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Iodine → 5-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde

HRID 1627158
Notes
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Reaction equation

HRID 1627158 reaction equation
[F:1][C:2]1[CH:7]=[N:6][C:5]2[NH:8][CH:9]=[CH:10][C:4]=2[C:3]=1[CH:11]=[O:12].[I:13]I.[I-].[Na+].[OH-].[Na+]>CCO.OS([O-])=O.[Na+]>[F:1][C:2]1[CH:7]=[N:6][C:5]2[NH:8][CH:9]=[C:10]([I:13])[C:4]=2[C:3]=1[CH:11]=[O:12]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 4

HCID 807IodineHCID 5238Sodium IodideHCID 14798Sodium HydroxideHCID 497616231H-Pyrrolo[2,3-b]pyridine-4-carboxaldehyde, 5-fluoro-

Product 1

HCID 866542075-fluoro-3-iodo-1H-pyrrolo[2,3-b]pyridine-4-carbaldehydeYield 151%

Reagents, catalysts & solvents 2

HCID 702
Ethanol
Solvent
HCID 23665763Sodium BisulfiteSolvent

Conditions

Temperature
25 °C

Procedure

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 C8H4FIN2O, 291; found, 291.5.

Workup

  1. filtrationAn orange precipitate was collected by filtration
  2. customdried under vacuum

Sources & evidence

ORD record
ord-a73d16bc99b24174b6f9b3f72e5ae241
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08785429B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes