HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-(1-Benzyl-4-piperidinyl)-3-methylcarbostyril hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | N-(alpha-methylcinnamoyl)-N-(1-benzyl-4-piperidinyl)aniline | HCID 54264746 | — |
| Solvent | Chlorobenzene | HCID 7964 | — |
| Product | 1-(1-Benzyl-4-piperidinyl)-3-methylcarbostyril hydrochloride | HCID 19030980 | 74.2% |
Reaction Conditions
| Temperature | 110 °C |
|---|
Reaction Steps
To grinded aluminum chloride (26 g) are added chlorobenzene (26 ml) and N-(α-methylcinnamoyl)-N-(1-benzyl-4-piperidinyl)aniline (8.7 g) and the mixture is heated at 110° C. for 1 hour. After cooling, the reaction mixture is poured into ice-water and made alkaline with an aqueous sodium hydroxide solution. After extraction with dichloromethane, the extract is concentrated and the resulting residue is purified by silica gel column chromatography (eluent; methylene chloride). The purified substance is converted into hydrochloride and then recrystallized from ethanol/water to give 1-(1-benzyl-4-piperidinyl)-3-methylcarbostyril hydrochloride (5.8 g) as colorless needles, m.p. 274°-276° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05436254 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-93b93f7de06f401c86f22ea800918403 |
| Source note | uspto-grants-1995_07 |