HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1968254Generated: October 29, 2026
Iodine → 5-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde
https://huagongshe.com/reaction/1968254
Participants
| Role | Name | HCID | Charge |
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| Reactant | Iodine | HCID 807 | — |
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1H-Pyrrolo[2,3-b]pyridine-4-carboxaldehyde, 5-fluoro- | HCID 49761623 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Sodium Bisulfite | HCID 23665763 | — |
| Product | 5-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde | HCID 86654207 | 151% |
Reaction Steps
To a solution of 5-fluoro-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde (2.45 g, 14.93 mmol) in EtOH (20 mL) was added iodine (4.55 g, 17.91 mmol), sodium iodide (2.68 g, 17.91 mmol) and aqueous NaOH (1N, 15 mL). The reaction mixture was stirred for 4 h at 25° C. and diluted with aqueous NaHSO3 (0.1N). An orange precipitate was collected by filtration and dried under vacuum to afford the title compound as a yellow solid (6.54 g, 82%). [M+H] calc'd for C8H4F1N2O, 291; found, 291.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08420816B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-4e2fb422f9cf464981dd4d9da251d01d |
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| Source note | uspto-grants-2013_04 |
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