HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → L 11204
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 3-(5,6-Dihydro[1,2,4]triazolo[5,1-a]isoquinolin-2-yl)phenol | HCID 134401 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | L 11204 | HCID 119282 | — |
Reaction Steps
2-(3-Hydroxyphenyl)-5,6-dihydro-s-triazolo-[5,1-a]isoquinoline (3.95 g.) is added to 60 ml. of ethanol containing one equivalent proportion of sodium ethoxide. To this mixture is added 1.57 ml. of ethyl iodide in 15 ml. of ethanol. After stirring for one hour at room temperature, a further 1.57 ml. of ethyl iodide is added and the mixture is refluxed for 18 hours. The solvent is distilled off and the residue is washed with water and extracted with dichloromethane. Evaporation of the solvent and crystallization of the residue from ethanol gives 3.87 g. of the title product; m.p. 102°-3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04075341 |
| Source dataset | uspto-grants-1978_02 |
| ORD ID | ord-7eb89bf05afa4e17aa7912120d86889f |
| Source note | uspto-grants-1978_02 |