HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-[3-(Methanesulfonyloxy)propylthio]imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5-[3-(Hydroxy)propylthio]imidazo[1,2-a]pyridine | HCID 23362890 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[3-(Methanesulfonyloxy)propylthio]imidazo[1,2-a]pyridine | HCID 23362949 | — |
Reaction Steps
To a solution of 5-[3-(hydroxy)propylthio]imidazo[1,2-a]pyridine (2.003 g, 9.62 mmoles) and triethylamine (2.01 ml, 14.4 mmoles) in methylene chloride (30 ml) was added methanesulfonyl chloride (0.89 ml, 12 mmoles) with stirring under ice-cooling and the mixture was further stirred under ice-cooling for 10 minutes. The reaction mixture was washed with water and the aqueous layer was extracted with methylene chloride (30 ml×3). The methylene chloride layers were combined and dried over anhydrous magnesium sulfate. Then, the solvent was distilled off to obtain crude 5-[3-(methanesulfonyloxy)propylthio]imidazo[1,2-a]pyridine as a yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244908 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-4e2651d7658c4004854f8e9660ba034f |
| Source note | uspto-grants-1993_09 |