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

HRID 1968254
Notes
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Reaction equation

HRID 1968254 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 C8H4F1N2O, 291; found, 291.5.

Workup

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

Sources & evidence

ORD record
ord-4e2fb422f9cf464981dd4d9da251d01d
Source dataset
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08420816B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes