HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-((Tert-butyldimethylsilyl)oxy)aniline → N-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1-cyclopropyl-1H-pyrazol-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-((Tert-butyldimethylsilyl)oxy)aniline | HCID 11715553 | — |
| Reactant | 4-Bromo-1-cyclopropyl-1H-pyrazole | HCID 52142099 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4-((tert-butyldimethylsilyl)oxy)phenyl)-1-cyclopropyl-1H-pyrazol-4-amine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09108983B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-9df8a3390e4d442e9440eff5da724df8 |
| Source note | uspto-grants-2015_08 |