HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591239Generated: October 29, 2026
4-Aminophenylsulphur pentafluoride → 2-ethyl-5-methyl-N-[4-(pentafluoro-lambda6-sulfanyl)phenyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine
https://huagongshe.com/reaction/591239
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Aminophenylsulphur pentafluoride | HCID 2779190 | — |
| Reactant | 7-Chloro-2-ethyl-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidine | HCID 30033447 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-ethyl-5-methyl-N-[4-(pentafluoro-lambda6-sulfanyl)phenyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine | HCID 51347397 | — |
Reaction Steps
A suspension of Intermediate 5 (80 mg, 0.407 mmol) and 4-aminophenylsulfur pentafluoride (MANCHESTER, 89 mg, 0.407 mmol) in ethanol (5 mL) was heated at 50° C. for 1 h, starting material dissolving during the process. The reaction mixture was concentrated under vacuum, redissolved in DCM (20 mL) and washed with aq. Na2CO3 (2×15 mL). The organic layer was dried over anhydrous Na2SO4, filtered and concentrated under vacuum to afford the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238653B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-5973ce8e9c10443fbe792214f837df38 |
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| Source note | uspto-grants-2016_01 |
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