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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1712368Generated: October 25, 2026

2-(3-Bromopropoxy)benzonitrile → tert-Butyl 4-{4-[3-(2-cyanophenoxy)propoxy]phenyl}-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/1712368

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Bromopropoxy)benzonitrileHCID 18755374—
ReactantTert-butyl 4-(4-hydroxyphenyl)-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylateHCID 68501561—
Producttert-Butyl 4-{4-[3-(2-cyanophenoxy)propoxy]phenyl}-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylateHCID 68635263—

Reaction Steps

Analogously to Method I, 0.100 g of tert-butyl 4-(4-hydroxyphenyl)-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylate (Example 44d) and 0.057 g of 2-(3-bromopropoxy)benzonitrile are used to prepare the title compound. Rf=0.18 (2:1 EtOAc-heptane); Rt=5.58.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07790715B2
Source datasetuspto-grants-2010_09
ORD IDord-6c53440ce5a74d5b940fd2115ec2a9ab
Source noteuspto-grants-2010_09