HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 10138421, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | 1-(4-Nitrophenyl)piperazine | HCID 80447 | — |
| Product | HCID 10138421 | HCID 10138421 | 2% |
Reaction Steps
Following the procedure outlined in Step 1 of Example 1, but substituting 9-[4-(piperazin-1-yl)phenyl]aminoacridine (Example 16) for N-(4-nitrophenyl)piperazine, and benzyl bromide for methyl iodide, afforded the title compound (15%, overall yield 2%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06593324B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-68e2c2fbeaea453a9d7b94344e0754ae |
| Source note | uspto-grants-2003_07 |