HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 3-(tert-butyl)-1-(1-methyl-1H-indol-5-yl)-1H-pyrazol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 3-Amino-5-tert-butylpyrazole | HCID 522787 | — |
| Reactant | 1-Methyl-1H-indole-5-boronic acid | HCID 2759867 | — |
| Catalyst | Cupric acetate | HCID 8895 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 3-(tert-butyl)-1-(1-methyl-1H-indol-5-yl)-1H-pyrazol-5-amine | HCID 117921683 | 48.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09242977B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-b2a73516c8834a8d8cfd3d9e5b650e87 |
| Source note | uspto-grants-2016_01 |