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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266657Generated: October 31, 2026

Cyanogen Bromide → HCID 86585882, compound

https://huagongshe.com/reaction/1266657

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantPotassium BicarbonateHCID 516893—
ReactantHCID 74990038HCID 74990038—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86585882HCID 8658588255.4%

Reaction Steps

To a solution of quinoxaline-2-carboxylic acid (1-benzyl-7-fluoro-4-hydrazinocarbonyl-2-hydroxy-7-methyl-octyl)-amide (110 mg, 0.228 mmol) in dioxane (0.5 mL) and water (0.5 mL) was added cyanogen bromide (31 mg, 0.296 mmol) and potassium hydrogencarbonate (31 mg, 0.310 mmol). The reaction was heated to reflux for 1 hour then cooled to ambient temperature. The dioxane/water was removed by adding benzene (5 mL) and concentrating (2×). The remaining solid was dissolved in ethyl acetate and water. The layers were separated and the aqueous layer extracted with ethyl acetate. The combined organics were dried over sodium sulfate and concentrated. Recrystallization of the crude product using a mixture of ethyl acetate, hexanes and methanol gave the title compound (64 mg, 55%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548671B2
Source datasetuspto-grants-2003_04
ORD IDord-248d28bfab694e82975300e81f08d775
Source noteuspto-grants-2003_04