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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890341Generated: October 31, 2026

Cyanogen Bromide → HCID 67312396, compound

https://huagongshe.com/reaction/1890341

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
ReactantHCID 67312740HCID 67312740—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 67312396HCID 6731239613.2%

Reaction Steps

A solution of 6-(benzyloxy)-N2-phenylpyridine-2,3-diamine (3.106 g, 10.66 mmol), and cyanogen bromide (1.694 g, 15.99 mmol) in EtOH (50 mL) was stirred overnight at room temperature. The mixture was diluted with EtOAc and saturated NaHCO3. The layers were separated and the aqueous phase was back-extracted with EtOAc. The organics were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by silica gel chromatography to give the title compound (446 mg). LCMS m/z=317.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507473B2
Source datasetuspto-grants-2013_08
ORD IDord-7c57e05abe944a13a0f942e4dc3bf626
Source noteuspto-grants-2013_08