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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenylsulphur pentafluorideHCID 2779190—
Reactant7-Chloro-2-ethyl-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidineHCID 30033447—
SolventEthanolHCID 702—
Product2-ethyl-5-methyl-N-[4-(pentafluoro-lambda6-sulfanyl)phenyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amineHCID 51347397—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238653B2
Source datasetuspto-grants-2016_01
ORD IDord-5973ce8e9c10443fbe792214f837df38
Source noteuspto-grants-2016_01