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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1076559Generated: November 1, 2026

Iodoethane → HCID 21537681, compound

https://huagongshe.com/reaction/1076559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodiumHCID 5360545—
ReactantHCID 178463030HCID 178463030—
SolventEthanolHCID 702—
ProductHCID 21537681HCID 21537681—

Reaction Steps

18.9 g. of 1-ethyl-6-hydroxy-1H-pyrazolo[3,4-b]-pyrazine-5-carbonitrile (0.1 mol.) are added to a solution of 2.3 g. of sodium (0.1 mol.) in 500 ml. of absolute ethanol and the mixture is stirred for 30 minutes at room temperature. Then the alcohol is distilled off in vacuo and the sodium salt is dissolved in dry dimethylformamide. Then 23.5 g. of ethyl iodide (0.15 mol.) are added and the solution is heated in an autoclave at 120° for 5 hours. After the dimethylformamide is removed in vacuo, the residual 6-ethoxy-1-ethyl-1H-pyrazolo[3,4-b]pyrazine-5-carbonitrile (19.1 g.) is recrystallized from hexane, yield 17 g. (78%), m.p. 73°-74°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03957782
Source datasetuspto-grants-1976_05
ORD IDord-5ad729be47fd4dd1b24ba30f9c6d45c5
Source noteuspto-grants-1976_05