Water → 3-Iodo-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridine

HRID 249807Notes

Reaction equation

HRID 249807 reaction equation
[I:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[NH:4][CH:3]=1.[H-].[Na+].[CH:13]([Si:16](Cl)([CH:20]([CH3:22])[CH3:21])[CH:17]([CH3:19])[CH3:18])([CH3:15])[CH3:14].O>CN(C)C=O>[I:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[CH:8][CH:9]=2)[N:4]([Si:16]([CH:20]([CH3:22])[CH3:21])([CH:17]([CH3:19])[CH3:18])[CH:13]([CH3:15])[CH3:14])[CH:3]=1

Participants

6

Reactant 4

HCID 962WaterHCID 24758Sodium hydrideHCID 139400Triisopropylsilyl chlorideHCID 53770783-Iodo-7-azaindole

Product 1

HCID 242292273-Iodo-1-[tris(1-methylethyl)silyl]-1H-pyrrolo[2,3-b]pyridineYield 98.2%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Procedure

3-Iodo-1H-pyrrolo[2,3-b]pyridine 36 (2.00 g, 8.20 mmol) was dissolved in N,N-dimethylformamide (50 mL). Sodium hydride (60% dispersion in mineral oil, 390 mg, 9.8 mmol) was added. After 20 minutes, triisopropylsilyl chloride (1.74 mL, 8.20 mmol) was added dropwise. After 1.5 hours, the reaction was poured into water and extracted with ethyl acetate, washed with saturated sodium bicarbonate and brine. The organic portions were dried over anhydrous sodium sulfate and concentrated. Purification by silica gel chromatography, 0-25% gradient ethyl acetate hexane gave compound 37 as a white solid (3.224 g, 98.2%). 1H-NMR was consistent with the desired compound.

Workup

  1. waitAfter 1.5 hours
  2. extractionextracted with ethyl acetate
  3. washwashed with saturated sodium bicarbonate and brine
  4. dry with materialThe organic portions were dried over anhydrous sodium sulfate
  5. concentrationconcentrated
  6. customPurification by silica gel chromatography, 0-25% gradient ethyl acetate hexane

Sources & evidence

ORD record
ord-e2e39c0b57c1481092ef7159f7d9be3b
Source dataset
uspto-grants-2011_01
Patent number
US07863289B2

Reaction notes

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