Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469323Generated: October 31, 2026

Tetrahydrofuran → 6-methoxy-3-piperidin-4-yl-1H-quinolin-2-one

https://huagongshe.com/reaction/469323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178488020HCID 178488020—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product6-methoxy-3-piperidin-4-yl-1H-quinolin-2-oneHCID 58181102—

Reaction Steps

A mixture of 160 mg (0.462 mmol) 3-(1-benzyl-1.2.3.6-tetrahydro-pyridin-4-yl)-6-methoxy-quinolin-2-ol and 20 mg palladium on charcoal (Pd/C 10%) in 30 mL MeOH was first of all hydrogenated for 17.5 h at 50° C. in a hydrogen atmosphere of 50 psi. Then 10 mL THF and 20 mg palladium on charcoal (Pd/C 10%) were added and hydrogenation continued for a further 2 h under the same conditions. Another 20 mg palladium on charcoal (Pd/C 10%) were added and the mixture was hydrogenated overnight at 50° C. in a hydrogen atmosphere of 60 psi. Then the reaction mixture was filtered, washed with DMF and the filtrate was evaporated down. The residue was added to EtOAc, triturated with PE and filtered. The precipitate was washed with DIPE and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629137B2
Source datasetuspto-grants-2014_01
ORD IDord-e5d13789f9e94fd384f4f98e8539b17d
Source noteuspto-grants-2014_01