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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500575Generated: November 1, 2026

Cyanogen Bromide → HCID 59424209, compound

https://huagongshe.com/reaction/500575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 68637515HCID 68637515—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 59424209HCID 59424209—

Reaction Steps

To a suspension of 4-amino-7-(4-bromo-2-fluorophenylamino)-8-fluorocinnoline-6-carboxylic acid hydrazide (1.00 equiv.) in 1,4-dioxane at room temperature is added BrCN (2.00 equiv.) followed by a solution of NaHCO3 (1.00 equiv.) in H2O. After stirring for 3 hours at room temperature, the reaction mixture is diluted with water and extracted with EtOAc. The organic layer is washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure to give the crude material that is purified by trituration or flash column chromatography to afford 6-(5-amino-[1,3,4]oxadiazol-2-yl)-N7-(4-bromo-2-fluoro-phenyl)-8-fluorocinnoline-4,7-diamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772234B2
Source datasetuspto-grants-2010_08
ORD IDord-7a5bb89ea27c4ebc9d5d42e260faa434
Source noteuspto-grants-2010_08