HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → 2-[[3-[[3-(4-Cyanophenoxy)-2-hydroxypropyl]ethylamino]propyl]thio]benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-[3-(Ethylamino)-2-hydroxypropoxy]-benzonitrile | HCID 15066841 | — |
| Reactant | 2-(3-Chloropropylthio)benzamide | HCID 15158818 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-[[3-[[3-(4-Cyanophenoxy)-2-hydroxypropyl]ethylamino]propyl]thio]benzamide | HCID 15158819 | — |
Reaction Steps
5.5 g 2-(3- chloropropylthio)benzamide, 5.3 g of 4-[3-(ethylamino) -2-hydroxypropoxy]- benzonitrile, 6.6 g potassium carbonate and 7.2 g sodiumiodide were mixed in 100 ml of acetonitrile and heated to reflux for two days. The mixture was filtered and evaporated and the residue was dissolved in 1 M sulphuric acid. The acidic water layer was then washed twice with ether, alkalized with 10 M sodiumhydroxide and extracted with dichlormethane. The organic layer was dried over sodiumsulphate, treated with active carbon, filtered and evaporated. The residue, 8.7 g, was separated by column chromatography. Yield: 4.5 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05034411 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-6ebdd1b9962f44d7b6f194ee28e645ab |
| Source note | uspto-grants-1991_07 |