HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargylamine → HCID 22028626, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargylamine | HCID 239041 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | HCID 67506234 | HCID 67506234 | — |
| Reactant | HCID 67507912 | HCID 67507912 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 22028626 | HCID 22028626 | — |
Reaction Steps
1-Benzyloxycarbonyl-4-[(methylthio)phenyliminomethyl]piperazine [product of Example 224 (2), 2.70 g] and propargylamine (2.3 mL) were dissolved in 1-butanol (25 mL), and p-toluenesulfonic acid monohydrate (156 mg) was added thereto. The mixture was refluxed for 20 hr. The reaction mixture was concentrated under reduced pressure, and saturated aqueous sodium hydrogencarbonate solution was added to the residue. The mixture was extracted with chloroform, and the extract was washed with brine, dried and concentrated under reduced pressure. The residue was purified by silica gel chromatography to give 1-benzyloxycarbonyl-4-(5-methyl-1-phenyl-2-imidazolyl)piperazine (1.82 g) as a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07060722B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-61bb031ddbbc475e9d738302ef3779e9 |
| Source note | uspto-grants-2006_06 |