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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755307Generated: November 2, 2026

Bromine → 4-Bromo-6-phenylpyridazin-3-amine

https://huagongshe.com/reaction/1755307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantSodium BicarbonateHCID 516892—
Reactant6-Phenylpyridazin-3-amineHCID 11958915—
SolventMethanolHCID 887—
Product4-Bromo-6-phenylpyridazin-3-amineHCID 5838636033.1%

Reaction Steps

In a 150 mL round bottom flask was placed 6-phenylpyridazin-3-amine (2.5 g, 14.5 mmol), NaHCO3 (2.44 g, 29 mmol) and methanol (50 mL) then to this suspension was added Br2 (2.317 g, 14.5 mmol) drop wise over about 30 minutes at room temperature. The mixture was stirred for 16 h, then filtered and concentrated in vacuo. The residue was purified by chromatography (silica gel, 200-300 mesh, petroleum ether:ethyl acetate=2:1) to give 4-bromo-6-phenylpyridazin-3-amine (1.2 g, 33%) as a light orange solid. LC-MS: [M+H]+, 250.0, tR=1.487 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169259B2
Source datasetuspto-grants-2015_10
ORD IDord-dc69f5c8911d47afb49c0a67735122db
Source noteuspto-grants-2015_10