HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ethanamine,2-(imidazo[1,2-a]pyridin-5-ylthio)-n-methyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-[2-(Methylsulfonyloxy)ethylthio]imidazo[1,2-a]pyridine | HCID 23362960 | — |
| Reactant | Monomethylamine methanol | HCID 57454252 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethanamine,2-(imidazo[1,2-a]pyridin-5-ylthio)-n-methyl- | HCID 23362988 | 47.1% |
Reaction Steps
A solution of 5-[2-(methylsulfonyloxy)ethylthio]imidazo[1,2-a]pyridine (2.18 g, 8 mmoles), triethylamine (2.24 ml, 16 mmoles) and a 40% methylamine-methanol solution (20 ml) in chloroform (20 ml) was heated at reflux for 3 hours. The reaction solution was washed with an aqueous 3N-sodium hydroxide solution and dried over anhydrous magnesium sulfate. After the solvent was distilled off, the residue was purified by column chromatography (eluent: methanol/chloroform=1:10) to obtain 781 mg of the desired product (47.1%, light brown oily product).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05587383 |
| Source dataset | uspto-grants-1996_12 |
| ORD ID | ord-3930444f2b074286bf53bac12cdd9ca6 |
| Source note | uspto-grants-1996_12 |