HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,5-Dinitrobenzoyl chloride → 7-(3,5-Dinitrobenzamido)-1-(4-methyl-1-piperazinyl)-naphthalene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,5-Dinitrobenzoyl chloride | HCID 7432 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 7-Amino-1-(4-methyl-1-piperazinyl)-naphthalene | HCID 23353484 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 7-(3,5-Dinitrobenzamido)-1-(4-methyl-1-piperazinyl)-naphthalene | HCID 23353499 | 63% |
Reaction Steps
The title product was prepared following the procedure of example 3 from 7-amino-1-(4-methyl-1-piperazinyl)-naphthalene (0.15 g, 0.622 mmol) and triethylamine (0.09 mL, 0.68 mmol) and 3,5-dinitrobenzoyl chloride (0.158 g, 0.684 mmol) in acetonitrile (10 mL) with overnight stirring at room temperature. The product was purified using chromatography and recrystallization from acetonitrile to yield 0.17 g (63%) of the title compound: mp 254°-256° C. Analysis calculated for C22H21N5O5 : C, 60.68; H, 4.86; N, 16.08. Found: C, 60.59; H, 4.73; N, 15.88.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05597826 |
| Source dataset | uspto-grants-1997_01 |
| ORD ID | ord-7d4b97a983d140cbb2edf104b0e327b0 |
| Source note | uspto-grants-1997_01 |