HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 13064787, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Benzylpiperidine | HCID 31738 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 14289478 | HCID 14289478 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13064787 | HCID 13064787 | 88% |
Reaction Steps
2.7 Grams of 7-(5-bromopentoxy)-3,4-dihydrocarbostyril, 2.0 g of 4-benzylpiperidine and 1.5 g of triethylamine were mixed with 30 ml of dimethylformamide and the mixture was heated at 60°-70° C. for 6 hours. The reaction mixture was then concentrated under a reduced pressure to dryness, and to the residue thus obtained was added a 5%-sodium hydrogencarbonate aqueous solution and stirred. The insoluble matters thus formed were collected by filtration, washed with water and dried. Recrystallization from ligroin to obtain 3.6 g (yield: 88%) of 7-[5-(4-benzyl-1-piperidyl)pentoxy]-3,4-dihydrocarbostyril as in the form of colorless plate-like crystals. Melting point: 100°-102° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04482560 |
| Source dataset | uspto-grants-1984_11 |
| ORD ID | ord-d4abbff3104442bfb2666db86f5fc95a |
| Source note | uspto-grants-1984_11 |