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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104187Generated: October 30, 2026

4-Methoxypiperidine → 2,2,2-Trifluoro-1-[4-(4-methanesulfonyl-phenyl)-6-(4-methoxy-piperidin-1-yl)-2-methyl-quinolin-3-yl]-ethanone

https://huagongshe.com/reaction/2104187

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxypiperidineHCID 77666—
Reactant1-[6-Bromo-4-(4-methanesulfonyl-phenyl)-2-methyl-quinolin-3-yl]-2,2,2-trifluoro-ethanoneHCID 11540085—
Product2,2,2-Trifluoro-1-[4-(4-methanesulfonyl-phenyl)-6-(4-methoxy-piperidin-1-yl)-2-methyl-quinolin-3-yl]-ethanoneHCID 1167781314%

Reaction Steps

The title compound was prepared from 1-[6-bromo-4-(4-methanesulfonyl-phenyl)-2-methyl-quinolin-3-yl]-2,2,2-trifluoro-ethanone [example 23] and 4-methoxy-piperidine according to the procedure of example 25. Yield: 14%; MS: m/z=507 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576217B2
Source datasetuspto-grants-2009_08
ORD IDord-5ce362a5c9db4f10ba803035b930a2cd
Source noteuspto-grants-2009_08