HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 14458863, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 14458805 | HCID 14458805 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14458863 | HCID 14458863 | — |
Reaction Steps
To a suspension of 50% sodium hydride in oil (300 mg) in dry dmethylformamide (16 ml) is added 3-(2-aminopyrazin-3-yl)-5-(2-furyl)-1,2,4-triazole (1.37 g) and the whole stirred under nitrogen at 60° until a solution forms. To this is added cyanogen bromide (700 mg) in dimethylformamide (9 ml) and the whole stirred under nitrogen over 66 hours at 60°. It is cooled to 0° and the solid collected, washed with dimethylformamide, then water, then ethanol and finally ether and air dried. It is recrystallized from dimethylacetamide (70 ml) to which methanol (50 ml) is added to form pure 5-amino-(2-furyl)-pyrazino[2,3-e][1,2,4]-triazolo[1,5-c]pyrimidine, melting in the range 347°-351°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831013 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-923b0cb3edf248329b99d924024b1ec5 |
| Source note | uspto-grants-1989_05 |