HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-[4-(4-Methoxybenzyl)-1-piperazinyl]-3,4-dihydrocarbostyril
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methyloxybenzyl chloride | HCID 69993 | — |
| Reactant | HCID 11630008 | HCID 11630008 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[4-(4-Methoxybenzyl)-1-piperazinyl]-3,4-dihydrocarbostyril | HCID 13236345 | 3.9% |
Reaction Steps
A mixture of 1.0 g of 5-(1-piperazinyl)-3,4-dihydrocarbostyril, 1.11 g of potassium carbonate, 760 mg of 4-methoxybenzyl chloride and 20 ml of DMF was stirred at 70°-80° C. for 4 hours. The reaction mixture was poured into a large amount of water and extracted with chloroform. After washing with water the extract was dried over anhydrous sodium sulfate. Chloroform was distilled off and the residue was purified through silica gel column chromatography. Recrystallization from methanol gave 60 mg of 5-[4-(4-methoxybenzyl)-1-piperazinyl]-3,4-dihydrocarbostyril, m.p. 194°-196° C., colorless needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04415572 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-8d040a85d93a49948cd8ec20593fa0cc |
| Source note | uspto-grants-1983_11 |