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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710079Generated: October 31, 2026

2-Bromopyridine → 2-Pyridinamine, N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-

https://huagongshe.com/reaction/1710079

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-BromopyridineHCID 7973—
Reactant3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amineHCID 10220561—
SolventChloroform methanolHCID 21584188—
Product2-Pyridinamine, N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-HCID 10019237—

Reaction Steps

3-[3-(Piperidinomethyl)phenoxy]propylamine (20 g) and 2-bromopyridine (12.64 g) were stirred at 125° C. for 31/2 days. The cooled reaction mixture was subjected to column chromatography on silica ((chloroform:methanol 10:1) to afford the title compound as an oil. This was treated with maleic acid in ethanol to give, on addition of diethyl ether, as a white solid 2-[3-[3-(piperidinomethyl)phenoxy]propylamino]pyridine dimaleate (11.40 g), m.p. 116°-7° C. (recrystallised from isopropanol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952589
Source datasetuspto-grants-1990_08
ORD IDord-d059df1e19904fdd9effda8132d2bc5e
Source noteuspto-grants-1990_08