HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-cyano-N'-(2-nitroxyethyl)pyrazinecarboximidamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethanol, 2-amino-, 1-nitrate, nitrate (1:1) | HCID 78397 | — |
| Reactant | Methyl N-cyanopyrazinecarboximidate | HCID 10057818 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-cyano-N'-(2-nitroxyethyl)pyrazinecarboximidamide | HCID 10331652 | 26% |
Reaction Steps
Methyl N-cyanopyrazinecarboximidate (0.49 g, 3.0 mmol) was dissolved in methanol (6 ml), 2-nitroxyethylamine nitrate (1.01 g, 6.0 mmol) and triethylamine (1.01 g, 10.0 mmol) were added. The mixture was stirred at room temperature for 46 hours. After the reaction was completed, the reaction solution was concentrated under reduced pressure, and the residue thus obtained was subjected to chromatography on a silica gel column (WAKO GEL C 200, 30 g) eluting with chloroform-methanol (300:1). The eluted fractions were concentrated under reduced pressure and crystallized from diethyl ether to give the title compound (0.18 g, 0.78 mmol, yield: 26%) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05166347 |
| Source dataset | uspto-grants-1992_11 |
| ORD ID | ord-c8529e887c1041cf90a5fa40260146ca |
| Source note | uspto-grants-1992_11 |