HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-Chloro-2-(methylthio)pyrazolo[1,5-a][1,3,5]triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 2-(Methylthio)pyrazolo[1,5-a][1,3,5]triazin-4(3H)-one | HCID 135444259 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Chloro-2-(methylthio)pyrazolo[1,5-a][1,3,5]triazine | HCID 12916115 | 71% |
Reaction Steps
In a round bottom flask equipped with a magnetic stirbar, 2-(methylthio)pyrazolo[1,5-a][1,3,5]triazin-4(3H)-one (1.0 eq, 10.43 g, 57.24 mmol) was suspended in acetonitrile (100 ml). Phosphorus oxychloride (4.0 eq, 21 ml, 229.4 mmol) and triethylamine (1.05 eq, 8.4 ml, 60.27 mmol) were added and the mixture stirred at reflux for 3.5 hours, at which time LCMS indicated completion of the reaction. The mixture was cooled down and slowly poured into crushed ice (final total volume of about 600 ml). The solid was filtered, washed with water and dried in a vacuum oven to afford 4-chloro-2-(methylthio)pyrazolo[1,5-a][1,3,5]triazine as a tan solid (8.15 g, 71% yield). LCMS (ES): >97% pure, m/z 201 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09303033B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-cd77b86bfe6c48ef917c8241596b5ffa |
| Source note | uspto-grants-2016_04 |