HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylenediamine → 2,3-Dichloro-N-[2-(3-{2-[4-(4,5-dihydro-1H-imidazol-2-yl) phenyl]ethyl}-2-oxoimidazolidin-1-yl)ethyl]-N-methylbenzenesulphonamide hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylenediamine | HCID 3301 | — |
| Reactant | Sulfur | HCID 5362487 | — |
| Reactant | 2,3-dichloro-N-(2-{3-[2-(4-cyanophenyl)ethyl]-2-oxoimidazolidin-1-yl}ethyl)-N-methylbenzenesulphonamide | HCID 69424668 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,3-Dichloro-N-[2-(3-{2-[4-(4,5-dihydro-1H-imidazol-2-yl) phenyl]ethyl}-2-oxoimidazolidin-1-yl)ethyl]-N-methylbenzenesulphonamide hydrochloride | HCID 69422960 | — |
Reaction Steps
A solution of 137 mg (0.29 mmol) of 2,3-dichloro-N-(2-{3-[2-(4-cyanophenyl)ethyl]-2-oxoimidazolidin-1-yl}ethyl)-N-methylbenzenesulphonamide, 2 ml of ethylenediamine and 4.6 mg (0.14 mmol) of sulphur was stirred at 100° C. for two hours. Water was then added, and the mixture was extracted with ethyl acetate. The organic extracts were washed with saturated sodium chloride solution, dried over sodium sulphate and concentrated. The crude product obtained in this manner was purified by column chromatography on silica gel (mobile phase: dichloromethane/methanol/NH3 13:1:0.1 to 8:1:0.1). Using etheral hydrochloric acid, the product was then converted into the hydrochloride and freeze-dried.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291642B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-40b7d3b4905546ae83aed4274c92ce92 |
| Source note | uspto-grants-2007_11 |