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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594202Generated: November 2, 2026

Ammonia → 3-(tert-butyl)-1-(1-methyl-1H-indol-5-yl)-1H-pyrazol-5-amine

https://huagongshe.com/reaction/594202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantDimethylformamideHCID 6228—
Reactant3-Amino-5-tert-butylpyrazoleHCID 522787—
Reactant1-Methyl-1H-indole-5-boronic acidHCID 2759867—
CatalystCupric acetateHCID 8895—
SolventPyridineHCID 1049—
Product3-(tert-butyl)-1-(1-methyl-1H-indol-5-yl)-1H-pyrazol-5-amineHCID 11792168348.2%

Reaction Steps

To a mixed solvent of dimethylformamide (8 mL) and pyridine (0.47 mL) were added 3-amino-5-tert-butylpyrazole (810 mg), N-methylindol-5-boronic acid (780 mg), copper (II) acetate (790 mg) and molecular sieves (400 mg). The reaction mixture was stirred overnight at room temperature. The reaction mixture was added with 10% aqueous ammonia and filtered through Celite®. The filtrate was added with ethyl acetate and separated. The obtained organic layer was washed with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. The obtained residue was purified on silica gel column chromatography (hexane:ethyl acetate=7:3→1:1→1:4) to give the titled compound (577 mg) having the following physical data.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242977B2
Source datasetuspto-grants-2016_01
ORD IDord-b2a73516c8834a8d8cfd3d9e5b650e87
Source noteuspto-grants-2016_01