HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → 2-[2-(3,4-Dimethoxy-phenyl)-3-methylsulfanyl-benzofuran-5-yl)-1-(4-phenyl-piperazin-1-yl)-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | [2-(3,4-Dimethoxy-phenyl)-3-methylsulfanyl-benzofuran-5-yl]-acetic acid | HCID 68473283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[2-(3,4-Dimethoxy-phenyl)-3-methylsulfanyl-benzofuran-5-yl)-1-(4-phenyl-piperazin-1-yl)-ethanone | HCID 68471151 | 554% |
Reaction Steps
Triethylamine and 12.992 mg of 1-phenyl-piperazine (0.080 mM) were added to the solution containing 35 mg of 3[2-(3,4-dimethoxy-phenyl)-3-methylsulfanyl-benzofuran-5-yl]-acetic acid (35a; 0.068 mM) dissolved in 2 ml of dichloromethane. The reaction mixture was stirred for 16 hours and the remaining solvent was removed. The remaining residue was purified with Silica gel column chromatography with a mobile phase (dichloromethane:methanol=20:1) to obtain white solid type of 2-[2-(3,4-dimethoxy-phenyl)-3-methylsulfanyl-benzofuran-5-yl)-1-(4-phenyl-piperazin-1-yl)-ethanone (37a; 223 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08263649B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-a60008956e7d4be580ce32f7e9056078 |
| Source note | uspto-grants-2012_09 |