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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 5-(Aminomethyl)-2-chloropyridine | HCID 7020927 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | [(6-Chloropyridin-3-yl)methyl]cyanamide | HCID 51342138 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09328068B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-dfe98bc203ff44248acc7b59710b20e9 |
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| Source note | uspto-grants-2016_05 |
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