HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 13531609, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | HCID 13531604 | HCID 13531604 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13531609 | HCID 13531609 | — |
Reaction Steps
Using the method of Example 1, 5-bromomethyl-2-nitro-3-phenylbenzofuran is reacted with N-phenylpiperazine in ethanol to provide yellow needles of 4-(2-nitro-3-phenyl-5-benzofuranylmethyl)-1-phenylpiperazine, m.p. 155°-157° C., having the structure ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04526896 |
| Source dataset | uspto-grants-1985_07 |
| ORD ID | ord-0b05f8064b234c5f8aa0d61d16b2ab5d |
| Source note | uspto-grants-1985_07 |