HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Phenylpiperazine → HCID 86742246, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Phenylpiperazine | HCID 7096 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 20133937 | HCID 20133937 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86742246 | HCID 86742246 | — |
Reaction Steps
1.1 g (6.5 mmol) of carbonyldiimidazole are added to 1.60 g (5 mmol) of 5-carboxymethyl-4-(2-chlorophenyl)-1,4-dihydro-2,6-dimethyl-pyridine-3-carboxylic acid suspended in 20 ml of absolute tetrahydrofuran. The mixture is stirred at room temperature for 30 minutes and at a reflux temperature for 30 minutes. 1.62 g (10 mmol) of phenylpiperazine in 5 ml of absolute tetrahydrofuran are added to the resulting solution. This mixture is heated to reflux for 3.5 hours and then evaporated, the residue is taken up in methylene chloride, and the solution is washed successively with 1N hydrochloric acid, 1N sodium hydroxide solution and water, dried with magnesium sulphate and again evaporated. The residue crystallizes from isopropanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04753936 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-054d7b9dd230437b8bd443a4da3528fc |
| Source note | uspto-grants-1988_06 |