HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → tert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | tert-Butyl 4-cyanopiperazine-1-carboxylate | HCID 14068968 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-butyl 4-(N-hydroxyamidino)-piperazine-1-carboxylate | HCID 178452346 | 100.7% |
Reaction Steps
To a solution of tert-butyl 4-cyanopiperazine-1-carboxylate (1.22 g, 5.77 mmol) in anhydrous ethanol (10 mL) were added hydroxylamine hydrochloride (420 mg, 6.04 mmol) and triethyl amine (843 L, 6.06 mmol). The reaction was heated to reflux for 45 min, after which TLC showed complete consumption of the starting material. The mixture was allowed to cool to room temperature overnight, and the resulting precipitate was removed by filtration. The filtrate was concentrated, yielding 1.42 g of a yellow gel that was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09260441B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-3c2ded138b444e7cb9954cadb0ff5ad5 |
| Source note | uspto-grants-2016_02 |