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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591247Generated: October 30, 2026

4-Aminophenylsulphur pentafluoride → 2-cyclopropyl-5-methyl-N-[4-(pentafluoro-lambda6-sulfanyl)phenyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amine

https://huagongshe.com/reaction/591247

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenylsulphur pentafluorideHCID 2779190—
Reactant7-Chloro-2-cyclopropyl-5-methyl-[1,2,4]triazolo[1,5-a]pyrimidineHCID 53391867—
SolventEthanolHCID 702—
Product2-cyclopropyl-5-methyl-N-[4-(pentafluoro-lambda6-sulfanyl)phenyl][1,2,4]triazolo[1,5-a]pyrimidin-7-amineHCID 51347546—

Reaction Steps

To a suspension of Intermediate 20 (0.04 g, 0.192 mmol) in ethanol (2.5 mL), 4-aminophenylsulfur pentafluoride (MANCHESTER, 0.042 g, 0.192 mmol) was added and the mixture was stirred under reflux overnight. Solvent was removed in vacuo and the crude mixture was purified by preparative HPLC (SunFire 19×150 mm, H2O 0.1% TFA-ACN 0.1% TFA gradient from 10 to 100%) to yield the title compound as a beige solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238653B2
Source datasetuspto-grants-2016_01
ORD IDord-a1603277a1ae49b2b9f61a4b92f3a6fc
Source noteuspto-grants-2016_01