HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-1,2,4-Triazole, 1-[[2-(2,4-dichlorophenyl)oxiranyl]methyl]- → 3-(4-[4-Aminophenyl]-cis-2,5-dimethylpiperazin-1-yl)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-1,2,4-Triazole, 1-[[2-(2,4-dichlorophenyl)oxiranyl]methyl]- | HCID 10423229 | — |
| Reactant | 4-Nitrophenyl-cis-2,5-dimethylpiperazine | HCID 70383030 | — |
| Solvent | 1-Pentanol | HCID 6276 | — |
| Product | 3-(4-[4-Aminophenyl]-cis-2,5-dimethylpiperazin-1-yl)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)propan-2-ol | HCID 70382687 | 23.1% |
Reaction Steps
A mixture of the product of part (i) (2.7 g, 11 mmole) and 2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl) oxirane (2.7 g, 10 mmole) in n-pentanol (30 ml) was heated under reflux for 48 hours. The solvent was then removed under reduced pressure and the residue suspended in hot ethyl acetate. After cooling, the insoluble material was removed by filtration to yield diastereomer I of the title compound (1.1 g, 22%), m.p. 212°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04885294 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-bb7d4381a4534f7d82255682c12012b9 |
| Source note | uspto-grants-1989_12 |