HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propylamino}-N,N-dimethylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-N,N-dimethylbenzamide | HCID 4778175 | — |
| Reactant | 3-(4-(2-Methoxyphenyl)piperazin-1-yl)propyl methanesulfonate | HCID 10806184 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-{3-[4-(2-methoxyphenyl)piperazin-1-yl]propylamino}-N,N-dimethylbenzamide | HCID 10572854 | 62.4% |
Reaction Steps
A mixture of 3-[4-(2-methoxyphenyl)piperazin-1-yl]propyl methanesulfonate (2 g, 6.06 mmol), 2-amino-N,N-dimethylbenzamide (1 g, 6.06 mmol), prepared as in Example 22, and potassium carbonate (2.1 g, 15 mmol) in 50 mL of acetonitrile was heated at reflux for 30 hours. The mixture was poured into water and extracted with ethyl acetate. The organic phase was dried (K2CO3) and concentrated. The residue was purified on silica gel by flash chromatography eluting with 6% methanol/methylene chloride to give 2-{3-[4-(2-methoxyphenyl)-piperazin-1-yl]propylamino}-N,N-dimethylbenzamide (1.5 g, 3.78 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688795 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-a35e787fc9cd4026ba396122fd1e6cab |
| Source note | uspto-grants-1997_11 |