HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen iodide → HCID 13106269, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen iodide | HCID 24841 | — |
| Reactant | HCID 14099940 | HCID 14099940 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 13106269 | HCID 13106269 | 70.3% |
Reaction Steps
In 50 ml of dioxane was dissolved 2.5 g of 5-{1-[2-(2-methoxyphenoxy)ethyl]aziridin-2-yl}-2-methylbenzenesulfonamide and after adding thereto 1 g of concentrated hydroiodic acid, the mixture was stirred overnight. After the reaction was over, the solvent was distilled off under reduced pressure and the residue was washed three with30 ml of water and then three with 200 ml of ether and crystallized by the addition of ethyl acetate. The crystals were recovered by filtration, washed with water, and dried to provide 1.7 g of 5-{1-iodo-2-[2-(2-methoxyphenoxy)ethylamino]ethyl}-2-methylbenzenesulfonamide hydroiodide. The product has the following physicochemical properties.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04868216 |
| Source dataset | uspto-grants-1989_09 |
| ORD ID | ord-e96980464fb548b988a01a5a345221cf |
| Source note | uspto-grants-1989_09 |