HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570333Generated: November 1, 2026
Cyanogen Bromide → HCID 86677454, compound
https://huagongshe.com/reaction/570333
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 71281043 | HCID 71281043 | — |
| Solvent | Water methylene chloride | HCID 21908982 | — |
| Product | HCID 86677454 | HCID 86677454 | — |
Reaction Steps
To a stirring mixture of N-(5-(5-(azetidin-3-yl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide hydrochloride (21) (200 mg, 0.487 mmol), potassium carbonate (202 mg, 1.46 mmol) and cyanogen bromide (103 mg, 0.974 mmol) in dichloromethane:water (1:1, 15 mL) were heated at 45° C. for 1.5 hours. The reaction was cooled to room temperature and the layers were separated. The aqueous layer was washed with 3 times with DCM and dried over anhydrous sodium sulfate. The combined organics were concentrated. The resulting solid was washed with hexanes to give N-(5-(5-(1-cyanoazetidin-3-yl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (82). MS m/z 400.14 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023839B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-8a668054eed148e39aabf04e65d68acf |
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| Source note | uspto-grants-2015_05 |
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