Tetrabutylammonium Fluoride → 4-Chloro-2-methyl-7-azaindole

HRID 2117164Notes

Reaction equation

HRID 2117164 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[N:8](COCC[Si](C)(C)C)[C:9]([CH3:11])=[CH:10][C:3]=12.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>>[Cl:1][C:2]1[CH:7]=[CH:6][N:5]=[C:4]2[NH:8][C:9]([CH3:11])=[CH:10][C:3]=12

Participants

3

Reactant 2

HCID 2724141Tetrabutylammonium FluorideHCID 210816744-Chloro-2-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine

Product 1

HCID 210816754-Chloro-2-methyl-7-azaindoleYield 60.6%

Procedure

A mixture of 4-chloro-2-methyl-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrrolo[2,3-b]pyridine (296.5 mg, 1 mmol) and TBAF (5 mL, 1 M in THF, Aldrich) was refluxed overnight. The THF was removed under reduced pressure and the residue was diluted with water (5 mL). The precipitate that formed was collected, washed with water and dried (MgSO4) to afford the title compound (101 mg, 60%). 1H NMR (CD3OD) δ 7.99 (d, 1H, J=5.5 Hz), 7.06 (d, 1H, J=5.5 Hz), 6.23 (s, 1H), 2.46 (s, 3H); MS(ESI+) m/z 167 and 169 (M+H, 1 Cl)+.

Workup

  1. temperaturewas refluxed overnight
  2. customThe THF was removed under reduced pressure
  3. additionthe residue was diluted with water (5 mL)
  4. customThe precipitate that formed
  5. customwas collected
  6. washwashed with water
  7. dry with materialdried (MgSO4)

Sources & evidence

ORD record
ord-be7a19ab17f941f581a3d2ca2a6a6929
Source dataset
uspto-grants-2008_10
Patent number
US07439246B2

Reaction notes

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