HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → 5-[3-(Amino)propylthio]imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Pseudourea, 2-(3-aminopropyl)-2-thio-, dihydrobromide | HCID 145992 | — |
| Reactant | 5-Chloroimidazo[1,2-A]pyridine | HCID 10953722 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-[3-(Amino)propylthio]imidazo[1,2-a]pyridine | HCID 23362849 | 64.3% |
Reaction Steps
To a mixed solution of 10% (w/w) potassium hydroxide (69.3 g, 105 mmoles) and dimethylsulfoxide (50 ml) was added S-(3-aminopropyl)isothiourea dihydrobromide (8.85 g, 39 mmoles) and the mixture was stirred at room temperature for 1.5 hours. To the reaction mixture was added 5-chloroimidazo[1,2-a]pyridine (3.05 g, 20 mmoles), followed by stirring at room temperature and additionally at 65° C. for 20 hours. Water was added to the reaction mixture, which was extracted with chloroform, washed with 1N sodium hydroxide several times and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off to obtain 2.66 g of the desired product (64.3%, pale yellow oily product).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244908 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-c26cb13241bf43e2bb978f5ffb81ffc1 |
| Source note | uspto-grants-1993_09 |