Potassium Carbonate → HCID 22907274, compound

HRID 2258582Notes

Reaction equation

HRID 2258582 reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([N:7]2[C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH:9]=[CH:8]2)[CH2:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+].Br[CH2:23][CH:24]1[CH2:26][CH2:25]1.C(=O)([O-])[O-]>C(O)C>[CH:24]1([CH2:23][N:1]2[CH2:6][CH2:5][CH:4]([N:7]3[C:15]4[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=4)[CH:9]=[CH:8]3)[CH2:3][CH2:2]2)[CH2:26][CH2:25]1

Participants

6

Procedure

To a solution of 1-N-(piperidin-4-yl)-indole (0.6 g, 3 mmol) in dry ethanol (4 mL) was added anhydrous potassium carbonate (680 mg, 4.9 mmol). After stirring for 15 minutes at ambient temperature, bromomethylcyclopropane (0.29 mL, 4.5 mmol) was added. Stirring was continued overnight. An additional amount of carbonate (0.22 g) and bromomethylcyclopropane (0.14 mL) was added. After 3 hours, the reaction mixture was quenched with water and extracted with ethyl acetate (3×). The combined organic phase was washed with water, dried, evaporated, and purified by column chromatography on silica gel eluting with methylene chloride/ethanol (98:2). Evaporation of the eluting solvent gave the title compound as an oil (480 mg, 63% yield).

Workup

  1. stirringStirring
  2. waitwas continued overnight
  3. waitAfter 3 hours
  4. customthe reaction mixture was quenched with water
  5. extractionextracted with ethyl acetate (3×)
  6. washThe combined organic phase was washed with water
  7. customdried
  8. customevaporated
  9. custompurified by column chromatography on silica gel eluting with methylene chloride/ethanol (98:2)
  10. customEvaporation of the eluting solvent

Sources & evidence

ORD record
ord-5e17a158cc6b408e8856571a237f25d8
Source dataset
uspto-grants-1997_08
Patent number
US05661173

Reaction notes

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