HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → N-[2-methyl-5(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-3-(4methylpiperazin-1-yl)-2-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | N-[2-methyl-5-(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-3-chloro-2-nitrobenzamide | HCID 22238140 | — |
| Product | N-[2-methyl-5(2-morpholinopyrid-4-ylcarbonylamino)phenyl]-3-(4methylpiperazin-1-yl)-2-nitrobenzamide | HCID 18422090 | — |
Reaction Steps
In an analogous procedure to that described in Example 15, N-[2-methyl-5-(2-morpholinopyrid-4ylcarbonylamino)phenyl]-3-chloro-2-nitrobenzamide was reacted with 1-methylpiperazine to give the title compound; NMR Spectrum: (DMSOd6) 2.84-2.89 (m, 4H), 2.92-3.08 (m, 4H), 3.58-3.61 (m, 4H), 3.81-3.84 (m, 4H), 6.95 (d, 1H), 7.09 (s, 1H), 7.10 (d, 1H), 7.41-7.44 (m, 2H), 7.53 (d, 1H), 7.76 (d, 1H), 7.96 (s, 1H), 8.04 (s, 1H), 8.3 (d, 1H); Mass Spectrum: M+H+ 560.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455520B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-2707102379fb413fa493256d929da9fb |
| Source note | uspto-grants-2002_09 |