Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 5-Phenyl-2,4-pentadienoic acid | HCID 73777 | — |
| Reactant | 4-Methoxy-3-(4-methylpiperazin-1-yl)aniline | HCID 10331101 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 54032034 | HCID 54032034 | 101.7% |
Reaction Steps
5-Phenylpenta-2,4-dienoic acid (270 mg, 1.55 mmol) was heated at reflux with thionyl chloride (3 ml) and toluene (40 ml) for 2 h, and then evaporated to dryness under reduced pressure. 4-Methoxy-3-(4-methyl-1-piperazinyl)phenylamine (340 mg, 1.55 mmol) in dry dichloromethane (40 ml) was added with triethylamine (1 ml) and the mixture stirred for 1 h. The solution was partitioned between dichloromethane (40 ml) and saturated aqueous potassium carbonate (40 ml), the organic solution dried (sodium sulphate) and evaporated to dryness under reduced pressure to afford an oil, which was purified by column chromatography (silica, chloroform/methanol 5%) to afford the title compound (595 mg, 100%) which was crystallised from methanol/diethyl ether as the oxalate salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05905080 |
|---|
| Source dataset | uspto-grants-1999_05 |
|---|
| ORD ID | ord-8d856fee9ad34efba26aeef91d32590a |
|---|
| Source note | uspto-grants-1999_05 |
|---|