Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229755Generated: October 30, 2026

Potassium Hydroxide → Zolmitriptan-2-carboxylic Acid

https://huagongshe.com/reaction/229755

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantZolmitriptan 2-carboxylic acid ethyl esterHCID 10498674—
SolventEthanolHCID 702—
ProductZolmitriptan-2-carboxylic AcidHCID 10449364299.8%

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of 1.4 g (24.9 mmoles) of KOH in 30 ml of ethanol was added 2.8 g (7.8 mmoles) of (S)-3-(2-dimethylaminoethyl)-5-[2-oxo-1,3-oxazolidin-4-ylmethyl]-1H-indol-2-carboxylic acid ethyl ester. The resulting solution was heated at reflux temperature for one hour. It was cooled and the solvent evaporated to dryness. The residue was dissolved in 6 ml of water and washed three times with 10 ml of dichloromethane. The aqueous solution was cooled to 5° C., adjusted to pH 6 with glacial acetic acid, stirred for 30 minutes at that temperature and the water evaporated to dryness. The residue was redissolved in 30 ml of water and 5 g of ionic exchange resin (Dowex 50WX8-400) added. The mixture was left under stirring at room temperature for 24 hours. The resin was filtered and it was washed with water. For desorption the resin was suspended with 20 ml of a 10% aqueous solution of ammonia and stirred at room temperature for 5 hours. Once that time had elapsed it was filtered and washed with water. The water was evaporated to dryness under reduced pressure to give 7.75 g (94%) of the title acid as a yellow crystalline solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563904B2
Source datasetuspto-grants-2009_07
ORD IDord-9e3e9dee3ce84e46b14656a3cd2d99a8
Source noteuspto-grants-2009_07