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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520754Generated: October 28, 2026

Cyanogen Bromide → [(6-Chloropyridin-3-yl)methyl]cyanamide

https://huagongshe.com/reaction/520754

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanogen BromideHCID 10476—
Reactant5-(Aminomethyl)-2-chloropyridineHCID 7020927—
SolventChloroformHCID 6212—
Product[(6-Chloropyridin-3-yl)methyl]cyanamideHCID 51342138—

Reaction Conditions

Temperature0 °C

Reaction Steps

Cyanogen bromide (220 mg, 2.09 mmol) was dissolved in 10 mL of anhydrous chloroform, and the solution was cooled to 0° C. To this was dropwise added a solution of 500 mg (3.49 mmol) of 2-chloro-5-aminomethylpyridine dissolved in 10 mL of anhydrous chloroform, and the resulting mixture was stirred at 0° C. for 1 hour. The reaction mixture was filtered, then water was added and liquid-liquid extraction was carried out, following which the chloroform phase was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The concentrate was purified by silica gel column chromatography (hexane/ethyl acetate=1:1), giving 122 mg (yield, 35%) of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328068B2
Source datasetuspto-grants-2016_05
ORD IDord-dfe98bc203ff44248acc7b59710b20e9
Source noteuspto-grants-2016_05