Iodine → 3-Iodo-5-methoxy-1-methyl-1H-indole

HRID 1854460Notes

Reaction equation

HRID 1854460 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2C(=[CH:10][CH:11]=1)NC=[CH:6]2.[OH-].[K+].[I:14]I.[H-].[Na+].IC.[CH3:20][N:21]([CH:23]=O)[CH3:22]>>[I:14][C:6]1[C:5]2[C:22](=[CH:10][CH:11]=[C:3]([O:2][CH3:1])[CH:4]=2)[N:21]([CH3:20])[CH:23]=1

Participants

7

Procedure

5-Methoxy-1H-indole (5.00 g, 34.0 mmol) in DMF (100 mL) was stirred with KOH (2.00 g, 35.7 mmol) for about 15 min then iodine (8.80 g, 34.7 mmol) was added. The mixture was stirred for about 30 min then NaH (60% dispersion in mineral oil, 1.63 g, 40.8 mmol) was added portion-wise. After stirring for about 15 min at ambient temperature, iodomethane (2.34 mL, 37.4 mmol) was added and the mixture was stirred for about 2 h. The solvents were removed under reduced pressure and the mixture was stirred with water (300 mL) for about 15 min. The slurry was treated with DCM (100 mL) and the layers were separated. The aqueous layer was extracted with DCM (50 mL) and the combined organics were dried over anhydrous MgSO4, filtered, and concentrated. The material was purified by silica gel chromatography eluting with DCM to give 3-iodo-5-methoxy-1-methyl-1H-indole (9.48 g, 97%): 1H NMR (400 MHz, DMSO-d6 δ 7.48 (s, 1H), 7.38 (d, 1H), 6.86 (dd, 1H), 6.72 (d, 1H), 3.79 (s, 3H), 3.76 (s, 3H); LC/MS (Table 2, Method a) Rt=2.50 min.

Workup

  1. stirringAfter stirring for about 15 min at ambient temperature
  2. stirringthe mixture was stirred for about 2 h
  3. customThe solvents were removed under reduced pressure
  4. stirringthe mixture was stirred with water (300 mL) for about 15 min
  5. additionThe slurry was treated with DCM (100 mL)
  6. customthe layers were separated
  7. extractionThe aqueous layer was extracted with DCM (50 mL)
  8. dry with materialthe combined organics were dried over anhydrous MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated
  11. customThe material was purified by silica gel chromatography
  12. washeluting with DCM

Sources & evidence

ORD record
ord-ff6a69bc084c4320971c1b59700a2ecc
Source dataset
uspto-grants-2015_02
Patent number
US08962629B2

Reaction notes

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