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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360677Generated: November 3, 2026

8-(1-tert-butyl-1,2,3,6-tetrahydropyridin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-one hydrochloride → 8-(1-tert-butylpiperidin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-one

https://huagongshe.com/reaction/1360677

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-(1-tert-butyl-1,2,3,6-tetrahydropyridin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-one hydrochlorideHCID 16064602—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventEthylacetate methanolHCID 21584119—
Product8-(1-tert-butylpiperidin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-oneHCID 16064604—

Reaction Steps

A solution of 8-(1-tert-butyl-1,2,3,6-tetrahydropyridin-4-yl)-6-(2-chlorophenyl)-1-(2,6-dichlorophenyl)-2H-quinolizin-2-one hydrochloride (Example 19, 24 mg) in methanol/ethyl acetate=1/5 was added platinum oxide (9 mg). The solution was hydrogenated under hydrogen (1 atm) for 1 h. The mixture was filtered though celite and concentrated. The residue was purified by silica gel (methylene chloride/methanol/2N ammonia=10/1/0.2) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07879875B2
Source datasetuspto-grants-2011_02
ORD IDord-4dd558562d2d4992965cd65f1b1dfbc2
Source noteuspto-grants-2011_02