mg, 0.36 mmol) synthesized in Reference Synthesis Example 3, 4-chlorobenzyl chloride (69 mg, 0.43 mmol), potassium carbonate (59 mg, 0.43 mmol), and sodium iodide (54 mg, 0.36 mmol) were added and the resultant mixture was stirred at 90° C. for 5 hours. The reaction solution was concentrated under reduced pressure and the resultant residue was purified by silica gel column chromatography to obtain the title compound (1 mg, yield: 1%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09403798B2 |
| Source dataset | uspto-grants-2016_08 |
| ORD ID | ord-ce9b40c17bc04a9fa5fdfecbcb968d46 |
| Source note | uspto-grants-2016_08 |