Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790465Generated: November 1, 2026

Hydrochloric Acid → HCID 22038143, compound

https://huagongshe.com/reaction/1790465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 22037901HCID 22037901—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
ProductHCID 22038143HCID 2203814324.6%

Reaction Steps

1-[1-(4-Fluorophenethyl)piperidin-4-yl]-6-[1-hydroxy-1-(2-pyridyl)methyl]indoline (0.321 g) was dissolved in ethanol (86.4 ml) f ollowed by the addition of 1 N hydrochloric acid (3.7 ml) and palladium carbon. Then the resultant mixture was catalytically reduced under atmospheric pressure for 3 hr. After filtering off the catalyst, the filtrate was concentrated under reduced pressure. To the residue were added a saturated aqueous solution of sodium bicarbonate and ethyl acetate and the layers were separated. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. Then the residue was purified by NH-silica gel column chromatography (hexane/ethyl acetate-methanol system) to give the title compound (0.076 g) as ayellow oil (yield: 24.6%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071201B2
Source datasetuspto-grants-2006_07
ORD IDord-d5f63a48d4ca4b87914def778f1304f4
Source noteuspto-grants-2006_07