HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 46916506, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-chloro-N-(3-quinoxalin-2-ylphenyl)acetamide | HCID 1485433 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 46916506 | HCID 46916506 | 39.4% |
Reaction Steps
A slurry of 2-chloro-N-(3-quinoxalin-2-ylphenyl)acetamide (100 mg, 0.336 mmol) and piperazine (58 mg, 0.672 mmol) in MeCN (5 mL) was heated at reflux for 48 hrs. The resulting precipitate was filtrated, washed with MeCN (10 mL) and submitted to preparative LCMS to afford 2-(piperazin-1-yl)-N-(3-(quinoxalin-2-yl)phenyl)acetamide (46 mg, 39% yield). LCMS calculated for C20H21N5O (M+H): 348.42. found 348. 1H-NMR (DMSO-d6, 400 Mhz) δH: 9.92 (1H, br.), 9.52 (1H, s), 8.55 (1H, m), 8.13-8.20 (2H, m), 8.05-8.08 (1H, m), 7.82-7.98 (3H, m), 7.55-7.60 (1H, m), 3.25-3.40 (NH and 6H, br.), 2.80-2.88 (4H, br.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08592415B2 |
| Source dataset | uspto-grants-2013_11 |
| ORD ID | ord-6c454742ae074821b1d7ac83a2c6ba43 |
| Source note | uspto-grants-2013_11 |