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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336557Generated: October 30, 2026

Potassium Hydroxide → HCID 68000203, compound

https://huagongshe.com/reaction/336557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
ReactantHCID 131732013HCID 131732013—
SolventWater ethanolHCID 19096565—
ProductHCID 68000203HCID 6800020395.8%

Reaction Conditions

Temperature110 °C

Reaction Steps

0.726 g (12.95 mmol) of potassium hydroxide is added, at room temperature, to a solution of 0.242 g (0.65 mmol) of ethyl[7-(6-chloroquinolin-2-yl)-7-azaspiro[3.5]non-2-yl]carbamate, obtained in step 12.5., in 3.25 mL of ethanol/water (1/1). The mixture is then heated at 110° C. for 12 hours. 0.363 g (6.47 mmol) of potassium hydroxide is added and the mixture is left stirring for 3 hours. The resulting mixture is allowed to cool to room temperature and is then concentrated under reduced pressure. The residue is taken up in dichloromethane and 1N hydrochloric acid solution. The acidic aqueous phase is washed with dichloromethane and then basified with aqueous 1N sodium hydroxide solution, which is extracted several times with dichloromethane. The combined organic phases are then dried over sodium sulfate and the filtrate is concentrated under reduced pressure. 0.188 g of expected product is thus obtained in the form of an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889702B2
Source datasetuspto-grants-2014_11
ORD IDord-db79ea0384814cb6a7396df9dd53d99d
Source noteuspto-grants-2014_11