HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118968Generated: October 27, 2026
2-Bromo-6-methoxypyridine → HCID 23035486, compound
https://huagongshe.com/reaction/2118968
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-6-methoxypyridine | HCID 256810 | — |
| Reactant | 3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine | HCID 10220561 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | HCID 23035486 | HCID 23035486 | 23% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04681883 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-aab9bb208052437db4a243970d118f3e |
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| Source note | uspto-grants-1987_07 |
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