HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-Tert-butyl-3-(4-chlorobenzyl)-1H-pyrazol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butylhydrazine monohydrochloride | HCID 81889 | — |
| Reactant | 4-(4-Chlorophenyl)-3-oxobutanenitrile | HCID 50988847 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-Tert-butyl-3-(4-chlorobenzyl)-1H-pyrazol-5-amine | HCID 57551173 | 115.6% |
Reaction Steps
A solution of 4-(4-chloro-phenyl)-3-oxo-butyronitrile (500 mg, 2 mmol, 1.0 equiv), triethylamine (1.16 mL, 8.3 mmol, 3.2 equiv), and tert-butylhydrazine hydrochloride (1.03 g, 8.3 mmol, 3.2 equiv) in 10 mL of ethanol was heated at 100° C. in a sealed tube. After 4 d, the reaction mixture was cooled to ambient temperature and concentrated in vacuo. The residue was purified via automated flash chromatography (40 g SiO2, gradient from hexanes to ethyl acetate) to afford the product as a yellow oil (610 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08124610B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-da5684ac0c8c47309f5c11f334e34c57 |
| Source note | uspto-grants-2012_02 |