HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenylsulphur pentafluoride → 2-isopropyl-5-methyl-N-[4-(pentafluoro-$l^{6}-sulfanyl)phenyl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenylsulphur pentafluoride | HCID 2779190 | — |
| Reactant | 7-Chloro-5-methyl-2-(1-methylethyl)[1,2,4]triazolo[1,5-a]pyrimidine | HCID 53391863 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-isopropyl-5-methyl-N-[4-(pentafluoro-$l^{6}-sulfanyl)phenyl]-[1,2,4]triazolo[1,5-a]pyrimidin-7-amine | HCID 51347540 | — |
Reaction Steps
To a suspension of Intermediate 18 (0.042 g, 0.199 mmol) in ethanol (5 mL), 4-aminophenylsulfur pentafluoride (MANCHESTER, 0.044 g, 0.199 mmol) was added and the mixture was stirred at room temperature overnight. Solvent was removed in vacuo and the crude mixture was purified by flash chromatography (Si, eluting with Hexane/EtOAc mixtures from 75:25 to 25:75%) to yield the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238653B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-3f393256bf0b40469a209d91f8179e31 |
| Source note | uspto-grants-2016_01 |