HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-[4-(Methanesulfonamido)butylthio]imidazo[1,2-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 5-[4-(Amino)butylthio]imidazo[1,2-a]pyridine | HCID 23362894 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 5-[4-(Methanesulfonamido)butylthio]imidazo[1,2-a]pyridine | HCID 23362862 | 50.8% |
Reaction Steps
To a solution of 5-[4-(amino)butylthio]imidazo[1,2-a]pyridine (440 mg, 1.99 mmoles) and triethylamine (0.42 ml, 3.01 mmoles) in methylene chloride (20 ml) was added methanesulfonyl chloride (0.19 ml, 2.45 mmoles) under ice-cooling with stirring and the mixture was stirred under ice-cooling for 1 hour. The reaction mixture was washed in turn with an aqueous saturated sodium bicarbonate solution and saturated saline and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: ethyl acetate) to obtain 302 mg of the desired product (50.8%, light red brown solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05244908 |
| Source dataset | uspto-grants-1993_09 |
| ORD ID | ord-9fd5a9c4f7704191a454c34da1b4dc2d |
| Source note | uspto-grants-1993_09 |