HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 1,3-Dimethyl-7-[4-(4-phenylpiperazinylmethylbenzoyl)benzyl]xanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 7-[4-(4-Bromomethylbenzoyl)benzyl]-1,3-dimethylxanthine | HCID 18918821 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1,3-Dimethyl-7-[4-(4-phenylpiperazinylmethylbenzoyl)benzyl]xanthine | HCID 69961138 | 14.7% |
Reaction Steps
A solution of 7-[4-(4-bromomethylbenzoyl)benzyl]-1,3-dimethylxanthine (232 mg), potassium carbonate (109 mg) and 1-phenylpiperazine (92 mg) in DMF (10 ml) was stirred at 60° C. for 5 hours. This reaction mixture was poured in water and extracted with ethyl acetate. The extract was washed with water, dried, and concentrated. The residue was purified by silica gel column chromatography (ethyl acetate: hexane: triethylamine =3:1:0.1) and recrystallized from chloroform-isopropyl ether to provide the title compound as colorless solid (20 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05753664 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-a5f9c9ab868846a293e2d88141f08a90 |
| Source note | uspto-grants-1998_05 |