HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-[2-(Diphenylmethoxy)ethyl]piperazine → HCID 54283397, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-[2-(Diphenylmethoxy)ethyl]piperazine | HCID 648525 | — |
| Reactant | HCID 53901538 | HCID 53901538 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54283397 | HCID 54283397 | 25.7% |
Reaction Steps
To a solution of 794 mg (2.68 mmol) of N-(2-benzhydroxyethyl)piperazine in dry dimethylformamide (4 ml) was added, under argon atmosphere, a solution of 1.15 g (2.61 mmol) of N[5-[3,5-dimethoxy-4-(β-methoxyethoxymethoxy)phenyl]-2,4-pentadienoyl)thiazolidine in dry dimethylformamide (4 ml), and the mixture was allowed to react at room temperature for 17 hours. At the end of this time, the reaction mixture was concentrated by evaporation under reduced pressure and the residue was subjected to silica gel column chromatography, eluted with chloroform-methanol (100:1), to give 413 mg (0.670 mmol) of N-[5-[3,5-dimethoxy-4-(β-methoxyethoxymethoxy)phenyl]-2,4-pentadienoyl]-N'-(2-benzhydroxyethyl)piperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04673684 |
| Source dataset | uspto-grants-1987_06 |
| ORD ID | ord-c40a10da124644e2a7d545e85c270daa |
| Source note | uspto-grants-1987_06 |