HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 5-Amino-1-cyclohexyl-1H-pyrazole-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Ethoxymethylene)propanedinitrile | HCID 67152 | — |
| Reactant | Cyclohexylhydrazine hydrochloride | HCID 207836 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Amino-1-cyclohexyl-1H-pyrazole-4-carbonitrile | HCID 690005 | — |
Reaction Steps
Firstly ethoxymethylenemalononitrile (2.43 g, 19.9 mmol) and then 8 ml of triethylamine are added to a solution of cyclohexylhydrazine hydrochloride (3 g, 19.9 mmol) in 36 ml of ethanol at room temperature. The mixture is refluxed for 20 min and then cooled. The solvent is stripped off in a rotary evaporator, and the residue is taken up in DCM, washed with aqueous sodium bicarbonate solution, dried over sodium sulfate, filtered and concentrated in vacuo. The crude product is chromatographed on silica gel (mobile phase: dichloromethane/methanol 0-10%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08158633B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-899cb114b1d14912aaee8f5c617b3260 |
| Source note | uspto-grants-2012_04 |