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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 334476Generated: October 26, 2026

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

https://huagongshe.com/reaction/334476

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 numberUS08883822B2
Source datasetuspto-grants-2014_11
ORD IDord-a98833bc412e4e35864eef7f746b99d9
Source noteuspto-grants-2014_11