HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(2-Aminoethyl)piperidine → N-[piperidino ethyl]-7-chloro-1,4-benzodioxane-5-carboxamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(2-Aminoethyl)piperidine | HCID 33944 | — |
| Reactant | 7-Chloro-1,4-benzodioxane-5-carbonyl chloride | HCID 20544703 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | N-[piperidino ethyl]-7-chloro-1,4-benzodioxane-5-carboxamide hydrochloride | HCID 70549227 | 129% |
Reaction Steps
150 ml of methyl ethyl ketone and 22 g of N-(aminoethyl)-piperidine were introduced into a 500 ml balloon flask provided with an agitator and a thermometer. The mixture was cooled and then a suspension of 35 g of 7-chloro-1,4-benzodioxane-5-carbonyl chloride in 200 ml of methyl ethyl ketone was added at a temperature of from 15°-20° C. After agitation the crystals formed were dried off and then washed with methyl ethyl ketone. 35 g of N-[piperidino ethyl]-7-chloro-1,4-benzodioxane-5-carboxamide hydrochloride was produced (M.P.: 192° C.; yield: 64.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04323503 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-00a13284245c4130b769362baab2cec7 |
| Source note | uspto-grants-1982_04 |