HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Hydroxide → 1-(2-methoxyethyl)-3-piperidinyl-1H-pyrrolo[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-[1-(2-methoxyethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidine-1-carboxylic acid ethyl ester | HCID 68894419 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-(2-methoxyethyl)-3-piperidinyl-1H-pyrrolo[2,3-b]pyridine | HCID 68895020 | — |
Reaction Steps
0.86 g (2.59 mmol) of 4-[1-(2-methoxyethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidine-1-carboxylic acid ethyl ester were added to a solution of 1.71 g (25.9 mmol) of potassium hydroxide in 25 ml of isopropanol. The mixture was refluxed for 20 hours. The solvent was distilled off and cold water was added. This solution was acidified with concentrated hydrochloric acid and then basified with 8 N aqueous sodium hydroxide solution. This aqueous solution was extracted twice with ethyl acetate. The organic phase was washed with water and brine, dried over magnesium sulphate, filtered and evaporated under reduced pressure. 0.42 g (68% of yield) of the expected product were obtained as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07622480B2 |
| Source dataset | uspto-grants-2009_11 |
| ORD ID | ord-cbbe3aad737847cf9b229461e22bf155 |
| Source note | uspto-grants-2009_11 |