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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515907Generated: October 26, 2026

4-((Tert-butyldimethylsilyl)oxy)aniline → N-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1-cyclopropyl-1H-pyrazol-4-amine

https://huagongshe.com/reaction/515907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((Tert-butyldimethylsilyl)oxy)anilineHCID 11715553—
Reactant4-Bromo-1-cyclopropyl-1H-pyrazoleHCID 52142099—
SolventTetrahydrofuranHCID 8028—
ProductN-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1-cyclopropyl-1H-pyrazol-4-amineHCID 131733318—

Reaction Steps

4-[tert-Butyl(dimethyl)silyl]oxyaniline (1.64 g, 7.3 mmol) and 4-bromo-1-cyclopropyl-1H-pyrazole (1.4 g, 7.3 mmol) dissolved in anhydrous tetrahydrofuran (30 mL) are stirred for 3 hours at ambient temperature in the presence of sodium tert-butylate (3.7 mL, 2M solution in THF) and chloro(2-di-tert-butylphosphino-2′,4′,6′-triisopropyl-1,1′-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) (101 mg, 0.146 mmol). The reaction mixture is filtered over Celite and then evaporated to dryness. The residue is purified by chromatography over silica gel using heptane and ethyl acetate as eluants to yield the expected product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108983B2
Source datasetuspto-grants-2015_08
ORD IDord-9df8a3390e4d442e9440eff5da724df8
Source noteuspto-grants-2015_08