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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1437164Generated: November 1, 2026

Potassium Hydroxide → 1-(2-ethoxyethyl)-3-piperidinyl-1H-pyrrolo[2,3-b]pyridine

https://huagongshe.com/reaction/1437164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant4-[1-(2-ethoxyethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidine-1-carboxylic acid ethyl esterHCID 68893879—
SolventIsopropanolHCID 3776—
Product1-(2-ethoxyethyl)-3-piperidinyl-1H-pyrrolo[2,3-b]pyridineHCID 68894782149.5%

Reaction Steps

1.1 g (3.18 mmol) of 4-[1-(2-ethoxyethyl)-1H-pyrrolo[2,3-b]pyridin-3-yl]-piperidine-1-carboxylic acid ethyl ester were added to a solution of 2.1 g (31.8 mmol) of potassium hydroxide in 30 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 affording 0.65 g (75% of yield) of 1-(2-ethoxyethyl)-3-piperidinyl-1H-pyrrolo[2,3-b]pyridine obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07622480B2
Source datasetuspto-grants-2009_11
ORD IDord-14aad1ed537d49b49c5a78d16aff7214
Source noteuspto-grants-2009_11