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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1762077Generated: November 2, 2026

Cyanogen Bromide → HCID 14458863, compound

https://huagongshe.com/reaction/1762077

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium hydrideHCID 24758—
ReactantHCID 14458805HCID 14458805—
SolventDimethylformamideHCID 6228—
ProductHCID 14458863HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04831013
Source datasetuspto-grants-1989_05
ORD IDord-923b0cb3edf248329b99d924024b1ec5
Source noteuspto-grants-1989_05