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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1916473Generated: November 2, 2026

Hydrazine hydrate (1:1) → 3-(Aminomethyl)-5-bromopyridine

https://huagongshe.com/reaction/1916473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-((5-Bromopyridin-3-yl)methyl)isoindoline-1,3-dioneHCID 22992261—
SolventEthanolHCID 702—
Product3-(Aminomethyl)-5-bromopyridineHCID 22992264115.8%

Reaction Steps

A solution of 2-((5-bromopyridin-3-yl)methyl)isoindoline-1,3-dione (LVII) (1.9 g, 6.0 mmol, 1 eq) and hydrazine hydrate (2.0 g, 40 mmol, 6 eq) in EtOH (20 mL) was heated at 70° C. for 3 h. The mixture was filtered through a Celite® pad and the filtrate was concentrated in vacuo, the crude product was dissolved in 1N HCl solution (15 mL) and concentrated to dryness, then it was washed with acetone (10 mL×3), the precipitate was collected by filtration, dried in vacuo to give (5-bromopyridin-3-yl)methanamine (LVIII) (1.3 g, 6.95 mmol, 97.7% yield) as a white solid. 1H NMR (D2O, 500 MHz) δ ppm 4.34 (s, 2H), 8.56 (s, 1H), 8.75 (d, J=1.2 Hz, 1H), 8.91 (d, J=1.6 Hz, 1H). ESIMS found for C6H7BrN2 m/z 187 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618128B1
Source datasetuspto-grants-2013_12
ORD IDord-13789d7639984e36a63cf614ae294c88
Source noteuspto-grants-2013_12