HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(2-Nitro-4-((4-phenylpiperazin-1-yl)methyl)phenylmethyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(4-chloromethyl-2-nitrophenylmethyl)acetamide | HCID 18423048 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2-Nitro-4-((4-phenylpiperazin-1-yl)methyl)phenylmethyl)acetamide | HCID 18423156 | — |
Reaction Steps
A solution of N-(4-chloromethyl-2-nitrophenylmethyl)acetamide (1.4 g), phenylpiperazine (0.8 ml) and potassium carbonate (0.6 g) in dimethylformamide (20 ml) was stirred at 60° C. for 4 hr. The reaction mixture was poured into water (150 ml) and extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give a pale-yellow solid. The obtained pale-yellow solid was crystallized from ethyl acetate to give the title compound (1.3 g) as pale-yellow white crystals, m.p.=135-136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455528B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-2e80df1a263b431a8db76cf703108157 |
| Source note | uspto-grants-2002_09 |