HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopropane → 1-[1-(1-Methylethyl)-4-piperidinyl]-1H-indole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-(Piperidin-4-yl)-1H-indole | HCID 14090755 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-[1-(1-Methylethyl)-4-piperidinyl]-1H-indole | HCID 22907267 | 36% |
Reaction Steps
To a solution of 1-(piperidin-4-yl)-indole (0.5 g, 2.5 mmol) in dry DMF (3 m) was added anhydrous potassium carbonate (360 mg, 2.6 mmol). After stirring for 15 minutes at ambient temperature, i-propyl bromide (0.84 mL, 9 mmol) was added. The reaction mixture was refluxed for 2 days with stirring, quenched with water, extracted with ethyl acetate (2×), dried, and evaporated. The remaining residue was chromatographed on silica gel eluting with a toluene/acetone gradient (90:10 to 70:30). Evaporation of the eluting solvent gave the title compound as an oil. (220 mg, 36% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05672618 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-e0732210b99b43c6a36b886a89c59fd1 |
| Source note | uspto-grants-1997_09 |