Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Piperazinone, 3-(2-chlorophenyl)- | HCID 54257827 | — |
| Reactant | HCID 54501257 | HCID 54501257 | — |
| Product | HCID 68668001 | HCID 68668001 | — |
Reaction Steps
A solution of 2-(-5-(4-cyanobenzyl)-imidazolyl)ethyl methanesulfonate (24 mg, 0.079 mmol) in DMF (0.2 ml) was added to 3-(chlorophenyl)piperazin-2-one (17.7 mg, 0.084 mmol), sodium iodide (50 mg, 0.336 mmol) and Hunigs base (0,0146 ml, 0.084 mmol). The mixture was stirred at 55° C. for 12 hours, and the solvent evaporated in vacuo. The residue was purified by preparative tic eluting with 10% saturated ammonia/acetonitrile to afford the title compound. 1H NMR δ CDCl3 (7.61 (2H, d, J=8.4 Hz), 7.56 (1H, s), 7.35-7.20 (7H, m), 7.16 (1H, d, J=8 Hz), 6.85 (1H, s), 4.03 (2H, s), 3.83 (2H, t, J=6.5 Hz),3.61 (2H, t, J=5.4 Hz), 3.27 (2H, s), 2.68 (2H, t, J=5.4 and 2.57 (2H, t, J=6.5 Hz) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05856326 |
|---|
| Source dataset | uspto-grants-1999_01 |
|---|
| ORD ID | ord-167674decc114e04b0696c6fccbfeb68 |
|---|
| Source note | uspto-grants-1999_01 |
|---|