Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176252Generated: October 27, 2026

tert-Butyl 3-hydroxy-4-{4-[4-(2-methoxyphenoxy)butoxy]phenyl}piperidine-1-carboxylate → tert-Butyl 4-{4-[4-(2-methoxyphenoxy)butoxy]phenyl}-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/1176252

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 3-hydroxy-4-{4-[4-(2-methoxyphenoxy)butoxy]phenyl}piperidine-1-carboxylateHCID 68499333—
Reactant7-chloromethyl-1-(3-methoxypropyl)-3,4-dihydro-1H-quinolin-2-oneHCID 68504434—
Producttert-Butyl 4-{4-[4-(2-methoxyphenoxy)butoxy]phenyl}-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylateHCID 68502972—

Reaction Steps

Analogously to Method D, 0.200 g of tert-butyl 3-hydroxy-4-{4-[4-(2-methoxyphenoxy)butoxy]phenyl}piperidine-1-carboxylate and 0.125 g of 7-chloromethyl-1-(3-methoxypropyl)-3,4-dihydro-1H-quinolin-2-one (Example 13b) are reacted. The title compound is obtained as a colourless oil. Rf=0.12 (1:1 EtOAc-heptane); Rt=5.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842688B2
Source datasetuspto-grants-2010_11
ORD IDord-0c6ff476c9d746e4af2ef06b94987c05
Source noteuspto-grants-2010_11