HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 7-(4-Chlorobenzamido)-1-(4-methyl-1-piperazinyl)-naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Chlorobenzoyl chloride | HCID 8501 | — |
| Reactant | 7-Amino-1-(4-methyl-1-piperazinyl)-naphthalene | HCID 23353484 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-(4-Chlorobenzamido)-1-(4-methyl-1-piperazinyl)-naphthalene | HCID 18967511 | 43.4% |
Reaction Steps
The title product was prepared following the procedure of example 3 from 7-amino-1-(4-methyl-1-piperazinyl)-naphthalene (0.249 g, 1.03 mmol) and triethylamine (0.151 mL, 1.14 mmol) and 4-chlorobenzoyl chloride (0.241 g, 1.14 mmol) in acetonitrile (10 mL) with overnight stirring at room temperature. The product was purified using chromatography and recrystallization from ethyl acetate to yield 0.17 g (43%) of the title compound as a white solid mp 174°-175° C. HRMS m/e calculated for C22H22ClN3O: 379.1448. Observed m/e: 379.1465. Analysis calculated for C22H22ClN3O: C, 69.56; H, 5.84; N, 11.06. Found: C, 69.38; H, 5.80; N, 10.96.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597826 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-09bd85beed084074b1d74caac5a4ce9e |
| Source note | uspto-grants-1997_01 |