HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → HCID 135674107, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | HCID 135674106 | HCID 135674106 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135674107 | HCID 135674107 | — |
Reaction Steps
At an ice-cooled temperature, gaseous ammonia was introduced into 2.0 mL of ethanol to prepare a saturated solution, and then 0.10 g of 6-fluoro-3-oxo-3,4-dihydro-2-pyrazinecarboximidoate and 2.0 mL of ethanol were added. After elevating the temperature to room temperature, the mixture was left to stand for 17 hours. The deposited solid product was collected by filtration and washed with ethanol. The residue thus obtained was purified by silica gel column chromatography [eluent: chloroform:methanol=10:1], ethanol was added to the purified product, and the solid product was collected by filtration. Thus, 20 mg of 6-fluoro-3-oxo-3,4-dihydro-2-pyrazinecarboximidamide was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800629B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-f7f4c34748e842308fd923b742864116 |
| Source note | uspto-grants-2004_10 |