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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1176367Generated: October 25, 2026

7-chloromethyl-1-(3-methoxypropyl)-3,4-dihydro-1H-quinolin-2-one → tert-Butyl 4-(4-{2-[2-(2-methoxyphenyl)ethoxy]ethoxy}phenyl)-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/1176367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-chloromethyl-1-(3-methoxypropyl)-3,4-dihydro-1H-quinolin-2-oneHCID 68504434—
Reactanttert-Butyl 3-hydroxy-4-(4-{2-[2-(2-methoxyphenyl)ethoxy]ethoxy}phenyl)piperidine-1-carboxylateHCID 68506643—
Producttert-Butyl 4-(4-{2-[2-(2-methoxyphenyl)ethoxy]ethoxy}phenyl)-3-[1-(3-methoxypropyl)-2-oxo-1,2,3,4-tetrahydroquinolin-7-ylmethoxy]piperidine-1-carboxylateHCID 68500681—

Reaction Steps

Analogously to Method D, 0.500 g of tert-butyl 3-hydroxy-4-(4-{2-[2-(2-methoxyphenyl)ethoxy]ethoxy}phenyl)piperidine-1-carboxylate (Example 100c) and 0.312 g of 7-chloromethyl-1-(3-methoxypropyl)-3,4-dihydro-1H-quinolin-2-one (Example 13b) are reacted. The title compound is obtained as an opaque oil. Rf=0.21 (1:1 EtOAc-heptane); Rt=5.80.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842688B2
Source datasetuspto-grants-2010_11
ORD IDord-8249f85d245949ea83dad7ac219c83a6
Source noteuspto-grants-2010_11