HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 20026881, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | (+-)-p-Methoxyamphetamine | HCID 31721 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 8-Benzyloxy-5-(2-bromoacetyl)-2-hydroxyquinoline | HCID 11667867 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20026881 | HCID 20026881 | 71.6% |
Reaction Steps
A mixture of 3.72 g of 5-bromoacetyl-8-benzyloxycarbostyril, 3.3 g of N-(2-(p-methoxyphenyl)-1-methylethyl)amine, 2.6 g of sodium bicarbonate, 10 ml of methylene chloride and 2 ml of dimethylformamide is refluxed for 30 minutes under stirring. The mixture is concentrated under reduced pressure to remove solvent. The residue is extracted with chloroform, and the extract is washed with 10% hydrochloric acid, dried and then concentrated under reduced pressure to remove solvent. The residue is rcrystallized form a mixture of ethanol and isopropanol. 3.53 g of 8-benzyloxy-5-{1-oxo-2-[N-(2-(p-methoxypheyl)-1-methylethyl)amino]ethyl}carbostyril hydrochloride are obtained as colorless needles. Yield: 71.6%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE033024 |
| Source dataset | uspto-grants-1989_08 |
| ORD ID | ord-cef943cdbcf946be86e46cc609d8e439 |
| Source note | uspto-grants-1989_08 |