HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503591Generated: October 30, 2026
Potassium Cyanide → 7-Chloro-furo[3,2-B]pyridine-2-carbonitrile
https://huagongshe.com/reaction/503591
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Cyanide | HCID 9032 | — |
| Reactant | HCID 66779473 | HCID 66779473 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 7-Chloro-furo[3,2-B]pyridine-2-carbonitrile | HCID 10511538 | — |
Reaction Steps
In a sealed tube 7-chloro-2-iodofuro[3,2-b]pyridine (0.200 g, 0.72 mmol), KCN (0.093 g, 1.4 mmol), and copper (I) iodide (0.014 g, 0.072 mmol) were dissolved in 2 mL DMF. Pd(Ph3P)4(0.041 g, 0.036 mmol) was added, the tube was flushed with nitrogen, and the reaction in the tube was stirred overnight at 100° C. The reaction was cooled to RT, diluted with DCM, and washed with water. The aqueous layer was extracted with DCM, and the combined organic layers were washed with brine, dried with sodium sulfate, filtered, and concentrated. The material was purified via column chromatography (gradient elution 0-50% EtOAc:Hex) to afford 7-chlorofuro[3,2-b]pyridine-2-carbonitrile as a white solid. MS: M+H+=179.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07776857B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-d7e2e1b42773452a8ec9920b30f76552 |
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| Source note | uspto-grants-2010_08 |
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