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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710080Generated: October 31, 2026

2-Bromo-6-methoxypyridine → HCID 23035486, compound

https://huagongshe.com/reaction/1710080

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-6-methoxypyridineHCID 256810—
Reactant3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amineHCID 10220561—
SolventHydrochloric AcidHCID 313—
ProductHCID 23035486HCID 2303548623%

Reaction Steps

3-[3-(Piperidinomethyl)phenoxy]propylamine (14.90 g) and 2-bromo-6-methoxypyridine (5.64 g) were heated with stirring in an oil bath at 165°-170° C. for 5 hours. The reaction mixture was cooled, dissolved in dilute hydrochloric acid to pH 3-4, washed with ether (5 times), taken to pH 9-10 with dilute sodium hydroxide, extracted into ether (5 times). The pH was adjusted after each extraction. The latter ether extracts were combined, dried (MgSO4), evaporated under reduced pressure, and subjected to medium pressure chromatography on silica using ethyl acetate as eluant, to yield the title compound as an oil (2.45 g). This was treated with maleic acid in ethanol to give 2-[3-[3-(piperidinomethyl)phenoxy]propylamino]-6-methoxypyridine dimaleate (2.71 g), m.p. 114.5°-115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952589
Source datasetuspto-grants-1990_08
ORD IDord-efc8c98e0e5c40aabdb76d1c2f0cd7c6
Source noteuspto-grants-1990_08